体外肠细胞模型:不同的共培养细胞产生不同的应用。

IF 4.3 4区 医学 Q1 PHARMACOLOGY & PHARMACY Journal of Drug Targeting Pub Date : 2024-06-01 Epub Date: 2024-03-27 DOI:10.1080/1061186X.2024.2333877
Xingyu Zou, Yue Liu, Mengyao Cui, Qing Wan, Xiaoqin Chu
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引用次数: 0

摘要

作为一种体外吸收模型,Caco-2 细胞来源于人类结肠腺癌,可分化成具有肠细胞特征的细胞层。Caco-2 细胞模型被广泛应用于探索药物转运机制、评估药物渗透性以及预测药物或生物活性物质在肠道的吸收。然而,由于缺乏粘液层、培养周期长以及无法准确模拟肠道环境等原因,Caco-2 细胞模型的应用存在局限性。要扩展 Caco-2 细胞模型并解决其局限性,最常用的方法是与其他细胞或物质共培养。本文回顾了围绕 Caco-2 细胞建立的三维和二维共培养细胞模型的培养方法和应用。最后还总结了模型的优缺点。
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The in vitro intestinal cell model: different co-cultured cells create different applications.

As a vitro absorption model, the Caco-2 cells originate from a human colon adenocarcinomas and can differentiate into a cell layer with enterocyte-like features. The Caco-2 cell model is popularly applied to explore drug transport mechanisms, to evaluate the permeability of drug and to predict the absorption of drugs or bioactive substances in the gut. However, there are limitations to the application of Caco-2 cell model due to lack of a mucus layer, the long culture period and the inability to accurately simulate the intestinal environment. The most frequent way to expand the Caco-2 cell model and address its limitations is by co-culturing it with other cells or substances. This article reviews the culture methods and applications of 3D and 2D co-culture cell models established around Caco-2 cells. It also concludes with a summary of model strengths and weaknesses.

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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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