Release study of selected terpenes from nanostructured lipid carriers

被引:20
|
作者
Lason, Elwira [1 ]
Sikora, Elzbieta [1 ]
Ogonowski, Jan [1 ]
Tabaszewska, Malgorzata [2 ]
Skoczylas, Lukasz [2 ]
机构
[1] Cracow Univ Technol, Inst Organ Chem & Technol, Warszawska 24, PL-31155 Krakow, Poland
[2] Univ Agr, Dept Fruit Vegetable & Mushroom Proc, Krakow, Poland
关键词
Nanostructured lipid carriers; Terpenes; Controlled release; Geranic acid; Forskolin; Ursolic acid; INTRAOCULAR-PRESSURE; GERANIC ACID; URSOLIC ACID; TOPICAL FORSKOLIN; OLEANOLIC ACID; AQUEOUS FLOW; NANOPARTICLES; NLC; PENETRATION; FORMULATION;
D O I
10.1016/j.colsurfa.2016.06.021
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The main objective of this study was to evaluate the potential of nanostructured lipid carriers (NLC) as a delivery system for mono-(geranic acid), di-(forskolin) and triterpenes (ursolic acid). The influence of the actives chemical structure on their release profile were investigated along with the physicochemical properties of terpene-loaded NLC. The formulations were prepared by ultrasound homogenization method using modified beeswax as a solid lipid and caprylic/capric trigliceryde as a liquid lipid. The systems were stabilized by alkylopolyglucoside. The average particle size for formulations with geranic acid (NLCGA), forskolin (NLCF) and ursolic acid (NLCUA) was 101.1 +/- 0.4, 106.4 +/- 1.4 and 97.6 +/- 0.9 nm, respectively. In vitro release studies of the terpenes were performed at the 32 degrees C, using cellulose membrane (Spectra/Porn((R)) Dialysis Membrane) and PBS/ethanol mixture as a receptor solution. The obtained results confirmed a high physical stability of the formulations and showed that the achieved systems are suitable carriers for all, mono- di- and triterpenes. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:87 / 92
页数:6
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