A:
Place a quantity of Oral Suspension, equivalent to about 100 mg of sulfamethoxazole, in a 50-mL centrifuge tube; add 5 mL of ammonium hydroxide; and shake gently. Add 25 mL of methanol, shake thoroughly for 3 minutes, centrifuge, decant the supernatant into a 50-mL volumetric flask, dilute with methanol to volume, and mix. Apply 50 µL of this solution and 50 µL of a solution prepared by dissolving 100 mg of
USP Sulfamethoxazole RS in 5 mL of ammonium hydroxide and diluting with methanol to 50.0 mL to a suitable thin-layer chromatographic plate (see
Chromatography 621) coated with a 0.25-mm layer of chromatographic silica gel. Allow the spots to dry, and develop the chromatogram in a solvent system consisting of a mixture of alcohol,
n-heptane, chloroform, and glacial acetic acid (25:25:25:7) until the solvent front has moved about three-fourths of the length of the plate. Remove the plate from the developing chamber, mark the solvent front, and allow the solvent to evaporate. Locate the spots on the plate by lightly spraying with a solution prepared by dissolving 0.10 g of
p-dimethylaminobenzaldehyde in 1 mL of hydrochloric acid and diluting with alcohol to 100 mL: the
RF value of the principal spot obtained from the test solution corresponds to that obtained from the Standard solution.