Fabrication and Optimization of Directly Compressible Self-Emulsifying Tablets Containing Cannabis Extract Obtained from Supercritical Carbon Dioxide Extraction

Chaowalit Monton, Natawat Chankana, Sureewan Duangjit, Jirapornchai Suksaeree, Ornchuma Naksuriya, L. Charoenchai, T. Songsak
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Abstract

Δ9-Tetrahydrocannabinol and cannabidiol, which are present in cannabis extract, exhibit low bioavailability when administered orally due to significant first-pass metabolism. The use of a self-emulsifying drug delivery system (SEDDS) can enhance their dissolution and bioavailability. However, liquid SEDDS formulations are prone to inadequate stability. To address this issue, the development of a solid SEDDS formulation was explored. This study aimed to optimize directly compressible self-emulsifying tablets containing cannabis extract obtained from supercritical carbon dioxide extraction. Initially, a liquid SEDDS of cannabis extract was solidified by adsorption onto solid carriers (colloidal silicon dioxide and microcrystalline cellulose). The resulting solid mixture was then combined with other pharmaceutical excipients and compressed into tablets. Three factors were optimized using the Box-Behnken design: compressional force (1,000–2,000 psi), quantity of hydroxypropyl methylcellulose (0–6%), and quantity of croscarmellose sodium (0–6%). The results revealed that a mass ratio of colloidal silicon dioxide, microcrystalline cellulose, and liquid SEDDS of cannabis extract at 0.65:2:1 successfully solidified the mixture. The optimal tablet formulation was achieved with a compressional force of 2,000 psi, without the addition of hydroxypropyl methylcellulose or croscarmellose sodium. Verification data indicated that the predictions made by the computer software were accurate and reliable. The developed tablets exhibited improved dissolution of the cannabis extract, with Δ9-tetrahydrocannabinol demonstrating higher dissolution compared to cannabidiol. Additionally, the compressed tablets were capable of emulsifying small nano-sized droplets (approximately 200 nm). However, the droplets exhibited a larger size and broader polydispersity index compared to the liquid SEDDS. In conclusion, the study successfully developed directly compressible self-emulsifying tablets that enhanced the dissolution of cannabis extract.
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超临界二氧化碳萃取大麻提取物直接可压缩自乳化片的制备与优化
Δ9-Tetrahydrocannabinol和大麻二酚,存在于大麻提取物中,由于显著的首过代谢,口服给药时表现出低生物利用度。使用自乳化给药系统(SEDDS)可以提高其溶出度和生物利用度。然而,液体SEDDS制剂容易存在稳定性不足的问题。为了解决这一问题,研究了固体SEDDS配方的开发。本研究旨在优化超临界二氧化碳萃取大麻提取物的直接可压缩自乳化片。最初,大麻提取物的液体SEDDS通过吸附在固体载体(胶体二氧化硅和微晶纤维素)上固化。然后将得到的固体混合物与其他药物赋形剂混合并压缩成片剂。使用Box-Behnken设计对三个因素进行了优化:压缩力(1,000-2,000 psi)、羟丙基甲基纤维素(0-6%)的量和交叉纤维素钠(0-6%)的量。结果表明,胶体二氧化硅、微晶纤维素和大麻提取物液体SEDDS的质量比为0.65:2:1,可以成功固化混合物。在不添加羟丙基甲基纤维素或交联纤维素钠的情况下,以2,000 psi的压缩力获得最佳片剂配方。验证数据表明,计算机软件预测准确可靠。开发的片剂表现出改善的大麻提取物的溶解,与Δ9-tetrahydrocannabinol相比,大麻二酚显示出更高的溶解。此外,压缩片剂能够乳化小纳米液滴(约200nm)。然而,与液态SEDDS相比,液滴表现出更大的尺寸和更广泛的多分散性指数。综上所述,本研究成功开发了可直接压缩的自乳化片,提高了大麻提取物的溶出度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Applied Science and Engineering Progress
Applied Science and Engineering Progress Engineering-Engineering (all)
CiteScore
4.70
自引率
0.00%
发文量
56
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