Rui Dong , Sijia Liu , Yuewu Li , Fan Gao , Keqiang Gao , Chunxiao Chen , Zhiyu Qian , Weitao Li , Yamin Yang
{"title":"Revisiting hemodynamics and blood oxygenation in a microfluidic microvasculature replica","authors":"Rui Dong , Sijia Liu , Yuewu Li , Fan Gao , Keqiang Gao , Chunxiao Chen , Zhiyu Qian , Weitao Li , Yamin Yang","doi":"10.1016/j.mvr.2023.104640","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>The complexity of microvascular circulation has led to the development of advanced imaging techniques and </span>biomimetic models. This study developed a multifaceted microfluidic-based microdevice as an </span><em>in vitro</em><span> model of microvasculature to replicate important geometric and functional features of </span><em>in vivo</em><span> perfusion in mice. The microfluidic device consisted of a microchannel for blood perfusion, mirroring the natural hierarchical branching vascular structures found in mice. Additionally, the device incorporated a steady gradient of oxygen (O</span><sub>2</sub><span><span><span>) which diffused through the polydimethylsiloxane (PDMS) layer, allowing for dynamic </span>blood oxygenation. The assembled multi-layered microdevice was accompanied by a dual-modal imaging system that combined laser speckle contrast imaging (LSCI) and intrinsic signal </span>optical imaging (ISOI) to visualize full-field blood flow distributions and blood O</span><sub>2</sub> profiles. By closely reproducing <em>in vivo</em><span> blood perfusion and oxygenation<span> conditions, this microvasculature model, in conjunction with numerical simulation results, can provide quantitative information on physiologically relevant hemodynamics and key O</span></span><sub>2</sub> transport parameters that are not directly measurable in traditional animal studies.</p></div>","PeriodicalId":18534,"journal":{"name":"Microvascular research","volume":"152 ","pages":"Article 104640"},"PeriodicalIF":2.9000,"publicationDate":"2023-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microvascular research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0026286223001668","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PERIPHERAL VASCULAR DISEASE","Score":null,"Total":0}
引用次数: 0
Abstract
The complexity of microvascular circulation has led to the development of advanced imaging techniques and biomimetic models. This study developed a multifaceted microfluidic-based microdevice as an in vitro model of microvasculature to replicate important geometric and functional features of in vivo perfusion in mice. The microfluidic device consisted of a microchannel for blood perfusion, mirroring the natural hierarchical branching vascular structures found in mice. Additionally, the device incorporated a steady gradient of oxygen (O2) which diffused through the polydimethylsiloxane (PDMS) layer, allowing for dynamic blood oxygenation. The assembled multi-layered microdevice was accompanied by a dual-modal imaging system that combined laser speckle contrast imaging (LSCI) and intrinsic signal optical imaging (ISOI) to visualize full-field blood flow distributions and blood O2 profiles. By closely reproducing in vivo blood perfusion and oxygenation conditions, this microvasculature model, in conjunction with numerical simulation results, can provide quantitative information on physiologically relevant hemodynamics and key O2 transport parameters that are not directly measurable in traditional animal studies.
期刊介绍:
Microvascular Research is dedicated to the dissemination of fundamental information related to the microvascular field. Full-length articles presenting the results of original research and brief communications are featured.
Research Areas include:
• Angiogenesis
• Biochemistry
• Bioengineering
• Biomathematics
• Biophysics
• Cancer
• Circulatory homeostasis
• Comparative physiology
• Drug delivery
• Neuropharmacology
• Microvascular pathology
• Rheology
• Tissue Engineering.