49 results about "Oral hypoglycemic agents" patented technology

The present invention provides a therapeutic agent for treatment of diabetes and hyperlipemia, especially a therapeutic agent for treatment of type II diabetes mellitus, which comprises as the active ingredient a neurotrophic factor such as BDNF (brain-derived neurotrophic factor), ligands of trkB or trkC receptors, NGF, NT-3, NT-4/5, CNTF, GDNF, HGF, etc. Different from conventional oral hypoglycemic agents being mainly used in the treatment of type II diabetes mellitus, the agent of the present invention exhibit blood lipid regulating effects and body fat accumulation regulating effects, in addition to the blood glucose regulating effects. Thus, the agent of the present invention are novel, and can reduce the risk factors in diabetes accompanied by hyperlipemia or obesity, without using any other agent.

Control of blood glucose is a fundamental goal in the treatment of diabetes mellitus. Glycation of l-lysine can lower blood glucose and advanced glycation end product (AGE) free adducts can be excreted in the urine. Lysine, an inexpensive amino acid, can be administered orally or parentally, and can be incorporated into a stereocomplex matrix as a time released preparation. In patients who suffer from diabetes and concomitant renal insufficiency who cannot clear sufficient quantities of AGE free adducts enantiomeric mixtures of lysine will lower blood glucose and AGEs since d-lysine has been shown to decrease protein glycation and lower hemoglobin Alc. This invention is not intended to replace insulin or oral hypoglycemic agents but is does offer patients a low cost and probably safe complementary therapy for the treatment of diabetes mellitus. In addition to the treatment of diabetes and its complications, this invention could lower AGE burden and slow or ameliorate some of the consequences of aging.

The Present invention relates to a process for the preparation of (RS) 3-methyl-1-(2-piperidinyl phenyl) butyl amine of formula 1. (RS) 3-Methyl-1-(2-piperidinyl phenyl butyl amine having formula 1 is an important key intermediate for the synthesis of repaglinide of formula 2 an oral hypoglycemic agent.

The present invention discloses a composition preparation for preventing and treating diabetes, which mainly contains oral hypoglycemic agents, Vitamin E, chromic pyridine formate, selenium, lutein, folic acid, Vitamin C, alpha_lipoic acid, lycopene, nicotinamide, coenzyme Q10, and vitamin complexes and mineral. The medicament of the invention can decrease oxidative stress in vivo, promote body immunity, repair the critical organs in vivo such as pancreas, by supplying the mineral, vitamins and other substances which are insufficient in the patient suffering from diabetes, to prevent and treat diabetes.

It is intended to provide a pyrimidyl indoline compound which structurally differs from compounds used as active ingredients in conventional oral hypoglycemic agents and has excellent hypoglycemic effect. The present invention provides a compound represented by the general formula (I) or a pharmaceutically acceptable salt thereof:

The invention relates to composite dietary fiber which is mainly prepared from 20-93 parts of dietary fiber, 10-30 parts of L-arabinose, 5-20 parts of isomaltulose, 1-5 parts of root of kudzu vine and 1-5 parts of folium mori in parts by weight. The composite dietary fiber has the beneficial effects that the composite dietary fiber is obvious in effect of controlling rise of postprandial blood sugar, improving sugar tolerance and other aspects; the composite dietary fiber, when being used, not only can be independently taken but also can be combined with other oral hypoglycemic drugs or insulin, and can take an excellent mutual promoting effect. The composite dietary fiber is simultaneously applicable to six groups: people of diabetes and instable postprandial blood sugar, people of cardiovascular and cerebrovascular diseases, people at risk of colitis, people of constipation, people of obesity, women, etc.

A method of treating Type II diabetes utilizing two off-the-shelf drugs.

Intravenous injection of one or both drugs, individually and in combination, can prevent and treat diabetes, restore damaged islet cell functions and reduce or stop the use of oral hypoglycemic agents and insulin.

The invention relates to the technical field of blood-sugar reducing healthcare products. The purpose of the invention is to provide a healthcare soft capsule with assistant blood-sugar reducing effect and a preparation method thereof, in order to solve the problems of drug dependence and occurrence of various complications caused by western-medicine control of diabetes treatment as well as side effects of oral blood-sugar reducing drugs which are commonly used in clinical treatment of diabetes. The healthcare soft capsule with assistant blood-sugar reducing effect is prepared from the following raw materials according to proportion: linseed oil, fagopyrum tataricum extract, American ginseng extract, chromium picolinate, beeswax, gelatin, glycerin, purified water, titanium dioxide, caramel color and so on. The preparation method comprises the following steps: preparing material solution of the soft capsule core, preparing glue solution of the soft capsule skin, preparing the soft capsules, shaping and drying the soft capsules, washing and drying the shaped soft capsules and selecting the prepared soft capsules, so that the healthcare soft capsules with assistant blood-sugar reducing effect are obtained. The healthcare soft capsule has scientific and rational production technology as well as stable and controllable quality, so that a safe, effective and reliable healthcare food is provided for the consumers. The healthcare soft capsule plays an important role in health care of Chinese residents, and has relatively high scientific values. Animal function and human trial tests have proven that the healthcare soft capsule has obvious assistant blood-sugar reducing effect.

The invention discloses a Chinese medical preparation assisting to adjusting blood sugar, relating to the field of traditional Chinese medicines. The medical preparation assisting to adjusting blood sugar is prepared from the following Chinese medical raw materials in percentage by weight: 1g of sealwort, 0.5-1.5g of polygonatum, 0.5-1.5g of salvia miltiorrhiza, 0.5-1.5g of radix astragali and 0.5-1.5g of fruit of glossy privet. Based on experiences for many years, the five Chinese medical herbs are proportionally prepared to effectively assist in adjusting the blood sugar of a patient, not only can the dosage of western medicines be reduced, but also complications caused by the microcirculatory disturbance of the patient can be improved. Proved by more than 30 clinical tests, the dosage of oral antidiabetic drugs in more than 80 percent of cases can be reduced by approximate one third to two thirds without toxic or side effect. The five Chinese medical herbs belong to pharmaceutical/food resources disclosed by the ministry of health, have reasonable prescription and low cost and are suitable for patients suffering from diabetes to use for a long time.

The present invention relates to a natural medicine composition for preparing medicine capable of curing diabetes. Said medicine composition is formed from ganoderma and ang-kak according to a certain ratio. Said composition can be used as oral sugar-reducing medicine and food additive of health-care food, and can made into various oral dosage forms.

The invention discloses a compound guava preparation and a manufacturing method thereof. The preparation is made from guava leaves, twigs of euonymus alatus, ficus hirta, mulberry leaves, kudzuvine roots, rhizoma coptidis, rhizoma atractylodis, rhizoma alismatis, hawthorn fruits and hongqu. The preparation has the efficacy of fortifying the spleen and resolving phlegm, reducing blood glucose and fat, and discharging the turbid and clearing heat, has an obvious effect on reduction of blood glucose, and can improve insulin resistance. In a clinical observation process, and in a compound guava preparation group, only three patients feel slight stomach discomfort and can self-relieve the discomfort without special treatment, and other patients have no untoward reaction. Therefore, the compound guava preparation is an efficient safe orally-administrated blood-glucose reducing medicine. The preparation is simple in formula and manufacturing method, convenient to consume, and suitable for industrial production and can be consumed for a long time.

A Chinese medicine for preventing and treating diabetes and its complications, and preventing arteriosclerosis and thrombosis is prepared from 6 Chinese-medicinal materials including mulberry leaf, gingko leaf, mulberry fruit, notoginseng, etc.

The invention discloses a market research method used for oral hypoglycemic agents. The method comprises the following steps that 1, a correlation information table of oral hypoglycemic agents on themarket is made; 2, sewage samples in a sewage treatment plant are collected, and refrigeration storage or heat preservation storage treatment is conducted on the sewage samples; 3, the collected sewage samples are subjected to separation and purification treatment, wherein by means of solid phase extraction, the sewage samples are subjected to separation and purification treatment; 4, different derivatization reagents are adopted for conducting derivatization reaction treatment on the sewage samples; 5, the sewage samples treated in the step 4 are subjected to samples analysis, liquid chromatography-mass spectrometry or gas chromatgraphy mass spectrometrometry is used for conducting qualitative and quantitative analysis, and then a consumption number per person, consumer group numbers, theprevalence rates and market shares of the oral hypoglycemic agents in the sewage samples are estimated; 6, data information obtained in the step 5 is analyzed, correlation parameters of the oral hypoglycemic agents are sorted out, and a market research report is drawn.

The invention discloses a prescribed tea for regulating hyperglycemia and a preparation method thereof, which comprises the following steps: the main raw materials and parts by weight of the prescribed tea for regulating hyperglycemia are respectively rhizoma polygonati 3-5 parts, dandelion portions 2-4 parts, black tea 1-2 parts, green tea 1-2 parts, medlar 2-3, hawthorn 2-3 parts, thistle 1-2, cassia seed 1-2 parts, yam 2-3 parts, tuckahoe 1-3 parts, and mint 1 part. The main raw materials and parts by weight of the prescribed tea are: 5 parts of Huang Jing, 4 parts of dandelion, 2 parts ofblack tea, 2 parts of green tea, and 3 parts of medlar, and 3 parts of hawthorn. The raw material of the invention is pure natural, has no additives, is a natural green health tea, the selected raw materials are all from the medicine and food homologous raw material catalogue approved by the State Health Planning Commission, which has high safety and will not produce toxic and side effects on human body, and solves the problem that the conventional drugs for treating diabetes, mainly oral hypoglycemic agents and insulin, have toxic and side effects to different degrees, and bring new diseasesand pains to diabetic patients.

The present application relates to pharmaceutical compositions for reducing glucose excursions in a normal subject or a subject having an insulin-related disorder or dysglycemia. The pharmaceutical composition contains one or more active agent-containing layers, which each contain a dry blended mixture including a therapeutically effective amount of a polar ionizable insulin-sensitizing oral hypoglycemic agent or a pharmaceutically acceptable salt thereof, and an amphipathic compound in monomelic form consisting of an amphipathic ionic compound in monomelic form. Each dry blended mixture contains a sufficient amount of the amphipathic ionic compound such that upon contact with an aqueous fluid, the amphipathic ionic compound forms a reverse micelle comprising the polar ionizable insulin-sensitizing oral hypoglycemic agent. The present invention also relates to a use of a modified release pharmaceutical composition comprising a therapeutically effective amount of an insulin-sensitizing oral hypoglycemic agent for sensitizing pre-prandial (basal) insulin levels and/or reducing postprandial glucose excursions in a normal patient or a patient having an insulin-related disorder.