Archaeosomes facilitate storage and oral delivery of cannabidiol

被引:9
|
作者
Sedlmayr, Viktor [1 ]
Horn, Christina [2 ]
Wurm, David Johannes [2 ]
Spadiut, Oliver [1 ]
Quehenberger, Julian [1 ,2 ]
机构
[1] TU Wien, Inst Chem Environm & Biosci Engn, Vienna, Austria
[2] NovoArc GmbH, Vienna, Austria
基金
奥地利科学基金会;
关键词
Archaeosomes; Cannabidiol; Oral drug delivery; Liposomes; Storage stability; LIPID-BASED FORMULATIONS; TETRAETHER LIPIDS; CELLULAR UPTAKE; LIPOSOMES;
D O I
10.1016/j.ijpharm.2023.123434
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cannabidiol (CBD) has received great scientific interest due to its numerous therapeutic applications. Degradation in the gastrointestinal (GI) tract, first-pass metabolism, and low water solubility restrain bioavailability of CBD to only 6% in current oral administration. Lipid-based nanocarriers are delivery systems that may enhance accessibility and solubility of hydrophobic payloads, such as CBD. Conventional lecithin-derived liposomes, however, have limitations regarding stability in the GI tract and long-term storage. Ether lipid-based archaeosomes may have the potential to overcome these problems due to chemical and structural uniqueness. In this study, we compared lecithin-derived liposomes with archaeosomes in their applicability as an oral delivery system of CBD. We evaluated drug load, storage stability, stability in a simulated GI tract, and in vitro particle uptake in Caco-2 cells. Loading capacity was 6-fold higher in archaeosomes than conventional liposomes while providing a stable formulation over six months after lyophilization. In a simulated GI tract, CBD recovery in archaeosomes was 57 +/- 3% compared to only 34 +/- 1% in conventional liposomes and particle uptake in Caco-2 cells was enhanced up to 6-fold. Our results demonstrate that archaeosomes present an interesting solution to tackle current issues of oral CBD formulations due to improved stability and endocytosis.
引用
收藏
页数:9
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