Loading…

Mitochondria-targeted theranostic nanoparticles for optical sensing of oxygen, photodynamic cancer therapy, and assessment of therapeutic efficacy

We report on a novel kind of mitochondria-targeted theranostic nanoparticles (NPs). The NPs are doped with the oxygen-sensitive probe Pt(II)-porphyrins (PtTFPP) which exerts a dual role in acting as a diagnostic tool that can sense oxygen via quenching of luminescence, but also acts as an agent in p...

Full description

Saved in:
Bibliographic Details
Published in:Mikrochimica acta (1966) 2016-10, Vol.183 (10), p.2723-2731
Main Authors: Wang, Xiao-Hui, Peng, Hong-Shang, Yang, Wei, Ren, Zhao-Di, Liu, Yuan-An
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:We report on a novel kind of mitochondria-targeted theranostic nanoparticles (NPs). The NPs are doped with the oxygen-sensitive probe Pt(II)-porphyrins (PtTFPP) which exerts a dual role in acting as a diagnostic tool that can sense oxygen via quenching of luminescence, but also acts as an agent in photodynamic therapy (PDT) of cancer. In addition, it allows therapeutic efficacy to be assessed in-situ. Upon appropriate high-energy photoirradiation, the NPs generate singlet oxygen by energy transfer from triplet PtTFPP to ground state oxygen, and cell death is induced via PDT. Under low-energy light irradiation, in contrast, the NPs can be utilized to detect oxygen consumption rate via time-resolved luminescence measurements in order to study the efficacy of PDT. This is the first report where a single nanoagent is used to stimulate PDT and also to assess the efficacy of PDT. In our perception, the method provides a promising platform for testing anti-cancer drugs. Graphical abstract We report on a kind of mitochondria-targeted theranostic nanoparticles (NPs) doped with Pt(II)-porphyrins for oxygen sensing via quenching of luminescence, efficient photodynamic therapy (PDT) of cancer and quantitative assessment of therapeutic response in-situ.
ISSN:0026-3672
1436-5073
DOI:10.1007/s00604-016-1917-1