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How to optimize binding of coated nanoparticles: coupling of physical interactions, molecular organization and chemical state

机译:如何优化涂层纳米颗粒的结合:物理相互作用,分子组织和化学状态的耦合

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One of the key challenges in the development of nano carriers for drug delivery and imaging is the design of a system that selectively binds to target cells. A common strategy is to coat the delivery device with specific ligands that bind strongly to overexpressed receptors. However such devices are usually unable to discriminate between receptors found on benign and malignant cells. We demonstrate, theoretically, how one can achieve enhanced binding to target cells by using multiple physical and chemical interactions. We study the effective interactions between a polymer decorated nano micelle or nanoparticle with three types of model lipid membranes that differ in the composition of their outer leaflet. They are: (i) lipid membranes with overexpressed receptors, (ii) membranes with a given fraction of negatively charged lipids and (iii) membranes with both overexpressed receptors and negatively charged lipids. The coating contains a mixture of two short polymers, one neutral for protection and the other a polybase with a functional end-group to optimize specific binding with the overexpressed receptors and electrostatic interactions with charged lipid head-groups. The strength of the binding for the combined system is much larger than the sum of the independent electrostatic or specific interactions binding. We find a range of distances where the addition of two effective repulsive interactions become an attraction in the combined case. The changes in the strength and shape of the effective interaction are due to the coupling that exists between molecular organization, physical interactions and chemical state, e.g., protonation. The predictions provide guidelines for the design of carrier devices for targeted drug and nanoparticle delivery and give insight in the competing and highly non-additive nature of the different effective interactions in nanoscale systems in constrained environments that are ubiquitous in synthetic and biological systems.
机译:开发用于药物递送和成像的纳米载体的主要挑战之一是选择性结合靶细胞的系统的设计。一种常见的策略是在递送装置上涂上与过度表达的受体强烈结合的特异性配体。然而,这样的装置通常不能区分良性和恶性细胞上发现的受体。从理论上讲,我们证明了如何通过使用多种物理和化学相互作用来实现与靶细胞的增强结合。我们研究了聚合物装饰的纳米胶束或纳米颗粒与三种类型的外部脂质组成不同的模型脂质膜之间的有效相互作用。它们是:(i)具有过表达的受体的脂质膜,(ii)具有给定比例的带负电荷的脂质的膜,以及(iii)具有过表达的受体和带负电荷的脂质的膜。该涂层包含两种短聚合物的混合物,一种是中性的,用于保护,另一种是具有功能性端基的多碱,以优化与过表达受体的特异性结合以及与带电脂质头基的静电相互作用。组合系统的结合强度远大于独立的静电或特异性相互作用结合的总和。我们发现了一个距离范围,在这种情况下,两个有效排斥相互作用的加和在组合情况下变得很有吸引力。有效相互作用的强度和形状的变化归因于在分子组织,物理相互作用和化学状态例如质子化之间存在的偶联。这些预测为靶向药物和纳米颗粒递送的载体设备的设计提供了指导,并提供了在合成和生物系统中普遍存在的受限环境中,纳米级系统中不同有效相互作用的竞争性和高度非累加性的见解。

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