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midazolam + fentanyl + rocuronium + propofol + remifentanil

Development stage
Unknown
Lead developer
AkzoNobel
Modality
Peptides, Small Molecules
Administration
Intravenous
01

Overview

This is a combination of five intravenous anesthetic and adjunct agents commonly used in anesthesia and critical care for induction, maintenance, and facilitation of procedures requiring deep sedation, analgesia, muscle relaxation, and rapid recovery. - **Midazolam** is a short-acting benzodiazepine that provides anxiolysis, amnesia, sedation, muscle relaxation, and anticonvulsant effects by enhancing GABAergic neurotransmission[2]. - **Fentanyl** is a potent synthetic opioid agonist at the μ-opioid receptor providing strong analgesia[3][6]. - **Rocuronium** is a non-depolarizing neuromuscular blocker that induces skeletal muscle paralysis by competitively inhibiting acetylcholine at the neuromuscular junction. - **Propofol** is an intravenous hypnotic agent acting primarily via potentiation of GABA-A receptors to induce rapid-onset anesthesia with antiemetic properties[4][5][7]. - **Remifentanil** is an ultra-short acting μ-opioid receptor agonist used for profound analgesia during surgery or intensive care; it has rapid onset/offset due to metabolism by plasma esterases[7][10]. This combination enables comprehensive control over consciousness (sedation/hypnosis), pain (analgesia), immobility (muscle relaxation), and autonomic responses during invasive procedures such as intubation or major surgery. The drugs are titrated according to patient needs; their pharmacokinetic profiles allow for precise control over depth of anesthesia and quick recovery.

02

Targets

BZD site (GABA-A receptor benzodiazepine site)MOR (Mu opioid receptor)Muscle-type nicotinic acetylcholine receptorGABRR (GABA-A receptor subunit rho)

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