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Merck
  • PLGA-PEG-PLGA hydrogel for ocular drug delivery of dexamethasone acetate.

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

Drug development and industrial pharmacy (2010-03-26)
Yuan Gao, Yan Sun, Fuzheng Ren, Shen Gao
摘要

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). 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. 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 microg/mL, which is sevenfold higher than that of the eye drop, along with greater area under the concentration-time curves (AUC). 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.

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Sigma-Aldrich
地塞米松 21-乙酸酯, ≥99%
醋酸地塞米松, European Pharmacopoeia (EP) Reference Standard