Amino groups are crucial for chitosan to stop bleeding

Joint Event on 11^th International Conference on Tissue Engineering & Regenerative Medicine & 4^th International Conference on Synthetic Biology and Tissue Engineering

October 18-20, 2018 Rome, Italy

Haibo Lu and Shibi Lu

First Affiliated Hospital of Chinese PLA General Hospital, China
General Hospital of Chinese PLA, China

Posters & Accepted Abstracts: J Tissue Sci Eng

Abstract :

Marine organisms adhere themselves onto wet surfaces by adhesive proteins containing L-3, 4-dihydroxyphenylalanine (DOPA). Several research groups have incorporated DOPA, or other compounds that contain 3, 4-dihydroxybenzene, into backbone of polymeric materials, and have found the improved adhesive properties. Although current positively charged chitosan hemostatic agents have limited adhesive property, especially to wet surfaces underneath blood pool, there is no report about modifying chitosan with 3, 4-dihydroxybenzene to achieve improved adhesive property so far, and the exact mechanism of chitosanâ??s positive charging is still unknown. Using two methods, we modified chitosan with 3, 4-dihydroxybenzene. One is modifying with 3, 4-dihydroxybenzaldehyde (DHBH), the other is with DOPA. The chemical structures of chitosan, Celox, DHBH, DMCTS, DOPA and DOPAMCTS were characterized with Fourier transform infrared (FTIR) spectroscopy. The coagulation test was performed to compare the hemostatic property of DMCTS and DOPAMCTS to that of chitin, chitosan and Celox. FTIR results revealed extreme similarity of chemical structures of chitosan and Celox, especially in presence of N-H bending vibration of primary amines, the incorporation of 3, 4-dihydroxybenzene from DMCTS and DOPA into backbone of chitosan. The coagulation time of chitosan, Celox and DOPAMCTS was significantly shorter than that of chitin and DMCTS. The blood drops touching Celox, chitosan and DOPAMCTS particles appeared significant surface-tension phenomenon. In conclusion, amino groups are crucial for chitosan to stop bleeding. Modification with 3, 4-dihydroxybenzene does not impair the hemostatic property of chitosan as long as the free or protonated amino group does not be modified. It is feasible to modify chitosan with 3, 4-dihydroxybenzene to develop a novel hemostatic dressing.

Biography :

E-mail: luhaibo304@163.com