Add like
Add dislike
Add to saved papers

Intrinsic Vascularization of Recombinant eADF4(C16) Spider Silk matrices in the AV Loop Model.

INTRODUCTION: The surgically induced angiogenesis by means of arteriovenous loops (AV loops) represents a powerful method to significantly enhance vascularization of biomaterials. Concerning Tissue Engineering applications, spider silk is a promising biomaterial with a good biocompatibility and slow biodegradation. The current study aims at investigating vascularization as well as de novo tissue formation of fibrous matrices made of electro- or wet-spun engineered ADF4(C16) spider silks in the rat AV loop model.

MATERIALS AND METHODS: Either electro- or wet-spun spider silk fibrous matrices were filled into Teflon chambers. Intrinsic vascularization was induced by means of an AV Loop. After 4 weeks vascularization, de novo tissue formation and biocompatibility were analyzed.

RESULTS: Regardless of their significantly differing fiber diameters, both electro- and wet-spun eADF4(C16) fiber matrices displayed a good biocompatibility and initiated de novo tissue formation as well as vessel formation. Both matrices demonstrated partial vascularization originating from the AV loop, with more vessels in spider silk matrices with lower fiber diameters.

CONCLUSION: We were able to demonstrate intrinsic vascularization of spider silk fibrous matrices by means of the AV loop. Moreover, our study indicates that the adjustment of the fiber diameter of engineered spider silks enables new possibilities to optimize vascularization.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app