Absorption, Disposition and Pharmacokinetics of Nanoemulsions

被引:62
作者
Lu, Yi [1 ]
Qi, Jianping [1 ]
Wu, Wei [1 ]
机构
[1] Fudan Univ, Dept Pharmaceut, Sch Pharm, Shanghai 201203, Peoples R China
关键词
Nanoemulsion; microemulsion; SMEDDS; absorption; pharmacokinetics; disposition; DRUG-DELIVERY SYSTEM; IN-OIL MICROEMULSIONS; FREE INTRAVENOUS MICROEMULSIONS; SELF-EMULSIFYING FORMULATION; OPHTHALMIC LIPID EMULSION; MOLECULAR-WEIGHT HEPARIN; ORAL DELIVERY; TRANSDERMAL DELIVERY; INTESTINAL-ABSORPTION; INTRANASAL DELIVERY;
D O I
10.2174/138920012800166544
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Nanoemulsions are composed of nanoscale droplets of one immiscible liquid dispersed within another, which have been the focus of extensive research worldwide due to their solubilization and transportation capacity of both hydrophobic and hydrophilic active compounds with unique physical properties. In a broad sense, submicron-emulsion, microemulsion, self-microemulsifing drug delivery system, lipid emulsion and cholesterol-rich microemulsion (LDE) all belong to nanoemulsions. The review starts with a brief introduction to the definition, formulation rationale, and types of nanoemulaions, and focused on, by different administration routes such as the oral, intravenous, transdermal, ocular nasal and rectal routes, the absorption, disposition, pharmacokinetics properties of nanoemulsions.
引用
收藏
页码:396 / 417
页数:22
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