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Article: Designing nanoparticle carriers for enhanced drug efficacy in photodynamic therapy

TitleDesigning nanoparticle carriers for enhanced drug efficacy in photodynamic therapy
Authors
Issue Date2014
Citation
Biomaterials Science, 2014, v. 2, n. 6, p. 827-832 How to Cite?
AbstractAlthough nanoparticles (NPs) have been proposed as carriers for photosensitizers (PS) in photodynamic therapy (PDT), how the design parameters of nanocarriers affect the final drug efficacy remains unclear. By designing SiO2-PS NPs with specific features (such as enabling easy release of PS from the nanocarriers, or introducing plasmonic Au NPs in the vicinity of the PS), and comparing the respective efficacy of PS to that of the conventional dense SiO2-PS NPs (PS were tightly confined into the silica matrix), we identified that both PS trapping-in/releasing from the silica nanocarriers and the Au plasmonic effect were responsible for the PS efficacy variation. The mechanistic study also disclosed that the different NP configurations would affect the cellular death pathway. These findings provide a general guideline for the design of NP-based PDT applications. This journal is © the Partner Organisations 2014.
Persistent Identifierhttp://hdl.handle.net/10722/265671
ISSN
2021 Impact Factor: 7.590
2020 SCImago Journal Rankings: 1.422
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChu, Zhiqin-
dc.contributor.authorZhang, Silu-
dc.contributor.authorYin, Chun-
dc.contributor.authorLin, Ge-
dc.contributor.authorLi, Quan-
dc.date.accessioned2018-12-03T01:21:20Z-
dc.date.available2018-12-03T01:21:20Z-
dc.date.issued2014-
dc.identifier.citationBiomaterials Science, 2014, v. 2, n. 6, p. 827-832-
dc.identifier.issn2047-4830-
dc.identifier.urihttp://hdl.handle.net/10722/265671-
dc.description.abstractAlthough nanoparticles (NPs) have been proposed as carriers for photosensitizers (PS) in photodynamic therapy (PDT), how the design parameters of nanocarriers affect the final drug efficacy remains unclear. By designing SiO2-PS NPs with specific features (such as enabling easy release of PS from the nanocarriers, or introducing plasmonic Au NPs in the vicinity of the PS), and comparing the respective efficacy of PS to that of the conventional dense SiO2-PS NPs (PS were tightly confined into the silica matrix), we identified that both PS trapping-in/releasing from the silica nanocarriers and the Au plasmonic effect were responsible for the PS efficacy variation. The mechanistic study also disclosed that the different NP configurations would affect the cellular death pathway. These findings provide a general guideline for the design of NP-based PDT applications. This journal is © the Partner Organisations 2014.-
dc.languageeng-
dc.relation.ispartofBiomaterials Science-
dc.titleDesigning nanoparticle carriers for enhanced drug efficacy in photodynamic therapy-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/c4bm00024b-
dc.identifier.scopuseid_2-s2.0-84900325581-
dc.identifier.volume2-
dc.identifier.issue6-
dc.identifier.spage827-
dc.identifier.epage832-
dc.identifier.eissn2047-4849-
dc.identifier.isiWOS:000335984000003-
dc.identifier.issnl2047-4830-

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