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dc.contributor.authorPolat, Baris E.
dc.contributor.authorLin, Shangchao
dc.contributor.authorMendenhall, Jonathan David
dc.contributor.authorVanVeller, Brett
dc.contributor.authorLanger, Robert
dc.contributor.authorBlankschtein, Daniel
dc.date.accessioned2013-05-07T17:52:31Z
dc.date.available2013-05-07T17:52:31Z
dc.date.issued2011-01
dc.date.submitted2010-12
dc.identifier.issn0022-3654
dc.identifier.issn1541-5740
dc.identifier.urihttp://hdl.handle.net/1721.1/78839
dc.description.abstractSulforhodamine B (SRB), a common fluorescent dye, is often considered to be a purely hydrophilic molecule, having no impact on bulk or interfacial properties of aqueous solutions. This assumption is due to the high water solubility of SRB relative to most fluorescent probes. However, in the present study, we demonstrate that SRB is in fact an amphiphile, with the ability to adsorb at an air/water interface and to incorporate into sodium dodecyl sulfate (SDS) micelles. In fact, SRB reduces the surface tension of water by up to 23 mN/m, and the addition of SRB to an aqueous SDS solution induces a significant decrease in the cmc of SDS. Molecular dynamics simulations were conducted to gain a deeper understanding of these findings. The simulations revealed that SRB has defined polar “head” and nonpolar “tail” regions when adsorbed at the air/water interface as a monomer. In contrast, when incorporated into SDS micelles, only the sulfonate groups were found to be highly hydrated, suggesting that the majority of the SRB molecule penetrates into the micelle. To illustrate the implications of the amphiphilic nature of SRB, an interesting case study involving the effect of SRB on ultrasound-mediated transdermal drug delivery is presented.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant EB-00351)en_US
dc.description.sponsorshipMassachusetts Institute of Technology. Institute for Soldier Nanotechnologies (Grant DAAD-19-02-D-002)en_US
dc.description.sponsorshipDuPont MIT Allianceen_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/jp109866qen_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePMCen_US
dc.titleAn Experimental and Molecular Dynamics Investigation into the Amphiphilic Nature of Sulforhodamine Ben_US
dc.typeArticleen_US
dc.identifier.citationPolat, Baris E. et al. “Experimental and Molecular Dynamics Investigation into the Amphiphilic Nature of Sulforhodamine B.” The Journal of Physical Chemistry B 115.6 (2011): 1394–1402. ©2013 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Civil and Environmental Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.mitauthorPolat, Baris E.
dc.contributor.mitauthorLin, Shangchao
dc.contributor.mitauthorMendenhall, Jonathan David
dc.contributor.mitauthorVanVeller, Brett
dc.contributor.mitauthorLanger, Robert
dc.contributor.mitauthorBlankschtein, Daniel
dc.relation.journalJournal of Physical Chemistryen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsPolat, Baris E.; Lin, Shangchao; Mendenhall, Jonathan D.; VanVeller, Brett; Langer, Robert; Blankschtein, Danielen
dc.identifier.orcidhttps://orcid.org/0000-0002-7836-415X
dc.identifier.orcidhttps://orcid.org/0000-0003-4255-0492
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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