Characterisation of products from EDC-mediated PEG substitution of chitosan allows optimisation of reaction conditions

被引:7
作者
Mushtaq, Asim [1 ]
Li, Li [2 ]
Anitha, A. [1 ]
Grondahl, Lisbeth [1 ]
机构
[1] Univ Queensland, Sch Chem & Mol Biosci, Cooper Rd, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Corner Coll & Cooper Rd, Brisbane, Qld 4072, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Chitosan; Polyethylene glycol; Carbodiimide; CHEMICAL-MODIFICATIONS; AMIDE FORMATION; PEGYLATION; CYTOTOXICITY; CARBODIIMIDE; NANOPARTICLES; ENHANCEMENT; DELIVERY;
D O I
10.1016/j.ijbiomac.2022.08.179
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
ABSTR A C T PEGylation is a common method use to modify the physiochemical properties and increase the solubility of chitosan (CHI). Knowledge of optimal reaction conditions for PEGylation of CHI underpins its ongoing use in nanomedicine. This study synthesised methoxy polyethyleneglycol grafted CHI (mPEG-CHI) using carbodiimide-mediated coupling. The effect of reagent concentrations and pH on the degree of substitution (DS) and the PEGylation yield (conversion of free PEG to conjugated PEG) was evaluated through detailed chemical char-acterisation. Within the parameter space investigated, optimised reaction conditions (NH2: COOH:NHS:EDC of 3.5:1:1:10, pH = 5) resulted in a DS of 24 % and a PEGylation yield of 84 %. An EDC-derived adduct formed at pH >= 5.5 and at a 15-fold excess of EDC relative to COOH. The adduct was evaluated to be a guanidine derivative formed by the reaction of the amine group of CHI directly with EDC. DS >= 12 % imparted water solubility to CHI at physiological pH and mPEG-CHI (0.2-1.0 mg/mL) was not cytotoxic against the breast cancer cell lines MCF-7 and MDA-MB-231, indicating its suitability for medical applications.
引用
收藏
页码:204 / 211
页数:8
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