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dc.contributor.authorRohrbach, Daniel J.
dc.contributor.authorSalem, Hakeem
dc.contributor.authorAksahin, Mehmet
dc.contributor.authorSunar, Ulas
dc.date.accessioned2019-08-02T12:01:55Z
dc.date.available2019-08-02T12:01:55Z
dc.date.issued2016
dc.identifier.issn2304-6732
dc.identifier.urihttps://www.mdpi.com/2304-6732/3/3/48
dc.identifier.urihttp://hdl.handle.net/11727/3794
dc.description.abstractOne of the main mechanisms of action for photodynamic therapy (PDT) is the destruction of tumor vasculature. We observed the PDT-induced vasculature destruction in a mouse model of skin cancer using two techniques: Photoacoustic microscopy (PAM) and diffuse correlation spectroscopy (DCS). PAM showed high-resolution images of the abnormal microvasculature near the establishing tumor area at pre-PDT, as well as the subsequent destruction of those vessels post-PDT. DCS indicated a significant blood flow decrease after PDT, confirming the vascular destruction. Noninvasive assessment of vascular changes may be indicative of therapy response.en_US
dc.language.isoengen_US
dc.relation.isversionof10.3390/photonics3030048en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectskin canceren_US
dc.subjectmicrovasculatureen_US
dc.subjectphotoacoustic microscopyen_US
dc.subjectblood flowen_US
dc.subjectphotodynamic therapyen_US
dc.titlePhotodynamic Therapy-Induced Microvascular Changes in a Nonmelanoma Skin Cancer Model Assessed by Photoacoustic Microscopy and Diffuse Correlation Spectroscopyen_US
dc.typearticleen_US
dc.relation.journalPHOTONICSen_US
dc.identifier.volume3en_US
dc.identifier.issue3en_US
dc.identifier.wos000381860400008en_US
dc.identifier.scopus2-s2.0-85013224002en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US


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