FORMULATION AND INVITRO EVALUATION OF TEMAZEPAM TABLETS FOR SUBLINGUAL DRUG DELIVERY SYSTEM
Navakoti Preethi* and Dr. M. Krishnaveni
Abstract
Temazepam, like many other similar and related benzodiazepines, acts
as a gamma-aminobutyric acid (GABA) modulator and is capable of
eliciting a variety of actions including sedation, hypnosis, skeletal
muscle relaxation, anticonvulsant activity, and anxiolytic action. In the
present work temazepam sublingual tablets using Locust bean gum,
Croscarmellose sodium and Crospovidone as super disintegrating
agents to enhance the solubility and dissolution rate of selected drug
molecule. All the formulations were prepared by direct compression
method using 6mm punch on 8 station rotary tablet punching machine.
The blend of all the formulations showed god flow properties such as
angle of repose, bulk density, tapped density. The prepared tablets
were shown good post compression parameters and they passed all the quality control
evaluation parameters as per I.P limits. Among all the formulations F3 formulation showed
maximum % drug release i.e., 98.13% in 8 min hence it is considered as optimized
formulation. The F3 formulation contains Locust bean gum as super disintegrate in the
concentration of 30 mg.
Keywords: Temazepam, sublingual tablets, Croscarmellose sodium, Locust bean gum and Crospovidone.
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