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用于抗生素治疗的有前途的亚 100nm 定制空心壳聚糖/聚丙烯酸纳米胶囊。

Promising sub-100 nm tailor made hollow chitosan/poly(acrylic acid) nanocapsules for antibiotic therapy.

机构信息

Université Paris Est, ICMPE (UMR7182), CNRS, UPEC, F-94320 Thiais, France.

Université Paris Est, ICMPE (UMR7182), CNRS, UPEC, F-94320 Thiais, France.

出版信息

J Colloid Interface Sci. 2018 Jul 15;522:183-190. doi: 10.1016/j.jcis.2018.03.061. Epub 2018 Mar 19.

DOI:10.1016/j.jcis.2018.03.061
PMID:29601960
Abstract

Herein, we report on the preparation of ultra-low sized (<100 nm in diameter) biodegradable polymeric capsules for potential applications as nanocontainers in antibiotic therapy. Hollow nanospheres based on the chitosan/poly(acrylic acid) pair are elaborated via (i) the layer-by-layer technique using gold nanoparticles (20 and 60 nm in size) as sacrificial templates, (ii) loading with amoxicillin, a betalactam antibiotic, and (iii) removal of the gold core via cyanide-assisted hydrolysis. Size, dispersity and concentration of the resulting nanocapsules are easily tuned by the nanoparticle templates, while wall thickness is controlled by the number of polyelectrolyte bilayers. Electrostatic interactions between the protonated amine groups of chitosan and the carboxyl groups of poly(acrylic acid) act as the driving attraction force allowing easy and fast design of robust and well-ordered multilayer films. Successful hydrolysis of the gold core is evidenced by time-dependent monitoring of the gold spectroscopic signature (absorbance at 519 nm and 539 nm for the gold nanoparticles with 20 and 60 nm, respectively). Crosslinked capsules are also prepared through crosslinking of the chitosan chains with glutaraldehyde. Chitosan-based nanocapsules are finally evidenced to be promising drug delivery vehicles of amoxicillin trihydrate with tuneable properties such as entrapment efficiency in the range of 62-75% and 3.5-5.5% concerning the drug loading.

摘要

本文报告了超小尺寸(直径<100nm)可生物降解聚合物胶囊的制备,这些胶囊可作为抗生素治疗中的纳米容器。基于壳聚糖/聚丙烯酸对的中空纳米球是通过(i)使用金纳米粒子(20 和 60nm 大小)作为牺牲模板的层层技术,(ii)负载阿莫西林(一种β-内酰胺抗生素),以及(iii)通过氰化物辅助水解去除金核来制备的。所得纳米胶囊的尺寸、分散性和浓度可以通过纳米粒子模板轻松调节,而壁厚度则由聚电解质双层的数量控制。壳聚糖的质子化氨基和聚丙烯酸的羧基之间的静电相互作用作为驱动力,允许快速设计坚固且有序的多层膜。通过对金纳米粒子的光谱特征(20nm 和 60nm 的金纳米粒子的 519nm 和 539nm 的吸光度)进行时变监测,证实了金核的成功水解。还通过戊二醛交联壳聚糖链来制备交联胶囊。壳聚糖基纳米胶囊最终被证明是阿莫西林三水合物的有前途的药物输送载体,其具有可调节的性质,例如包封效率在 62-75%之间,药物载量在 3.5-5.5%之间。

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