Development of curcumin-loaded lipid nanocapsules for drug delivery across mucus

被引:0
|
作者
Tiatragoon, Worawan [1 ,2 ]
Laffleur, Flavia [3 ]
Netsomboon, Kesinee [2 ]
机构
[1] Thailand Inst Sci & Technol Res TISTR, Expert Ctr Innovat Herbal Prod InnoHerb, Pathum Thani 12130, Thailand
[2] Thammasat Univ, Fac Pharm, Div Pharmaceut Sci, Rangsit Campus,Phahonyothin Rd, Khlong Luang 12120, Pathumthani, Thailand
[3] Univ Innsbruck, Inst Pharm, Dept Pharmaceut Technol, A-6020 Innsbruck, Austria
关键词
Curcumin; Nanoparticles; Mucopenetration; Mucus; Particulate drug delivery; ANTICANCER ACTIVITY; NANOPARTICLES; PERMEATION; DESIGN;
D O I
10.1016/j.jddst.2024.106014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study aimed to develop and characterize lipid nanocapsules (LNCs) for mucosal delivery. Curcumin loaded-LNCs (CCM-LNCs) were prepared by phase inversion temperature (PIT) method. Particle characteristics, morphology, entrapment efficiency (EE) and loading capacity were determined. Mucopenetration studies were conducted by Transwell (R) (R) plate and tube methods. CCM solution served as control.Particle size and zeta-potential of the CCM-loaded LNCs were 67.47 f 0.15 nm and-32.86 f 2.51 mV. EE and loading capacity of CCM-LNCs was found to be 98.38 f 0.45 % and 42.24 f 2.24 %, respectively. No significant change on stability of CCM-LNCs was found after 30 days storage. CCM-LNCs could penetrate mucus 3 times deeper than CCM solution. Moreover, the delivered amount of CCM across mucus layer was 6 folds higher compared with CCM solution. LNCs with negative charge could be used as a promising particulate delivery system for delivering BCS class IV drug such as CCM across mucus.
引用
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页数:8
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