Please use this identifier to cite or link to this item: https://doi.org/10.1073/pnas.1717552115
Title: In vivo wireless photonic photodynamic therapy
Authors: Bansal, Akshaya
Yang, Fengyuan
Xi, Tian
ZHANG YONG 
Ho, John S
Keywords: Science & Technology
Multidisciplinary Sciences
Science & Technology - Other Topics
photodynamic therapy
wireless powering
bioelectronics
phototherapy
UP-CONVERSION NANOPARTICLES
LIGHT-SOURCES
BIOCOMPATIBILITY
PHOTOSENSITIZERS
CELLS
PDT
DELIVERY
TUMORS
BRAIN
Issue Date: 13-Feb-2018
Publisher: NATL ACAD SCIENCES
Citation: Bansal, 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
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.
Source Title: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
URI: https://scholarbank.nus.edu.sg/handle/10635/169757
ISSN: 0027-8424
1091-6490
DOI: 10.1073/pnas.1717552115
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