Hemp has been grown and cultivated for centuries throughout the world. In the 1930’s, concerns about tetrahydrocannabinol intoxication in people resulted in regulation of hemp production by the Bureau of Narcotics and Dangerous Drugs and eventually the US Drug Enforcement Agency (DEA). However, the 2014 Farm Bill allowed for the research based cultivation and production of industrial hemp [Cannabis sativa containing < 0.3%Tetrahydrocannabinol (THC)] for fiber and phytocannabinoid production. The 2018 Farm Bill took the additional step of removing industrial hemp (IH) from the DEA list of Schedule I drugs renewing interest in hemp cultivation as a novel agricultural commodity. Hemp plants, and their by-products, are considered to have nutritional and potentially therapeutic value when used as a feed source in livestock. However, the absence of published data describing the disposition of bioactive phytocannabinoid compounds including cannabidiol (CBD), cannabigerol (CBG), tetrahydrocannabinolic acid (THCA-A), and cannabidiolic acid (CBDA) in edible tissues after hemp consumption is a significant impediment to future animal health and production research in this field.

Pharmacokinetic data for cannabinoids has been published in humans, mice, and swine1,2,3,4. These studies were aimed at providing toxicological data for illicit cannabis use or data from animal models for disease syndromes. There are no published studies investigating the pharmacokinetics of cannabinoids in ruminant species, such as cattle. Cattle can utilize industrial hemp byproducts as they can digest cellulose plant materials in their rumens. The objective of this study was to describe the pharmacokinetics of the cannabinoid, CBDA, and to describe the presences of other cannabinoids found in plasma after administration of industrial hemp with known cannabinoid content to cattle.


No adverse effects (reactions and behavioral changes) were observed following oral dosing of IH. The final mean (± SD) CBDA dose administered to the cattle was 5.4 ± 0.4 mg/kg. The total mg of each cannabinoid dosed are listed in Table 1. Only 5 of the 11 detected cannabinoids in the hemp plant material administered to the cattle were detected in the plasma following oral administration. Cannabidiol (CBD) was detected in four samples from two calves. The psychoactive cannabinoid 9-THC was not detected in any plasma samples. The cannabinoids ( ±)-cis-11-Nor-9-carboxy-Δ9-tetrahydrocannabinol glucuronide (THC-glu), ( ±)-11-Hydroxy-Δ9-tetrahydrocannabinol (THC-OH), , cannabidivarin (CBDV), Δ9-Tetrahydrocannabinolic acid A (THCA-A), cannabigerolic acid (CBGA), cannabigerol (CBG), Δ9-tetrahydrocannabinol (9-THC), Δ8-tetrahydrocannabinol (8-THC), cannabichromene (CBC), Δ9-tetrahydrocannabivarin (THCV), cannabinol (CBN), and (-)-11-nor-9-Carboxy-Δ9-tetrahydrocannabinol (THC-acid).were not detected in any sample at any time points.

Table 1 Individual animal weights (kg), total industrial hemp administered (g), and doses (mg) of individual cannabinoids administered to each animal.

Plasma CBDA, THCA-A, CBCA, and CBDVA concentrations over time are shown in Fig. 1. The pharmacokinetic parameters of CBDA are summarized in Table 2. Following oral administration of IH, CBDA reached a geometric mean maximum concentration of 72.7 ng/mL, which was observed at 11.8 h after dosing. A geometric mean apparent half-life (T½) of 14.1 h was recorded. The geometric mean AUC0-∞ was 2718.6 h × ng/mL. A geometric mean residence time of 30.6 h was determined. The arithmetic mean observed maximum concentrations of THCA-A, CBCA, and CBDVA were 12.1 ng/mL, 12.3 ng/mL, and 13.1 ng/mL respectively. The times of the mean maximum concentrations were observed at 25.2 h, 23.2 h, and 13.6 h for THCA-A, CBCA, and CBDVA.

Figure 1
figure 1

Mean plasma concentrations (ng/mL) of cannadibiolic acid (CBDA) at 5.4 mg/kg, tetrahydrocannabinolic acid-A (THCA-A) at 0.6 mg/kg, cannabidivarinic acid (CBDVA) at 0.02 mg/kg, and cannabichromenic acid (CBCA) at 0.5 mg/kg over time in cattle exposed to industrial hemp (n = 8).

Table 2 Pharmacokinetic parameters of cannabidiolic acid (CBDA) following oral administration of industrial hemp to achieve a 5.4 mg/kg dose (n = 8).

Mean serum biochemical analysis are summarized in Table 3. Glucose and alkaline phosphatase (ALP) were elevated pre- and post-dosing. Additionally, blood urea nitrogen (BUN) were lower than reference ranges pre- and post-dosing. Other changes in the biochemical profiles of calves following IH administration were observed, but these changes remained within the normal limits of the tests. There were no significant changes in serum biochemical analytes observed.

Table 3 Results of serum blood chemistry profiles pre- and post-industrial hemp administration.


This is the first report describing the pharmacokinetics of cannabinoids in cattle after administration of industrial hemp. Specifically, this is the first report to focus on CBDA pharmacokinetics in cattle. Cannabidiolic acid is a precursor of cannabidiol (CBD), and present in high concentrations in industrial hemp. Cannabidiolic acid is converted to CBD via a decarboxylation reaction5.

In cattle, CBDA is absorbed from the rumen. The target dose of 5.0 mg/kg was chosen as it is the starting dose of cannabidiol for patients with seizures due to Lennox-Gastaut or Dravet syndromes6. The actual dose administered was 5.4 mg/kg or a mean of 1142.9 g per animal. This difference is due to the hemp boluses being prefilled and weighed prior to study commencement.

The pharmacokinetics of cannabinoids has been studied in mice as part of research to examine therapeutic control of seizures. Following intraperitoneal injection, cannabidiolic acid is rapidly absorbed reaching peak concentrations within 15 min; and has a relatively short half-life of 45 min. This is in contrast to cannabidiolic acid following oral dosing in cattle. In cattle, cannabidiolic acid is slowly absorbed from the rumen, and has a longer half-life. These pharmacokinetic data are needed to further design studies to investigate multiple daily doses, tissue residue kinetics, and eventual clinical studies to evaluate CBDA therapeutic and production effects in cattle.

The absorption of cannabinoids appears to be influenced by the chemistry of the cannabinoid. Acidic cannabinoids (CBDA, THCA-A, CBDVA, CBCA) were predominantly detected in the plasma after dosing. Cannabidiol (CBD) despite having a similar dose on a total mg basis as THCA-A, was only detected in four total samples. Interestingly, CBDVA was the lowest dosed cannabinoid on a total milligram basis (mean 3.5 mg per animal) yet it was found in all calves with maximum concentrations similar to THCA-A and CBCA. This suggests that CBDVA may have a higher oral bioavailability than the other compounds examined. However, a prospective study involving IV administration, is required to determine bioavailability. A similar pattern of the acidic forms of cannabinoids (CBDA and THCA-A) was observed in humans administered oral cannabis. Study participants were administered cannabis oil containing 2.3 mg/mL THCA-A, 2.2 mg/mL 9-THC, 4.4 mg CBDA, and 2.4 mg/mL CBD. The maximum concentrations (Cmax) of the four cannabinoids were 48.9 ng/mL, 1.4 ng/mL, 74.6 ng/mL and 4.4 ng/mL for THCA-A, 9-THC, CBDA, and CBD respectively7. These values are similar to others published for human cannabis users8.

Moreover, the impact of the rumen on the fate of oral cannabinoids requires further investigation. Rumen microbes could potentially degrade or metabolize cannabinoids causing alterations in the cannabinoids available for absorption. Merrick et al., reported the in vitro conversion of cannabidiol (CBD) to 9-tetrahydrocannabinol (9-THC) in simulated gastric fluid9. Although these findings were not supported in vivo10; there is still potential for rumen microbes to play a significant role in the conversion of fatty-acids through biohydrogenation.

Blood serum chemistry were taken prior to IH administration and 96 h after IH administration. There were no changes observed. The liver enzyme alkaline phosphatase was elevated in all animals prior to IH administration. Sorbitol dehydrogenase, a liver associated enzyme, was elevated prior to IH dosing, but returned to normal levels 96 h after dosing. However the change in sorbitol dehydrogenase was not statistically significant. Mean blood urea nitrogen (BUN) levels were below the reference range. This is likely due to the lower protein diet the calves were consuming. Further investigation into the impact of abnormal serum biochemical analytes is warranted, however the serum total proteins and albumin were within normal limits. The cattle in used in the study were on-site for five months prior to study commencement and were considered healthy on examination by a veterinarian.

The results of the finding of this study have implications for IH as an agriculture commodity. In the short-term, these findings can be used to develop strategies for cattle accidently exposed to IH and hemp by-products, as the U.S. Food and Drug Administration (FDA) has explicitly stated cannabinoids are considered adulterants in food production species. However, cattle and other ruminants are ideally suited to utilize IH and the byproducts of cannabinoid production from IH as a novel source of nutrition. Understanding of plasma half-lives for cannabinoids will allow veterinarians to work with cattle producers to establish withdrawal intervals to ensure exposed cattle can enter the food supply. Additionally, understanding of cannabinoid pharmacology is needed if IH and hemp byproducts are to be considered by the US FDA and the Association of American Feed Control Officials (AAFCO) for inclusion into animal diets.

The bulk of this report is centered on the pharmacokinetics of CBDA, but the absorption of THCA-A, CBCA, and CBDVA was observed. This work is an important first step towards follow-up studies that are needed to characterize cannabinoid absorption, distribution, metabolism, and excretion in cattle. Specifically, additional work is required to determine edible tissue residue profiles for cannabinoids in cattle. Evaluation of the role rumen microflora may have on the metabolism and degradation of cannabinoids administered to cattle either by direct exposure of specific cannabinoids or via hemp products is needed.

Materials and methods

Subjects and housing

Eight Holstein castrated males 10 months of age and weighing (± SD) 214 ± 23 kg were enrolled onto the study. Calves were acclimated to the research facility and halter trained for 1 week prior to study commencement. These calves were group housed in outdoor dirt pens with access to shelter. Pen size per calf exceeded the recommendations set forth in the Guide for the Care and Use of Agricultural Animals in Research and Teaching11. Calves were fed a custom grain mix at 8:00 and 16:00 h. Calves had ad libitum access to grass hay and water via self-filling trough for the entire duration of the study.

This study was performed in accordance with all relevant legislative and regulatory requirements in the United States, the State of Kansas, and AAALAC. All experimental procedures were approved by the Institutional Animal Care and Use Committee at Kansas State University (IACUC# 4326). Industrial hemp was grown and handled under license of the Kansas Department of Agriculture Industrial Hemp Research Program (licenses numbers: KDA-0621466839 and KDA-0302873296).

Industrial hemp dosing and cattle sampling

Cannabinoid content of the IH was determined using ULPC-MS methods prior to the start of the study to determine cannabinoid dosage. As CBDA was the highest cannabinoid found in the IH, and considered the target cannabinoid for dosing. The target dose of CBDA was 5.0 mg/kg. For dosing, IH flower material was placed into gelatin capsules and the weight of each filled capsule was recorded. At the time of dosing cattle were administered four IH filled capsules. The weight of each capsule was recorded and a total weight of the IH administered was determined. Calves were monitored by study personnel for rejection (spitting out) the hemp boluses for 15 min following dose administration to confirm delivery.

Calves had a sterile jugular catheter placed 12 h prior to IH dosing to facilitate serial blood sampling for the first 12 h of the study. Blood samples for plasma cannabinoid analysis were obtained via the jugular catheter or jugular venipuncture prior to IH administration, and at 0.25, 0.5, 0.75, 1, 1.5, 2, 4, 6, 8, 12, 24, 36, 48, 72, and 96 h. Blood was placed into prelabeled vacutainer tubes containing lithium heparin and the contents mixed. After collection, whole blood was placed on ice and transported to the laboratory within 1 h of collection. Blood tubes were centrifuged at 1500 g for 10 min. Each plasma sample was harvested into individual cryovials and placed in − 80 °C freezer until analyzed.

Additionally, prior to IH dosing and at 96 h, blood was obtained and placed into vacutainers with no additive for serum biochemical analysis. Serum samples were submitted to the Kansas State Veterinary Diagnostic Laboratory for biochemical analysis by photometric methods (Cobas 501, Roche Diagnostics, Indianapolis, IN, USA).

Cannabinoid analysis

Plasma cannabinoid concentrations were determined using UPLC-MS methods adapted from Zhang et al.12. All solvents used such as methanol, acetonitrile, isopropanol, formic acid were LC–MS grade. Cannabinoids standards were purchased in individual solutions in methanol (Cerilliant Corporation, Round Rock, TX), including: ( ±)-cis-11-Nor-9-carboxy- Δ 9-tetrahydrocannabinol glucuronide (THC-glu), ( ±)-11-Hydroxy-Δ9-tetrahydrocannabinol (THC-OH), cannabidivarinic acid (CBDVA), cannabidivarin (CBDV), cannabidiol (CBD), cannabidiolic acid (CBDA), Δ9-Tetrahydrocannabinolic acid A (THCA-A), cannabigerolic acid (CBGA), cannabigerol (CBG), Δ9-tetrahydrocannabinol (9-THC), Δ8-tetrahydrocannabinol (8-THC), cannabichromene (CBC), Δ9-tetrahydrocannabivarin (THCV), cannabichromenic Acid (CBCA), cannabinol (CBN), (-)-11-nor-9-Carboxy-Δ 9-tetrahydrocannabinol (THC-acid). Cannabinoid analogs used as internal standards were also purchased in solution in methanol at 100 µg/mL (Cerilliant Corporation, Round Rock, TX): ( ±)-cis-11-Nor-9-carboxy-Δ9-tetrahydrocannabinol glucuronide (THC-glu-d3), Cannabidiol-d3 (CBD-d3), Δ9-Tetrahydrocannabinol-d3 (9-THC-d3), ( ±)-11-nor-9-Carboxy-D9-tetrahydrocannabinol-d9 (THC-acid-d9), ( ±)-11-Hydroxy-Δ9-tetrahydrocannabinol-d3 (THC-OH-d3), Cannabichromene-d9 (CBC-d9). All cannabinoids standards were kept in the freezer at − 20 °C.

On the day of analysis, plasma samples were allowed to thaw. Once thawed, 0.1 mL of plasma (samples, quality controls or negative control plasma) were mixed with 0.1 mL of internal standard mixture at 200 ng/mL (not added to the negative control sample) and 0.1 mL of acetonitrile with 0.1% formic acid to each samples to precipitate the proteins. The mixture was vortexed for 5 s and centrifuge for 5 min at 7000 g. The supernatant was then diluted with 0.4 mL of ultra-pure 18 Ω water before clean-up. The sample was loaded on a solid phase extraction plate using positive pressure nitrogen. Each well was washed twice with 0.25 mL of a mixture of methanol–water (25:75). The compounds were eluted with two-25 µL aliquots of acetonitrile-methanol (90:10) and diluted with 50 µL of water before analysis.

Cannabinoid analysis was performed using an Acquity H UPLC and a TQ-S triple quadrupole mass spectrometer (Waters Corp., Milford, MA). The chromatographic separation was performed with a UPLC column (Eclipse Plus C18, Agilent Technologies, Santa Clara, CA) 100 × 2.1 mm, 1.8 µ, heated at 55 °C. The flow rate was set at 0.5 mL/min, the mobile phase consisted of a gradient of acetonitrile (B) and water containing 0.1% formic acid (A) as follow: 0 min: 60%B, 6.50 min: 86% B, 7.50 min-9 min: 100%B, 9.01 m in12 min: 60%B. The total run time was 12 min. The injection volume was 5 µL. The data acquisition was performed by electrospray ionization in positive and negative mode using multiple reaction monitoring. The capillary voltage was 3.0 kV, the source temperature 150 °C, the desolvation temperature 500 °C, the desolvation nitrogen flow at 1000 L/h, and the cone nitrogen flow at 150 L/h. Linear regression with a weighing factor of 1/X was used and accepted if the coefficient of correlation R2 was > 0.99. Calibration curves were linear from 0.1 to 100 ng/mL for all cannabinoids. The lower limit of detection, lower limit of quantification, intra-day precisions, inter-day precisions, and inter-day accuracies for each cannabinoid analyte are summarized in Table 4.

Table 4 Lower level of detection (LOD), lower limit of quantification (LOQ), intra-day precisions, inter-day precisions, and inter-day accuracies for each cannabinoid analyte analyzed following oral administration of industrial hemp.

Pharmacokinetic analysis

Individual animal pharmacokinetic parameters were calculated for CBDA concentration vs. time data using computer software (Phoenix 8.2, Certara, Inc., Princeton, NJ, USA). Non-compartmental approach based on statistical moment theory was used for the analysis. The area under the plasma concentration versus time curve (AUC) and area under the first moment of the concentration vs time curve (AUMC) were determined using the linear trapezoidal linear interpolation method. The AUC0-last and AUMC0-last of CBDA, the time range from the time of drug administration to the last quantifiable drug concentration were extrapolated to infinity to determine AUC0-, AUMC0-. The mean residence times (MRT0-) of CBDA following administration was calculated from AUC0- and AUMC0- (i.e., MRT0- = AUMC0-/AUC0-). The elimination rate constants (λz) associated with the terminal elimination phase was estimated by using linear regression of the terminal phase of the log plasma concentration vs. time curve. The elimination half-lives (λz-HL) were calculated using the equation = \(\frac{0.693}{{\lambda }_{z}}\). The maximum plasma concentration (Cmax) and time to obtain maximum concentration (Tmax) were reported as observed values. The apparent volume of distribution per fraction of the dose absorbed based on the terminal phase (Vz/F) and apparent total body clearance per fraction of dose absorbed (CL/F) were calculated. Pharmacokinetic parameters are presented as geometric means, medians, and ranges based on the consideration of log-normal distributions.