以羧甲基-卡帕-卡拉胶-壳聚糖为载体的聚电解质复合物持续给药的人工神经网络建模

S. Lefnaoui, S. Rebouh, M. Bouhedda, M. M. Yahoum, S. Hanini
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引用次数: 6

摘要

由带相反电荷的生物聚合物结合形成的聚电解质复合物(PECs)已被证明是开发药用辅料的一种广泛使用的方法。本研究的目的是利用人工神经网络(ANN)模拟抗高血压活性药物缬沙坦从羧甲基卡帕卡拉胶(CMKC)和壳聚糖(CTS)合成的PEC基质片中的缓释谱。用人工神经网络预测和描述了动力学释放曲线和速率。已经开发了几种配方,并对粉末混合物的药效学和流变性能进行了研究。流变试验表明,该材料具有良好的流动性和压实性。Carr指数和Hausner指数表示的可压缩性百分比表明具有良好的流动性。直接压缩粉末混合物后得到的片剂在最佳压缩力下显示出可接受的硬度和脆性水平。体外溶出试验结果表明,缬沙坦的释放动力学主要取决于形成片剂的亲水性基质中PEC的浓度。对人工神经网络模型进行了优化,得到了$2.09\乘以10^{-17}$的均方根值。本研究证实了人工神经网络在药物释放剂型开发中的作用,它可以描述制剂参数与药物释放谱之间的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Artificial Neural Network Modeling of Sustained Antihypertensive Drug Delivery using Polyelectrolyte Complex based on Carboxymethyl-kappa-carrageenan and Chitosan as Prospective Carriers
The polyelectrolyte complexes (PECs) formed by the combination of opposing charge biopolymers proves to be a widely used method for the development of excipients for pharmaceutical use. The aim of this work is the use of an artificial neural network (ANN) to modeling the prolonged release profile of an antihypertensive active agent: Valsartan from a matrix tablet formed from PEC based on carboxymethyl-kappa-carrageenan (CMKC) and chitosan (CTS). ANN is used to predict and describe the kinetic release profile and rate. Several formulas have been developed and a study of the pharmacotechnical and rheological properties of pulverulent mixtures has been carried out. Rheological tests showed satisfactory flowability and compaction. The percentage of compressibility expressed by the Carr index and the Hausner index indicates a good flowability. The tablets obtained after direct compression of the pulverulent mixtures showed acceptable levels of hardness and friability at optimum compression forces. The results of the in vitro dissolution test showed that the release kinetics of Valsartan depend essentially on the concentration of PEC in the hydrophilic matrix forming the tablets. The ANN model is optimized and a root mean square value of the order of $2.09\times 10^{-17}$ is reached. In this work, the efficacy of ANN to contribute to the development of release dosage forms has been demonstrated, it could describe the relationship that connect the formulation parameters and the drug release profile.
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