## Abstract In this article we describe our preliminary work involving the use of depolymerized, low molecular weight chitosan nanoparticles as carriers for proteins and peptides. We hypothesized that the molecular weight of chitosan could favorably modulate the particle and protein release charact
Quaternized chitosan/alginate nanoparticles for protein delivery
โ Scribed by Tao Li; Xiao-Wen Shi; Yu-Min Du; Yu-Feng Tang
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 176 KB
- Volume
- 83A
- Category
- Article
- ISSN
- 1549-3296
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โฆ Synopsis
Abstract
Quaternized chitosan (QCS)/alginate (AL) nanoparticles (QCS/AL) were successfully prepared in neutral condition for the oral delivery of protein. The physicochemical structure of the QCS/AL nanoparticles was characterized by IR spectroscopy and transmission electron microscopy. The diameter of the nanoparticles with a positive surface charge was about 200 nm. The load of bovine serum albumin (BSA) was affected by the concentration and the molecular parameters, i.e. degree of substitution (DS) and weightโaverage molecular weight (M~w~) of QCS, as well as the concentration of BSA. The release of BSA from nanoparticles was pHโdependent. Quick release occurred in 0.1__M__ phosphate buffer solution (PBS, pH = 7.4), while the release was slow in 0.1__M__ HCl (pH = 1.2). The DS and M~w~ of QCS play important roles in the release of BSA in vitro. QCS with high M~w~ accelerated the release of BSA in acid, while high DS retarded the release of BSA in both 0.1__M__ HCl and 0.1__M__ PBS. ยฉ 2007 Wiley Periodicals, Inc. J Biomed Mater Res 2007
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