• 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

超临界流体技术的药物递送应用

Drug delivery applications of supercritical fluid technology.

作者信息

Kompella U B

机构信息

UNMC College of Pharmacy, Omaha, NE 68198-6025, USA.

出版信息

IDrugs. 1999 Jan;2(1):33-4.

PMID:16180167
Abstract

At the 1998 annual meeting of the American Association of Pharmaceutical Scientists (AAPS) held in San Francisco, a symposium entitled 'Drug Delivery Applications of Supercritical Fluid Technology' was presented. Five speakers presented the advances made by their research groups in this area. Various approaches using supercritical fluids as solvents, antisolvents or mechanical agents were employed in forming particles or delivery systems of various drugs, including antibiotics, steroids and macromolecules. The particles obtained with this technology were small, free-flowing, easily wettable and have minimal surface charges. A coating unit employing supercritical CO2 to fluidize the substrates and to remove solvent has been reported. Nasal delivery of insulin was enhanced when the formulations were processed with supercritical CO2. Macromolecules such as insulin and trypsin dissolved in a carrier liquid could be incorporated in preformed microspheres upon supercritical fluid exposure. Thus supercritical fluid technology appears to be a promising new approach to process drugs and their dosage forms.

摘要

在1998年于旧金山举行的美国药物科学家协会(AAPS)年会上,举办了一场题为“超临界流体技术的药物递送应用”的研讨会。五位演讲者介绍了他们的研究小组在该领域取得的进展。使用超临界流体作为溶剂、抗溶剂或机械剂的各种方法被用于形成包括抗生素、类固醇和大分子在内的各种药物的颗粒或递送系统。用该技术获得的颗粒小、流动性好、易于润湿且表面电荷最小。据报道,有一种包衣装置采用超临界二氧化碳使底物流化并去除溶剂。当制剂用超临界二氧化碳处理时,胰岛素的鼻腔递送得到增强。溶解在载液中的胰岛素和胰蛋白酶等大分子在暴露于超临界流体时可被纳入预制微球中。因此,超临界流体技术似乎是一种有前途的加工药物及其剂型的新方法。

相似文献

1
Drug delivery applications of supercritical fluid technology.超临界流体技术的药物递送应用
IDrugs. 1999 Jan;2(1):33-4.
2
Preparation of drug delivery systems using supercritical fluid technology.使用超临界流体技术制备药物递送系统。
Crit Rev Ther Drug Carrier Syst. 2001;18(2):173-99.
3
Supercritical fluid technology for enhanced drug delivery.用于增强药物递送的超临界流体技术。
Expert Opin Drug Deliv. 2005 Jul;2(4):747-61. doi: 10.1517/17425247.2.4.747.
4
A supercritical fluid-based coating technology 1: process considerations.
J Microencapsul. 2003 Jan-Feb;20(1):87-96.
5
Disposition of non-viral gene delivery systems and oligonucleotides.
IDrugs. 1999 Jan;2(1):31-2.
6
[Development of antituberculous drugs: current status and future prospects].[抗结核药物的研发:现状与未来前景]
Kekkaku. 2006 Dec;81(12):753-74.
7
Supercritical fluid technologies: an innovative approach for manipulating the solid-state of pharmaceuticals.超临界流体技术:一种操控药物固态的创新方法。
Adv Drug Deliv Rev. 2008 Feb 14;60(3):399-410. doi: 10.1016/j.addr.2007.08.030. Epub 2007 Oct 5.
8
Application of supercritical fluid to preparation of powders of high-molecular weight drugs for inhalation.超临界流体在制备用于吸入的高分子量药物粉末中的应用。
Adv Drug Deliv Rev. 2008 Feb 14;60(3):433-46. doi: 10.1016/j.addr.2007.02.002. Epub 2007 Oct 9.
9
Nanoparticle formulations in pulmonary drug delivery.肺部药物递送中的纳米颗粒制剂
Med Res Rev. 2009 Jan;29(1):196-212. doi: 10.1002/med.20140.
10
Biodegradable particle formation for drug and gene delivery using supercritical fluid and dense gas.利用超临界流体和致密气体制备用于药物和基因递送的可生物降解颗粒
Adv Drug Deliv Rev. 2008 Feb 14;60(3):411-32. doi: 10.1016/j.addr.2007.02.003. Epub 2007 Oct 11.

引用本文的文献

1
Direct incorporation of nano graphene oxide (nGO) into hydrophobic drug crystals for enhanced aqueous dissolution.将纳米石墨烯氧化物(nGO)直接掺入疏水性药物晶体中,以提高其在水中的溶解性能。
Colloids Surf B Biointerfaces. 2020 May;189:110827. doi: 10.1016/j.colsurfb.2020.110827. Epub 2020 Feb 1.
2
Impact of Dendrimers on Solubility of Hydrophobic Drug Molecules.树枝状聚合物对疏水性药物分子溶解度的影响
Front Pharmacol. 2017 May 16;8:261. doi: 10.3389/fphar.2017.00261. eCollection 2017.
3
Drug solubility: importance and enhancement techniques.
药物溶解度:重要性及增强技术
ISRN Pharm. 2012;2012:195727. doi: 10.5402/2012/195727. Epub 2012 Jul 5.
4
Chapter 9 - Nanoliposomal dry powder formulations.第9章 - 纳米脂质体干粉制剂
Methods Enzymol. 2009;464:167-91. doi: 10.1016/S0076-6879(09)64009-X.
5
Monitoring tablet surface roughness during the film coating process.在薄膜包衣过程中监测片剂表面粗糙度。
AAPS PharmSciTech. 2006 Apr 7;7(2):E31. doi: 10.1208/pt070231.
6
Preparation of budesonide- and indomethacin-hydroxypropyl-beta-cyclodextrin (HPBCD) complexes using a single-step, organic-solvent-free supercritical fluid process.采用一步法、无有机溶剂的超临界流体工艺制备布地奈德和吲哚美辛-羟丙基-β-环糊精(HPBCD)复合物。
Eur J Pharm Sci. 2004 Oct;23(2):159-68. doi: 10.1016/j.ejps.2004.06.007.
7
Preparation of budesonide and budesonide-PLA microparticles using supercritical fluid precipitation technology.使用超临界流体沉淀技术制备布地奈德及布地奈德-聚乳酸微粒。
AAPS PharmSciTech. 2002;3(3):E18. doi: 10.1208/pt030318.