Self-nanoemulsifying drug delivery systems: formulation insights, applications and advances

被引:223
作者
Date, Abhijit A. [1 ]
Desai, Neha [1 ]
Dixit, Rahul [1 ]
Nagarsenker, Mangal [1 ]
机构
[1] Bombay Coll Pharm, Dept Pharmaceut, Bombay 400098, Maharashtra, India
关键词
nanoemulsion; oral delivery; poor bioavailability; self-nanoemulsification; solid SNEDDS; SNEDDS; NANO-EMULSION FORMATION; IN-VIVO EVALUATION; ENERGY EMULSIFICATION METHODS; IMPROVED ORAL DELIVERY; INTESTINAL-ABSORPTION; LIPID DIGESTION; DROPLET SIZE; PHARMACEUTICAL EXCIPIENTS; EMULSIFYING FORMULATION; VITRO CHARACTERIZATION;
D O I
10.2217/NNM.10.126
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
There has been a resurgence of interest in nanoemulsions for various pharmaceutical applications since low-energy emulsification methods, such as spontaneous or self-nanoemulsification, have been described. Self-nanoemulsifying drug delivery systems (SNEDDS) are anhydrous homogenous liquid mixtures consisting of oil, surfactant, drug and coemulsifier or solubilizer, which spontaneously form oil-in-water nanoemulsion of approximately 200 nm or less in size upon dilution with water under gentle stirring. The physicochemical properties, drug solubilization capacity and physiological fate considerably govern the selection of the SNEDDS components. The composition of the SNEDDS can be optimized with the help of phase diagrams, whereas statistical experimental design can be used to further optimize SNEDDS. SNEDDS can improve oral bioavailability of hydrophobic drugs by several mechanisms. The conversion of liquid SNEDDS to solid oral dosage forms or solid SNEDDS has also been achieved by researchers. Solid SNEDDS can offer better patient compliance and minimize problems associated with capsules filled with liquid SNEDDS.
引用
收藏
页码:1595 / 1616
页数:22
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