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            <subfield code="0">(orcid)0000-0002-2576-6382</subfield>
            <subfield code="a">Prieto, Martín</subfield>
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            <subfield code="a">Light emitting photon-upconversion nanoparticles in the generation of transdermal reactive oxygen species</subfield>
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        <datafield tag="260" ind1=" " ind2=" ">
            <subfield code="c">2017</subfield>
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            <subfield code="a">Common photosensitizers used in photodynamic therapy do not penetrate the skin effectively. In addition, the visible blue and red lights used to excite such photosensitizers have shallow penetration depths through tissue. To overcome these limitations, we have synthesized ultraviolet- and visible-light-emitting, energy-transfer-based upconversion nanoparticles and coencapsulated them inside PLGA-PEG (methoxy poly(ethylene glycol)-b-poly(lactic-co-glycolic acid)) nanoparticles with the photosensitizer protoporphyrin IX. Nd3+ has been introduced as a sensitizer in the upconversion nanostructure to allow its excitation at 808 nm. The subcytotoxic doses of the hybrid nanoparticles have been evaluated on different cell lines (i.e., fibroblasts, HaCaT, THP-1 monocytic cell line, U251MG (glioblastoma cell line), and mMSCs (murine mesenchymal stem cells). Upon NIR (near infrared)-light excitation, the upconversion nanoparticles emitted UV and VIS light, which consequently activated the generation of reactive-oxygen species (ROS). In addition, after irradiating at 808 nm, the resulting hybrid nanoparticles containing both upconversion nanoparticles and protoporphyrin IX generated 3.4 times more ROS than PLGA-PEG nanoparticles containing just the same dose of protoporphyrin IX. Their photodynamic effect was also assayed on different cell cultures, demonstrating their efficacy in selectively killing treated and irradiated cells. Compared to the topical application of the free photosensitizer, enhanced skin permeation and penetration were observed for the nanoparticulate formulation, using an ex vivo human-skin-permeation experiment. Whereas free protoporphyrin IX remained located at the outer layer of the skin, nanoparticle-encapsulated protoporphyrin IX was able to penetrate through the epidermal layer slightly into the dermis.</subfield>
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            <subfield code="a">All rights reserved</subfield>
            <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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            <subfield code="a">Nanoscience and Nanotechnology</subfield>
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        <datafield tag="700" ind1=" " ind2=" ">
            <subfield code="a">Rwei, Alina Y.</subfield>
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            <subfield code="0">(orcid)0000-0002-9324-0446</subfield>
            <subfield code="a">Alejo, Teresa</subfield>
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            <subfield code="a">Wei, Tuo</subfield>
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            <subfield code="a">López-Franco, María Teresa</subfield>
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            <subfield code="a">Mendoza, Gracia</subfield>
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            <subfield code="a">Sebastián, Víctor</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="a">Kohane, Daniel S.</subfield>
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            <subfield code="a">Arruebo, Manuel</subfield>
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            <subfield code="a">Universidad de Zaragoza</subfield>
            <subfield code="b">Dpto. Ing.Quím.Tecnol.Med.Amb.</subfield>
            <subfield code="c">Área Ingeniería Química</subfield>
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            <subfield code="g">9, 48 (2017), 41737-41747</subfield>
            <subfield code="p">ACS appl. mater. interfaces</subfield>
            <subfield code="t">ACS Applied Materials &amp; Interfaces</subfield>
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