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dc.contributor.authorZani, Brett
dc.contributor.authorStanley, James
dc.contributor.authorMuraj, Benny
dc.contributor.authorKnutson, Jennifer
dc.contributor.authorKohler, Robert
dc.contributor.authorMarkham, Peter
dc.contributor.authorNikanorov, Alexander
dc.contributor.authorTzafriri, A Rami
dc.contributor.authorGarcia Polite, Fernando
dc.contributor.authorEdelman, Elazer R
dc.date.accessioned2017-12-14T16:56:46Z
dc.date.available2017-12-14T16:56:46Z
dc.date.issued2017-09
dc.date.submitted2017-08
dc.identifier.issn0168-3659
dc.identifier.urihttp://hdl.handle.net/1721.1/112760
dc.description.abstractBackground: Calcific atherosclerosis is a major challenge to intraluminal drug delivery in peripheral artery disease (PAD). Objectives: We evaluated the effects of orbital atherectomy on intraluminal paclitaxel delivery to human peripheral arteries with substantial calcified plaque. Methods: Diagnostic angiography and 3-D rotational imaging of five fresh human lower limbs revealed calcification in all main arteries. The proximal or distal segment of each artery was treated using an orbital atherectomy system (OAS) under simulated blood flow and fluoroscopy. Explanted arterial segments underwent either histomorphometric assessment of effect or tracking of [superscript 14]C-labeled or fluorescent–labeled paclitaxel. Radiolabeled drug quantified bulk delivery and fluorescent label established penetration of drug over finer spatial domain in serial microscopic sections. Results: were interpreted using a mathematical model of binding-diffusion mediated arterial drug distribution. Results Lesion composition affected paclitaxel absorption and distribution in cadaveric human peripheral arteries. Pretreatment imaging calcium scores in control femoropopliteal arterial segments correlated with a log-linear decline in the bulk absorption rate-constant of [superscript 14]C-labeled, declining 5.5-fold per calcified quadrant (p = 0.05, n = 7). Compared to controls, OAS-treated femoropopliteal segments exhibited 180 μm thinner intima (p < 0.001), 45% less plaque calcification, and 2 log orders higher paclitaxel bulk absorption rate-constants. Correspondingly, fluorescent paclitaxel penetrated deeper in OAS-treated femoropopliteal segments compared to controls, due to a 70% increase in diffusivity (p < 0.001). Conclusions These data illustrate that calcified plaque limited intravascular drug delivery, and controlled OAS treatment of calcific plaques resulted in greater drug permeability and improved adjunct drug delivery to diseased arteries.Peripheral artery disease Keywords: Drug coated balloons, Drug eluting stents, Atherectomy, Orbital atherectomy, calcified plaque, Paclitaxelen_US
dc.description.sponsorshipNational Institute of Mental Health (U.S.) (Grant R01 GM-49039)en_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.jconrel.2017.08.037en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourceElsevieren_US
dc.titleCalcified plaque modification alters local drug delivery in the treatment of peripheral atherosclerosisen_US
dc.typeArticleen_US
dc.identifier.citationTzafriri, Abraham R., et al. “Calcified Plaque Modification Alters Local Drug Delivery in the Treatment of Peripheral Atherosclerosis.” Journal of Controlled Release, vol. 264, Oct. 2017, pp. 203–10.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.mitauthorTzafriri, A Rami
dc.contributor.mitauthorGarcia Polite, Fernando
dc.contributor.mitauthorEdelman, Elazer R
dc.relation.journalJournal of Controlled Releaseen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2017-12-14T16:08:21Z
dspace.orderedauthorsTzafriri, Abraham R.; Garcia-Polite, Fernando; Zani, Brett; Stanley, James; Muraj, Benny; Knutson, Jennifer; Kohler, Robert; Markham, Peter; Nikanorov, Alexander; Edelman, Elazer R.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-7832-7156
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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