Table 1.
Summary of the cited research work.
Single object manipulation and assembly in 1D | |||
---|---|---|---|
Concept | Device | Particle/cell type | References |
Object trapping within nodes of standing waves | Mainly IDTs on LiNbO3, PDMS channels or Petri dishes |
Microparticles, red blood cells, Escherichia coli, Caenorhabditis elegans |
[29,30,52,53] |
Acoustic vortices and streaming forces to trap objects | IDTs of different shape and configuration on LiNbO3, PDMS channels or Petri dishes |
Microparticles, microbubbles, exosomes | [53,54] |
Acoustic tweezers to move objects along defined trajectories |
IDTs of different shape and configuration on LiNbO3, PDMS channels or Petri dishes |
Microparticles, breast cancer cells, zebrafish embryos |
[[55], [56], [57], [58]] |
Manipulation in 2D and assembly of multiple objects | |||
Concept |
Device |
Particle/cell type |
References |
Spheroid formation and cell aggregation | Mainly IDTs on LiNbO3, PDMS channels or Petri dishes ZnO/Si piezoelements |
Microparticles, yeast cells, tumor spheroids, neurospheroids | [33,[62], [63], [64], [65],69] |
Spatial positioning of cells and co-culture systems | Mainly IDTs on LiNbO3, PDMS channels |
HMVEC-d, HeLa, epithelial cells, fibroblasts, Schwann cells, DRG | [[66], [67], [68]] |
Cell patterning within hydrogels |
Mainly IDTs on LiNbO3, PDMS channels or open-top chambers |
hASC, PC12, HUVEC, hMSC, NRVC, iPSC-CM, C2C12, neuroprogenitor cells |
[27,28,31,45,48,[70], [71], [72], [73], [74], [75]] |
Assembly in 2.5D or 3D and acoustic patterning of building blocks | |||
Concept |
Particle/cell type |
Outcome |
References |
Spheroid assembly into engineered constructs | HUVEC and hMSC | Perfusable microvasculature | [45] |
Multicellular assembly into 3D structures | Fibroblasts, HUVEC, hepatocytes | Liver organoids; cellu-robots | [80,81] |
In situ cell–polymer biograft assembly |
HeLa, MC3T3-E1, P12 |
Macroscopic fibers/building blocks for tissue engineering |
[32] |
Short-term acoustic manipulation—effect after seconds | |||
Concept |
Particles/cells |
Outcome |
References |
Cell seeding with acoustic waves | Primary osteoblast-like cells, yeast cells | Fast, homogeneous cell seeding | [82,83] |
Acoustic stimulation of cells | Cortical neurons | Altered excitability and action potential | [84] |
Acoustic waves for laboratory practice |
Cryopreservation of hUCM-MSCs |
Increased viability |
[85] |
Midterm acoustic manipulation—from seconds to minutes to trap and sort objects | |||
Concept |
Device/strategy |
Particles/cells |
References |
Object trapping and sorting | Acoustofluidics, mainly PDMS microchannels assembled on IDTs and LiNbO3 | Microparticles, nanoparticles, spheroids | [37,86,87,90] |
Acoustofluidics for diagnostics | Mainly PDMS microchannels assembled on IDTs and LiNbO3 | Red blood cells, lymphocytes, circulating tumor cells | [88,89,91] |
Biomaterial design by acoustic waves/Chemical reactions |
Topographical structuring of polymer precursors or extracellular matrix proteins |
PEGDA or PDMS beads, O2 and CO2 as reactive agents, collagen, fibrinogen |
[[92], [93], [94], [95], [96], [97]] |
Long-term acoustic manipulation—the effect of sound waves on cell fate | |||
Concept |
Particles/cells |
Outcome |
References |
Cell viability after prolonged acoustic stimulation | HeLa, human B cells | Confirmed cell viability | [99,100] |
Cell differentiation under acoustic stimulation | hASC | Chondrogenesis, osteogenesis | [[101], [102], [103]] |
Effect of acoustic waves on microorganisms |
Escherichia coli; Pseudomonas aeruginosa |
Biofilm formation; susceptibility to antibiotics |
[34,110] |
Abbreviations: hUCM-MSC: human umbilical cord matrix mesenchymal stem cells; PDMS: polydimethylsiloxan; IDT: interdigital transducers; PEGDA: poly(ethylene glycol)di-acryloyl; HeLa: Henriette Lacks cervical cancer cell line; hASC: human adipose tissue-derived stem cells; hMSC: human mesenchymal stem cells; HMVEC-d: human dermal vascular endothelial cells; DRG: dorsal route ganglion (neurons); PC12: cell line of neuroblasts and eosinophilic cells; HUVEC: human umbilical vein endothelial cells; NRVC: neonatal rat ventricular cardiomyocytes; iPSC-CM: induced pluripotent stem cell-derived cardiomyocytes; C2C12: murine skeletal myoblasts.