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以生物聚合物聚(3-羟基丁酸酯)为平台用于地塞米松控释的薄膜。

Films based on the biopolymer poly(3-hydroxybutyrate) as platforms for the controlled release of dexamethasone.

作者信息

Villegas Mercedes, Cid Alicia Graciela, Briones Cintia Alejandra, Romero Analía Irma, Pistán Florencia Alejandra, Gonzo Elio Emilio, Gottifredi Juan Carlos, Bermúdez José María

机构信息

Instituto de Investigaciones para la Industria Química, Universidad Nacional de Salta - Consejo Nacional de Investigaciones Científicas y Técnicas, Av. Bolivia 5150, Salta Capital 4400, Argentina.

Facultad de Ingeniería, Universidad Nacional de Salta, Av. Bolivia 5150, Salta Capital 4400, Argentina.

出版信息

Saudi Pharm J. 2019 Jul;27(5):694-701. doi: 10.1016/j.jsps.2019.04.004. Epub 2019 Apr 2.

Abstract

Controlled drug delivery aims to achieve an effective drug concentration in the action site for a desired period of time, while minimizing side effects. In this contribution, biodegradable poly(3-hydroxybutyrate) films were evaluated as a reservoir platform for dexamethasone controlled release. These systems were morphological and physicochemically characterized. release assays were performed for five different percentages of drug in the films and data were fitted by a mathematical model developed and validated by our research group. When the profiles were normalized, a single curve properly fitted all the experimental data. Using this unique curve, the dissolution efficiency (), the time to release a given amount of drug ( ), and the mean dissolution time were calculated. Furthermore, the dissolution rate, the initial dissolution rate ( and the intrinsic dissolution rate were determined. The mean value was 1.968 × 10% released/min, was about 14 days, and the was 59.6% at 14 days and 66.5% at 20 days. After 2 days, when approximately 40% of the drug was released, the dissolution rate decreased about 60% respect to the initial value. The poly(3-hydroxybutyrate) platforms behaved as an appropriate system to release and control the dexamethasone delivery, suggesting that they could be an alternative to improve drug therapy.

摘要

控释药物旨在在期望的时间段内在作用部位达到有效的药物浓度,同时将副作用降至最低。在本研究中,对可生物降解的聚(3-羟基丁酸酯)薄膜作为地塞米松控释的储库平台进行了评估。对这些系统进行了形态学和物理化学表征。对薄膜中五种不同药物百分比进行了释放测定,并通过我们研究小组开发和验证的数学模型对数据进行拟合。当曲线归一化后,一条单一曲线能很好地拟合所有实验数据。利用这条独特的曲线,计算了溶出效率()、释放给定剂量药物的时间()和平均溶出时间。此外,还测定了溶出速率、初始溶出速率()和固有溶出速率。平均释放速率为1.968×10%/分钟,约为14天,14天时溶出率为59.6%,20天时为66.5%。2天后,当约40%的药物释放时,溶出速率相对于初始值下降了约60%。聚(3-羟基丁酸酯)平台表现为一种合适的地塞米松释放和控释系统,表明它们可能是改善药物治疗的一种替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10a0/6598214/3c9a8fc30772/ga1.jpg

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