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提高桦树皮提取物生物利用度的创新方法:与其他分散体系对比的新型油凝胶开发方法

Innovative Approach to Enhance Bioavailability of Birch Bark Extracts: Novel Method of Oleogel Development Contrasted with Other Dispersed Systems.

作者信息

Andze Laura, Vitolina Sanita, Berzins Rudolfs, Rizikovs Janis, Godina Daniela, Teresko Arturs, Grinberga Solveiga, Sevostjanovs Eduards, Cirule Helena, Liepinsh Edgars, Paze Aigars

机构信息

Latvian State Institute of Wood Chemistry, 27 Dzerbenes Street, LV-1006 Riga, Latvia.

ZS DOKTUS, 22 Pavila Street, LV-4101 Cesis, Latvia.

出版信息

Plants (Basel). 2024 Jan 4;13(1):145. doi: 10.3390/plants13010145.

Abstract

Birch outer bark extract (BBE), containing pentacyclic triterpenes such as betulin, lupeol, and betulinic acid, is a widely recognized natural product renowned for its diverse pharmacological effects. However, its limited water solubility restricts its bioavailability. Therefore, the main objective is to enhance the bioavailability of BBE for pharmaceutical use. In this study, we aimed to develop a dispersion system utilizing a unique oleogel-producing method through the recrystallization of BBE from an ethanol solution in the oil phase. We generated an oleogel that demonstrates a notable 42-80-fold improvement in betulin and lupeol peroral bioavailability from BBE in Wistar rats, respectively. A physical paste-like BBE hydrogel developed with antisolvent precipitation showed a 16-56-fold increase in the bioavailability of betulin and lupeol from BBE in rat blood plasma, respectively. We also observed that the repeated administration of the BBE oleogel did not exhibit any toxicity at the tested dose (38.5 mg/kg betulin, 5.2 mg/kg lupeol, 1.5 mg/kg betulinic acid daily for 7 days). Betulin and betulinic acid were not detected in rat heart, liver, kidney, or brain tissues after the peroral administration of the oleogel daily for 7 days. Lupeol was found in rat heart, liver, and kidney tissues.

摘要

桦树外树皮提取物(BBE)含有五环三萜类化合物,如桦木醇、羽扇豆醇和桦木酸,是一种因具有多种药理作用而被广泛认可的天然产物。然而,其有限的水溶性限制了其生物利用度。因此,主要目标是提高BBE在药物应用中的生物利用度。在本研究中,我们旨在通过从油相中的乙醇溶液中重结晶BBE,利用一种独特的油凝胶生产方法开发一种分散体系。我们制备了一种油凝胶,在Wistar大鼠中,该油凝胶使BBE中桦木醇和羽扇豆醇的口服生物利用度分别显著提高了42至80倍。通过反溶剂沉淀法制备的物理糊状BBE水凝胶,使大鼠血浆中BBE中桦木醇和羽扇豆醇的生物利用度分别提高了16至56倍。我们还观察到,重复给予BBE油凝胶在测试剂量(每天38.5毫克/千克桦木醇、5.2毫克/千克羽扇豆醇、1.5毫克/千克桦木酸,持续7天)下未表现出任何毒性。连续7天每天口服油凝胶后,在大鼠心脏、肝脏、肾脏或脑组织中未检测到桦木醇和桦木酸。在大鼠心脏、肝脏和肾脏组织中发现了羽扇豆醇。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d907/10780823/1fa1d2ed5016/plants-13-00145-g001.jpg

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