Testing a novel nanofibre scaffold for utility in bone tissue regeneration.
Testing a novel nanofibre scaffold for utility in bone tissue regeneration.
复制标题
DOI:
10.1002/term.2740
复制
发表时间:
2018-10
影响因子:
3.3
通讯作者:
Cray J
中科院分区:
文献类型:
--
作者:
Howie RN;Durham E;Oakes B;Grey Z;Smith J;Campbell P;LaRue A;Steed M;Muise-Helmericks R;Cray J
Many variables serve to alter the process of bone remodeling and diminish regeneration including the size and nature of the wound bed and health status of the individual. To overcome these inhibitory factors, tissue engineered osteoconductive scaffolds paired with various growth factors have been utilized clinically. However, many limitations still remain, for example, bone morphogenetic protein 2 (BMP2), can lead to rampant inflammation, ectopic bone formation, and graft failure. Here we studied the ability for a nanofiber scaffold (Talymed) to accelerate BMP2 growth factor induced bone healing compared to the traditional absorbable collagen sponge (ACS) delivery system. 155 adult wild-type mice were arranged in 16 groups by time, 4 and 8 week, and treatment, ACS or Talymed, loaded with control, low, medium or high dosages of BMP2. Skulls were subjected to microCT, biomechanical, and histological analysis to assess bone regeneration. The use of Talymed within the defect site was found to decrease the bone volume, bone formation rate, and ALP activity compared to ACS/BMP2 combinations. Interestingly, though Talymed regenerated less bone, the regenerate was found to have a greater hardness value than that of bone within the ACS groups. However, the difference in bone hardness between scaffolds was not detectable by 8 weeks. Based on these results, we found that the nanofiber scaffold generated a better quality of bone regenerate at 4 weeks but, due to the lack of overall bone formation and the inhibition of normal remodeling processes, was not as efficacious as the current clinical standard ACS/BMP2 therapy.
登录
查看更多内容
影响因子:
3.6
作者:
Cooper GM;Mooney MP;Gosain AK;Campbell PG;Losee JE;Huard J
通讯作者:
Huard J
影响因子:
6.2
作者:
Dayer, Romain;Badoud, Isabelle;Ammann, Patrick
通讯作者:
Ammann, Patrick
影响因子:
14
作者:
Li, Bing;Yoshii, Toshitaka;Guelcher, Scott A.
通讯作者:
Guelcher, Scott A.
影响因子:
4.1
作者:
Herberg, Samuel;Kondrikova, Galina;Cray, James J.
通讯作者:
Cray, James J.
DOI:
10.1038/nrrheum.2014.164
发表时间:
2015-01
期刊:
Nature reviews. Rheumatology
影响因子:
--
作者:
通讯作者:
--