Development of Resistant Starch-Pectin Microsphere for Improving Oral Colon-specific Drug Delivery of 5-Fluorouracil

Nushrat Jahan Ema, S. Hossain, S. Shahriar, M. Islam, J. A. Chowdhury
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Abstract

Conventional chemotherapy is ineffective for colorectal cancer as the drug moiety does not reach its intended site. 5-Fluorouracil (5-FU) microspheres aimed at colon-specific drug delivery have been developed by using the solvent evaporation technique in this study. The influence of utilizing different percentages of resistant starch-pectin polymer on the drug loading, encapsulation efficiency, and release behavior of the drug was investigated. The characterization of prepared microspheres was done by shape, surface morphology, drug loading, encapsulation efficiency and in vitro drug release studies. Drug-polymer interactions and drug stability were investigated by Differential Scanning Calorimetry (DSC) and FTIR spectroscopy. The 5-Fluorouracil polymeric microspheres that were formulated utilizing a resistant starch (RS) and pectin polymer displayed ideal physicochemical properties and spherical particles. The targeted microspheres demonstrated a high drug loading, encapsulation efficiency, and a satisfactory drug release pattern over the time period of 8 hours. Studies on drug release conducted under conditions that simulate stomach to colon transit have demonstrated that the drug was prevented from being released in the physiological conditions of the stomach and small intestine. Creating a new multiparticulate system using RS-pectin microspheres in order to forecast the protection that the combination might provide to the dosage form that will ensure localized drug release in the colon. Finally, it was found that the 5-Fluorouracil polymeric microsphere is a suitable microcarrier for effective colon-specific drug delivery tools with increased chemotherapeutic efficacy. Bangladesh Pharmaceutical Journal 26(1): 36-44, 2023 (January)
改善5-氟尿嘧啶口服结肠特异性给药的耐药淀粉-果胶微球的研制
常规化疗对结直肠癌无效,因为药物部分未到达预定部位。本研究利用溶剂蒸发技术制备了5-氟尿嘧啶(5-FU)微球,用于结肠特异性给药。研究了使用不同比例的抗性淀粉-果胶聚合物对药物的载药量、包封效率和释放行为的影响。通过微球的形状、表面形貌、载药量、包封率和体外释药研究对制备的微球进行表征。采用差示扫描量热法(DSC)和傅里叶红外光谱(FTIR)研究了药物-聚合物相互作用和药物稳定性。利用抗性淀粉(RS)和果胶聚合物配制的5-氟尿嘧啶聚合物微球具有理想的物理化学性质和球形颗粒。该微球具有较高的载药量和包封效率,在8小时内具有良好的释药模式。在模拟胃到结肠转运的条件下进行的药物释放研究表明,药物在胃和小肠的生理条件下被阻止释放。使用rs -果胶微球创建一个新的多颗粒系统,以预测该组合可能为剂型提供的保护,以确保药物在结肠中的局部释放。最后,我们发现5-氟尿嘧啶聚合物微球是一种合适的微载体,可以作为有效的结肠特异性药物递送工具,提高化疗疗效。孟加拉国医药杂志26(1):36- 44,2023(1月)
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