Human barrier models for the in vitro assessment of drug delivery

被引:0
|
作者
Matthias Schweinlin
Angela Rossi
Nina Lodes
Christian Lotz
Stephan Hackenberg
Maria Steinke
Heike Walles
Florian Groeber
机构
[1] University Hospital Wuerzburg,Department of Tissue Engineering and Regenerative Medicine (TERM)
[2] University Hospital Wuerzburg,Department of Oto
[3] Translational Center Wuerzburg “Regenerative Therapies for Oncology and Musculoskeletal Diseases”,Rhino
[4] Würzburg branch of the Fraunhofer IGB,Laryngology, Plastic, Aesthetic and Reconstructive Head and Neck Surgery
来源
Drug Delivery and Translational Research | 2017年 / 7卷
关键词
Human barrier tissue; Tissue engineering; In vitro model; Alternative to animal testing; Drug delivery;
D O I
暂无
中图分类号
学科分类号
摘要
In vitro test systems gain increasing importance in preclinical studies to increase the predictivity and reduce animal testing. Of special interest herein are barrier tissues that guard into the human body. These barriers are formed by highly specialized tissues such as the skin, the airways, and the intestine. However, to recapitulate these tissues, researchers are currently restricted by a lack of suitable supporting scaffolds. In this study, we present biological scaffolds based on decellularized porcine gut segments that offer a natural environment for cell growth and differentiation. Employing these scaffolds, human barrier models of the skin, the airways, and the intestine that mimic the natural histological architecture of the respective tissue are generated. These models show tissue specific barrier properties, such as the stratification of the skin, the mucociliary phenotype of the airways, and polarization of the intestinal epithelium. To investigate the transport characteristics of the intestinal test system, we incubated the tissue models with fluorescein (Papp <1 × 106 cm/s), propranolol (Papp >7 × 106 cm/s), and rhodamin123 (ratio 2.45). The here presented biological scaffolds facilitate the in vitro generation of human barrier models that might represent useful tools for drug delivery studies.
引用
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页码:217 / 227
页数:10
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