Sustained-release therapeutic agent for hypertension and renal dysfunction
A kidney function and slow-release technology, applied in the direction of organic active ingredients, cardiovascular system diseases, skin care preparations, etc., can solve problems such as ignorance, and achieve a strong therapeutic effect
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Embodiment 1
[0062] The effects of immediate-release and sustained-release administration of febuxostat in a model of naturally occurring hypertension were confirmed.
[0063] A 12-week-old male SHR (Spontaneously Hypertensive Rat: spontaneously hypertensive rat) was used as a sample after being quarantined for more than 1 week. From the age of 13 weeks, blood pressure measurement was carried out by Tail-Cuff sphygmomanometer (BP-2000, Visitech systems, Napa Place, NC, USA) for 2 weeks. After the adaptation, the blood pressure was measured at the age of 15 weeks, and the samples were divided into 3 groups (10 rats in each group) so that there was no deviation in the systolic blood pressure, and then the administration was started. The control group of the first group was given tap water. Febuxostat was given to the drinking water of group 2. Febuxostat was administered orally compulsorily to Group 3.
[0064] Drinking water administration was performed by allowing them to freely drink a...
Embodiment 2
[0069] The effects of immediate-release and sustained-release administration of febuxostat in adriamycin-induced nephropathy mouse models were confirmed. The doxorubicin-induced nephropathy model is known as a renal insufficiency model in which glomerular epithelial cells are damaged and proteinuria is exhibited.
[0070] Seven-week-old male BALB / cAnNCrlCrlj mice were quarantined for more than one week and used as specimens.
[0071] Urine storage was carried out for 24 hours at the age of 8 weeks, and the amount of albumin in the urine obtained from the storage was measured by the ELISA method. After the samples were divided into three groups so that there was no variation in the amount of urinary albumin excretion, the administration was started. The control group of the first group was given tap water. Febuxostat was given to the drinking water of group 2. Febuxostat was administered orally compulsorily to Group 3.
[0072] Drinking water administration was performed by...
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