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A mixture theory model of fluid and solute transport in the microvasculature of normal and malignant tissues. II: Factor sensitivity analysis, calibration, and validation.
Schuff, M M; Gore, J P; Nauman, E A.
Afiliação
  • Schuff MM; School of Mechanical Engineering, Purdue University, 585 Purdue Mall, West Lafayette, IN, 47907-2088, USA, meller@purdue.edu.
J Math Biol ; 67(6-7): 1307-37, 2013 Dec.
Article em En | MEDLINE | ID: mdl-23108729
The treatment of cancerous tumors is dependent upon the delivery of therapeutics through the blood by means of the microcirculation. Differences in the vasculature of normal and malignant tissues have been recognized, but it is not fully understood how these differences affect transport and the applicability of existing mathematical models has been questioned at the microscale due to the complex rheology of blood and fluid exchange with the tissue. In addition to determining an appropriate set of governing equations it is necessary to specify appropriate model parameters based on physiological data. To this end, a two stage sensitivity analysis is described which makes it possible to determine the set of parameters most important to the model's calibration. In the first stage, the fluid flow equations are examined and a sensitivity analysis is used to evaluate the importance of 11 different model parameters. Of these, only four substantially influence the intravascular axial flow providing a tractable set that could be calibrated using red blood cell velocity data from the literature. The second stage also utilizes a sensitivity analysis to evaluate the importance of 14 model parameters on extravascular flux. Of these, six exhibit high sensitivity and are integrated into the model calibration using a response surface methodology and experimental intra- and extravascular accumulation data from the literature (Dreher et al. in J Natl Cancer Inst 98(5):335-344, 2006). The model exhibits good agreement with the experimental results for both the mean extravascular concentration and the penetration depth as a function of time for inert dextran over a wide range of molecular weights.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Eritrócitos / Microvasos / Modelos Biológicos / Neoplasias Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Eritrócitos / Microvasos / Modelos Biológicos / Neoplasias Idioma: En Ano de publicação: 2013 Tipo de documento: Article