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Lidocaine hydrochloride absorption from a subcutaneous site
Journal of Pharmaceutical Sciences
|May 1, 1975
Summary
Researchers studied lidocaine hydrochloride absorption in rats using a closed cell. Unexpected pH shifts occurred, preventing simple pharmacokinetic modeling and suggesting potential lidocaine base precipitation during subcutaneous drug absorption.
Area of Science:
- Pharmacokinetics
- Drug Absorption
- Animal Models
Background:
- Lidocaine hydrochloride absorption is influenced by solution pH.
- Open-cell systems show pH increase due to carbon dioxide loss.
- Closed systems were designed to prevent atmospheric gas exchange.
Purpose of the Study:
- To investigate subcutaneous lidocaine hydrochloride disappearance over time in rats.
- To assess the impact of a closed absorption cell on drug solution pH.
- To determine if a simple pharmacokinetic absorption model could be derived.
Main Methods:
- Utilized a "closed" subcutaneous absorption cell on anesthetized rats.
- Monitored lidocaine hydrochloride solution over time.
- Measured changes in solution pH within the closed cell.
Main Results:
- pH shifts to higher values were observed within the closed cell.
- The observed pH changes prevented the development of a simple pharmacokinetic absorption model.
- Data suggest potential precipitation of lidocaine base due to pH shifts.
Conclusions:
- The closed absorption cell did not maintain stable pH conditions for lidocaine hydrochloride.
- Subcutaneous drug absorption studies can be complicated by unexpected solution chemistry changes.
- Further investigation is needed to understand lidocaine base precipitation in vivo.