• 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

The use of oil-in-water emulsions as a vehicle for parenteral drug administration.

作者信息

Prankerd R J, Stella V J

机构信息

Department of Pharmaceutical Chemistry, University of Kansas, Lawrence.

出版信息

J Parenter Sci Technol. 1990 May-Jun;44(3):139-49.

PMID:2196363
Abstract

Oil-in-water emulsion formulations are useful for the parenteral administration of drugs which have significant delivery problems. Drugs may be incorporated into emulsion formulations either by emulsification of the drug dissolved in the oil phase, or by extemporaneous addition of a concentrated solution in a cosolvent to a commercial i.v. emulsion. Examples are given of the use of parental emulsion dosage forms for the delivery of drugs which have low water solubility, lack stability to hydrolysis, are irritant or have substantial affinity for plastic infusion sets. These examples are largely drawn from studies of novel cytotoxic agents. Emulsion dosage forms may also have some potential for site-directed drug delivery or for sustained release applications. The potential hazards of parenteral emulsions and some of the means of size determination of the dispersed oil droplets are also examined.

摘要

相似文献

1
The use of oil-in-water emulsions as a vehicle for parenteral drug administration.
J Parenter Sci Technol. 1990 May-Jun;44(3):139-49.
2
Oil-in-water lipid emulsions: implications for parenteral and ocular delivering systems.水包油型脂质乳剂:对肠外和眼部给药系统的影响。
Prog Lipid Res. 2004 Nov;43(6):489-533. doi: 10.1016/j.plipres.2004.09.001.
3
The role of solid nanoparticle technology in the parenteral delivery of poorly water-soluble drugs.固体纳米颗粒技术在难溶性药物肠胃外给药中的作用。
Int J Pharm. 2004 Oct 13;284(1-2):109-22. doi: 10.1016/j.ijpharm.2004.07.019.
4
Topical delivery of lipophilic drugs from o/w Pickering emulsions.亲脂性药物从水包油型皮克林乳液的局部递送。
Int J Pharm. 2009 Apr 17;371(1-2):56-63. doi: 10.1016/j.ijpharm.2008.12.017. Epub 2008 Dec 24.
5
The potential of lipid emulsion for ocular delivery of lipophilic drugs.脂质乳剂用于亲脂性药物眼部给药的潜力。
Eur J Pharm Biopharm. 2004 Sep;58(2):357-68. doi: 10.1016/j.ejpb.2004.03.033.
6
Emulsion forming drug delivery system for lipophilic drugs.用于亲脂性药物的乳液形成给药系统。
Acta Pol Pharm. 2012 Mar-Apr;69(2):179-91.
7
Preparation and physical characterization of a novel marine oil emulsion as a potential new formulation vehicle for lipid soluble drugs.
Int J Pharm. 2006 Nov 15;325(1-2):180-5. doi: 10.1016/j.ijpharm.2006.06.033. Epub 2006 Jun 29.
8
Microemulsions as transdermal drug delivery vehicles.微乳剂作为透皮给药载体
Adv Colloid Interface Sci. 2006 Nov 16;123-126:369-85. doi: 10.1016/j.cis.2006.05.014. Epub 2006 Jul 14.
9
Study of the preparation of sustained-release microspheres containing zedoary turmeric oil by the emulsion-solvent-diffusion method and evaluation of the self-emulsification and bioavailability of the oil.采用乳化-溶剂扩散法制备莪术油缓释微球及其自乳化和油的生物利用度研究。
Colloids Surf B Biointerfaces. 2006 Mar 1;48(1):35-41. doi: 10.1016/j.colsurfb.2005.12.011. Epub 2006 Feb 9.
10
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.

引用本文的文献

1
The preclinical pharmacological study on HX0969W, a novel water-soluble pro-drug of propofol, in rats.新型水溶性丙泊酚前体药物HX0969W在大鼠中的临床前药理学研究。
PeerJ. 2020 Apr 16;8:e8922. doi: 10.7717/peerj.8922. eCollection 2020.
2
Oil-in-water emulsion formulated with eucalyptus leaves extract inhibit influenza virus binding and replication in vitro.含有桉树叶提取物的水包油乳剂在体外可抑制流感病毒的结合与复制。
AIMS Microbiol. 2017 Nov 7;3(4):899-907. doi: 10.3934/microbiol.2017.4.899. eCollection 2017.
3
Computed tomography-guided screening of surfactant effect on blood circulation time of emulsions: application to the design of an emulsion formulation for paclitaxel.
计算机断层扫描引导下评估表面活性剂对乳剂血液循环时间的影响:应用于紫杉醇乳剂制剂的设计
Pharm Res. 2014 Aug;31(8):2022-34. doi: 10.1007/s11095-014-1304-8. Epub 2014 Feb 19.
4
Preparation and evaluation of novel mixed micelles as nanocarriers for intravenous delivery of propofol.新型混合胶束作为丙泊酚静脉给药纳米载体的制备与评价
Nanoscale Res Lett. 2011 Mar 31;6(1):275. doi: 10.1186/1556-276X-6-275.
5
Complexities of particulate matter measurement in parenteral formulations of small-molecule amphiphilic drugs.小分子两亲药物的注射制剂中颗粒物质测量的复杂性。
AAPS PharmSciTech. 2011 Mar;12(1):248-54. doi: 10.1208/s12249-010-9574-x. Epub 2011 Jan 14.
6
Influence of incorporation methods on partitioning behavior of lipophilic drugs into various phases of a parenteral lipid emulsion.包封方法对亲脂性药物在肠外脂质乳剂各相中的分配行为的影响。
AAPS PharmSciTech. 2008;9(2):684-92. doi: 10.1208/s12249-008-9089-x. Epub 2008 May 22.
7
4D-QSAR analysis of a set of propofol analogues: mapping binding sites for an anesthetic phenol on the GABA(A) receptor.一组丙泊酚类似物的4D-QSAR分析:麻醉性酚类在GABA(A)受体上的结合位点映射
J Med Chem. 2002 Jul 18;45(15):3210-21. doi: 10.1021/jm010461a.
8
A novel in vitro release method for submicron sized dispersed systems.一种用于亚微米级分散体系的新型体外释放方法。
AAPS PharmSci. 1999;1(3):E11. doi: 10.1208/ps010311.
9
Evidence for phospholipid bilayer formation in solid lipid nanoparticles formulated with phospholipid and triglyceride.
Pharm Res. 1996 Sep;13(9):1406-10. doi: 10.1023/a:1016090420759.
10
A method for the early evaluation of the effects of storage and additives on the stability of parenteral fat emulsions.一种用于早期评估储存和添加剂对肠外脂肪乳剂稳定性影响的方法。
Pharm Res. 1993 Apr;10(4):535-41. doi: 10.1023/a:1018941801368.