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Controlled release of neurotrophin-3 from fibrin-based tissue engineering scaffolds enhances neural fiber sprouting following subacute spinal cord injury

✍ Scribed by Philip J. Johnson; Stanley R. Parker; Shelly E. Sakiyama-Elbert


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
363 KB
Volume
104
Category
Article
ISSN
0006-3592

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✦ Synopsis


Abstract

This study investigated whether delayed treatment of spinal cord injury with controlled release of neurotrophin‐3 (NT‐3) from fibrin scaffolds can stimulate enhanced neural fiber sprouting. Long Evans rats received a T9 dorsal hemisection spinal cord injury. Two weeks later, the injury site was re‐exposed, and either a fibrin scaffold alone, a fibrin scaffold containing a heparin‐based delivery system with different concentrations of NT‐3 (500 and 1,000 ng/mL), or a fibrin scaffold containing 1,000 ng/mL of NT‐3 (no delivery system) was implanted into the injury site. The injured spinal cords were evaluated for morphological differences using markers for neurons, astrocytes, and chondroitin sulfate proteoglycans 2 weeks after treatment. The addition of 500 ng/mL of NT‐3 with the delivery system resulted in an increase in neural fiber density compared to fibrin alone. These results demonstrate that the controlled release of NT‐3 from fibrin scaffolds can enhance neural fiber sprouting even when treatment is delayed 2 weeks following injury. Biotechnol. Bioeng. 2009; 104: 1207–1214. © 2009 Wiley Periodicals, Inc.


📜 SIMILAR VOLUMES


Fibrin-based tissue engineering scaffold
✍ Philip J. Johnson; Stanley R. Parker; Shelly E. Sakiyama-Elbert 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 558 KB

## Abstract The purpose of this study was to evaluate the effects of fibrin scaffolds on subacute rat spinal cord injury (SCI). Long–Evans rats were anesthetized and underwent a dorsal hemisection injury; two weeks later, the injury site was re‐exposed, scar tissue was removed, and a fibrin scaffol