Medicinal composition with hemostatic function
A pharmaceutical composition and functional technology, applied in the field of pharmaceutical compositions with hemostatic function, can solve the problems of unstable conditions, life-threatening, vascular obstruction and the like, and achieve the effect of reducing the amount of bleeding
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Embodiment 1
[0034] Methods of microparticle formation without fibrinogen:
[0035] Put human albumin powder into 0.9% sodium chloride solution, and add a surfactant with a concentration of 0.05mg / ml-15mg / ml, such as tetradecyl sodium sulfate, Tween-80 or TritonX-151, to form a concentration Protein solution at 5-20% w / v. 2 ml of glutaraldehyde diluted in sodium chloride solution ranging from 0.01 to 3.0% was then added to a series of test tubes containing 2 ml of the above protein solution containing different concentrations of surfactant. After 10 minutes, add 10ml of ethanol [dilute to 80% (volume ratio) with water], and the solution will appear cloudy immediately. After another 10 minutes, dilute with 5 times the volume of sodium chloride solution to observe whether the suspension is clear, and the result is negative. Thereafter, the suspension was observed under a microscope at 1000 times, and it was found that the diameter of the particles in the suspension was less than 1 micron. ...
Embodiment 2
[0038] The method of linking fibrinogen to protein particles as tracer particles:
[0039] Using the same conditions as in Example 1, human albumin with a marker of 1-125 was used. The spheres were pelleted by centrifugation, and the number of radioactive protein particles contained in the pellet and the supernatant were measured, and it was found that 95% of the albumin particles formed spheres. If the solute of the solution is raised 2 times by the concentration of 0.9% sodium chloride solution, it becomes 1.8% sodium chloride solution or the 0.9% sodium chloride solution is reduced to 0.09% sodium chloride solution. The yield of spheroids was not greatly affected. If the pH of the buffer solution was lowered below 4, it was found that more alcohol was required for the formation of spheres than at pH 8, and pH below 4 slightly reduced the yield of spheres. decline.
Embodiment 3
[0041] Example 2 was repeated under the most preferred conditions, except that human albumin was coated with fluorescent isothiocyanate, and the optimal conditions of Example 1 were used, and the fibrinogen Added to the spheroid suspension, it was found that adding fibrinogen within fifteen minutes of spheroid formation stabilized the spheroids and gave the best mix. In addition, the sphere suspension must be further processed, including dilution, filtration, dialysis, re-filtration, centrifugation, electrophoresis separation, and column separation, which are completed after vacuum freeze-drying and reconstitution of frozen powder, among which Add or change buffers or preservatives during the process.
[0042] According to McGill et al.'s "Platelet cavity can reduce the bleeding time of platelet-deficient rabbits" on J.Lab.Clin.Med.1987,109:127-133, using platelet-deficient rabbits for pharmacological tests, 70mg The bleeding time of ten rabbits treated by the Busulfan method...
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