Modified Cellulose Nanocrystal for Vitamin C Delivery

被引:25
作者
Akhlaghi, Seyedeh Parinaz [1 ]
Berry, Richard M. [2 ]
Tam, Kam Chiu [1 ]
机构
[1] Univ Waterloo, Waterloo Inst Nanotechnol, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
[2] CelluForce Inc, Montreal, PQ H3A 1K2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
cellulose nanocrystals; chitosan oligosaccharide; controlled release; vitamin C antioxidant activity; L-ASCORBIC-ACID; CHITOSAN OLIGOSACCHARIDE; ANTIOXIDATIVE PROPERTIES; MOLECULAR-WEIGHT; IN-VITRO; NANOPARTICLES; DERIVATIVES; COSMECEUTICALS; MICROSPHERES; EVALUATE;
D O I
10.1208/s12249-014-0218-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cellulose nanocrystal grafted with chitosan oligosaccharide (CNC-CSOS) was used to encapsulate vitamin C and prepare CNCS/VC complexes using tripolyphosphte via ionic complexation. The stability of vitamin C and the antioxidant activity of the CNCS/VC complexes were elucidated. The formation of the complex was confirmed using DSC and UV-vis spectrophotometry, and TEM was used to study the morphology of the complexes. The encapsulation efficiency of vitamin C at pH 3 and 5 was 71.6% +/- 6.8 and 91.0 +/- 1.0, respectively. Strong exothermic peaks observed in isothermal titration calorimetric (ITC) studies at pH 5 could be attributed to additional electrostatic interactions between CNC-CSOS and vitamin C at pH 5. The in vitro release of vitamin C from CNCS/VC complexes showed a sustained release of up to 20 days. The vitamin C released from CNCS/VC complex displayed higher stability compared with the control vitamin C solution, and this was also confirmed from the ITC thermograms. CNC-CSOS possessed a higher scavenging activity and faster antioxidant activity compared with its precursors, i.e., oxidized CNC and CSOS and their physical mixtures. Complexing vitamin C into CNC-CSOS particles yielded a dynamic antioxidant agent, where the vitamin C is released over time and displayed sustained antioxidant properties. Therefore, CNCS/VC can potentially be used in cosmeceutical applications as topical formulations.
引用
收藏
页码:306 / 314
页数:9
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