X-ray Activated Nanoplatforms for Deep Tissue Photodynamic Therapy

Photodynamic therapy (PDT), the use of light to excite photosensitive molecules whose electronic relaxation drives the production of highly cytotoxic reactive oxygen species (ROS), has proven an effective means of oncotherapy. However, its application has been severely constrained to superficial tis...

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Main Authors: Jeffrey S. Souris, Lara Leoni, Hannah J. Zhang, Ariel Pan, Eve Tanios, Hsiu-Ming Tsai, Irina V. Balyasnikova, Marc Bissonnette, Chin-Tu Chen
Format: Article
Language:English
Published: MDPI AG 2023-02-01
Series:Nanomaterials
Subjects:
Online Access:https://www.mdpi.com/2079-4991/13/4/673
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author Jeffrey S. Souris
Lara Leoni
Hannah J. Zhang
Ariel Pan
Eve Tanios
Hsiu-Ming Tsai
Irina V. Balyasnikova
Marc Bissonnette
Chin-Tu Chen
author_facet Jeffrey S. Souris
Lara Leoni
Hannah J. Zhang
Ariel Pan
Eve Tanios
Hsiu-Ming Tsai
Irina V. Balyasnikova
Marc Bissonnette
Chin-Tu Chen
author_sort Jeffrey S. Souris
collection DOAJ
description Photodynamic therapy (PDT), the use of light to excite photosensitive molecules whose electronic relaxation drives the production of highly cytotoxic reactive oxygen species (ROS), has proven an effective means of oncotherapy. However, its application has been severely constrained to superficial tissues and those readily accessed either endoscopically or laparoscopically, due to the intrinsic scattering and absorption of photons by intervening tissues. Recent advances in the design of nanoparticle-based X-ray scintillators and photosensitizers have enabled hybridization of these moieties into single nanocomposite particles. These nanoplatforms, when irradiated with diagnostic doses and energies of X-rays, produce large quantities of ROS and permit, for the first time, non-invasive deep tissue PDT of tumors with few of the therapeutic limitations or side effects of conventional PDT. In this review we examine the underlying principles and evolution of PDT: from its initial and still dominant use of light-activated, small molecule photosensitizers that passively accumulate in tumors, to its latest development of X-ray-activated, scintillator–photosensitizer hybrid nanoplatforms that actively target cancer biomarkers. Challenges and potential remedies for the clinical translation of these hybrid nanoplatforms and X-ray PDT are also presented.
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spelling doaj.art-a72c74d1fa3a445982e75c854b77d9862023-11-16T22:27:23ZengMDPI AGNanomaterials2079-49912023-02-0113467310.3390/nano13040673X-ray Activated Nanoplatforms for Deep Tissue Photodynamic TherapyJeffrey S. Souris0Lara Leoni1Hannah J. Zhang2Ariel Pan3Eve Tanios4Hsiu-Ming Tsai5Irina V. Balyasnikova6Marc Bissonnette7Chin-Tu Chen8Department of Radiology, The University of Chicago, Chicago, IL 60637, USAIntegrated Small Animal Imaging Research Resource, Office of Shared Research Facilities, The University of Chicago, Chicago, IL 60637, USADepartment of Radiology, The University of Chicago, Chicago, IL 60637, USADepartment of Radiology, The University of Chicago, Chicago, IL 60637, USADepartment of Radiology, The University of Chicago, Chicago, IL 60637, USAIntegrated Small Animal Imaging Research Resource, Office of Shared Research Facilities, The University of Chicago, Chicago, IL 60637, USADepartment of Neurological Surgery, Northwestern University, Chicago, IL 60611, USADepartment of Medicine, The University of Chicago, Chicago, IL 60637, USADepartment of Radiology, The University of Chicago, Chicago, IL 60637, USAPhotodynamic therapy (PDT), the use of light to excite photosensitive molecules whose electronic relaxation drives the production of highly cytotoxic reactive oxygen species (ROS), has proven an effective means of oncotherapy. However, its application has been severely constrained to superficial tissues and those readily accessed either endoscopically or laparoscopically, due to the intrinsic scattering and absorption of photons by intervening tissues. Recent advances in the design of nanoparticle-based X-ray scintillators and photosensitizers have enabled hybridization of these moieties into single nanocomposite particles. These nanoplatforms, when irradiated with diagnostic doses and energies of X-rays, produce large quantities of ROS and permit, for the first time, non-invasive deep tissue PDT of tumors with few of the therapeutic limitations or side effects of conventional PDT. In this review we examine the underlying principles and evolution of PDT: from its initial and still dominant use of light-activated, small molecule photosensitizers that passively accumulate in tumors, to its latest development of X-ray-activated, scintillator–photosensitizer hybrid nanoplatforms that actively target cancer biomarkers. Challenges and potential remedies for the clinical translation of these hybrid nanoplatforms and X-ray PDT are also presented.https://www.mdpi.com/2079-4991/13/4/673photodynamic therapynanoparticleX-ray activateddeep tissuereactive oxygen speciesdosimetry
spellingShingle Jeffrey S. Souris
Lara Leoni
Hannah J. Zhang
Ariel Pan
Eve Tanios
Hsiu-Ming Tsai
Irina V. Balyasnikova
Marc Bissonnette
Chin-Tu Chen
X-ray Activated Nanoplatforms for Deep Tissue Photodynamic Therapy
Nanomaterials
photodynamic therapy
nanoparticle
X-ray activated
deep tissue
reactive oxygen species
dosimetry
title X-ray Activated Nanoplatforms for Deep Tissue Photodynamic Therapy
title_full X-ray Activated Nanoplatforms for Deep Tissue Photodynamic Therapy
title_fullStr X-ray Activated Nanoplatforms for Deep Tissue Photodynamic Therapy
title_full_unstemmed X-ray Activated Nanoplatforms for Deep Tissue Photodynamic Therapy
title_short X-ray Activated Nanoplatforms for Deep Tissue Photodynamic Therapy
title_sort x ray activated nanoplatforms for deep tissue photodynamic therapy
topic photodynamic therapy
nanoparticle
X-ray activated
deep tissue
reactive oxygen species
dosimetry
url https://www.mdpi.com/2079-4991/13/4/673
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