Comparative release studies of two cationic model drugs from different cellulose nanocrystal derivatives

被引:44
作者
Akhlaghi, Seyedeh Parinaz [1 ]
Tiong, Daryl [1 ]
Berry, Richard M. [2 ]
Tam, Kam Chiu [1 ]
机构
[1] Univ Waterloo, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
[2] CelluForce Inc, Montreal, PQ, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Cellulose nanocrystals; Drug selective electrode; Isothermal titration calorimetry; In vitro drug release; Procaine hydrochloride; Imipramine hydrochloride; NANOPARTICLES; BINDING;
D O I
10.1016/j.ejpb.2014.04.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Native cellulose nanocrystal (CNC), oxidized CNC (CNC-OX) and chitosan oligosaccharide grafted CNC (CNC-CSOS) were evaluated as potential drug delivery carriers for two model drug compounds, procaine hydrochloride (PrHy) and imipramine hydrochloride (IMI). The loading of PrHy and IMI was performed at pH 8 and 7, respectively. IMI displayed higher binding to CNC derivatives than PrHy. Drug selective membranes were prepared for each model drug and a drug selective electrode system was used to measure the drug concentration in the filtrate and release medium. Isothermal Titration Calorimetry (ITC) was used to elucidate the types of interactions between model drugs and CNC and its derivatives. The complexation between model drugs and CNC derivatives was confirmed by zeta potential and transmittance measurements. The binding and release of these drugs correlated with the nature and types of interactions that exist between the CNC and drug molecules. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:207 / 215
页数:9
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