Nap R J, Szleifer I
Department of Biomedical Engineering, Department of Chemistry and Chemistry of Life Processes Institute, Northwestern University, 2145 Sheridan Road, Evanston, Illinois, 60208-3100, United States.
Biomater Sci. 2013 Aug 1;1(8):814-823. doi: 10.1039/C3BM00181D.
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 mixtures 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, , 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.
用于药物递送和成像的纳米载体开发中的关键挑战之一是设计一种能够选择性结合靶细胞的系统。一种常见策略是用与过表达受体强烈结合的特定配体包覆递送装置。然而,此类装置通常无法区分良性和恶性细胞上的受体。我们从理论上证明了如何通过利用多种物理和化学相互作用来增强与靶细胞的结合。我们研究了一种聚合物修饰的纳米胶束或纳米颗粒与三种模型脂质膜之间的有效相互作用,这三种脂质膜的外层小叶组成不同。它们分别是:i)具有过表达受体的脂质膜,ii)具有给定比例带负电荷脂质的膜,iii)同时具有过表达受体和带负电荷脂质的膜。包覆物包含两种短聚合物的混合物,一种是中性的用于保护,另一种是带有功能性端基的聚碱,以优化与过表达受体的特异性结合以及与带电荷脂质头部基团的静电相互作用。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强度之和。我们发现了一系列距离,在这些距离下,两种有效排斥相互作用在组合情况下会变成吸引作用。有效相互作用的强度和形状变化是由于分子组织、物理相互作用和化学状态(质子化)之间存在的耦合。这些预测为靶向药物和纳米颗粒递送的载体装置设计提供了指导,并深入了解了在合成和生物系统中普遍存在的受限环境下纳米尺度系统中不同有效相互作用的竞争和高度非加和性质。