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2-甲基丙烯酰氧乙基磷酰胆碱与甲基丙烯酸正丁酯共聚物提高药物溶解度和吸收。

Enhancement of drug solubility and absorption by copolymers of 2-methacryloyloxyethyl phosphorylcholine and n-butyl methacrylate.

机构信息

Faculty of Pharmacy, Takasaki University of Health and Welfare, Takasaki, Japan.

出版信息

Drug Metab Pharmacokinet. 2011;26(1):79-86. doi: 10.2133/dmpk.dmpk-10-rg-070. Epub 2010 Nov 12.

DOI:10.2133/dmpk.dmpk-10-rg-070
PMID:21084766
Abstract

Poly[2-methacryloyloxyethyl phosphorylcholine-co-n-butyl methacrylate]s (PMBs) are water-soluble solid copolymers of 2-methacryloyloxyethyl phosphorylcholine (MPC) and n-butyl methacrylate with a molecular weight of 30,000 (PMB50T) or 100,000 (PMB100T). Here, we characterized the solubilizing properties of PMBs using miconazole (MCZ), vidarabine (Ara-A) and griseofulvin (GRF), which are class 2, 3 and 4 compounds, respectively, in the Biopharmaceutics Classification System (BCS). Moreover, we evaluated the enhancement of gastric absorption of GRF dissolved in PMB solutions and the toxicity of PMBs in rats. PMB50T solution dramatically increased the solubility of GRF and MCZ compared with Ara-A, and these drugs became more soluble as the concentration of PMB50T was increased. The solubility of GRF in 10% PMB solutions was higher than with any other tested aqueous solubilizer. When a solution of GRF (20 mg/10 mL/kg) in 10% PMB was orally administered to rats, GRF absorption was greatly increased compared with that following administration of a suspension in water or Gelucire. After repeated oral administration of PMBs once daily for 14 successive days, no organ lesions or changes in biochemical parameters were observed. Thus, the polymers are expected to be useful and safe solubilizers and oral absorption enhancers for poorly soluble lipophilic drugs.

摘要

聚[2-(甲基丙烯酰氧)乙基磷酰胆碱-co-正丁基甲基丙烯酸酯](PMB)是 2-(甲基丙烯酰氧)乙基磷酰胆碱(MPC)和正丁基甲基丙烯酸酯的水溶性固体共聚物,分子量为 30,000(PMB50T)或 100,000(PMB100T)。在这里,我们使用米康唑(MCZ)、阿昔洛韦(Ara-A)和灰黄霉素(GRF)来表征 PMB 的增溶特性,它们分别是生物药剂学分类系统(BCS)中的 2 类、3 类和 4 类化合物。此外,我们评估了 GRF 在 PMB 溶液中的胃吸收增强作用和 PMB 在大鼠中的毒性。与 Ara-A 相比,PMB50T 溶液显著增加了 GRF 和 MCZ 的溶解度,并且随着 PMB50T 浓度的增加,这些药物的溶解度更高。10% PMB 溶液中 GRF 的溶解度高于任何其他测试的水溶性增溶剂。当以 10% PMB 溶液(20 mg/10 mL/kg)口服给予 GRF 溶液时,与水悬浮液或 Gelucire 相比,GRF 吸收大大增加。连续 14 天每天口服给予 PMB 一次后,未观察到器官损伤或生化参数变化。因此,这些聚合物有望成为用于脂溶性差的药物的有用且安全的增溶剂和口服吸收增强剂。

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