Exploiting the Thermotropic Behavior of Hydroxypropyl Cellulose to Produce Edible Photonic Pigments
Source abstract
Abstract
Abstract Hydroxypropyl cellulose (HPC) is a widely commercialized cellulose derivative. While it is typically used as a binder or stabilizer for foods and pharmaceuticals, it can also form a cholesteric liquid crystal in aqueous solution. Moreover, at high HPC concentrations this lyotropic and thermotropic mesophase is known to reflect structural color. However, it remains a challenge to retain this vibrant coloration into the solid state. Herein, by combining the emulsification of a HPC mesophase with drying at elevated temperature, solid microparticles are produced that can reflect color across the visible spectrum, from blue to green and red. This method provides a facile and scalable pathway to fabricate structurally colored, edible pigments, which can displace existing synthetic additives used in a wide range of foods and cosmetics.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Pickering emulsions and particle stabilization · Advanced Cellulose Research Studies · Advanced Materials and Mechanics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Yusuf Hamied Department of Chemistry University of Cambridge Lensfield Road Cambridge CB2 1EW UK
Funding
H2020 European Research Council · Biotechnology and Biological Sciences Research Council
References (43)
Show source-provided references
1. 10.1038/s41566-018-0152-110.1038/s41566-018-0152-1 ↗
2. 10.1007/s10570-020-03674-w10.1007/s10570-020-03674-w ↗
3. 10.1002/adma.20210211210.1002/adma.202102112 ↗
4. 10.1081/DDC-10010227810.1081/DDC-100102278 ↗
5. 10.1016/j.ajps.2016.05.00410.1016/j.ajps.2016.05.004 ↗
6. 10.1023/A:101897591959810.1023/A:1018975919598 ↗
7. 10.1007/978-1-4615-3552-210.1007/978-1-4615-3552-2 ↗
8. 10.1016/j.foodhyd.2012.07.00510.1016/j.foodhyd.2012.07.005 ↗
9. Werbowyj R. S. · Macromol. Chem. · 1980 · 13 · 69
10. Godinho M. H. · Eur. Phys. J.: Spec. Top. · 2016 · 39 · 89
11. 10.1080/1542140760808389410.1080/15421407608083894 ↗
12. 10.1038/s41467-022-31079-910.1038/s41467-022-31079-9 ↗
13. 10.1002/adom.20210212510.1002/adom.202102125 ↗
14. Guido S. · Macromol. Chem. · 1995 · 28 · 4530
15. 10.1002/adfm.20210856610.1002/adfm.202108566 ↗
16. 10.1002/adfm.20190272010.1002/adfm.201902720 ↗
17. 10.1002/adom.20160045110.1002/adom.201600451 ↗
18. 10.1002/ange.20200821010.1002/ange.202008210 ↗
19. 10.1038/s41467-018-07048-610.1038/s41467-018-07048-6 ↗
20. Wei J. · Adv. Mater. Technol. · 2022
21. 10.1002/app.1988.07036040210.1002/app.1988.070360402 ↗
22. 10.1007/BF0072015110.1007/BF00720151 ↗
23. 10.1002/adfm.20030438310.1002/adfm.200304383 ↗
24. 10.1023/A:102084572631410.1023/A:1020845726314 ↗
25. 10.1002/adma.20190515110.1002/adma.201905151 ↗
26. Gray D. G. · J. Appl. Polym. Sci.: Appl. Polym. Symp. · 1983 · 37 · 179
27. 10.1021/ma00195a05010.1021/ma00195a050 ↗
28. 10.1021/ma00167a00710.1021/ma00167a007 ↗
29. 10.1295/polymj.32.66510.1295/polymj.32.665 ↗
30. 10.1134/S0965545X0705012410.1134/S0965545X07050124 ↗
31. 10.1007/BF0115307110.1007/BF01153071 ↗
32. 10.1021/ma400601b10.1021/ma400601b ↗
33. 10.1007/s00396-010-2367-710.1007/s00396-010-2367-7 ↗
34. 10.1038/ncomms1252010.1038/ncomms12520 ↗
35. 10.1021/acsnano.6b0335510.1021/acsnano.6b03355 ↗
36. 10.1039/C3TC32055C10.1039/C3TC32055C ↗
37. 10.1021/acs.macromol.7b0228810.1021/acs.macromol.7b02288 ↗
38. 10.1295/koron.43.22310.1295/koron.43.223 ↗
39. 10.1021/ma00009a04410.1021/ma00009a044 ↗
40. Godinho M. H. · Liq. Cryst. · 2017 · 44 · 2108
41. 10.1016/j.cpc.2021.10825610.1016/j.cpc.2021.108256 ↗
42. 10.1111/1541-4337.1224410.1111/1541-4337.12244 ↗
43. 10.1016/j.procbio.2013.10.00810.1016/j.procbio.2013.10.008 ↗