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Sbt apparatus

Manufactured by Erweka
Sourced in Germany

The SBT apparatus is a laboratory equipment designed for the disintegration testing of solid dosage forms, such as tablets and capsules. It operates based on the disintegration test method specified in pharmacopoeial regulations. The apparatus provides a standardized environment for the test, ensuring consistent and reproducible results.

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2 protocols using sbt apparatus

1

Evaluation of Suppository Hardness

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The hardness measurements were performed using an SBT apparatus (Erweka, Germany) at room temperature (22 ± 0.5 °C) to evaluate the mechanical resistance of the suppositories to crushing, i.e., to determine the mass at which the suppository breaks or crushes at room temperature [21 (link)]. One suppository of each dosage per formula was placed between two jaws applying a mass of 600 g, and a mass of 200 g was added to the rod attached to the upper jaw every minute until the suppository was crushed. The time taken to crush each tested suppository was recorded. This test was adapted from monograph 2.9.24 of the Ph. Eur. [22 ].
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2

Uniformity, Softening, and Disintegration of Suppositories

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The uniformity of mass of single-dose preparation test was carried out as follows: twenty suppositories were individually weighted (Mettler AT201 FACT Switzerland) from each formula. Average mass and standard deviation (SD) were calculated.
The softening time determination of lipophilic suppositories test was conducted using apparatus for measuring the softening time of suppositories (n = 3).
The disintegration of suppositories test was performed in water maintained at 37 °C ± 0.5 °C using ST30 apparatus (Erweka, Germany) (n = 3).
The resistance to rupture of suppositories test was carried out on 10 suppositories using SBT apparatus (Erweka, Germany) at room temperature (22 °C ± 0.5 °C). Results of above tests are shown in Table 2.
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