Effect of CaCl2 Crosslinker Concentration On The Characteristics, Release and Stability of Ciprofloxacin HCl-Alginate-Carrageenan Microspheres

Amiruddin, Muh. Agus Syamsur Rijal, Dewi Melani Hariyadi
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Abstract

Background: Ciprofloxacin HCl is a broad-spectrum fluoroquinolone antibiotic that has the lowest MIC against Mycobacterium tuberculosis but has limitations in oral use, so inhalation microspheres are made. Objective: This study aimed to investigate the effect of CaCl2 crosslinker concentration on the characteristics, release and stability of ciprofloxacin-alginate-carrageenan microspheres. Methods: Microspheres were prepared by ionotropic gelation using aerosolization with calcium chloride 0.5M (F1), 1.0M (F2), 1.5M (F3), 2.0M (F4) as crosslinker and then dried using freeze dryer. Results: Ciprofloxacin-alginate-carrageenan microspheres formed of yellowish-white powder, smooth morphology and excellent flow properties with the particle size of less than 5µm, drug loading and entrapment efficiency were between    2.05% - 2.42% and 75.34% - 98.09%, yield was between 84.69% - 97.57%, moisture content of less than 10%. Ciprofloxacin-alginate-carrageenan microspheres with 1.5M crosslinker (F3) was the optimal formula. For 12 hours, ciprofloxacin released was 49.89% - 63.78% at pH 7.4, and the kinetics of drug release showed that of Korsmeyer-peppas with a mechanism based on fickian diffusion. The microspheres were discovered to be stable for up to 28 days of storage. Conclusion: The increased concentration of the CaCl2 crosslinker from 0.5M to 2.0M decreased the particle size and drug release but increased the yield, drug loading and entrapment efficiency.
CaCl2 交联剂浓度对盐酸环丙沙星-藻酸盐-卡拉胶微球的特性、释放和稳定性的影响
背景:盐酸环丙沙星是一种广谱氟喹诺酮类抗生素:盐酸环丙沙星是一种广谱氟喹诺酮类抗生素,对结核分枝杆菌的 MIC 值最低,但口服使用有局限性,因此制成了吸入微球。研究目的本研究旨在探讨 CaCl2 交联剂浓度对环丙沙星-精氨酸-卡拉胶微球的特性、释放和稳定性的影响。制备方法以氯化钙 0.5M (F1)、1.0M (F2)、1.5M (F3)、2.0M (F4) 作为交联剂,采用离子凝胶法制备微球,然后用冷冻干燥机干燥。结果结果表明:环丙沙星-阿糖胞苷-卡拉胶微球为黄白色粉末,形态光滑,流动性好,粒径小于 5µm,载药量和包埋效率分别为 2.05% - 2.42% 和 75.34% - 98.09%,得率为 84.69% - 97.57%,含水量小于 10%。含有 1.5M 交联剂的环丙沙星-阿胶酸盐-卡拉胶微球(F3)是最佳配方。在 pH 值为 7.4 的条件下,12 小时内环丙沙星的释放量为 49.89% - 63.78%,药物释放动力学显示为 Korsmeyer-peppas 动力学,其机制是基于费克扩散。研究发现,这种微球在 28 天的储存期内都很稳定。结论将 CaCl2 交联剂的浓度从 0.5M 增加到 2.0M,会减小微球的粒径和药物释放量,但会增加微球的产量、载药量和包埋效率。
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