Aggregation-Enhanced Asymmetric Heptamethine Cyanine Nanoplatform for Imaging-Guided Synergistic Phototherapy and Ferroptosis

Mengyuan Cui , Wenqing Li , Yanli Chen , Huijia Liu , Li Liu , Min Ji , Peng Wang

Aggregate ›› 2025, Vol. 6 ›› Issue (12) : e70211

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Aggregate ›› 2025, Vol. 6 ›› Issue (12) :e70211 DOI: 10.1002/agt2.70211
RESEARCH ARTICLE
Aggregation-Enhanced Asymmetric Heptamethine Cyanine Nanoplatform for Imaging-Guided Synergistic Phototherapy and Ferroptosis
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Abstract

Current phototherapeutic agents based on heptamethine cyanine dyes often rely on symmetric structures, limiting their photodynamic therapy (PDT) efficiency. Herein, we report a novel asymmetric heptamethine cyanine dye (Cyp-TPE) that features a twisted tetraphenylethylene moiety. This design facilitates the formation of stable aggregate nanoparticles (NPs) with a cross-arranged structure, as revealed by molecular dynamics simulations. This specific aggregation mode promotes exciton delocalization and dramatically enhances spin-orbit coupling, leading to an unprecedented ROS quantum yield of 154.54%. Under 808 nm laser irradiation, the Cyp-TPE NPs demonstrate potent synergistic photodynamic and photothermal activity, concurrently triggering ferroptosis and lysosomal dysfunction, thereby achieving multimodal death of cancer cells. Furthermore, the excellent NIR absorption and photothermal conversion of these aggregates enable precise photothermal imaging (PTI) and photoacoustic imaging (PAI). This work highlights the potential of asymmetric molecular design to overcome the limitations of conventional photosensitizers, offering a robust nanoplatform for imaging-guided cancer therapy.

Keywords

asymmetric heptamethine dyes / cancer / ferroptosis / photodynamic therapy / photothermal therapy

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Mengyuan Cui, Wenqing Li, Yanli Chen, Huijia Liu, Li Liu, Min Ji, Peng Wang. Aggregation-Enhanced Asymmetric Heptamethine Cyanine Nanoplatform for Imaging-Guided Synergistic Phototherapy and Ferroptosis. Aggregate, 2025, 6(12): e70211 DOI:10.1002/agt2.70211

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References

[1]

L. Fang, Z. Chen, J. Dai, et al., “Recent Advances in Strategies to Enhance Photodynamic and Photothermal Therapy Performance of Single-Component Organic Phototherapeutic Agents,” Advanced Science 12 (2025): 2409157.

[2]

X. Miao, W. Yao, R. Chen, et al., “Excimer-Mediated Ultrafast Intermolecular Nonradiative Decay Enables Giant Photothermal Performance for Optimized Phototheranostic,” Advanced Materials 35 (2023): 2301739.

[3]

E. S. Day, P. A. Thompson, L. Zhang, et al., “Nanoshell-Mediated Photothermal Therapy Improves Survival in a Murine Glioma Model,” Journal of Neuro-Oncology 104 (2011): 55–63.

[4]

Y. Liu, P. Bhattarai, Z. Dai, and X. Chen, “Photothermal Therapy and Photoacoustic Imaging via Nanotheranostics in Fighting Cancer,” Chemical Society Reviews 48 (2019): 2053–2108.

[5]

L. Li, J. Li, X. Huang, et al., “Construction of a Novel D-π-A Type Photosensitizer for NIR-II Fluorescence and Photoacoustic Dual-Mode Imaging Guided PDT/PTT Synergistic Cancer Therapy Through Extending the Conjugation Length,” Sensors and Actuators B: Chemical 443 (2025): 138295.

[6]

H. Chen, S. Yan, L. Zhang, et al., “A Self-Degrading and NIR-II Emissive Type I/II Photosensitizer With Synergistic Photodynamic and Photothermal Properties for Antibacterial and Anticancer,” Sensors and Actuators B: Chemical 405 (2024): 135346.

[7]

M. Cui, D. Tang, B. Wang, H. Zhang, G. Liang, and H. Xiao, “Bioorthogonal Guided Activation of cGAS-STING by AIE Photosensitizer Nanoparticles for Targeted Tumor Therapy and Imaging,” Advanced Materials 35 (2023): e2305668.

[8]

J. Yi, L. Liu, W. Gao, et al., “Advances and Perspectives in Phototherapy-Based Combination Therapy for Cancer Treatment,” Journal of Materials Chemistry B 12 (2024): 6285–6304.

[9]

Z. C. Yang, Q. S. Gu, J. J. Chao, et al., “Glutathione-Activated Biotin-Targeted Dual-Modal Imaging Probe With Improved PDT/PTT Synergistic Therapy,” Analytica Chimica Acta 1316 (2024): 342860.

[10]

H. Gu, W. Liu, W. Sun, J. Du, J. Fan, and X. Peng, “Single-Molecule Photosensitizers for NIR-II Fluorescence and Photoacoustic Imaging Guided Precise Anticancer Phototherapy,” Chemical Science 13 (2022): 9719–9726.

[11]

M. Overchuk, R. A. Weersink, B. C. Wilson, and G. Zheng, “Photodynamic and Photothermal Therapies: Synergy Opportunities for Nanomedicine,” ACS Nano 17 (2023): 7979–8003.

[12]

Y. Chen, Z. Lu, and D. Wang, “Multifunctional Nanoplatform for Single NIR Laser-Regulated Efficient PDT/PTT/Chemotherapy,” Biomacromolecules 25 (2024): 1038–1046.

[13]

Z. Li, X. Lai, S. Fu, et al., “Immunogenic Cell Death Activates the Tumor Immune Microenvironment to Boost the Immunotherapy Efficiency,” Advanced Science 9 (2022): e2201734.

[14]

X. Jiang, M. Yang, Y. Fang, et al., “A Photo-Activated Thermoelectric Catalyst for Ferroptosis-/Pyroptosis-Boosted Tumor Nanotherapy,” Advanced Healthcare Materials 12 (2023): 2300699.

[15]

X. Chen, R. Kang, G. Kroemer, and D. Tang, “Broadening Horizons: The Role of Ferroptosis in Cancer,” Nature Reviews Clinical Oncology 18 (2021): 280–296.

[16]

T. A. Mishchenko, I. V. Balalaeva, M. V. Vedunova, and D. V. Krysko, “Ferroptosis and Photodynamic Therapy Synergism: Enhancing Anticancer Treatment,” Trends in Cancer 7 (2021): 484–487.

[17]

Y. Li, R. Zhang, Q. Wan, et al., “Trojan Horse-Like Nano-AIE Aggregates Based on Homologous Targeting Strategy and Their Photodynamic Therapy in Anticancer Application,” Advanced Science 8 (2021): e2102561.

[18]

X. Zhao, H. Zhao, S. Wang, et al., “A Tumor-Targeting Near-Infrared Heptamethine Cyanine Photosensitizer With Twisted Molecular Structure for Enhanced Imaging-Guided Cancer Phototherapy,” Journal of the American Chemical Society 143 (2021): 20828–20836.

[19]

F. Wu, Y. Lu, X. Mu, et al., “Intriguing H-Aggregates of Heptamethine Cyanine for Imaging-Guided Photothermal Cancer Therapy,” ACS Applied Materials & Interfaces 12 (2020): 32388–32396.

[20]

C. Zhang, L. Long, and C. Shi, “Mitochondria-Targeting IR-780 Dye and Its Derivatives: Synthesis, Mechanisms of Action, and Theranostic Applications,” Advanced Therapeutics 1 (2018): 1800069.

[21]

X. Zhao, Z. Fan, Y. Qiao, et al., “AIEgens Conjugation Improves the Photothermal Efficacy and Near-Infrared Imaging of Heptamethine Cyanine IR-780,” ACS Applied Materials & Interfaces 12 (2020): 16114–16124.

[22]

Y. Xu, M. Cui, W. Zhang, et al., “A Sulfatase-Activatable AIEgen Nanoprobe for Inhalation Imaging-Guided Surgical Excision of Lung Cancer,” Chemical Engineering Journal 428 (2022): 132514.

[23]

K.-X. Teng, L.-Y. Niu, and Q.-Z. Yang, “Supramolecular Photosensitizer Enables Oxygen-Independent Generation of Hydroxyl Radicals for Photodynamic Therapy,” Journal of the American Chemical Society 145 (2023): 4081–4087.

[24]

P. He, M. Jia, L. Yang, et al., “Zwitterionic Photosensitizer-Assembled Nanocluster Produces Efficient Photogenerated Radicals via Autoionization for Superior Antibacterial Photodynamic Therapy,” Advanced Materials 37 (2025): 2418978.

[25]

R. Ackroyd, C. Kelty, N. Brown, and M. Reed, “The History of Photodetection and Photodynamic Therapy,” Photochemistry and Photobiology 74 (2001): 656–669.

[26]

S. Shui, Z. Zhao, H. Wang, M. Conrad, and G. Liu, “Non-Enzymatic Lipid Peroxidation Initiated by Photodynamic Therapy Drives a Distinct Ferroptosis-Like Cell Death Pathway,” Redox Biology 45 (2021): 102056.

[27]

K. Bersuker, J. M. Hendricks, Z. Li, et al., “The CoQ Oxidoreductase FSP1 Acts Parallel to GPX4 to Inhibit Ferroptosis,” Nature 575 (2019): 688–692.

[28]

S. Kaushik and A. M. Cuervo, “Chaperone-Mediated Autophagy: A Unique Way to Enter the Lysosome World,” Trends in Cell Biology 22 (2012): 407–417.

[29]

J. F. Dice, “Peptide Sequences That Target Cytosolic Proteins for Lysosomal Proteolysis,” Trends in Biochemical Sciences 15 (1990): 305–309.

[30]

H. L. Chiang, S. R. Terlecky, C. P. Plant, and J. F. Dice, “A Role for a 70-Kilodalton Heat Shock Protein in Lysosomal Degradation of Intracellular Proteins,” Science 246 (1989): 382–385.

[31]

A. M. Cuervo and J. F. Dice, “A Receptor for the Selective Uptake and Degradation of Proteins by Lysosomes,” Science 273 (1996): 501–503.

[32]

B. Tian, C. Wang, Y. Du, et al., “Near Infrared-Triggered Theranostic Nanoplatform With Controlled Release of HSP90 Inhibitor for Synergistic Mild Photothermal and Enhanced Nanocatalytic Therapy With Hypoxia Relief,” Small 18 (2022): e2200786.

[33]

S. Doll, B. Proneth, Y. Y. Tyurina, et al., “ACSL4 Dictates Ferroptosis Sensitivity by Shaping Cellular Lipid Composition,” Nature Chemical Biology 13 (2016): 91–98.

[34]

X. Wang, Y. Chen, X. Yang, et al., “Activation of ALOX12 by a Multi-Organelle-Orienting Photosensitizer Drives ACSL4-Independent Cell Ferroptosis,” Cell Death & Disease 13 (2022): 1040.

[35]

B. A. Ball and V. O. Anthony, “Detection of Lipid Peroxidation in Equine Spermatozoa Based Upon the Lipophilic Fluorescent Dye C11-BODIPY 581/591,” Journal of Andrology 23 (2013): 259–269.

[36]

C. Kong and X. Chen, “Combined Photodynamic and Photothermal Therapy and Immunotherapy for Cancer Treatment: A Review,” International Journal of Nanomedicine 17 (2022): 6427–6446.

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2025 The Author(s). Aggregate published by SCUT, AIEI, and John Wiley & Sons Australia, Ltd.

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