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利用新型自乳化药物递送系统(SEDDS)VESIsorb 制剂技术提高健康受试者中β-石竹烯的口服生物利用度。

Enhanced Oral Bioavailability of β-Caryophyllene in Healthy Subjects Using the VESIsorb Formulation Technology, a Novel Self-Emulsifying Drug Delivery System (SEDDS).

机构信息

BioTeSys GmbH, Schelztorstraße 54-56, 73728 Esslingen, Germany.

Interlabor Belp AG, Aemmenmattstrasse. 16, 3123 Belp, Switzerland.

出版信息

Molecules. 2022 Apr 30;27(9):2860. doi: 10.3390/molecules27092860.

DOI:10.3390/molecules27092860
PMID:35566210
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9104399/
Abstract

β-Caryophyllene (BCP), a common constituent of many spice and food plants, is gaining increased attention due to recent research identifying numerous potential health benefits. Due to limited oral bioavailability observed in preclinical models, the described benefits of BCP may be maximized by using a suitable delivery system. Additionally, human pharmacokinetics (PK) remain unknown. This study evaluates the relative oral bioavailability of BCP formulated in a self-emulsifying drug delivery system (SEDDS) based on VESIsorb formulation technology (BCP-SEDDS) compared to BCP neat oil. Hence, a randomized, double-blind, cross-over design, single oral dose study (100 mg BCP) in 24 healthy subjects (12 men/12 women) was performed under fasting conditions. Pharmacokinetic parameters were analyzed from individual concentration-time curves. The data show that BCP-SEDDS resulted in a 2.2/2.0-fold increase in AUC/AUC and a 3.6-fold increase in C compared to BCP neat oil. Moreover, BCP was absorbed faster from BCP-SEDDS (T: 1.43 h) compared to BCP neat oil (T: 3.07 h). Gender analysis revealed that there is no significant difference between men and women for both the investigated formulations and all investigated PK endpoints. In conclusion, BCP-SEDDS offers a well-tolerated and effective oral delivery system to significantly enhance the oral bioavailability of BCP in humans.

摘要

β-石竹烯(BCP)是许多香料和食用植物的常见成分,由于最近的研究确定了许多潜在的健康益处,因此越来越受到关注。由于在临床前模型中观察到有限的口服生物利用度,因此通过使用合适的递送系统可以最大程度地发挥 BCP 的描述益处。此外,人类药代动力学(PK)仍然未知。本研究评估了基于 VESIsorb 制剂技术的自乳化药物递送系统(SEDDS)中配制的 BCP(BCP-SEDDS)与 BCP 纯油相比的相对口服生物利用度。因此,在禁食条件下,对 24 名健康受试者(12 名男性/12 名女性)进行了一项随机、双盲、交叉设计、单次口服剂量研究(100mg BCP)。从个体浓度-时间曲线分析药代动力学参数。数据表明,与 BCP 纯油相比,BCP-SEDDS 使 AUC/AUC 增加了 2.2/2.0 倍,C 增加了 3.6 倍。此外,与 BCP 纯油(T:3.07h)相比,BCP-SEDDS 中 BCP 的吸收更快(T:1.43h)。性别分析表明,对于两种研究制剂和所有研究的 PK 终点,男性和女性之间没有显着差异。总之,BCP-SEDDS 提供了一种耐受良好且有效的口服递送系统,可显着提高人类 BCP 的口服生物利用度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/738e/9104399/1f057cd09420/molecules-27-02860-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/738e/9104399/227835cf695b/molecules-27-02860-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/738e/9104399/1366174ba033/molecules-27-02860-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/738e/9104399/1f057cd09420/molecules-27-02860-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/738e/9104399/227835cf695b/molecules-27-02860-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/738e/9104399/1366174ba033/molecules-27-02860-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/738e/9104399/1f057cd09420/molecules-27-02860-g003.jpg

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