Construction of a Linear Cell Cross-Linker with Multivalent Glycyrrhetinic Acid Ligands for Rapid Formation of Hepatocyte Spheroids
Source abstract
Abstract
We report herein the development of a novel cellular cross-linker further employed in the construction of hepatocellular spheroids based on multivalent strategy. The linker structure consists of a glycyrrhetinic acid derivative (GA-N(CH3)2) modified alginate (ALG). GA-N(CH3)2 is selected as the recognition ligand due to its high affinity toward hepatocyte, whereas ALG represents the linear backbone accounting for its good biocompatibility and flexible structure. These features endow the cellular cross-linker with the ability to flexibly interact with the cell through multiple binding sites, providing superior binding force between the cell and cross-linker, and subsequently rapidly combining multiple cells into cellular spheroids.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: 3D Printing in Biomedical Research · Pharmacological Effects of Natural Compounds · Liver physiology and pathology
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Functional Polymer Materials of Ministry of Education, Institute of Polymer Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China
Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300071, China
Funding
Natural Science Foundation of Tianjin City · Changjiang Scholar Program of Chinese Ministry of Education · National Natural Science Foundation of China
References (33)
Show source-provided references
1. 10.1038/nrm185810.1038/nrm1858 ↗
2. 10.1096/fasebj.13.14.188310.1096/fasebj.13.14.1883 ↗
3. 10.1177/09636897950040030310.1177/096368979500400303 ↗
4. 10.1007/s10544-007-9125-810.1007/s10544-007-9125-8 ↗
5. 10.1016/j.biomaterials.2010.07.05010.1016/j.biomaterials.2010.07.050 ↗
6. 10.1016/j.jconrel.2016.09.01410.1016/j.jconrel.2016.09.014 ↗
7. 10.1158/0008-5472.CAN-12-207110.1158/0008-5472.CAN-12-2071 ↗
8. 10.1089/ten.tec.2008.051610.1089/ten.tec.2008.0516 ↗
9. 10.1038/bjc.2014.16010.1038/bjc.2014.160 ↗
10. 10.3727/00000000310874703710.3727/000000003108747037 ↗
11. 10.1046/j.1525-1594.2002.06836.x10.1046/j.1525-1594.2002.06836.x ↗
12. 10.2217/rme.11.10110.2217/rme.11.101 ↗
13. 10.1039/b618439a10.1039/b618439a ↗
14. 10.1002/(SICI)1097-0290(19960520)50:4<349::AID-BIT1>3.3.CO;2-D10.1002/(SICI)1097-0290(19960520)50:4<349::AID-BIT1>3.3.CO;2-D ↗
15. 10.1016/j.actbio.2009.04.01510.1016/j.actbio.2009.04.015 ↗
16. 10.1016/j.colsurfb.2012.06.03310.1016/j.colsurfb.2012.06.033 ↗
17. 10.1016/j.biomaterials.2010.06.02010.1016/j.biomaterials.2010.06.020 ↗
18. 10.1002/anie.20100344510.1002/anie.201003445 ↗
19. 10.1016/j.colsurfb.2017.03.04910.1016/j.colsurfb.2017.03.049 ↗
20. 10.1016/j.biomaterials.2013.01.00310.1016/j.biomaterials.2013.01.003 ↗
21. 10.1016/j.biomaterials.2007.04.03410.1016/j.biomaterials.2007.04.034 ↗
22. 10.1016/j.biomaterials.2008.05.01910.1016/j.biomaterials.2008.05.019 ↗
23. 10.1002/jbm.a.3530610.1002/jbm.a.35306 ↗
24. 10.1007/s11426-015-5451-510.1007/s11426-015-5451-5 ↗
25. 10.1016/j.biomaterials.2011.11.04510.1016/j.biomaterials.2011.11.045 ↗
26. 10.1016/j.biomaterials.2017.05.02810.1016/j.biomaterials.2017.05.028 ↗
27. 10.1021/ja027184x10.1021/ja027184x ↗
28. 10.1021/am504533910.1021/am5045339 ↗
29. 10.7503/cjcu2016031610.7503/cjcu20160316 ↗
30. 10.1016/S0142-9612(02)00445-310.1016/S0142-9612(02)00445-3 ↗
31. 10.1021/bm900784x10.1021/bm900784x ↗
32. 10.1007/s11426-009-0178-910.1007/s11426-009-0178-9 ↗
33. 10.1016/j.nano.2011.11.00210.1016/j.nano.2011.11.002 ↗