Tissue sealant in which collagen and fibrin are mixed, and method for preparing same
A fibrin and fibrinogen technology, applied in peptide/protein components, medical preparations containing active ingredients, pharmaceutical formulations, etc., can solve the problems of lack of physical properties and high biodegradation rate of fibrin glue, and improve the quality and reliability, high viability, good growth rate effect
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Embodiment 1
[0061] Comparison of physical properties between the present invention and prior art
[0062] In order to verify the physical properties of the present invention, the maximum stress, gel strength and tensile strength were measured using a physical property meter.
[0063] 1. Sample preparation
[0064] 1) In the prior art, Greenplast products are used.
[0065] 2) For the components of the present invention, Greenplast's dried fibrinogen and thrombin were dissolved in aprotinin solution and added calcium solution, respectively. Here, a thrombin solution is mixed with a 3% collagen solution. The resulting solution was loaded into a two-way syringe.
[0066] 3) For the measurement of physical properties, each sample was put into a cylindrical mold (Φ12X 15mm) to make a shape.
[0067] 2. Measurement of physical properties
[0068] 1) Physical property instrument: Rheometer (CR-500DX, Sun scientific rheometer)
[0069] 2) Test items: maximum stress (N), gel strength (g-cm),...
Embodiment 2
[0075] Comparison of degradability (long term / short term) between products of the invention and prior art
[0076] In order to verify the degradability of the compositions of the invention, fibrin glue products and materials were tested for degradability for a predetermined period of time.
[0077] 1. Degradability (short term)
[0078] 1) Sample preparation
[0079] - In the prior art, Greenplast products are used.
[0080] - For the composition of the invention, Greenplast's dried fibrinogen and thrombin were dissolved in aprotinin and added calcium solution, respectively. Here, a thrombin solution is mixed with a 3% collagen solution. The resulting solution was loaded into a two-way syringe.
[0081] - For the measurement of physical properties, each sample was put into a cylindrical mold (Φ8X 5mm) to make a shape.
[0082] 2) Processing conditions for degradability verification
[0083] - Confirm both conditions for the solvent. The condition of using only DEME medi...
Embodiment 3
[0097] Electron Microscopy Analysis of the Invention
[0098] Observation of the structure of the composition of the present invention by electron microscopy
[0099] 1. Sample preparation
[0100] - For the preparation of the composition, a fibrinogen solution of Greenplast and a thrombin solution / calcium solution containing collagen are prepared. The concentration of the collagen solution was 3% (weight / volume).
[0101] - For electron microscopy, each prepared solution was applied to a two-way syringe for distribution on trays.
[0102] 2. Method
[0103] - The composition of the invention is critically dried and then observed with an electron microscope.
[0104] -Critical point drying of the composition was performed by treating ethanol in a critical point dryer (Hitachi, HCP-2).
[0105] - The sample for electron microscope observation was cut and gold plated, followed by observation with SEM (Hitachi, S3500).
[0106] - Electron microscopy analysis was performed a...
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