journal article·2025-05Open access

Chiral Sensing of Amino Acids under Visible Light via Hydroxypropyl Cellulose Gels

Luyao Huang, Xianzhe Zhang, Cheng Xu, Jiwei Wang, Allen Zhang, Yongmin Liu, Hongli Zhu

Advanced Optical Materials· Volume 13· Issue 15

Abstract

Abstract The identification of Chiral molecules is essential in pharmaceutical and food science. However, conventional methods are complex and cost‐prohibitive. This study introduces a sustainable method using hydroxypropyl cellulose (HPC) gel to identify amino acids enantiomers, such as phenylalanine and alanine, through visible light. By integrating the structural color properties of HPC, this research demonstrates the HPC gel's capability to distinguish L (Levo)‐phenylalanine (L‐Phe), D (Dextro)‐phenylalanine (D‐Phe), and DL (racemic mixture)‐phenylalanine (DL‐Phe) supplemented with visible circular dichroism (CD) spectra or hydrochloric acid (HCl) as visual indicators. Similar chiral sensing results are observed with D‐alanine, L‐alanine, and DL‐alanine. Unlike traditional UV‐based detection requiring expensive equipment, this approach simplifies the process while maintaining sensitivity. Varying phenylalanine concentrations altered the CD response without disrupting the gel's helical structure, and color changes in response to HCl addition facilitated visual identification of enantiomers. Furthermore, adding various salts generates colorful HPC/Phe gels, demonstrating their suitability for 3D printing. Meanwhile, the HPC gels remained functional for three months, indicating long‐term stability. These advancements are significant for pharmaceutical and biotechnological industries, facilitating efficient low‐concentration chirality detection (0.2 wt.%). Continued development and refinement of this technology are expected to expand its applications and improve analytical capabilities for future chirality‐related studies and photonic gel 3D printing.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Molecular Sensors and Ion Detection · Analytical Chemistry and Chromatography · Supramolecular Self-Assembly in Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Mechanical and Industrial Engineering Northeastern University Boston MA 02115 USA

Department of Electrical and Computer Engineering Northeastern University Boston MA 02115 USA

Funding

National Science Foundation

References (32)

Show source-provided references
1. 10.1002/1521-3773(20020617)41:12<2008::AID-ANIE2008>3.0.CO;2-410.1002/1521-3773(20020617)41:12<2008::AID-ANIE2008>3.0.CO;2-4 ↗
2. 10.1038/s41570-023-00476-z10.1038/s41570-023-00476-z ↗
3. 10.1016/0026-0495(94)90123-610.1016/0026-0495(94)90123-6 ↗
4. Walsh N. E. · Arch. Phys. Med. Rehabil. · 1986 · 67 · 436
5. 10.3727/03601298281695209910.3727/036012982816952099 ↗
6. 10.1038/ncomms1418010.1038/ncomms14180 ↗
7. 10.1016/j.aca.2017.03.02110.1016/j.aca.2017.03.021 ↗
8. 10.1016/j.trac.2019.07.01110.1016/j.trac.2019.07.011 ↗
9. 10.3390/molecules2108105610.3390/molecules21081056 ↗
10. 10.1017/S003358351500007410.1017/S0033583515000074 ↗
11. 10.1063/1.493222910.1063/1.4932229 ↗
12. 10.1039/C9NR08433A10.1039/C9NR08433A ↗
13. 10.1021/acs.nanolett.0c0350610.1021/acs.nanolett.0c03506 ↗
14. 10.1021/acs.nanolett.0c0193810.1021/acs.nanolett.0c01938 ↗
15. 10.1021/acsphotonics.8b0136510.1021/acsphotonics.8b01365 ↗
16. 10.1002/adma.20210211210.1002/adma.202102112 ↗
17. 10.1002/adfm.20210724210.1002/adfm.202107242 ↗
18. 10.1021/acsnano.3c1143210.1021/acsnano.3c11432 ↗
19. 10.1021/ja00093a04210.1021/ja00093a042 ↗
20. 10.1007/978-3-642-35943-9_629-110.1007/978-3-642-35943-9_629-1 ↗
21. 10.1021/acsami.0c0513910.1021/acsami.0c05139 ↗
22. 10.1039/C7BM00882A10.1039/C7BM00882A ↗
23. 10.1021/bm400752k10.1021/bm400752k ↗
24. 10.1021/acs.jproteome.8b0056710.1021/acs.jproteome.8b00567 ↗
25. 10.1016/j.carbpol.2005.11.02210.1016/j.carbpol.2005.11.022 ↗
26. 10.1016/j.apmt.2020.10091210.1016/j.apmt.2020.100912 ↗
27. 10.1295/polymj.34.14910.1295/polymj.34.149 ↗
28. 10.1021/bm060567t10.1021/bm060567t ↗
29. 10.1021/mz400372210.1021/mz4003722 ↗
30. 10.1021/acs.molpharmaceut.1c0083210.1021/acs.molpharmaceut.1c00832 ↗
31. 10.17352/abse.00001510.17352/abse.000015 ↗
32. 10.1364/OL.17.00088610.1364/OL.17.000886 ↗