Investigation of the Diels–Alder reaction as a cross-linking mechanism for degradable poly(ethylene glycol) based hydrogels
Source abstract
Abstract
The Diels-Alder (DA) reaction was investigated as a cross-linking mechanism for poly(ethylene glycol) (PEG) based hydrogels. Two complementary macromonomers were synthesized by functionalizing star-shaped PEG with furyl and maleimide groups. Gel formation occurred in water at 37 °C; the gelation time ranged between 171 ± 25 min and 14 ± 1 min depending on the used hydrogel formulation. The complex shear modulus was dependent on the concentration, branching factor and molecular weight of the macromonomers; values between 2821 ± 1479 Pa and 37097 ± 6698 Pa were observed. Hydrogel swelling and degradation were influenced by the same parameters; the degradation time varied between a few days and several weeks. Gel dissolution was found to occur by retro-DA reaction and subsequent hydrolysis of maleimide groups. Calculations of the network mesh size revealed that the prepared hydrogels would be suitable for the controlled release of therapeutic proteins.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Hydrogels: synthesis, properties, applications · Advanced Polymer Synthesis and Characterization · Surfactants and Colloidal Systems
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (46)
Show source-provided references
1. Slaughter · Adv. Mater. · 2009 · 21 · 330710.1002/adma.200802106 ↗
2. Boateng · J. Pharm. Sci. · 2008 · 97 · 289210.1002/jps.21210 ↗
3. Hoare · Polymer · 2008 · 49 · 199310.1016/j.polymer.2008.01.027 ↗
4. Qiu · Adv. Drug Delivery Rev. · 2001 · 53 · 32110.1016/S0169-409X(01)00203-4 ↗
5. Vermonden · Chem. Rev. · 2012 · 112 · 285310.1021/cr200157d ↗
6. Lin · Pharm. Res. · 2009 · 26 · 63110.1007/s11095-008-9801-2 ↗
7. Deligkaris · Sens. Actuators, B · 2010 · 147 · 76510.1016/j.snb.2010.03.083 ↗
8. Hoffman · Adv. Drug Delivery Rev. · 2002 · 54 · 310.1016/S0169-409X(01)00239-3 ↗
9. Tessmar · Macromol. Biosci. · 2007 · 7 · 2310.1002/mabi.200600096 ↗
10. Huebsch · Nat. Mater. · 2010 · 9 · 51810.1038/nmat2732 ↗
11. Anseth · J. Controlled Release · 2002 · 78 · 19910.1016/S0168-3659(01)00500-4 ↗
12. Gilbert · Science · 2010 · 329 · 107810.1126/science.1191035 ↗
13. Mann · Cel. Mol. Bioeng. · 2010 · 3 · 4010.1007/s12195-010-0108-0 ↗
14. Brandl · Biomaterials · 2007 · 28 · 13410.1016/j.biomaterials.2006.09.017 ↗
15. Engler · Cell · 2006 · 126 · 67710.1016/j.cell.2006.06.044 ↗
16. Kloxin · Adv. Mater. · 2010 · 22 · 348410.1002/adma.200904179 ↗
17. Huisgen · Pure Appl. Chem. · 1989 · 61 · 61310.1351/pac198961040613 ↗
18. Kolb · Angew. Chem., Int. Ed. Engl. · 2001 · 40 · 200410.1002/1521-3773(20010601)40:11<2004::AID-ANIE2004>3.0.CO;2-5 ↗
19. Gaetke · Toxicology · 2003 · 189 · 14710.1016/S0300-483X(03)00159-8 ↗
20. Yigit · Chem.–Asian J. · 2011 · 6 · 264810.1002/asia.201100440 ↗
21. Yang · J. Polym. Sci., Part A: Polym. Chem. · 2011 · 49 · 404410.1002/pola.24847 ↗
22. Zheng · ACS Macro Lett. · 2012 · 1 · 107110.1021/mz3003775 ↗
23. Gandini · Prog. Polym. Sci. · 2013 · 38 · 110.1016/j.progpolymsci.2012.04.002 ↗
24. Nicolaou · Angew. Chem., Int. Ed. · 2002 · 41 · 166810.1002/1521-3773(20020517)41:10<1668::AID-ANIE1668>3.0.CO;2-Z ↗
25. Tan · Macromol. Rapid Commun. · 2011 · 32 · 90510.1002/marc.201100125 ↗
26. Marref · Polym. Int. · 2013 · 62 · 8710.1002/pi.4287 ↗
27. Nimmo · Biomacromolecules · 2011 · 12 · 82410.1021/bm101446k ↗
28. Wei · Polymer · 2009 · 50 · 283610.1016/j.polymer.2009.04.032 ↗
29. Wei · J. Appl. Polym. Sci. · 2011 · 120 · 97410.1002/app.33116 ↗
30. Kozlowski · J. Controlled Release · 2001 · 72 · 21710.1016/S0168-3659(01)00277-2 ↗
31. Brandl · Adv. Eng. Mater. · 2007 · 9 · 114110.1002/adem.200700221 ↗
32. Kim · Chem. Mater. · 2008 · 20 · 585910.1021/cm801623a ↗
33. Rulíšek · J. Org. Chem. · 2005 · 70 · 629510.1021/jo050759z ↗
34. Sankaran · Macromolecules · 2010 · 43 · 553010.1021/ma100234j ↗
35. Mantovani · J. Am. Chem. Soc. · 2005 · 127 · 296610.1021/ja0430999 ↗
36. Keller · Tetrahedron Lett. · 2005 · 46 · 118110.1016/j.tetlet.2004.12.067 ↗
37. Bray · J. Appl. Polym. Sci. · 1973 · 17 · 377910.1002/app.1973.070171219 ↗
38. Elbert · J. Controlled Release · 2001 · 76 · 1110.1016/S0168-3659(01)00398-4 ↗
39. Canal · J. Biomed. Mater. Res. · 1989 · 23 · 118310.1002/jbm.820231007 ↗
40. Raeber · Biophys. J. · 2005 · 89 · 137410.1529/biophysj.104.050682 ↗
41. Metters · Biomacromolecules · 2005 · 6 · 29010.1021/bm049607o ↗
42. Lutolf · Biomacromolecules · 2003 · 4 · 71310.1021/bm025744e ↗
43. Oliva · J. Chromatogr., B: Biomed. Sci. Appl. · 2000 · 749 · 2510.1016/S0378-4347(00)00374-1 ↗
44. Armstrong · Biophys. J. · 2004 · 87 · 425910.1529/biophysj.104.047746 ↗
45. McElhanon · Langmuir · 2005 · 21 · 325910.1021/la047074z ↗
46. Koehler · Biomacromolecules · 2013 · 14 · 53810.1021/bm301789d ↗