Elimination of Terbinafine Hydrochloride Antifungal Drug Traces from Water, Pharmaceutical Formulations and Blood Plasma using Low-Cost Bio and Synthetic Sorbents

Samah Ali, B. Alharbi, A. Mohamed
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引用次数: 1

Abstract

: Chitosan (CS) biosorbent and polyurethane foam (PUF) synthetic sorbent have been utilized to eliminate terbinafine hydrochloride (TRB HCl) antifungal drug in its pure and pharmaceutical forms from both contaminated aqueous and biological media using a batch process. The experimental conditions for efficient removal of TRB HCl for both CS and PUF were optimized depending on various experimental parameters such as the pH of the solution, contact periods, initial TRB HCl concentration, and sorbents dosage in the solution.SEM, FT-IR, and XRD characterizations were carried out to study the adsorption of a drug by both sorbents. The optimum conditions for removing TRB HCl by CS and PUF were achieved at a pH of 8.5 and a contact time of 60 min at 250 rpm, using 0.4 g for both sorbents. The measured spectrophotometric absorbance at λmax of TRB HCl was 242 nm. In addition, the zero-point charge (pHpzc) was determined for the studied sorbents. The pHpzc of the surface of sorbents has shown that electrostatic attraction is one of the mechanisms in TRB HCl sorption. The adsorption process was modeled using the pseudo-first-order, pseudo-second-order, Elovich, and intraparticle diffusion kinetic models. The results indicated that the adsorption of TRB HCl on CS and PUF does follow a pseudo-first-order type of reaction kinetics. The adsorption process was modeled using Langmuir and Freundlich isotherms. The adsorption data found that the Freundlich isotherm model was more suitable for the PUF sorbent, while the Langmuir isotherm model better fit the CS biosorbent.Evaluation of the experimental data using the Langmuir equation revealed that the maximum adsorption capacities of PUF and CS were 2.807 and 1.2297 mg. g-1, respectively. The solution was also used to estimate TRB HCl in its pharmaceutical form, and the assessed recoveries were 97.25 and 98.437% for CS and PUF, respectively. The proposed procedure was validated for other complex mediums by removing TRB HCl from spiked human blood plasma. In-silico aquatic toxicity forecast of TRB HCl was also carried out.
利用低成本生物和合成吸附剂去除水、制剂和血浆中的盐酸特比萘芬抗真菌药物痕迹
研究了壳聚糖(CS)生物吸附剂和聚氨酯泡沫(PUF)合成吸附剂对盐酸特比萘芬(TRB HCl)抗真菌药物的间歇处理。根据溶液的pH、接触时间、初始TRB HCl浓度和溶液中吸附剂的用量等实验参数,对CS和PUF有效去除TRB HCl的实验条件进行了优化。通过SEM, FT-IR和XRD表征研究了两种吸附剂对药物的吸附作用。CS和PUF去除TRB HCl的最佳条件为pH为8.5,接触时间为60 min,转速为250 rpm,两种吸附剂用量均为0.4 g。测得TRB HCl在λmax处的吸光度为242 nm。此外,还测定了所研究吸附剂的零点电荷(pHpzc)。吸附剂表面的pHpzc表明静电吸引是吸附TRB HCl的机理之一。采用拟一阶、拟二阶、Elovich和颗粒内扩散动力学模型对吸附过程进行了建模。结果表明,TRB HCl在CS和PUF上的吸附符合准一级反应动力学。采用Langmuir等温线和Freundlich等温线模拟了吸附过程。吸附数据发现Freundlich等温线模型更适合PUF吸附剂,Langmuir等温线模型更适合CS生物吸附剂。用Langmuir方程对实验数据进行评价,PUF和CS的最大吸附量分别为2.807和1.2297 mg。分别g1。该溶液还用于测定药物形式的盐酸三氯甲烷(TRB HCl), CS和PUF的回收率分别为97.25%和98.437%。通过从人血浆中去除TRB HCl,验证了该方法在其他复杂培养基中的有效性。对TRB HCl的水生毒性进行了计算机预测。
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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