Chiral assemblies for enantioselective nano-bio interactions and therapeutic translation

Chiral assemblies for enantioselective nano-bio interactions and therapeutic translation

Qianyun Ye
,
Xiyuan Li
,
Xiaohuan Sun
*
,
Jie Han
*
*Correspondence to: Xiaohuan Sun, Jiangsu Provincial Key Laboratory of Green & Functional Materials and Environmental Chemistry, School of Chemistry and Materials, Yangzhou University, Yangzhou 225002, Jiangsu, China. E-mail: xhuansun@yzu.edu.cn
Jie Han, Jiangsu Provincial Key Laboratory of Green & Functional Materials and Environmental Chemistry, School of Chemistry and Materials, Yangzhou University, Yangzhou 225002, Jiangsu, China. E-mail: hanjie@yzu.edu.cn
Chiral Chem. 2027;3:202638. 10.70401/cc.2026.0048
Received: August 10, 2026Accepted: November 02, 2026Published: November 04, 2026
Tips Icon
This manuscript is made available in its unedited form to allow early access to the reported findings. Further editing will be completed before final publication. As such, the content may include errors, and standard legal disclaimers are applicable.

Abstract

Living systems possess intrinsic homochirality, yet this stereochemical characteristic is frequently neglected in conventional nanomedicine design. Chiral assemblies are capable of regulating nano-bio interactions in an enantioselective fashion, offering a promising strategy to boost anticancer therapeutic efficacy. This review systematically outlines recent progress in chiral assemblies, with a core focus on the enantioselective modulation of nano-bio interfacial affinity across three key aspects: biomolecule recognition, protein adsorption, cellular uptake and subcellular organelle targeting. We further summarize chirality-dependent anticancer modalities, including catalytic therapy, chemotherapy, phototherapy, and immunotherapy. Overall, the discussed studies illustrate how interfacial stereochemical effects can influence therapeutic outcomes, while also highlighting the remaining challenges in translating these concepts into practical nanomedicine.

Keywords

Chiral assemblies, enantioselectivity, nano-bio interaction, cancer therapy, chirality

References

  • 1. Mahmoudi M, Landry MP, Moore A, Coreas R. The protein corona from nanomedicine to environmental science. Nat Rev Mater. 2023;1-17.
    [DOI] [PubMed] [PMC]
  • 2. Baimanov D, Wang J, Zhang J, Liu K, Cong Y, Shi X, et al. In situ analysis of nanoparticle soft corona and dynamic evolution. Nat Commun. 2022;13(1):5389.
    [DOI] [PubMed] [PMC]
  • 3. Song L, Chen P, Shi B, Qu A, Xu C, Kuang H, et al. Dual signals of chiral and fluorescent copper sulphide nanoparticles boost tumor cell autophagy. Adv Funct Mater. 2026;36(16):e06926.
    [DOI]
  • 4. Shi Y, Liao J, Zhang C, Wu Q, Hu S, Yang T, et al. Cascade-responsive size/charge bidirectional-tunable nanodelivery penetrates pancreatic tumor barriers. Chem Sci. 2024;15(38):15647-15658.
    [DOI] [PubMed] [PMC]
  • 5. Pan X, Yan KH, Wang MD, Zhou LX, Liu KM, An JY, et al. Boosting tumor retention via water solubility and molecular charge engineering for enhanced photoimmunotherapy. Chin Chem Lett. 2026;37(12):112291.
    [DOI]
  • 6. Kramarenko GC, Casas CG, Dang MN, Demetriou ND, Day ES. Loading density influences the tumor cell targeting and signaling inhibition capabilities of antibody nanoconjugates. ACS Omega. 2026;11(5):8836-8847.
    [DOI] [PubMed] [PMC]
  • 7. Zheng X, Wang X, Feng Q, Jiang L. Immunoregulatory dendritic lipopeptide nanoparticles for high-capacity cisplatin delivery and pancreatic cancer chemo-immunotherapy. ACS Appl Mater Interfaces. 2026;18(29):39771-39784.
    [DOI] [PubMed]
  • 8. Li Z, Xiao C, Yang X, Li Z. Progress in the mechanical properties of nanoparticles for tumor-targeting delivery. Chem Soc Rev. 2025;54(11):5698-5734.
    [DOI] [PubMed]
  • 9. Xu L, Wang X, Wang W, Sun M, Choi WJ, Kim JY, et al. Enantiomer-dependent immunological response to chiral nanoparticles. Nature. 2022;601(7893):366-373.
    [DOI] [PubMed]
  • 10. Cho NH, Guerrero-Martínez A, Ma J, Bals S, Kotov NA, Liz-Marzán LM, et al. Bioinspired chiral inorganic nanomaterials. Nat Rev Bioeng. 2023;1(2):88-106.
    [DOI]
  • 11. Cho NH, Kim H, Kim JW, Lim YC, Kim RM, Lee YH, et al. Chiral inorganic nanomaterials for biomedical applications. Chem. 2024;10(4):1052-1070.
    [DOI]
  • 12. Zhang NN, Mychinko M, Gao SY, Yu L, Shen ZL, Wang L, et al. Self-matching assembly of chiral gold nanoparticles leads to high optical asymmetry and sensitive detection of adenosine triphosphate. Nano Lett. 2024;(41):13027-13036.
    [DOI] [PubMed]
  • 13. Li M, Jiang S, Wang X, Xu W, Du C, Wei Y, et al. Chirality and curvature on protein adsorption and osteogenesis. Angew Chem Int Ed. 2024;63(45):e202411733.
    [DOI] [PubMed]
  • 14. Qin Y, Hu J, Kuai Z, Jiang W, Zhu D, Song A, et al. Peptide-directed chiral gold nanozymes for asymmetric polymerization and chirality-selective cytotoxicity. Biomacromolecules. 2026;27(3):2137-2147.
    [DOI]
  • 15. Liu J, Deng C, Yang L, Ma H, Gao C, Li S, et al. Decoding chiral interactions: Molecular insights into the selective binding of nanoparticles at biological interfaces. J Phys Chem Lett. 2025;16(24):6040-6051.
    [DOI]
  • 16. Vitagliano CM, Camilli A, Moldoveanu VG, Di Sabato A, Feroci M, Sturabotti E, et al. Selective interaction of chiral carbon dots with nucleic acids: A promising nanosensing platform. Chemistry A European J. 2024;30(70):e202402787.
    [DOI]
  • 17. García F, Gómez R, Sánchez L. Chiral supramolecular polymers. Chem Soc Rev. 2023;52(21):7524-7548.
    [DOI]
  • 18. Xing C, Dou X, Gao L, Xu P, Peng Y, Yang K, et al. Chiral artificial antigen-presenting cells enhancing tumor immunotherapy: Evasion of macrophage uptake through inhibition of serum protein corona formation. ACS Nano. 2025;19(31):28204-28217.
    [DOI]
  • 19. Wang J, Gao N, Wei J, Liao L. Chiral gold nanoparticles manipulate osteoimmune microenvironment via macrophage autophagy for bone regeneration. Mater Today Bio. 2025;34:102131.
    [DOI] [PubMed] [PMC]
  • 20. Chen L, Zhou X, Huang Y, Wang X, Gao X, Cao Y, et al. Chirality interplay of peptide and saccharide on glycopeptide self-assembly. Nano Lett. 2025;25(4):1558-1566.
    [DOI] [PubMed]
  • 21. Klawa SJ, Lee M, Riker KD, Jian T, Wang Q, Gao Y, et al. Uncovering supramolecular chirality codes for the design of tunable biomaterials. Nat Commun. 2024;15(1):788.
    [DOI] [PubMed] [PMC]
  • 22. Li J, Cui Y, Lu YL, Zhang Y, Zhang K, Gu C, et al. Programmable supramolecular chirality in non-equilibrium systems affording a multistate chiroptical switch. Nat Commun. 2023;14(1):5030.
    [DOI] [PubMed] [PMC]
  • 23. Luo B, Ma M, Hao A, Xing P. Arene-perfluoroarene force driven chiral transfer, chiral amplification and chiral inversion. Chin Chem Lett. 2026;37(1):111736.
    [DOI]
  • 24. Chen W, Li B, Gao G, Sun T. Chiral supramolecular nanomaterials: From chirality transfer and amplification to regulation and applications. Interdiscip Mater. 2023;2(5):689-713.
    [DOI]
  • 25. Wang Y, Liu Z, Liu D, Liu G, Ren K, Bai J, et al. Ultra-narrowband circular dichroism in chiral nanopore arrays based on bound states in the continuum: Implications for ultrasensitive detection of chiral molecules. ACS Appl Nano Mater. 2025;8(2):962-973.
    [DOI]
  • 26. Su X, Fang S, Zhang Y, Liu P, Pan R, Xu X, et al. Shining light on group II-VI chiral quantum dots: Synthesis, chirality induction, and applications. ACS Appl Mater Interfaces. 2026;18(9):13344-13370.
    [DOI] [PubMed]
  • 27. Fa S, Tomita T, Wada K, Yasuhara K, Ohtani S, Kato K, et al. CPL on/off control of an assembled system by water soluble macrocyclic chiral sources with planar chirality. Chem Sci. 2022;13(20):5846-5853.
    [DOI] [PubMed] [PMC]
  • 28. Idrees A, Reuven B, Markovich G. High enantioselectivity in adsorption of chiral molecules on the surface of chiral terbium phosphate nanocrystals. J Am Chem Soc. 2025;147(17):14191-14197.
    [DOI] [PubMed] [PMC]
  • 29. Li X, Yang X, Hu J, Li J, Zhu H, He S, et al. Surfactant-mediated synthesis of twisted Cu 2–xS nanobowties with chirality continuum toward enantioselective catalysis. J Am Chem Soc. 2026;148(13):14016-14027.
    [DOI]
  • 30. Wu X, Xi Z, Zhao C, Zhang M, Lyu Y, Sun Q, et al. Mesopore-confined self-assembly of chiral supramolecular nanohelices as highly durable asymmetric catalysts. ACS Catal. 2026;16(6):5816-5824.
    [DOI]
  • 31. Wang Z, Zhang R, Hu Y, Song Q, Fu X, Wang Y, et al. Chiral metal nanozyme-enabled SOD2 activation and siRNA delivery cooperatively mitigating chronic heart failure. Bioact Mater. 2026;58:203-220.
    [DOI]
  • 32. Zhang H, Chen P, Shi W, Qu A, Sun M, Kuang H. Renal clearable chiral manganese oxide supraparticles for in vivo detection of metalloproteinase-9 in early cancer diagnosis. Adv Mater. 2025;37(7):2415656.
    [DOI]
  • 33. Zhang Y, Zheng H, Zhao Y, Du C, Zhang J, Liu J, et al. Deciphering the distinct roles of molecular and supramolecular chirality in osteogenic differentiation of mesenchymal stem cells in 3D hydrogels. ACS Nano. 2025;19(22):20564-20577.
    [DOI]
  • 34. Li X, Xu PH, Lu Q, Zhang J, Chen J, Dong L, et al. Confined chiral center stacking induced twisted silica nanoribbons for tumor cell proliferation regulation. Angew Chem Int Ed. 2026;65(5):e22375.
    [DOI] [PubMed]
  • 35. Li Y, Wang Y, Ao Q, Li X, Huang Z, Dou X, et al. Unique chirality selection in neural cells for D-matrix enabling specific manipulation of cell behaviors. Adv Mater. 2023;35(36):e2301435.
    [DOI] [PubMed]
  • 36. Duan H, Yang T, Li Q, Cao F, Wang P, Cao L. Recognition and chirality sensing of guanosine-containing nucleotides by an achiral tetraphenylethene-based octacationic cage in water. Chin Chem Lett. 2024;35(1):108878.
    [DOI]
  • 37. Guo N, Shi X, Sun X, Hu L, Jiao L, Zhai Y, et al. Chirality-matching in Au-S oriented assembly induces highly selective recognition of glucose enantiomers. Small. 2026;22(39):e73913.
    [DOI]
  • 38. Zhu M, Pang X, Wang K, Sun L, Wang Y, Hua R, et al. Enantioselective effect of chiral prothioconazole on the conformation of bovine serum albumin. Int J Biol Macromol. 2023;240:124541.
    [DOI] [PubMed]
  • 39. Banreti A, Bhattacharya S, Wien F, Matsuo K, Réfrégiers M, Meinert C, et al. Biological effects of the loss of homochirality in a multicellular organism. Nat Commun. 2022;13:7059.
    [DOI]
  • 40. Ding C, Min J, Tan Y, Zheng L, Ma R, Zhao R, et al. Combating atherosclerosis with chirality/phase dual-engineered nanozyme featuring microenvironment-programmed senolytic and senomorphic actions. Adv Mater. 2024;36(29):e2401361.
    [DOI] [PubMed]
  • 41. Liu Y, Wu Z, Armstrong DW, Wolosker H, Zheng Y. Detection and analysis of chiral molecules as disease biomarkers. Nat Rev Chem. 2023;7(5):355-373.
    [DOI] [PubMed] [PMC]
  • 42. Li S, Cortez-Jugo C, Ju Y, Caruso F. Approaching two decades: Biomolecular coronas and bio-nano interactions. ACS Nano. 2024;18(49):33257-33263.
    [DOI] [PubMed]
  • 43. Cortez-Jugo C, Czuba-Wojnilowicz E, Tan A, Caruso F. A focus on “bio” in bio-nanoscience: The impact of biological factors on nanomaterial interactions. Adv Health Mater. 2021;10(16):2100574.
    [DOI]
  • 44. Liu J, Yang L, Qin P, Zhang S, Yung KKL, Huang Z. Recent advances in inorganic chiral nanomaterials. Adv Mater. 2021;33(50):2005506.
    [DOI]
  • 45. Niu X, Liu Y, Zhao R, Yuan M, Zhao H, Li H, et al. Mechanisms for translating chiral enantiomers separation research into macroscopic visualization. Adv Colloid Interface Sci. 2025;335:103342.
    [DOI] [PubMed]
  • 46. Wang C, Yuan G, Wang C, Sun X, Hang P, Xi Z, et al. Supramolecular chiral nanozymes with high and switchable enantioselectivity. Small Struct. 2023;4(8):2200405.
    [DOI]
  • 47. Suzuki Y, Mizuta Y, Mikagi A, Misawa-Suzuki T, Tsuchido Y, Sugaya T, et al. Recognition of d-glucose in water with excellent sensitivity, selectivity, and chiral selectivity using γ-cyclodextrin and fluorescent boronic acid inclusion complexes having a Pseudo-diboronic acid moiety. ACS Sens. 2023;8(1):218-227.
    [DOI] [PubMed]
  • 48. Ouyang YC, Yeom BJ, Zhao Y, Ma W. Progress and prospects of chiral nanomaterials for biosensing platforms. Rare Met. 2024;43(6):2469-2497.
    [DOI]
  • 49. Liu Y, Ren S, Wang S, Guo J, Lin F, Hu R, et al. Specific detection of CA242 by antibody-modified chiral symmetric double “N” metasurface biosensor. Spectrochim Acta A Mol Biomol Spectrosc. 2024;309:123811.
    [DOI] [PubMed]
  • 50. Mo X, Li H, Zhong X, Li M, Jia M, Wu H, et al. Dual-signal probing of molecular subtypes of breast cancer: Synergistic chirality and charge-transfer effect enable enhanced accuracy. Anal Chem. 2025;97(21):11298-11306.
    [DOI]
  • 51. Wang X, Zhang X, Zhao Y, Wu X, Yang G, Zhao Y, et al. Biomimetic chiral recognition of biothiols by enantiomeric nanoclusters in plasma. Adv Mater. 2026;38(3):e14158.
    [DOI]
  • 52. Peng AP, Liang YL, Wu GW, Zeng J, Li Y, Gu SX, et al. Efficient synergistic recognition of D/L-cysteine and zinc ions using a chiral chemosensor. Sens Actuators B Chem. 2025;442:138062.
    [DOI]
  • 53. Bera S, Lawrence E, Kamalesh S, Sithaiyan V, Sayyad US, Mondal S, et al. Chiral and bright green fluorescent MXene quantum dots as “on/off/on” nanoprobe for the selective and ultrasensitive detection of hypochlorite and glutathione. ACS Appl Nano Mater. 2026;9(17):7565-7578.
    [DOI]
  • 54. Wang N, Zhao L, Liu C, Zhang J, He Y, Yang H, et al. Chiral detection of glucose: An amino acid-assisted surface-enhanced Raman scattering strategy showing opposite enantiomeric effects on SERS signals. Anal Chem. 2022;94(42):14565-14572.
    [DOI] [PubMed]
  • 55. Jun YW, Kim KH, Yang YJ, Jung Y, Kim KT, Kim H, et al. Discrimination of invasive human skin tumor using an ultrafast ATP-proton AND-gate probe. ACS Sens. 2022;7(4):1068-1074.
    [DOI] [PubMed]
  • 56. Mei M, Mu L, Wang Y, Liang S, Zhao Q, Huang L, et al. Simultaneous monitoring of the adenosine triphosphate levels in the cytoplasm and nucleus of a single cell with a single nanowire-based fluorescent biosensor. Anal Chem. 2022;94(34):11813-11820.
    [DOI] [PubMed]
  • 57. Chen X, Jiang Z, Liang L, Li YF, Huang CZ, Gao PF. Dark-field imaging monitoring of adenosine triphosphate in live cells by Au NBPs@ZIF-8 nanoprobes. Anal Chem. 2022;94(51):18107-18113.
    [DOI] [PubMed]
  • 58. Yang B, Tian R, Guo T, Qu W, Lu J, Li Y, et al. Mitochondrial-targeted AIE-active fluorescent probe based on tetraphenylethylene fluorophore with dual positive charge recognition sites for monitoring ATP in cells. Anal Chem. 2023;95(11):5034-5044.
    [DOI] [PubMed]
  • 59. Ding Q, Yang W, Xing X, Lin H, Xu C, Xu L, et al. Modulation by co (II) ion of optical activities of L/D-glutathione (GSH)-modified chiral copper nanoclusters for sensitive adenosine triphosphate detection. Angew Chem Int Ed. 2024;63(17):e202401032.
    [DOI] [PubMed]
  • 60. Zou Y, Ito S, Fujiwara M, Komatsu N. Probing the role of charged functional groups on nanoparticles grafted with polyglycerol in protein adsorption and cellular uptake. Adv Funct Mater. 2022;32(22):2111077.
    [DOI]
  • 61. Dolci M, Wang Y, Nooteboom SW, Soto Rodriguez PED, Sánchez S, Albertazzi L, et al. Real-time optical tracking of protein corona formation on single nanoparticles in serum. ACS Nano. 2023;17(20):20167-20178.
    [DOI] [PubMed] [PMC]
  • 62. Liu X, Zhao Y, Gao C, Sun X, Li S, Han J. Effect of supramolecular chirality on nano-protein/cell interaction: An experimental and computational investigation. Int J Biol Macromol. 2024;283:137613.
    [DOI]
  • 63. Carney CP, Pandey N, Kapur A, Saadi H, Ong HL, Chen C, et al. Impact of targeting moiety type and protein corona formation on the uptake of Fn14-targeted nanoparticles by cancer cells. ACS Nano. 2023;17(20):19667-19684.
    [DOI] [PubMed] [PMC]
  • 64. Olivieri PH, Hayashi JY, Torquato RJS, Lima AF, Pereira TP, Lima IF, et al. Heparin-binding proteins in the nanoparticle corona enhance cellular uptake through glycocalyx interactions. ACS Nano. 2025;19(51):42964-42978.
    [DOI]
  • 65. Qu S, Qiao Z, Zhong W, Liang K, Jiang X, Shang L. Chirality-dependent dynamic evolution of the protein corona on the surface of quantum dots. ACS Appl Mater Interfaces. 2022;14(39):44147-44157.
    [DOI] [PubMed]
  • 66. Hu M, He Y, Wu L, Su W, Zhang W, Yu X, et al. Chiral polyproline enables functional stealth for simultaneous long circulation and endoplasmic reticulum-targeted antigen presentation. ACS Nano. 2026;20(9):7908-7927.
    [DOI]
  • 67. Jiang H, Liu R, Wang L, Wang X, Zhang M, Lin S, et al. Chiral-selective antigen-presentation by supramolecular chiral polymer micelles. Adv Mater. 2023;35(5):2208157.
    [DOI]
  • 68. Zhou J, Gu J, Sun X, Ye Q, Wu X, Xi J, et al. Supramolecular chiral binding affinity-achieved efficient synergistic cancer therapy. Adv Sci. 2024;11(16):e2308493.
    [DOI] [PubMed] [PMC]
  • 69. Tian Y, Hao J, Lin C, Han D, Zhu N, Li Z, et al. Enantioselective modulation of inflammatory response through MAPK pathway by wavelike chiral nanoparticles. Environ Health. 2025;3(11):1311-1319.
    [DOI] [PubMed] [PMC]
  • 70. Shi B, Zhao J, Xu Z, Chen C, Xu L, Xu C, et al. Chiral nanoparticles force neural stem cell differentiation to alleviate Alzheimer’s disease. Adv Sci. 2022;9(29):e2202475.
    [DOI] [PubMed] [PMC]
  • 71. Sun X, Ye Q, Liang Y, Yuan Y, Zhu L, Zhang Q, et al. Chiral cysteine-copper ion-based assemblies for improved phototherapy. J Colloid Interface Sci. 2024;657:993-1002.
    [DOI]
  • 72. Huang Q, Ruan X, Mao X, Hu X, Li J, Wang W, et al. L-DNA-based framework nucleic acid nanodevice for lysosomal ATP imaging. Anal Chem. 2026;98(23):17353-17360.
    [DOI] [PubMed]
  • 73. Wang W, Zhao J, Hao C, Hu S, Chen C, Cao Y, et al. The development of chiral nanoparticles to target NK cells and CD8+ T cells for cancer immunotherapy. Adv Mater. 2022;34(16):e2109354.
    [DOI] [PubMed]
  • 74. Hu T, Zou J, Zhu Z, Zhang Z, Pan Y, Lu Y, et al. Cell chirality in cancer: Emerging roles in malignant progression and tumor metastasis. Biochim Biophys Acta Rev Cancer. 2026;1881(4):189658.
    [DOI] [PubMed]
  • 75. Wang X, Wu B, Zhang Y, Dou X, Zhao C, Feng C. Polydopamine-doped supramolecular chiral hydrogels for postoperative tumor recurrence inhibition and simultaneously enhanced wound repair. Acta Biomater. 2022;153:204-215.
    [DOI] [PubMed]
  • 76. Zheng W, Lin H, Chen J, Zeng A, Wu R, Qiu Y, et al. Tumor microenvironment-activate chiral copper hydroxide nanoreactors for breast cancer suppression via NIR II triggered synergistic therapy. Mater Today Chem. 2026;51:103312.
    [DOI]
  • 77. Dong L, Yang W, Li X, Ma Y, Huang X, Fan Y, et al. Self-assembled two-dimensional chiral meso-topography determines the balance of cellular and humoral immunity against tumors. Adv Mater. 2026;38(12):e20552.
    [DOI] [PubMed]
  • 78. Ye Q, Liang Y, Yuan Y, Sun X, Zhu L, Wu X, et al. pH-responsive chiral supramolecular cysteine-Zn2+-indocyanine green assemblies for triple-level chirality-specific anti-tumor efficacy. Chin Chem Lett. 2025;36(5):110432.
    [DOI]
  • 79. Raj G, Vasantha AP, Sreekumar VD, Beena AV, Dommeti VKK, Perozhy H, et al. Bimetallic DNAsome decorated with G4-DNA as a nanozyme for targeted and enhanced chemo/chemodynamic cancer therapy. Adv Healthc Mater. 2024;13(20):e2400256.
    [DOI] [PubMed]
  • 80. Wang S, Zhao Y, Yao S, Wang Z, Zhang Z, Wen K, et al. Chirality of copper-amino acid nanoparticles determines chemodynamic cancer therapeutic outcome. Small. 2024;20(28):e2309328.
    [DOI] [PubMed]
  • 81. Hao C, Huang L, Zhang H, Xu L, Sun M, Kuang H, et al. Chiral CuxOS@Fe-MOFs for enhanced cancer therapy. Adv Funct Mater. 2024;34(10):2312795.
    [DOI]
  • 82. Yuan G, Wang C, Xi Z, Li S, Sun X, Hang P, et al. Supramolecular polyaniline-metal ion as chiral nanozymes for enantioselective catalysis. Small. 2023;19(47):e2303739.
    [DOI] [PubMed]
  • 83. Hang P, Tong J, Xi Z, Li S, Tao S, Sun X, et al. Precise control of polyaniline nanohelices with chirality continuum and their correlation on catalytic performance. Nano Lett. 2024;24(48):15428-15435.
    [DOI] [PubMed]
  • 84. Gao P, Chen S, Liu S, Liu H, Xie Z, Zheng M. Chiral carbon dots-enzyme nanoreactors with enhanced catalytic activity for cancer therapy. ACS Appl Mater Interfaces. 2021;13(47):56456-56464.
    [DOI] [PubMed]
  • 85. Kang H, Yu S, Kim RM, Kim Y, Shin SC, Jang D, et al. Optically tunable catalytic cancer therapy using enzyme-like chiral plasmonic nanoparticles. Nat Commun. 2025;16(1):2562.
    [DOI]
  • 86. Xing S, Lan X, Zhang J, Li M, Wang B. High-order framework nucleic acid for targeted-delivery of antisense peptide nucleic acids to overcome drug resistance. Chem Commun. 2023;59(88):13223-13226.
    [DOI]
  • 87. Giancola JB, Raines RT. Endosomolytic peptides enable the cellular delivery of peptide nucleic acids. Chem Commun. 2024;60(100):15019-15022.
    [DOI] [PubMed] [PMC]
  • 88. Chen C, Li Y, Wang Q, Cai N, Wu L, Yan X. Single-particle assessment of six different drug-loading strategies for incorporating doxorubicin into small extracellular vesicles. Anal Bioanal Chem. 2023;415(7):1287-1298.
    [DOI]
  • 89. Malfanti A, Sami H, Balasso A, Marostica G, Arpac B, Mastrotto F, et al. Control of cell penetration enhancer shielding and endosomal escape-kinetics crucial for efficient and biocompatible siRNA delivery. J Control Release. 2023;363:101-113.
    [DOI]
  • 90. Wang Z, Yue L, Min J, Liu H, Zhang Y, Du Y, et al. Control the gene delivery and anticancer efficacy of peptides through chiral modulation. Nano Lett. 2025;25(7):2693-2701.
    [DOI] [PubMed]
  • 91. Joo HS, Suh JH, So CM, Jeon HJ, Yoon SH, Lee JM. Emerging roles of using small extracellular vesicles as an anti-cancer drug. Int J Mol Sci. 2023;24(18):14063.
    [DOI] [PubMed] [PMC]
  • 92. Zhang Q, Cao K, Ren TJ, Wu H, Xu ZR. Exploring the homing effect and enhanced drug delivery potential of small extracellular vesicles. Chem Commun. 2025;61(18):3708-3711.
    [DOI] [PubMed]
  • 93. Hettich BF, Bader JJ, Leroux JC. Encapsulation of hydrophilic compounds in small extracellular vesicles: Loading capacity and impact on vesicle functions. Adv Healthc Mater. 2022;11(5):e2100047.
    [DOI] [PubMed] [PMC]
  • 94. Xu H, Liu R, Zhou H, Kong B, Shen K, Zhao T, et al. Engineered small extracellular vesicles as bioactive materials: Integrating engineering strategies for cargo loading and targeted delivery systems. Bioact Mater. 2026;59:96-134.
    [DOI] [PubMed] [PMC]
  • 95. Zhang Y, Kim G, Zhu Y, Wang C, Zhu R, Lu X, et al. Chiral graphene quantum dots enhanced drug loading into small extracellular vesicles. ACS Nano. 2023;17(11):10191-10205.
    [DOI] [PubMed]
  • 96. Zhao Y, An F, Wu J, Li H, Wang X, Jiao L, et al. Chiral-induced highly efficient NIR-photothermal conversion of perylene diimide@silica nanocapsules for photothermal therapy. Aggregate. 2024;5(6):e630.
    [DOI]
  • 97. Sun X, Ye Q, Zhou J, Han J, Guo R. Host-guest assemblies for improved photothermal cancer therapy. Chem Synth. 2023;3(2):16.
    [DOI]
  • 98. Zhou X, Cai Q, Zhao S, Ling F, Xiang G, Li L, et al. CDs-ICG@BSA nanoparticles for excellent phototherapy and in situ bioimaging. Talanta. 2024;271:125661.
    [DOI]
  • 99. Zhao X, Sun M, Cao X, Xu J, Li X, Zhao X, et al. Near-infrared light-driving organic photothermal agents with an 88.9% photothermal conversion efficiency for image-guided synergistic phototherapy. Adv Healthc Mater. 2024;13(19):e2400201.
    [DOI] [PubMed]
  • 100. Sun X, Yuan Y, Lu Y, Ye Q, Liu X, Liu X, et al. Porphyrin-based supramolecular chiral assembly for enantioselective interaction and augmented photodynamic therapy. J Colloid Interface Sci. 2025;699(p2):138235.
    [DOI]
  • 101. Liu X, Lu Y, Li X, Luo L, You J. Nanoplatform-enhanced photodynamic therapy for the induction of immunogenic cell death. J Control Release. 2024;365:1058-1073.
    [DOI]
  • 102. Wang H, Jing G, Niu J, Yang L, Li Y, Gao Y, et al. A mitochondria-anchored supramolecular photosensitizer as a pyroptosis inducer for potent photodynamic therapy and enhanced antitumor immunity. J Nanobiotechnology. 2022;20(1):513.
    [DOI] [PubMed] [PMC]
  • 103. Ding YN, Ding HY, Li H, Yang R, Huang JY, Chen H, et al. Photosensitive small extracellular vesicles regulate the immune microenvironment of triple negative breast cancer. Acta Biomater. 2023;167:534-550.
    [DOI] [PubMed]
  • 104. He M, Zhang M, Xu T, Xue S, Li D, Zhao Y, et al. Enhancing photodynamic immunotherapy by reprograming the immunosuppressive tumor microenvironment with hypoxia relief. J Control Release. 2024;368:233-250.
    [DOI] [PubMed]
  • 105. Lu Y, Ye Q, Gao C, Li X, Gao P, Sun X, et al. Enantioselective induction of immunogenic cell death: A type-I photodynamic therapy enabled by chiral porphyrin/arginine self-assemblies. Langmuir. 2026;42(17):12325-12337.
    [DOI] [PubMed]
  • 106. Zhang Y, Li Y, Wang G, Ullah A. One-pot synthesis of chiral cysteine-capped gold nanoparticles for use as vaccine adjuvants in mice. J Drug Deliv Sci Technol. 2024;102(Part A):106333.
    [DOI]
  • 107. Zhao R, Liu H, Xie Z, Zheng M. Targeting chiral carbon dots to enhance melanoma immunotherapy. J Colloid Interface Sci. 2026;703(Part 1):139093.
    [DOI]
  • 108. Zhang Y, Cui T, Yang J, Huang Y, Ren J, Qu X. Chirality-dependent reprogramming of macrophages by chiral nanozymes. Angew Chem Int Ed. 2023;62(34):e202307076.
    [DOI] [PubMed]
  • 109. Hu YP, Xiao K, Si MC, Wang CX, Miao Y, Hu ZQ. Chiral hydrogels facilitate rapid diabetic wound healing by promoting macrophage M2 polarization and cellular proliferation. J Mater Chem C. 2024;12(19):6961-6973.
    [DOI]
  • 110. Wen JH, Li DY, Liang S, Yang C, Tang JX, Liu HF. Macrophage autophagy in macrophage polarization, chronic inflammation and organ fibrosis. Front Immunol. 2022;13:946832.
    [DOI] [PubMed] [PMC]
  • 111. Cassetta L, Pollard JW. A timeline of tumour-associated macrophage biology. Nat Rev Cancer. 2023;23(4):238-257.
    [DOI] [PubMed]
  • 112. Mu Z, Shen T, Deng H, Zeng B, Huang C, Mao Z, et al. Enantiomer-dependent supramolecular immunosuppressive modulation for tissue reconstruction. ACS Nano. 2024;18(6):5051-5067.
    [DOI] [PubMed]
  • 113. Li X, Ma S, Gao T, Mai Y, Song Z, Yang J. The main battlefield of mRNA vaccine–Tumor immune microenvironment. Int Immunopharmacol. 2022;113(Part A):109367.
    [DOI]
  • 114. Zhao T, Cai Y, Jiang Y, He X, Wei Y, Yu Y, et al. Vaccine adjuvants: Mechanisms and platforms. Signal Transduct Target Ther. 2023;8(1):283.
    [DOI] [PubMed] [PMC]
  • 115. Ding J, Wang T, Lin Z, Li Z, Yang J, Li F, et al. Chiral polypeptide hydrogels regulating local immune microenvironment and anti-tumor immune response. Nat Commun. 2025;16(1):1222.
    [DOI] [PubMed] [PMC]

© The Author(s) 2026. This is an Open Access article licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Publisher’s Note

Science Exploration remains a neutral stance on jurisdictional claims in published maps and institutional affiliations. The views expressed in this article are solely those of the author(s) and do not reflect the opinions of the Editors or the publisher.

Share And Cite

Science Exploration Style
Ye Q, Li X, Sun X, Han J. Chiral assemblies for enantioselective nano-bio interactions and therapeutic translation. Chiral Chem. 2027;3:202638. https://doi.org/10.70401/cc.2026.0048

Submit a Manuscript
Author Instructions
Cite this Article
Export Citation
Article Metrics
0
View
0
Download
Cited
Article Updates
Citation Icon Get citation