Université Catholique de Louvain, Louvain Drug Research Institute, Unit of Pharmaceutics, UCL-FARG 7320, Avenue E. Mounier, B-1200, Brussels, Belgium.
J Control Release. 2010 Dec 1;148(2):135-46. doi: 10.1016/j.jconrel.2010.08.027. Epub 2010 Aug 24.
Because of the particular characteristics of the tumor microenvironment and tumor angiogenesis, it is possible to design drug delivery systems that specifically target anti-cancer drugs to tumors. Most of the conventional chemotherapeutic agents have poor pharmacokinetics profiles and are distributed non-specifically in the body leading to systemic toxicity associated with serious side effects. Therefore, the development of drug delivery systems able to target the tumor site is becoming a real challenge that is currently addressed. Nanomedicine can reach tumor passively through the leaky vasculature surrounding the tumors by the Enhanced Permeability and Retention effect whereas ligands grafted at the surface of nanocarriers allow active targeting by binding to the receptors overexpressed by cancer cells or angiogenic endothelial cells. This review is divided into two parts: the first one describes the tumor microenvironment and the second one focuses on the exploitation and the understanding of these characteristics to design new drug delivery systems targeting the tumor. Delivery of conventional chemotherapeutic anti-cancer drugs is mainly discussed.
由于肿瘤微环境和肿瘤血管生成的特殊性质,可以设计专门将抗癌药物输送到肿瘤部位的药物传递系统。大多数传统的化疗药物药代动力学特征不佳,在体内分布不均匀,导致与严重副作用相关的全身毒性。因此,开发能够针对肿瘤部位的药物传递系统正成为一个真正的挑战,目前正在解决这个问题。纳米医学可以通过肿瘤周围渗漏的血管系统被动地到达肿瘤部位,这是通过增强的通透性和保留效应实现的,而接枝在纳米载体表面的配体可以通过与癌细胞或血管内皮细胞过度表达的受体结合来实现主动靶向。这篇综述分为两部分:第一部分描述了肿瘤微环境,第二部分重点介绍了利用和理解这些特性来设计针对肿瘤的新型药物传递系统。主要讨论了传统化疗抗癌药物的传递。
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