首页> 外国专利> ORAL DOSAGE FORM OF TETRAHYDROCANNABINOL AND A METHOD OF AVOIDING AND/OR SUPPRESSING HEPATIC FIRST PASS METABOLISM VIA TARGETED CHYLOMICRON/LIPOPROTEIN DELIVERY

ORAL DOSAGE FORM OF TETRAHYDROCANNABINOL AND A METHOD OF AVOIDING AND/OR SUPPRESSING HEPATIC FIRST PASS METABOLISM VIA TARGETED CHYLOMICRON/LIPOPROTEIN DELIVERY

机译:四氢大麻酚的口服剂量形式和靶向的氯霉素/脂蛋白的递送避免和/或抑制肝第一代谢的方法

摘要

An oral dosage form of cannabinoids and/or standardized marijuana extracts in a self-emulsifying system operable to avoid hepatic first pass metabolism via targeted chylomicron/lipoprotein delivery for promoting lymphatic transport. The oral dosage form includes: (a) a pharmacologically active form of cannabinoids and/or standardized marijuana extracts; and (b) an oily medium consisting of: (i) about 15 to 85 wt % of one or more triglycerides formed from long chain fatty having from C13 to C24 carbon atoms; (ii) about 15 to 85 wt % of one or more mixed glycerides formed from long chain fatty having from C13 to C24 carbon atoms; and (iii) one or more free fatty acids formed from un-esterified long chain fatty acids having from C13 to C24 carbon atoms; and (c) about 10 to 70 wt % of a surfactant which promotes self-emulsification.
机译:自乳化系统中的大麻素和/或标准化大麻提取物的口服剂型,可通过靶向乳糜微粒/脂蛋白输送来避免肝首过代谢,从而促进淋巴运输。口服剂型包括:(a)大麻素和/或标准化大麻提取物的药理活性形式; (b)由以下组成的油性介质:(i)约15至85 wt%的一种或多种由C 13 至C 24 的长链脂肪形成的甘油三酸酯碳原子(ii)约15至85 wt%的一种或多种由具有C 13 至C 24 个碳原子的长链脂肪形成的混合甘油酯; (iii)一种或多种由具有C 13 到C 24 个碳原子的未酯化的长链脂肪酸形成的游离脂肪酸; (c)约10至70重量%的促进自乳化的表面活性剂。

著录项

  • 公开/公告号US2014357708A1

    专利类型

  • 公开/公告日2014-12-04

    原文格式PDF

  • 申请/专利权人 MURTY PHARMACEUTICALS INC.;

    申请/专利号US201414454145

  • 发明设计人 RAM B. MURTY;SANTOS B. MURTY;

    申请日2014-08-07

  • 分类号A61K31/352;A61K47/12;A61K9/127;A61K47/14;A61K47/10;A61K47/44;A61K47/22;

  • 国家 US

  • 入库时间 2022-08-21 15:20:55

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