Current Limitations and Recent Progress in Nanomedicine for Clinically Available Photodynamic Therapy

Photodynamic therapy (PDT) using oxygen, light, and photosensitizers has been receiving great attention, because it has potential for making up for the weakness of the existing therapies such as surgery, radiation therapy, and chemotherapy. It has been mainly used to treat cancer, and clinical tests...

Full description

Bibliographic Details
Main Authors: Jooho Park, Yong-Kyu Lee, In-Kyu Park, Seung Rim Hwang
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/9/1/85
_version_ 1797410677921415168
author Jooho Park
Yong-Kyu Lee
In-Kyu Park
Seung Rim Hwang
author_facet Jooho Park
Yong-Kyu Lee
In-Kyu Park
Seung Rim Hwang
author_sort Jooho Park
collection DOAJ
description Photodynamic therapy (PDT) using oxygen, light, and photosensitizers has been receiving great attention, because it has potential for making up for the weakness of the existing therapies such as surgery, radiation therapy, and chemotherapy. It has been mainly used to treat cancer, and clinical tests for second-generation photosensitizers with improved physicochemical properties, pharmacokinetic profiles, or singlet oxygen quantum yield have been conducted. Progress is also being made in cancer theranostics by using fluorescent signals generated by photosensitizers. In order to obtain the effective cytotoxic effects on the target cells and prevent off-target side effects, photosensitizers need to be localized to the target tissue. The use of nanocarriers combined with photosensitizers can enhance accumulation of photosensitizers in the tumor site, owing to preferential extravasation of nanoparticles into the tumor vasculature by the enhanced permeability and retention effect. Self-assembly of amphiphilic polymers provide good loading efficiency and sustained release of hydrophobic photosensitizers. In addition, prodrug nanomedicines for PDT can be activated by stimuli in the tumor site. In this review, we introduce current limitations and recent progress in nanomedicine for PDT and discuss the expected future direction of research.
first_indexed 2024-03-09T04:33:44Z
format Article
id doaj.art-2f705abf723141f1ba5e3f02be154d7e
institution Directory Open Access Journal
issn 2227-9059
language English
last_indexed 2024-03-09T04:33:44Z
publishDate 2021-01-01
publisher MDPI AG
record_format Article
series Biomedicines
spelling doaj.art-2f705abf723141f1ba5e3f02be154d7e2023-12-03T13:31:55ZengMDPI AGBiomedicines2227-90592021-01-01918510.3390/biomedicines9010085Current Limitations and Recent Progress in Nanomedicine for Clinically Available Photodynamic TherapyJooho Park0Yong-Kyu Lee1In-Kyu Park2Seung Rim Hwang3Department of Biomedical Chemistry, College of Biomedical and Health Science, Konkuk University, Chungju 27478, KoreaDepartment of Chemical and Biological Engineering, Korea National University of Transportation, Chungju 27469, KoreaDepartment of Biomedical Sciences, Chonnam National University Medical School, Hwasun 58128, KoreaCollege of Pharmacy, Chosun University, Gwangju 61452, KoreaPhotodynamic therapy (PDT) using oxygen, light, and photosensitizers has been receiving great attention, because it has potential for making up for the weakness of the existing therapies such as surgery, radiation therapy, and chemotherapy. It has been mainly used to treat cancer, and clinical tests for second-generation photosensitizers with improved physicochemical properties, pharmacokinetic profiles, or singlet oxygen quantum yield have been conducted. Progress is also being made in cancer theranostics by using fluorescent signals generated by photosensitizers. In order to obtain the effective cytotoxic effects on the target cells and prevent off-target side effects, photosensitizers need to be localized to the target tissue. The use of nanocarriers combined with photosensitizers can enhance accumulation of photosensitizers in the tumor site, owing to preferential extravasation of nanoparticles into the tumor vasculature by the enhanced permeability and retention effect. Self-assembly of amphiphilic polymers provide good loading efficiency and sustained release of hydrophobic photosensitizers. In addition, prodrug nanomedicines for PDT can be activated by stimuli in the tumor site. In this review, we introduce current limitations and recent progress in nanomedicine for PDT and discuss the expected future direction of research.https://www.mdpi.com/2227-9059/9/1/85nanomedicinephotodynamic therapyphotosensitizernanocarrierself-assemblyprodrug
spellingShingle Jooho Park
Yong-Kyu Lee
In-Kyu Park
Seung Rim Hwang
Current Limitations and Recent Progress in Nanomedicine for Clinically Available Photodynamic Therapy
Biomedicines
nanomedicine
photodynamic therapy
photosensitizer
nanocarrier
self-assembly
prodrug
title Current Limitations and Recent Progress in Nanomedicine for Clinically Available Photodynamic Therapy
title_full Current Limitations and Recent Progress in Nanomedicine for Clinically Available Photodynamic Therapy
title_fullStr Current Limitations and Recent Progress in Nanomedicine for Clinically Available Photodynamic Therapy
title_full_unstemmed Current Limitations and Recent Progress in Nanomedicine for Clinically Available Photodynamic Therapy
title_short Current Limitations and Recent Progress in Nanomedicine for Clinically Available Photodynamic Therapy
title_sort current limitations and recent progress in nanomedicine for clinically available photodynamic therapy
topic nanomedicine
photodynamic therapy
photosensitizer
nanocarrier
self-assembly
prodrug
url https://www.mdpi.com/2227-9059/9/1/85
work_keys_str_mv AT joohopark currentlimitationsandrecentprogressinnanomedicineforclinicallyavailablephotodynamictherapy
AT yongkyulee currentlimitationsandrecentprogressinnanomedicineforclinicallyavailablephotodynamictherapy
AT inkyupark currentlimitationsandrecentprogressinnanomedicineforclinicallyavailablephotodynamictherapy
AT seungrimhwang currentlimitationsandrecentprogressinnanomedicineforclinicallyavailablephotodynamictherapy