dc.contributorUniversidad EAFIT. Departamento de Ciencias
dc.contributorLógica y Computación
dc.creatorSimon, Laurent
dc.creatorOspina, Juan
dc.creatorSimon, Laurent
dc.creatorOspina, Juan
dc.date.accessioned2021-03-26T21:32:04Z
dc.date.accessioned2022-09-23T22:00:30Z
dc.date.available2021-03-26T21:32:04Z
dc.date.available2022-09-23T22:00:30Z
dc.date.created2021-03-26T21:32:04Z
dc.date.issued2013-07-01
dc.identifier00255564
dc.identifier18793134
dc.identifierWOS;000320747800007
dc.identifierPUBMED;23624255
dc.identifierSCOPUS;2-s2.0-84878458631
dc.identifierhttp://hdl.handle.net/10784/27331
dc.identifier10.1016/j.mbs.2013.04.004
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3537750
dc.description.abstractA transient percutaneous drug absorption model was solved in two dimensions. Clearance of the topically-applied pharmaceutical occured at the skin-capillary boundary. Timolol penetration profiles in the dermal tissue were produced revealing concentration gradients in the directions normal and parallel to the skin surface. Ninety-eight percent of the steady-state flux was reached after 85. h or four time constants. The analytical solution procedure agreed with published results. As the clearance rate increased relative to diffusion, the delivery rate and amount of drug absorbed into the bloodstream increased while the time to reach the equilibrium flux decreased. Researchers can apply the closed-form expressions to simulate the process, estimate key parameters and design devices that meet specific performance requirements. © 2013 Elsevier Inc.
dc.publisherELSEVIER SCIENCE INC
dc.relationhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84878458631&doi=10.1016%2fj.mbs.2013.04.004&partnerID=40&md5=2dfbe5dc61c0f65ec156f760e91ffb58
dc.rightshttps://v2.sherpa.ac.uk/id/publication/issn/0025-5564
dc.sourceMATHEMATICAL BIOSCIENCES
dc.subjectClosed-form expression
dc.subjectConcentration gradients
dc.subjectPenetration profiles
dc.subjectPercutaneous absorption
dc.subjectPercutaneous drug absorption
dc.subjectPerformance requirements
dc.subjectSolution procedure
dc.subjectTime constants
dc.subjectLaplace transforms
dc.subjectPartial differential equations
dc.subjectTissue
dc.subjectTwo dimensional
dc.subjecttimolol
dc.subjectabsorption
dc.subjectblood
dc.subjectboundary condition
dc.subjectdiffusion
dc.subjectdrug
dc.subjectequation
dc.subjectLaplace transform
dc.subjectskin
dc.subjectarticle
dc.subjectblood flow
dc.subjectcapillary
dc.subjectconcentration (parameters)
dc.subjectcontrolled study
dc.subjectdrug absorption
dc.subjectdrug clearance
dc.subjectdrug delivery system
dc.subjectdrug diffusion
dc.subjectdrug transport
dc.subjectequipment design
dc.subjectmathematical model
dc.subjectperformance
dc.subjectskin
dc.subjectsteady state
dc.subjecttransdermal drug administration
dc.subjectAdministration, Cutaneous
dc.subjectCapillaries
dc.subjectModels, Biological
dc.subjectSkin
dc.subjectSkin Absorption
dc.subjectTimolol
dc.titleTwo-dimensional transport analysis of transdermal drug absorption with a non-perfect sink boundary condition at the skin-capillary interface
dc.typearticle
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typepublishedVersion


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