首页> 外文期刊>American Journal of Translational Research >Dietary fats and pharmaceutical lipid excipients increase systemic exposure to orally administered cannabis and cannabis-based medicines
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Dietary fats and pharmaceutical lipid excipients increase systemic exposure to orally administered cannabis and cannabis-based medicines

机译:膳食脂肪和药用脂质赋形剂增加了口服大麻和基于大麻的药物的全身暴露

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There has been an escalating interest in the medicinal use of Cannabis sativa in recent years. Cannabis is often administered orally with fat-containing foods, or in lipid-based pharmaceutical preparations. However, the impact of lipids on the exposure of patients to cannabis components has not been explored. Therefore, the aim of this study is to elucidate the effect of oral co-administration of lipids on the exposure to two main active cannabinoids, Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD). In this study, oral co-administration of lipids enhanced the systemic exposure of rats to THC and CBD by 2.5-fold and 3-fold, respectively, compared to lipid-free formulations. In vitro lipolysis was conducted to explore the effect of lipids on the intestinal solubilisation of cannabinoids. More than 30% of THC and CBD were distributed into micellar fraction following lipolysis, suggesting that at least one-third of the administered dose will be available for absorption following co-administration with lipids. Both cannabinoids showed very high affinity for artificial CM-like particles, as well as for rat and human CM, suggesting high potential for intestinal lymphatic transport. Moreover, comparable affinity of cannabinoids for rat and human CM suggests that similar increased exposure effects may be expected in humans. In conclusion, co-administration of dietary lipids or pharmaceutical lipid excipients has the potential to substantially increase the exposure to orally administered cannabis and cannabis-based medicines. The increase in patient exposure to cannabinoids is of high clinical importance as it could affect the therapeutic effect, but also toxicity, of orally administered cannabis or cannabis-based medicines.
机译:近年来,人们对药用大麻的使用越来越感兴趣。大麻通常与含脂肪的食物一起口服,或以脂质为基础的药物制剂中使用。但是,尚未探讨脂质对患者接触大麻成分的影响。因此,本研究的目的是阐明口服脂质共同给药对两种主要活性大麻素(Δ9-四氢大麻酚(THC)和大麻二酚(CBD))的暴露作用。在这项研究中,与不含脂质的制剂相比,口服脂质的共同给药分别使大鼠对THC和CBD的全身暴露分别增加了2.5倍和3倍。进行体外脂解以研究脂质对大麻素在肠道中的增溶作用。脂质分解后,超过30%的THC和CBD被分配到胶束级分中,这表明与脂质共同给药后,至少有三分之一的给药剂量可用于吸收。两种大麻素对人造CM样颗粒以及大鼠和人CM均显示出极高的亲和力,表明肠道淋巴运输的潜力很高。此外,大麻素对大鼠和人CM的可比亲和力表明,预期在人类中会有类似的增加的暴露效应。总之,饮食脂质或药物脂质赋形剂的共同给药可能会大大增加口服大麻和基于大麻的药物的暴露量。增加患者对大麻素的接触具有重要的临床意义,因为它可能影响口服大麻或基于大麻的药物的治疗效果,但也会影响其毒性。

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