NALBUPHINE

NALBUPHINE Chemische Eigenschaften,Einsatz,Produktion Methoden

• Originator

  Nubain,Du Pont,US,1979

• Manufacturing Process

  To a slurry of 110.5 g of 14-hydroxydihydronormorphinone in 2.5 liters of methylene chloride and 280 ml of triethylamine was added a solution of 106 g of cyclobutanecarboxylic acid chloride in 500 ml of methylene chloride. The temperature of the reaction mixture was maintained at 20°C to 25°C during the addition. After 5 minutes the reaction mixture was brought to reflux and heated for 5 hours.
  It was then cooled, washed with water, dried over sodium sulfate and evaporated to dryness. The residue was crystallized from benzene and pentane to give 138.5 g of the dicyclobutanecarbonyl derivative, melting point about 112°C (dec.).
  The dicyclobutanecarbonyl derivative (136.7 g) was dissolved in 200 ml of tetrahydrofuran and added dropwise to a suspension of 34.2 g of lithium aluminum hydride in 1 liters of tetrahydrofuran. The temperature of the mixture rose to reflux during the addition. Reflux was maintained for 2 hours after the addition was completed. After cooling, 110 ml of ethyl acetate was added dropwise, followed by 30 ml of water, followed by a solution of 53 g of ammonium chloride in 125 ml of water. The resulting mixture was filtered and the inorganic precipitate was washed with methanol. Evaporation of the combined filtrates gave 66 g of N-cyclobutylmethyl-14-hydroxydihydronormorphinone, melting point 229°C to 231°C.

• Therapeutic Function

  Analgesic

• Biologische Funktion

  Nalbuphine (Nubain) is a mixed agonist–antagonist that is similar in structure to both the antagonist naloxone and the agonist oxymorphone. It is administered parenterally and is equipotent to morphine and 5 times as potent as pentazocine.Although the pharmacological effects (analgesia, respiratory depression, sedation, and so on) are similar to those produced by pentazocine, nalbuphine produces fewer psychotomimetic effects. It differs from pentazocine in that it has far greater antagonist than agonist effect.Thus, its use is likely to precipitate severe withdrawal in opioid-dependent patients. It is used much as pentazocine is, that is, for moderate to severe pain, postsurgical anesthesia, and obstetrical analgesia. Nalbuphine’s abuse potential is less than that of codeine and propoxyphene, although tolerance and dependence have been shown following chronic administration. High doses are perceived by addicts as being like those of the barbiturates.Drug interactions and contraindications are similar to those for pentazocine and morphine.

• Allgemeine Beschreibung

  Nalbuphine (Nubain) is structurally a member of thephenanthrene class of compounds and resembles oxymorphonewith a cyclobutyl methyl group on the nitrogen,equivalent to naloxone’s substitution. It was introduced in1979 as an agonist/antagonist with the hope of becoming aneffective pain reliever with little abuse potential. Althoughthe abuse potential of nalbuphine is low, it is not zero, andincreasing reports of diversion and abuse can be found in theliterature and the Internet. At low parenteral doses(<0.5 mg), it has an analgesic potency approximately twothirds that of morphine, and it has a similar degree of respiratorydepression. However, escalating doses above 30 mgdoes not produce further respiratory depression. The oralbioavailability of nalbuphine is only 12%, and the drug isonly marketed as an injectable. Patents have been filed foran oral extended-release formulation, and it is presently inphase II testing. The pharmacologic profile of nalbuphinein animal studies includes agonist activity at the κ-receptorand antagonist activity at the μ-receptor. Clinical studieshave shown that nalbuphine, and κ-agonists in general, mayhave better analgesic activity in female patients comparedwith male patients. Used as the sole opioid agent, nalbuphinehas been used successfully to treat the pain of labor,cesarean section, dental extraction, hip replacement, andhysterectomy surgery. Nalbuphine also may have a role intreating opioid-induced pruritus, because it can reverse thepruritus without reversing the analgesic effect when used inlow doses. Nalbuphine is marketed as an injectable (10 and20 mg/mL).

NALBUPHINE Upstream-Materialien And Downstream Produkte