首页> 外文会议>Controlled Release Society annual meeting >COEFFECT OF AQUEOUS SOLUBILITY OF DRUGS AND GLYCOLIDE MONOMER ON INVITRO RELEASE RATES FROM POLY(D,L-LACTIDE-CO-GLYCOLIDE) DISCS ANDPOLYMER DEGRADATION
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COEFFECT OF AQUEOUS SOLUBILITY OF DRUGS AND GLYCOLIDE MONOMER ON INVITRO RELEASE RATES FROM POLY(D,L-LACTIDE-CO-GLYCOLIDE) DISCS ANDPOLYMER DEGRADATION

机译:药物和乙交酯单体的水溶性对聚(D,L-丙交酯-乙交酯)圆盘体外释放速率和聚合物降解的影响

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摘要

The objective of this study was to investigate theeffect of aqueous solubility of model drugs andglycolide monomer (GM) from 50:50 PLGA discs onin vitro release rates and polymer degradation. 5-Flurouracil (5-FU) release was found to be increasingin proportion to drug loading amount with an initialburst for 5 days, while dexamethasone (DEX)showed absolute antithesis release profiles. However,the discs containing GM showed faster release ratesthan control discs (without GM), respectively and didnot show lag periods during in vitro release test dueto GM.
机译:本研究的目的是研究50:50 PLGA光盘中模型药物和乙交酯单体(GM)的水溶性对体外释放速率和聚合物降解的影响。发现5-氟尿嘧啶(5-FU)释放与药物装载量成比例地增加,初始爆发持续5天,而地塞米松(DEX)显示绝对的对映体释放曲线。但是,含有GM的光盘分别比对照光盘(不含GM)显示出更快的释放速率,并且由于GM而在体外释放测试中没有显示滞后时间。

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