Gerges Abdelsayed , Danish Ali , Andrew Malone , Jemil Saidi , Manoj Myneni , Keshava Rajagopal , Faisal H. Cheema , Aamir Hameed
{"title":"2D and 3D in-Vitro models for mimicking cardiac physiology","authors":"Gerges Abdelsayed , Danish Ali , Andrew Malone , Jemil Saidi , Manoj Myneni , Keshava Rajagopal , Faisal H. Cheema , Aamir Hameed","doi":"10.1016/j.apples.2022.100115","DOIUrl":null,"url":null,"abstract":"<div><p>Cardiovascular diseases are the leading cause of morbidity and mortality and a huge economic burden on the healthcare system globally. Both pharmacological and device based treatment options have emerged over the years, however, it is still a ‘holy grail’ to effectively treat some cardiovascular conditions, for example, heart failure. Any treatment option whether it is drug therapy or a device therapy, has to go through a rigorous regulatory approval process. This requires robust pre-clinical research and clinical trial results. In order to proceed to the clinical trials, pre-clinical research is very important and may take methodologies which are at the interface of biology and engineering, for example, <em>in-vitro, ex-vivo</em> and <em>in-vivo</em> models. This paper focusses on the 2D and 3D <em>in-vitro</em> models to mimic the pathophysiology of a specific cardiovascular disease and their advantages and limitations.</p></div>","PeriodicalId":72251,"journal":{"name":"Applications in engineering science","volume":"12 ","pages":"Article 100115"},"PeriodicalIF":2.2000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666496822000310/pdfft?md5=c71c8e10aebfcff1d89ba5dcbec1da2c&pid=1-s2.0-S2666496822000310-main.pdf","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applications in engineering science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666496822000310","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 3
Abstract
Cardiovascular diseases are the leading cause of morbidity and mortality and a huge economic burden on the healthcare system globally. Both pharmacological and device based treatment options have emerged over the years, however, it is still a ‘holy grail’ to effectively treat some cardiovascular conditions, for example, heart failure. Any treatment option whether it is drug therapy or a device therapy, has to go through a rigorous regulatory approval process. This requires robust pre-clinical research and clinical trial results. In order to proceed to the clinical trials, pre-clinical research is very important and may take methodologies which are at the interface of biology and engineering, for example, in-vitro, ex-vivo and in-vivo models. This paper focusses on the 2D and 3D in-vitro models to mimic the pathophysiology of a specific cardiovascular disease and their advantages and limitations.