Sustained Release of Antimicrobial Peptide from Self-Assembling Hydrogel Enhanced Osteogenesis
Sustained Release of Antimicrobial Peptide from Self-Assembling Hydrogel Enhanced Osteogenesis
复制标题
自组装水凝胶持续释放抗菌肽增强成骨作用
DOI:
10.1080/09205063.2018.1504191
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发表时间:
2018-09
期刊:
影响因子:
--
通讯作者:
Lingling Dong
中科院分区:
文献类型:
--
作者:
Guoli Yang;Tingben Huang;Ying Wang;Huiming Wang;Yongzheng Li;Ke Yu;Lingling Dong
Abstract Biomaterials have been widely used in bone infection and osteomyelitis resulting from their versatile functionalities. As far as we know, the appearance of osteomyelitis was mainly caused by bacteria. Therefore, a biomaterial that can cure bone infection and promote osteogenesis may become an ideal candidate for the treatment of osteomyelitis. Cationic antimicrobial peptides (AMPs) have been proved to have an excellent ability to kill bacteria, fungi, viruses, and parasites. However, the application of AMPs in bone infection and osteomyelitis is quite limited. Here, we designed a new hydrogel that has an inhibitory effect on the proliferation of S. aureus and enhances osteogenesis. RADA16 self-assembling peptide has been applied for AMPs delivery. In this study, we demonstrated that RADA16 could form a stable structure and afford the sustained release of AMPs. The interwoven nanofiber morphology was detected by field emission scanning electron microscopy. The sustained release study revealed that the release of AMPs could be obtained until 28 days. In vitro research showed this new self-assembling hydrogel could promote the proliferation of bone mesenchymal stem cells (BMSCs) and inhibited the growth of S. aureus. More importantly, the results in vivo also proved that RADA16-AMP self-assembling peptide had an excellent effect on bone formation. Our findings implied that we successfully combined RADA16 and AMPs together and laid the foundation for the application of this new hydrogel and open new avenues for biomaterials.
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影响因子:
--
作者:
I. Marriott;Jeremy Miller;Mahnaz Sahraei
通讯作者:
I. Marriott;Jeremy Miller;Mahnaz Sahraei
DOI:
10.2147/dddt.s109545
发表时间:
2016
期刊:
Drug design, development and therapy
影响因子:
--
作者:
Zhou A;Chen S;He B;Zhao W;Chen X;Jiang D
通讯作者:
Jiang D
影响因子:
4.9
作者:
Steinberg, DA;Hurst, MA;Fiddes, JC
通讯作者:
Fiddes, JC
DOI:
10.1073/pnas.97.12.6728
发表时间:
2000-06-06
影响因子:
11.1
作者:
Holmes, TC;de Lacalle, S;Zhang, SG
通讯作者:
Zhang, SG
影响因子:
3.7
作者:
Ni N;Hu Y;Ren H;Luo C;Li P;Wan JB;Su H
通讯作者:
Su H