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利用白蛋白纳米包封抗炎药物开发用于评估上皮屏障功能的3D生物打印结肠炎模拟模型

Development of 3D-Bioprinted Colitis-Mimicking Model to Assess Epithelial Barrier Function Using Albumin Nano-Encapsulated Anti-Inflammatory Drugs.

作者信息

Almutary Abdulmajeed G, Alnuqaydan Abdullah M, Almatroodi Saleh A, Bakshi Hamid A, Chellappan Dinesh Kumar, Tambuwala Murtaza M

机构信息

Department of Medical Biotechnology, College of Applied Medical Sciences, Qassim University, Buraydah 51452, Saudi Arabia.

Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah 51452, Saudi Arabia.

出版信息

Biomimetics (Basel). 2023 Jan 18;8(1):41. doi: 10.3390/biomimetics8010041.

Abstract

Physiological barrier function is very difficult to replicate in vitro. This situation leads to poor prediction of candidate drugs in the drug development process due to the lack of preclinical modelling for intestinal function. By using 3D bioprinting, we generated a colitis-like condition model that can evaluate the barrier function of albumin nanoencapsulated anti-inflammatory drugs. Histological characterization demonstrated the manifestation of the disease in 3D-bioprinted Caco-2 and HT-29 constructs. A comparison of proliferation rates in 2D monolayer and 3D-bioprinted models was also carried out. This model is compatible with currently available preclinical assays and can be implemented as an effective tool for efficacy and toxicity prediction in drug development.

摘要

生理屏障功能很难在体外复制。由于缺乏肠道功能的临床前模型,这种情况导致在药物开发过程中对候选药物的预测不佳。通过使用3D生物打印,我们生成了一种结肠炎样病症模型,该模型可以评估白蛋白纳米包封的抗炎药物的屏障功能。组织学特征证明了3D生物打印的Caco-2和HT-29构建体中疾病的表现。还对2D单层模型和3D生物打印模型中的增殖率进行了比较。该模型与目前可用的临床前试验兼容,可作为药物开发中疗效和毒性预测的有效工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3370/9944493/1837ba42a0eb/biomimetics-08-00041-g001.jpg

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