PLGA-PEG-PLGA hydrogel for ocular drug delivery of dexamethasone acetate

被引:96
|
作者
Gao, Yuan [1 ]
Sun, Yan [2 ]
Ren, Fuzheng [3 ]
Gao, Shen [1 ]
机构
[1] Second Mil Med Univ, Changhai Hosp, Shanghai 200433, Peoples R China
[2] Shanghai Inst Mat Med, Shanghai, Peoples R China
[3] E China Univ Sci & Technol, Shanghai 200237, Peoples R China
关键词
Dexamethasone; in situ gelling; ocular drug delivery; PLGA-PEG-PLGA; thermosensitive copolymer; BIODEGRADABLE BLOCK-COPOLYMERS; TRIBLOCK COPOLYMERS; THERMOREVERSIBLE GELATION; FORMING HYDROGELS; MICRODIALYSIS; PHARMACOKINETICS; SYSTEMS;
D O I
10.3109/03639041003680826
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Aim: This study aims to investigate the suitability of thermosensitive triblock polymer poly-(DL-lactic acid-co- glycolic acid) (PLGA)-polyethylene glycol (PEG)-PLGA as a matrix material for ocular delivery of dexamethasone acetate (DXA). Methods: The copolymer was synthesized and evaluated for its thermosensitive and gelation properties. DXA in situ gel-forming solution based on PLGA-PEG-PLGA copolymer of 20% (w/w) was prepared and evaluated for ocular pharmacokinetics in rabbit according to the microdialysis method, which was compared to the normal eye drop. Result: The copolymer with 20% (w/w) had a low critical solution temperature of 32 degrees C, which is close to the surface temperature of the eye. The C-max of DXA in the anterior chamber for the PLGA-PEG-PLGA solution was 125.2 mu g/mL, which is sevenfold higher than that of the eye drop, along with greater area under the concentration-time curves (AUC). Conclusion: These results suggest that the PLGA-PEG-PLGA copolymer is potential thermosensitive in situ gel-forming material for ocular drug delivery, and it may improve the bioavailability, efficacy of some eye drugs.
引用
收藏
页码:1131 / 1138
页数:8
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