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有机聚合物与无机超顺磁性氧化铁胶体晶体的共包封需要匹配的扩散时间尺度。

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

作者信息

Wilson Brian K, Prud'homme Robert K

机构信息

Department of Chemical and Biological Engineering, ACE34 Engineering Quadrangle, Princeton University, 41 Olden Street, Princeton, NJ, 08544, USA.

出版信息

Soft Matter. 2024 Oct 23;20(41):8312-8325. doi: 10.1039/d4sm00935e.

Abstract

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)--poly(ethylene glycol) (1600 Da--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 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.

摘要

在同一纳米颗粒核心中同时包含有机分子和无机金属或金属氧化物胶体的纳米颗粒(NPs)是“复合纳米颗粒”,其在许多应用中都备受关注,尤其是在生物医学领域作为“治疗诊断剂”,用于胶体诊断成像剂与治疗药物的联合递送。快速沉淀技术——闪式纳米沉淀法(FNP)能够连续且可扩展地生产流体动力学直径在40至200纳米(nm)之间的复合纳米颗粒,这些颗粒包含疏水性超顺磁性氧化铁初级胶体。复合纳米颗粒共包封这些初级胶体(直径分别为6纳米、15纳米或29纳米)、一种荧光染料(600道尔顿)以及聚(苯乙烯)均聚物(1800、50000或200000道尔顿),纳米颗粒由聚(苯乙烯)-聚(乙二醇)(1600道尔顿-5000道尔顿)嵌段共聚物稳定。FNP中的纳米颗粒组装是通过疏水核心成分的扩散限制聚集,随后是稳定聚合物疏水嵌段的吸附来实现的。塌陷的有机物种与初级胶体之间的流体动力学直径不匹配(0.5 - 5纳米对6 - 29纳米)导致各成分之间的扩散 - 聚集时间尺度不匹配,这可能导致最终纳米颗粒中非化学计量的共包封;一些纳米颗粒是包含与有机物共包封的初级胶体的复合材料,而另一些则不含初级胶体,仅包含有机物种。我们使用磁捕获过程从仅含有机物的纳米颗粒中分离出磁性复合纳米颗粒,并对每种配方的磁性和非磁性部分中的氧化铁胶体和疏水性荧光染料的量(作为总疏水聚合物含量的替代指标)进行定量。通过透射电子显微镜(TEM)成像和成分测量对超过1100个单个纳米颗粒的微观结构进行分析,确定了产生不含共包封磁性氧化铁胶体的非化学计量复合纳米颗粒群体的条件。当无机初级胶体与有机核心成分之间的特征扩散 - 聚集时间尺度之比小于30且分散体中的所有纳米颗粒都含有大致相同比例的有机和无机物种时,就会产生化学计量的磁响应复合纳米颗粒。这些将胶体和有机成分组装成均匀复合纳米颗粒的规则具有广泛的适用性。

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