利福昔明海藻酸凝胶珠的制备及评价

Prasad Deshmukh, M. Tawar, Vaishnavi Chandak, Rachana Hallale, Alisha Hirani, Omkar Rajurkar
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引用次数: 1

摘要

任何最佳的药物输送系统都可以将治疗量的药物输送到身体的正确部位,以实现快速反应并保持所需的药物浓度。在作用部位静脉输注药物超过一段期望的时间可以提供这种最佳的药物输送。近年来,科学家和工程师已经开发出速率控制的口服药物输送装置。这些配方以受控和预定的速率提供药物,使其在循环中保持治疗有效浓度。大多数受限制的物质是药片。对制备的水凝胶藻酸盐微球进行药物释放后发现,在03小时的时间内,药物释放率(%)在0.81 ~ 4.81%之间。这一发现是由于发现药物释放(%)在0.81 ~ 4.81%的范围内。根据药物释放数据,发现fz4批次相对于其他批次具有最高的持续药物释放。根据药物释放规律,随着制剂中聚合物浓度的增加,药物释放速度减慢。该制剂延长药物释放,增加生物利用度和治疗活性。具有释放调节剂的海藻酸钠微球可作为药物载体。这种工业规模的工艺需要进行初步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation and Evaluation of Hydrogel Alginate Beads of Rifaximin
Any optimal medication delivery system provides a therapeutic amount of medicine to the correct spot in the body to achieve quick reaction and maintain the desired drug concentration. Intravenous drug infusion at the site of action over a desired time period can provide this optimal drug delivery. In recent years, scientists and engineers have developed rate-controlled oral medication delivery devices. These formulations provide the medicine at a controlled and predetermined rate, keeping its therapeutically effective concentration in circulation. Most restricted substances are pills. After carrying out the drug release of prepared hydrogel alginate microbeads, it was discovered that the drug release (%) was found to be in the range of 0.81 to 4.81% for the time period of 03 hours. This finding was made possible by the fact that the drug release (%) was found to be in the range of 0.81 to 4.81%. According to the data on drug release, it was discovered that the batch of fz4 had the highest sustained drug release in comparison to the other batches. According to the pattern of drug release, the rate of drug release slows down as the concentration of polymer in the formulation increases. This formulation prolongs medication release, increasing bioavailability and therapeutic activity. Sodium alginate micro beads with a release modifier could be employed as a medication carrier. The industrial-scale process needs a pilot study.
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