journal article·2024-08

Chiral-functionalized membranes for chiral drugs sieving

Sijia He, Yaqian Zhang, Sravan Baddi, Changli Zhao, Xiaoqiu Dou, Chuanliang Feng

Science China Materials· Volume 67· Issue 8
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OpenAlex topics: Analytical Chemistry and Chromatography · Lipid Membrane Structure and Behavior · Analytical Chemistry and Sensors

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References (51)

Show source-provided references
1. Brandt JR, Salerno F, Fuchter MJ. The added value of small-molecule chirality in technological applications. Nat Rev Chem, 2017, 1: 004510.1038/s41570-017-0045 ↗
2. Yang Y, Zhang Y, Wei Z. Supramolecular helices: Chirality transfer from conjugated molecules to structures. Adv Mater, 2013, 25: 6039–604910.1002/adma.201302448 ↗
3. Du C, Li Z, Zhu X, et al. Hierarchically self-assembled homochiral helical microtoroids. Nat Nanotechnol, 2022, 17: 1294–130210.1038/s41565-022-01234-w ↗
4. Peng Y, Gong T, Zhang K, et al. Engineering chiral porous metal-organic frameworks for enantioselective adsorption and separation. Nat Commun, 2014, 5: 440610.1038/ncomms5406 ↗
5. Coelho MM, Fernandes C, Remião F, et al. Enantioselectivity in drug pharmacokinetics and toxicity: Pharmacological relevance and analytical methods. Molecules, 2021, 26: 311310.3390/molecules26113113 ↗
6. Candelaria L, Frolova LV, Kowalski BM, et al. Surface-modified three-dimensional graphene nanosheets as a stationary phase for chromatographic separation of chiral drugs. Sci Rep, 2018, 8: 1474710.1038/s41598-018-33075-w ↗
7. Qian HL, Yang CX, Yan XP. Bottom-up synthesis of chiral covalent organic frameworks and their bound capillaries for chiral separation. Nat Commun, 2016, 7: 1210410.1038/ncomms12104 ↗
8. Gassmann E, Kuo JE, Zare RN. Electrokinetic separation of chiral compounds. Science, 1985, 230: 813–81410.1126/science.230.4727.813 ↗
9. Chan JY, Zhang H, Nolvachai Y, et al. Incorporation of homochirality into a zeolitic imidazolate framework membrane for efficient chiral separation. Angew Chem, 2018, 130: 17376–1738010.1002/ange.201810925 ↗
10. Torsi L, Farinola GM, Marinelli F, et al. A sensitivity-enhanced field-effect chiral sensor. Nat Mater, 2008, 7: 412–41710.1038/nmat2167 ↗
11. Chen X, Kang Y, Zeng S. Analysis of stereoisomers of chiral drug by mass spectrometry. Chirality, 2018, 30: 609–61810.1002/chir.22833 ↗
12. Zhu YY, Wu XD, Gu SX, et al. Free amino acid recognition: A bisbinaphthyl-based fluorescent probe with high enantioselectivity. J Am Chem Soc, 2018, 141: 175–18110.1021/jacs.8b07803 ↗
13. Zhang QP, Wang Z, Zhang ZW, et al. Triptycene-based chiral porous polyimides for enantioselective membrane separation. Angew Chem Int Ed, 2021, 60: 12781–1278510.1002/anie.202102350 ↗
14. Wang X, Wolfbeis OS. Optical methods for sensing and imaging oxygen: Materials, spectroscopies and applications. Chem Soc Rev, 2014, 43: 3666–376110.1039/C4CS00039K ↗
15. Vespalec R, Boček P. Chiral separations in capillary electrophoresis. Chem Rev, 2000, 100: 3715–375410.1021/cr9411583 ↗
16. Tian H, Zheng N, Li S, et al. Characterization of chiral amino acids from different milk origins using ultra-performance liquid chromatography coupled to ion-mobility mass spectrometry. Sci Rep, 2017, 7: 4628910.1038/srep46289 ↗
17. Das S, Xu S, Ben T, et al. Chiral recognition and separation by chirality-enriched metal-organic frameworks. Angew Chem Int Ed, 2018, 57: 8629–863310.1002/anie.201804383 ↗
18. Lu Y, Zhang H, Chan JY, et al. Homochiral MOF–polymer mixed matrix membranes for efficient separation of chiral molecules. Angew Chem Int Ed, 2019, 131: 16928–1693510.1002/anie.201910408 ↗
19. Qi Y, Xia Y, Li P, et al. Plastic-swelling preparation of functional graphene aerogel fiber textiles. Adv Fiber Mater, 2023, 5: 2016–202710.1007/s42765-023-00316-1 ↗
20. Liu J, Wang N, Yu LJ, et al. Bioinspired graphene membrane with temperature tunable channels for water gating and molecular separation. Nat Commun, 2017, 8: 201110.1038/s41467-017-02198-5 ↗
21. Guo J, Zhang Y, Yang F, et al. Ultra-permeable dual-mechanism-driven graphene oxide framework membranes for precision ion separations. Angew Chem Int Ed, 2023, 62: e20230293110.1002/anie.202302931 ↗
22. Zhu Y, Murali S, Cai W, et al. Graphene and graphene oxide: Synthesis, properties, and applications. Adv Mater, 2010, 22: 3906–392410.1002/adma.201001068 ↗
23. Chen D, Feng H, Li J. Graphene oxide: Preparation, functionalization, and electrochemical applications. Chem Rev, 2012, 112: 6027–605310.1021/cr300115g ↗
24. Chung C, Kim YK, Shin D, et al. Biomedical applications of graphene and graphene oxide. Acc Chem Res, 2013, 46: 2211–222410.1021/ar300159f ↗
25. Thebo KH, Qian X, Zhang Q, et al. Highly stable graphene-oxide-based membranes with superior permeability. Nat Commun, 2018, 9: 148610.1038/s41467-018-03919-0 ↗
26. Wang Y, Wu N, Wang Y, et al. Graphite phase carbon nitride based membrane for selective permeation. Nat Commun, 2019, 10: 250010.1038/s41467-019-10381-z ↗
27. Shen B, Kim Y, Lee M. Supramolecular chiral 2D materials and emerging functions. Adv Mater, 2020, 32: 190566910.1002/adma.201905669 ↗
28. Lewis RV. Spider silk: Ancient ideas for new biomaterials. Chem Rev, 2006, 106: 3762–377410.1021/cr010194g ↗
29. Sun M, Li J. Graphene oxide membranes: Functional structures, preparation and environmental applications. Nano Today, 2018, 20: 121–13710.1016/j.nantod.2018.04.007 ↗
30. Liu G, Jin W, Xu N. Two-dimensional-material membranes: A new family of high-performance separation membranes. Angew Chem Int Ed, 2016, 55: 13384–1339710.1002/anie.201600438 ↗
31. Marcano DC, Kosynkin DV, Berlin JM, et al. Improved synthesis of graphene oxide. ACS Nano, 2010, 4: 4806–481410.1021/nn1006368 ↗
32. Qin M, Li Y, Zhang Y, et al. Solvent-controlled topological evolution from nanospheres to superhelices. Small, 2020, 16: 200475610.1002/smll.202004756 ↗
33. Liu G, Zhang D, Feng C. Control of three-dimensional cell adhesion by the chirality of nanofibers in hydrogels. Angew Chem Int Ed, 2014, 53: 7789–779310.1002/anie.201403249 ↗
34. Lu H, Zhao Y, Qin S, et al. Fluorine substitution tunes the nanofiber chirality of supramolecular hydrogels to promote cell adhesion and proliferation. Adv Fiber Mater, 2023, 5: 377–38710.1007/s42765-022-00232-w ↗
35. Qian X, Li N, Wang Q, et al. Chitosan/graphene oxide mixed matrix membrane with enhanced water permeability for high-salinity water desalination by pervaporation. Desalination, 2018, 438: 83–9610.1016/j.desal.2018.03.031 ↗
36. Zhang Y, Zhang M, Jiang H, et al. Bio-inspired layered chitosan/graphene oxide nanocomposite hydrogels with high strength and pH-driven shape memory effect. Carbohydr Polyms, 2017, 177: 116–12510.1016/j.carbpol.2017.08.106 ↗
37. Khan YH, Islam A, Sarwar A, et al. Novel green nano composites films fabricated by indigenously synthesized graphene oxide and chitosan. Carbohydr Polyms, 2016, 146: 131–13810.1016/j.carbpol.2016.03.031 ↗
38. Mehwish N, Dou X, Zhao C, et al. Chirality transfer in supramolecular co-assembled fibrous material enabling the visual recognition of sucrose. Adv Fiber Mater, 2020, 2: 204–21110.1007/s42765-020-00028-w ↗
39. Yang D, Duan P, Liu M. Dual upconverted and downconverted circularly polarized luminescence in donor-acceptor assemblies. Angew Chem Int Ed, 2018, 130: 9357–936110.1002/anie.201804402 ↗
40. Zhu X, Li Y, Duan P, et al. Self-assembled ultralong chiral nanotubes and tuning of their chirality through the mixing of enantiomeric components. Chem Eur J, 2010, 16: 8034–804010.1002/chem.201000595 ↗
41. Fan H, Wang L, Zhao K, et al. Fabrication, mechanical properties, and biocompatibility of graphene-reinforced chitosan composites. Biomacromolecules, 2010, 11: 2345–235110.1021/bm100470q ↗
42. Zhu G, Zhu X, Fan Q, et al. Raman spectra of amino acids and their aqueous solutions. SpectroChim Acta Part A-Mol Biomol Spectr, 2011, 78: 1187–119510.1016/j.saa.2010.12.079 ↗
43. Nagatomo S, Nagai M, Ogura T, et al. Near-UV circular dichroism and UV resonance raman spectra of tryptophan residues as a structural marker of proteins. J Phys Chem B, 2013, 117: 9343–935310.1021/jp404685x ↗
44. Koch H, Polepil S, Eisen K, et al. Raman microspectroscopy and multivariate data analysis: Optical differentiation of aqueous D- and L-tryptophan solutions. Phys Chem Chem Phys, 2017, 19: 30533–3053910.1039/C7CP02321A ↗
45. Yeom J, Guimaraes PPG, Ahn HM, et al. Chiral supraparticles for controllable nanomedicine. Adv Mater, 2020, 32: 190387810.1002/adma.201903878 ↗
46. Feng W, Kim JY, Wang X, et al. Assembly of mesoscale helices with near-unity enantiomeric excess and light-matter interactions for chiral semiconductors. Sci Adv, 2017, 3: e160115910.1126/sciadv.1601159 ↗
47. Shen J, Okamoto Y. Efficient separation of enantiomers using stereo-regular chiral polymers. Chem Rev, 2016, 116: 1094–113810.1021/acs.chemrev.5b00317 ↗
48. Gumustas M, Ozkan SA, Chankvetadze B. Analytical and preparative scale separation of enantiomers of chiral drugs by chromatography and related methods. Curr Med Chem, 2018, 25: 4152–418810.2174/0929867325666180129094955 ↗
49. Han D, Yan L, Chen W, et al. Preparation of chitosan/graphene oxide composite film with enhanced mechanical strength in the wet state. Carbohydr Polyms, 2011, 83: 653–65810.1016/j.carbpol.2010.08.038 ↗
50. Hamley I, Castelletto V. Small-angle scattering of block copolymersin the melt, solution and crystal states. Prog Polym Sci, 2004, 29: 909–948
51. Zhang S, Zheng Y, An H, et al. Covalent organic frameworks with chirality enriched by biomolecules for efficient chiral separation. Angew Chem Int Ed, 2018, 57: 16754–1675910.1002/anie.201810571 ↗