Background: Because the valproic derivates are frequently used in the treatment of epilepsy, bipolar disorders, major depression cases, migraines and other neurological disorders at children, the rectal administration is a real advantage.
Aim: In this study we aimed to assess the influence of the formulation on the rheological characteristics of lipophilic suppository bases Suppocire NAI, Witepsol W35, Massa Estarinum299, Lipex403, containing Cetyl alcohol and Solutol HS15, respectively.
Methods: Spreadability was determined by the Pozo Ojeda-Sune Arbussa method. Half a gram suppository was placed on the bottom plaque of the extensiometer, and the upper plaque was added over it. After equal intervals of time (1 minute) different weights (2, 5, 10, 20, 30, 40, 50, 100, 150, 200, 250, 300, 350, 400, 500 g) were placed. Following each weight addition, the diameters of the obtained circles were measured, and the corresponding area was calculated. The viscosity was determined using the Brookfield (DV-II +Pro) rotational viscosimeter. The measurements were performed at 37±0.5°C and 5, 10, 20, 50, 100, 50, 20, 10, 5 rpm.
Results: The experimental results demonstrated that sodium valproate as active substance induces an increase in viscosity and consequently a decrease in the spreading capacity of the lipophilic suppository bases used. Lipex403 (a base consisting in fatty acids) manifests the lowest viscosity compared to the bases consisting in mixtures of glycerides (Suppocire NAI, Witepsol W35, Massa Estarinum 299). Solutol HS15 as emulsifier determines a higher decrease in viscosities and a better spreading capacity than Cetyl alcohol. Sodium valproate suppositories obtained with Lipex403 as excipient base show plastic flow characteristics without thixotropy.
Conclusions: The experimental results demonstrated that sodium valproate as active substance induces an increase in viscosity and consequently a decrease in the spreading capacity of the lipophilic suppository bases used. Solutol HS15 determines a higher decrease in viscosities and a better spreading capacity than Cetyl alcohol.
Tag Archives: suppositories
Formulation and Evaluation of Valproic Acid Suppositories for Children
Introduction: Rectal suppositories of valproic acid were prepared using different lipophilic excipients: Suppocire NAI, Adeps solidus 50, Adeps solidus 3, Lipex 403, Cacao oleum. Each prepared suppository has been evaluated for various physical parameters like weight variation, disintegration and softening time and crushing (breaking) strength.
Methods: Suppositories were prepared by fusion method. The quantity of active drug (valproic acid) added to the suppositories was 200 mg, thus resulting 1.0 g suppositories. Prepared suppositories were visually inspected. Randomly selected suppositories were cut longitudinally and the surfaces were examined with naked eye. For determination of weight variation, 20 suppositories were weighed and the average weight was determined. Disintegration time, softening time and breaking strength of the prepared suppositories were determined according to the 5th European Pharmacopoeia.
Results: All the suppositories were free from pits, fissures and cracks. All formulas studied were disintegrated in less than 30 minutes. Valproic acid decreased the disintegration time of suppositories. The used excipient also influences the disintegration time, with a greater effect on the F1 formula (Suppocire NAI). After one month of preservation, the disintegration time of all formulas increased, but was less than 30 minutes. The softening time of the suppositories was the largest for the F1 formula (Suppocire NAI). The softening time decreases in the presence of valproic acid. The softening time and breaking strength increased for all formulas after one month.
Conclusions: The prepared suppositories were within the permissible range of physical parameters. The results obtained allow the selection of excipients in order to assure the optimum characteristics for prepared suppositories.