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Anesth Analg 1986; 65:159-165
© 1986 International Anesthesia Research Society
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Fundamental Properties of Local Anesthetics I. The Dependence of Lidocaine's Ionization and Octanol

Buffer Partitioning on Solvent and Temperature

Virgil Sanchez, MD, G. Richard Arthur, PhD, and Gary R. Strichartz, PhD

Anesthesia Research Laboratories, Brigham and Women's Hospital, and the Department of Pharmacology, Harvard Medical School, Boston, Massachusetts.

Abstract

The protonation equilibrium and hydrophobic character of lidocaine were characterized by its pKa and the octanol:buffer partition coefficients of the charged (P+) and neutral (P0) drug species. These measurements were accomplished by ultraviolet spectrophotometry of pure lidocaine HO solutions at different temperatures, ionic strengths, and buffer concentrations. Corroboration of the pKa determination by the potentiometric method and of the partition coefficients by gas chromatography validated the general application of the spectrophotometric technique. The pKa increased with decreasing temperature (7.61 ± 0.06 at 36°C; 7.94 ± 0.04 at 26°C, in water; mean ± SD), increasing ionic strength (8.06 ± 0.02 at 26°C in 0.165 M NaCl) and increasing buffer capacity (8.28 ± 0.06 at 25°C in 0.15 M NaCl + 20 mM buffer). Octanol:buffer partition coefficients for both the protonated and the neutral species (expressed as mole fractions) increased upon warming: 0.55 ± 0.04 and 2666 ± 202, respectively, at 25°C, and 0.75 ± 0.09 and 3210 ± 272, respectively, at 36°C. Ionic strength and buffer concentration had no significant effect on either P value. The increase in pKa at lower temperatures coupled with the decreased partition coefficients resulted in a nearly constant concentration of the protonated species in octanol as the system was cooled, whereas the concentration of the neutral species fell by more than 80%. This finding may explain the large increase in the impulse blocking potency of lidocaine observed upon nerve cooling, if the protonated anesthetic species is the more active form of the drug competing with the neutral species for a common binding site.

Key Words: ANESTHETICS, local—physical properties.







Lippincott, Williams & Wilkins Anesthesia & Analgesia® is published for the International Anesthesia Research Society® by Lippincott Williams & Wilkins with the assistance of Stanford University Libraries' HighWire Press®. Copyright 2006 by the International Anesthesia Research Society. Online ISSN: 1526-7598   Print ISSN: 0003-2999 HighWire Press
Copyright © 1986 by the International Anesthesia Research Society.