Diazoxide Oral Suspension
» Diazoxide Oral Suspension contains not less than 90.0 percent and not more than 110.0 percent of the labeled amount of diazoxide (C8H7ClN2O2S).
Packaging and storage Preserve in tight, light-resistant containers.
A: Place a portion of Oral Suspension, equivalent to about 50 mg of diazoxide, in a 50-mL volumetric flask, add 30 mL of 0.1 N sodium hydroxide, shake for 30 minutes, dilute with 0.1 N sodium hydroxide to volume, and mix: the solution so obtained responds to the Thin-Layer Chromatographic Identification Test 201, a solvent system consisting of a mixture of ethyl acetate, methanol, and ammonium hydroxide (17:4:3) being used.
B: The retention time of the major peak in the chromatogram of the Assay preparation corresponds to that in the chromatogram of the Standard preparation, both relative to the internal standard, as obtained in the Assay.
Uniformity of dosage units 905
for oral suspension packaged in single-unit containers: meets the requirements.
Deliverable volume 698
for oral suspension packaged in multiple-unit containers: meets the requirements.
Mobile phase, Internal standard solution, Standard preparation, and Chromatographic system Prepare as directed in the Assay under Diazoxide.
Assay preparation Transfer an accurately measured volume of freshly mixed Oral Suspension, equivalent to about 100 mg of diazoxide, to a 50-mL centrifuge tube, add 2 mL of water and 35 mL of methanol, shake for 15 minutes, and centrifuge for 5 minutes. Transfer the supernatant to a 200-mL volumetric flask. Repeat the extraction process two times, beginning with the addition of 2 mL of water, combine the extracts in the 200-mL volumetric flask, dilute with methanol to volume, and mix. Transfer 10.0 mL of this solution to a 100-mL volumetric flask, add 2.0 mL of Internal standard solution, dilute with a mixture of water and methanol (4:1) to volume, and mix.
Procedure Proceed as directed for Procedure in the Assay under Diazoxide. Calculate the quantity, in mg, of diazoxide (C8H7ClN2O2S) in each mL of the Oral Suspension taken by the formula:
2(C/V)(RU / RS)in which C is the concentration, in µg per mL, of USP Diazoxide RS in the Standard preparation; V is the volume, in mL, of Oral Suspension taken; and RU and RS are the peak response ratios obtained from the Assay preparation and the Standard preparation, respectively.
Auxiliary Information Please check for your question in the FAQs before contacting USP.Chromatographic Column
USP32NF27 Page 2117Pharmacopeial Forum: Volume No. 29(6) Page 1870
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.