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METHOD AND PHARMACEUTICAL COMPOSITIONS FOR TREATMENT OF POST-PRANDRANDIAL HYPERGLYCEMIA TYPE II DIABETES BY INTRODUCTION THROUGH THE MURAL ORAL CAVITY

机译:通过口腔内腔导入治疗餐后血糖过高的II型糖尿病的方法和药物组合物

摘要

1. A pharmaceutical composition, characterized in that it has the form of an aqueous-alcoholic solution in which at least one hypoglycemic / insulinotropic active substance is stably and completely dissolved in a dosage reduced by at least 30-50% compared to a conventional a single dose for oral administration, for its use by administration through the mucous membrane of the oral cavity as a medicine in the precise treatment of postprandial hyperglycemia of type II diabetes in humans or animals. 2. The pharmaceutical composition according to claim 1, wherein the strength is at least 30 °. The pharmaceutical composition according to claim 1 or 2, which is based on water and ethanol. The pharmaceutical composition according to claim 1 or 2, wherein the hypoglycemic active ingredient is present in base form and / or in salt form. The pharmaceutical composition according to claim 1 or 2, which has the form of an aqueous-alcoholic solution with a volume of less than 2 ml, in which an amount less than or equal to 250 mg of at least one hypoglycemic active substance is stably and completely dissolved. The pharmaceutical composition according to claim 1 or 2, in which the hypoglycemic active ingredient in a dosage reduced by 30-50% compared with the usual single dose when administered orally, is selected from among lipophilic or amphiphilic active substances, such as glycazide, metformin, glibenclamide, clayey and incretins. 7. The pharmaceutical composition according to claim 1 or 2, which further comprises a pH adjusting agent. The pharmaceutical composition according to claim 7, in which the pH-adjusting substance is selected from among carbonates and bicarbonates
机译:1.一种药物组合物,其特征在于它具有水-醇溶液的形式,其中与常规药物相比,至少一种降血糖/促胰岛素活性物质稳定和完全溶解,其剂量减少了至少30-50%。单次口服给药,通过口腔粘膜给药,可作为药物精确治疗人或动物的II型糖尿病餐后高血糖。 2.根据权利要求1所述的药物组合物,其中所述强度为至少30°。 3.根据权利要求1或2的药物组合物,其基于水和乙醇。 3.根据权利要求1或2所述的药物组合物,其中所述降血糖活性成分以碱形式和/或盐形式存在。 3.根据权利要求1或2所述的药物组合物,其为体积小于2ml的醇水溶液的形式,其中,稳定地形成小于或等于250mg的至少一种降血糖活性物质。完全溶解。 3.根据权利要求1或2所述的药物组合物,其中,与口服时相比通常的单次剂量降低30-50%的降血糖活性成分选自亲脂性或两亲性活性物质,例如,叠氮化物,二甲双胍。 ,格列本脲,黏土和肠降血糖素。 7.根据权利要求1或2的药物组合物,其还包含pH调节剂。 8.根据权利要求7所述的药物组合物,其中所述pH调节物质选自碳酸盐和碳酸氢盐。

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