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Acta anaesthesiologica Taiwanica : official journal of the Taiwan Society of Anesthesiologists 2005-Jun

The antinociceptive and anti-inflammatory effects of five depot formulations of ketorolac propyl ester in rats.

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Li-Kai Wang
Pei-Jung Wang
Chia-Hui Hou
Chin-Chen Chu
Jann-Inn Tzeng
Ja-Ping Shieh
Jhi-Joung Wang

Nøgleord

Abstrakt

BACKGROUND

Ketorolac is a potent nonsteroidal anti-inflammatory drug. Recently, a ketorolac prodrug, ketorolac propyl ester, was synthesized in our laboratory. The aim of the study was to evaluate the antinociceptive and anti-inflammatory effects of ketorolac propyl ester in five depot formulations. The vehicles used in these formulations were injectable vegetable oils, i.e., sesame oil, peanut oil, soybean oil, castor oil, and cottonseed oil. The traditional therapentic form of ketorolac tromethamine in saline was used as control.

METHODS

Six studies were carried out to test the antinociceptive and anti-inflammatory effects of intramuscular ketorolac tromethamine (in saline) and its propyl ester (in five depot formulations) 240 micromol/kg on Sprague-Dawley rats treated with intraplantar carrageenin.

RESULTS

Ketorolac tromethamine (in saline) produced an 8 h duration of action on both antinociception and anti-inflammation, whereas ketorolac propyl ester in five oily vehicles produced 54- to 78-h durations of actions in both antinociception and anti-inflammation. Ketorolac propyl ester in cottonseed oil produced a duration of action of 78h in both antinociception and anti-inflammation.

CONCLUSIONS

All five depot formulations of ketorolac propyl ester produced longer durations of antinociceptive and anti-inflammatory effects.

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