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用于提高他克莫司溶解度的氨基烷基甲基丙烯酸酯共聚物。I:固体分散体配方的评估。

Aminoalkyl methacrylate copolymers for improving the solubility of tacrolimus. I: Evaluation of solid dispersion formulations.

机构信息

Pharmaceutical Research and Technology Labs, Astellas Pharma Inc., 180 Ozumi, Yaizu, Shizuoka 425-0072, Japan.

出版信息

Int J Pharm. 2012 May 30;428(1-2):18-24. doi: 10.1016/j.ijpharm.2012.02.041. Epub 2012 Mar 3.

Abstract

The aim of this study was to investigate the effect of Eudragit E/HCl (E-SD) on the reprecipitation of a poorly water-soluble drug, tacrolimus. To evaluate the inhibition of reprecipitation of E-SD, reprecipitation studies on tacrolimus were conducted using a dissolution test method. Solubility of tacrolimus was measured at regular intervals in a dissolution media, in which tacrolimus was dissolved in ethanol, and the test media contained additives for inhibiting precipitation. Supersaturation profiles of tacrolimus were observed, and were maintained for 24h only with E-SD. Solid dispersion formulations of tacrolimus prepared with hydroxypropylmethylcellulose (HPMC) or E-SD in different drug/carrier ratios were also investigated. Solid dispersions prepared with E-SD showed higher solubility of tacrolimus compared with that of HPMC. In the E-SD formulation, the drug solubility influences to drug/carrier ratio. The formulation of drug/E-SD (1/5) showed the highest drug solubility. Thus, it may be inferred that a definite drug/carrier ratio exists to increase drug solubility. Further, by mixing E-SD the solid dispersion prepared with HPMC showed enhanced drug solubility.

摘要

本研究旨在探讨 Eudragit E/HCl (E-SD) 对难溶性药物他克莫司再沉淀的影响。为了评估 E-SD 对再沉淀的抑制作用,采用溶解试验法对他克莫司的再沉淀进行了研究。在溶解介质中定期测量他克莫司的溶解度,其中他克莫司溶解在乙醇中,试验介质中含有抑制沉淀的添加剂。观察到他克莫司的过饱和度曲线,仅用 E-SD 就可维持 24 小时。还研究了用羟丙甲纤维素(HPMC)或 E-SD 以不同药物/载体比制备的他克莫司固体分散体配方。用 E-SD 制备的固体分散体显示出比 HPMC 更高的他克莫司溶解度。在 E-SD 配方中,药物溶解度随药物/载体比的变化而变化。药物/E-SD(1/5)的配方显示出最高的药物溶解度。因此,可以推断存在一个确定的药物/载体比来增加药物溶解度。此外,通过混合 E-SD,用 HPMC 制备的固体分散体显示出增强的药物溶解度。

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