{"title":"Modeling of interstitial fluid pressure in solid tumor","authors":"Jani Pusenjak, Damijan Miklavcic","doi":"10.1016/S0928-4869(00)00003-3","DOIUrl":null,"url":null,"abstract":"<div><p>Interstitial fluid pressure (IFP) is one of the main obstacles for macromolecular agents uptake and distribution in solid tumors. It has been demonstrated to reduce effectiveness of different macromolecular agents used in <em>in vivo</em> anti-tumor therapies, which on the other hand showed very good anti-tumor properties in <em>in vitro</em> conditions [L.T. Baxter, R.K. Jain, Microvascular Research 37 (1989) 77–104]. With an appropriate model we demonstrated the correlation between different physiological properties of solid tumor and IFP. The model which we present showed high correlation with results from literature and thus represents a good simulation of physiological processes that govern fluid dynamics in solid tumors. One of the potential uses of presented model is drafting of future experiments which would lead to more effective chemo- or immuno-therapy of solid tumors. This model could also serve as an aid to the interpretation of different experimental results concerning IFP.</p></div>","PeriodicalId":101162,"journal":{"name":"Simulation Practice and Theory","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2000-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0928-4869(00)00003-3","citationCount":"20","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Simulation Practice and Theory","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0928486900000033","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 20
Abstract
Interstitial fluid pressure (IFP) is one of the main obstacles for macromolecular agents uptake and distribution in solid tumors. It has been demonstrated to reduce effectiveness of different macromolecular agents used in in vivo anti-tumor therapies, which on the other hand showed very good anti-tumor properties in in vitro conditions [L.T. Baxter, R.K. Jain, Microvascular Research 37 (1989) 77–104]. With an appropriate model we demonstrated the correlation between different physiological properties of solid tumor and IFP. The model which we present showed high correlation with results from literature and thus represents a good simulation of physiological processes that govern fluid dynamics in solid tumors. One of the potential uses of presented model is drafting of future experiments which would lead to more effective chemo- or immuno-therapy of solid tumors. This model could also serve as an aid to the interpretation of different experimental results concerning IFP.