File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Efficient Triplet-Triplet Annihilation-Based Upconversion for Nanoparticle Phototargeting

TitleEfficient Triplet-Triplet Annihilation-Based Upconversion for Nanoparticle Phototargeting
Authors
Keywordsupconverting micelles
shielding
phototargeted
photoresponsive
photocleavage
Caged ligands
Issue Date2015
Citation
Nano Letters, 2015, v. 15, n. 10, p. 6332-6338 How to Cite?
Abstract© 2015 American Chemical Society.High-efficiency upconverted light would be a desirable stimulus for triggered drug delivery. Here we present a general strategy to achieve photoreactions based on triplet-triplet annihilation upconversion (TTA-UC) and Förster resonance energy transfer (FRET). We designed PLA-PEG micellar nanoparticles containing in their cores hydrophobic photosensitizer and annihilator molecules which, when stimulated with green light, would undergo TTA-UC. The upconverted energy was then transferred by FRET to a hydrophobic photocleavable group (DEACM), also in the core. The DEACM was bonded to (and thus inactivated) the cell-binding peptide cyclo-(RGDfK), which was bound to the PLA-PEG chain. Cleavage of DEACM by FRET reactivated the PLA-PEG-bound peptide and allowed it to move from the particle core to the surface. TTA-UC followed by FRET allowed photocontrolled binding of cell adhesion with green light LED irradiation at low irradiance for short periods. These are attractive properties in phototriggered systems.
Persistent Identifierhttp://hdl.handle.net/10722/236724
ISSN
2021 Impact Factor: 12.262
2020 SCImago Journal Rankings: 4.853
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWang, Weiping-
dc.contributor.authorLiu, Qian-
dc.contributor.authorZhan, Changyou-
dc.contributor.authorBarhoumi, Aoune-
dc.contributor.authorYang, Tianshe-
dc.contributor.authorWylie, Ryan G.-
dc.contributor.authorArmstrong, Patrick A.-
dc.contributor.authorKohane, Daniel S.-
dc.date.accessioned2016-12-02T03:07:29Z-
dc.date.available2016-12-02T03:07:29Z-
dc.date.issued2015-
dc.identifier.citationNano Letters, 2015, v. 15, n. 10, p. 6332-6338-
dc.identifier.issn1530-6984-
dc.identifier.urihttp://hdl.handle.net/10722/236724-
dc.description.abstract© 2015 American Chemical Society.High-efficiency upconverted light would be a desirable stimulus for triggered drug delivery. Here we present a general strategy to achieve photoreactions based on triplet-triplet annihilation upconversion (TTA-UC) and Förster resonance energy transfer (FRET). We designed PLA-PEG micellar nanoparticles containing in their cores hydrophobic photosensitizer and annihilator molecules which, when stimulated with green light, would undergo TTA-UC. The upconverted energy was then transferred by FRET to a hydrophobic photocleavable group (DEACM), also in the core. The DEACM was bonded to (and thus inactivated) the cell-binding peptide cyclo-(RGDfK), which was bound to the PLA-PEG chain. Cleavage of DEACM by FRET reactivated the PLA-PEG-bound peptide and allowed it to move from the particle core to the surface. TTA-UC followed by FRET allowed photocontrolled binding of cell adhesion with green light LED irradiation at low irradiance for short periods. These are attractive properties in phototriggered systems.-
dc.languageeng-
dc.relation.ispartofNano Letters-
dc.subjectupconverting micelles-
dc.subjectshielding-
dc.subjectphototargeted-
dc.subjectphotoresponsive-
dc.subjectphotocleavage-
dc.subjectCaged ligands-
dc.titleEfficient Triplet-Triplet Annihilation-Based Upconversion for Nanoparticle Phototargeting-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/acs.nanolett.5b01325-
dc.identifier.pmid26158690-
dc.identifier.scopuseid_2-s2.0-84944339302-
dc.identifier.volume15-
dc.identifier.issue10-
dc.identifier.spage6332-
dc.identifier.epage6338-
dc.identifier.eissn1530-6992-
dc.identifier.isiWOS:000363003100008-
dc.identifier.issnl1530-6984-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats