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影响胶体药物递送系统隐身性的参数。

Parameters influencing the stealthiness of colloidal drug delivery systems.

作者信息

Vonarbourg Arnaud, Passirani Catherine, Saulnier Patrick, Benoit Jean-Pierre

机构信息

INSERM U646, Ingénierie de la Vectorisation Particulaire, Université d'Angers, Immeuble IBT, 10, rue André Boquel, 49100 Angers, France.

出版信息

Biomaterials. 2006 Aug;27(24):4356-73. doi: 10.1016/j.biomaterials.2006.03.039. Epub 2006 May 2.

Abstract

Over the last few decades, colloidal drug delivery systems (CDDS) such as nano-structures have been developed in order to improve the efficiency and the specificity of drug action. Their small size permits them to be injected intravenously in order to reach target tissues. However, it is known that they can be rapidly removed from blood circulation by the immune system. CDDS are removed via the complement system and via the cells of the mononuclear phagocyte system (MPS), after their recognition by opsonins and/or receptors present at the cell surface. This recognition is dependent on the physicochemical characteristics of the CDDS. In this study, we will focus on parameters influencing the interactions of opsonins and the macrophage plasma membrane with the surface of CDDS, whereby parameters of the polymer coating become necessary to provide good protection.

摘要

在过去几十年中,为了提高药物作用的效率和特异性,已经开发了诸如纳米结构之类的胶体药物递送系统(CDDS)。它们的小尺寸允许它们通过静脉注射以到达靶组织。然而,众所周知,它们可以被免疫系统迅速从血液循环中清除。CDDS在被存在于细胞表面的调理素和/或受体识别后,通过补体系统和单核吞噬细胞系统(MPS)的细胞被清除。这种识别取决于CDDS的物理化学特性。在本研究中,我们将专注于影响调理素和巨噬细胞质膜与CDDS表面相互作用的参数,由此聚合物涂层的参数对于提供良好的保护变得必要。

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