胞吞作用:通过生物屏障增强纳米颗粒外渗的有效机制。

Qianyi Zhang, Jiamian Wang, Zhiyang Chen, Hao Qin, Qichen Zhang, Bo Tian, Xilei Li
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引用次数: 0

摘要

纳米颗粒(NPs)作为治疗肿瘤和中枢神经系统(CNS)疾病以及口服给药的药物载体已被探索。然而,由于其通过生物屏障向靶组织外渗和浸润能力差,临床疗效不理想。大多数临床抗肿瘤NPs都是基于增强的渗透性和保留作用而设计的,这在人类肿瘤中是不充分和不均匀的。血脑屏障(BBB)和小肠上皮的紧密连接(TJs)分别严重阻碍NPs进入中枢神经系统和血液循环。相比之下,胞吞作用使NPs能够绕过这些生理障碍,并通过主动运输增强其渗入目标组织。本文系统综述了NP胞吞靶向肿瘤和中枢神经系统组织的作用机制和可能的应用,探讨了NP口服给药,并提出了NP胞吞领域未来的研究方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcytosis: an effective mechanism to enhance nanoparticle extravasation and infiltration through biological barriers.

Nanoparticles (NPs)1have been explored as drugs carriers for treating tumors and central nervous system (CNS)2diseases and for oral administration. However, they lack satisfactory clinical efficacy due to poor extravasation and infiltration through biological barriers to target tissues. Most clinical antitumor NPs have been designed based on enhanced permeability and retention effects which are insufficient and heterogeneous in human tumors. The tight junctions33TJs: tight junctionsof the blood-brain barrier44BBB: blood-brain barrierand the small intestinal epithelium severely impede NPs from being transported into the CNS and blood circulation, respectively. By contrast, transcytosis enables NPs to bypass these physiological barriers and enhances their infiltration into target tissues by active transport. Here, we systematically review the mechanisms and putative application of NP transcytosis for targeting tumor and CNS tissues, explore oral NP administration, and propose future research directions in the field of NP transcytosis.

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