Development of Ultrasmall Chitosan/Succinyl β-Cyclodextrin Nanoparticles as a Sustained Protein-Delivery System

被引:14
作者
Taranejoo, Shahrouz [1 ,2 ]
Monemian, Seyedali [3 ]
Moghri, Mehdi [4 ]
Derakhshankhah, Hossein [4 ]
机构
[1] Monash Univ, Dept Chem Engn, Melbourne, Vic 3004, Australia
[2] Shahid Beheshti Univ Med Sci, Med Nanotechnol & Tissue Engn Res Ctr, Tehran, Iran
[3] Case Western Reserve Univ, Dept Macromol Sci & Engn, Cleveland, OH 44106 USA
[4] Islamic Azad Univ, Kashan Branch, Kashan, Iran
关键词
biodegradable; biopolymers; drug-delivery systems; DRUG-DELIVERY; CHITOSAN NANOPARTICLES; IN-VITRO; POLYMERS; RELEASE; MONODISPERSE; PROTECTION; STABILITY; CARRIERS; INSULIN;
D O I
10.1002/app.39648
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this article, we introduce a new method for preparing ultrasmall chitosan (CS)/succinyl beta-cyclodextrin (SCD) nanoparticles (NPs) intended for loading bovine serum albumin (BSA) as a model protein. The proposed method is based on the complex coacervation technique followed by ionotropic gelation with tripolyphosphate. SCD, an anionic derivative of cyclodextrin, was synthesized and used in CS-based NPs to enhance the entrapment efficiency of BSA. The results show that with this approach, ultrasmall, compact, and neutralized NPs with a mean particle size near 30 nm were obtained. A high degree of protein entrapment in the NPs led to a significant improvement in the BSA release profile with a low initial burst release (ca. 3% w/v of the initially loaded BSA) and a sustained release over time. This enabled a suitable nanocarrier for long-term protein delivery (30% release over 120 h). (C) 2013 Wiley Periodicals, Inc.
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页数:6
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