Processing method capable of sufficiently maintaining activity of cartialgenous
A processing method and technology of velvet antler, applied in the field of processing that can fully maintain the activity of fresh velvet velvet, can solve the problems of loss of active ingredients, easy deterioration in storage, difficult transportation of velvet antler, etc., and achieve the effect of increasing activity and reducing dosage
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0022] Take the freshly cut velvet antler, cut it into pieces quickly before the blood in the velvet velvet coagulates, put it in a colloid mill and pulverize it to a powder with a particle size below 0.01mm, and then add it to a tube centrifuge and centrifuge at a high speed of 10,000 rpm After 20 minutes, discard the precipitate, take the supernatant and freeze-dry. The freeze-drying conditions are: the freeze-drying pressure is 26.6Pa, the thickness of the material layer is 18-20mm, and the temperature is -40°C. into capsules. The SOD activity measurement result was 1290U / g.
Embodiment 2
[0024] Take the freshly cut velvet antler, cut it into pieces quickly before the blood in the velvet antler coagulates, put it in a colloid mill and crush it to a powder with a particle size below 0.01mm, and then add it to a tube centrifuge and centrifuge at a high speed of 5000 rpm After 30 minutes, discard the precipitate, take the supernatant and freeze-dry. The freeze-drying conditions are: the freeze-drying pressure is 26.6Pa, the thickness of the material layer is 18-20mm, and the temperature is -40°C. After freeze-drying, a light brown powder is obtained, which is directly pressed piece. The SOD activity measurement result was 1220U / g.
Embodiment 3
[0026] Take the freshly cut velvet antler, cut it into pieces quickly before the blood in the velvet velvet coagulates, put it in a colloid mill and pulverize it to a powder with a particle size below 0.01mm, and then add it to a tube centrifuge and centrifuge at a high speed of 10,000 rpm After 10 minutes, the precipitate was discarded, and the supernatant was taken for freeze-drying. The freeze-drying conditions were as follows: the pressure of the freeze-drying chamber was 26.6 Pa, the thickness of the material layer was 18-20 mm, and the freeze-drying temperature was -40°C. After freeze-drying, a light brown powder is obtained, which can be made into granules by adding auxiliary materials. The SOD activity assay result was 1260U / g.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 