Cucurbit[n]urils-Mediated Structural Regulation of AIE Supramolecular Assemblies and D–π–A Structure-Driven Ion Recognition and Selective Cytotoxicity Applications

Yang Luo , Mao-Qin Liu , Jin-Shan Xiong , Jin-Liang Zhuang , Xin Xiao , Wei Zhang

Aggregate ›› 2025, Vol. 6 ›› Issue (12) : e70199

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Aggregate ›› 2025, Vol. 6 ›› Issue (12) :e70199 DOI: 10.1002/agt2.70199
RESEARCH ARTICLE
Cucurbit[n]urils-Mediated Structural Regulation of AIE Supramolecular Assemblies and D–π–A Structure-Driven Ion Recognition and Selective Cytotoxicity Applications
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Abstract

The precise control of supramolecular assembly to achieve multifunctional integration remains a significant challenge in materials science. In this study, we synthesized a novel, previously unreported AIE-active molecule (BA) through an exceptionally simple procedure. Subsequently, we constructed two cucurbituril-mediated assemblies (Q[8]-BA and Q[10]-BA) using BA as the building block. These assemblies were systematically investigated for their differences in ion recognition, cellular imaging, and cytotoxicity. The Q[8]-BA assembly exhibited enhanced fluorescence intensity, pH sensitivity, and high specificity for Co2+ detection (LOD = 4.8 × 10−7 M), making it a promising candidate for environmental sensing and cell imaging. In contrast, the Q[10]-BA assembly demonstrated selective cytotoxicity toward melanoma cells while protecting normal cells, highlighting its potential in cancer theranostics. These findings reveal the critical role of cavity size and assembly mode in regulating material properties, providing new insights for designing multifunctional supramolecular systems with tailored functionalities for environmental monitoring and biomedical applications.

Keywords

aggregation-induced emission / cell imaging / cucurbit[n]uril / ion recognition / selective cytotoxicity

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Yang Luo, Mao-Qin Liu, Jin-Shan Xiong, Jin-Liang Zhuang, Xin Xiao, Wei Zhang. Cucurbit[n]urils-Mediated Structural Regulation of AIE Supramolecular Assemblies and D–π–A Structure-Driven Ion Recognition and Selective Cytotoxicity Applications. Aggregate, 2025, 6(12): e70199 DOI:10.1002/agt2.70199

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References

[1]

W. Zhang, M.-Q. Liu, and Y. Luo, “Supramolecular Light-Harvesting Systems Based on Cucurbit[n]urils: SS-FRET and TS-FRET Mechanisms and Functional Applications,” Coordination Chemistry Reviews 533 (2025): 216555.

[2]

W.-L. Zhou, W. Lin, Y. Chen, X.-Y. Dai, and Y. Liu, “Tunable Multicolor Lanthanide Supramolecular Assemblies With White Light Emission Confined by Cucurbituril[7],” Small 19 (2023): 2304009.

[3]

M. Tang, Z. Zhong, and C. Ke, “Advanced Supramolecular Design for Direct Ink Writing of Soft Materials,” Chemical Society Reviews 52 (2023): 1614–1649.

[4]

R. Zheng, M. Zhao, J. S. Du, et al., “Assembly of Short Amphiphilic Peptoids Into Nanohelices With Controllable Supramolecular Chirality,” Nature Communications 15 (2024): 3264.

[5]

J.-X. Liu, K. Chen, and C. Redshaw, “Stimuli-Responsive Mechanically Interlocked Molecules Constructed From Cucurbit[n]uril Homologues and Derivatives,” Chemical Society Reviews 52 (2023): 1428–1455.

[6]

J.-H. Hu, Y. Huang, C. Redshaw, Z. Tao, and X. Xiao, “Cucurbit[n]uril-Based Supramolecular Hydrogels: Synthesis, Properties and Applications,” Coordination Chemistry Reviews 489 (2023): 215194.

[7]

S. Song, H. Zhang, and Y. Liu, “Light-Controlled Macrocyclic Supramolecular Assemblies and Luminescent Behaviors,” Accounts of Materials Research 5 (2024): 1109–1120.

[8]

Y. Yang, D. Li, and S. Qie, et al., “Cucurbit[6]uril-Based Supramolecular Assembly: Its Syntheses, Structures, Capture of Heavy Metal Ions, and Sensing Properties,” Science China Chemistry 68 (2024): 891–899.

[9]

Y. Jiang, H. Qi, M. Wang, K. Chen, C. Chen, and H. Xie, “Chlorogenic Acid-Cucurbit[n]uril Nanocomplex Delivery System: Synthesis and Evaluations for Potential Applications in Osteoporosis Medication,” International Journal of Nanomedicine 19 (2024): 11577–11592.

[10]

K. de la Vega-Hernández, M. G. Suero, and P. Ballester, “Investing in Entropy: The Strategy of Cucurbit[n]urils to Accelerate the Intramolecular Diels–Alder Cycloaddition Reaction of Tertiary Furfuryl Amines,” Chemical Science 15 (2024): 8841–8849.

[11]

M. Li, F. Wen, Y.-N. Jiang, N. Sun, S. Xing, and B. Wang, “Emerging Trends in Cucurbit[n]uril-Based Sensing,” Coordination Chemistry Reviews 542 (2025): 216870.

[12]

J. Yu, H. Yu, J. Niu, Z. Lei, and Y. Liu, “Tunable Nano-Supramolecules Based on Cucurbiturils for Near-Infrared Phosphorescence Imaging,” Nano Letters 24 (2024): 16124–16131.

[13]

S. Jiang, J. Yang, L. Ling, S. Wang, and D. Ma, “Supramolecular Fluorescent Probes for the Detection of Reactive Oxygen Species Discovered via High-Throughput Screening,” Analytical Chemistry 94 (2022): 5634–5641.

[14]

C. Hu, T. Jochmann, P. Chakraborty, et al., “Further Dimensions for Sensing in Biofluids: Distinguishing Bioorganic Analytes by the Salt-Induced Adaptation of a Cucurbit[7]uril-Based Chemosensor,” Journal of the American Chemical Society 144 (2022): 13084–13095.

[15]

X. Chen, H. K. Bisoyi, X.-F. Chen, et al., “Hierarchical Self-Assembly of an Excitation-Wavelength-Dependent Emissive Fluorophore and Cucurbiturils for Secondary Encryption,” Matter (2022): 3883–3900.

[16]

X. Zhou, X. Bai, F. Shang, et al., “Supramolecular Assembly Activated Single-Molecule Phosphorescence Resonance Energy Transfer for Near-Infrared Targeted Cell Imaging,” Nature Communications 15 (2024): 4787.

[17]

A. A. Bhosle, M. Banerjee, S. D. Hiremath, et al., “A Combination of a Graphene Quantum Dots–Cationic Red Dye Donor–Acceptor Pair and Cucurbit[7]uril as a Supramolecular Sensor for Ultrasensitive Detection of Cancer Biomarkers Spermine and Spermidine,” Journal of Materials Chemistry B 10 (2022): 8258–8273.

[18]

Y. Xia, Q. Bai, Y. Jiang, Q. Li, D. Wang, and X. Xiao, “Supramolecular Self-Assembly and Metal–Ligand-Enhanced Organic Room-Temperature Phosphorescence for Live Cell Imaging,” ACS Applied Materials & Interfaces 17 (2025): 22375–22383.

[19]

W. Zhang, L. Yang, Y. Luo, et al., “AIE Biofluorescent Probe Based on Twisted Cucurbit[14]uril for the Detection of Fe(CN)63-Anion in Solutions and Live Kidney Cells,” Sensors and Actuators B: Chemical 379 (2023): 133255.

[20]

X. Yu, Z. Duan, H. Yang, N. Peng, Z. Zhao, and S. Liu, “Supramolecular Assemblies With Aggregation-Induced Emission for In Situ Active Imaging-Guided Photodynamic Therapy of Cancer Cells,” Talanta 280 (2024): 126722.

[21]

R. Zhang, Z. Lei, Z. Yu, Y. Chen, and Y. Liu, “Multicolor Luminescent Supramolecular Bidirectional Shuttles Driven by Light,” Advanced Science 12 (2025): e07090.

[22]

R. Sasmal, A. Som, P. Kumari, et al., “Supramolecular Guest Exchange in Cucurbit[7]uril for Bioorthogonal Fluorogenic Imaging Across the Visible Spectrum,” ACS Central Science 10 (2024): 1945–1959.

[23]

D. Kim, M. L. Bossi, V. N. Belov, and S. W. Hell, “Supramolecular Complex of Cucurbit[7]uril With Diketopyrrolopyrole Dye: Fluorescence Boost, Biolabeling and Optical Microscopy,” Angewandte Chemie International Edition 63 (2024): e202410217.

[24]

C. Zhang, S. Chen, Y. Zhao, and J. Meng, “Cucurbit[6]uril Builds a Water Channel for Improving the Water/Salt Selectivity of Polybenzimidazole,” Journal of Membrane Science 694 (2024): 122411.

[25]

X. Qiu, T. Zheng, M. Runowski, et al., “Constructing [2.2]Paracyclophane-Based Ultrasensitive Optical Fluorescent-Phosphorescent Thermometer With Cucurbit[8]uril Supramolecular Assembly,” Advanced Functional Materials 34 (2024): 2313517.

[26]

X. Chen, R. Yang, K. Liu, et al., “From Natural Product Derivative to Hexagonal Prism Supermolecule: Potent Biofilm Disintegration, Enhanced Foliar Affinity, and Effective Management of Tomato Bacterial Canker,” Angewandte Chemie 137 (2025): e202416079.

[27]

X. Hu, J. Yang, F. Gao, Z. Zhao, and S. Liu, “Highly Selective [4+4] Cross-Photodimerization of (4a-Azonia)Anthracenes Driven by Confinement of D–A Hetero–Guest Pair in Cucurbit[10]uril Host,” Chinese Chemical Letters 36 (2025): 109967.

[28]

D. Wu, X. Du, Q. Xue, et al., “Supramolecular Porphyrin Photosensitizers Based on Host−Guest Recognition for In Situ Bacteria-Responsive Near-Infrared Photothermal Therapy,” Advanced Healthcare Materials 13 (2024): 2401662.

[29]

Y. Wang, J. Liao, Y. Lyu, et al., “An AIE Photosensitizer With Simultaneous Type I and Type II ROS Generation: Efficient Bacterial Elimination and Hypoxic Tumor Ablation,” Advanced Functional Materials 33 (2023): 2301692.

[30]

X.-L. Li, D.-L. Cheng, K.-K. Niu, et al., “Construction of Supramolecular Dimer Photosensitizers Based on Triphenylamine Derivatives and Cucurbit [8]uril for Photocatalysis,” Journal of Materials Chemistry A 11 (2023): 24911–24917.

[31]

Z. Sun, J. Wang, M. Xiao, et al., “A Straightforward Strategy to Modulate ROS Generation of AIE Photosensitizers for Type-I PDT,” Chemical Engineering Journal 499 (2024): 155782.

[32]

S. Li, T. Liu, W. Zhang, et al., “Highly Efficient Anion Exchange Membrane Water Electrolyzers via Chromium-Doped Amorphous Electrocatalysts,” Nature Communications 15 (2024): 3416.

[33]

S. Chen, T. Luo, J. Wang, et al., “Tuning Proton Affinity on Co−N−C Atomic Interface to Disentangle Activity-Selectivity Trade-Off in Acidic Oxygen Reduction to H2O2,” Angewandte Chemie 137 (2025): e202418713.

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

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