Table 1. Summary of different drug carriers integrated into microfluidic platforms.
Drug Carrier Type | Main Material | Size | Synthetic Method | Drug | Target/Application | Ref. | ||
---|---|---|---|---|---|---|---|---|
Microcapsules | P(NIPAM-co-AAPBA-co-AAc) | ID ∼240 μm; OD ∼360 μm | Microfluidic double emulsion | Rhodamine B; insulin | Glucose-responsive controlled release | [99] | ||
PAA-b-PMMA | OD ∼120-150 μm | Microfluidic double emulsion | -- | pH-responsive controlled release | [100] | |||
PDM | ID ∼294 μm; OD ∼402 μm | Microfluidic double emulsion | -- | pH-responsive controlled release | [101] | |||
Alginate; chitosan | OD 472-740 μm | Electrostatic microfluidic droplets | Ampicillin; diclofenac | pH-responsive controlled release; Dual-drug carriers | [102] | |||
Ca-alginate | OD 60-105 μm | gradient-microfluidic droplets | BSA | Pharmaceutical area; Therapeutic proteins | [103] | |||
Ca-alginate | ID ∼383 μm; OD ∼467 μm | Microfluidic double emulsion | BSA | Pharmaceutical area; Therapeutic proteins | [104] | |||
PVA, PCL, PEG | OD 23-47 μm | Microfluidic double emulsion | BSA | Pharmaceutical area; Therapeutic proteins | [105] | |||
PAH, PSS, FITC | OD 50-80 μm | Microfluidic droplet merging and droplet storage functions | MnCO3 | Drug effects on specific cells | [106] | |||
Nanoemulsions | Six dietary lipids (corn oil, canola oil, olive oil, palm oil, coconut oil, MCTs) | ∼160-180 nm | Micro-fluidization | BC | Caco-2 cells | [133] | ||
Labrafil M, Tween 80, ethanol | ∼30-50 nm | Spontaneous emulsification | AB | Heart | [134] | |||
Soybean oil, PEGylated lipids, oleic acid-coated FeO, Cy7 | 50 nm | Immediate evaporation | PAV | Kidney, liver | [138] | |||
PFPE | 180 nm | Self-assembly and high energy emulsification | Celecoxib | FSDCs | [139] | |||
PAM | 20-32 nm | Rapid microfluidic mixing | Ketoprofen | Gastro intestinal tract | [140] | |||
NPs | Lipid NPs | POPC, cholesterol, triglyceride triolein | 20-50 nm | Rapid microfluidic mixing | Doxorubicin | Pharmaceutical area | [132] | |
DLinKC2-DMA, phospholipid, cholesterol, PEG | ∼80 nm | Rapid microfluidic mixing | siRNA | Therapeutic siRNA | [152] | |||
Polymer NPs | Chitosan | 75-122 nm | Rapid microfluidic mixing | Paclitaxel | Anticancer drug | [155] | ||
Chitosan | ∼73-216 nm | Rapid microfluidic mixing | Paclitaxel | Anticancer drug | [156] | |||
Chitosan | 200-300 nm | Rapid microfluidic mixing | Clindamycin phosphate; tretinoin | Transdermal multidrug delivery | [157] | |||
PLGA-PEG | 25-200 nm | Rapid microfluidic mixing | Docetaxel | Drug discovery and clinical translation | [175] | |||
Ag@CD NPs | 20-60 nm | Conventional method | Dihydro-artemisinin | Monitoring of drug effect on cancer cells | [177] | |||
Carboxymethyl chitosan, PAMAM dendrimer | ∼50 nm | Conventional method | -- | Monitoring of drug effect on cancer cells | [178] | |||
Nano-sized polymeric conjugates | FA, RA | 130 nm | Rapid microfluidic mixing | Heparin | KB and A549 cells | [169] | ||
PEG, PCL, PEI | 179 ± 11 nm | Rapid microfluidic mixing | siRNA | SKOV3 cells | [171] | |||
Hybrid NPs | PLGA, cholesterol | ∼103-106 nm | Rapid microfluidic mixing | Doxorubicin; combretastatin A4 | Anticancer drug | [174] |
Note, chemical structures and formulas of small molecular drugs are shown in supplementary Table S2.