Packaging and storage
Preserve in tight, light-resistant containers. Store at 25
, excursions permitted between 15
and 30
.
Identification
B:
Transfer about 50 mg of it to a 500-mL volumetric flask, add water to volume, and mix. Transfer 10.0 mL of the resulting solution to a 100-mL volumetric flask, add 2.0 mL of 0.1 N hydrochloric acid, dilute with water to volume, and mix to obtain a 1 in 100,000 solution: the UV absorption spectrum of the solution so obtained exhibits maxima and minima only at the same wavelengths as that of a similar solution of
USP Isoniazid RS, concomitantly measured.
Assay
Mobile phase
Dissolve 4.4 g of docusate sodium in 600 mL of methanol, add 400 mL of water, adjust with 2 N sulfuric acid to a pH of 2.5, and mix. Make adjustments if necessary (see
System Suitability under
Chromatography 621).
Standard preparation
Dissolve an accurately weighed quantity of
USP Isoniazid RS in
Mobile phase, and quantitatively dilute with
Mobile phase to obtain a solution having a known concentration of about 0.32 mg per mL.
Assay preparation
Transfer about 16 mg of Isoniazid, accurately weighed, to a 50-mL volumetric flask, dissolve in and dilute with Mobile phase to volume, and mix.
Chromatographic system (see Chromatography 621)
The liquid chromatograph is equipped with a 254-nm detector and a 4.6-mm × 25-cm column that contains packing L1. The flow rate is about 1.5 mL per minute. Chromatograph the
Standard preparation, and record the peak responses as directed for
Procedure: the column efficiency determined from the isoniazid peak is not less than 1800 theoretical plates; the tailing factor for the isoniazid peak is not more than 2.0; and the relative standard deviation for replicate injections is not more than 2.0%.
Procedure
Separately inject equal volumes (about 10 µL) of the
Standard preparation and the
Assay preparation into the chromatograph, record the chromatograms, and measure the responses for the major peaks. Calculate the quantity, in mg, of C
6H
7N
3O in the portion of Isoniazid taken by the formula:
50C(rU / rS),
in which
C is the concentration, in mg per mL, of
USP Isoniazid RS in the
Standard preparation; and
rU and
rS are the peak responses of isoniazid obtained from the
Assay preparation and the
Standard preparation, respectively.