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Modification of microbial polymers by thiol-ene click reaction: Nanoparticle formation and drug encapsulation

机译:通过硫醇-烯点击反应修饰微生物聚合物:纳米颗粒形成和药物包封

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Comb-like amphiphilic polymers were obtained by grafting long paraffinic chains on microbial poly(gamma,DL-glutamic acid) and poly(beta,L-malic acid) through two steps, i.e. allylation of the carboxylic side groups followed by UV-initiated thiol-ene click reaction with 1-alkanethiols bearing 8,12 and 16 carbon atoms, and their characterization was accomplished by H-1 NMR, GPC and DSC. The grafted polymers were capable of self-assembling in nanoparticles with diameters in the 80-240 nm range. Incubation in water under physiological conditions led to hydrolysis of the lateral ester bonds followed by scission of the polyamide or polyester main chain. The model drugs, Theophylline and Carbamazepine, were efficiently encapsulated.in these systems with much better results attained for the later. Drug release from nanoparticles incubated under physiological conditions occurred with a burst effect and were completely discharged in 24 h. Release profiles recorded from drug-loaded films suggested that the drug was delivered in both cases through a diffusion process. (C) 2016 Elsevier B.V. All rights reserved.
机译:通过两个步骤将长链烷烃链接枝到微生物聚(γ,DL-谷氨酸)和聚(β,L-苹果酸)上,获得梳状两亲聚合物,即羧基侧基的烯丙基化,然后由紫外线引发的硫醇与带有8,12和16个碳原子的1-链烷硫醇的α-烯点击反应,其表征通过H-1 NMR,GPC和DSC进行。接枝的聚合物能够在直径在80-240 nm范围内的纳米颗粒中自组装。在生理条件下在水中温育导致侧酯键水解,随后切断聚酰胺或聚酯主链。模型药物茶碱和卡马西平被有效地封装在这些系统中,随后获得了更好的结果。在生理条件下温育的纳米颗粒释放出的药物具有爆发效应,并在24小时内完全排出。从载有药物的薄膜记录的释放曲线表明,在两种情况下,药物都是通过扩散过程递送的。 (C)2016 Elsevier B.V.保留所有权利。

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