水凝聚法制备盐酸地尔硫卓酪蛋白-壳聚糖微球

M.A. Bayomi, S.A. Al-Suwayeh, A.M. El-Helw, A.F. Mesnad
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引用次数: 89

摘要

采用胶体凝聚法制备了含盐酸地尔硫卓(DTZ)的酪蛋白-壳聚糖缓释微球。壳聚糖溶液(5% v/v)与酪蛋白溶液(0.5 M氢氧化钠)的相互作用是微球形成的基础。甲醛通过交联使液滴表面硬化,从而固定形成的微球的形状和表面形态。不同制备条件下,微球的包封效率可达14.5 ~ 53.7%。制备的微球的休止角在31.9 ~ 42.0°之间,具有良好的自由流动特性,而DTZ粉则不具有流动性。酪蛋白-壳聚糖微球对DTZ的溶出曲线显示药物在蒸馏水中的缓释。酪蛋白和壳聚糖浓度、初始药物浓度和搅拌时间是影响微球性能的主要参数。随着酪蛋白浓度的增加和搅拌时间的延长,DTZ的缓释速度加快。另一方面,增加壳聚糖浓度和采用高初始载药量可以使药物快速释放。
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Preparation of casein–chitosan microspheres containing diltiazem hydrochloride by an aqueous coacervation technique

Sustained release casein–chitosan microspheres containing diltiazem hydrochloride (DTZ) were prepared with colloidal coacervation technique in a completely aqueous environment. The interaction between chitosan solution in dilute acetic acid (5% v/v) and casein solution in 0.5 M sodium hydroxide was the basis for the microspheres formation. Formaldehyde was used for the surface hardening of the droplets by cross-linking and thus fixing the shape and surface morphology of the formed microspheres. The entrapment efficiencies of the microspheres were variables (14.5–53.7%) depending on the preparation conditions. The prepared microspheres exhibited an angle of repose values between 31.9–42.0° indicating good free flowing nature, whereas DTZ powder as such was non-flowable. The dissolution profiles of DTZ from casein–chitosan microspheres showed retarded release pattern of the drug into distilled water. Casein and chitosan concentrations, initial drug concentration and stirring time were found to be the main parameters that affect the properties and the performance of the prepared microspheres. The retarded release of DTZ was increased by increasing casein concentration, and stirring time. On the other hand, increasing chitosan concentration and using high initial drug loading showed a fast drug release.

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