Application of vaccarin in preparation of drug for preventing angiosteosis
A technology of flavonoid glycosides and anti-vascular calcification, which is applied in drug combinations, cardiovascular system diseases, and pharmaceutical formulations, can solve problems such as accelerating the healing speed of open wounds, and achieve the effect of expanding options and improving vascular calcification
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Embodiment 1
[0010] The replication of embodiment 1 vascular calcification model
[0011] The production method of vascular calcification model rats: referring to authoritative journals at home and abroad, we used 8-week-old male SD rats for intramuscular injection of vitamin D3. Weeks later, intramuscular injection of vitamin DB 300,000 units / kg was given again, and extensive vascular calcification appeared in the rats after 4 weeks.
Embodiment 2
[0012] Example 2 Experimental Grouping and Vaccina flavonoid glycoside (VAC) intervention
[0013] The 8-week-old SD rats were randomly divided into three groups:
[0014] (1) Normal control-normal saline group: as the normal control group, normal diet and drinking water were given all the time, and after 2 weeks, normal saline was subcutaneously infused for 2 weeks as a control of vaccinia flavonoid glycosides (VAC);
[0015] (2) Vascular calcification group-normal saline group was treated with vitamin D3 combined with nicotine to induce vascular calcification, and 2 weeks later, normal saline (saline) was injected intraperitoneally for 2 weeks as a control of flavonoid glycoside (VAC) of wangbuliuxing;
[0016] (3) Vascular calcification-flavone glycoside group (10mg / kg): Vitamin D3 combined with nicotine was used to induce vascular calcification, and 2 weeks later, vaccinia flavone glycoside (VAC, 10mg / kg) was injected intraperitoneally for 2 weeks.
Embodiment 3
[0017] Example 3 von Kossa staining and Alizarin red S staining
[0018] Referring to authoritative literature at home and abroad, rats were anesthetized with pentobarbital sodium, the chest cavity was opened, the heart was exposed, the ascending aorta was intubated through the left ventricle, the wall of the abdominal aorta was clipped, a small outlet was cut from the left atrial appendage, and 0.01M PBS was rapidly perfused. (37° C.) rinse until the effluent is clear, and then perfuse with pre-cooled (4° C.) 4% paraformaldehyde for fixation (first fast and then slow, slow down after the rat’s limbs are stretched). The thoracic aorta was taken out, fixed in 4% paraformaldehyde at 4°C for 24 hours, dehydrated, embedded in paraffin, sectioned, and subjected to routine vonKossa staining and Alizarin red S staining.
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