首页> 外国专利> PROCESSES FOR PRODUCING 6-0-PALMITOYL-3-0-BETA-P-D-GLUCOPYRANOS YL-CAMPESTEROL, EXTRACTS AND FRACTIONS, FROM THE WILD-TYPE PLANT AND IN VITRO CULTURES OF LOPEZIA RACEMES CAV., AND THE APPLICATION THEREOF AS ANTI-INFLAMMATORY AGENTS IN COSMETIC AND PHARMACEUTICAL COMPOSITIONS.

PROCESSES FOR PRODUCING 6-0-PALMITOYL-3-0-BETA-P-D-GLUCOPYRANOS YL-CAMPESTEROL, EXTRACTS AND FRACTIONS, FROM THE WILD-TYPE PLANT AND IN VITRO CULTURES OF LOPEZIA RACEMES CAV., AND THE APPLICATION THEREOF AS ANTI-INFLAMMATORY AGENTS IN COSMETIC AND PHARMACEUTICAL COMPOSITIONS.

机译:从野豌豆属植物的体外和体外培养物中提取6-0-棕榈基-3-0- [BETA] -PD-葡糖基内酯,提取物和馏分的方法及其在动物身上的应用化妆品和药物组合物中的炎症代理。

摘要

The invention relates to the method for producing the compound 6-0-palmitoyl-3-0-[beta]-P-D-glucopyranosyl-campesterol(6-O-PGC) with a novel structure and with in vivo anti-inflammatory activity, from plant extracts obtained from in vitro cultures and wild-type plants of Lopezia racemosa. The invention also relates to the method for producing extracts and fractions with anti-inflammatory activity, obtained from in vitro cultures and wild plants of Lopezia racemosa with different organic solvents, and to the use of said extracts as anti-inflammatory agents.; The invention further relates to the application of the extracts which contain, as active principle, 6-0-palmitoyl-3-0-[beta]-D-glucopyranosyl-campesterol (6-O-PGC), and extracts or fractions of Lopezia racemes, for the effective treatment of inflammatory disorders, in various pharmaceutical or cosmetic compositions formulated for the oral or topical administration thereof. Another aim of the invention is to use the biotechnologica l process in order to improve the yield of the anti-inflammatory active principles and to establish an alternative for obtaining plant material via the micropropagation of the plant Lopezia racemosa. This process includes the production of axenic seedlings by means of in vitro germination, and the direct and indirect induction of morphogenesis.
机译:本发明涉及一种由新颖的结构和具有体内抗炎活性的化合物6-0-棕榈酰基-3-0-β-PD-吡喃葡萄糖基-菜油甾醇(6-O-PGC)的制备方法。植物提取物,得自苦艾草的体外培养物和野生型植物。本发明还涉及生产具有抗炎活性的提取物和级分的方法,所述提取物和级分得自异种果木的体外培养物和野生植物,并具有不同的有机溶剂,并且涉及所述提取物作为抗炎剂的用途。本发明还涉及含有作为活性成分的6-0-棕榈酰基-3-0-β-D-吡喃葡萄糖基-菜油甾醇(6-O-PGC)的提取物,以及洛佩齐亚提取物或级分的应用。为了有效治疗炎性疾病的外消旋体,配制成用于口服或局部给药的各种药物或化妆品组合物。本发明的另一个目的是使用生物技术方法,以提高抗炎活性成分的产量,并建立一种通过对植物紫花苜蓿进行微繁殖而获得植物材料的替代方法。此过程包括通过体外萌发生产树莓种子,以及直接和间接诱导形态发生。

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