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Calcium Chloride Modified Alginate Microparticles Formulated by the Spray Drying Process: A Strategy to Prolong the Release of Freely Soluble Drugs

机译:通过喷雾干燥过程配制的氯化钙改性海藻酸盐微粒:延长可自由溶解的药物释放的策略

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摘要

Alginate (ALG) cross-linking by CaCl2 is a promising strategy to obtain modified-release drug delivery systems with mucoadhesive properties. However, current technologies to produce CaCl2 cross-linked alginate microparticles possess major disadvantages, such as a poor encapsulation efficiency of water-soluble drugs and a difficulty in controlling the process. Hence, this study presents a novel method that streamlines microparticle production by spray drying; a rapid, continuous, reproducible, and scalable technique enabling obtainment of a product with low moisture content, high drug loading, and a high production yield. To model a freely water-soluble drug, metformin hydrochloride (MF) was selected. It was observed that MF was successfully encapsulated in alginate microparticles cross-linked by CaCl2 using a one-step drying process. Modification of ALG provided drug release prolongation—particles obtained from 2% ALG cross-linked by 0.1% CaCl2 with a prolonged MF rate of dissolution of up to 12 h. Cross-linking of the ALG microparticles structure by CaCl2 decreased the swelling ratio and improved the mucoadhesive properties which were evaluated using porcine stomach mucosa.
机译:藻酸盐(ALG)CaCl2的交联是具有粘膜粘附性质的改性释放药物递送系统的有希望的策略。然而,产生CaCl2交联藻酸盐微粒的当前技术具有主要的缺点,例如水溶性药物的封装效率差,难以控制过程。因此,本研究提出了一种新的方法,其通过喷雾干燥流动微粒产生;一种快速,连续,可重复和可伸缩的技术,可获得具有低水分含量,高药物载荷和高产量的产品。为了模拟自由水溶性药物,选择盐酸二甲双胍(MF)。观察到MF使用一步干燥过程成功地包装在CaCl 2交联的海藻酸盐微粒中。 ALG的改性提供了从2%ALG获得的药物释放延长颗粒,其交叉连接的0.1%CaCl 2,延长的MF溶解速率最高12小时。通过CaCl2的ALG微粒结构的交联减少了溶胀比,并改善了使用猪胃粘膜评价的粘膜粘附性质。

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