地氯雷他定光分散膜的研制初探。

Özden Çakmakyapan, Fatma Nur Tuğcu Demiröz, Zeynep Şafak Teksin
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引用次数: 0

摘要

目的:口服分散膜(odf)是新一代的剂型,增加了患者的依从性,为许多患者群体,如儿童、老年、生理和精神疾病患者提供了给药的便利。本研究的目的是对含有低水溶性和氧化敏感性药物地氯雷他定(DL)的ODF进行初步研究。材料与方法:本研究采用溶剂铸造法制备的20种薄膜配方,对其配方、工艺参数及表征方法进行了研究。对膜的外观、力学性能、厚度、崩解时间和含量均匀性进行了表征。采用各种策略来提高DL在配方中的化学稳定性,从而选择合适的抗氧化剂,并使用差示扫描量热法进行形态和相容性研究。为了增加载药量,还对不同的膜组成进行了评价。结果:浇注高度为400 μm的初步配方均质良好,抗拉强度在6.21 ~ 10.34 MPa之间,柔韧性好,odf崩解时间小于60s。通过增加DL与所选组分在制剂中的溶解度,将载药量提高到所需水平的3%。结论:其中一种使能配方F20无颗粒,膜厚均匀性(相对标准偏差=4.6%)、含量均匀性(接受值=5)适宜。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preliminary Study on the Development of Orodispersible Film Containing Desloratadine.

Objectives: Orodispersible films (ODFs) are new-generation dosage forms that increase patient compliance, providing ease of drug administration in many patient groups, such as pediatric, geriatric, and patients with physiological and psychiatric disorders. The aim of this study was to conduct preliminary studies to develop ODF containing the poorly water-soluble and oxidation-sensitive drug desloratadine (DL).

Materials and methods: In this study, the formulation and process parameters, as well as the characterization method were investigated using 20 film formulations manufactured by the solvent casting method. The films were characterized in terms of their appearance, mechanical properties, thickness, disintegration time, and content uniformity. Various strategies have been applied to increase the chemical stability of DL in the formulations and, therefore to choose suitable antioxidants, and morphological and compatibility studies using differential scanning calorimetry were performed. For increasing drug loading, different film compositions were also evaluated.

Results: Among the preliminary formulations tested with a casting height of 400 μm, homogeneous, good mechanical properties with tensile strength values between 6.21-10.34 MPa, flexibility, and ODFs with a disintegration time of less than 60s ODFs were developed. By increasing the solubility of DL in the formulation with the selected components, the drug loading capacity was increased to 3% by the desired level.

Conclusion: One of the enabling formulations, F20, was particle-free with a suitable thickness uniformity (relative standard deviation =4.6%) and content uniformity (acceptance values =5) films were developed.

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