Design and Optimization of Elanzapine Drug Release with Polyoxazoline Based Hydrogel

Zabiulllah Zalmay, Ruhullah Hanif, Shirullah Rahmani, Sayad Amiry, Wahidullah Enayat
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Abstract

Due to the fact that Elanzapine is prescribed orally and by injection for psychotic and schizophrenic disorders, and depending on the type of disease, these people are prevented from swallowing the drug; therefore, checking the injectable form of the drug with controlled release, which increases the release of the drug to one week with a single injection, is important. On the other hand, one of the most important biodegradable polymers that have the adhesive property of Elanzapine is Polyoxazoline, so the aim of this study is to design a slow release system, considering the short half-life of this drug and the need for a large number of doses and the patient's lack of cooperation for treatment. The drug is based on Polyoxazoline, which can reduce the consumption and, consequently, the toxicity and accumulation of the drug in the body. Mathematical heart direction, the forecast of different conditions will be presented, and also obtaining the optimal conditions and the final formulation is one of the main goals of this study. In this research, the release of olanzapine on the matrix loaded with olanzapine, the morphological characteristics of the matrix, the thermal characteristics of the matrix and the rheological characteristics of the matrix have been investigated. The release of olanzapine in the examined gels lasted for more than 168 hours, which was a sign of the slow release system, which is the main goal of this project. Several models were used to investigate the release kinetics of olanzapine, and among them, the Higuchi equation showed the best degree of regression with experimental data. By increasing the percentage of Elanzapine, the process of changes in viscosity goes out of the linear state; on the other hand, the difference between the optimum matrix viscosity of 3 and 4% of Elanzapine is small.
聚恶唑啉基水凝胶释放依氮平的设计与优化
由于依氮平是用于治疗精神病和精神分裂症的口服和注射处方,并且根据疾病的类型,这些人不能吞咽这种药物;因此,检查具有控释的药物的可注射形式是很重要的,这将药物的释放增加到单次注射一周。另一方面,聚恶唑啉是具有依氮平黏附性能的最重要的可生物降解聚合物之一,因此考虑到该药物半衰期短、需要大量剂量以及患者治疗缺乏配合,本研究的目的是设计一种缓释系统。该药物以聚恶唑啉为基础,可以减少消耗,从而减少药物在体内的毒性和积累。数学心脏方向,预测不同的条件将提出,并获得最优条件和最终配方是本研究的主要目标之一。在本研究中,研究了奥氮平在负载奥氮平的基质上的释放、基质的形态特征、基质的热特性和基质的流变特性。奥氮平在被测凝胶中的释放持续时间超过168小时,这是一个缓释系统的标志,这是本项目的主要目标。采用多种模型研究奥氮平的释放动力学,其中以Higuchi方程与实验数据的回归程度最好。通过增加依氮平的百分比,粘度的变化过程脱离线性状态;另一方面,依氮平的最佳基质粘度为3%和4%之间的差异很小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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