Excretion of Delta 9 tetrahydrocannabinol in sweat

Excretion of Delta 9 tetrahydrocannabinol in sweat

Academia – Summary of this paper

Excretion of Delta 9-tetrahydrocannabinol in sweat. Our Machine-Learning algorithms scan the text for the most important phrases or passages. These highlights, alongside their respective section titles, are shown below.

Introduction

Saito et al. reported a validated gas chromatography-mass spectrometry (GC/MS) method with a LOQ of 0.4 ng THC/patch and found concentrations of 0.9 to 3.1 ng THC/patch in several 24-hour sweat patches from one cannabis user [20]. The expected disposition of THC in sweat from chronic cannabis users has not been reported.

Subjects And Study Design

Exact times of dosing were recorded, but target times each day were 0800, 1300 and 1730 h. After five consecutive dosing days, there was a 10-day washout period prior to the next dosing condition. Subjects had five dosing conditions involving placebo, low-dose liquid hemp oil (9 μg/g or a daily dose of 0.39 mg THC), low-dose hemp oil in capsules (92 μg/g or a daily dose of 0.47 mg THC), high-dose hemp oil (347 μg/g or a daily dose of 14.8 mg THC) and dronabinol (2.5 mg/capsule or a daily dose of 7.5 mg THC). Sweat patches were stored at −20°C until THC analysis.

Gc/Ms Analysis

Percent recovery from patches was 44-46%, LOQ was 0.4 ng THC/patch and coefficients of variation were < 10%. All weekly patches were tested. Some daily patches were not tested if no THC was found in the corresponding weekly patch.

When you are ready to start a business or protect your business. Michigan’s top referred Cannabis Business Services and Licensing law firm. Komorn Law PLLC800-656-3557.

Results

Prior to receiving their first THC dose, frequent cannabis users (Group 2) produced their first negative urine specimen, i.e. less than 10 μg/L, within one to three weeks. During this washout phase, the first weekly sweat patch from two of seven subjects had THC above the assay LOQ. One weekly patch contained 0.93 ng THC/patch, with none of the seven daily sweat patches worn this week positive for THC.

Discussion

The manufacturer recommends that the patches be worn for one week. In the present study, sweat patches worn by daily cannabis users the first week of monitored abstinence had THC concentrations averaging 3.85 ng/patch. There are no other published studies reporting sweat patch THC concentrations after cessation of use for comparison.

Conclusions

Results of our clinical study indicate that daily cannabis users will excrete THC into sweat in concentrations above the SAMHSA cutoff of 1 ng/patch. During abstinence, negative patches are expected after one week, but some may have a longer washout period of four weeks or more. The sensitivity of sweat patches to detect new drug use following cannabis smoking is not known and requires an independent controlled smoked cannabis administration study.


Author

Marilyn Huestis

University of Maryland School of Medicine – Faculty Member

Professor Dr. Dr. (h.c.) Marilyn A. Huestis recently retired as a tenured senior investigator and Chief, Chemistry and Drug Metabolism Section, National Institute on Drug Abuse, National Institutes of Health, after 23 years of conducting controlled drug administration studies. She is an Adjunct Professor, University of Maryland Baltimore School of Medicine. 

Source

Delta 9 in human plasma after controlled administration

Delta 9 in human plasma after controlled administration

Delta(9)-tetrahydrocannabinol, 11-hydroxy-delta(9)-tetrahydrocannabinol and 11-nor-9-carboxy-delta(9)-tetrahydrocannabinol in human plasma after controlled oral administration of cannabinoids

Summary of this paper

Our Machine-Learning algorithms scan the text for the most important phrases or passages. These highlights, alongside their respective section titles, are shown below.

Section 1

Although there are several pharmacokinetic studies of THC and its metabolites in plasma or urine after smoked cannabis, [25][26][27][28][29][30] few studies have investigated their disposition in plasma after oral administration. [13][14][15] The objectives of this study were to determine plasma profiles of THC, 11-hydroxy-D 9 -tetrahydrocannabinol (11-OH-THC), and THCCOOH after controlled ingestion of natural cannabinoids in hemp oil and synthetic THC (dronabinol) and to relate these concentrations to ongoing physiological and subjective effects.Go To Passage 

Participants

Six healthy participants with a history of cannabis use resided in the secure clinical research unit of the National Institute on Drug Abuse (NIDA) Intramural Research Program, National Institutes of Health while participating in a protocol designed to characterize the pharmacokinetics and pharmacodynamics of oral THC. The NIDA Institutional Review Board approved the study. All participants provided written informed consent, were under continuous medical supervision, and were financially compensated for their time and inconvenience.Go To Passage 

Drug Administration

A total daily dose of 14.8 mg THC was achieved with the high-dose hemp oil (concentration 347 mg THC/g hemp oil). Dronabinol (synthetic THC in sesame oil), 2.5 mg THC per capsule, was administered as a positive control with a daily total dose of 7.5 mg. For safety reasons, only 2 doses (5.0 mg THC) were administered on the first dosing day of the session. Doses administered reflected concentrations of THC in commercially available hemp oil at the time of study design.Go To Passage 

Clinical Specimen Analysis

Blood was collected on ice, centrifuged, and plasma removed within 2 hour; specimens were stored at À 201C until analysis. A previously published procedure for the simultaneous extraction and quantification of THC, 11-OH-THC, and THCCOOH was employed. Escherichia coli b-glucuronidase hydrolysis cleaved glucuronic acid moieties to capture total cannabinoid concentrations.Go To Passage 

When you need an attorney to represent your Cannabis Business who has the experience and intimate knowledge of the industry – Take a good look at Komorn Law PLLC – a law firm that has been on the front line defending the future of cannabis both medical, recreational and in the justice system providing legal defense services.

Statistical Analysis

Plasma THC, 11-OH-THC, and THCCOOH concentrations were compared between the 7.5 and 14.8 mg THC/d dosing sessions with analysis of variance (ANOVA) and Wilcoxon Signed Ranks Test for Areas Under the Curve. Correlations of body mass index (BMI) and C max and for the number of specimens positive for THC and 11-OH-THC were analyzed by Spearman’s rank correlation coefficient.Go To Passage 

Results

The number of specimens positive for THCCOOH during and after the 0.39 and 0.47 mg THC/d regimens varied widely, ranging from 0 to 23, out of a possible 28 per participant. Participant N had 9 of 15 specimens positive for THC and 6 of 18 positive for 11-OH-THC during dosing with the high potency oil and capsules (Fig. 1), considerably more than any other subject. Participants A, H, P, L, and O had 11,8,8,, and 0 of 36 positive specimens, respectively.Go To Passage 

Discussion

In the present study, concentrations of THC and 11-OH-THC were similar during the 7.5 mg THC/d dronabinol and 14.8 mg THC/d hemp oil doses, never exceeding 6.1 ng/mL. No specimens had measurable THC or 11-OH-THC during or after the 0.39 or 0.47 mg THC/ d dosing sessions. The lower dose regimens are reflective of THC concentrations in hemp oil currently produced by US manufacturers, indicating that consumption of these hemp oils according to manufacturer’s instructions should not lead to positive THC or 11-OH-THC plasma tests.Go To Passage 

Conclusions

Nearly all specimens had measurable THCCOOH. There was a significant correlation between BMI and the number of specimens positive for THC and 11-OH-THC and between BMI and C max for both analytes, possibly indicating greater deposition in adipose tissue and release to plasma of THC and metabolites in obese individuals. These controlled drug administration data should assist in the interpretation of plasma cannabinoid results and provide clinicians with valuable information for future pharmacological studies.Go To Passage