Please use this identifier to cite or link to this item: https://doi.org/10.1073/pnas.1717552115
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dc.titleIn vivo wireless photonic photodynamic therapy
dc.contributor.authorBansal, Akshaya
dc.contributor.authorYang, Fengyuan
dc.contributor.authorXi, Tian
dc.contributor.authorZHANG YONG
dc.contributor.authorHo, John S
dc.date.accessioned2020-06-15T02:47:36Z
dc.date.available2020-06-15T02:47:36Z
dc.date.issued2018-02-13
dc.identifier.citationBansal, Akshaya, Yang, Fengyuan, Xi, Tian, ZHANG YONG, Ho, John S (2018-02-13). In vivo wireless photonic photodynamic therapy. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 115 (7) : 1469-1474. ScholarBank@NUS Repository. https://doi.org/10.1073/pnas.1717552115
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/169757
dc.description.abstract© 2018 National Academy of Sciences.All Rights Reserved. An emerging class of targeted therapy relies on light as a spatially and temporally precise stimulus. Photodynamic therapy (PDT) is a clinical example in which optical illumination selectively activates light-sensitive drugs, termed photosensitizers, destroying malignant cells without the side effects associated with systemic treatments such as chemotherapy. Effective clinical application of PDT and other light-based therapies, however, is hindered by challenges in light delivery across biological tissue, which is optically opaque. To target deep regions, current clinical PDT uses optical fibers, but their incompatibility with chronic implantation allows only a single dose of light to be delivered per surgery. Here we report a wireless photonic approach to PDT using a miniaturized (30 mg, 15 mm3) implantable device and wireless powering system for light delivery. We demonstrate the therapeutic efficacy of this approach by activating photosensitizers (chlorin e6) through thick (>3 cm) tissues inaccessible by direct illumination, and by delivering multiple controlled doses of light to suppress tumor growth in vivo in animal cancer models. This versatility in light delivery overcomes key clinical limitations in PDT, and may afford further opportunities for light-based therapies.
dc.language.isoen
dc.publisherNATL ACAD SCIENCES
dc.sourceElements
dc.subjectScience & Technology
dc.subjectMultidisciplinary Sciences
dc.subjectScience & Technology - Other Topics
dc.subjectphotodynamic therapy
dc.subjectwireless powering
dc.subjectbioelectronics
dc.subjectphototherapy
dc.subjectUP-CONVERSION NANOPARTICLES
dc.subjectLIGHT-SOURCES
dc.subjectBIOCOMPATIBILITY
dc.subjectPHOTOSENSITIZERS
dc.subjectCELLS
dc.subjectPDT
dc.subjectDELIVERY
dc.subjectTUMORS
dc.subjectBRAIN
dc.typeArticle
dc.date.updated2020-06-11T05:19:55Z
dc.contributor.departmentBIOMEDICAL ENGINEERING
dc.description.doi10.1073/pnas.1717552115
dc.description.sourcetitlePROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
dc.description.volume115
dc.description.issue7
dc.description.page1469-1474
dc.published.statePublished
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