Dexmedetomidine Chemische Eigenschaften,Einsatz,Produktion Methoden
Beschreibung
Dexmedetomidine has an eight times increased affinity for the α2-receptor
compared with clonidine and therefore produces less cardiovascular
instability at comparable doses.
Verwenden
Dexmedetomidine is principally used as a sedative in
mechanically ventilated patients in ICU. I t is particularly useful in those
patients with delirium.
Mechanism of action
Dexmedetomidine is metabolised via hepatic glucuronidation, and clearance is reduced in patients with liver impairment. Very lile unchanged drug reaches the urine, but 95% of degradation products are excreted this way (4% in faeces). There is a theoretical possibility of accumulation of metabolites in patients with renal failure, but toxicity has not been described because active metabolites of dexmedetomidine have not been identified at present.
Pharmakokinetik
Dexmedetomidine is freely soluble in water and has a pKa of 7.1. The pharmaceutical formulation is a clear, colourless preservative-free solution with a pH of 4.5–8. Protein binding of dexmedetomidine is 94%, with negligible displacement by drugs commonly used in anaesthetic and I CU practice. The elimination half-life is approximately 2h and the steady-state volume of distribution is 118 l. There are no significant differences in the pharmacokinetic profile in the elderly, but an enhanced clinical response is seen.
Dexmedetomidine Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
