Medicine composition for preventing or curing degenerative disease caused by oxidative stress
A technology for degenerative diseases and oxidative stress, applied in the direction of drug combination, active ingredients of fluorine compounds, active ingredients of iodine compounds, etc., can solve the problems of metabolism in vitro, easy disappearance of antioxidant activity, and inability to fully exert the effect of eliminating free radicals , to achieve the effect of high safety and few side effects
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[0089] In the preparation of the pharmaceutical compositions, preparations and medicaments of the present invention, pharmaceutical adjuvants and / or carriers (excipients) may be used. For example, coloring agents, sweeteners, flavoring agents, binders, adsorbents, lubricants, disintegrants, softeners, suspending agents, emulsifiers, surfactants, stabilizers, pH regulators, dispersants, etc. can be used Osmotic agents, humectants, dissolving agents, solubilizers, and / or absorption enhancers are used as pharmaceutical adjuvants. These different forms can be prepared by conventional methods under sterile conditions.
[0090] In addition, in the administration form, according to the conditions of use, a functional coating such as an enteric coating may be further provided. In the case of administration in solid form, enteric coatings and shells can be used to complete the preparation. Additionally, such administration forms are capable of releasing the drug to certain parts of t...
Embodiment 1
[0125] Example 1: Injection solution
[0126] A mixture of hydroxylated antioxidant groups* with a hydroxylation rate of 86% (by mole conversion) and hydroxylated bioelement groups** with a hydroxylation rate of 87% (by mole conversion) at a weight ratio of 2:8. , after being completely dissolved in 1000cc of Ringer's solution for medicine at a concentration of 5 ppm, the sterile filter was used for the manufacture of injections to perform sterile filtration to prepare an injection solution as the cell optimizer for intravenous injection of the present invention.
[0127] * Hydroxylated Antioxidant Groups: Superoxide Dismutase (SOD), Catalase (CAT), Glutathione Peroxidase (GSH-Px), Glutathione, Melatonin, Fertility Trienols, Alpha Lipoic Acid
[0128] ** Hydroxylated bioelement groups: Bioelements (macro / trace elements)
Embodiment 2
[0129] Example 2: Powder for oral administration
[0130] A mixture of hydroxylated antioxidant groups* with a hydroxylation rate of 86% (mole conversion) and hydroxylated bioelement groups** with a hydroxylation rate of 87% (mole conversion) at a weight ratio of 2:8 , a cell-optimized complex formed by mixing 95% by weight and 5% by weight of dibenzofluoranthene (C20H10), diluted in mannitol at a concentration of 1% by weight, to prepare the following degenerative diseases Oral powder for prevention and treatment, including but not limited to myocardial infarction, ischemic heart disease, heart failure, angina pectoris, arrhythmia, arteriosclerosis, hepatic lipid metabolism disorder, hyperlipidemia, hypertension , arteriosclerosis, coronary arteriosclerosis, thrombosis, arteriosclerosis obliterans, vascular disease, peripheral vascular disease, cholestasis, hypercholesterolemia, limb injury, internal organ failure, acute and chronic hepatitis, stomach stains , duodenal ulce...
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