Related Experiment Video
Updated: Aug 11, 2026

Assessing Changes in Volatile General Anesthetic Sensitivity of Mice after Local or Systemic Pharmacological Intervention
Published on: October 16, 2013
[Pharmacodynamics of two different propofol formulations]
H Ihmsen1, C Jeleazcov, J Schüttler
1Anästhesiologische Klinik, Friedrich-Alexander-Universität Erlangen-Nürnberg, Krankenhausstrasse 12, 91054 Erlangen. Harald.Ihmsen@kfa.imed.uni-erlangen.de
Two propofol lipid formulations showed no difference in pharmacodynamics, measured by EEG and clinical signs. This suggests that the lipid base does not impact propofol's effects.
Area of Science:
- Anesthesiology
- Pharmacology
- Neuroscience
Background:
- Propofol is available in multiple lipid formulations.
- Comparing the pharmacodynamics of different propofol formulations is crucial for clinical practice.
Purpose of the Study:
- To compare the pharmacodynamics of two different propofol lipid formulations.
- To evaluate the influence of lipid formulations on propofol's effects on EEG and clinical signs.
Main Methods:
- Ten volunteers received computer-controlled infusions of Diprivan 1% and Propofol 1% MCT Fresenius.
- Pharmacodynamics were assessed using EEG median frequency and clinical reflexes.
- A sigmoid Emax model was used to analyze propofol plasma concentrations and effects.
Main Results:
- No significant differences in pharmacodynamics were observed between the two propofol formulations.
- EEG analysis (EC50 values) and clinical signs showed comparable effects for both drugs.
- A steep concentration-effect relationship and hysteresis were noted in the pharmacodynamic model.
Conclusions:
- The investigated lipid formulations do not influence the pharmacodynamics of propofol.
- Clinical outcomes related to propofol's effects are similar across different lipid formulations.
Related Concept Videos
Parenteral Anesthetics: Overview
Factors Affecting Drug Distribution: Organ Perfusion Rate
Perfusion rate-limited distribution relies on the...
One-Compartment Open Model for IV Bolus Administration: General Considerations
The drug's presence in the body is defined by an equation representing the difference between the rates of drug entry and exit. Key parameters—elimination rate constant, half-life,...
Pharmaceutical Alternatives: Stability-Related Therapeutic Nonequivalence
Measurement of Bioavailability: Pharmacodynamic Methods
Local Anesthetics: Pharmacokinetics