Scientific illustration for Cannabidiol lymphatic transport after oral administration assessed using a novel thoracic lymph duct cannulated conscious pig model.

Cannabidiol lymphatic transport after oral administration assessed using a novel thoracic lymph duct cannulated conscious pig model.

Drug delivery β€’ β€’ Highly Relevant
πŸ€–

AI Summary

Researchers wanted to understand how cannabidiol (CBD), a major component of cannabis, moves through the body's lymphatic systemβ€”a network of vessels that absorbs fats and other substances from food and supplements. Most previous studies on this process used anesthetized rats, but rats are quite different from humans in their anatomy and physiology. In this innovative study, scientists surgically placed a small tube into the thoracic lymph duct (a major lymphatic vessel) in conscious pigs, which are considered a better biological model for understanding human physiology. They then gave pigs two different forms of CBDβ€”one dissolved in sesame oil and one as a modern nanoemulsion formulationβ€”and measured how much CBD ended up in the bloodstream and lymph over time.

The results showed that CBD has relatively low overall bioavailability (the amount that actually enters the bloodstream) at around 6-9%, but surprisingly, a significant portion of the CBD that does get absorbed travels through the lymphatic system rather than directly into the blood. Notably, the lymphatic transport patterns differed between pigs and rats, suggesting that previous rat studies may not accurately predict how CBD moves through the human body. The nanoemulsion formulation showed more consistent results between species, which has important implications for how CBD products are formulated and absorbed.

These findings are significant for both researchers and cannabis users because they highlight how formulation mattersβ€”different ways of preparing CBD can substantially affect how your body absorbs it. The research also suggests that animal models closer to humans (like pigs) are essential for accurately predicting how cannabinoid medicines will work in people, potentially leading to better CBD products and more reliable dosing guidelines in the future.

πŸ’‘ Key Findings

1
Lymphatic transport is a major absorption route for CBD after oral administration, accounting for 11-20% of systemically available drug, demonstrating that this pathway plays an important physiological role in CBD bioavailability.
High
85%
2
CBD bioavailability in pigs was low (6.1-9.2%), highlighting the poor oral absorption of cannabidiol and suggesting that formulation strategies are needed to improve drug delivery.
High
90%
3
Lymphatic transport patterns for CBD differ significantly between rodents and larger mammals (pigs), indicating that rat models may not accurately predict human CBD absorption and supporting the need for larger animal studies.
High
80%
4
Nanoemulsion formulations of CBD showed more consistent lymphatic transport between species compared to oil solutions, suggesting this formulation approach may be more predictable for human use.
Good
75%

πŸ“„ Original Abstract

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.

Explore More Research

Stay informed about the latest cannabis science.

Track your cannabis journey with AI

Get personalized strain recommendations based on your preferences