Skip to main content
Micromachines logoLink to Micromachines
. 2021 Jun 15;12(6):700. doi: 10.3390/mi12060700

Secure Air Traffic Control at the Hub of Multiplexing on the Centrifugo-Pneumatic Lab-on-a-Disc Platform

Jens Ducrée 1
Editor: Wim De Malsche1
PMCID: PMC8232791  PMID: 34203926

Abstract

Fluidic larger-scale integration (LSI) resides at the heart of comprehensive sample-to-answer automation and parallelization of assay panels for frequent and ubiquitous bioanalytical testing in decentralized point-of-use/point-of-care settings. This paper develops a novel “digital twin” strategy with an emphasis on rotational, centrifugo-pneumatic flow control. The underlying model systematically connects retention rates of rotationally actuated valves as a key element of LSI to experimental input parameters; for the first time, the concept of band widths in frequency space as the decisive quantity characterizing operational robustness is introduced, a set of quantitative performance metrics guiding algorithmic optimization of disc layouts is defined, and the engineering principles of advanced, logical flow control and timing are elucidated. Overall, the digital twin enables efficient design for automating multiplexed bioassay protocols on such “Lab-on-a-Disc” (LoaD) systems featuring high packing density, reliability, configurability, modularity, and manufacturability to eventually minimize cost, time, and risk of development and production.

Keywords: centrifugal microfluidics, Lab-on-a-Disc, centrifugo-pneumatic flow control, integration, sample-to-answer automation, multiplexing, parallelization, reliability, tolerances, design-for-manufacture, digital twin, event triggering, timing

1. Introduction

There is a strong market need for providing rather complex bioanalytical testing capabilities that are currently carried out by well-trained personnel in professional facilities, for manifold decentralized use cases. Main applications are found in biomedical point-of-care and global diagnostics, liquid handling automation for the life sciences, process analytical techniques, and cell line development for biopharma, as well as monitoring the environment, infrastructure, industrial processes, and agrifood. Since the early 1990s, microfluidic “Lab-on-a-Chip”, also—now quite synonymously—referred to as Micro Total Analysis Systems (“µTAS”), have been proposed to cater for these strong demands [1,2,3,4,5].

Since these pioneering days, centrifugal microfluidic technologies have played a significant role in the scientific community [6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29], and, even more, in commercially directed initiatives [30,31,32,33,34,35,36,37,38,39,40,41,42]; as common in pioneering technologies, many of these companies have experienced significant success, while others were absorbed or discontinued in the meantime. The development of such “Lab-on-a-Disc” (LoaD) systems involves the well-coordinated development of fluidic, manufacturing, instrumentation, software, detection, and, last but not least, bioassay capabilities. The latter two elements of the LoaD technology stack are often closely derived from established reagent kits, and optical or electrochemical sensing techniques. However, the degrees of freedom for fluidic layouts are significantly restricted, chiefly owing to the typical, single-use character of the carrier chip as the multi-branched channel networks can typically not be regenerated.

To still mitigate the cost, the disposable chips are usually produced in polymer materials by (compression-)injection molding, which is a well-established technique in optical data storage manufacturing, and thus often adopt geometries such as Compact DiscTM (CD), Digital Video Disc (DVD), or Blu-ray formats (or sections thereof) with their standard 12 cm diameter, thickness of about 1.2 mm, and a central, 15 mm diameter hole for coupling to the spindle. The disc shape is also commensurate with the rotational symmetry of the centrifugal field. While centrifugal microfluidic devices have been implemented on many other shapes, e.g., circular segments, semicircle, standard (rectangular) microscope slides, and even tubes, for the sake of this work, the popular term “disc” will represent all types of chip formats attached to a rotor.

Similar to a CD player or Discman, LoaD systems usually feature a modular setup with a rather rugged, possibly portable, and widely autonomous instrument taking up the fluidic carrier chip, which is equipped with the spindle motor, control, detection, display, and communication units. For immersion with most point-of-use scenarios outside professional laboratory infrastructure, all (liquid or dry) reagents need to be (pre-)stored on the chip so that only the (bio-)sample needs to be loaded by the end-user.

While the physical representation, i.e., pits and lands, on optical storage media are of micron- and sub-micron size, the channels and chamber in microfluidic systems commonly need to handle volumes in the upper microliter range, at least on the inlet side, corresponding to milli- to centimeter lateral dimensions. Such multi-scale manufacture of the low-aspect-ratio discs imposes significant challenges on manufacturing and assembly, which need to be addressed separately for each fluidic design and fabrication technology. Furthermore, as with other conventional Lab-on-a-Chip technologies, the development of LoaD applications goes through several stages, often starting from prototyping for initial proof-of-concept, pilot series, e.g., to establish sufficient statistics for fluidic and bioanalytical validation, and substantial optimization towards commercially viable mass production.

Each fabrication scheme, along with the scale-up, e.g., precision milling in prototyping and subsequent tool-based replication, involves restrictions on geometries, manufacturing tolerances, artefacts, and often entails considerable efforts for setting up the process [43]. Typically, any change in the fluidic layout, materials, manufacturing processes, detection concepts, instrumentation, software, reagents, and assay protocol may induce mutual interference. Consequently, diligently following Design-for-Manufacture (DfM) guidelines and proper interface management are thus key for reaching high Technology Readiness Levels (TRLs) within reasonable techno-economical boundary conditions.

Most centrifugal microfluidic platforms operate in a batch-wise “stop-and-go” fashion, meaning that Laboratory Unit Operations (LUOs) for sample preconditioning, such as metering/aliquoting [44,45,46], removal of bioparticles [29,47,48,49,50,51], incubation, purification/concentration/extraction [52,53], homogenization [54,55], resuspension of dry, and mixing with liquid reagents [56,57,58,59] are gated by normally closed valves. Upon completion of each LUO, the liquid is forwarded to the next step. These centrifugal LUOs and their connected downstream detection methods have been surveyed before [7,8,12,19,20,21,22,23,24,25,26,27,60,61,62,63,64,65,66,67].

Techniques for such valving can be broadly distinguished by their retention and release mechanisms [68,69]. Initial LoaD concepts were mainly based on siphoning [31,32] and capillary burst valves [6], typically requiring the precise definition of geometrical features or surface coatings. Concepts based on sacrificial materials, for instance, wax [70,71,72,73], membranes [74], or stick-packaging [75], provide a liquid and vapor barrier, thus making them suitable for longer-term onboard storage of liquid buffers or reagents; yet, they either require an externally powered unit [67,76] or very high, often poorly defined release rates. Rudimentary centrifugo-pneumatic (CP) flow control mechanisms were introduced [77,78], which tend to require large, rotationally induced pressure heads for opening; therefore, they are primarily suitable for valving the penultimate LUO in a liquid handling sequence.

Subsequent work refined the release mechanism of these CP valving techniques by venting their compression chamber. Other than removing the seal by instrument-based units such as lasers [74] or xurography [79], (water) dissolvable films (DFs) covering outlets that are pneumatically coupled to the compression chamber were opened by ancillary liquids [80]. With this strategy, complex, highly multiplexed networks offering “handshake” as well as logical flow control, such as AND, OR, and IF conditionals, could be developed, which operate widely independently of the spin protocol [49,81,82,83,84].

This paper investigates key design features gearing centrifugo-pneumatically coupled valving networks towards larger-scale integration (LSI) of parallelized, multi-step bioassay panels. Note that the notion of fluidic LSI has previously been used by Quake et al. [85,86] in a different context of a pneumatically multiplexed liquid handling on a stationary, elastomeric platform, which is to be distinguished from the centrifugal technology be presented here. For the first time, the approach presented here also factors in experimental tolerances to deliver high predictability for batch-mode operated microfluidic LoaD platforms [68]. In pursuit of this novel objective, a “digital twin” [87,88], i.e., a model-based representation that serves as the virtual counterpart of a physical object or process [68,87,88], is developed for optimizing the fluidic performance, robustness, packing density, and manufacturability of rotationally controlled valving schemes for LoaD platforms.

First, the basic principles of centrifugal microfluidic liquid handling are briefly reviewed to establish the mathematical framework of the digital twin. Then a set of performance metrics is introduced along which fluidic layouts can be systematically optimized for given design objectives. The next section elaborates on the fluidic multiplexing in the context of real space and band widths in the frequency domain induced by standard deviations experimental input parameters. The method is illustrated by an exemplary bioassay. In the next section, the digital twin concept is applied to advanced flow control schemes allowing enhanced multiplexing and flexible timing before concluding.

2. Basics of Rotational Flow Control

2.1. Centrifugal Field

According to classical mechanics, an object of (uniform) density ϱpart and volume V with a center of mass located at a distance R from the axis of rotation experiences a centrifugal field density

fω=Fω/V=ϱpartRω2 (1)

at the angular spin rate ω=2πν. Note that in typical microfluidic scenarios, a (bio-) particle suspended in a liquid of density ϱ experiences buoyancy, so the ϱpart in fω (1) would refer to the difference between the densities ϱΔ=ϱpartϱ of the object and its surrounding medium.

While not relevant to the immediate context of this paper focusing on valving, the rotationally induced Coriolis (pseudo) force |fv|=2ϱωv acts on objects traveling at a speed v=ωr in the non-inertial frame spinning at ω. In common LoaD systems, fv is directed opposite to the direction of motion in the plane of the disc, and has been used for agitating advective mixing [57,59] and routing [89].

2.2. Pressure Contributions

Rather than forces, the response of liquids as continuous media to a field fω (1) is better captured by pressures p=F/A, i.e., force F per unit (cross-sectional) area A. In the context of the essentially hydrostatic approximation underlying the mainstay of this paper, flow-induced effects relating to the viscosity of the liquid are neglected. A valve is represented by a geometrical structure Γ which is composed of chambers and interconnecting channels holding a liquid of total volume U0.

On LoaD systems, the distribution of the (contiguous) liquid Λ(𝜔) within Γ forms under the impact of the centrifugal pressure head

pω=ϱr¯Δrω2 (2)

scaling with the square of the spin rate ω and the radial product

r¯Δr=12(r2r02) (3)

composed of its mean radial position

r¯Δr=12(r2r02) (4)

and its radial extension

Δr=rr0 (5)

which is (radially) confined by its inner and outer menisci r0 and r, respectively. For typical values ϱ=103 kg m3, r¯=3 cm, and Δr=1 cm, spin rates ν=ω/2π=10 Hz and 50 Hz, rotationally induced pressure heads pω (2) of roughly 12 hPa and 300 hPa are obtained, the latter corresponding to about 1/3 of the standard atmospheric pressure pstd=1013.25 hPa.

The net counterpressure in the axial z-direction opposing pω can be compounded to pz=pp with (the gradients of) the pressures pointing parallel p and opposite p to the main (axial) direction of the channel. Based on the hydrostatic equilibrium

pω+p=ppω=pz (6)

and the continuity of liquid volume

ddtΛdV=0 (7)

the two (radial) positions r and r0 of its confining menisci, and thus the distribution Λ throughout Γ, can hence, either algebraically or numerically, be calculated.

The contributions p and p might be generated externally [11,74,76,83,90,91,92,93], e.g., by compressed air bottles, onboard pumps, or mechanical valves (corresponding to p); for more common, rotationally controlled valving mainly investigated in the mainstay of this work, pneumatic pressures

pV=p0V0V (8)

linked to the compression of a gas volume enclosed by the liquid from their original size V0 at the ambient atmospheric pressure p0 to V<V0, e.g., by mechanical work or temperature change. Through shrinking V, pV (8) may, theoretically, be made randomly large.

Capillary action is associated with a pressure

pΘ=4σDcosΘ (9)

governed by the diameter D of the channel (with a round cross section) and the contact angle Θ of its inner wall with a liquid of surface tension σ. have been implemented. Typical values D=100 µm, σ72.8×103 N m1 and Θ=120° yield pΘ15 hPa (9), which corresponds to rather low spin rates in the regime of ν=ω/2π10 Hz.

2.3. Angular Acceleration

Certain LUOs, e.g., for mixing by chaotic advection [56] and or mechanical cell lysis [94] with obstacles or (magnetic) beads, benefit from rotational accelerations dv/dt=Rdω/dt. Assuming a solid disc of mass mdisc and radius Rdisc, and thus a moment of inertia Idisc0.5mdiscRdisc2 and resulting angular momentum Ldisc=Idiscω, the steepness of the ramps dω/dt=τspindle/Idisc is limited by the maximum torque τspindle of the spindle motor. Such angular accelerations might be approximated by an inertially induced pressure term

pm=ϱURdω/dtAϱURτspindleAIdisc (10)

for a fluid volume U of density ϱ traveling at a speed v=Rω at a radial position R through a channel of cross-section A.

Note that LoaD systems feature cavities, i.e., channels and chambers, through which the liquids move along the assay protocol; the moment of inertia I=I(t) thus increases over time t with the centrifugally outbound motion of (the center of mass of) the liquid distribution Λ(t) .

2.4. Critical Spin Rate

The common, normally closed valving schemes of LoaD systems can be described by a first retention phase when the outer meniscus of Λ at r is retained upstream of a critical point in Γ. Subsequently, the rotationally induced release of (part of) the liquid volume U0 to an outlet is prompted through shifting the spin protocol ω(t) across a critical frequency Ω. For spin-rate independent axial pressure heads p and p, and thus also pz, we derive a critical frequency

Ω=ppϱr¯Δr=pzϱr¯Δr (11)

by combining (2) and (6). High- and low-pass valves distinguish by whether the release is triggered by lifting or lowering ω(t) across Ω (11), respectively.

As an alternative to modulating ω(t), the hydrostatic equilibrium (6) may also be altered by adding a liquid volume VΔ to the inner end of Λ for elevating Δr (and possibly also r¯) in pω (2). Furthermore, in centrifugo-pneumatic valves delineated by p=p0 and p=pV (8), the outer compression chamber may be enlarged or vented, i.e., p=pVp0, for prompting liquid release.

Note that for highly dynamic systems, inertial effects will have to be included in calculating the frequency Ω (11), e.g., by introducing an inertial pressure term pm>0 (10) in p, which would thus lower the effective retention rate Ω compared to the quasi-hydrostatic case mainly considered in the course of this work.

2.5. Siphon Valving

From the early days of LoaD systems, siphoning principles have been utilized for centrifugal flow control. In these geometries, Γ, a (usually larger) inlet reservoir is connected by an outlet channel featuring inbound and outbound segments with an inner crest point at Rcrest to a receiving chamber. During retention, the front meniscus at r resides in the inbound segment where the centrifugal pressure pω (2) points antiparallel to the direction of pz, thus effectively stabilizing the retention of the distribution Λ(Ω) against perturbations, such as inertial effects or droplet break-off. This phase is characterized by a Δr between the front meniscus in the inbound section r and the liquid level in the inlet reservoir at r0, so that pz(r)=pωr¯Δr (3). The axial direction of pz determines the sign of Δr during retention of Λ, i.e., whether r is elevated or depressed with respect to r0.

In many cases, siphons connect two vented (or very large) chambers, thus neutralizing the impact of the ambient pressure p0 applying at either end. In macroscopic setups, priming of the siphon channel is then triggered by the addition of a sufficient volume VΔ to the inlet for the liquid distribution Λ to progress (sufficiently) past the crest point at Rcrest. While such release mechanisms can also be deployed for miniaturized systems, LoaD technologies have mainly resorted to priming by capillary action, i.e., p=pΘcosΘ (9), energized by a hydrophilically coated siphon outlet with Θ90°. Furthermore, pneumatic pumping through compression of a volume in a side chamber connected to the inlet has been explored [20,28]. In both of these low-pass constructs, either an overflow mechanism, or a continuous liquid “pulley” effect [95] sets in once the condition Δr>0 is met between the menisci in the inner reservoir and the outbound segment; at this stage, also pω (2) works in tandem with pz>0 to drag the liquid radially outwards, thus further increasing Δr in a self-amplifying pumping mechanism.

In centrifugo-pneumatic (CP) siphon valving (Figure 1), p=p0 and p=pV (8), i.e., pz=p0(V0/V1), so that Δr>0 is needed to drive the liquid past the inner crest point at Rcrest all the way to the outlet chamber against shrinking compression volume V, and thus growing pV1/V (8). Instead of a self-propelling pulley effect promoted by a narrow outlet, advancement of the outbound meniscus requires a steady increase of the spin rate ω(t), and, as long as there is a positive Δr>0, the centrifugal pressure pωΔr ω2 (2) can, at least mathematically, match any counteracting pV (8).

Figure 1.

Figure 1

CP-DF siphon valving. The measures of the default geometry Γ (linearized display, not to scale) are compiled in Appendix A, Table A1. The structure consists of an inlet reservoir of cross-section A0=d0w0 with depth w0 and width w0, which is connected through a (narrow) isoradial channel of volume Uiso=disoLisohiso positioned at R to an inbound section of radial extension Z and cross-section A=dw of depth d and width w. (For the sake of simplicity, d0=diso=d=1 mm is chosen in this rudimentary layout.) During retention, the outer part represents the gas-filled compression chamber, with a main compartment of volume VC,0, isoradial and radial sections of aggregate volume Vint (with VintVC,0) connecting to a shallow round chamber of volume VDF (with VDFVC,0) centered at RDF. This outer compartment of volume VDF features a dissolvable-film (DF) membrane. This DF intermittently covers a centrally placed vertical via leading to an outlet in a lower layer until a liquid volume UDF=βVDF with geometry-dependent coefficient 0<β<1 (here: α=1/2) has arrived. A fraction αVDF with α<β remains in the receiving chamber after transfer.

For a sufficiently narrow outlet channel, the integrity of the liquid plug might be preserved by the surface tension σ along the entire path until the front meniscus at r reaches the entrance of the outer chamber at the radial position Rcham; thereafter, the liquid is transferred. However, for larger cross-sections A of the outbound segment of the siphon and high spin rates, the liquid will creep or drip after passing the crest segment Rcrest into the outer chamber until Δr=0, rather than showing a quasi-solid, piston-like behavior. There are thus critical frequencies Ω and Ω* (11) characterizing the retention and release into the outer chamber, which depend on whether the liquid plug is cut at Rcrest or Rcham. In either case, a volume Uloss remains in the upstream part of the valve.

Note that the critical frequency Ω (11) of CP valves, i.e., their basic as well as their siphon variants, can be widely configured by the original compression volume VC; its permanently gas-filled parts can be located at “anywhere”, e.g., where disc real estate is still available, if the fractional volume of its sub-compartments remains pneumatically interconnected.

2.6. Centrifugo-Pneumatic Siphon Valving with Dissolvable-Film Membranes

In order to supersede the prerequisite for external actuation to induce venting, CP valves have integrated sacrificial, fluidically impermeable [51] membranes in their final receiving chamber (Figure 1); these seal the compression chamber until they come into contact with their specific solvent, usually an aqueous bioliquid. The opening of these dissolvable films (DFs) requires the transfer of sufficient liquid UDF to raise the filling level above its location.

3. Performance Metrics

In this section, quantitative characteristics for rotationally controlled valving are specified to play a pivotal role in fluidic LSI requiring high packing density that is tightly interwoven with system-level reliability. These metrics are run along with the example of CP-DF siphon valving (Figure 1), but can also be readily employed for further valve types.

3.1. High Field Strengths for LUOs

LUOs, such as plasma separation, become most efficient at high field strengths fω (1). Given a medium of (differential) density ϱ retained by a valve of critical spin rate Ω (11) at a given position R, we obtain

f^ω=ϱRΩ2 (12)

for the maximum field strength available for the LUO. As shifting RR in (12) mostly impacts r¯ in the radial product r¯Δr (11), the primary parameter towards maximizing f^ω (12) for a given retention rate ωΩ1/r¯Δr (11) is Δr, i.e., the liquid distribution Λ(Ω) extending between r0 and r, which can be trimmed by the geometry Γ for a given U0. The dimensionless metric

f¯ω=RRmaxΩ2ωmax2 (13)

references f^ω (12) to the largest available field strength at the maximum radial position Rmax and (safe) rotational frequency ωmax that can be produced by the spindle motor.

3.2. Radial Space

Due to the unidirectional nature of the centrifugal field fω (1), (the center of gravity of) a liquid distribution Λ must always advance in the radially outbound direction. At least in the absence of externally powered centripetal pumping, the processing chambers of subsequent LUOs must thus be staggered radially.

As part of such serial arrangement, the outwards pointing field fω (1) puts a price tag on the radial position

R¯=RRminRmaxRmin (14)

echoing that a central placement is most favorable, i.e., R¯ (14) minimized, to keep sufficient room for downstream LUOs. Note that small R¯ (14) might interfere with requirements on maximizing the local field strength f¯ω (13) for LUOs. Further, the overall consumption of radial space

ΔR¯=r^rˇRmaxRmin (15)

with the inner and outer boundaries rˇ and r^ of the structure Γ, respectively, should be taxed towards an optimization of the packing density.

3.3. Spatial Footprint

The real estate available for patterning Γ on a discoid carrier is limited, e.g., between Rmin=7.5 mm outside the 15 mm central hole and Rmax=5.5 cm to leave an outer rim for bonding a lid, e.g., with a radial extension of 5 mm, for chip geometries derived from conventional optical data storage formats. This makes central real estate, where space is the smallest and most precious.

If we consider a function of the full (azimuthal) width W(r) of Γ along the radial direction r, a simple measure of the spatial footprint would be the entire surface area enclosed by its outer contours confined by rˇ and r^. Considering the scarcity of central space, we introduce the metric

A¯=1RmaxRminrˇr^W(r)2πrdr (16)

which relates the spatial footprint of Γ at R with respect to the total area 2πrdr contained within the ring of (infinitesimal) radial extension dr at a radial location r.

3.4. Volume Definition and Loss

Liquid transfer through an LUO and its connected downstream valve may be associated with a volume Uloss left behind in the structure Γ after completion. Depending on the fluidic process of emptying a CP-DF siphon valve, the lost amount of liquid

0Uloss(A0+A)(RRcrest)+Uiso (17)

might vanish for a perfect “pulley” mechanism, which maintains a continuous liquid column until the entire liquid in Γ is dragged through the crest channel, and in a pure “overspill” mode until r=Rcrest and Δr=0 (Figure 1d). For serial processing, the volume arriving at the next valve U0=U0Uloss can be factored into its retention rate Ω=Ω(U0), and also into the mixing ratio of a quantitative bioassay.

The metric

Uloss¯=UlossU0 (18)

is useful to quantify volume loss with respect to the loaded volume U0. For siphoning, where a significant fraction of the liquid remains in Γ, Uloss¯ may be minimized through reduction of Uiso and AZ. As any uncertainty ΔUloss directly impacts the spread of the retention rate ΔΩ=ΔΩ(ΔUloss), minimizing the relative fluctuation

ΔUloss¯=ΔUlossUloss (19)

is critical for assuring reliability towards fluidic LSI.

3.5. Reliability and Band Width

In practice, all experimental input parameters {γk} impacting the liquid distribution Λ=Λ(R,Γ,U0,ω), and thus Ω (11), are subject to random spreads of standard deviations {Δγk} delineated by a Gaussian distribution. This statistical spread implies that at a given spin speed ω, the actual (radial) position of the meniscus r(ω) will statistically vary around its target value r(ω). So, to make sure that the conditions for operationally reliable flow control are guaranteed, e.g., r>Rcrest during retention, the spin rate ω has to stay outside the corridor ΩMΔΩ<ω<Ω+MΔΩ; in other words, ω has to be lifted or lowered through this entire frequency band Ω±MΔΩ for assuring proper retention and release for high- and low-pass valves, respectively.

The factor M{1,2,3,4} represents the degree of (component-level) reliability, with probabilities PM=erf(M/2){68%, 95%, 99.7%, 99.99%,} (and “erf” representing the error function) that the actual values  Ω are found in this frequency interval. Above M=6 and M=7, reliability of this (single) valving step is in the range of 10 and 1 defects per million opportunities (DPMO); for M=8, faults are practically absent.

At least in case that the input parameters {γk} are (widely) independent and their spreads {Δγk} comparatively small, Gaussian error propagation provides an analytical formula to calculate the standard deviation

ΔΩ({γk},{Δγk})k(ΩγkΔγk)2 (20)

of Ω (11), which is a very suitable method for optimization routines. Figure 2 reveals the scaling of Ω and its standard deviation ΔΩ with three impact parameters defined in Figure 1. For a given Γ, the volume of the main compression compartment VC,0 (a) and the radial position R (b) are varied; in (c), the field strength fω. (1) is kept constant while R shifted, e.g., to mimic translocating a particle sedimentation structure requiring a minimum fω to a radial position R where space is still available in a multiplexed layout.

Figure 2.

Figure 2

Variation of retention rate Ω (11) and its standard deviation ΔΩ (20) with (a) the volume of the main, permanently gas-filled compartment of the compression chamber VC,0 and (b) the radial position R while leaving (the remainder of) the structure Γ unchanged. The retention rate Ω sharply increases towards shrinking compression volumes VC,0 and central placements R; this comes at the expense of widening the tolerance ΔΩ. The gridlines represent the default volume VC,0=200 µL, at a radial position R=30 mm and retention rate Ω/2π22 Hz. (c) Ω and ΔΩ vs. R while maintaining the field strength fω (1), originally evaluated for its default geometry Γ (Table A1), critical spin rate Ω/2π=30 Hz, ϱ=1000 kg m3  and R=3 cm, while varying the radial position R.

Alternatively, Monte Carlo (MC) methods can be interpreted as virtual manufacturing and testing by running a large number of iterations, where a set of values {γk} is obtained from a random number generator assuming Gaussian distributions of {γk} of standard deviations {Δγk} around their nominal values {γk} and inserted into Equation (11) for obtaining a histogram for Ω in the simulated experiment.

The resulting band widths 2MΔΩ (20), which are associated with concurrently loaded valves, and thus change over the course of an LUO sequence, need to “fit” into the practically available envelope of spin rates ω between ωmin and ωmax; these boundaries are, on the lower end at ωmin, constrained by a minimum centrifugal field fω (1) or pressure pω (2) required to stabilize a liquid distribution Λ, e.g., to suppress unwanted capillary motion (9); the upper value at ωmax is imposed by factors such as the limited torque of the spindle motor τspindle (10), the pressure tightness of the (bonded) lid, and operational safety.

Towards multiplexing, the metric

ΔΩ¯=ΔΩωmaxωmin (21)

rewards minimum use of band width 2MΔΩ (20) with respect to the available frequency envelope.

4. Multiplexing

4.1. System-Level Robustness

Towards microfluidic LSI, many such serial and parallelized valving steps need to be coordinated on the LoaD device; each component failure might affect the overall reliability. For N independently operating, concurrently loaded valves {i,j} in a given step i, the probability for consistent system-level function amounts to (PM)N; for the example of M=2, and thus PM=95%, (PM=2)N drops from approximately 90% to 86%, 77% and 60% for N={2,3,5,10}, respectively, in case the bands Ωi,jMΔΩi,j<ω<Ωi,j+MΔΩi,j must be avoided for properly controlling each valve {i,j}. For N=5 loaded valves, extending the protected frequency intervals from M=2 to M=3 would significantly improve the (fluidic) reliability at the system level from (PM=2)5=77% to (PM=3)5=98.5%.

Note that the above considerations apply to each step i separately, i.e., after opening a particular valve of the cohort {i,j} at a point in time Ti, a new group of loaded valves emerges; this fresh set consists of the valves that remained closed in step i, plus the ones next in line to receive the released liquid, excluding “unvalved”, e.g., end-point chambers. The protected areas {Ωi,j±MΔΩi,j} in the frequency domain thus change over the course of the centrifugally multiplexed assay protocol ω(t).

4.2. Frequency Corridor

We consider serial valving in steps {i} with critical spin rates {Ωi} that are activated at points in time {Ti}; each Ωi controls a subset of concurrently loaded and opened valves {i,j}. Retention is assured while the spin rate ω(t) does neither surpass nor drop below the (aggregate) band widths 2Mmaxj{ΔΩi,j} centered at the critical frequencies {Ω^i} and {Ωˇi} where t<Ti for high- and low-pass valves, respectively. Figure 3a displays the scenario in frequency space for rotational actuation. An initial retention corridor between Ωˇ1 and Ω^2 successively broadens as further valves are triggered, with Ω^i<Ω^i+1 and Ωˇi>Ωˇi+1.

Figure 3.

Figure 3

Multiplexing of concurrently loaded valves in frequency vs. time domain. High- and low-pass valving takes place at points in time {Ti}. With each step i, a certain frequency corridor (green) that is available for LUOs rearranges. (a) For rotational actuation, reliable opening of valves {i,j} in a given step i is triggered by fully crossing their linked frequency bands {Ωi,j±MΔΩi,j}. (b) In venting mode, the concurrently loaded valves serially release according to the order of opening their compression chamber, i.e., VC,0,i and pVp0.

For the case of actuating (high-pass) CP valves by venting at {Ti} with i{2,4,5} in the exemplary scenario portrayed in Figure 3b, the retention zone for the spin rate curve ω(t) is also defined by the innermost limits of the allowed bands {Ωi,j±MΔΩi,j} of the valves still loaded at a given point in time Ti. Nevertheless, the order of release is merely imposed by the venting sequence, and does hence not necessitate steadily rising or decreasing critical retention rates Ω^i and Ωˇi at Ti, respectively.

4.3. Configuration in Real and Frequency Space

Theoretically, the geometry Γ can always be modified to minimize the radial product r¯Δr (3), thus allowing any randomly large retention rate Ω1/r¯Δr (11) for a given radial position R and liquid volume U0. Yet, its standard deviation ΔΩ (20) might become too broad to still be able to sufficiently multiplex flow control within the confinement of the practical spin rate envelope between ωmin and ωmax (Figure 2 and Figure 3). Furthermore, there would be additional restrictions to parameter spaces, e.g., on the smallest feature sizes and tolerances {Δγk} (20) associated with the manufacturing technology, or minimum liquid volumes, for instance, as prescribed by the loading and metering technique, the bioassay protocol, or the detection technology.

It also needs to be considered that, especially towards concentrated packing of LoaD substrates, it is wise to leave the liquid carrying parts of geometries Γ, that may have already been thoroughly validated in terms of design-for-manufacture (DfM), fluidic and assay performance, untouched. For CP valving techniques, it is therefore advantageous to only alter larger, uncritical features, e.g., the main volume VC,0 of the permanently gas-filled part of the compression chamber (Figure 2a), for tuning Ω (11). Different U0 may simply be accommodated by adjusting the width w0 of the inlet reservoir (Figure 1). Nonetheless, the paucity of central disc space may necessitate shifting the radial location R, while the retention rate Ω (11) still needs to comply with the planned valving sequence (Figure 4).

Figure 4.

Figure 4

Representative scenarios underpinning multiplexing. The critical retention rates {Ωi,j} (11) of concurrently loaded (high-pass) valves {i,j} to be rotationally actuated at a time Ti may be preserved while shifting the radial positions {Ri,j} of the structures {Γi,j}. This might be, for instance, required to meet spatial needs towards more crowded disc layouts, by adjusting the (permanently gas-filled part) of the compression chamber of volume VC,0,i,j, while observing proper arrangement in the frequency domain 𝜔, e.g., to avoid overlapping bands by Ωi+MΔΩi<Ωi+1MΔΩi+1.

Figure 4 shows distinctive scenarios for CP-DF siphon valves commonly encountered when seeking the best compromise in real and frequency space. We again investigate simultaneous actuation of valves {i,j} at times {Ti}, and sequential firing with isoradial as well as radially inbound and outbound staggering on the given disc. The ordering of Ωi (11) is accomplished by adjusting the main compression volume VC,0, while leaving all other parts of Γ and U0 untouched. Note, again, that without non-rotationally powered pumping mechanisms, (the center of gravity of) a given liquid distribution Λi can only migrate radially outbound, i.e., Ri+1>Ri.

Figure 5 displays the distribution of the frequency bands {Ωi±MΔΩi} in the different rotational actuation scenarios for simultaneous and sequential release (Figure 4) through adjusting the main volume of the compression chamber VC,0,i,j. Note that the requirement to create non-overlapping bands Ω±MΔΩ for serial opening even leads to a slight increase in VC,0 towards the highest spin rate ω (Figure 5b), and a huge widening of frequency bands Ω±MΔΩ in the radially outbound release sequence (Figure 5d).

Figure 5.

Figure 5

Distribution of bands in frequency space ω with required volumes of the main compression chamber VC,0,i for the different radial staggering and release scenarios as portrayed in Figure 4. CP-DF siphon valves {i,j} to be released simultaneously, i.e., Ti=Ti+1, or sequentially, i.e., Ti<Ti+1; the valves, which have similar geometries Γi,j of their liquid-occupied sectors and downstream compression volumes VC,0,i,j, are placed isoradially, i.e., at R=3 cm, or staggered over radial positions R={2,3,4,5} cm. The reliability factor is M=4. (a) A set of radially staggered valves {i,j} with Ri,j>Ri,j1 has been tuned through their VC,0,i,j to simultaneously burst in the same step i once ω>Ωi+MΔΩi with ΔΩi=max{ΔΩi,j}. There are three representative cases for sequential actuation with ΩiMΔΩi>Ωi1+MΔΩi1 for successive steps i according to Ωi>Ωi1. (b) For identical Γi,j and VC,i,j, the valves will open according to their radially inbound order Ri<Ri1. (c) For isoradial alignment Ri=R=const., the valve with the largest VC opens first: VC,i<VC,i1. (d) Further, a radially outbound opening sequence Ri>Ri1 can be achieved, for which VC,i needs to be drastically reduced along successive steps i to suppress premature release from by the high pressure pω (2) at distal locations R, which comes at the expense of huge bandwidth ΔΩ (20).

4.4. Exemplary Bioassay Panel

Figure 6 illustrates the rotational automation of a typical bioassay protocol. Plasma P is separated from a (blood) sample S before mixing with a first, onboard stored liquid reagent L1. This mixture P&L1 is then released to a final detection chamber, where it is successively combined with reagents L2 and L3. The liquid handling is coordinated by high-pass valves opening after their respective bands Ωi±MΔΩi are crossed, thus creating an ω- corridor with a successively growing upper limit over time t. Intermediate mixing steps are implemented by zig-zag patterns in ω(t). The domains available in real and frequency space are confined by Rmin and Rmax, and ωmin and ωmax, respectively.

Figure 6.

Figure 6

Exemplary bioassay implementing the loading of blood sample, plasma separation, and mixing with three prestored liquid reagents {Li}. Flow is controlled by five high-pass valves with release rates ωmin<Ωi<ωmax located at Rmin<Ri<Rmax and opening for ω>Ωi at points in time Ti. (a) Plasma (P) is extracted from the sample (S) in a peripheral position RP at high field strength fωRPω2 (1). While owing to the unidirectional nature of the centrifugal field fω (1), the course of the assay requires RS<RP<RD and RL1<RP, a radially inbound staggering RL1>RL2>RL3 (Figure 5b) has been chosen for the serial release of {Li} through their high-pass valves opening at ΩL1<ΩL2<ΩL3. (b) A blood sample S is loaded and released at ΩS<ω<ΩP. Separation of plasma P proceeds at ΩP<ω<ΩL1. Onboard liquid reagent L1 is then forwarded at ΩL1<ω<ΩL2 into the separation chamber where it is mixed with the plasma P within ωmin<ω<ΩL2. The mixture P&L1 then progresses to the final detection chamber for ΩP<ω<ΩL2, followed by addition of and mixing with L2 within Ω2<ω<Ω3 and ωmin<ω<ΩL3, respectively. Finally, L3 is added at Ω3<ω<ωmax and blended to obtain S&L1&L2 within ωmin<ω<ωmax. The green background marks the allowed frequency corridor at each point in time t=Ti, with its upper limit expanding according to ωmin<ΩS<ΩP<ΩL1<ΩL2<ΩL3<ωmax. Note that, for the sake of simplicity, the frequency thresholds {Ωi} are meant to refer to their associated bands Ωi±MΔΩi.

The unidirectional nature of the centrifugal field fω (1) requires that the positions of the serial processing of the sample through loading, separation, and detection chambers need to follow RS<RP<RD, while the release rates of the high-pass valves need to continuously increase along ωmin<ΩS<ΩP<ΩL1<ΩL2<ΩL3<ωmax, so that overlap of their associated bands Ωi±MΔΩi is avoided. In the portrayed exemplary assay protocol, high quality and speedy plasma separation is linked to a large field strength fωRPω2 (1), which is limited by ω<ΩP (11), thus making an outer position RP most favorable. On the other hand (Figure 2a), high retention rates ΩP<ΩL,i1/r¯iΔri (11) for the onboard reagents within the narrow corridor ΩP<ω<ωmax are best achieved for their more central placement (when estimating r¯iRL,i and Δriconst.).

Overall, the structures {Γi,j} presenting LUOs with their downstream valves need to meet several, partially contradictory demands on the maximum retention rate Ω (11), disc real estate A¯ (16), maximum field strength f^ω (12), and footprints in radial R¯ (14), ΔR¯ (15), and frequency space ΔΩ¯ (21).

Figure 7 shows the release rates {Ωi} for given ΩS/2π=15 Hz and ΩP/2π=30 Hz (at RP=4 cm) of CP-DF siphon valves with the same default geometries Γi, except for their (main) compression volumes VC,0,i, which are varied to guarantee disjunct tolerance intervals {2MΔΩi} for a given M=3. The two distributions represent sets of identical {Ωi} with their radial positions {Ri} shifted by 0.5 cm as a possible way to increase the functional integration density on a given disc cartridge. Note that the rotational actuation of these high-pass valves “squeezes” the release rates for the onboard reagents {ΩL,i} in the narrow ω strip within ΩP+MΔΩP<ω<ωmax (see also Figure 6b).

Figure 7.

Figure 7

Rotational automation of an exemplary bioassay featuring sequential release of sample and separated plasma as well as pre-stored liquid onboard reagents L1, L2, and L3 with high-pass CP-DF siphon valves of release rates {Ωi} with ΩS/2π=15 Hz and ΩP/2π=30 Hz. The release rates {Ωi} are tuned by the dead volumes of the main compression chamber {VC,0,i}, as displayed on the vertical axis. (a) Radial positions (blue) Ri={3,4,3.5,3,2.5} cm and (orange) Ri=Ri+0.5 cm mimick concurrent processing of the same bioassay protocols requiring identical {Ωi} for concurrent valving (M=3), while increasing their spatial packing density towards microfluidic LSI.

4.5. Assay Parallelization

A straight-forward method to replicate several simultaneously processed, identical assay protocols on the same LoaD carrier, e.g., for testing different samples for the same analytes, or for redundancies for controls, calibration, or statistics, is to set equal release frequencies {Ωi}, which are crossed synchronously {Ti}. The packing density might be augmented by the radial staggering of the structures Γ, for which Figure 2 shows the required adjustments of the main compression volumes VC,0,i,j, and their impact of the total band width 2MΔΩi. Concurrent processing of homologous assay protocols with the (primary) variation of inlet volumes U0,i may be readily achieved by adjusting the cross-sections A0 of the inlet reservoirs (Figure 1). In the general case of diverging multiplexing protocols, each release step must comply with the frequency corridor required to reliably shut the concurrently loaded valves.

5. Advanced Rotational Flow Control

We now expand on the actuation mode of CP-DF siphon valves by venting (Figure 1d). Instead of the various mechanical, radiation-induced, or thermal methods to open the compression chamber, a second (ancillary) liquid volume wets a DF placed at a remote location to effectuate pVp0. First, a handshake mechanism called “event triggering” is introduced, which also enables fluidic conditionals logical flow control. Afterward, the timing of event triggering, e.g., to comply with mixing or incubation periods of bioassays, through delay elements and rotational pulsing, is outlined.

5.1. Event Triggering

Two DFs are attached to the compression chamber of CP-DF siphon valves (Figure 8). In an exemplary assembly of upper and lower layers displaying the microfluidic conduits sandwiching a sealing sheet containing a set of DFs, the first “Load Film” (LF) initially blocks the outlet for the liquid through a vertical via into a lower layer; a second “Control Film” (CF) is placed in a pneumatically connected, distal compartment [81]. Below a critical spin rate Ω (11), the pneumatic counterpressure pV (8) prevents the liquid from reaching the LF.

Figure 8.

Figure 8

Principle of event-triggered flow control. (a) Basic valve configuration with the control film (CF), which is opened by a first liquid to vent the compression chamber of a pneumatic valve. Consequently, a second liquid is released through the load film (LF) (Adopted from [81] with permission from The Royal Society of Chemistry). (b) Extended corridor for the spin rate ω(t) in case of the event-triggered versus the rotationally actuated (Figure 6a) high-pass valves. After the sample is released at ω>ΩS, the upper boundary is defined by the, e.g., common, retention rate Ω= shared by all LUOs. Release from their chambers is prompted by event-triggered venting, rather than raising the spin rate ω.

The remote CF can be accessed by another ancillary liquid through a channel, e.g., situated in the lower layer, to open the DF, to thus massively expand the enclosed gas volume VC. With pVp0, the main liquid advances into the chamber containing the LF, which then disintegrates for release through the exit channel.

Event triggering (Figure 8) refers to the constellation when a liquid received from a preceding stage of an assay protocol takes on the role of the ancillary liquid to establish a “handshake” type flow control; instead of rotational cues or external power, the sequential release follows a “domino effect” that proceeds broadly independent of the spin rate ω(t). The frequency corridor (Figure 3), and especially the maximum field strength f^ω (12) that is available for LUOs along the assay procedure, are thus only restricted by the (minimum) retention rate Ω (11) of concurrently loaded (high-pass) valves, or ωmax.

Figure 9 illustrates the benefits of event-triggered flow control regarding configurability and packing density in real and frequency space. As opposed to the implementation of the exemplary bioassays with the rotationally actuated high-pass CP-DF siphon valves (Figure 7), the liquid reagents {Li} may all be released ω>ΩP+MΔΩP with respect to the plasma separation at ΩP. Overall, the speed (and quality) of plasma separation in the initial stages of common assay protocols may hence be significantly improved.

Figure 9.

Figure 9

Event-triggered flow control in exemplary bioassay protocol. (a) The set of valves {Γi} at their default (blue) positions {Ri}, and radially shifted outwards by 0.5 cm (orange), which is a common requirement towards microfluidic LSI. All frequency bands {Ωi±MΔΩi} are centered at identical rates Ωi=Ω. (b) The same radial distribution {Ri} is operated at different spin rates Ωi=ΩP, showing that event triggering is advantageous for enabling high spin rates ω, e.g., for improving and accelerating plasma separation.

5.2. Logical Flow Control

Such an event-triggered relay may also be considered as a logical “IF” condition, in a way that a (subsequent) valve only fires “if” another liquid has arrived to dissolve the CF in a designated pneumatic compartment [81]. This concept has been further refined by placing the CF at critical radial positions RDF (Figure 1a) in a way that a minimum liquid volume UCF must arrive in the DF chamber to dissolve the membrane, and thus vent and open the next valve. Based on such a logical “IF” condition, closed-loop “handshake” flow control has been implemented. Alternatively, the DF in the receiving chamber may be placed at a radial position that is only reached after a minimum amount of liquid has entered from (at least) two incoming channels, thus establishing an “AND” element. In a similar way, a logical “OR” may be defined by positioning the DF so that it is wetted after the arrival of a minimum liquid volume from a defined subset of incoming channels.

5.3. Delay Elements

Bioassay protocols usually require certain time spans, e.g., to account for reaction kinetics between bioentities that are dissolved, suspended, or bound to surfaces on cells and beads of walls. However, event triggering “hard-wires” process intervals in the network of valving structures in a direct “knock-on” fashion. To this end, delay elements have been incorporated into event-triggered fluidic systems for bioassay integration [96]. Examples are hydrodynamic flow resistances imposed by narrow and long channel segments, or paper strips, which have also been utilized for other purposes [15,97]. Through imbibition at defined wicking speed, these timers slow down the transfer of the main or ancillary liquids compared to open channels. While, in theory, also reducing the spin speed during transfer periods would be an option, such action would require rather complex “closed-loop” coordination between monitoring liquid flow on the disc and the frequency of the spindle motor ω.

5.4. Pulsing of Spin Rate

Commonly, the aggregate time spans for dissolution and liquid transfer range on the second- to minute scale, while bioassays normally require processing times of minutes to an hour. So, while such physical delay elements prolong the intervals available for LUOs, the timing still faces upper limits, and it is also ‘inscribed’ in the layout and material characteristics, such as the dissolution time of the sacrificial membrane or the imbibition speed of the paper strip. In addition, the requirement of the rotational actuation mode to steadily increase the critical spin rates Ωi along successive steps i managed by high-pass CP valves compromises the flexibility that may be required for enabling microfluidic LSI.

For situations when liquid volumes {Ui,j} are synchronously transferred between serial steps {i} at {Ωi} and {Ti}, the concept of rotational pulsing (Figure 10) has been presented [82]. This flow control mechanism exploits that within the interval ΔTi=Ti+1Ti, the subsequent valve i+1 is not fully loaded with U0, yet, thus intermittently increasing is retention rate Ωi+1 (Figure 10c) to allow jumps in the spin rate ω(t) that only need to stay inside the corridor required to retain the (other) concurrently loaded liquids; furthermore, the spin rate ω may be reduced below Ωi, thus alleviating the requirement for a steady increase (Figure 7) or constant spin rate ω (Figure 8 and Figure 9) while sequentially progressing the release steps {i}.

Figure 10.

Figure 10

Pulse-actuated CP-DF valving (Adopted from [82]). (a) Photo and concept of the fluidic structure. (b) Spin protocol ω(t) and (c) decrease of the retention frequency Ω(U0) with the arrival of the liquid volume U0(t). In conventional CP-DF siphon valving (Figure 1), a group of liquids is sequentially released through stepping up the spin rate ω across their critical burst frequencies {Ωi}. Digital pulse actuation considers the time ΔTi it takes a liquid volume U0 to advance through the outlet channel between valve opening at the burst frequency Ωi, and its arrival at the following valve featuring Ωi+1. During this interval ΔTi, which is primarily determined by the centrifugally induced pressure head pω (2), the flow resistance of the connecting channel on the viscosity of the liquid, and the dissolution time of the DF, the subsequent valve i+1 is only partially loaded, so its effective retention rate Ωi+1(Ti<t<Ti+1) is transiently be lifted above Ωi+1(U0) that is nominally calculated after the arrival of the full volume U0 (c). The spin rate ω(t) can thus be spiked well above Ωi+1(U0) during this interval ΔTi, and also allow Ωi+1<Ωi to squash the requirement of steadily growing retention rates Ωi+1>Ωi for the high-pass valves along the serial assay protocol ω(t).

In a similar way as ‘venting’, rotational pulsing allows retaining liquid menisci at sufficiently “safe” spacing at r=r(ΩMΔΩ) from the DF during retention. It can also be used to synchronize parallel processes, e.g., when the same protocol needs to be run on several patient samples. However, in heterogeneous assay panels where each channel would run a different protocol, the height of the rotational pulse for the CP-DF valve i to be released is confined by the lowest critical frequency of the concurrently loaded valves {κ} that need to stay closed, i.e., ωpulse,i<minκi {ΩκMΔMκ}.

6. Conclusions and Outlook

“Lab-on-a-Disc” (LoaD) systems are highly promising candidates for enabling cost-efficient and robust commercial solutions for decentralized testing, especially in low-resource settings and minimally trained operators. Underlying sample-to-answer automation and parallelization of bioassay protocols roots in fluidic large(r)-scale integration (LSI) of Laboratory Unit Operations (LUOs) and their control valves at tight packing densities.

This work has elaborated the basic principles of centrifugal flow control to directly connect experimental parameters such as liquid volumes, geometrical dimensions, and the ambient atmospheric pressure to the retention and release rates of rotationally actuated valves at the pivot of LSI. In the wake of such “digital-twin” modeling, frequency bands are calculated from tolerances in the input variables to quantify operational robustness. As the practically limited real and frequency spaces of LoaD systems severely restrict fluidic LSI, a suite of metrics has been elaborated to algorithmically guide performance optimization. Furthermore, the principles of advanced rotational valving schemes enabling conditional, closed-loop flow control and random timing by “digital” pulsing were systematically explored. With the availability of extended fabrication capabilities that are beyond the reach of most academic laboratories, larger numbers of LoaD devices can be provided for statistically relevant validation and refinement of the digital-twin model.

Future work will expand the design tool to allow for the simulation of mixed layouts synergistically combining various types of high- and low-pass valves, for refined geometries exhibiting rounded edges and contours, for incorporating dynamic fluid effects and bioassay kinetics, for onboard storage and release of reagents, for bead-based multiplexing techniques [24], and for externally powered, onboard pumping and control modules [76]. The degree of multiplexing might be markedly enhanced by multi-disc stack architectures.

Furthermore, manufacturing processes may be virtualized, e.g., through mold flow analysis for commercial polymer replication techniques, which commonly indicates the need for fairly even distributions of fluidic structures and flow resistances (for the centrally injected hot melt), minimum draft angles, and surface roughness to facilitate proper demolding. Design guidelines are also proving to be important for assembly and bonding.

With its high predictive power, the presented work and the suggested follow-ups can enable the computational generation and validation of disc layouts regarding fluidic functionality and compliance with design-for-manufacture (DfM) guidelines and related scale-up of mass fabrication. Such software might then create an effective interface for foundry services as a hallmark of mature industrial supply chains in task-sharing economies. Superior control and knowledge of manufacturing tolerances can also empower anti-counterfeit strategies protecting genuine medical products and their users [98].

Most foundational patents on centrifugal microfluidics that were primarily filed throughout the 1990s and early 2000s have expired, thus creating substantial wiggle room in the intellectual property (IP) space. Apart from classical exploitation, such opportunity might also resonate well with the present highly disruptive socio-economic and technological trends in the technological ecosystem of LoaD, such as Maker/Fab Labs, hackathons, science as a service (SaaS), cloud computing, Machine Learning (ML)/Artificial Intelligence (AI), Big Data, Internet of Things (IoT), and decentralization. Overall, this development may enable novel open platform concepts, e.g., to usher a new era of blockchain-backed participatory research models and crowdsourcing of ideas, expertise, skills, workforce, infrastructure, and equipment may be established [99,100,101,102].

Appendix A. Default Geometry of CP-DF Siphon Valves

The structure Γ, loaded liquid volumes U0, and radial positions R can be varied across a multi-dimensional parameter space, e.g., to tune retention rates Ω of other key performance indicators. Table A1 gives of overview or generic values which can be used to initiate the optimization.

Table A1.

Default geometrical parameters and relationships of CP-DF siphon valves (Figure 1). The resulting critical spin rate Ω(R,Γ,U0)/2π22 Hz. Minimum lateral dimensions are given by the smallest practical diameter of milling tools (200 µm). As tools for injection molding are often adopted from optical data storage (e.g., CD, DVD, Blu-ray), a central, 1.5 cm diameter hole and a disc radius of 6 cm with thickness around 1.2 mm, fluidic structures Γ may need to stay within the radial interval between Rmin=1.5 cm and Rmax=5.5 cm, and an upper limit for the depth of about 1 mm. The lowest depth of cavities is often restricted by the sealing technology; for large lateral extensions or small aspect ratios, sagging of the lid, which is often a foil, may significantly change the nominal volume capacity, also in response to the pressure, and might even lead to sticking to the bottom of the cavity.

R=3 cm Rmin=1.5 cm Rmax=5.5 cm RDF=3.15 cm>R
A0=d0w0 d0=1 mm w0=5 mm
U0=100 µL<A0(RRmin)
Uiso=d0hLU0 diso=1 mm hiso=1 mm Liso=15 mm>w0+w 
UZ=dwZ d=500 µm w=800 µmw0 Z=10 mm
VC,0=dCwChCUZ dC=1 mm wC=20 mm hC=10 mm
Vint=dinthintLintVC dint=200 µm hint=300 µm Lint=1 cm>2w
VDF=0.25πdDFDDF2VC dDF=190 µm DDF=3 mm α=0.45, β=0.5

Funding

This research received no external funding.

Conflicts of Interest

The author declares no conflict of interest.

Footnotes

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Manz A., Graber N., Widmer H. Miniaturized total chemical analysis systems: A novel concept for chemical sensing. Sensors Actuators B Chem. 1990;1:244–248. doi: 10.1016/0925-4005(90)80209-I. [DOI] [Google Scholar]
  • 2.Reyes D.R., Iossifidis D., Auroux P.-A., Manz A. Micro Total Analysis Systems. 1. Introduction, Theory, and Technology. Anal. Chem. 2002;74:2623–2636. doi: 10.1021/ac0202435. [DOI] [PubMed] [Google Scholar]
  • 3.Auroux P.-A., Iossifidis D., Reyes D.R., Manz A. Micro Total Analysis Systems. 2. Analytical Standard Operations and Applications. Anal. Chem. 2002;74:2637–2652. doi: 10.1021/ac020239t. [DOI] [PubMed] [Google Scholar]
  • 4.Whitesides G.M. The origins and the future of microfluidics. Nat. Cell Biol. 2006;442:368–373. doi: 10.1038/nature05058. [DOI] [PubMed] [Google Scholar]
  • 5.Yager P., Edwards T., Fu E., Helton K., Nelson K., Tam M.R., Weigl B.H. Microfluidic diagnostic technologies for global public health. Nat. Cell Biol. 2006;442:412–418. doi: 10.1038/nature05064. [DOI] [PubMed] [Google Scholar]
  • 6.Madou M.J., Kellogg G.J. LabCD: A centrifuge-based microfluidic platform for diagnostics; Proceedings of the BiOS ‘98 International Biomedical Optics Symposium; San Jose, CA, USA. 27–29 January 1998; pp. 80–93. [DOI] [Google Scholar]
  • 7.Ducrée J., Haeberle S., Lutz S., Pausch S., Von Stetten F., Zengerle R. The centrifugal microfluidic Bio-Disk platform. J. Micromech. Microeng. 2007;17:S103–S115. doi: 10.1088/0960-1317/17/7/S07. [DOI] [Google Scholar]
  • 8.Gorkin R., Park J., Siegrist J., Amasia M., Lee B.S., Park J.-M., Kim J., Kim H., Madou M., Cho Y.-K. Centrifugal microfluidics for biomedical applications. Lab Chip. 2010;10:1758–1773. doi: 10.1039/b924109d. [DOI] [PubMed] [Google Scholar]
  • 9.Park J.-M., Cho Y.-K., Lee B.-S., Lee J.-G., Ko C. Multifunctional microvalves control by optical illumination on nanoheaters and its application in centrifugal microfluidic devices. Lab Chip. 2007;7:557–564. doi: 10.1039/b616112j. [DOI] [PubMed] [Google Scholar]
  • 10.Watts A.S., Urbas A.A., Moschou E., Gavalas V.G., Zoval J.V., Madou M., Bachas L. Centrifugal Microfluidics with Integrated Sensing Microdome Optodes for Multiion Detection. Anal. Chem. 2007;79:8046–8054. doi: 10.1021/ac0709100. [DOI] [PubMed] [Google Scholar]
  • 11.Clime L., Geissler M., Veres T., Brassard D. Active pneumatic control of centrifugal microfluidic flows for lab-on-a-chip applications. Lab Chip. 2015;15:2400–2411. doi: 10.1039/C4LC01490A. [DOI] [PubMed] [Google Scholar]
  • 12.Strohmeier O., Keller M., Schwemmer F., Zehnle S., Mark D., von Stetten F., Zengerle R., Paust N. Centrifugal microfluidic platforms: Advanced unit operations and applications. Chem. Soc. Rev. 2015;44:6187–6229. doi: 10.1039/C4CS00371C. [DOI] [PubMed] [Google Scholar]
  • 13.Thompson B.L., Birch C., Nelson D.A., Li J., Duvall J.A., Le Roux D., Tsuei A.-C., Mills D.L., Root B.E., Landers J.P. A centrifugal microfluidic device with integrated gold leaf electrodes for the electrophoretic separation of DNA. Lab Chip. 2016;16:4569–4580. doi: 10.1039/C6LC00953K. [DOI] [PubMed] [Google Scholar]
  • 14.Smith S., Mager D., Perebikovsky A., Shamloo E., Kinahan D., Mishra R., Delgado S.M.T., Kido H., Saha S., Ducrée J., et al. CD-Based Microfluidics for Primary Care in Extreme Point-of-Care Settings. Micromachines. 2016;7:22. doi: 10.3390/mi7020022. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Hwang H., Kim S.-H., Kim T.-H., Park J.-K., Cho Y.-K. Paper on a disc: Balancing the capillary-driven flow with a centrifugal force. Lab Chip. 2011;11:3404–3406. doi: 10.1039/c1lc20445a. [DOI] [PubMed] [Google Scholar]
  • 16.Kim T.-H., Hwang H., Gorkin R., Madou M., Cho Y.-K. Geometry effects on blood separation rate on a rotating disc. Sens. Actuators B Chem. 2013;178:648–655. doi: 10.1016/j.snb.2013.01.011. [DOI] [Google Scholar]
  • 17.Hwang H., Kim H.-H., Cho Y.-K. Elastomeric membrane valves in a disc. Lab Chip. 2011;11:1434–1436. doi: 10.1039/c0lc00658k. [DOI] [PubMed] [Google Scholar]
  • 18.Roy E., Stewart G., Mounier M., Malic L., Peytavi R., Clime L., Madou M., Bossinot M., Bergeron M.G., Veres T. From cellular lysis to microarray detection, an integrated thermoplastic elastomer (TPE) point of care Lab on a Disc. Lab Chip. 2014;15:406–416. doi: 10.1039/C4LC00947A. [DOI] [PubMed] [Google Scholar]
  • 19.Kong L.X., Perebikovsky A., Moebius J., Kulinsky L., Madou M. Lab-on-a-CD. J. Lab. Autom. 2016;21:323–355. doi: 10.1177/2211068215588456. [DOI] [PubMed] [Google Scholar]
  • 20.Hess J.F., Zehnle S., Juelg P., Hutzenlaub T., Zengerle R., Paust N. Review on pneumatic operations in centrifugal microfluidics. Lab Chip. 2019;19:3745–3770. doi: 10.1039/C9LC00441F. [DOI] [PubMed] [Google Scholar]
  • 21.Aeinehvand M.M., Magaña P., Aeinehvand M.S., Aguilar O., Madou M.J., Martinez-Chapa S.O. Ultra-rapid and low-cost fabrication of centrifugal microfluidic platforms with active mechanical valves. RSC Adv. 2017;7:55400–55407. doi: 10.1039/C7RA11532F. [DOI] [Google Scholar]
  • 22.Aeinehvand M.M., Weber L., Jiménez M., Palermo A., Bauer M., Loeffler F.F., Ibrahim F., Breitling F., Korvink J., Madou M., et al. Elastic reversible valves on centrifugal microfluidic platforms. Lab Chip. 2019;19:1090–1100. doi: 10.1039/C8LC00849C. [DOI] [PubMed] [Google Scholar]
  • 23.Van Nguyen H., Nguyen V.D., Nguyen H.Q., Chau T.H.T., Lee E.Y., Seo T.S. Nucleic acid diagnostics on the total integrated lab-on-a-disc for point-of-care testing. Biosens. Bioelectron. 2019;141:111466. doi: 10.1016/j.bios.2019.111466. [DOI] [PubMed] [Google Scholar]
  • 24.Rombach M., Hin S., Specht M., Johannsen B., Lüddecke J., Paust N., Zengerle R., Roux L., Sutcliffe T., Peham J.R., et al. RespiDisk: A point-of-care platform for fully automated detection of respiratory tract infection pathogens in clinical samples. Analyst. 2020;145:7040–7047. doi: 10.1039/D0AN01226B. [DOI] [PubMed] [Google Scholar]
  • 25.Miyazaki C., Carthy E., Kinahan D. Biosensing on the Centrifugal Microfluidic Lab-on-a-Disc Platform. Processes. 2020;8:1360. doi: 10.3390/pr8111360. [DOI] [Google Scholar]
  • 26.Madadelahi M., Acosta-Soto L.F., Hosseini S., Martinez-Chapa S.O., Madou M.J. Mathematical modeling and computational analysis of centrifugal microfluidic platforms: A review. Lab Chip. 2020;20:1318–1357. doi: 10.1039/C9LC00775J. [DOI] [PubMed] [Google Scholar]
  • 27.Homann A.R., Niebling L., Zehnle S., Beutler M., Delamotte L., Rothmund M.-C., Czurratis D., Beller K.-D., Zengerle R., Hoffmann H., et al. A microfluidic cartridge for fast and accurate diagnosis of Mycobacterium tuberculosis infections on standard laboratory equipment. Lab Chip. 2021;21:1540–1548. doi: 10.1039/D1LC00035G. [DOI] [PubMed] [Google Scholar]
  • 28.Zehnle S., Schwemmer F., Bergmann R., von Stetten F., Zengerle R., Paust N. Pneumatic siphon valving and switching in centrifugal microfluidics controlled by rotational frequency or rotational acceleration. Microfluid. Nanofluidics. 2015;19:1259–1269. doi: 10.1007/s10404-015-1634-9. [DOI] [Google Scholar]
  • 29.Zehnle S., Rombach M., Zengerle R., Von Stetten F., Paust N. Network simulation-based optimization of centrifugo-pneumatic blood plasma separation. Biomicrofluidics. 2017;11:024114. doi: 10.1063/1.4979044. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Abaxis. [(accessed on 14 June 2021)]; Available online: https://www.abaxis.com/
  • 31.Schembri C.T., Ostoich V., Lingane P.J., Burd T.L., Buhl S.N. Portable Simultaneous Multiple Analyte Whole-Blood Analyzer for Point-of-Care Testing. Clin. Chem. 1992;38:1665–1670. doi: 10.1093/clinchem/38.9.1665. [DOI] [PubMed] [Google Scholar]
  • 32.Schembri C.T., Burd T.L., Kopf-Sill A.R., Shea L.R., Braynin B. Centrifugation and capillarity integrated into a multiple analyte whole blood analyser. J. Autom. Chem. 1995;17:99–104. doi: 10.1155/S1463924695000174. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Gyros Protein Technologies. [(accessed on 14 June 2021)]; Available online: https://www.gyrosproteintechnologies.com/
  • 34.Shea M., Ommert S., Gleich L., Towle T., Haspel H., Schmid N., Jindal H., Kellogg G., Carvalho B., Contarino M., et al. ADMET Assays on Tecan’s LabCD-ADMET System. J. Lab. Autom. 2003;8:74–77. doi: 10.1016/S1535-5535-04-00260-6. [DOI] [Google Scholar]
  • 35.Biosurfit S.A. [(accessed on 14 June 2021)]; Available online: https://www.biosurfit.com/
  • 36.Burstein Technologies, Inc. [(accessed on 31 May 2021)];2006 Available online: https://web.archive.org/web/20061209052345/http://www.bursteintechnologies.com.
  • 37.Mian A., Kieffer-Higgins S.G., Corey G.D. US6319469B1–Devices and methods for using centripetal acceleration to drive fluid movement in a microfluidics system. [(accessed on 14 June 2021)];1996 Available online: https://patents.google.com/patent/US6319469B1/en.
  • 38.Radisens Diagnostics. [(accessed on 14 June 2021)]; Available online: www.radisens.com.
  • 39.LaMotte Chemical Products Co. [(accessed on 14 June 2021)]; Available online: https://www.lamotte.com.
  • 40.Blusense Diagnostics. [(accessed on 14 June 2021)]; Available online: https://blusense-diagnostics.com/
  • 41.Spindiag GmbH. [(accessed on 14 June 2021)]; Available online: http://www.spindiag.de.
  • 42.RotaPrep Inc. [(accessed on 19 April 2021)]; Available online: https://rotaprep.com/
  • 43.Ducrée J. Efficient Development of Integrated Lab-On-A-Chip Systems Featuring Operational Robustness and Manufacturability. Micromachines. 2019;10:886. doi: 10.3390/mi10120886. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Mark D., Haeberle S., Metz T., Lutz S., Ducrée J., Zengerle R., von Stetten F. Aliquoting structure for centrifugal micro-fluidics based on a new pneumatic valve; Proceedings of the MEMS 2008, 21st IEEE International Conference on Micro Electro Mechanical Systems; Tucson, AZ, USA. 13–17 January 2008. [Google Scholar]
  • 45.Schwemmer F., Hutzenlaub T., Buselmeier D., Paust N., Von Stetten F., Mark D., Zengerle R., Kosse D. Centrifugo-pneumatic multi-liquid aliquoting—Parallel aliquoting and combination of multiple liquids in centrifugal microfluidics. Lab Chip. 2015;15:3250–3258. doi: 10.1039/C5LC00513B. [DOI] [PubMed] [Google Scholar]
  • 46.Keller M., Wadle S., Paust N., Dreesen L., Nuese C., Strohmeier O., Zengerle R., von Stetten F. Centrifugo-thermopneumatic fluid control for valving and aliquoting applied to multiplex real-time PCR on off-the-shelf centrifugal thermocycler. RSC Adv. 2015;5:89603–89611. doi: 10.1039/C5RA16095B. [DOI] [Google Scholar]
  • 47.Haeberle S., Brenner T., Zengerle R., Ducrée J. Centrifugal extraction of plasma from whole blood on a rotating disk. Lab Chip. 2006;6:776–781. doi: 10.1039/B604145K. [DOI] [PubMed] [Google Scholar]
  • 48.Steigert J., Brenner T., Grumann M., Riegger L., Lutz S., Zengerle R., Ducrée J. Integrated siphon-based metering and sedimentation of whole blood on a hydrophilic lab-on-a-disk. Biomed. Microdevices. 2007;9:675–679. doi: 10.1007/s10544-007-9076-0. [DOI] [PubMed] [Google Scholar]
  • 49.Kinahan D.J., Kearney S.M., Kilcawley N.A., Early P.L., Glynn M., Ducrée J. Density-Gradient Mediated Band Extraction of Leukocytes from Whole Blood Using Centrifugo-Pneumatic Siphon Valving on Centrifugal Microfluidic Discs. PLoS ONE. 2016;11:e0155545. doi: 10.1371/journal.pone.0155545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Dimov N., Gaughran J., McAuley D., Boyle D., Kinahan D.J., Ducree J. Centrifugally automated solid-phase purification of RNA; Proceedings of the 2014 IEEE 27th International Conference on Micro Electro Mechanical Systems (MEMS); San Francisco, CA, USA. 26–30 January 2014; pp. 260–263. [DOI] [Google Scholar]
  • 51.Gaughran J., Boyle D., Murphy J., Kelly R., Ducrée J. Phase-selective graphene oxide membranes for advanced microfluidic flow control. Microsystems Nanoeng. 2016;2:16008. doi: 10.1038/micronano.2016.8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Strohmeier O., Keil S., Kanat B., Patel P., Niedrig M., Weidmann M., Hufert F., Drexler J., Zengerle R., von Stetten F. Automated nucleic acid extraction from whole blood, B. subtilis, E. coli, and Rift Valley fever virus on a centrifugal microfluidic LabDisk. RSC Adv. 2015;5:32144–32150. doi: 10.1039/C5RA03399C. [DOI] [Google Scholar]
  • 53.Brassard D., Geissler M., Descarreaux M., Tremblay D., Daoud J., Clime L., Mounier M., Charlebois D., Veres T. Extraction of nucleic acids from blood: Unveiling the potential of active pneumatic pumping in centrifugal microfluidics for integration and automation of sample preparation processes. Lab Chip. 2019;19:1941–1952. doi: 10.1039/C9LC00276F. [DOI] [PubMed] [Google Scholar]
  • 54.Karle M., Miwa J., Röth G., Zengerle R., Von Stetten F. A Novel Microfluidic Platform for Continuous DNA Extraction and Purification using Laminar Flow Magnetophoresis; Proceedings of the 2009 IEEE 22nd International Conference on Micro Electro Mechanical Systems; Sorrento, Italy. 25–29 January 2009; pp. 276–279. [DOI] [Google Scholar]
  • 55.Kido H., Micic M., Smith D., Zoval J., Norton J., Madou M. A novel, compact disk-like centrifugal microfluidics system for cell lysis and sample homogenization. Colloids Surfaces B Biointerfaces. 2007;58:44–51. doi: 10.1016/j.colsurfb.2007.03.015. [DOI] [PubMed] [Google Scholar]
  • 56.Grumann M., Geipel A., Riegger L., Zengerle R., Ducrée J. Batch-mode mixing on centrifugal microfluidic platforms. Lab Chip. 2005;5:560–565. doi: 10.1039/b418253g. [DOI] [PubMed] [Google Scholar]
  • 57.Ducrée J., Brenner T., Haeberle S., Glatzel T., Zengerle R. Multilamination of flows in planar networks of rotating microchannels. Microfluid. Nanofluidics. 2006;2:78–84. doi: 10.1007/s10404-005-0056-5. [DOI] [Google Scholar]
  • 58.Burger R., Kinahan D.J., Cayron H., Reis N., Fonseca J., Ducrée J. Siphon-Induced Droplet Break-Off for Enhanced Mixing on a Centrifugal Platform. Inventions. 2019;5:1. doi: 10.3390/inventions5010001. [DOI] [Google Scholar]
  • 59.Ducrée J., Haeberle S., Brenner T., Glatzel T., Zengerle R. Patterning of flow and mixing in rotating radial microchannels. Microfluid. Nanofluidics. 2005;2:97–105. doi: 10.1007/s10404-005-0049-4. [DOI] [Google Scholar]
  • 60.Lutz S., Mark D., Roth G., Zengerle R., von Stetten F. Centrifugal Microfluidic Platforms for Molecular Diagnostics. Clin. Chem. Lab. Med. 2011;49:S608. [Google Scholar]
  • 61.Tang M., Wang G., Kong S.-K., Ho H.-P. A Review of Biomedical Centrifugal Microfluidic Platforms. Micromachines. 2016;7:26. doi: 10.3390/mi7020026. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Maguire I., O’Kennedy R., Ducrée J., Regan F. A review of centrifugal microfluidics in environmental monitoring. Anal. Methods. 2018;10:1497–1515. doi: 10.1039/C8AY00361K. [DOI] [Google Scholar]
  • 63.Burger R., Amato L., Boisen A. Detection methods for centrifugal microfluidic platforms. Biosens. Bioelectron. 2016;76:54–67. doi: 10.1016/j.bios.2015.06.075. [DOI] [PubMed] [Google Scholar]
  • 64.Duffy D.C., Gillis H.L., Lin J., Sheppard N.F., Kellogg G.J. Microfabricated Centrifugal Microfluidic Systems: Characterization and Multiple Enzymatic Assays. Anal. Chem. 1999;71:4669–4678. doi: 10.1021/ac990682c. [DOI] [Google Scholar]
  • 65.Azimi-Boulali J., Madadelahi M., Madou M.J., Martinez-Chapa S.O. Droplet and Particle Generation on Centrifugal Microfluidic Platforms: A Review. Micromachines. 2020;11:603. doi: 10.3390/mi11060603. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Brennan D., Coughlan H., Clancy E., Dimov N., Barry T., Kinahan D., Ducrée J., Smith T.J., Galvin P. Development of an on-disc isothermal in vitro amplification and detection of bacterial RNA. Sensors Actuators B Chem. 2017;239:235–242. doi: 10.1016/j.snb.2016.08.018. [DOI] [Google Scholar]
  • 67.Delgado S.M.T., Kinahan D.J., Sandoval F.S., Julius L.A.N., Kilcawley N.A., Ducrée J., Mager D. Fully automated chemiluminescence detection using an electrified-Lab-on-a-Disc (eLoaD) platform. Lab Chip. 2016;16:4002–4011. doi: 10.1039/C6LC00973E. [DOI] [PubMed] [Google Scholar]
  • 68.Ducrée J. Systematic review of centrifugal valving based on digital twin modelling towards highly integrated Lab-on-a-Disc systems. Nat. Microsyst. Nanoeng. 2021 doi: 10.20944/preprints202105.0683.v2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Ducrée J. Design optimization of centrifugal microfluidic “Lab-on-a-Disc” systems towards fluidic larger-scale integration. Appl. Sci. 2021 doi: 10.20944/preprints202105.0282.v2. [DOI] [Google Scholar]
  • 70.Abi-Samra K., Hanson R., Madou M., Iii R.A.G. Infrared controlled waxes for liquid handling and storage on a CD-microfluidic platform. Lab Chip. 2011;11:723–726. doi: 10.1039/C0LC00160K. [DOI] [PubMed] [Google Scholar]
  • 71.Kong L.X., Parate K., Abi-Samra K., Madou M. Multifunctional wax valves for liquid handling and incubation on a microfluidic CD. Microfluid. Nanofluidics. 2015;18:1031–1037. doi: 10.1007/s10404-014-1492-x. [DOI] [Google Scholar]
  • 72.Al-Faqheri W., Ibrahim F., Thio T.H.G., Moebius J., Joseph K., Arof H., Madou M. Vacuum/Compression Valving (VCV) Using Parrafin-Wax on a Centrifugal Microfluidic CD Platform. PLoS ONE. 2013;8:e58523. doi: 10.1371/journal.pone.0058523. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Wang Y., Li Z., Huang X., Ji W., Ning X., Liu K., Tan J., Yang J., Ho H.-P., Wang G. On-board control of wax valve on active centrifugal microfluidic chip and its application for plasmid DNA extraction. Microfluid. Nanofluidics. 2019;23:112. doi: 10.1007/s10404-019-2278-y. [DOI] [Google Scholar]
  • 74.Garcia-Cordero J.L., Kurzbuch D., Benito-Lopez F., Diamond D., Lee L.P., Ricco A.J. Optically addressable single-use microfluidic valves by laser printer lithography. Lab Chip. 2010;10:2680–2687. doi: 10.1039/c004980h. [DOI] [PubMed] [Google Scholar]
  • 75.Stumpf F., Schwemmer F., Hutzenlaub T., Baumann D., Strohmeier O., Dingemanns G., Simons G., Sager C., Plobner L., von Stetten F., et al. LabDisk with complete reagent prestorage for sample-to-answer nucleic acid based detection of respiratory pathogens verified with influenza A H3N2 virus. Lab Chip. 2015;16:199–207. doi: 10.1039/C5LC00871A. [DOI] [PubMed] [Google Scholar]
  • 76.Delgado S.M.T., Kinahan D.J., Julius L.A.N., Mallette A., Ardila D.S., Mishra R., Miyazaki C.M., Korvink J., Ducrée J., Mager D. Wirelessly powered and remotely controlled valve-array for highly multiplexed analytical assay automation on a centrifugal microfluidic platform. Biosens. Bioelectron. 2018;109:214–223. doi: 10.1016/j.bios.2018.03.012. [DOI] [PubMed] [Google Scholar]
  • 77.Iii R.G., Nwankire C.E., Gaughran J., Zhang X., Donohoe G.G., Rook M., O’Kennedy R., Ducrée J. Centrifugo-pneumatic valving utilizing dissolvable films. Lab Chip. 2012;12:2894–2902. doi: 10.1039/c2lc20973j. [DOI] [PubMed] [Google Scholar]
  • 78.Godino N., Iii R.G., Linares A.V., Burger R., Ducrée J. Comprehensive integration of homogeneous bioassays via centrifugo-pneumatic cascading. Lab Chip. 2013;13:685–694. doi: 10.1039/C2LC40722A. [DOI] [PubMed] [Google Scholar]
  • 79.Kinahan D.J., Early P.L., Vembadi A., MacNamara E., Kilcawley N.A., Glennon T., Diamond D., Brabazon D., Ducrée J. Xurography actuated valving for centrifugal flow control. Lab Chip. 2016;16:3454–3459. doi: 10.1039/C6LC00568C. [DOI] [PubMed] [Google Scholar]
  • 80.Mishra R., Gaughran J., Kinahan D., Ducrée J. Functional Membranes for Enhanced Rotational Flow Control on Centrifugal Microfluidic Platforms. Ref. Modul. Mater. Sci. Mater. Eng. 2017 doi: 10.1016/b978-0-12-803581-8.04041-8. [DOI] [Google Scholar]
  • 81.Kinahan D.J., Kearney S.M., Dimov N., Glynn M.T., Ducrée J. Event-triggered logical flow control for comprehensive process integration of multi-step assays on centrifugal microfluidic platforms. Lab Chip. 2014;14:2249–2258. doi: 10.1039/C4LC00380B. [DOI] [PubMed] [Google Scholar]
  • 82.Kinahan D.J., McConville K., Henderson B., McCaul M., McNamara E., Diamond D., Ducrée J. Digital pulse actuated flow control on a centrifugal disc towards multiparameter water quality monitoring. In: Pamme N., Ducrée J., editors. Proceedings of the 20th International Conference on Miniaturized Systems for Chemistry and Life Sciences (μTAS 2016); Dublin, Ireland. 9–13 October 2016; Dublin, Ireland: CBMS; 2016. pp. 871–872. [Google Scholar]
  • 83.Kinahan D.J., Renou M., Kurzbuch D., Kilcawley N.A., Bailey Éanna, Glynn M., McDonagh C., Ducrée J. Baking Powder Actuated Centrifugo-Pneumatic Valving for Automation of Multi-Step Bioassays. Micromachines. 2016;7:175. doi: 10.3390/mi7100175. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84.Mishra R., Reilly G., Agnew M., Garvey A., Rogers C., Andrade E., Ma H., Fitzgerald S., Zapatero J., O’Kennedy R., et al. Laser-actuated centrifugo-pneumatic flow control towards ‘sample-to-answer’ integrated detection of multi-marker panels at the point-of-care; Proceedings of the 2018 IEEE Micro Electro Mechanical Systems (MEMS); Dublin, Ireland. 21–25 January 2018; pp. 1185–1188. [DOI] [Google Scholar]
  • 85.Unger M.A., Chou H.-P., Thorsen T., Scherer A., Quake S.R. Monolithic Microfabricated Valves and Pumps by Multilayer Soft Lithography. Science. 2000;288:113–116. doi: 10.1126/science.288.5463.113. [DOI] [PubMed] [Google Scholar]
  • 86.Thorsen T., Maerkl S.J., Quake S.R. Microfluidic Large-Scale Integration. Science. 2002;298:580–584. doi: 10.1126/science.1076996. [DOI] [PubMed] [Google Scholar]
  • 87.Digital Twin. [(accessed on 25 May 2021)];2021 Available online: https://en.wikipedia.org/wiki/Digital_twin.
  • 88.Marr B. What Is Digital Twin Technology—And Why Is It So Important? [(accessed on 25 May 2021)];2017 Available online: https://www.forbes.com/sites/bernardmarr/2017/03/06/what-is-digital-twin-technology-and-why-is-it-so-important/
  • 89.Brenner T., Glatzel T., Zengerle R., Ducrée J. Frequency-dependent transversal flow control in centrifugal microfluidics. Lab Chip. 2004;5:146–150. doi: 10.1039/B406699E. [DOI] [PubMed] [Google Scholar]
  • 90.Clime L., Daoud J., Brassard D., Malic L., Geissler M., Veres T. Active pumping and control of flows in centrifugal microfluidics. Microfluid. Nanofluidics. 2019;23:29. doi: 10.1007/s10404-019-2198-x. [DOI] [Google Scholar]
  • 91.Noroozi Z., Kido H., Madou M.J. Electrolysis-Induced Pneumatic Pressure for Control of Liquids in a Centrifugal System. J. Electrochem. Soc. 2011;158:P130–P135. doi: 10.1149/2.028111jes. [DOI] [Google Scholar]
  • 92.Abi-Samra K., Clime L., Kong L., Gorkin R., Kim T.-H., Cho Y.-K., Madou M. Thermo-pneumatic pumping in centrifugal microfluidic platforms. Microfluid. Nanofluidics. 2011;11:643–652. doi: 10.1007/s10404-011-0830-5. [DOI] [Google Scholar]
  • 93.Haeberle S., Schmitt N., Zengerle R., Ducrée J. Centrifugo-magnetic pump for gas-to-liquid sampling. Sens. Actuators A Phys. 2007;135:28–33. doi: 10.1016/j.sna.2006.09.001. [DOI] [Google Scholar]
  • 94.Siegrist J., Gorkin R., Bastien M., Stewart G., Peytavi R., Kido H., Bergeron M., Madou M. Validation of a centrifugal microfluidic sample lysis and homogenization platform for nucleic acidextraction with clinical samples. Lab Chip. 2009;10:363–371. doi: 10.1039/B913219H. [DOI] [PubMed] [Google Scholar]
  • 95.Soroori S., Kulinsky L., Kido H., Madou M. Design and implementation of fluidic micro-pulleys for flow control on centrifugal microfluidic platforms. Microfluid. Nanofluidics. 2014;16:1117–1129. doi: 10.1007/s10404-013-1277-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Kinahan D.J., Kearney S.M., Faneuil O.P., Glynn M.T., Dimov N., Ducrée J. Paper imbibition for timing of multi-step liquid handling protocols on event-triggered centrifugal microfluidic lab-on-a-disc platforms. RSC Adv. 2014;5:1818–1826. doi: 10.1039/C4RA14887H. [DOI] [Google Scholar]
  • 97.Godino N., Vereshchagina E., Gorkin R., Ducrée J. Centrifugal automation of a triglyceride bioassay on a low-cost hybrid paper-polymer device. Microfluid. Nanofluidics. 2014;16:895–905. doi: 10.1007/s10404-013-1283-9. [DOI] [Google Scholar]
  • 98.Ducrée J. Anti-counterfeit technologies for centrifugal microfluidic “Lab-on-a-Disc” systems: An analysis. 2021 in press. [Google Scholar]
  • 99.Ducrée J., Etzrodt M., Bartling S., Walshe R., Harrington T., Wittek N., Posth S., Wittek K., Ionita A., Prinz W., et al. Unchaining Collective Intelligence for Science, Research, and Technology Development by Blockchain-Boosted Community Participation. Front. Blockchain. 2021;4:631648. doi: 10.3389/fbloc.2021.631648. [DOI] [Google Scholar]
  • 100.Ducrée J. Research—A blockchain of knowledge? Blockchain Res. Appl. 2020;1:100005. doi: 10.1016/j.bcra.2020.100005. [DOI] [Google Scholar]
  • 101.Ducrée J., Gravitt M., Walshe R., Bartling S., Etzrodt M., Harrington T. Open Platform Concept for Blockchain-Enabled Crowdsourcing of Technology Development and Supply Chains. Front. Blockchain. 2020;3:386525. doi: 10.3389/fbloc.2020.586525. [DOI] [Google Scholar]
  • 102.Ducrée J., Etzrodt M., Gordijn B., Gravitt M., Bartling S., Walshe R., Harrington T. Blockchain for Organizing Effective Grass-Roots Actions on a Global Commons: Saving the Planet. Front. Blockchain. 2020;3:33. doi: 10.3389/fbloc.2020.00033. [DOI] [Google Scholar]

Articles from Micromachines are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES