利用盒式贝肯设计设计、优化和表征用于牙周炎局部给药的盐酸二甲双胍载体生物可降解微球

M. Gambhire, V. Gambhire, Abhijit Kulkarni, R. Dolas, Anuja Mulay, Manali Bhide
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摘要

本研究制备了盐酸二甲双胍微球,用于填充到有或没有植牙的牙周袋中,以治疗牙周炎。为此,研究人员选择壳聚糖作为聚合物,并采用乳液交联法以不同的药物/聚合物比例制备微球。通过实施三因素、三水平盒-贝肯设计进行了优化。通过回归分析生成了粒度(PS)和包埋效率(EE)响应的数学模型。实验设计考虑到了在微球制剂的最佳工艺条件下,通过减少化学品用量和制剂时间,以经济的方式制备出EE%最大、PS最小的优化配方。根据可取函数选择了优化配方,并进一步评估了粒度、包埋效率、体外药物释放、差示扫描量热法(DSC)、傅立叶变换红外光谱(FTIR)和表面形态研究。对释放研究结果进行了动力学和统计学评估。发现所选批次的粒度和夹带效率分别在 40.2 至 59.6 μm 和 85 至 95% 之间。DSC 研究显示药物分子分散并转化为无定形形式。扫描电子显微镜(SEM)分析了微球的表面形态,发现微球呈球形,表面光滑。优化批次的平均粒径、EE 和体外药物释放率分别为 51.4 ± 4.8 μm、96.5 ± 1.42% 和 79.8 ± 3.1%。释放动力学表明,释放遵循 Peppas 模型,药物释放的主要机制是扩散。这些缓释壳聚糖微球可作为局部给药盐酸二甲双胍治疗牙周炎的给药系统。
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Design, Optimization and Characterization of Metformin Hydrochloride Loaded Biodegradable Microspheres using Box Behnken design for Local Delivery in Periodontitis
In the present study, metformin hydrochloride-loaded microspheres were prepared for filling into the periodontal pockets with or without grafts for the treatment of periodontitis. For this purpose, chitosan was chosen as a polymer and used at different drug/polymer ratios in the preparation of microspheres by emulsion cross-linking method. Optimization was carried out by implementing a three-factor, three-level Box–Behnken design. Mathematical models were generated by regression analysis for responses of particle size (PS) and entrapment efficiency (EE). The experimental design took into account the preparation of optimized formulation with maximum %EE and minimum PS at optimum process conditions for the microsphere formulation by reducing chemical use and formulation time, in an economical way. The optimized formulation was selected on the basis of the desirability function and was further evaluated with respect to the particle size, entrapment efficiency, in-vitro drug release, differential scanning calorimetry (DSC), fourier transform infrared (FTIR) spectroscopy and surface morphology studies. The results of release studies were evaluated kinetically and statistically. Particle size and entrapment efficiency of the selected batch were found to be in the range of 40.2 to 59.6 μm and 85 to 95%, respectively. The DSC studies revealed molecular dispersion and conversion of the drug into an amorphous form. Surface morphology of microspheres was analyzed by scanning electron microscopy (SEM) and found to be spherical in shape with a smooth surface. The mean particle size, EE, and in-vitro drug release of the optimized batch were found to be 51.4 ± 4.8 μm, 96.5 ± 1.42%, and 79.8 ± 3.1%, respectively. The release kinetics showed that the release followed the Peppas model, and the main mechanism of drug release was diffusion. These sustained-release chitosan microspheres could be a promising drug delivery system for local delivery of metformin hydrochloride in the treatment of periodontitis.
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