Suppr超能文献

甲硝唑与高岭土相互作用的测定与表征

Determination and characterization of metronidazole-kaolin interaction.

作者信息

Aleanizy Fadilah Sfouq, Alqahtani Fulwah, Al Gohary Omaimah, El Tahir Eram, Al Shalabi Rania

机构信息

Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

Pharmacy Department, King Faisal Specialized Hospital, Riyadh, Saudi Arabia.

出版信息

Saudi Pharm J. 2015 Apr;23(2):167-76. doi: 10.1016/j.jsps.2014.06.006. Epub 2014 Jul 8.

Abstract

The needs for safe, therapeutically effective antidiarrheal combination continuously lead to effective treatment. When administered simultaneously, metronidazole-kaolin interactions have been reported by FDA but not studied. This paper is the first to study metronidazole-kaolin interactions. Adsorption isotherms of a metronidazole-kaolin antidiarrheal combination from aqueous solutions at an in vivo simulated pH conditions were obtained at 37 ± 0.5 °C. Langmuir constants for the adsorption are 10.8225, 41.3223 mg g(-1) and 11.60, 2.56 l g(-1) aimed at the monolayer capacity, and the equilibrium constant at pH 1.2 and 6.8, respectively. pH effect on adsorption of known concentration of metronidazole by kaolin was also studied over the range 1.2-8. A gradual increase in the adsorbed amount was noted with increasing the pH. Elution studies by different eluents showed that drug recovery from adsorbent surface was pH-dependent via competitive mechanism. The elution followed the sequence: 0.1 M HCl > 0.1 M NaCl > H2O. Adsorption-desorption studies revealed physical adsorption. The equilibrium concentration of metronidazole decreased as the adsorbent concentration was increased in the systems. The dissolution profiles (USP) of commercially available tablets (Riazole® 500 mg) were obtained alone and in the presence of either (ORS®) rehydration salts and 9 or 18 g of kaolin powder. The percentage drug released versus time: 95.01% in 25 min, 101.02% in 30 min, 67.63% in 60 min, 60.59% in 60 min, respectively. The percentage drug released versus time was increased with ORS® due to common ion effect [Cl(-)], while, it was decreased with kaolin due to adsorption. The mechanism of reaction of Riazole® (500 mg) tablets in the different dissolution media, confirms with Korsmeyer-Peppas model. The interaction between metronidazole and kaolin was characterized by melting point determinations, differential scanning calorimetry analysis and infrared spectroscopy. The results obtained were suggestive of physical interaction between metronidazole and kaolin.

摘要

对安全、治疗有效的止泻组合的需求持续推动有效治疗的发展。FDA曾报告过甲硝唑与高岭土同时给药时存在相互作用,但未进行研究。本文首次对甲硝唑与高岭土的相互作用展开研究。在37±0.5°C的体内模拟pH条件下,测定了甲硝唑 - 高岭土止泻组合在水溶液中的吸附等温线。该吸附的朗缪尔常数分别为10.8225、41.3223mg g⁻¹和11.60、2.56l g⁻¹,分别针对pH 1.2和6.8时的单层容量及平衡常数。还研究了在1.2 - 8范围内pH对高岭土吸附已知浓度甲硝唑的影响。随着pH升高,吸附量逐渐增加。不同洗脱剂的洗脱研究表明,通过竞争机制,药物从吸附剂表面的回收率取决于pH。洗脱顺序为:0.1M HCl>0.1M NaCl>H₂O。吸附 - 解吸研究表明为物理吸附。在体系中,随着吸附剂浓度增加,甲硝唑的平衡浓度降低。单独以及在存在口服补液盐(ORS®)和9或18g高岭土粉末的情况下,获得了市售片剂(Riazole®500mg)的溶出曲线(USP)。药物释放百分比随时间变化分别为:25分钟时95.01%,30分钟时101.02%,60分钟时67.63%,60分钟时60.59%。由于共同离子效应[Cl⁻],ORS®使药物释放百分比随时间增加,而高岭土因吸附作用使药物释放百分比降低。Riazole®(500mg)片剂在不同溶出介质中的反应机制符合Korsmeyer - Peppas模型。通过熔点测定、差示扫描量热分析和红外光谱对甲硝唑与高岭土之间的相互作用进行了表征。所得结果表明甲硝唑与高岭土之间存在物理相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0f6/4421081/0f196485aa48/fx1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验