• 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

聚乙二醇化油在自乳化制剂中的乳化和增溶特性。

The emulsification and solubilisation properties of polyglycolysed oils in self-emulsifying formulations.

作者信息

Devani Manisha, Ashford Marianne, Craig Duncan Q M

机构信息

GlaxoSmithKline, Park Road, Ware, Hertfordshire, SG12 0DP, UK.

出版信息

J Pharm Pharmacol. 2004 Mar;56(3):307-16. doi: 10.1211/0022357022872.

DOI:10.1211/0022357022872
PMID:15025855
Abstract

Self-emulsifying drug delivery systems (SEDDS), whereby drugs are dispersed in an oil-surfactant mix that emulsifies on contact with water, represent a highly promising approach for enhancing oral bioavailability. However, the choice of formulation is, at present, largely empirical both in terms of the composition dependence of the emulsification process and the solubilisation of the drug in the initial oil-surfactant mixture. In this investigation, a range of chemically related self-emulsifying systems have been studied, based on the Labrafil family of polyglycolysed oils, using Tween 80 and Tween 20 as surfactants. The ease of emulsification, the particle size distribution and the appearance of the emulsion droplets were studied as a function of composition, while the solubility of danazol and mefenamic acid in the various oil-surfactant mixes was measured. It was noted that dilution of the emulsions led to apparent change in particle size distribution. The more hydrophilic oil-surfactant mixes showed a greater ease of emulsification and a lower particle size. It was also noted that multiple emulsions could be formed using systems of lower polarity. A linear relationship was observed between the hydrophile-lipophile balance (HLB) of the mix and the solubility of both danazol and mefenamic acid, with more hydrophilic mixes showing greater drug solubility values. The study has indicated that, within the range studied, more hydrophilic mixes tend to result in superior emulsification properties and greater drug solubility.

摘要

自乳化药物递送系统(SEDDS)是将药物分散在油-表面活性剂混合物中,该混合物在与水接触时会乳化,是提高口服生物利用度的一种极具前景的方法。然而,目前在选择制剂时,无论是在乳化过程的成分依赖性方面,还是在药物在初始油-表面活性剂混合物中的溶解方面,很大程度上都是凭经验。在本研究中,基于聚乙二醇化油的Labrafil家族,以吐温80和吐温20作为表面活性剂,研究了一系列化学相关的自乳化系统。研究了乳化的难易程度、粒径分布以及乳液滴的外观随成分的变化,同时测定了达那唑和甲芬那酸在各种油-表面活性剂混合物中的溶解度。注意到乳液的稀释导致粒径分布明显变化。亲水性更强的油-表面活性剂混合物乳化更容易且粒径更小。还注意到使用较低极性的系统可以形成多重乳液。观察到混合物的亲水亲油平衡(HLB)与达那唑和甲芬那酸的溶解度之间存在线性关系,亲水性更强的混合物显示出更高的药物溶解度值。该研究表明,在所研究的范围内,亲水性更强的混合物往往会导致更好的乳化性能和更高的药物溶解度。

相似文献

1
The emulsification and solubilisation properties of polyglycolysed oils in self-emulsifying formulations.聚乙二醇化油在自乳化制剂中的乳化和增溶特性。
J Pharm Pharmacol. 2004 Mar;56(3):307-16. doi: 10.1211/0022357022872.
2
Enhanced oral bioavailability of Coenzyme Q10 by self-emulsifying drug delivery systems.自乳化药物递送系统提高辅酶Q10的口服生物利用度。
Int J Pharm. 2009 Jun 5;374(1-2):66-72. doi: 10.1016/j.ijpharm.2009.03.008. Epub 2009 Mar 19.
3
Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs.用于改善亲脂性药物口服给药的自乳化药物递送系统(SEDDS)。
Biomed Pharmacother. 2004 Apr;58(3):173-82. doi: 10.1016/j.biopha.2004.02.001.
4
Nano-emulsion formulation using spontaneous emulsification: solvent, oil and surfactant optimisation.采用自发乳化法的纳米乳液配方:溶剂、油和表面活性剂的优化
Int J Pharm. 2004 Aug 6;280(1-2):241-51. doi: 10.1016/j.ijpharm.2004.05.016.
5
Formulation optimization of self-emulsifying preparations of puerarin through self-emulsifying performances evaluation in vitro and pharmacokinetic studies in vivo.通过体外自乳化性能评价和体内药代动力学研究对葛根素自乳化制剂进行处方优化
Yao Xue Xue Bao. 2007 Aug;42(8):886-91.
6
Impact of emulsion-based drug delivery systems on intestinal permeability and drug release kinetics.基于乳剂的药物传递系统对肠道通透性和药物释放动力学的影响。
J Control Release. 2010 Feb 25;142(1):22-30. doi: 10.1016/j.jconrel.2009.10.005. Epub 2009 Oct 20.
7
Liquid spray formulations of xibornol by using self-microemulsifying drug delivery systems.使用自微乳化药物递送系统的喜保宁液体喷雾制剂。
Int J Pharm. 2007 Aug 1;340(1-2):84-91. doi: 10.1016/j.ijpharm.2007.03.021. Epub 2007 Mar 30.
8
[Design, optimization and quality evaluation of curcumin self-emulsifying drug delivery system (SEDDS)].姜黄素自乳化药物递送系统(SEDDS)的设计、优化及质量评价
Zhong Yao Cai. 2010 Dec;33(12):1933-7.
9
The influence of cosurfactants and oils on the formation of pharmaceutical microemulsions based on PEG-8 caprylic/capric glycerides.助表面活性剂和油对基于聚乙二醇8辛酸/癸酸甘油酯的药物微乳形成的影响
Int J Pharm. 2008 Mar 20;352(1-2):231-9. doi: 10.1016/j.ijpharm.2007.10.041. Epub 2007 Nov 4.
10
Influence of cryogenic grinding on properties of a self-emulsifying formulation.低温研磨对自乳化制剂性质的影响。
Int J Pharm. 2004 Jun 18;278(1):79-89. doi: 10.1016/j.ijpharm.2004.02.033.

引用本文的文献

1
Self-Emulsifying Drug Delivery Systems (SEDDS): Transition from Liquid to Solid-A Comprehensive Review of Formulation, Characterization, Applications, and Future Trends.自乳化药物递送系统(SEDDS):从液体到固体的转变——制剂、表征、应用及未来趋势的全面综述
Pharmaceutics. 2025 Jan 5;17(1):63. doi: 10.3390/pharmaceutics17010063.
2
Lipid Horizons: Recent Advances and Future Prospects in LBDDS for Oral Administration of Antihypertensive Agents.脂质前沿:用于口服抗高血压药物的脂质体药物递送系统的最新进展与未来前景
Int J Hypertens. 2024 Feb 19;2024:2430147. doi: 10.1155/2024/2430147. eCollection 2024.
3
Self-Emulsifying Formulation of Indomethacin with Improved Dissolution and Oral Absorption.
具有改善溶出度和口服吸收的吲哚美辛自乳化制剂。
Turk J Pharm Sci. 2017 Aug;14(2):108-119. doi: 10.4274/tjps.60352. Epub 2017 Aug 15.
4
Localized delivery of ibuprofen via a bilayer delivery system (BiLDS) for supraspinatus tendon healing in a rat model.通过双层递药系统(BiLDS)局部递送布洛芬促进大鼠冈上肌腱愈合。
J Orthop Res. 2020 Nov;38(11):2339-2349. doi: 10.1002/jor.24670. Epub 2020 Apr 7.
5
In vitro evaluation of a self-emulsifying drug delivery system (SEDDS) for nasal administration of dimenhydrinate.经鼻给予茶苯海明自乳化药物传递系统(SEDDS)的体外评价。
Drug Deliv Transl Res. 2019 Oct;9(5):945-955. doi: 10.1007/s13346-019-00634-1.
6
Biopharmaceutical Development of a Bifonazole Multiple Emulsion for Enhanced Epidermal Delivery.用于增强表皮递送的联苯苄唑多重乳液的生物制药开发。
Pharmaceutics. 2019 Feb 2;11(2):66. doi: 10.3390/pharmaceutics11020066.
7
Calcium-alginate microparticles for sustained release of catechin prepared via an emulsion gelation technique.通过乳液凝胶化技术制备的用于儿茶素缓释的海藻酸钙微粒。
Food Sci Biotechnol. 2016 Oct 31;25(5):1337-1343. doi: 10.1007/s10068-016-0210-8. eCollection 2016.
8
Development and Evaluation of Novel Self-Nanoemulsifying Drug Delivery Systems Based on a Homolipid from Capra hircus and Its Admixtures with Melon Oil for the Delivery of Indomethacin.基于来自山羊的单一脂质及其与甜瓜油的混合物用于吲哚美辛递送的新型自纳米乳化药物递送系统的开发与评价
J Pharm (Cairo). 2014;2014:340486. doi: 10.1155/2014/340486. Epub 2014 Mar 20.
9
In vitro digestion of the self-emulsifying lipid excipient Labrasol(®) by gastrointestinal lipases and influence of its colloidal structure on lipolysis rate.自乳化脂质辅料 Labrasol(®)在胃肠脂肪酶中的体外消化及其胶体结构对脂肪酶解速率的影响。
Pharm Res. 2013 Dec;30(12):3077-87. doi: 10.1007/s11095-013-1053-0. Epub 2013 May 2.
10
Lipid-based formulations for danazol containing a digestible surfactant, Labrafil M2125CS: in vivo bioavailability and dynamic in vitro lipolysis.含可消化表面活性剂Labrafil M2125CS的达那唑脂质体制剂:体内生物利用度及体外动态脂解作用
Pharm Res. 2008 Dec;25(12):2769-77. doi: 10.1007/s11095-008-9641-0. Epub 2008 Jul 1.