(4) Various additives complexing with PLGA with increased drug loading and/or sustained release profiles | ||||
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Additives | Encapsulated drug | Drug loading or EE | Drug release profile | References |
POE/PLGA | BSA | 9–11% and EE 60–90% | 95% over 30 days | Shi et al., 2003 |
POE/PLGA | Cyclosporin A | 6–10% and EE 60–90% | 14% over 15 days followed by 78% over the next 27 days | Shi et al., 2003 |
Alginate and chitosan-PLGA double walled | BSA | EE at 75% c.f. 65% compared with single-walled systems | 5–10% in 30 min c.f. 30% for single-walled systems | Zheng and Liang, 2010 |
Alginate-PLGA double walled | Metoclopramide HCl | EE increase from 30% to 60% c.f. single walled system | Improved release profile | Lim et al., 2013 |
4% w/w chitosan/PLGA | Resveratrol | EE 40–52% Particle size: 11 to 20 μm and more stable | Improved controlled release | Sanna et al., 2015 |
Caffeic acid grafted PLGA (g-CA-PLGA) | Ovalbumin | EE increased from 35 to 95% c.f. PLGA alone (size 15–50 μm) | Unchanged | Selmin et al., 2015 |
Mixed copolymer of PLGA 50:50 (Mr 100,000 and 14,000) 1:7 | Pentamidine | 23.7%, whereas only 9.8 and 13.9 %, when prepared with either of them alone | Produced microcapsules with desired release profiles | Graves et al., 2004 |
Aqueous core-PLGA shell | Risedronate sodium | 2.5-fold increase: 31.6% c.f. 12.7% for classical PLGA microspheres | Sustained release according to diffusion-controlled Higuchi model | Abulateefeh and Alkilany, 2015 |
Porous silicon oxide (pSiO2)-PLGA | Daunorubicin | Slightly increased loading (3.1–4.6%) c.f. 2.7% for PLGA-daunorubicin microspheres | A 2-5 fold longer duration of release c.f. PLGA-daunorubicin microspheres | Nan et al., 2014 |
BSA, Bovine serum albumin; EE, Encapsulation efficiency; hGH, Human growth hormone; Mr, Molecular weight; OHR1031, a small molecule for the treatment of glaucoma; PLA, poly(lactic acid); PLGA, poly(lactic-co-glycolic acid); POE, poly(ortho esters).