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体内纳米颗粒递呈的一种数学描述方法。

A proposed mathematical description of in vivo nanoparticle delivery.

机构信息

Institute of Biomedical Engineering, University of Toronto, Toronto, ON M5S 3G9, Canada; Terrence Donnelly Centre for Cellular & Biomolecular Research, University of Toronto, Toronto, ON M5S 3E1, Canada.

Institute of Biomedical Engineering, University of Toronto, Toronto, ON M5S 3G9, Canada; Terrence Donnelly Centre for Cellular & Biomolecular Research, University of Toronto, Toronto, ON M5S 3E1, Canada; Department of Chemical Engineering & Applied Chemistry, University of Toronto, Toronto, ON M5S 3E5, Canada; Department of Materials Science & Engineering, University of Toronto, Toronto, ON M5S 1A1, Canada; Department of Chemistry, University of Toronto, Toronto, ON M5S 3H6, Canada.

出版信息

Adv Drug Deliv Rev. 2022 Oct;189:114520. doi: 10.1016/j.addr.2022.114520. Epub 2022 Aug 27.

Abstract

Nanoparticles are promising vehicles for the precise delivery of molecular therapies to diseased sites. Nanoparticles interact with a series of tissues and cells before they reach their target, which causes less than 1% of administered nanoparticles to be delivered to these target sites. Researchers have been studying the nano-bio interactions that mediate nanoparticle delivery to develop guidelines for designing nanoparticles with enhanced delivery properties. In this review article, we describe these nano-bio interactions with a series of mathematical equations that quantitatively define the nanoparticle delivery process. We employ a compartment model framework to describe delivery where nanoparticles are either (1) at the site of administration, (2) in the vicinity of target cells, (3) internalized by the target cells, or (4) sequestered away in off-target sites or eliminated from the body. This framework explains how different biological processes govern nanoparticle transport between these compartments, and the role of intercompartmental transport rates in determining the final nanoparticle delivery efficiency. Our framework provides guiding principles to engineer nanoparticles for improved targeted delivery.

摘要

纳米粒子是将分子疗法精确递送到病变部位的有前途的载体。纳米粒子在到达目标之前与一系列组织和细胞相互作用,导致只有不到 1%的给药纳米粒子递送到这些目标部位。研究人员一直在研究介导纳米粒子递送到目标的纳米-生物相互作用,以制定设计具有增强递送特性的纳米粒子的指南。在这篇综述文章中,我们使用一系列定量定义纳米粒子递送过程的数学方程来描述这些纳米-生物相互作用。我们采用隔室模型框架来描述递送,其中纳米粒子要么 (1) 在给药部位,要么 (2) 在靶细胞附近,要么 (3) 被靶细胞内化,要么 (4) 被隔离在非靶部位或从体内消除。该框架解释了不同的生物过程如何控制这些隔室之间的纳米粒子转运,以及隔室间转运率在确定最终纳米粒子递送效率中的作用。我们的框架为工程纳米粒子以实现改进的靶向递送提供了指导原则。

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