Novel functionalized biodegradable polymers for nanoparticle drug delivery systems

被引:127
|
作者
Kallinteri, P
Higgins, S
Hutcheon, GA
St Pourçain, CB
Garnett, MC
机构
[1] Univ Nottingham, Sch Pharm, Nottingham NG7 2RD, England
[2] Liverpool John Moores Univ, Sch Pharm & Chem, Liverpool L3 3AF, Merseyside, England
[3] Aston Univ, Sch Engn & Appl Sci, Birmingham B4 7ET, W Midlands, England
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1021/bm049200j
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have prepared and screened a library of novel functionalized polymers for development of nanoparticle drug delivery systems. The polymer backbone consisting of two ester-linked, nontoxic, biological monomers, Glycerol and adipic acid, was prepared using a hydrolytic enzyme. The specificity of the chosen enzyme yields a linear polymer with one free pendant hydroxyl group per repeat unit, which can be further functionalized. This protocol gives control over the backbone polymer molecular weight, together with the ability to incorporate various amounts of different fatty acyl substituents. These functionalized polymers are able to self-assemble into well-defined small particles of high homogeneity with a very low toxicity. They are able to incorporate a water soluble drug, dexamethasone phosphate, with a high efficiency and drug loading which varies with the polymer specification. The above characteristics strongly suggest that these polymers could be developed into useful nanoparticulate drug delivery systems.
引用
收藏
页码:1885 / 1894
页数:10
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