Solubilising and Aerosolising Cannabidiol Using Methyl β-Cyclodextrin and Human Serum Albumin

IF 3.4 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Waiting Tai, Dipesh Khanal, Jonathon Carl Arnold, Hak-Kim Chan, Philip Chi Lip Kwok
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Abstract

Pulmonary delivery can deliver cannabidiol (CBD) with high bioavailability and fast onset of action. One formulation obstacle is the low aqueous solubility of CBD, so solubilsers are necessary. This study aimed to develop inhalable CBD powders using excipients that help dissolving CBD. The solubilisation effects of human serum albumin (HSA), β-cyclodextrin, 2-hydroxypropyl-β-cyclodextrin, and methyl-β-cyclodextrin (mbCD) were investigated with phase solubility test. MbCD showed the highest CBD solubilisation ability at all tested concentrations, followed by HSA. Therefore, mbCD and HSA were co-spray freeze dried with CBD to obtain CBD + mbCD and CBD + HSA powders, respectively. Both powders were amorphous, had < 3% residual solvent, and contained CBD in complexes. CBD + mbCD maintained its amorphicity at < 70% relative humidity. On the other hand, CBD + HSA resisted recrystallisation even at 90% relative humidity. However, although both formulations emitted about 90% of CBD, CBD + HSA was less dispersible than CBD + mbCD (fine particle fraction < 5 µm: 30.2 ± 1.0% vs 53.5 ± 1.5%). The higher level of CBD solubility enhancement and better aerosol performance from mbCD indicated that it was an effective excipient to deliver CBD and potentially other cannabinoids in the future.

Graphical Abstract

甲基β-环糊精和人血清白蛋白对大麻二酚的增溶和雾化作用
肺输送大麻二酚(CBD)具有高生物利用度和快速起效。一个配方障碍是CBD的水溶解度低,因此需要增溶剂。这项研究旨在开发可吸入的CBD粉末,使用辅料来帮助溶解CBD。采用相溶解度法研究了人血清白蛋白(HSA)、β-环糊精、2-羟丙基-β-环糊精和甲基-β-环糊精(mbCD)的增溶作用。在所有测试浓度下,MbCD对CBD的溶解能力最高,其次是HSA。因此,将mbCD和HSA与CBD共喷雾冷冻干燥,分别得到CBD + mbCD和CBD + HSA粉末。这两种粉末都是无定形的,有<; 3%的残余溶剂,并在配合物中含有CBD。CBD + mbCD在70%的相对湿度下保持非晶性。另一方面,CBD + HSA即使在90%的相对湿度下也能抵抗再结晶。然而,尽管两种配方都释放了约90%的CBD,但CBD + HSA的分散性不如CBD + mbCD(细颗粒分数<; 5µm: 30.2±1.0% vs 53.5±1.5%)。mbCD具有较高的CBD溶解度增强和更好的气溶胶性能,表明它是一种有效的赋形剂,可以在未来输送CBD和其他大麻素。图形抽象
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来源期刊
AAPS PharmSciTech
AAPS PharmSciTech 医学-药学
CiteScore
6.80
自引率
3.00%
发文量
264
审稿时长
2.4 months
期刊介绍: AAPS PharmSciTech is a peer-reviewed, online-only journal committed to serving those pharmaceutical scientists and engineers interested in the research, development, and evaluation of pharmaceutical dosage forms and delivery systems, including drugs derived from biotechnology and the manufacturing science pertaining to the commercialization of such dosage forms. Because of its electronic nature, AAPS PharmSciTech aspires to utilize evolving electronic technology to enable faster and diverse mechanisms of information delivery to its readership. Submission of uninvited expert reviews and research articles are welcomed.
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