Engineering star-shaped lactic acid oligomers to develop novel functional adhesives
Source abstract
Abstract
Direct polycondensation of L-lactic acid with a comonomer allows tailoring the properties of the product from the very first step. The viscous L-lactic acid co-oligomers with star-shaped architectures obtained were modified with three different acrylate monomers. Regardless the functionalization agent, UV curing was fast and all materials were cell compatible and promoted cell adhesion. The physical properties of the three star-shaped films exhibited a consistent trend as swelling capacity, hydrolytic instability, and gel content decreased simultaneously. A higher network density increased crosslinking degree and gel content among the films with an isocyanate group. The methacrylic end group functionalized material, lowest molecular weight, consistently exhibited the higher hydrolytic instability. Comparison of physical properties of these films with the corresponding linear materials reported previously confirmed the influence of precursor molecular architecture on the final material. The methodology developed herein is prone to scale-up and lead to the industrial production of new bioadhesives.
Source: expertdata · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: biodegradable polymer synthesis and properties · Photopolymerization techniques and applications · Advanced Polymer Synthesis and Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (35)
Show source-provided references
1. 10.1021/bm101505r10.1021/bm101505r ↗
2. 10.1016/j.biomaterials.2005.04.01210.1016/j.biomaterials.2005.04.012 ↗
3. 10.1002/mabi.20110019810.1002/mabi.201100198 ↗
4. 10.1016/j.jconrel.2010.06.00510.1016/j.jconrel.2010.06.005 ↗
5. 10.1002/mabi.20120033210.1002/mabi.201200332 ↗
6. 10.1016/S0142-9612(98)00059-310.1016/S0142-9612(98)00059-3 ↗
7. 10.1016/j.msec.2015.09.00910.1016/j.msec.2015.09.009 ↗
8. 10.1002/jbm.a.3301610.1002/jbm.a.33016 ↗
9. 10.3390/polym303137710.3390/polym3031377 ↗
10. 10.1021/bm201261d10.1021/bm201261d ↗
11. 10.1016/j.ijpharm.2007.10.02610.1016/j.ijpharm.2007.10.026 ↗
12. Xiao · 2012 · 248
13. 10.1016/j.progpolymsci.2011.12.00310.1016/j.progpolymsci.2011.12.003 ↗
14. Vidovic · 2006
15. 10.1002/pola.2836810.1002/pola.28368 ↗
16. 10.1016/S0168-583X(02)00647-X10.1016/S0168-583X(02)00647-X ↗
17. Multifunctional chondroitin sulphate for cartilage tissue-biomaterial integration10.1038/nmat1890 ↗
18. 10.1016/j.ijbiomac.2011.08.01010.1016/j.ijbiomac.2011.08.010 ↗
19. 10.1016/j.ijbiomac.2008.06.00210.1016/j.ijbiomac.2008.06.002 ↗
20. 10.1166/jbn.2014.185610.1166/jbn.2014.1856 ↗
21. 10.1016/j.progpolymsci.2014.02.00110.1016/j.progpolymsci.2014.02.001 ↗
22. 10.1002/marc.20029001410.1002/marc.200290014 ↗
23. 10.1080/00914037.2015.112996210.1080/00914037.2015.1129962 ↗
24. 10.1016/j.reactfunctpolym.2015.07.00310.1016/j.reactfunctpolym.2015.07.003 ↗
25. 10.1021/bm060869v10.1021/bm060869v ↗
26. 10.1016/j.reactfunctpolym.2012.10.00210.1016/j.reactfunctpolym.2012.10.002 ↗
27. 10.1002/app.1119310.1002/app.11193 ↗
28. 10.1021/cr60134a00410.1021/cr60134a004 ↗
29. 10.1002/app.3080010.1002/app.30800 ↗
30. 10.1021/bm050375i10.1021/bm050375i ↗
31. 10.3390/ijms1401187010.3390/ijms14011870 ↗
32. 10.1007/978-1-4757-9510-3_2010.1007/978-1-4757-9510-3_20 ↗
33. 10.1038/ncb206210.1038/ncb2062 ↗
34. 10.1016/j.carbpol.2014.04.09310.1016/j.carbpol.2014.04.093 ↗
35. 10.1089/ten.2007.009310.1089/ten.2007.0093 ↗