TY - JOUR
T1 - Aggregation-Induced Emission Luminogen Based Wearable Visible-Light Penetrator for Deep Photodynamic Therapy
AU - Zhou, Kun
AU - Yu, Ying
AU - Xu, Letian
AU - Wang, Siyuan
AU - Li, Zhuojian
AU - Liu, Yong
AU - Kwok, Ryan T.K.
AU - Sun, Jianwei
AU - Lam, Jacky W.Y.
AU - He, Gang
AU - Zhao, Zheng
AU - Tang, Ben Zhong
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/10/29
Y1 - 2024/10/29
N2 - Photodynamic therapy (PDT) has emerged as a preferred nonsurgical treatment in clinical applications due to its capacity to selectively eradicate diseased tissues while minimizing damage to normal tissue. Nevertheless, its clinical efficacy is constrained by the limited penetration of visible light. Although near-infrared (NIR) lasers offer enhanced tissue penetration, the dearth of suitable photosensitizers and a pronounced imaging-treatment disparity pose challenges. Additionally, clinical implementation via optical fiber implantation carries infection risks and necessitates minimally invasive surgery, contradicting PDT’s noninvasive advantage. In this study, we introduce a brilliant approach utilizing aggregation-induced emission luminogens (AIEgen) to develop a visible-light penetrator (VLP), coupled with wireless light emitting diodes (LEDs), enabling deep photodynamic therapy. We validate the therapeutic efficacy of this visible-light penetrator in tissues inaccessible to conventional PDT, demonstrating significant suppression of inflammatory diffusion in vivo using AIEgen TBPPM loaded within the VLP, which exhibits a transmittance of 86% in tissues with a thickness of 3 mm. This innovative visible-light penetrator effectively overcomes the substantial limitations of PDT in clinical settings and holds promise for advancing phototherapy.
AB - Photodynamic therapy (PDT) has emerged as a preferred nonsurgical treatment in clinical applications due to its capacity to selectively eradicate diseased tissues while minimizing damage to normal tissue. Nevertheless, its clinical efficacy is constrained by the limited penetration of visible light. Although near-infrared (NIR) lasers offer enhanced tissue penetration, the dearth of suitable photosensitizers and a pronounced imaging-treatment disparity pose challenges. Additionally, clinical implementation via optical fiber implantation carries infection risks and necessitates minimally invasive surgery, contradicting PDT’s noninvasive advantage. In this study, we introduce a brilliant approach utilizing aggregation-induced emission luminogens (AIEgen) to develop a visible-light penetrator (VLP), coupled with wireless light emitting diodes (LEDs), enabling deep photodynamic therapy. We validate the therapeutic efficacy of this visible-light penetrator in tissues inaccessible to conventional PDT, demonstrating significant suppression of inflammatory diffusion in vivo using AIEgen TBPPM loaded within the VLP, which exhibits a transmittance of 86% in tissues with a thickness of 3 mm. This innovative visible-light penetrator effectively overcomes the substantial limitations of PDT in clinical settings and holds promise for advancing phototherapy.
KW - aggregation-induced emission
KW - antibacterial
KW - deep tissue infection
KW - photodynamic therapy
KW - visible-light penetrator
UR - https://www.scopus.com/pages/publications/85207134787
U2 - 10.1021/acsnano.4c10452
DO - 10.1021/acsnano.4c10452
M3 - 文章
C2 - 39423317
AN - SCOPUS:85207134787
SN - 1936-0851
VL - 18
SP - 29930
EP - 29941
JO - ACS Nano
JF - ACS Nano
IS - 43
ER -