Resum
We evaluated the anti-edema/antinociceptive effects of subcutaneous free and liposomal morphine in rats with carrageenan-induced inflammation of the paw. We assessed antinociception by the paw pressure test and edema by plethysmography. Unilamellar liposomes (150–200 nm) with 0.3% morphine hydrochloride were used; encapsulation signifcantly reduced the rate for release of morphine in vitro. During inflammation, the antinociceptive potency of free, but not liposomal morphine increased 2.5 times; moreover, duration of the effects was prolonged by encapsulation (p < 0.001). The anti-edema effects of liposomal morphine were more pronounced (p < 0.001) and of longer duration (p < 0.05). All the effects were reversed by naloxone. The results show that morphine encapsulation enhances the anti-edema effects and prolongs antinociception.
Idioma original | No s'ha definit/desconegut |
---|---|
Pàgines (de-a) | 121-127 |
Nombre de pàgines | 7 |
Revista | Pharmacology |
Volum | 60 |
Número | 3 |
DOIs | |
Estat de la publicació | Publicada - d’abr. 2000 |
Paraules clau
- Opioids
- Liposomal morphine
- Acute inflammation
- Antinociception
- Antiedema effect
- Anti-inflammatory effect