Taranalli Sangmesh S, Dandagi Panchaxari M, Mastiholimath Vinayak S
Department of Pharmaceutics, KLEU's College of Pharmacy, Belgaum, 590010, Karnataka, India,
Eur J Drug Metab Pharmacokinet. 2015 Jun;40(2):225-33. doi: 10.1007/s13318-014-0194-9. Epub 2014 Apr 18.
The purpose of this work was to develop hollow calcium pectinate beads for floating pulsatile release of metoprolol tartrate intended for chronopharmacotherapy. Floating pulsatile concept was applied to increase the gastric residence of the dosage form having lag phase followed by a burst release. To overcome limitations of various approaches for imparting buoyancy, hollow/porous beads were prepared by simple process of acid-base reaction during ionotropic cross-linking using low methoxy pectin, xanthan gum, sodium carboxy methyl cellulose, guar gum, locust bean, gellan gum and calcium chloride as a cross-linking agent. Based on the preliminary studies optimized polymers were selected for formulation design with different polymers ratio concentrations. The obtained floating beads were studied for entrapment efficiency, buoyancy study, swelling index, surface morphology, in vitro release, stability studies and in vivo floating study. The floating beads obtained were porous, float up to 12-24 h. The radiological studies (X-rays) pointed out the capability of the system to release drug in lower parts of GIT after a programmed lag time for hypertension. The floating beads provided expected two-phase release pattern with initial lag time during floating in acidic medium followed by rapid pulse release in phosphate buffer. From the accelerated stability studies, it was observed that the formulations are quite stable. All formulations followed first-order release kinetics by diffusion mechanism. This approach suggested the use of hollow calcium pectinate microparticles as promising floating pulsatile drug delivery system for site- and time-specific release of drugs acting as per chronotherapy of diseases.
本研究旨在开发中空果胶酸钙微球,用于酒石酸美托洛尔的漂浮脉冲释放,以实现时辰治疗。应用漂浮脉冲概念来增加具有滞后相随后爆发释放的剂型在胃中的滞留时间。为了克服赋予浮力的各种方法的局限性,使用低甲氧基果胶、黄原胶、羧甲基纤维素钠、瓜尔胶、刺槐豆胶、结冷胶和氯化钙作为交联剂,通过离子交联过程中的酸碱反应简单工艺制备中空/多孔微球。基于初步研究,选择优化的聚合物用于不同聚合物比例浓度的制剂设计。对所得漂浮微球进行包封率、浮力、溶胀指数、表面形态、体外释放、稳定性研究和体内漂浮研究。所得漂浮微球为多孔结构,可漂浮12 - 24小时。放射学研究(X射线)表明,该系统能够在设定的滞后时间后在胃肠道下部释放药物用于治疗高血压。漂浮微球呈现出预期的两相释放模式,在酸性介质中漂浮时有初始滞后时间,随后在磷酸盐缓冲液中快速脉冲释放。从加速稳定性研究中观察到,制剂相当稳定。所有制剂均遵循扩散机制的一级释放动力学。该方法表明,中空果胶酸钙微粒有望作为漂浮脉冲给药系统,用于根据疾病的时辰疗法实现药物的位点和时间特异性释放。