Elkomy Mohammed H, Abou-Taleb Heba A, Eid Hussein M, Yassin Heba A
Department of Pharmaceutics, College of Pharmacy, Jouf University, Sakaka 72341, Saudi Arabia.
Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Merit University (MUE), Sohag 82755, Egypt.
Pharmaceutics. 2022 Apr 14;14(4):863. doi: 10.3390/pharmaceutics14040863.
is thought to be the most common cause of peptic and duodenal ulcers. Eradication of this organism is now considered one of the lines of treatment of gastric and duodenal ulcers. This can be achieved via local delivery of antibacterial agents in high concentrations. Accordingly, our objective was to fabricate and evaluate sustained release floating tablets for metronidazole to extend the gastric residence period and control the release rate of metronidazole. Floating tablets containing cellulose derivatives and Avicel were prepared using direct compression. The rate of metronidazole release from the floating tablets (K = 6.278 mg min) was significantly lower than that from conventional tablets (K = 10.666 mg min), indicating sustained drug release, according to the Higuchi model, for more than 6 h in an acidic medium of 0.1 N HCl. In vivo study in healthy volunteers revealed significantly improved bioavailability; increased Tmax, AUC, and MRT; and significantly lower absorption rate constant after a single oral dose of 150 mg metronidazole as floating tablets. In addition, the significant increase in MRT indicated an in vivo sustained drug release. The floating tablets provided several benefits, including ease of preparation, absence of effervescent ingredients, and reliance on a pH-independent gel-forming agent to deliver metronidazole in a sustained manner. In conclusion, the prepared tablets could be promising for enhancing both local and systemic metronidazole efficacy.
被认为是消化性溃疡和十二指肠溃疡最常见的病因。根除这种微生物现在被视为治疗胃溃疡和十二指肠溃疡的方法之一。这可以通过局部递送高浓度抗菌剂来实现。因此,我们的目标是制备并评估甲硝唑缓释漂浮片,以延长其在胃内的停留时间并控制甲硝唑的释放速率。采用直接压片法制备了含有纤维素衍生物和微晶纤维素的漂浮片。根据 Higuchi 模型,在 0.1 N HCl 酸性介质中,甲硝唑从漂浮片中的释放速率(K = 6.278 mg/min)显著低于从普通片中的释放速率(K = 10.666 mg/min),表明药物持续释放超过 6 小时。在健康志愿者身上进行的体内研究显示,单次口服 150 mg 甲硝唑漂浮片后,生物利用度显著提高;Tmax、AUC 和 MRT 增加;吸收速率常数显著降低。此外,MRT 的显著增加表明药物在体内持续释放。漂浮片具有多种优点,包括易于制备、不含泡腾成分以及依赖与 pH 无关的凝胶形成剂来持续递送甲硝唑。总之,所制备的片剂有望提高甲硝唑的局部和全身疗效。