Bioactive Pore‐Forming Bone Adhesives Facilitating Cell Ingrowth for Fracture Healing
Source abstract
Abstract
Abstract The effectiveness of commercial bone adhesives is known to be hampered by the weak efficacy of cell ingrowth. The strategy of macropore‐forming, especially bioactive macropores, holds considerable promise to circumvent this problem, thereby promoting fracture healing. Herein, a class of bioactive glass‐involved macropore‐embedded bone adhesives is developed, which is capable of facilitating the migration of bone‐derived mesenchymal stromal cells into the adhesive layer and differentiation into osteocytes. The integration of bioactive glass‐particle‐encapsulated porogens in the bone adhesives is key to this approach. A robust instant bonding on the bone adhesive and a high efficiency of bone regeneration on a mouse skull are observed, both of which are vital for clinical applications and personalized surgical procedures. This work represents a general strategy to design biomaterials with high cell‐ingrowth efficacy.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Bone Tissue Engineering Materials · Polymer Surface Interaction Studies · Orthopaedic implants and arthroplasty
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Beijing National Laboratory for Molecular Sciences State Key Laboratory of Polymer Physics and Chemistry CAS Research/Education Center for Excellence in Molecular Sciences Institute of Chemistry Chinese Academy of Sciences Beijing 100190 China
School of Chemical Sciences University of Chinese Academy of Sciences Beijing 100190 China
Department of Orthopedics Peking University Third Hospital Beijing 100191 China
Funding
National Basic Research Program of China · National Natural Science Foundation of China
References (38)
Show source-provided references
1. 10.1038/nature2100510.1038/nature21005 ↗
2. 10.1002/adfm.20180037210.1002/adfm.201800372 ↗
3. 10.1038/nmat446310.1038/nmat4463 ↗
4. 10.1016/j.biomaterials.2016.10.01010.1016/j.biomaterials.2016.10.010 ↗
5. 10.1002/adfm.20180084810.1002/adfm.201800848 ↗
6. 10.1002/adma.20090238010.1002/adma.200902380 ↗
7. 10.1038/nmat453910.1038/nmat4539 ↗
8. 10.1002/adma.20160474310.1002/adma.201604743 ↗
9. 10.1002/adma.20170464010.1002/adma.201704640 ↗
10. 10.1016/j.actbio.2018.03.00810.1016/j.actbio.2018.03.008 ↗
11. 10.1126/sciadv.aax315510.1126/sciadv.aax3155 ↗
12. 10.1016/0142-9612(89)90022-710.1016/0142-9612(89)90022-7 ↗
13. 10.1016/S0161-6420(93)31674-X10.1016/S0161-6420(93)31674-X ↗
14. 10.1016/j.dental.2006.06.02710.1016/j.dental.2006.06.027 ↗
15. 10.1016/j.ijadhadh.2011.11.00910.1016/j.ijadhadh.2011.11.009 ↗
16. 10.1126/sciadv.170005310.1126/sciadv.1700053 ↗
17. 10.1111/edt.1232810.1111/edt.12328 ↗
18. 10.1016/j.rbo.2016.12.00710.1016/j.rbo.2016.12.007 ↗
19. 10.1039/b618409j10.1039/b618409j ↗
20. 10.1073/pnas.100644210710.1073/pnas.1006442107 ↗
21. 10.1073/pnas.100786210810.1073/pnas.1007862108 ↗
22. 10.1038/nmat440710.1038/nmat4407 ↗
23. 10.1002/adma.20180546010.1002/adma.201805460 ↗
24. 10.1039/C8MH00937F10.1039/C8MH00937F ↗
25. 10.1002/adhm.20150044710.1002/adhm.201500447 ↗
26. 10.1002/adhm.20180154210.1002/adhm.201801542 ↗
27. 10.1515/bglass-2017-000510.1515/bglass-2017-0005 ↗
28. 10.3390/jfb901002510.3390/jfb9010025 ↗
29. 10.1126/science.106740410.1126/science.1067404 ↗
30. 10.1016/j.biomaterials.2011.01.00410.1016/j.biomaterials.2011.01.004 ↗
31. 10.1126/sciadv.aax694610.1126/sciadv.aax6946 ↗
32. 10.1016/j.biomaterials.2006.01.03910.1016/j.biomaterials.2006.01.039 ↗
33. 10.1016/j.biomaterials.2009.11.05010.1016/j.biomaterials.2009.11.050 ↗
34. 10.1007/s10856-011-4464-710.1007/s10856-011-4464-7 ↗
35. 10.1111/j.1445-2197.2007.04020.x10.1111/j.1445-2197.2007.04020.x ↗
36. 10.1126/science.167.3916.27910.1126/science.167.3916.279 ↗
37. 10.1021/acsami.6b1208910.1021/acsami.6b12089 ↗
38. 10.1002/adma.20130058410.1002/adma.201300584 ↗