TY - JOUR
T1 - Theranostic NIR-active Conjugated Polymer Nanoparticles
AU - Zhao, Miao
AU - Leggett, Edward
AU - Bourke, Struan
AU - Poursanidou, Souzana
AU - Carter-Searjeant, Sadie
AU - Po, Steve
AU - Palma do Carmo, Marciano
AU - Dailey, Lea Ann
AU - Manning, Philip
AU - Ryan, Sean
AU - Urbano, Laura
AU - Green, Mark
AU - Rakovich, Aliaksandra
N1 - © 2021 American Chemical Society. This is the accepted manuscript version of an article which has been published in final form at https://doi.org/10.1021/acsnano.1c01257
PY - 2021/5/12
Y1 - 2021/5/12
N2 - Conjugated polymer nanoparticles (CPNs) based on a common solar cell material (PTB7) have been prepared, and their potential in theranostic applications based on bioimaging and photosensitizing capabilities has been evaluated. The main absorption and emission bands of the prepared CPN particles both fell within the NIR-I (650-950 nm) transparency window, allowing facile and efficient implementation of our CPNs as bioimaging agents, as demonstrated in this work for A549 human lung cancer cell cultures. The prepared CPN samples were also shown to produce reactive oxygen species (ROS) upon photoexcitation in the near infrared or ultraviolet spectral regions, both in aqueous solutions and in HaCaT keratinocyte cell cultures. Importantly, we show that the photosensitizing ability of our CPNs was largely determined by the nature of the stabilizing shell: coating the CPNs with a pluronic F127 copolymer led to an improvement of photoinitiated ROS production, while using PSMA instead completely quenched said process. To best of our knowledge, this work is the first to demonstrate the modulation of the photosensitizing capability of CPNs via an appropriate selection of stabilizing material and one that opens a new gateway to the design of theranostic probes based on CPNs.
AB - Conjugated polymer nanoparticles (CPNs) based on a common solar cell material (PTB7) have been prepared, and their potential in theranostic applications based on bioimaging and photosensitizing capabilities has been evaluated. The main absorption and emission bands of the prepared CPN particles both fell within the NIR-I (650-950 nm) transparency window, allowing facile and efficient implementation of our CPNs as bioimaging agents, as demonstrated in this work for A549 human lung cancer cell cultures. The prepared CPN samples were also shown to produce reactive oxygen species (ROS) upon photoexcitation in the near infrared or ultraviolet spectral regions, both in aqueous solutions and in HaCaT keratinocyte cell cultures. Importantly, we show that the photosensitizing ability of our CPNs was largely determined by the nature of the stabilizing shell: coating the CPNs with a pluronic F127 copolymer led to an improvement of photoinitiated ROS production, while using PSMA instead completely quenched said process. To best of our knowledge, this work is the first to demonstrate the modulation of the photosensitizing capability of CPNs via an appropriate selection of stabilizing material and one that opens a new gateway to the design of theranostic probes based on CPNs.
KW - conjugated polymer nanoparticles
KW - theranostic probe
KW - NIR-I
KW - reactive oxygen species
KW - photodynamic therapy
U2 - 10.1021/acsnano.1c01257
DO - 10.1021/acsnano.1c01257
M3 - Article
SN - 1936-0851
VL - 15
SP - 8790
EP - 8802
JO - ACS Nano
JF - ACS Nano
IS - 5
ER -