Cannabidiol lymphatic transport after oral administration assessed using a novel thoracic lymph duct cannulated conscious pig model
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
41459703
PubMed Central
PMC12777811
DOI
10.1080/10717544.2025.2608913
Knihovny.cz E-zdroje
- Klíčová slova
- Cannabinoids, animal model development, interspecies comparison, lymph sampling, oral bioavailability, pharmacokinetics,
- MeSH
- aplikace orální MeSH
- biologická dostupnost MeSH
- biologický transport MeSH
- ductus thoracicus * metabolismus MeSH
- emulze MeSH
- kanabidiol * aplikace a dávkování farmakokinetika metabolismus MeSH
- klinické křížové studie MeSH
- krysa rodu Rattus MeSH
- lymfa * metabolismus MeSH
- lymfatický systém metabolismus MeSH
- modely u zvířat MeSH
- potkani Sprague-Dawley MeSH
- prasata MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- emulze MeSH
- kanabidiol * MeSH
Lymphatic transport of drugs after oral administration is an important physiological process in highly lipophilic compounds, such as cannabidiol (CBD). The majority of lymphatic transport studies have been historically conducted in anesthetized rats. However, this animal model differs significantly from the humans regarding both anatomical and physiological features. The aim of this study was therefore to develop a novel animal model using pigs and to provide an interspecies comparison for the lymphatic transport of CBD. The thoracic lymph duct was cannulated via thoracotomy in three pigs and lymph and blood were sampled from conscious animals to assess the lymphatic transport parameters and basic pharmacokinetic parameters of CBD administered in two distinct drug formulations (sesame oil-based solution and nanoemulsion) using a two-period cross-over study design. The mean ± SD oral bioavailability (F) was 6.1 ± 0.9% for the oil solution and 9.2 ± 6.6% for the nanoemulsion. The relative bioavailability via lymph (FRL), i.e. the percentage of the systemically available drug that has been transported through the mesenteric lymph, was 20 ± 10% and 11 ± 13%, respectively. Whereas the FRL for the oil solution was 2.3-fold lower in pigs compared to rats, the FRL for the nanoemulsion was almost identical for both species. In conclusion, the lymphatic transport of CBD plays an important role after its oral administration. The particular parameters differed significantly between the rodent and higher non-rodent species. The use of higher species models is therefore warranted for the lymphatic transport assessment in settings close to humans.
Deparment of Analytical Chemistry Faculty of Science Charles University Prague Prague Czech Republic
Deparment of Cardiac Surgery Masaryk Hospital in Ústí nad Labem Ústí nad Labem Czech Republic
Institute of Physiology 1st Faculty of Medicine Charles University Prague Prague Czech Republic
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