journal article·2021-04-09

Toward Renewable and Functional Biomedical Polymers with Tunable Degradation Rates Based on Itaconic Acid and 1,8-Octanediol

Yufeng Shou, Scott B. Campbell, Angus Lam, Alexander J. Lausch, J. Paul Santerre, Milica Radisic, Locke Davenport Huyer

ACS Applied Polymer Materials· Volume 3· Issue 4
Publisher page

Abstract

Biomedical polymers face rigid requirements for the biocompatibility of their monomers, the final polymeric product, and their residual reagents from their synthesis schemes. However, their preparation still heavily relies on nonrenewable resources. Itaconate (ITA) is an organic acid that is used as a platform chemical for the production of numerous value-added chemicals and serves as a valuable green chemistry alternative to petrochemical derivatives. In recent years, the multiple roles of this molecule in cell metabolism have generated great attention, particularly as a modulator of inflammation and infection. Recently, we developed a family of ITA polyesters that leverage hydrolytically driven degradation to recapitulate its biofunctionality. This renewable-based material platform warrants characterization of material properties based on synthesis conditions in order to advance their potential application. In this work, we describe the development of ITA polyesters relying on defined reaction feed ratios and reaction times. Material characterization highlighted the significant impact of changing molar feed on molecular weight, which corresponded to increased viscosity and decreased percent degradation. Using 20% excess ITA monomers in the reaction led to optimal outcomes, suggesting opportunities in future material design. Leveraging this characterization, ITA polyesters can be altered through synthesis conditions to achieve appropriate and specific biopolymer applications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: biodegradable polymer synthesis and properties · Chemistry and Chemical Engineering · Carbon dioxide utilization in catalysis

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

Affiliations

Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, Ontario M5S3E5, Canada

Toronto General Research Institute, University Health Network, Toronto, Ontario M5G2C4, Canada

Institute of Biomedical Engineering, University of Toronto, Toronto, Ontario M5S3G9, Canada

Faculty of Dentistry, University of Toronto, Toronto, Ontario M5G2L3, Canada

Funding

Canadian Institutes of Health Research · Canada Foundation for Innovation · Canada Research Chairs · Natural Sciences and Engineering Research Council of Canada · Heart and Stroke Foundation of Canada

References (66)

Show source-provided references
1. 10.4172/ijbbd.100011910.4172/ijbbd.1000119 ↗
2. 10.1007/s00253-010-2642-z10.1007/s00253-010-2642-z ↗
3. 10.1016/j.biortech.2012.11.14110.1016/j.biortech.2012.11.141 ↗
4. 10.1038/pj.2013.6210.1038/pj.2013.62 ↗
5. 10.1021/ma025796w10.1021/ma025796w ↗
6. 10.1039/c9re00338j10.1039/c9re00338j ↗
7. 10.1007/s00253-009-2132-310.1007/s00253-009-2132-3 ↗
8. 10.1007/s00253010068510.1007/s002530100685 ↗
9. 10.1039/c6gc00605a10.1039/c6gc00605a ↗
10. 10.1021/ja207088910.1021/ja2070889 ↗
11. 10.1021/pr101054m10.1021/pr101054m ↗
12. 10.1007/s11306-011-0353-910.1007/s11306-011-0353-9 ↗
13. 10.1038/ni.350910.1038/ni.3509 ↗
14. 10.1073/pnas.121859911010.1073/pnas.1218599110 ↗
15. 10.1016/j.cmet.2016.06.00410.1016/j.cmet.2016.06.004 ↗
16. 10.1038/nature2598610.1038/nature25986 ↗
17. 10.1038/s41586-018-0052-z10.1038/s41586-018-0052-z ↗
18. 10.1038/s41467-019-13078-510.1038/s41467-019-13078-5 ↗
19. 10.3390/molecules1410402210.3390/molecules14104022 ↗
20. 10.1002/app.1981.07026020610.1002/app.1981.070260206 ↗
21. 10.1081/MA-10010336610.1081/MA-100103366 ↗
22. 10.1021/acs.macromol.5b0005210.1021/acs.macromol.5b00052 ↗
23. 10.1002/pi.557310.1002/pi.5573 ↗
24. 10.1039/c9py00463g10.1039/c9py00463g ↗
25. 10.1021/ma502006610.1021/ma5020066 ↗
26. 10.1016/j.eurpolymj.2018.04.01710.1016/j.eurpolymj.2018.04.017 ↗
27. 10.1021/acsami.8b1463610.1021/acsami.8b14636 ↗
28. 10.1016/b978-0-408-70310-9.50011-310.1016/b978-0-408-70310-9.50011-3 ↗
29. 10.1016/S0165-2370(98)00128-410.1016/S0165-2370(98)00128-4 ↗
30. 10.1016/j.polymdegradstab.2005.04.03010.1016/j.polymdegradstab.2005.04.030 ↗
31. 10.1016/S0141-3910(00)00139-710.1016/S0141-3910(00)00139-7 ↗
32. 10.1016/s0032-3861(02)00433-010.1016/s0032-3861(02)00433-0 ↗
33. 10.1021/acsbiomaterials.0c0091510.1021/acsbiomaterials.0c00915 ↗
34. 10.1007/s10118-021-2498-y10.1007/s10118-021-2498-y ↗
35. 10.1016/j.matchemphys.2016.11.03610.1016/j.matchemphys.2016.11.036 ↗
36. 10.1002/adfm.20200334110.1002/adfm.202003341 ↗
37. 10.1002/adhm.20190024510.1002/adhm.201900245 ↗
38. 10.3390/ijms16071491210.3390/ijms160714912 ↗
39. 10.1002/pola.2907910.1002/pola.29079 ↗
40. 10.1021/acs.biomac.7b0004410.1021/acs.biomac.7b00044 ↗
41. 10.1021/jo971176v10.1021/jo971176v ↗
42. 10.3390/app1006216310.3390/app10062163 ↗
43. 10.3389/fchem.2019.0050110.3389/fchem.2019.00501 ↗
44. 10.1039/c5py01729g10.1039/c5py01729g ↗
45. 10.1021/ma010986c10.1021/ma010986c ↗
46. 10.1021/jo01377a01510.1021/jo01377a015 ↗
47. Wang, H.; Siow, K. S. Effects of Interfacial Residual Stress on Tg of Epoxy Resin. Proceedings of the 1997 1st Electronic Packaging Technology Conference, 1997; pp 228–232.
48. 10.1021/ma000125o10.1021/ma000125o ↗
49. 10.1007/s11998-018-0146-410.1007/s11998-018-0146-4 ↗
50. 10.1080/0091403060086509310.1080/00914030600865093 ↗
51. 10.1021/acsbiomaterials.0c0054510.1021/acsbiomaterials.0c00545 ↗
52. 10.1002/app.1984.07029020110.1002/app.1984.070290201 ↗
53. 10.1002/app.1986.07031060310.1002/app.1986.070310603 ↗
54. 10.1295/polymj.26.18710.1295/polymj.26.187 ↗
55. 10.1002/macp.20090018910.1002/macp.200900189 ↗
56. 10.1021/ma047537810.1021/ma0475378 ↗
57. 10.1002/jbm.82028100910.1002/jbm.820281009 ↗
58. 10.1016/j.aca.2013.11.00110.1016/j.aca.2013.11.001 ↗
59. 10.1021/acssuschemeng.8b0560910.1021/acssuschemeng.8b05609 ↗
60. 10.1039/c8py01655k10.1039/c8py01655k ↗
61. 10.1016/0014-3057(89)90152-310.1016/0014-3057(89)90152-3 ↗
62. 10.1007/s10924-019-01368-410.1007/s10924-019-01368-4 ↗
63. 10.3390/ijms1009403310.3390/ijms10094033 ↗
64. 10.1016/j.progpolymsci.2017.10.00110.1016/j.progpolymsci.2017.10.001 ↗
65. Molitor, E. J.; Mullen, B. D. Method of Manufacture of Octanedioic Acid, Precursors, and Derivatives, 2020. https://patentimages.storage.googleapis.com/49/e5/0e/17cf3e53c84b20/US20160031790A1.pdf.
66. 10.1016/j.ymben.2015.01.00710.1016/j.ymben.2015.01.007 ↗