Rice bran phospholipid-based nanovesicles for enhanced oral and topical delivery of capsaicinoids

被引:5
|
作者
Abulencia, Anabel B. [1 ,2 ]
Vidallon, Mark Louis P. [1 ,3 ]
Almeda, Ronaniel A. [1 ,4 ]
Salamanez, Kevin C. [1 ]
Rodriguez, Evelyn B. [1 ]
机构
[1] Univ Philippines Los Banos, Coll Arts & Sci, Inst Chem, Smart Funct Biomat Lab, Laguna 4031, Philippines
[2] Univ Philippines Diliman, Coll Sci, Inst Chem, Quezon City 1101, Philippines
[3] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
[4] Univ Philippines Los Banos, Coll Engn & Agroind Technol, Inst Agr & Biosyst Engn, UPLB Nanotechnol Program,Agr Bioproc Div, Los Banos 4031, Laguna, Philippines
关键词
Anti-inflammatory; Capsaicinoids; Chorioallantoic membrane assay; Controlled release; Nanoencapsulation; Rice bran phospholipids; DRUG-DELIVERY; SKIN; CAPSICUM; TRANSFERSOMES; PEPPERS;
D O I
10.1016/j.jddst.2020.102005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The current work aimed to fabricate a rice bran phospholipid-based nanovesicular system for oral and topical delivery of capsaicinoids from Capsicum annuum. Using a modified thin film-hydration method, capsaicinoid-loaded nanovesicles (CLNVs) with encapsulation efficiency of 92.31 +/- 5.35% and a mean diameter of 134 +/- 2 nm, were produced. Based on in vitro release studies, the produced CLNVs exhibited a slow and limited release in both simulated salivary and gastric fluids, and selective release in simulated intestinal fluid, suggesting the opportunity for targeting release via the gastro-intestinal tract during oral delivery. Furthermore, the observed limited release of capsaicinoids in surfactant solution is a desirable property for topical delivery formulations. The fabricated delivery vehicle has also shown a masked and reduced irritation effect that co-occur with the strong anti-inflammatory activity of the capsaicinoids. Using a modified duck egg chorioallantoic membrane (CAM) assays, it was demonstrated that encapsulation into nanovesicles was able to reduce the irritancy of capsaicinoids by almost 50% and, at the same time, improve the anti-inflammatory activity by up to 10 folds. These results demonstrated the potential of CLNVs to be developed as oral and topical delivery systems for capsaicinoids.
引用
收藏
页数:9
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