Isomer Engineering of NIR-II Aggregation-Induced Emission for the Theranostics of MRSA-Induced Abscess

Wentian Zhang , Haifei Wen , Ximing Chen , Tianxing Liu , Yuanyuan Li , Zhiliang Yu , Linjie Tan , Shichuang Xu , Parvej Alam , Zheng Zhao , Ying Li , Junfeng Dong , Ben Zhong Tang

Aggregate ›› 2026, Vol. 7 ›› Issue (6) : e70376

PDF (9019KB)
Aggregate ›› 2026, Vol. 7 ›› Issue (6) :e70376 DOI: 10.1002/agt2.70376
RESEARCH ARTICLE
Isomer Engineering of NIR-II Aggregation-Induced Emission for the Theranostics of MRSA-Induced Abscess
Author information +
History +
PDF (9019KB)

Abstract

The escalating crisis of antimicrobial resistance poses an urgent threat to global public health. Conventional photodynamic therapy (PDT) is limited by oxygen dependence and restricted light penetration, which can compromise its therapeutic efficacy in the hypoxic microenvironment of deep abscesses. Herein, we report a positional isomer engineering strategy that transforms a thioxanthene (THX) scaffold into aggregation-induced emission luminogens (AIEgens) with fluorescence extending into the second near-infrared (NIR-II) window and dual-modal therapeutic capability. Theoretical and photophysical studies revealed that the para-configured isomer (Ph-p-THX) exhibited a smaller energy gap and higher oscillator strength than its meta-counterpart (Ph-m-THX). These electronic features provide more favorable singlet-triplet energy alignment, thereby supporting triplet-involved Type-I-dominant mixed reactive oxygen species (ROS) generation under hypoxic-relevant conditions associated with abscess microenvironments. In parallel, the narrowed energy gap and enhanced light-harvesting capability contribute to efficient photothermal conversion. As a result, Ph-p-THX enabled NIR-II imaging-guided treatment and exhibited superior antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) abscesses in vivo. Overall, this study highlights positional isomerization as an effective strategy for optimizing THX-based AIE photosensitizers for antimicrobial theranostic applications.

Keywords

aggregation-induced emission luminogens / MRSA abscess / photodynamic therapy / photothermal therapy / positional isomer engineering

Cite this article

Download citation ▾
Wentian Zhang, Haifei Wen, Ximing Chen, Tianxing Liu, Yuanyuan Li, Zhiliang Yu, Linjie Tan, Shichuang Xu, Parvej Alam, Zheng Zhao, Ying Li, Junfeng Dong, Ben Zhong Tang. Isomer Engineering of NIR-II Aggregation-Induced Emission for the Theranostics of MRSA-Induced Abscess. Aggregate, 2026, 7 (6) : e70376 DOI:10.1002/agt2.70376

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

A. Abbas, A. Barkhouse, D. Hackenberger, and G. D. Wright, “Antibiotic Resistance: A Key Microbial Survival Mechanism That Threatens Public Health,” Cell Host & Microbe 32 (2024): 837-851.

[2]

C. Lei, S. Kumar, and H. Y. Wu, “A Review of Current Antibiotic Resistance and Promising Antibiotics With Novel Modes of Action to Combat Antibiotic Resistance,” Archives of Microbiology 205 (2023): 356.

[3]

G. P. Allen and L. M. Deshpande, “Determination of the Mutant Selection Window for Clindamycin, Doxycycline, Linezolid, Moxifloxacin and Trimethoprim/Sulfamethoxazole Against Community-Associated Meticillin-Resistant Staphylococcus aureus (MRSA),” International Journal of Antimicrobial Agents 35 (2010): 45-49.

[4]

M. R. Earls, E. J. Steinig, S. Monecke, et al., “Exploring the Evolution and Epidemiology of European CC1-MRSA-IV: Tracking a Multidrug-Resistant Community-Associated Meticillin-Resistant Staphylococcus aureus Clone,” Microbial Genomics 7 (2021): 000601.

[5]

Y. Lv, M. Zhao, Q. Lin, et al., “Bacterial DNA-Targeting AIE Photosensitizer for Efficient Eradication of Intracellular Bacteria and Biofilm-Associated Infections,” Aggregate 6 (2025): e70214.

[6]

R. Sauermann, R. Karch, H. Langenberger, et al., “Antibiotic Abscess Penetration: Fosfomycin Levels Measured in Pus and Simulated Concentration-Time Profiles,” Antimicrobial Agents and Chemotherapy 49 (2005): 4448-4454.

[7]

X. Gu, X. Zhang, H. Ma, et al., “Corannulene-Incorporated AIE Nanodots With Highly Suppressed Nonradiative Decay for Boosted Cancer Phototheranostics In Vivo,” Advanced Materials 30 (2018): 1801065.

[8]

M. J. Jiang, J. Kang, and A. Dong, “Aggregation-Induced Emission Luminogens for Intracellular Bacteria Imaging and Elimination,” Biosensors and Bioelectronics 267 (2025): 116873.

[9]

L. Shen, Q. Zhang, Y. Yao, et al., “Alkyl Chain Length-Regulated In Situ Intelligent Nano-Assemblies With AIE-Active Photosensitizers for Photodynamic Cancer Therapy,” Asian Journal of Pharmaceutical Sciences 19 (2024): 100967.

[10]

Y. Wu, J. Li, L. Zhu, et al., “Photosensitive AIEgens Sensitize Bacteria to Oxidative Damage and Modulate the Inflammatory Responses of Macrophages to Salvage the Photodynamic Therapy Against MRSA,” Biomaterials 309 (2024): 122583.

[11]

H. Wang, E. G. Zhao, J. W. Y. Lam, and B. Z. Tang, “AIE Luminogens: Emission Brightened by Aggregation,” Materials Today 18 (2015): 365-377.

[12]

M. Jiang, X. Gu, R. T. K. Kwok, et al., “Multifunctional AIEgens: Ready Synthesis, Tunable Emission, Mechanochromism, Mitochondrial, and Bacterial Imaging,” Advanced Functional Materials 28 (2018): 1704589.

[13]

D. Li, P. Liu, Y. Tan, et al., “Type I Photosensitizers Based on Aggregation-Induced Emission: A Rising Star in Photodynamic Therapy,” Biosensors 12 (2022): 722.

[14]

K. Anguluri, S. Bagherpour, A. C. Calpena, et al., “Rose Bengal-Incorporated Supramolecular Gels as a Topical Platform for Localized Antimicrobial Photodynamic Therapy,” International Journal of Molecular Sciences 26 (2025): 11455.

[15]

P. Chowdhury, A. Banerjee, B. Saha, K. Bauri, and P. De, “Stimuli-Responsive Aggregation-Induced Emission (AIE)-Active Polymers for Biomedical Applications,” ACS Biomaterials Science & Engineering 8 (2022): 4207-4229.

[16]

C. Li, J. Li, Y. Pang, et al., “Harnessing Donor Cyclization Strategy: Converting Type II to Type I Photosensitizers and Enhancing AIE Performance for NIR-II FL/MR Imaging-Guided Photodynamic Therapy Under Hypoxia Condition,” Chemical Engineering Journal 498 (2024): 155471.

[17]

M. M. Lee, D. Yan, J. H. Chau, et al., “Highly Efficient Phototheranostics of Macrophage-Engulfed Gram-Positive Bacteria Using a NIR Luminogen With Aggregation-Induced Emission Characteristics,” Biomaterials 261 (2020): 120340.

[18]

G. Qi, X. Liu, H. Li, et al., “A Dual-Mechanism Luminescent Antibiotic for Bacterial Infection Identification and Eradication,” Science Advances 11 (2025): e9448.

[19]

H. Yu, B. Chen, H. Huang, et al., “AIE-Active Photosensitizers: Manipulation of Reactive Oxygen Species Generation and Applications in Photodynamic Therapy,” Biosensors 12 (2022): 348.

[20]

S. Zhen, Z. Xu, M. Suo, et al., “NIR-II AIE Liposomes for Boosting Type-I Photodynamic and Mild-Temperature Photothermal Therapy in Breast Cancer Treatment,” Advanced Materials 37 (2025): 2411133.

[21]

K. Wen, H. Tan, Q. Peng, et al., “Achieving Efficient NIR-II Type-I Photosensitizers for Photodynamic/Photothermal Therapy Upon Regulating Chalcogen Elements,” Advanced Materials 34 (2022): 2108146.

[22]

C. Wang, Y. Xiao, W. Zhu, et al., “Photosensitizer-Modified MnO2 Nanoparticles to Enhance Photodynamic Treatment of Abscesses and Boost Immune Protection for Treated Mice,” Small 16 (2020): 2000589.

[23]

M. Tavakkoli Yaraki, M. Wu, E. Middha, et al., “Gold Nanostars-AIE Theranostic Nanodots With Enhanced Fluorescence and Photosensitization Towards Effective Image-Guided Photodynamic Therapy,” Nano-Micro Letters 13 (2021): 58.

[24]

B. Li, W. Wang, L. Zhao, et al., “Multifunctional AIE Nanosphere-Based “Nanobomb” for Trimodal Imaging-Guided Photothermal/Photodynamic/Pharmacological Therapy of Drug-Resistant Bacterial Infections,” ACS Nano 17 (2023): 4601-4618.

[25]

C. Wang, J. Wang, K. Xue, M. Xiao, Z. Sun, and C. Zhu, “A Receptor-Targeting AIE Photosensitizer for Selective Bacterial Killing and Real-Time Monitoring of Photodynamic Therapy Outcome,” Chemical Communications 58 (2022): 7058-7061.

[26]

F. Wang, Y. Zhong, O. Bruns, Y. Liang, and H. Dai, “In Vivo NIR-II Fluorescence Imaging for Biology and Medicine,” Nature Photonics 18 (2024): 535-547.

[27]

H. Wang, X. D. Chen, G. Xie, et al., “Inverse Opal Photonic Hydrogels for Blue-Edge Slow Photon-Enhanced Photodynamic Antibacterial Therapy,” Advanced Functional Materials 33 (2023): 102225.

[28]

S. Huang, Z. Wang, Q. Wu, et al., “Top-Down Assembly of Photosensitizable Flexible Wood Dressing With Synergistic Effect of Anti-Infection and Moisture Management,” Advanced Functional Materials 35 (2025): 2423123.

[29]

P. Manivasagan, T. Thambi, A. Joe, et al., “Progress in Nanomaterial-Based Synergistic Photothermal-Enhanced Chemodynamic Therapy in Combating Bacterial Infections,” Progress in Materials Science 144 (2024): 101292.

[30]

J. Gong, L. Liu, C. Li, et al., “Oxidization Enhances Type I ROS Generation of AIE-Active Zwitterionic Photosensitizers for Photodynamic Killing of Drug-Resistant Bacteria,” Chemical Science 14 (2023): 4863-4871.

[31]

Z. Chang, J. Cai, C. Liu, et al., “Strong Exciton Emission and Ultra-Photostable Near Infrared-II Fluorescent Protein for In Vivo Imaging,” Advanced Functional Materials 35 (2025): 2416366.

[32]

Z. Feng, T. Tang, T. Wu, et al., “Perfecting and Extending the Near-Infrared Imaging Window,” Light: Science & Applications 10 (2021): 197.

[33]

F. Yu, Y. Zhong, B. Zhang, et al., “A New Theranostic Platform Against Gram-Positive Bacteria Based on Near-Infrared-Emissive Aggregation-Induced Emission Nanoparticles,” Small 20 (2024): 2308071.

[34]

H. Wang, B. Li, Y. Sun, et al., “NIR-II AIE Luminogen-Based Erythrocyte-Like Nanoparticles With Granuloma-Targeting and Self-Oxygenation Characteristics for Combined Phototherapy of Tuberculosis,” Advanced Materials 36 (2024): e2406143.

[35]

T. Huang, K. Yang, W. Hu, et al., “Manipulation of Intramolecular Charge Transfer in NIR-II Emissive Organic Diradicaloids via a Symmetry-Breaking Design,” Chem 11 (2025): 102659.

[36]

G. Su, Y. Liu, W. Chou, et al., “Facile Crystallized-AIE-Photosensitizer Functionalized Hydrogel for Antimicrobial Photodynamic Therapy and Wound Recovery,” European Journal of Medicinal Chemistry 298 (2025): 118016.

[37]

Z. Zhou, K. Yang, L. He, et al., “Sulfone-Functionalized Chichibabin's Hydrocarbons: Stable Diradicaloids With Symmetry Breaking Charge Transfer Contributing to NIR Emission Beyond 900 nm,” Journal of the American Chemical Society 146 (2024): 6763-6772.

[38]

W. Wang, G. Zhang, Y. Wang, et al., “An Injectable and Thermosensitive Hydrogel With Nano-Aided NIR-II Phototherapeutic and Chemical Effects for Periodontal Antibacteria and Bone Regeneration,” Journal of Nanobiotechnology 21 (2023): 367.

[39]

L. Yang, J. Zhuang, J. Chen, X. Wu, N. Li, and N. Zhao, “Molecularly Engineered Lipid Droplet-Targeted NIR-II Type I AIE Photosensitizers Trigger Ferroptosis and Apoptosis for Cancer Therapy,” Science China Materials 68 (2025): 3808-3818.

[40]

S. Liu, B. Wang, Y. Yu, et al., “Cationization-Enhanced Type I and Type II ROS Generation for Photodynamic Treatment of Drug-Resistant Bacteria,” ACS Nano 16 (2022): 9130-9141.

[41]

R. Jia, H. Xu, C. Wang, et al., “NIR-II Emissive AIEgen Photosensitizers Enable Ultrasensitive Imaging-Guided Surgery and Phototherapy to Fully Inhibit Orthotopic Hepatic Tumors,” Journal of Nanobiotechnology 19 (2021): 419.

[42]

H. Peng, X. Zheng, T. Han, et al., “Dramatic Differences in Aggregation-Induced Emission and Supramolecular Polymerizability of Tetraphenylethene-Based Stereoisomers,” Journal of the American Chemical Society 139 (2017): 10150-10156.

[43]

W. Zhu, Y. Li, S. Guo, et al., “Stereoisomeric Engineering of Aggregation-Induced Emission Photosensitizers Towards Fungal Killing,” Nature Communications 13 (2022): 7046.

[44]

J. Zhuang, Q. Pan, C. Zhou, Z. Cai, N. Li, and N. Zhao, “The Cyano Positional Isomerism Strategy for Constructing Mitochondria-Targeted AIEgens With Type I Reactive Oxygen Species Generation Capability,” Journal of Materials Chemistry B 12 (2024): 11359-11367.

[45]

H. Wen, Z. Deng, R. Dong, et al., “Sulfur-π Interaction: A New Strategy for Designing NIR-II AIE Photosensitizer for Wound Healing,” Advanced Functional Materials 35 (2025): 2508015.

[46]

S. Deng, Z. Peng, F. Zhou, et al., “Elaborately Engineered Au(I)-Based AIEgens: Robust and Broad-Spectrum Elimination Abilities Toward Drug-Resistant Bacteria,” Aggregate 5 (2024): e575.

RIGHTS & PERMISSIONS

2026 The Author(s). Aggregate published by SCUT, AIEI, and John Wiley & Sons Australia, Ltd.

PDF (9019KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/