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Pharmacokinetics and Concentration-Effect Relationship of Oral LSD in Humans

Patrick C. Dolder, Yasmin Schmid, Manuel Haschke, Katharina Rentsch, Matthias E. Liechti

The International Journal of Neuropsychopharmacology June 24, 2015 DOI: 10.1093/ijnp/pyv072 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Pharmacokinetic study Peer reviewed
Population Healthy adults
Intervention Lysergic acid diethylamide
Topics LSD
Keywords Pharmacokinetics Urine Pharmacology Active metabolite Oral administration Pharmacodynamics
Citations 110
Key points LSD exhibits dose-proportional pharmacokinetics with a terminal half-life of 3.6 hours and effects lasting up to 12 hours.

Abstract

These first data on the pharmacokinetics and concentration-effect relationship of oral lysergic acid diethylamide are relevant for further clinical studies and serve as a reference for the assessment of intoxication with lysergic acid diethylamide.

Comparable studies

Other experimental studies on LSD, most cited first.

Study Year Design Participants
Neural correlates of the LSD experience revealed by multimodal neuroimaging. Human participants 2016 Experimental study
Crystal structure of an LSD-bound human serotonin receptor 2017 Experimental study with structural biology and molecular dynamics simulations
Lysergic Acid Diethylamide: Sensitive Neuronal Units in the Midbrain Raphe Midbrain neurons containing serotonin 1968 Experimental study
Connectome-harmonic decomposition of human brain activity reveals dynamical repertoire re-organization under LSD. Human brain 2017 Experimental study
LSD-Assisted Psychotherapy in Patients with Terminal Cancer Cancer patients 1973 Experimental study n = 60

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