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Librium (Chlordiazepoxide Hydrochloride) - Description and Clinical Pharmacology

 
 



LIBRIUM® C-IV
(chlordiazepoxide HCl)
CAPSULES

DESCRIPTION

Librium, the original chlordiazepoxide HCl and prototype for the benzodiazepine compounds, was synthesized and developed at Hoffmann-La Roche Inc.  It is a versatile therapeutic agent of proven value for the relief of anxiety.  Librium is among the safer of the effective psychopharmacologic compounds available, as demonstrated by extensive clinical evidence.

Librium is available as capsules containing 5 mg, 10 mg or 25 mg chlordiazepoxide HCl.  Each capsule also contains corn starch, lactose and talc.  Gelatin capsule shells may contain methyl and propyl parabens and potassium sorbate, with the following dye systems:  5-mg capsules – FD&C Yellow No. 6 plus D&C Yellow No. 10 and either FD&C Blue No. 1 or FD&C Green No. 3.  10-mg capsules – D&C Yellow No. 10 and either FD&C Blue No. 1 plus FD&C Red No. 3 or FD&C Green No. 3 plus FD&C Red No. 40.  25-mg capsules– D&C Yellow No. 10 and either FD&C Green No. 3 or FD&C Blue No. 1.

Chlordiazepoxide hydrochloride is 7-chloro-2- (methylamino) -5-phenyl-3H-1,4-benzodiazepine 4-oxide hydrochloride.  A white to practically white crystalline substance, it is soluble in water.  It is unstable in solution and the powder must be protected from light.  The molecular weight is 336.22.  The structural formula of chlordiazepoxide hydrochloride is as follows:

CLINICAL PHARMACOLOGY

Librium (chlordiazepoxide HCl) has antianxiety, sedative, appetite-stimulating and weak analgesic actions.  The precise mechanism of action is not known.  The drug blocks EEG arousal from stimulation of the brain stem reticular formation.  It takes several hours for peak blood levels to be reached and the half-life of the drug is between 24 and 48 hours.  After the drug is discontinued plasma levels decline slowly over a period of several days.  Chlordiazepoxide is excreted in the urine, with 1% to 2% unchanged and 3% to 6% as conjugate.

Animal Pharmacology

The drug has been studied extensively in many species of animals and these studies are suggestive of action on the limbic system of the brain, which recent evidence indicates is involved in emotional responses.

Hostile monkeys were made tame by oral drug doses which did not cause sedation. Chlordiazepoxide HCl revealed a “taming” action with the elimination of fear and aggression.  The taming effect of chlordiazepoxide HCl was further demonstrated in rats made vicious by lesions in the septal area of the brain.  The drug dosage which effectively blocked the vicious reaction was well below the dose which caused sedation in these animals.

The LD50 of parenterally administered chlordiazepoxide HCl was determined in mice (72 hours) and rats (5 days), and calculated according to the method of Miller and Tainter, with the following results:  mice, IV, 123±12mg/kg; mice, IM, 366±7mg/kg; rats, IV, 120±7 mg/kg; rats, IM, >160 mg/kg.

Effects on Reproduction

Reproduction studies in rats fed 10, 20 and 80 mg/kg daily and bred through one or two matings showed no congenital anomalies, nor were there adverse effects on lactation of the dams or growth of the newborn.  However, in another study at 100 mg/kg daily there was noted a significant decrease in the fertilization rate and a marked decrease in the viability and body weight of off-spring which may be attributable to sedative activity, thus resulting in lack of interest in mating and lessened maternal nursing and care of the young.  One neonate in each of the first and second matings in the rat reproduction study at the 100 mg/kg dose exhibited major skeletal defects.  Further studies are in progress to determine the significance of these findings.

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