用于心血管研究和药物开发的3D生物打印模型的现状和未来

IF 3.4 Q2 CHEMISTRY, MEDICINAL ADMET and DMPK Pub Date : 2021-08-25 DOI:10.5599/admet.951
L. Polonchuk, C. Gentile
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引用次数: 1

摘要

在过去的十年中,3D生物打印技术已经成为再生医学和药物开发的一种创新的组织工程方法。本文旨在概述最常用的生物工程组织,重点介绍3D生物打印的心脏细胞以及它们如何用于药物发现和开发。该综述指出,虽然该领域仍在发展,但心血管研究可能受益于实验室工程心脏组织,该组织由特定细胞类型构建,具有精确的3D结构,模仿天然心脏微环境。它还描述了监管机构所扮演的角色,以及使用3D生物打印心脏组织从实验室直接转化为临床研究的潜在商业化途径。
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Current state and future of 3D bioprinted models for cardiovascular research and drug development
In the last decade, 3D bioprinting technology has emerged as an innovative tissue engineering approach for regenerative medicine and drug development. This article aims at providing an overview about the most commonly used bioengineered tissues, focusing on 3D bioprinted cardiac cells and how they have been utilized for drug discovery and development. The review describes that, while this field is still developing, cardiovascular research may benefit from laboratory-engineered heart tissues built of specific cell types with precise 3D architecture mimicking the native cardiac microenvironment. It also describes the role played by regulatory agencies and potential commercialization pathways for direct translation from the bench to the bedside of studies using 3D bioprinted cardiac tissues.
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来源期刊
ADMET and DMPK
ADMET and DMPK Multiple-
CiteScore
4.40
自引率
0.00%
发文量
22
审稿时长
4 weeks
期刊介绍: ADMET and DMPK is an open access journal devoted to the rapid dissemination of new and original scientific results in all areas of absorption, distribution, metabolism, excretion, toxicology and pharmacokinetics of drugs. ADMET and DMPK publishes the following types of contributions: - Original research papers - Feature articles - Review articles - Short communications and Notes - Letters to Editors - Book reviews The scope of the Journal involves, but is not limited to, the following areas: - physico-chemical properties of drugs and methods of their determination - drug permeabilities - drug absorption - drug-drug, drug-protein, drug-membrane and drug-DNA interactions - chemical stability and degradations of drugs - instrumental methods in ADMET - drug metablic processes - routes of administration and excretion of drug - pharmacokinetic/pharmacodynamic study - quantitative structure activity/property relationship - ADME/PK modelling - Toxicology screening - Transporter identification and study
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