Anesth Analg 2006;103:882-887
© 2006 International Anesthesia Research Society
doi: 10.1213/01.ane.0000237126.57445.80
ANESTHETIC PHARMACOLOGY
Anesthetic Properties of a Propofol Microemulsion in Dogs
Timothy E. Morey, MD*,
Jerome H. Modell, MD, DSc (Hon)* ,
Dushyant Shekhawat, BS ,
Dinesh O. Shah, PhD* ,
Brian Klatt, BS ,
George P. Thomas, MSc, PhD ,
Frank A. Kero, BS*||,
Matthew M. Booth, PhD*, and
Donn M. Dennis, MD, FAHA*¶#
From the Departments of *Anesthesiology, Chemical Engineering, ||Chemistry, ¶Pharmacology and Experimental Therapeutics, and #Psychiatry, University of Florida, Gainesville, Florida; NanoMedex, Inc., Alachua, Florida; and Calvert Laboratories, Inc., Olyphant, Pennsylvania.
Address correspondence and reprint requests to Donn M. Dennis, MD, FAHA, Department of Anesthesiology, University of Florida, PO Box 100254, Gainesville, FL 32610-0254. Address e-mail to DDennis{at}ufl.edu.
Microemulsions of propofol with nanometer droplet diameter are alternatives to soybean macroemulsions for inducing anesthesia, and may have important advantages. We used a propofol (10 mg/mL) microemulsion (particle diameter 24.5 ± 0.5 nm) and a commercial macroemulsion to induce anesthesia in dogs (n = 10) using a randomized, crossover design separated by a 7-day rest interval. The end points were loss of leg withdrawal after a toe pinch and changes in vital signs. Venous blood samples were acquired at multiple times to measure plasma propofol concentrations and indices of erythrocytes, leukocytes, and coagulation. All dogs were rendered insensitive to pain followed by successful recovery without noticeable complications. Comparing indices between microemulsion and macroemulsion formulations, no differences were noted with respect to dose (10.3 ± 1.2 and 9.7 ± 1.6 mg/kg, respectively, P = 0.39), time to induction (1.0 ± 0.1 and 1.0 ± 0.2 min, P = 0.39), time to recovery (17.4 ± 4.6 and 18.2 ± 3.8 min, P = 0.70), heart rate (P = 0.62), arterial blood pressure (P = 0.81), respiratory rate (P = 0.60), hemogram variables, prothrombin time (P = 0.89), activated partial thromboplastin time (P = 0.76), fibrinogen concentration (P = 0.52), platelet concentration (P = 0.55), or plasma propofol concentrations (P = 0.20). Induction with a propofol microemulsion or macroemulsion did not significantly vary with respect to vital signs, the hemogram, clotting variables, and plasma propofol concentrations.
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J. G. Bovill
Anesthetic Pharmacology: Reflections of a Section Editor
Anesth. Analg.,
November 1, 2007;
105(5):
1186 - 1190.
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