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Ketamine hydrochloride is Off-White Solid

Ketanest,Parke Davis,W. Germany,1969

Anesthetic (intravenous). Controlled substance (depressant).

ChEBI: The hydrochloride salt of ketamine.

ketamine: A vetinary anaesthetic that is used illegally as a club drug. Itis a class A drug in the UK.

The 1-hydroxycyclopentyl-(o-chlorophenyl)-ketone N-methylimine used as an intermediate is prepared as follows. To the Grignard reagent prepared from 119.0 g of cyclopentyl bromide and 19.4 g of magnesium is added 55.2 g of o-chlorobenzonitrile. The reaction mixture is stirred for 3 days and thereafter hydrolyzed in the usual manner. From the hydrolysis there is obtained ochlorophenylcyclopentylketone, BP 96° to 97°C (0.3 mm), nD251.5452. To 21.0 g of the ketone is added 10.0 g of bromine in 80 ml of carbon tetrachloride.
1-Bromocyclopentyl-(o-chlorophenyl)-ketone, BP 111° to 114°C (0.1 mm) is isolated in the usual manner. Since it is unstable, it must be used immediately. The bromoketone (29.0 g) is dissolved in 50 ml of liquid methylamine. After one hour, the excess liquid methylamine is allowed to evaporate. The organic residue is dissolved in pentane, and upon evaporation of the solvent, 1-hydroxycyclopentyl-(o-chlorophenyl)-ketone N-methylimine, MP 62°C, is isolated.
1-Hydroxycyclopentyl-(o-chlorophenyl)-ketone N-methylimine (2.0 g) is dissolved in 15 ml of Decalin and refluxed for 2,5 hours. After evaporation of the Decalin under reduced pressure, the residue is extracted with dilute hydrochloric acid, the solution treated with decolorizing charcoal, and the resulting acidic solution is made basic. The liberated product, 2-methylamino- 2-(o-chlorophenyl)-cyclohexanone, after crystallization from pentane-ether, has MP 92° to 93°C. The hydrochloride of this compound has MP 262° to 263°C.

Ketalar (Parkdale).

Anesthetic

Ketamine is a cyclohexanone derivative whose pharmacological actions are quite different from those of the other IV anesthetics. The state of unconsciousness it produces is trancelike (i.e., eyes may remain open until deep anesthesia is obtained) and cataleptic; it has frequently been characterized as dissociative (i.e., the patient may appear awake and reactive but does not respond to sensory stimuli). The term dissociative anesthesia is used to describe these qualities of profound analgesia, amnesia, and superficial level of sleep.

Ketamine is formulated as an acidic solution, pH 3.5 to 5.5,available with or without 0.1 mg/mL benzethonium chloridepreservative. Ketamine is marketed as the racemic mixtureand some properties of the individual isomers have beenelucidated. Ketamine is a rapid-acting agent that can beused for induction, used as the sole agent for general anesthesiaor combined with other agents. Unlike the proposedmechanism of action for most anesthetics, ketamine doesnot act at the GABAA receptor. Ketamine acts as a noncompetitiveantagonist at the glutamate, NMDA receptor, anonspecific ion channel receptor. The NMDA receptor is locatedthroughout the brain and contains four well-studiedbinding sites. The primary binding site binds L-glutamate,NMDA, and aspartate. The allosteric site binds glycine,which facilitates primary ligand binding. There is also amagnesium binding site that blocks ion flow through thechannel and a phencyclidine (PCP) binding site that blocksthe ion channel when occupied. Ketamine is believed tobind to the PCP site in a stereoselective manner and blockthe ion flow in the channel. By blocking the flow ofcalcium ions into the cell, ketamine prevents the calcium concentration from building and triggering excitatorysynaptic transmissions in the brain and spinal cord.

Non-competitive NMDA receptor antagonist (EC 50 values are 13.6 and 17.6 μ M for NR1/NR2A and NR1/NR2B subunit combinations respectively). Dissociative anesthetic.

Selective NMDA glutamate receptor antagonist; veterinary anesthetic.

Slow IV administration of ketamine does not cause gradual loss of airway reflexes, apnea, or general muscular relaxation.The onset of the ketamine-induced “anesthetic state” is accompanied by a gradual, mild increase in muscle tone (which greatly resembles catatonia), continued maintenance of pharyngeal and laryngeal reflexes, and opening of the eyes (usually accompanied by nystagmus). Although reflexes may be maintained, the airway still must be protected, since ketamine sensitizes laryngeal and pharyngeal muscles to mucous or foreign substances, and laryngospasm may occur.
Ketamine also can be contrasted to other intravenous drugs in its ability to cause cardiovascular stimulation rather than depression. The observed increases in heart rate and blood pressure appear to be mediated through stimulation of the sympathetic nervous system. In a healthy, normovolemic, unpremedicated patient, the initial induction dose of ketamine maintains or stimulates cardiovascular function. In contrast, patients with poor cardiac reserve, compromised autonomic control, or hypovolemia may undergo a precipitous fall in blood pressure after induction of anesthesia with ketamine. If selection of the patient and preoperative preparation are carefully done, however, ketamine may be an excellent drug for the induction of anesthesia in individuals who cannot tolerate compromise of their cardiovascular system.
The analgesia induced by ketamine also is a property that separates it from other IV anesthetic drugs. Analgesia is obtained without a deep level of anesthesia. When subdissociative doses of ketamine are given either IV or intramuscularly (IM), they provide adequate analgesia for postoperative pain relief as well as analgesia for brief operations on the skin, such as debridement of third-degree burns. Because it can be regarded as a nearly complete anesthetic (hypnosis and analgesia), does not require anesthesia equipment, and is relatively protective of hemodynamics, ketamine also can be very useful outside of normal operating room conditions, such as may be found during painful radiographic procedures.
A most important advantage of ketamine over other anesthetic agents is its potential for administration by the IM route.This is particularly useful in anesthetizing children, since anesthesia can be induced relatively quickly in a child who resists an inhalation induction or the insertion of an IV line. Ketamine has a limited but useful role as an IM induction agent and in pediatrics.

Like other dissociative anesthetics, ketamine isabused for its hallucinatory effects. Most of the illegallyused ketamine comes from stolen legitimate sources, particularlyfrom veterinary clinics or smuggled in fromMexico.
Ketamine is metabolized via N-demethylation to formthe main metabolite norketamine. Norketamine has aboutone third the potency of the parent compound. Minor metabolicpathways include hydroxylation of the cyclohexanonering; hydroxylation followed by glucuronide conjugation,and hydroxylation followed by dehydration to the cyclohexenonederivative.

The most serious disadvantage to the use of ketamine is its propensity to evoke excitatory and hallucinatory phenomena as the patient emerges from anesthesia. Patients in the recovery period may be agitated, scream and cry, hallucinate, or experience vivid dreams. These episodes may be controlled to some extent by maintaining a quiet reassuring atmosphere in which the patient can awaken or if necessary by administering tranquilizing doses of diazepam.
Other reported side effects include vomiting, salivation, lacrimation, shivering, skin rash, and an interaction with thyroid preparations that may lead to hypertension and tachycardia. Ketamine also may raise intracranial pressure and elevate pulmonary vascular resistance, especially in children with trauma or congenital heart disease. Increases in intraocular pressure also may occur, and vigilance is required if ketamine is used in ocular surgery.

Molecular weight (daltons) 274.2 (as hydrochloride) % Protein binding 20-50 % Excreted unchanged in urine 2 (88% as metabolites) Volume of distribution (L/kg) 4 Half-life - normal/ESRF (hrs) 2-4 / Unchanged

After intravenous boluses, ketamine shows a bi- or triexponential pattern of elimination. The alpha phase which lasts about 45 minutes, represents ketamine's anaesthetic action, and is terminated by redistribution from the CNS to peripheral tissues and hepatic biotransformation to an active metabolite norketamine. Other metabolic pathways include hydroxylation of the cyclohexone ring and conjugation with glucuronic acid. Ketamine is excreted mainly in the urine as metabolites.

Store at RT