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聚(丙交酯-乙交酯)-嵌段-聚乙二醇纳米颗粒作为药物递送载体的内部结构的小角中子散射研究

Small angle neutron scattering studies on the internal structure of poly(lactide-co-glycolide)-block-poly(ethylene glycol) nanoparticles as drug delivery vehicles.

作者信息

Yang Bin, Lowe John P, Schweins Ralf, Edler Karen J

机构信息

Department of Chemistry, University of Bath , Claverton Down, Bath, BA2 7AY, U.K.

出版信息

Biomacromolecules. 2015 Feb 9;16(2):457-64. doi: 10.1021/bm501519u. Epub 2015 Jan 14.

DOI:10.1021/bm501519u
PMID:25539145
Abstract

Poly(lactide-co-glycolide)-block-poly(ethylene glycol) (PLGA-PEG) nanoparticles are commonly used as drug carriers in controlled drug release and targeting. To achieve predictable and clinically relevant volumes of drug distribution, nanoparticle size, surface charge, and especially composition and structure must be controlled. Understanding the internal structures within the particles is fundamentally important to explain differences in drug loading and variations in drug release rate. We prepared nanoparticles from ester-terminated PLGA-PEG polymers via nanoprecipitation, and studied the effects of altering the solvent-water miscibility (THF, acetone, and acetonitrile). Morphology, size, polydispersity, and ζ-potential of PLGA-PEG nanoparticles were characterized. Small angle neutron scattering measurements and fitted models revealed the internal nanoparticle structure: PLGA blocks of 7-9 nm are encapsulated inside a fairly dense PEG/water network in a fractal geometry. Particles with a larger PLGA block volume and higher PEG volume fraction in the particle interior result in greater retention of the hydrophilic anticancer drug carboplatin.

摘要

聚(丙交酯-共-乙交酯)-嵌段-聚(乙二醇)(PLGA-PEG)纳米颗粒通常用作药物载体,用于药物控释和靶向给药。为了实现可预测的、与临床相关的药物分布体积,必须控制纳米颗粒的大小、表面电荷,尤其是组成和结构。了解颗粒内部结构对于解释药物负载差异和药物释放速率变化至关重要。我们通过纳米沉淀法由酯端基PLGA-PEG聚合物制备了纳米颗粒,并研究了改变溶剂与水的混溶性(四氢呋喃、丙酮和乙腈)的影响。对PLGA-PEG纳米颗粒的形态、大小、多分散性和ζ电位进行了表征。小角中子散射测量和拟合模型揭示了纳米颗粒的内部结构:7-9纳米的PLGA嵌段包裹在具有分形几何形状的相当致密的PEG/水网络中。颗粒内部具有较大PLGA嵌段体积和较高PEG体积分数的颗粒会导致亲水性抗癌药物卡铂的保留率更高。

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