TY - JOUR
T1 - Pharmacokinetics and tolerability of liposomal synthetic cannabidiol subcutaneous depot in Holstein dairy calves
AU - Shilo-Benjamini, Y.
AU - dos Santos Silva, P.
AU - Cern, A.
AU - Aroch, I.
AU - Abu Ahmad, W.
AU - Barasch, D.
AU - Lavy, E.
AU - Barenholz, Y.
AU - Zachut, M.
N1 - Publisher Copyright:
© 2026 American Dairy Science Association
PY - 2026/2
Y1 - 2026/2
N2 - As animal welfare concerns and pain management awareness in cattle increase, long-term analgesics can become a solution for the treatment of painful husbandry procedures. Cannabidiol (CBD) has anti-inflammatory and analgesic properties. Nevertheless, poor gastrointestinal absorption and first-pass liver metabolism results in low oral bioavailability in humans. The use of injected liposomal-CBD facilitates slow-drug-release, providing prolonged CBD plasma concentrations, with increased bioavailability. Study objectives were to determine preliminary pharmacokinetics and tolerability of a single subcutaneous injection of liposomal synthetic CBD (L-sCBD; 5 mg/kg) in 6 Holstein female neonatal calves. Blood was sampled for CBD and its metabolites, complete blood count, serum chemistry and serum amyloid A up to 6 wk. Vital signs and adverse effects were monitored. Data over time were compared with baseline using linear regression mixed effects. Plasma CBD concentrations were detected up to a median of 4.5 wk; with median peak plasma concentration (Cmax) 44.1 ng/mL, median time to Cmax 1 d and median half-life 5.3 d. The primary metabolite, 7-carboxy-CBD, exceeded CBD exposure by 9-fold (4–16) based on the area under the curve. A short-term significant neutrophil count increase was observed 2 d after injection. Serum amyloid A decreased after injection. The main adverse reaction was local swelling, which spontaneously resolved. Subcutaneous injection of L-sCBD produced detectable CBD plasma concentrations for several weeks and was well tolerated by calves. The use of injectable L-sCBD as an additional long-term analgesic in calves undergoing routine painful procedures (e.g., disbudding, castration) appears to have potential to decrease suffering and promote animal welfare, although further research is required to evaluate efficacy.
AB - As animal welfare concerns and pain management awareness in cattle increase, long-term analgesics can become a solution for the treatment of painful husbandry procedures. Cannabidiol (CBD) has anti-inflammatory and analgesic properties. Nevertheless, poor gastrointestinal absorption and first-pass liver metabolism results in low oral bioavailability in humans. The use of injected liposomal-CBD facilitates slow-drug-release, providing prolonged CBD plasma concentrations, with increased bioavailability. Study objectives were to determine preliminary pharmacokinetics and tolerability of a single subcutaneous injection of liposomal synthetic CBD (L-sCBD; 5 mg/kg) in 6 Holstein female neonatal calves. Blood was sampled for CBD and its metabolites, complete blood count, serum chemistry and serum amyloid A up to 6 wk. Vital signs and adverse effects were monitored. Data over time were compared with baseline using linear regression mixed effects. Plasma CBD concentrations were detected up to a median of 4.5 wk; with median peak plasma concentration (Cmax) 44.1 ng/mL, median time to Cmax 1 d and median half-life 5.3 d. The primary metabolite, 7-carboxy-CBD, exceeded CBD exposure by 9-fold (4–16) based on the area under the curve. A short-term significant neutrophil count increase was observed 2 d after injection. Serum amyloid A decreased after injection. The main adverse reaction was local swelling, which spontaneously resolved. Subcutaneous injection of L-sCBD produced detectable CBD plasma concentrations for several weeks and was well tolerated by calves. The use of injectable L-sCBD as an additional long-term analgesic in calves undergoing routine painful procedures (e.g., disbudding, castration) appears to have potential to decrease suffering and promote animal welfare, although further research is required to evaluate efficacy.
KW - analgesia
KW - cannabidiol (CBD)
KW - liposomes
KW - slow release
KW - welfare
UR - https://www.scopus.com/pages/publications/105028556357
U2 - 10.3168/jds.2025-27373
DO - 10.3168/jds.2025-27373
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C2 - 41349822
AN - SCOPUS:105028556357
SN - 0022-0302
VL - 109
SP - 1936
EP - 1950
JO - Journal of Dairy Science
JF - Journal of Dairy Science
IS - 2
ER -