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可溶胀和惰性聚合物混合物基质的压缩特性、药物释放动力学和前沿运动研究。II. 不同甲氧基/羟丙基取代度的 HPMC 的影响。

Compaction properties, drug release kinetics and fronts movement studies from matrices combining mixtures of swellable and inert polymers. II. Effect of HPMC with different degrees of methoxy/hydroxypropyl substitution.

机构信息

Dpto. Farmacia y Tecnología Farmacéutica, Facultad de Farmacia, Universidad de Sevilla, C/Profesor García González n 2, 41012 Sevilla, Spain.

出版信息

Int J Pharm. 2010 Mar 15;387(1-2):56-64. doi: 10.1016/j.ijpharm.2009.12.001. Epub 2009 Dec 5.

Abstract

The aim of this paper is the modification of the release behaviour of hydrophilic HPMC-based matrices of different substitution degree (E4M, F4M, K4M) by the introduction of a new inert polymeric excipient hydroxypropylcellulose-methyl methacrylate (HCMMA) at different proportions (75:25, 50:50 and 25:75). The product (HCMMA) was dried either in a vacuum oven--OD copolymers--or freeze-dried-FD copolymers. HPMC E4M formulations showed the worst compaction properties. All mixtures presented a percentage of theophylline release between 47% and 32% at 1440 min. The drying methods employed had only influence over the drug release in E4M and K4M formulations, at higher proportions of HCMMA, showing the highest release the mixtures containing OD-HCMMA. Combinations of diffusion and erosion release mechanisms were found to matrix tablets. All mixtures with F4M did not modify relaxation rate constant values of Peppas and Shalin equation (k(r)) respect to F4M 100%. However, all mixtures with K4M showed the highest k(r) values, which decreased when HCMMA proportion decreased. Only K4M mixtures showed a different diffusion front movement than the other mixtures. The modulation of theophylline monoaxial release was obtained using a high percentage of HCMMA, and HPMCs with a substantial difference of hydroxypropyl groups (F4M and K4M or E4M).

摘要

本文的目的是通过在不同比例(75:25、50:50 和 25:75)下引入新的惰性聚合物赋形剂羟丙甲纤维素-甲基丙烯酸甲酯(HCMMA)来修饰不同取代度的亲水性 HPMC 基质(E4M、F4M、K4M)的释放行为。将产物(HCMMA)在真空烘箱(OD 共聚物)或冷冻干燥(FD 共聚物)中干燥。HPMC E4M 制剂表现出最差的压缩性能。所有混合物在 1440 分钟内的茶碱释放百分比在 47%到 32%之间。所采用的干燥方法仅对 E4M 和 K4M 制剂中的药物释放有影响,在 HCMMA 比例较高时,OD-HCMMA 混合物的释放最高。发现扩散和侵蚀释放机制组合存在于基质片剂中。所有与 F4M 混合的混合物均未改变 Peppas 和 Shalin 方程(k(r))的 Peppas 和 Shalin 方程(k(r))的松弛率常数值(k(r))相对于 F4M 100%。然而,所有与 K4M 混合的混合物均显示出最高的 k(r)值,当 HCMMA 比例降低时,k(r)值降低。只有 K4M 混合物显示出与其他混合物不同的扩散前沿运动。使用 HCMMA 的高比例和羟丙基基团有很大差异的 HPMCs(F4M 和 K4M 或 E4M)来调节茶碱单轴释放。

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