TY - JOUR
T1 - A Nanotherapeutic Agent for Synergistic Tumor Therapy
T2 - Co-Activation of Photochemical-Biological Effects
AU - Liu, Junwei
AU - Liu, Yang
AU - Zhi, Songsong
AU - Yang, Yonggang
AU - Kim, Heejeong
AU - Wu, Dapeng
AU - Wang, Ge
AU - James, Tony D.
AU - Yoon, Juyoung
AU - Zhang, Hua
N1 - Publisher Copyright:
© 2025 The Author(s). Angewandte Chemie International Edition published by Wiley-VCH GmbH.
PY - 2025/4/17
Y1 - 2025/4/17
N2 - Single-mode photodynamic therapy (PDT) based on photochemical reactions is limited by the tumor microenvironment, which reduces the ablation efficiency for solid tumors. Making it vital to seek ways to improve the tumor therapeutic effect. Based on this, we propose a dual-mode intelligent nanotherapeutic system (HAP@BMPns) based on photochemical-biological effects. HAP@BMPns is composed of an acid-responsive high-calcium biomimetic nanomaterial (HAP) and photosensitizer (BMP), which can spontaneously activate photochemical (Type-I PDT) and biological effects for synergistic cancer therapy. HAP@BMPns breaks down upon entering tumor cells under acidic conditions, releasing a large amount of Ca2+ and BMP. Triggering intracellular Ca2+ overload, which induces mitochondrial damage, leading to apoptosis. Synchronously, Type-I PDT of BMP under two-photon (800 nm) laser irradiation becomes activated, resulting in enhanced destruction of tumor cells by the photochemical effect. Cell studies have indicated that HAP@BMPns (41.6 μg/mL) exhibits a strong inhibitory efficiency on tumor cells growth, with low (22.4 %) survival rate. However, the individual components, i. e. BMP (5.0 μM) and HAP (41.6 μg/mL) display low inhibitory efficiency with high survival rates (55.9 % and 63.0 % respectively). Therefore, this dual-mode synergistic treatment strategy using acid-triggered photochemical-biological effects significantly enhances the ablation of solid tumors, realizing the synergistic effect. We hope that this design strategy can provide guidance for the design and development of a tumor therapeutic platform.
AB - Single-mode photodynamic therapy (PDT) based on photochemical reactions is limited by the tumor microenvironment, which reduces the ablation efficiency for solid tumors. Making it vital to seek ways to improve the tumor therapeutic effect. Based on this, we propose a dual-mode intelligent nanotherapeutic system (HAP@BMPns) based on photochemical-biological effects. HAP@BMPns is composed of an acid-responsive high-calcium biomimetic nanomaterial (HAP) and photosensitizer (BMP), which can spontaneously activate photochemical (Type-I PDT) and biological effects for synergistic cancer therapy. HAP@BMPns breaks down upon entering tumor cells under acidic conditions, releasing a large amount of Ca2+ and BMP. Triggering intracellular Ca2+ overload, which induces mitochondrial damage, leading to apoptosis. Synchronously, Type-I PDT of BMP under two-photon (800 nm) laser irradiation becomes activated, resulting in enhanced destruction of tumor cells by the photochemical effect. Cell studies have indicated that HAP@BMPns (41.6 μg/mL) exhibits a strong inhibitory efficiency on tumor cells growth, with low (22.4 %) survival rate. However, the individual components, i. e. BMP (5.0 μM) and HAP (41.6 μg/mL) display low inhibitory efficiency with high survival rates (55.9 % and 63.0 % respectively). Therefore, this dual-mode synergistic treatment strategy using acid-triggered photochemical-biological effects significantly enhances the ablation of solid tumors, realizing the synergistic effect. We hope that this design strategy can provide guidance for the design and development of a tumor therapeutic platform.
KW - Ca Overload
KW - Photodynamic Therapy
KW - Synergistic Effects
KW - Theranostics
KW - Tumor Therapy
UR - https://www.scopus.com/pages/publications/105003156509
U2 - 10.1002/anie.202425631
DO - 10.1002/anie.202425631
M3 - Article
C2 - 39936628
AN - SCOPUS:105003156509
SN - 1433-7851
VL - 64
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 17
M1 - e202425631
ER -