Polydopamine-Decorated Black Phosphorous to Enhance Stability in polymer scaffold

2021 ◽  
Author(s):  
Guoyong Wang ◽  
Guowen Qian ◽  
Jia Yao ◽  
Weiliang Cai ◽  
Shuping Peng ◽  
...  
2021 ◽  
Vol 435 ◽  
pp. 213826
Author(s):  
Abhijeet Pandey ◽  
Ajinkya Nitin Nikam ◽  
Bharath Singh Padya ◽  
Sanjay Kulkarni ◽  
Gasper Fernandes ◽  
...  

2020 ◽  
Vol 4 (8) ◽  
pp. 2398-2408 ◽  
Author(s):  
Cijun Shuai ◽  
Li Yu ◽  
Pei Feng ◽  
Yancheng Zhong ◽  
Zhenyu Zhao ◽  
...  

KH550 organic modified MMT was incorporated into PCL to enhance the interfacial bonding and restricted the movement of PCL molecular chains in galleries through the interlayer locking effect.


2018 ◽  
Vol 3 (3) ◽  
pp. 2473011418S0053
Author(s):  
Jianying Zhang ◽  
Daibang Nie ◽  
Guangyi Zhao ◽  
Susheng Tan ◽  
MaCalus Hogan ◽  
...  

Category: Hindfoot Introduction/Purpose: Entheses have a special fibrocartilage transition zone where tendons and ligaments attach to bone. Enthesis injury is very common, and the reattachment of tendon to bone is a great challenge because healing takes place between a soft tissue (tendon) and a hard tissue (bone). We have now developed a kartogene (KGN)-containing polymer scaffold (KGN-P) that can precisely deliver KGN to damaged enthesis area. The effects of the KGN-containing polymer on the healing of wounded TBJ were investigated in vitro and in vivo. Methods: The proliferation and chondrogenesis of rat Achilles tendon stem cells (TSCs) grown in four conditions were measured: normal medium (Control); normal medium with 100 nM KGN (KGN); lysine diisocyanate (LDI)-glycerol scaffold with normal medium (LDI-P); LDI-glycerol-KGN scaffold with normal medium (KGN-P).A wound (1 mm) was created on each hind leg Achilles enthesis of all 8 rats (3 months old). The wounds were then treated either with 10 ul saline (Wound); or 10 ul of 10 uM KGN (KGN); or LDI polymer scaffold (LDI-P); or KGN-containing polymer scaffold (KGN-P). The rats were sacrificed on day 15 and 30 post-surgery, and their Achilles entheses were collected for gross inspection and histochemical analysis. Results: KGN-containing polymers have sponge-like structures (Fig. 1A-D), and release KGN in a time- and temperature-dependent manner (Fig. 1E). KGN-P scaffold induced chondrogenesis of TSCs (Fig. 2D, 2H) without changing cell proliferation (Fig. 2I), and enhanced fibrocartilage-like tissue formation (Fig. 3E). KGN (Fig. 3C) and LDI-P (Fig. 3D) treated groups exhibited unhealed wound areas as in saline group (Fig. 3B). Finally, KGN-P and KGN treated rat TSCs underwent chondrogenesis by upregulating collagen II, aggrecan, and SOX-9 expression (Fig. 3F). Conclusion: Our results showed that KGN-containing polymer scaffold enhanced wounded enthesis healing by inducing TSC chondrogenesis and promoting the formation of the fibrocartilage in the wound site. The KGN-P may be used for regeneration of wounded entheses in clinical settings. Future research will focus on optimizing KGN concentration and releasing rate in the polymer scaffold during enthesis healing.


2019 ◽  
Vol 32 (2) ◽  
pp. 238-247 ◽  
Author(s):  
L. Durai ◽  
A. Gopalakrishnan ◽  
Nandimalla Vishnu ◽  
Sushmee Badhulika

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