• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

微生理系统的崛起以解决药物测试困境。

The ascendance of microphysiological systems to solve the drug testing dilemma.

作者信息

Dehne Eva-Maria, Hasenberg Tobias, Marx Uwe

机构信息

TissUse GmbH, Oudenarder Straße 16, 13347 Berlin, Germany.

出版信息

Future Sci OA. 2017 Mar 31;3(2):FSO185. doi: 10.4155/fsoa-2017-0002. eCollection 2017 Jun.

DOI:10.4155/fsoa-2017-0002
PMID:28670475
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5481853/
Abstract

The development of drugs is a process obstructed with manifold security and efficacy concerns. Although animal models are still widely used to meet the diligence required, they are regarded as outdated tools with limited predictability. Novel microphysiological systems intend to create systemic models of human biology. Their ability to host 3D organoid constructs in a controlled microenvironment with mechanical and electrophysiological stimuli enables them to create and maintain homeostasis. These platforms are, thus, envisioned to be superior tools for testing and developing substances such as drugs, cosmetics and chemicals. We will present reasons why microphysiological systems are required for the emerging demands, highlight current technological and regulatory obstacles, and depict possible solutions from state-of-the-art platforms from major contributors.

摘要

药物研发是一个充满诸多安全性和有效性问题的过程。尽管动物模型仍被广泛用于满足所需的严谨性,但它们被视为预测性有限的过时工具。新型微生理系统旨在创建人类生物学的系统模型。它们能够在具有机械和电生理刺激的可控微环境中培养三维类器官构建体,从而能够创建并维持体内平衡。因此,这些平台被视为测试和开发药物、化妆品及化学品等物质的卓越工具。我们将阐述为何新兴需求需要微生理系统,突出当前的技术和监管障碍,并描述主要贡献者的前沿平台可能提供的解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a93b/5481853/f55a5a9f206a/fsoa-03-185-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a93b/5481853/e24792a3ce37/fsoa-03-185-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a93b/5481853/1a54cd708559/fsoa-03-185-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a93b/5481853/f55a5a9f206a/fsoa-03-185-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a93b/5481853/e24792a3ce37/fsoa-03-185-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a93b/5481853/1a54cd708559/fsoa-03-185-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a93b/5481853/f55a5a9f206a/fsoa-03-185-g3.jpg

相似文献

1
The ascendance of microphysiological systems to solve the drug testing dilemma.微生理系统的崛起以解决药物测试困境。
Future Sci OA. 2017 Mar 31;3(2):FSO185. doi: 10.4155/fsoa-2017-0002. eCollection 2017 Jun.
2
Biology-inspired microphysiological system approaches to solve the prediction dilemma of substance testing.受生物学启发的微生理系统方法解决物质测试的预测困境。
ALTEX. 2016;33(3):272-321. doi: 10.14573/altex.1603161. Epub 2016 May 15.
3
Liver microphysiological platforms for drug metabolism applications.用于药物代谢应用的肝脏微生理平台。
Cell Prolif. 2021 Sep;54(9):e13099. doi: 10.1111/cpr.13099. Epub 2021 Jul 22.
4
Microphysiological Systems: Next Generation Systems for Assessing Toxicity and Therapeutic Effects of Nanomaterials.微生理系统:用于评估纳米材料毒性和治疗效果的下一代系统。
Small Methods. 2020 Jan 16;4(1). doi: 10.1002/smtd.201900589. Epub 2019 Nov 11.
5
Farewell to Animal Testing: Innovations on Human Intestinal Microphysiological Systems.告别动物实验:人类肠道微生理系统的创新
Micromachines (Basel). 2016 Jun 27;7(7):107. doi: 10.3390/mi7070107.
6
Organoids and Microphysiological Systems: New Tools for Ophthalmic Drug Discovery.类器官与微生理系统:眼科药物研发的新工具
Front Pharmacol. 2020 Apr 3;11:407. doi: 10.3389/fphar.2020.00407. eCollection 2020.
7
Microphysiological Systems (Tissue Chips) and their Utility for Rare Disease Research.微生理系统(组织芯片)及其在罕见病研究中的应用。
Adv Exp Med Biol. 2017;1031:405-415. doi: 10.1007/978-3-319-67144-4_23.
8
Self-contained, low-cost Body-on-a-Chip systems for drug development.用于药物研发的独立式低成本芯片人体系统。
Exp Biol Med (Maywood). 2017 Nov;242(17):1701-1713. doi: 10.1177/1535370217694101. Epub 2017 Feb 17.
9
Tissue Chips and Microphysiological Systems for Disease Modeling and Drug Testing.用于疾病建模和药物测试的组织芯片与微生理系统
Micromachines (Basel). 2021 Jan 28;12(2):139. doi: 10.3390/mi12020139.
10
Organ on Chip Technology to Model Cancer Growth and Metastasis.用于模拟癌症生长和转移的芯片器官技术
Bioengineering (Basel). 2022 Jan 11;9(1):28. doi: 10.3390/bioengineering9010028.

引用本文的文献

1
Embryoid Body Test: A Simple and Reliable Alternative Developmental Toxicity Test.胚状体试验:一种简单可靠的替代性发育毒性试验。
Int J Mol Sci. 2024 Dec 18;25(24):13566. doi: 10.3390/ijms252413566.
2
Organ-On-A-Chip: An Emerging Research Platform.器官芯片:一种新兴的研究平台。
Organogenesis. 2023 Dec 31;19(1):2278236. doi: 10.1080/15476278.2023.2278236. Epub 2023 Nov 15.
3
Engineering in vitro immune-competent tissue models for testing and evaluation of therapeutics.用于测试和评估治疗方法的体外免疫活性组织工程模型。

本文引用的文献

1
High-throughput compound evaluation on 3D networks of neurons and glia in a microfluidic platform.在微流控平台上的神经元和神经胶质的 3D 网络上进行高通量化合物评估。
Sci Rep. 2016 Dec 9;6:38856. doi: 10.1038/srep38856.
2
Acute Neurologic Disorder from an Inhibitor of Fatty Acid Amide Hydrolase.脂肪酸酰胺水解酶抑制剂引发的急性神经障碍
N Engl J Med. 2016 Nov 3;375(18):1717-1725. doi: 10.1056/NEJMoa1604221.
3
Validation of Alternative In Vitro Methods to Animal Testing: Concepts, Challenges, Processes and Tools.动物试验替代体外方法的验证:概念、挑战、流程与工具
Adv Drug Deliv Rev. 2022 Mar;182:114111. doi: 10.1016/j.addr.2022.114111. Epub 2022 Jan 11.
4
A pharmacokinetic-pharmacodynamic model based on multi-organ-on-a-chip for drug-drug interaction studies.一种基于多器官芯片的药代动力学-药效学模型用于药物相互作用研究。
Biomicrofluidics. 2020 Jul 23;14(4):044108. doi: 10.1063/5.0011545. eCollection 2020 Jul.
5
3D cell culture models: Drug pharmacokinetics, safety assessment, and regulatory consideration.3D 细胞培养模型:药物药代动力学、安全性评估和监管考虑。
Clin Transl Sci. 2021 Sep;14(5):1659-1680. doi: 10.1111/cts.13066. Epub 2021 Jun 16.
6
Current EU regulatory requirements for the assessment of chemicals and cosmetic products: challenges and opportunities for introducing new approach methodologies.当前欧盟化学品和化妆品评估的监管要求:引入新方法学的挑战和机遇。
Arch Toxicol. 2021 Jun;95(6):1867-1897. doi: 10.1007/s00204-021-03034-y. Epub 2021 Apr 13.
7
Oncoimmunology Meets Organs-on-Chip.肿瘤免疫学与器官芯片技术的结合。
Front Mol Biosci. 2021 Mar 26;8:627454. doi: 10.3389/fmolb.2021.627454. eCollection 2021.
8
Bioethical, Reproducibility, and Translational Challenges of Animal Models.动物模型的生物伦理、可重复性和转化挑战。
ILAR J. 2021 Dec 31;62(1-2):60-65. doi: 10.1093/ilar/ilaa027.
9
Characterizing the reproducibility in using a liver microphysiological system for assaying drug toxicity, metabolism, and accumulation.描述使用肝微生理系统测定药物毒性、代谢和积累的可重复性。
Clin Transl Sci. 2021 May;14(3):1049-1061. doi: 10.1111/cts.12969. Epub 2021 Apr 3.
10
The evolution of strategies to minimise the risk of human drug-induced liver injury (DILI) in drug discovery and development.在药物发现和开发中,降低人类药物诱导肝损伤(DILI)风险策略的演变。
Arch Toxicol. 2020 Aug;94(8):2559-2585. doi: 10.1007/s00204-020-02763-w. Epub 2020 May 6.
Adv Exp Med Biol. 2016;856:65-132. doi: 10.1007/978-3-319-33826-2_4.
4
Screening out irrelevant cell-based models of disease.筛选与疾病无关的基于细胞的模型。
Nat Rev Drug Discov. 2016 Nov;15(11):751-769. doi: 10.1038/nrd.2016.175. Epub 2016 Sep 12.
5
Good Cell Culture Practice for stem cells and stem-cell-derived models.良好的干细胞和干细胞衍生模型的细胞培养规范。
ALTEX. 2017;34(1):95-132. doi: 10.14573/altex.1607121. Epub 2016 Aug 23.
6
Assessment of whole blood thrombosis in a microfluidic device lined by fixed human endothelium.在由固定的人内皮细胞衬里的微流控装置中评估全血血栓形成。
Biomed Microdevices. 2016 Aug;18(4):73. doi: 10.1007/s10544-016-0095-6.
7
Genetic variability in a frozen batch of MCF-7 cells invisible in routine authentication affecting cell function.MCF-7 细胞冻存批次中的遗传变异在常规鉴定中不可见,影响细胞功能。
Sci Rep. 2016 Jul 26;6:28994. doi: 10.1038/srep28994.
8
Human Upcyte Hepatocytes: Characterization of the Hepatic Phenotype and Evaluation for Acute and Long-Term Hepatotoxicity Routine Testing.人Upcyte肝细胞:肝表型特征及急性和长期肝毒性常规检测评估
Toxicol Sci. 2016 Jul;152(1):214-29. doi: 10.1093/toxsci/kfw078. Epub 2016 May 4.
9
Biology-inspired microphysiological system approaches to solve the prediction dilemma of substance testing.受生物学启发的微生理系统方法解决物质测试的预测困境。
ALTEX. 2016;33(3):272-321. doi: 10.14573/altex.1603161. Epub 2016 May 15.
10
Design and demonstration of a pumpless 14 compartment microphysiological system.无泵式14腔微生理系统的设计与演示
Biotechnol Bioeng. 2016 Oct;113(10):2213-27. doi: 10.1002/bit.25989. Epub 2016 Apr 29.