用于控制药物释放的壳聚糖-TPP 微胶囊

Yaridé Pérez-Pacheco, Tiziano Alimandi, B. Tylkowski, M. Sisteré, R. García-Valls
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摘要

通过喷雾干燥法生产壳聚糖/三聚磷酸钠(CS/TPP)微胶囊,需要将含有壳聚糖、三聚磷酸钠、乙酸(AcOH)和叶酸(FA)的乳液雾化成细小液滴,暴露在高温、低压气流中。溶剂在干燥室内蒸发,形成固体颗粒。喷雾干燥法对于制造固体 CS/TPP 微胶囊非常有价值。通过精确调整设备参数(如入口温度和气体流速),可以研究微胶囊的形态、尺寸和特性。这种适应性允许根据特定的 pH 溶解范围进行定制。通过修改喷雾干燥器参数(包括入口温度和吸气压力),研究了生产方法对 CS/TPP 微胶囊的影响,从而加深了对其在不同生产条件下溶液行为的理解。在壳聚糖给药系统中,有多种方法可以封装叶酸等药剂,叶酸是癌症治疗药物甲氨蝶呤的类似物。药剂可以在交联前添加到壳聚糖溶液中,也可以在与壳聚糖预先混合的凝胶诱导剂中加入,或者包含在交联混合物中。实验评估了 CS/TPP 微胶囊在封装叶酸等药物时的行为。分析了释放曲线,以了解其药物输送能力和作为控释载体的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chitosan-TPP microcapsules for controlled drug release
Production of chitosan/sodium tripolyphosphate (CS/TPP) microcapsules via spray drying involves atomizing an emulsion containing CS, TPP, acetic acid (AcOH), and folic acid (FA) into fine droplets exposed to high-temperature, low-pressure gas flow. Solvent evaporation within the drying chamber leads to solid particle formation. Spray drying is valuable for creating solid CS/TPP microcapsules. Precise equipment parameter adjustments, like inlet temperature and gas flow rate, enable the study of microcapsule morphology, size, and properties. This adaptability allows for customization to specific pH dissolution ranges. The production method's impact on CS/TPP microcapsules was studied by modifying spray drier parameters, including inlet temperature and aspirator pressure, to enhance understanding of their behavior in solution under varied production conditions. In chitosan delivery systems, various approaches can encapsulate drug agents like folic acid, an analog to the cancer treatment drug methotrexate. Agents can be added to the chitosan solution pre-crosslinking, incorporated into gelation-inducing agents pre-mixing with chitosan, or included in the crosslinking mixture. Experiments were conducted to assess CS/TPP microcapsules' behavior when encapsulating agents like folic acid. Release profiles were analyzed to understand their drug delivery capabilities and potential as controlled release carriers.
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