以盐酸小檗碱包埋壳聚糖为基础的新型漂浮微球:优化、表征和体内抗溃疡潜力

Q2 Pharmacology, Toxicology and Pharmaceutics Drug Delivery Letters Pub Date : 2022-06-02 DOI:10.2174/2210303112666220602123548
R. Rani, Manish Kumar, R. Verma, Pravin Gupta, B. Kumari, R. Pahwa, Vineet Mittal, S. Bhatt, Deepak Kaushik
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引用次数: 1

摘要

微球是受控药物递送系统(CDDS),因为它们具有封装各种药物、核酸和蛋白质的潜力。它们的优点包括生物相容性、更高的生物利用度和可控释放。目前,现有的抗溃疡剂存在严重的副作用,这限制了它们的用途,并鼓励人们对无害和熟练的新型抗溃疡剂的需求。目前研究工作的基本原理是在胃中吸收药物,以获得更好的抗溃疡潜力和更少的副作用。目前研究工作的基本原理是使用盐酸黄连素制备和检查漂浮微球,以增加胃滞留,而不与胃内粘膜相互作用。毛细管挤出技术是在壳聚糖(一种聚合物)和十二烷基硫酸钠(一种交联剂)的帮助下使用的。扫描电子显微镜表征了制备的微球的表面形态。有效地评估了聚合物浓度以及交联剂浓度对产率、体外漂浮行为和体外药物释放的影响。扩散已被视为大多数发射的流行机制。在制备的微球中观察到药物释放延长(12小时),并且在约10小时内保持浮力。成功进行了体内评估研究。根据不同组的溃疡指数值,确定保护率。治疗组(F-2制剂)显示出97.29%的最大保护率。因此,所制备的漂浮微球可以说服潜在的候选者适应任何胃内条件下的多单元递送装置。
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Berberine hydrochloride embedded chitosan-based novel floating microspheres: Optimization, characterization and in vivo anti-ulcer potential
Microspheres are controlled drug delivery systems (CDDS) because they have the potential to encapsulate various drugs, nucleic acids, and proteins. Their benefits include biocompatiblity, greater bioavailability, and controlled release. Presently, existing antiulcer agents suffer from severe side effects which restricted their utility and encouraged the requirement of a harmless and proficient new antiulcer agent. The rationale of the present research work was to absorb the drug in the stomach for better antiulcer potential and fewer side effects. The rationale of the current investigational effort is to prepare and examine floating microspheres using berberine hydrochloride to increase gastric retention without interaction with the mucosa inside the stomach. The capillary extrusion technique was used with the aid of chitosan, a polymer in addition to sodium lauryl sulphate, a crosslinking agent. Scanning electron microscopy characterized the surface morphology of the prepared microspheres. The effects of polymeric concentration as well as the concentration of cross-link agent on percent yield, in vitro floating behavior, and in vitro drug release were efficiently assessed. Diffusion has been observed as a popular mechanism for most launches. Prolonged drug release (12 hrs) has been seen in the prepared microspheres and they also remained buoyant for around 10 hrs. In vivo evaluation study was successfully performed. From the values of ulcer indexes for various groups, percentage protection was determined. The treatment group (F-2 formulation) showed the maximum percentage protection of 97.29%. The prepared floating microspheres can thus persuade potential candidates to be adaptable to any intra-gastric conditions for multiple-unit delivery devices.
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来源期刊
Drug Delivery Letters
Drug Delivery Letters Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
1.70
自引率
0.00%
发文量
30
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