KURUTMA SICAKLIĞININ KURKUMİN VE PİPERİN ÇÖZÜNMESİNE VE KATI DİSPERSİYON BAZLI MİKROPARTİKÜLLERİN SALINIM KİNETİĞİNE ETKİLERİ: BİR ÖN ÇALIŞMA

Q4 Pharmacology, Toxicology and Pharmaceutics Ankara Universitesi Eczacilik Fakultesi Dergisi Pub Date : 2023-08-25 DOI:10.33483/jfpau.1253561
Monica Octaviani Tiara Dewi̇, Dewi Setyani̇ngsi̇h
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Abstract

Objective: One of the major challenges in developing curcumin as a pharmaceutical agent is its low bioavailability after oral administration. Co-administration of curcumin-piperine combined with employing solid dispersions (SD) approach has been shown to enhance curcumin dissolution and bioavailability. Understanding the influence of the processing temperature during spray drying is crucial in SDs preparations; the purpose of this study is to inquire the effect of inlet temperature spray-dryer on dissolution behavior and the best-fit kinetic model of dissolution itself. Material and Method: The SD powder was prepared using a spray-drying method by varying the inlet temperature (105°C; 115°C; 125°C) and involved polyvinyl alcohol (PVA) as a carrier. The SD were prepared at 30% Curcuma longa and 10% Piper nigrum extracts. Yield (%) of the dried powder resulted from the spray drying process was monitored, and dissolution behavior of curcumin and piperine were analyzed using a dissolution efficiency (DE) value. Furthermore, mathematical model describing the release mechanism of curcumin and piperine from the dissolution were evaluated using a DDSolver software. Result and Discussion: The variation of drying temperature on the spray dryer affects the dissolution behavior and the % yield of the PVA-based SD containing C. longa and P. nigrum extract. The most ideal mathematical model of kinetic release for curcumin and piperine were the Quadratic model, indicating that the mechanism of dissolution is diffusion through a gap between the PVA particle and the surrounding medium.
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目的:开发姜黄素作为药物制剂的主要挑战之一是其口服后的生物利用度低。姜黄素-哌啶联合应用固体分散体(SD)方法已被证明可以提高姜黄素的溶解性和生物利用度。了解喷雾干燥过程中加工温度的影响对SDs的制备至关重要;本研究的目的是探讨入口温度喷雾干燥器对溶解行为的影响以及溶解本身的最佳拟合动力学模型。材料和方法:采用喷雾干燥法,通过改变入口温度(105°C;115°C;125°C),以聚乙烯醇(PVA)为载体制备SD粉末。SD是用30%的姜黄和10%的胡椒提取物制备的。监测喷雾干燥过程产生的干燥粉末的产率(%),并使用溶解效率(DE)值分析姜黄素和胡椒碱的溶解行为。此外,使用DDSolver软件评估了描述姜黄素和哌啶从溶解中释放机制的数学模型。结果与讨论:喷雾干燥器干燥温度的变化会影响PVA基SD的溶解行为和产率。姜黄素和胡椒碱最理想的动力学释放数学模型是二次模型,表明溶解机制是通过PVA颗粒和周围介质之间的间隙扩散。
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来源期刊
Ankara Universitesi Eczacilik Fakultesi Dergisi
Ankara Universitesi Eczacilik Fakultesi Dergisi Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
0.80
自引率
0.00%
发文量
70
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