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

机译:药物和乙酰胺单体对来自聚(D,L-丙交酯 - 共乙酰化)圆盘和聚合物降解的体外释放速率的水溶性的系数

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摘要

The objective of this study was to investigate the effect of aqueous solubility of model drugs and glycolide monomer (GM) from 50:50 PLGA discs on in vitro release rates and polymer degradation. 5- Flurouracil (5-FU) release was found to be increasing in proportion to drug loading amount with an initial burst for 5 days, while dexamethasone (DEX) showed absolute antithesis release profiles. However, the discs containing GM showed faster release rates than control discs (without GM), respectively and did not show lag periods during in vitro release test due to GM.
机译:本研究的目的是探讨模型药物和乙酰胺单体(GM)的水溶性从50:50 PLGA圆盘对体外释放率和聚合物降解的影响。 5-鳞片(5-FU)释放的释放与药物负载量成比例地增加,初始爆发5天,而DexameLasone(DEX)显示出绝对的抗衡释放曲线。然而,含有GM的光盘分别显示出比对照盘(没有GM)的速度释放率更快,并且在由于GM的体外释放试验期间没有显示出滞后期。

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