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Nanosystem drug targeting: Facing up to complex realities

机译:纳米系统药物靶向:面对复杂现实

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摘要

This review considers some of the obstacles to successful drug targeting and delivery of therapeutic agents to desired target sites in the body, in the context of the sometimes overblown claims made for nanoparticle and nanosystem based delivery. It covers aspects of issues surrounding the instability of particles in vivo through flocculation and aggregation, their complex flow and adhesion patterns in the capillary network, particle jamming and bridging, the heterogeneity of access of drugs to some sites such as tumours even in their free molecular state, the diffusion of free drug and nanoparticles in tumour tissue and in single cells. There are the fundamental laws of physics and materials, especially in relation to diffusion, adsorption, adhesion and hydrodynamics, which apply and these cannot be denied in our attempts to target carriers to anatomically distant targets, tumours being the archetypal target experiencing most of the barriers which prevent quantitative carrier and hence drug uptake. The paper closes with a discussion of some of the unmet challenges which must be addressed before quantitative delivery and targeting is achieved in many disease states. It is clear that if progress is to be made an International System for testing nanoparticulate delivery systems should be established. In this way data from different laboratories will be comparable. The International protocol should cover both in vitro and in vivo testing.
机译:这篇综述考虑了在基于纳米粒子和纳米系统的递送有时被夸大的主张的背景下成功进行药物靶向和将治疗剂递送至体内所需靶点的一些障碍。它涵盖了以下方面的问题:通过絮凝和聚集体内颗粒的不稳定性,毛细管网络中颗粒的复杂流动和粘附模式,颗粒卡塞和桥接,药物进入某些部位(例如肿瘤,甚至是游离分子)的异质性状态,游离药物和纳米颗粒在肿瘤组织和单个细胞中的扩散。存在物理和材料的基本定律,尤其是与扩散,吸附,粘附和流体动力学有关的定律,这些定律在我们尝试将载体靶向解剖学上距离较远的目标的尝试中不可否认,肿瘤是经历了大多数障碍的原型目标这会阻止定量载体,从而阻止药物吸收。本文结束时讨论了许多疾病状态下尚未实现的定量挑战和针对性目标之前必须解决的一些挑战。显然,如果要取得进展,就应该建立一个国际系统来测试纳米颗粒传递系统。这样,来自不同实验室的数据将具有可比性。国际协议应涵盖体外和体内测试。

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