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Assessment of hemostatic ability of biomaterial based on chitosan and Eclipta prostrata L. extract

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Abstract The biomaterials based on chitosan and Eclipta prostrata L. extract have been prepared by microemulsion method and solution method (with and without sodium tripolyphosphate (STPP) as a cross-linking agent). The main component in Eclipta prostrata L. extract is flavonoid groups. The structure of the chitosan/extract biomaterials was studied by infrared spectroscopy. The chitosan/extract biomaterial using STPP cross-linker appeared an absorption band at 1152 cm−1 attributed to the vibrations of C–O–P bonds, which proved that chitosan has crosslinked with STPP. The morphology of the biomaterials was investigated by the dynamic light scattering technique and field emission scanning electron microscopy. The obtained results showed that the particle size of the chitosan/extract biomaterials prepared by microemulsion method and solution method with STPP ranged from 68.06 nm to 1484 nm, with an average particle size of 304.9–1019 nm. The microemulsion method produced biomaterials with much smaller average particle size than the solution method using cross-linkers. The hemostatic ability of the biomaterials was better than that of the control sample based on the time of blood clotting formation and glomerular aggregation ability. The sample with the ratio of E. prostrata L. extract: chitosan of 1:30 had the lowest hemostasis time (6 min 46 s) and its glomerular aggregation rate after 5 min was 13.05%. This indicated that the biomaterials based on chitosan and E. prostrata L. extract are promising for application in biomedicine as hemostatic materials.
Title: Assessment of hemostatic ability of biomaterial based on chitosan and Eclipta prostrata L. extract
Description:
Abstract The biomaterials based on chitosan and Eclipta prostrata L.
extract have been prepared by microemulsion method and solution method (with and without sodium tripolyphosphate (STPP) as a cross-linking agent).
The main component in Eclipta prostrata L.
extract is flavonoid groups.
The structure of the chitosan/extract biomaterials was studied by infrared spectroscopy.
The chitosan/extract biomaterial using STPP cross-linker appeared an absorption band at 1152 cm−1 attributed to the vibrations of C–O–P bonds, which proved that chitosan has crosslinked with STPP.
The morphology of the biomaterials was investigated by the dynamic light scattering technique and field emission scanning electron microscopy.
The obtained results showed that the particle size of the chitosan/extract biomaterials prepared by microemulsion method and solution method with STPP ranged from 68.
06 nm to 1484 nm, with an average particle size of 304.
9–1019 nm.
The microemulsion method produced biomaterials with much smaller average particle size than the solution method using cross-linkers.
The hemostatic ability of the biomaterials was better than that of the control sample based on the time of blood clotting formation and glomerular aggregation ability.
The sample with the ratio of E.
prostrata L.
extract: chitosan of 1:30 had the lowest hemostasis time (6 min 46 s) and its glomerular aggregation rate after 5 min was 13.
05%.
This indicated that the biomaterials based on chitosan and E.
prostrata L.
extract are promising for application in biomedicine as hemostatic materials.

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