Review Article

Recent Trends in Preparation of Poly(lactide-co-glycolide) Nanoparticles by Mixing Polymeric Organic Solution with Antisolvent

Table 1

Summary of processing conditions of o/w emulsion methods and major characteristics of PLGA nanoparticles.

Polymer (grade)SolventPolymer (%)DrugD/PSize (nm)EE (%)Reference

RG502H (0.16–0.24 dL/g)DCM-DMSO2.5Amphotericin B5.615453[14]
PLGA50 : 50 (40–75 kDa)EA2Betamethasone-17-valerate6028185[15]
mPEG-PLGA (11 kDa)DCM2Bufalin516482 [16]
RG502H (7–17 kDa)DCM5β-Carotene10200∼8001[17]
PLGA75 : 25 (66–107 kDa)DCM-acetone0.1, 0.2Celecoxib25, 50115∼43631∼86[18]
PLGA50 : 50 (10 kDa)EA, PC2Coumarin-6556∼306.641∼52[19]
RG 50 : 50 H (40–75 kDa)EA-DCM2.5Cucumin10 16277[20]
RG 503 (n/a)DCM1.67Cyclosporine A2022090[21]
PLGA50 : 50 (20–23 kDa)DCM1Exemestanen/a16964[22]
PLGA50 : 50 (0.36∼037 dL/g)DCM3.3Haloperidol2.5∼552423∼37[23]
PLGA (n/a)DCM2.5∼5.0Nimesulide5∼10212∼28925∼100[24]
RH503 (35–40 kDa)EA1Paclitaxel512147[25]
PLGA50 : 50 (25 kDa)DCM2.5Paclitaxel531889[26]
Antibody-PLGA50 : 50 (40 kDa)Chloroform3Paclitaxel2031991[27]
R503H (0.32–0.44 dL/g)DCM5Pirfenidone5022531[28]
PLGA50 : 50 (40–100 kDa)DCM1.25∼5.0Praziquantel10∼30243∼36082[29]
mPEG-PLGA-PLL (n/a)DCM-TFE2Rhodamine119890[30]
PGA-PLGA (103.4 kDa)PC0.1Saquinavir10120∼30077[31]
PLGA (n/a)DCM1tPA0.1266∼32066∼71[32]
APRPG-PEG-PLA (n/a)DCM1Fumagillin analog513066[33]
PLGA85 : 15 (50–75 kDa)DCM12.5Voriconazole8∼100207∼6058∼63[34]

Note: n/a, not available, not specified.
Polymer %, polymer concentration in an organic solvent; D/P, the weight ratio of drug to polymer; EE, drug encapsulation efficiency; DCM, dichloromethane; DMSO, dimethylsulfoxide; EA, ethyl acetate; TFE, trifluoroethanol; PC, propyl carbonate; tPA, tissue-type plasminogen activator.