Effects of Hydrotropic Phenomenon on Solubility Enhancement of Ebastine; Formulation and Characterization

Anum Saif, Rashid Ali, Khan, S. Zaman, Muhammad Ali Shahbaz, Atif Sarwar, Muhammad Nouman Arif
{"title":"Effects of Hydrotropic Phenomenon on Solubility Enhancement of Ebastine; Formulation and Characterization","authors":"Anum Saif, Rashid Ali, Khan, S. Zaman, Muhammad Ali Shahbaz, Atif Sarwar, Muhammad Nouman Arif","doi":"10.55627/pharma.001.001.0180","DOIUrl":null,"url":null,"abstract":"Hydrotropes are the nontoxic small organic molecules that at certain concentrations result in solubility enhancement of poorly water-soluble compounds. In this study various hydrotropes including nicotinamide, sodium acetate and trisodium citrate were used at varying ratios to observe the effect on solubility enhancement of Ebastine. Various combinations of drug-hydrotrope complexes were prepared with each above mentioned hydrotropes using solvent evaporation technique. The resultant residues were subjected to various analytical and characterization techniques for verification of complexation and solubility enhancement. These techniques included Powder X-ray diffraction studies, FTIR and UV spectroscopy. Three different formulations were prepared using various hydrotrop-drug complexes and their stability studies along with in-vitro release were carried out using simulated environment in dissolution apparatus and then later UV spectrophotometric studies were conducted.Standard curve was constructed for UV Spectroscopic analysis and the UV analysis of %age drug release from final suspension dosage form revealed 67.56%, 55.04 % and 66.76 % for the complex containing drug-nicotinamide at ratio of 3:1, drug- sodium acetate at 2:2and drug-trisodium citrate at 2:2 respectively. This release profile clearly indicated the increment in water solubility of the said insoluble drug in the prepared suspension formulated from the drug-hydrotrope complex","PeriodicalId":123783,"journal":{"name":"Pharmaceutical Communications","volume":"63 39","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmaceutical Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55627/pharma.001.001.0180","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Hydrotropes are the nontoxic small organic molecules that at certain concentrations result in solubility enhancement of poorly water-soluble compounds. In this study various hydrotropes including nicotinamide, sodium acetate and trisodium citrate were used at varying ratios to observe the effect on solubility enhancement of Ebastine. Various combinations of drug-hydrotrope complexes were prepared with each above mentioned hydrotropes using solvent evaporation technique. The resultant residues were subjected to various analytical and characterization techniques for verification of complexation and solubility enhancement. These techniques included Powder X-ray diffraction studies, FTIR and UV spectroscopy. Three different formulations were prepared using various hydrotrop-drug complexes and their stability studies along with in-vitro release were carried out using simulated environment in dissolution apparatus and then later UV spectrophotometric studies were conducted.Standard curve was constructed for UV Spectroscopic analysis and the UV analysis of %age drug release from final suspension dosage form revealed 67.56%, 55.04 % and 66.76 % for the complex containing drug-nicotinamide at ratio of 3:1, drug- sodium acetate at 2:2and drug-trisodium citrate at 2:2 respectively. This release profile clearly indicated the increment in water solubility of the said insoluble drug in the prepared suspension formulated from the drug-hydrotrope complex
嗜水现象对碱溶解度增强的影响配方与表征
亲水化合物是一种无毒的小有机分子,在一定浓度下可提高水溶性差的化合物的溶解度。本研究采用烟酰胺、乙酸钠和柠檬酸三钠等不同比例的水变性物,观察其对埃巴斯丁溶解度的增强作用。采用溶剂蒸发技术制备了不同的药物-亲水配合物组合。所得残留物进行了各种分析和表征技术,以验证络合和溶解度的增强。这些技术包括粉末x射线衍射研究,FTIR和UV光谱。采用不同的水合药物配合物制备了3种不同的制剂,并在溶出仪模拟环境下对其稳定性和体外释放度进行了研究,然后进行了紫外分光光度法的研究。建立标准曲线进行紫外光谱分析,最终混悬剂型的药物释放率为:药物与烟酰胺的比例为3:1,药物与乙酸钠的比例为2:2,药物与柠檬酸三钠的比例为2:2,其释放率分别为67.56%、55.04%和66.76%。该释放谱清楚地表明,所述不溶性药物在由药物-水络合物配制的制备悬浮液中的水溶性增加
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信