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pharmaceutical and veterinary compositions in micro and nanostructured forms and forming micro and nanostructures in the gastrointestinal tract containing benznidazole and its derivatives and their biological applications

机译:含有苯并硝唑及其衍生物的微和纳米结构形式的药物和兽医学组合物,以及在胃肠道中形成微和纳米结构的药物及其生物学应用

摘要

Pharmaceutical and veterinary compositions in micro and nanostructured forms and forming micro and nanostructures in the gastrointestinal tract containing benznidazole and its derivatives and their biological applications The present invention describes the methods of preparing micro and nanometric polymeric dosage forms by encapsulating benznidazole for parenteral and parenteral use. oral dosage forms that self-emulsify in contact with biological fluids, forming micro or nanoemulsions. include microcapsules, microspheres, microemulsions, nanocapsules, nanospheres, nanoemulsions, solid, semi-solid and liquid lipid nanoparticles, lipid core nanocapsules and self-emulsifying systems that form micro and nanoemulsions. Formulations to be patented include pharmaceutical forms having emulsified cell structure coated or not with benznidazole-containing polymers and / or one of nitroimidazole derivatives. The developed pharmaceutical compositions improve the dissolution profile of benznidazole, control drug release and promote increased plasma bioavailability, with consequent improvement in pharmacological activity.
机译:含有苯并硝唑及其衍生物的微和纳米结构形式的药物和兽医学组合物,以及在胃肠道中形成微和纳米结构的药物及其生物学应用本发明描述了通过包封苯并硝唑用于胃肠外和胃肠外用途制备微和纳米聚合物剂型的方法。口服剂型,在与生物液体接触时会自行乳化,形成微乳或纳米乳。包括微胶囊,微球,微乳剂,纳米胶囊,纳米球,纳米乳剂,固体,半固体和液体脂质纳米颗粒,脂质核心纳米胶囊和形成微乳和纳米乳剂的自乳化系统。待获得专利的制剂包括具有乳化细胞结构的药物形式,该药物结构的乳化细胞结构被含或不含苯并咪唑的聚合物和/或硝基咪唑衍生物之一包覆或未包覆。所开发的药物组合物改善了苯并咪唑的溶出度,控制了药物的释放并提高了血浆的生物利用度,从而改善了药理活性。

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