增强激素片剂的崩解性:壳聚糖在雌二醇片剂中作为替代崩解剂的作用

Q4 Medicine
Mikael Ham Sembiring, Taufik Riadi, Arsyadi
{"title":"增强激素片剂的崩解性:壳聚糖在雌二醇片剂中作为替代崩解剂的作用","authors":"Mikael Ham Sembiring, Taufik Riadi, Arsyadi","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The vital regulatory role of estradiol in diverse physiological systems, encompassing the menstrual cycle, cardiovascular, neurologic, skeletal, and vascular systems, underscores its importance. Consequently, this compound is frequently incorporated into diverse pharmaceutical formulations, particularly those in tablet form. Typical inactive ingredients used in estradiol tablet formulations include lactose monohydrate, magnesium stearate, microcrystalline cellulose, and sodium starch glycolate. Chitosan, recognized as a novel excipient, is emerging as a promising alternative to microcrystalline cellulose (MCC). In contrast to MCC, chitosan exhibits noteworthy properties, such as excellent solubility in aqueous solutions, a pleasant odor, superdisintegrant effects, increased porosity, and enhanced liquid absorption. The utilization of chitosan as a tablet disintegrant not only enhances tablet bioavailability but also facilitates the formulation of water-soluble tablet formulations and augments cell penetration in nanoparticle chitosan without any chitosan-estradiol interaction. This article will conduct an in-depth examination of the characteristics of chitosan and its disintegration properties, drawing comparisons with those of microcrystalline cellulose. Furthermore, we will investigate potential formulation strategies for the development of effective tablet formulations employing chitosan as a disintegrant. Additionally, attention will be given to several prior studies on the utilization of chitosan as a disintegrant, providing an analysis of their advantages and limitations in diverse pharmaceutical contexts.</p>","PeriodicalId":14381,"journal":{"name":"International journal of pharmaceutical compounding","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Enhancing Hormonal Tablets Disintegration: The Role of Chitosan as an Alternative Disintegrant in Estradiol Tablet Formulation.\",\"authors\":\"Mikael Ham Sembiring, Taufik Riadi, Arsyadi\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The vital regulatory role of estradiol in diverse physiological systems, encompassing the menstrual cycle, cardiovascular, neurologic, skeletal, and vascular systems, underscores its importance. Consequently, this compound is frequently incorporated into diverse pharmaceutical formulations, particularly those in tablet form. Typical inactive ingredients used in estradiol tablet formulations include lactose monohydrate, magnesium stearate, microcrystalline cellulose, and sodium starch glycolate. Chitosan, recognized as a novel excipient, is emerging as a promising alternative to microcrystalline cellulose (MCC). In contrast to MCC, chitosan exhibits noteworthy properties, such as excellent solubility in aqueous solutions, a pleasant odor, superdisintegrant effects, increased porosity, and enhanced liquid absorption. The utilization of chitosan as a tablet disintegrant not only enhances tablet bioavailability but also facilitates the formulation of water-soluble tablet formulations and augments cell penetration in nanoparticle chitosan without any chitosan-estradiol interaction. This article will conduct an in-depth examination of the characteristics of chitosan and its disintegration properties, drawing comparisons with those of microcrystalline cellulose. Furthermore, we will investigate potential formulation strategies for the development of effective tablet formulations employing chitosan as a disintegrant. Additionally, attention will be given to several prior studies on the utilization of chitosan as a disintegrant, providing an analysis of their advantages and limitations in diverse pharmaceutical contexts.</p>\",\"PeriodicalId\":14381,\"journal\":{\"name\":\"International journal of pharmaceutical compounding\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International journal of pharmaceutical compounding\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of pharmaceutical compounding","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

雌二醇在月经周期、心血管、神经、骨骼和血管系统等多种生理系统中发挥着重要的调节作用,这一点凸显了它的重要性。因此,这种化合物经常被用于各种药物制剂中,尤其是片剂。雌二醇片剂中使用的典型非活性成分包括一水乳糖、硬脂酸镁、微晶纤维素和淀粉乙醇酸钠。壳聚糖被认为是一种新型辅料,正在成为微晶纤维素(MCC)的一种有前途的替代品。与微晶纤维素相比,壳聚糖具有值得注意的特性,例如在水溶液中具有极佳的溶解性、气味宜人、具有超微崩解作用、孔隙率增加以及液体吸收能力增强。利用壳聚糖作为片剂崩解剂,不仅能提高片剂的生物利用度,还能方便配制水溶性片剂,并能增强纳米颗粒壳聚糖的细胞渗透性,且壳聚糖与雌二醇不会发生任何相互作用。本文将深入研究壳聚糖的特性及其崩解性能,并将其与微晶纤维素进行比较。此外,我们还将研究采用壳聚糖作为崩解剂开发有效片剂配方的潜在配方策略。此外,我们还将关注之前关于使用壳聚糖作为崩解剂的几项研究,分析其在不同制药环境中的优势和局限性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancing Hormonal Tablets Disintegration: The Role of Chitosan as an Alternative Disintegrant in Estradiol Tablet Formulation.

The vital regulatory role of estradiol in diverse physiological systems, encompassing the menstrual cycle, cardiovascular, neurologic, skeletal, and vascular systems, underscores its importance. Consequently, this compound is frequently incorporated into diverse pharmaceutical formulations, particularly those in tablet form. Typical inactive ingredients used in estradiol tablet formulations include lactose monohydrate, magnesium stearate, microcrystalline cellulose, and sodium starch glycolate. Chitosan, recognized as a novel excipient, is emerging as a promising alternative to microcrystalline cellulose (MCC). In contrast to MCC, chitosan exhibits noteworthy properties, such as excellent solubility in aqueous solutions, a pleasant odor, superdisintegrant effects, increased porosity, and enhanced liquid absorption. The utilization of chitosan as a tablet disintegrant not only enhances tablet bioavailability but also facilitates the formulation of water-soluble tablet formulations and augments cell penetration in nanoparticle chitosan without any chitosan-estradiol interaction. This article will conduct an in-depth examination of the characteristics of chitosan and its disintegration properties, drawing comparisons with those of microcrystalline cellulose. Furthermore, we will investigate potential formulation strategies for the development of effective tablet formulations employing chitosan as a disintegrant. Additionally, attention will be given to several prior studies on the utilization of chitosan as a disintegrant, providing an analysis of their advantages and limitations in diverse pharmaceutical contexts.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
0.40
自引率
0.00%
发文量
62
期刊介绍: The International Journal of Pharmaceutical Compounding (IJPC) is a bi-monthly, scientific and professional journal emphasizing quality pharmaceutical compounding. IJPC is the only publication that covers pharmaceutical compounding topics relevant and necessary to empower pharmacists to meet the needs of today"s patients. No other publication features hands-on, how-to compounding techniques or the information that contemporary pharmacists need to provide individualized care.
×
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:481959085
Book学术官方微信