Sentence examples for usp test from inspiring English sources

Exact(1)

To this end, we have developed an expedited tablet friability test method, using the existing USP test apparatus.

Similar(59)

The USP tests also failed to pinpoint the clinical interaction between content uniformity and dissolution variability.

The quantum yield standard, quinine sulfate (CAS: 207671-44-1, meetestingtespecificationsations), was purchased from Sigma-Aldrich.

The dissolution rates of the different SD were determined using 900 mL of phosphate buffer solution (pH 6.8) at 37 ± 0.5°C using a type II USP dissolution test apparatus (EDT-08L-Electrolab, Mumbai, India) run at 75 rpm.

The present work aims to predict drug release from novel site-specific release isoniazid pellets, in USP dissolution test apparatus 3, using the response surface methodology (RS M.

The ex vivo absorption profile of each formulation was determined using the modified apparatus and type II USP dissolution test apparatus (EDT-08L, Electrolab, Mumbai, India).

Dissolution study of curcumin microsponges was carried out in USP dissolution test apparatus II stirred at 100 rpm and temperature of 37 ± 0.5°C (Paddle type, Electro lab. EDT-08 11LX).

The most common dissolution testing system for solid dosage forms is the United States Pharmacopeia (USP) Dissolution Testing Apparatus 2. This apparatus is very sensitive to the initial location of the tablet, which cannot be controlled because the tablet is dropped into the vessel at the beginning of the test and it may rest at random locations at the vessel's bottom.

In all cases suture size 3-0 United States Pharmocopeia (USP) was tested.

In the pharmaceutical industry, the United States Pharmacopeia (USP) dissolution testing is commonly used for evaluating drug tablets, capsules, and nutritional dietary supplements, which also involves mixing sample with simulated gastric juice to cause the dissolution of active ingredients.

The results came as a surprise in comparison with traditional USP II tests, which were performed with 900 mL of simple buffered media, where the pH was raised by the buffered formulations only to values around 4, thus prohibiting discrimination between the two formulation designs (unpublished results).

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