AG-331注射用冻干粉的产品开发。

C C Chiang, D Fessler, K Freebern, R Thirucote, P Tyle
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引用次数: 0

摘要

AG-331是一种潜在抗癌药物的水溶性葡萄糖酸盐,是用一种被称为“基于蛋白质结构的药物设计”的技术合成的。研制了一种含有44.4% (w/w) AG-331、55.6% (w/w)甘露醇和微量水的冻干制剂,用于AG-331的肠外给药。预冻干溶液含有2.0% (w/v)的AG-331和2.5% (w/v)的甘露醇,可通过常用的0.2微米过滤器进行无菌过滤,没有明显的AG-331损失。选用聚四氟乙烯(PTFE)膜作为过滤材料。冻干产品在加速条件下至少稳定6个月。该产品可以用γ辐照灭菌。5%葡萄糖注射液中AG-331重组溶液在5℃和30℃下在PVC输液袋中至少稳定2天。
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Product development of AG-331 lyophilized powder for injection.

AG-331, a water-soluble glucuronate salt of a potential anticancer drug, was synthesized using a technology described as "Protein Structure-based Drug Design." A lyophilized product containing 44.4% (w/w) of AG-331, 55.6% (w/w) of mannitol and trace of water was developed for parenteral delivery of AG-331. The pre-lyophilized solution, which contains 2.0% (w/v) of AG-331 and 2.5% (w/v) mannitol can be aseptically filtered through commonly used 0.2-micron filters without significant AG-331 loss. The filter of choice was made of PTFE (polytetrafluoroethylene) membrane. The lyophilized product is stable under accelerated conditions for at least 6 months. The product can be sterilized with gamma-irradiation. The AG-331 reconstituted solution in 5% Dextrose Injection, USP is stable in PVC infusion bags for at least 2 days at 5 degrees C and 30 degrees C.

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