• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

固体分散体系统的药物应用:灰黄霉素-琥珀酸低共熔混合物的溶出度

Pharmaceutical applications of solid dispersion systems: dissolution of griseofulvin-succinic acid eutectic mixture.

作者信息

Chiou W L, Niazi S

出版信息

J Pharm Sci. 1976 Aug;65(8):1212-4. doi: 10.1002/jps.2600650820.

DOI:10.1002/jps.2600650820
PMID:978439
Abstract

The dissolution profile of the griseofulvin-succinic acid eutectic mixture system was evaluated using the powder and constant-surface are tablet methods. Factors contributing to the enhancement of griseofulvin dissolution from the dispersion in succinic acid are discussed. Contrary to the original proposal of Sekiguchi and coworkers, dissolution rates of driseofulvin from solid dispersions were found to be markedly affected by the particle size of solid dispersions.

摘要

采用粉末法和恒定表面积片法对灰黄霉素-琥珀酸共熔混合物体系的溶出曲线进行了评估。讨论了有助于提高灰黄霉素从其在琥珀酸中的分散体中溶出的因素。与关口及其同事最初的提议相反,发现灰黄霉素从固体分散体中的溶出速率明显受固体分散体粒径的影响。

相似文献

1
Pharmaceutical applications of solid dispersion systems: dissolution of griseofulvin-succinic acid eutectic mixture.固体分散体系统的药物应用:灰黄霉素-琥珀酸低共熔混合物的溶出度
J Pharm Sci. 1976 Aug;65(8):1212-4. doi: 10.1002/jps.2600650820.
2
The use of ordered mixtures for improving the dissolution rate of low solubility compounds.使用有序混合物提高低溶解度化合物的溶解速率。
J Pharm Pharmacol. 1986 Mar;38(3):161-5. doi: 10.1111/j.2042-7158.1986.tb04537.x.
3
Comparison of polyethylene glycol and polyoxyethylene stearate as excipients for solid dispersion systems of griseofulvin and tolbutamide II: dissolution and solubility studies.
J Pharm Sci. 1980 Nov;69(11):1321-6. doi: 10.1002/jps.2600691122.
4
Effect of the solid-dispersion method on the solubility and crystalline property of tacrolimus.固体分散体法对他克莫司溶解度和结晶性质的影响。
Int J Pharm. 2010 Aug 16;395(1-2):161-6. doi: 10.1016/j.ijpharm.2010.05.023. Epub 2010 May 24.
5
Pharmaceutical applications of solid dispersion systems: X-ray diffraction and aqueous solubility studies on griseofulvin-polyethylene glycol 6000 systems.固体分散体系统的药物应用:灰黄霉素-聚乙二醇6000系统的X射线衍射及水溶性研究
J Pharm Sci. 1977 Jul;66(7):989-91. doi: 10.1002/jps.2600660722.
6
Influence of spray drying and dispersing agent on surface and dissolution properties of griseofulvin micro and nanocrystals.喷雾干燥和分散剂对灰黄霉素微米和纳米晶体的表面及溶解性能的影响
Drug Dev Ind Pharm. 2016 Nov;42(11):1842-50. doi: 10.1080/03639045.2016.1178770. Epub 2016 May 4.
7
Factors affecting the formation of eutectic solid dispersions and their dissolution behavior.影响低共熔固体分散体形成及其溶解行为的因素。
J Pharm Sci. 2007 Feb;96(2):294-304. doi: 10.1002/jps.20754.
8
Comparative dissolution studies for mefenamic acid-polyethylene glycol solid dispersion systems and tablets.甲芬那酸-聚乙二醇固体分散体系统与片剂的比较溶出度研究
Pharm Dev Technol. 1998 Aug;3(3):405-12. doi: 10.3109/10837459809009868.
9
Development of prednisone:polyethylene glycol 6000 fast-release tablets from solid dispersions: solid-state characterization, dissolution behavior, and formulation parameters.泼尼松:聚乙二醇6000速释片固体分散体的研制:固态表征、溶出行为及处方参数
AAPS PharmSciTech. 2007 Dec 14;8(4):E108. doi: 10.1208/pt0804108.
10
Investigation of the interactions of enteric and hydrophilic polymers to enhance dissolution of griseofulvin following hot melt extrusion processing.研究肠溶聚合物和亲水性聚合物之间的相互作用,以提高灰黄霉素在热熔挤出加工后的溶出度。
J Pharm Pharmacol. 2015 Jul;67(7):918-38. doi: 10.1111/jphp.12388. Epub 2015 Feb 3.

引用本文的文献

1
Formulation and Pharmacokinetic Evaluation of Polymeric Dispersions Containing Valsartan.含有缬沙坦的聚合物分散体的制剂与药代动力学评价
Eur J Drug Metab Pharmacokinet. 2016 Oct;41(5):517-26. doi: 10.1007/s13318-015-0290-5.