Show simple item record

dc.contributor.authorMartin, Gregory T
dc.contributor.authorWeaver, James C
dc.contributor.authorGowrishankar, Thiruvallur R.
dc.contributor.authorStewart, Donald A., Jr.
dc.date.accessioned2010-10-05T21:13:12Z
dc.date.available2010-10-05T21:13:12Z
dc.date.issued2004-11
dc.date.submitted2004-04
dc.identifier.issn1475-925X
dc.identifier.urihttp://hdl.handle.net/1721.1/58885
dc.description.abstractBackground: Investigation of bioheat transfer problems requires the evaluation of temporal and spatial distributions of temperature. This class of problems has been traditionally addressed using the Pennes bioheat equation. Transport of heat by conduction, and by temperature-dependent, spatially heterogeneous blood perfusion is modeled here using a transport lattice approach. Methods: We represent heat transport processes by using a lattice that represents the Pennes bioheat equation in perfused tissues, and diffusion in nonperfused regions. The three layer skin model has a nonperfused viable epidermis, and deeper regions of dermis and subcutaneous tissue with perfusion that is constant or temperature-dependent. Two cases are considered: (1) surface contact heating and (2) spatially distributed heating. The model is relevant to the prediction of the transient and steady state temperature rise for different methods of power deposition within the skin. Accumulated thermal damage is estimated by using an Arrhenius type rate equation at locations where viable tissue temperature exceeds 42°C. Prediction of spatial temperature distributions is also illustrated with a two-dimensional model of skin created from a histological image. Results: The transport lattice approach was validated by comparison with an analytical solution for a slab with homogeneous thermal properties and spatially distributed uniform sink held at constant temperatures at the ends. For typical transcutaneous blood gas sensing conditions the estimated damage is small, even with prolonged skin contact to a 45°C surface. Spatial heterogeneity in skin thermal properties leads to a non-uniform temperature distribution during a 10 GHz electromagnetic field exposure. A realistic two-dimensional model of the skin shows that tissue heterogeneity does not lead to a significant local temperature increase when heated by a hot wire tip. Conclusions: The heat transport system model of the skin was solved by exploiting the mathematical analogy between local thermal models and local electrical (charge transport) models, thereby allowing robust, circuit simulation software to obtain solutions to Kirchhoff's laws for the system model. Transport lattices allow systematic introduction of realistic geometry and spatially heterogeneous heat transport mechanisms. Local representations for both simple, passive functions and more complex local models can be easily and intuitively included into the system model of a tissue.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant RO1-GM63857)en_US
dc.publisherBioMed Central Ltden_US
dc.relation.isversionofhttp://dx.doi.org/10.1186/1475-925X-3-42en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.0en_US
dc.sourceBioMed Central Ltden_US
dc.titleTransport lattice models of heat transport in skin with spatially heterogeneous, temperature-dependent perfusionen_US
dc.typeArticleen_US
dc.identifier.citationBioMedical Engineering OnLine. 2004 Nov 17;3(1):42en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.mitauthorGowrishankar, Thiruvallur R.
dc.contributor.mitauthorMartin, Gregory T.
dc.contributor.mitauthorWeaver, James C.
dc.contributor.mitauthorStewart, Donald A., Jr.
dc.relation.journalBioMedical Engineering Onlineen_US
dc.eprint.versionFinal published versionen_US
dc.identifier.pmid15548324
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2010-09-03T16:19:03Z
dc.language.rfc3066en
dc.rights.holderGowrishankar et al.; licensee BioMed Central Ltd.
dspace.orderedauthorsGowrishankar, TR; Stewart, Donald A; Martin, Gregory T; Weaver, James Cen
dc.identifier.orcidhttps://orcid.org/0000-0002-9016-5962
dspace.mitauthor.errortrue
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record