有机聚合物和无机超顺磁性氧化铁胶体晶体的共封装需要匹配的扩散时间尺度。

IF 2.9 3区 化学 Q3 CHEMISTRY, PHYSICAL Soft Matter Pub Date : 2024-10-08 DOI:10.1039/D4SM00935E
Brian K. Wilson and Robert K. Prud’homme
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引用次数: 0

摘要

在同一纳米粒子内核中既含有有机分子又含有无机金属或金属氧化物胶体的纳米粒子(NPs)被称为 "复合纳米粒子",在许多应用领域,特别是在生物医学领域作为 "治疗学 "将胶体诊断成像剂与治疗药物联合输送时,这种复合纳米粒子都具有重要意义。闪速纳米沉淀(FNP)快速沉淀技术可以连续、规模化地生产出水动力直径在 40-200 纳米之间的复合纳米粒子,其中含有疏水性超顺磁性氧化铁原胶体。复合纳米粒子共同封装了这些原胶体(直径为 6 纳米、15 纳米或 29 纳米)、荧光染料(600 道尔顿)和聚(苯乙烯)均聚物(1800、50000 或 200000 道尔顿),纳米粒子由聚(苯乙烯)-嵌段-聚(乙二醇)(1600 Da-b-5000 Da)嵌段共聚物稳定。FNP 中纳米粒子的组装是通过疏水性核心成分的扩散受限聚集,然后吸附稳定聚合物的疏水嵌段实现的。坍缩的有机物与原胶体之间的流体力学直径不匹配(0.5-5 nm 与 6-29 nm)造成了各组分之间扩散-聚集时间尺度的不匹配,从而导致最终纳米粒子中出现非等比共包囊;一些纳米粒子是原胶体与有机物共包囊的复合体,而另一些则没有原胶体,只含有有机物。我们使用磁性捕获工艺将磁性复合纳米粒子与纯有机纳米粒子分离,并对每种配方的磁性和非磁性馏分中氧化铁胶体和疏水荧光染料(作为疏水聚合物总含量的代表)的含量进行量化。通过 TEM 成像和成分测量分析了 1100 多个单个纳米粒子的微观结构,确定了产生无共包磁性氧化铁胶体的非等比复合 NP 群体的条件。当无机主胶体和有机核心成分之间的特征扩散-聚集时间尺度之比小于 30,并且分散体中的所有 NP 都含有比例大致相同的有机和无机物种时,就会产生化学计量的磁响应复合 NP。这些将胶体和有机成分组装成均质复合纳米粒子的规则具有广泛的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Co-encapsulation of organic polymers and inorganic superparamagnetic iron oxide colloidal crystals requires matched diffusion time scales†

Nanoparticles (NPs) that contain both organic molecules and inorganic metal or metal oxide colloids in the same NP core are “composite nanoparticles” which are of interest in many applications, particularly in biomedicine as “theranostics” for the combined delivery of colloidal diagnostic imaging agents with therapeutic drugs. The rapid precipitation technique Flash NanoPrecipitation (FNP) enables continuous and scalable production of composite nanoparticles with hydrodynamic diameters between 40–200 nanometers (nm) that contain hydrophobic superparamagnetic iron oxide primary colloids. Composite NPs co-encapsulate these primary colloids (diameters of 6 nm, 15 nm, or 29 nm), a fluorescent dye (600 Daltons), and poly(styrene) homopolymer (1800, 50 000, or 200 000 Daltons) with NPs stabilized by a poly(styrene)-block-poly(ethylene glycol) (1600 Da-b-5000 Da) block copolymer. Nanoparticle assembly in FNP occurs by diffusion limited aggregation of the hydrophobic core components followed by adsorption of the hydrophobic block of the stabilizing polymer. The hydrodynamic diameter mismatch between the collapsed organic species and the primary colloids (0.5–5 nm versus 6–29 nm) creates a diffusion-aggregation time scale mismatch between components that can lead to nonstoichiometric co-encapsulation in the final nanoparticles; some nanoparticles are composites with primary colloids co-encapsulated alongside organics while others are devoid of the primary colloids and contain only organic species. We use a magnetic capture process to separate magnetic composite nanoparticles from organic-only nanoparticles and quantify the amount of iron oxide colloids and hydrophobic fluorescent dye (as a proxy for total hydrophobic polymer content) in the magnetic and nonmagnetic fractions of each formulation. Analysis of the microstructure in over 1100 individual nanoparticles by TEM imaging and composition measurements identifies the conditions that produce nonstoichiometric composite NP populations without co-encapsulated magnetic iron oxide colloids. Stoichiometric magnetically responsive composite NPs are produced when the ratio of characteristic diffusion-aggregation time scales between the inorganic primary colloid and the organic core component is less than 30 and all NPs in a dispersion contain organic and inorganic species in approximately the same ratio. These rules for assembly of colloids and organic components into homogeneous composite nanoparticles are broadly applicable.

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来源期刊
Soft Matter
Soft Matter 工程技术-材料科学:综合
CiteScore
6.00
自引率
5.90%
发文量
891
审稿时长
1.9 months
期刊介绍: Where physics meets chemistry meets biology for fundamental soft matter research.
期刊最新文献
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