» Isradipine Capsules contain not less than 90.0 percent and not more than 110.0 percent of the labeled amount of isradipine (C19H21N3O5).
Packaging and storage Store in a tight container at controlled room temperature. Protect from light.
USP Reference standards 11
USP Isradipine RS.
USP Isradipine Related Compound A RS.
A: Ultraviolet Absorption 197U
Solution Transfer the contents of 1 Capsule into a suitable volumetric flask, dissolve the contents in the Medium by mechanical shaking for 15 minutes, and dilute with Medium to obtain a solution containing 25 µg of isradipine per mL.
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, as obtained in the Assay.
Medium: 0.1% aqueous solution of lauryl dimethyl amine oxide (prepared by transferring 500 mL of deaerated water into the dissolution vessel, adding 1.65 mL of 30% lauryl dimethyl amine oxide, and mixing); 500 mL.
Apparatus 2: 50 rpm.
Time: 45 minutes.
Procedure Determine the amount of C19H21N3O5 dissolved by employing UV absorption at the wavelength of maximum absorbance at about 328 nm on filtered portions of the solution under test, suitably diluted with Medium, if necessary, in comparison with a Standard solution having a known concentration of USP Isradipine RS in the same Medium.
Tolerances Not less than 75% (Q) of the labeled amount of C19H21N3O5 is dissolved in 45 minutes.
Uniformity of dosage units 905: meet the requirements.
noteIsradipine is light sensitive. Throughout the following procedures, protect test or assay specimens, the Reference Standards, and solutions containing them from unnecessary exposure to light. Use low-actinic glassware, unless otherwise directed.
Mobile phase, Resolution solution, and Chromatographic system Proceed as directed in the test for Chromatographic purity under Isradipine.
Standard solution Dissolve an accurately weighed quantity of USP Isradipine RS in Mobile phase, with the aid of sonication if necessary, and dilute quantitatively, and stepwise if necessary, with Mobile phase to obtain a solution having a known concentration of about 1 µg per mL. [noteIf necessary, use 1 mL of methanol per 20 mL of Mobile phase to dissolve the Reference Standard prior to diluting with Mobile phase.]
Test solution Use the Assay preparation.
Procedure Separately inject equal volumes (about 25 µL) of the Standard solution and the Test solution into the chromatograph, record the chromatograms, and measure the responses for all the peaks: the sum of all peak responses, other than that of isradipine, from the Test solution is not more than four times the isradipine response obtained from the Standard solution (2.0%); and no single peak response is greater than that of the isradipine peak response obtained from the Standard solution (0.5%).
Mobile phase, Standard preparation, and Chromatographic system Proceed as directed in the Assay under Isradipine.
Assay preparation Remove, as completely as possible, the contents of not fewer than 20 Capsules, and mix the combined contents. Transfer an accurately weighed quantity, equivalent to about 25 mg of isradipine, to a 100-mL volumetric flask. Add 5.0 mL of methanol and 5.0 mL of Mobile phase, and sonicate at room temperature for 15 minutes. Shake for 15 minutes in a mechanical shaker. Dilute with Mobile phase to volume, mix, and filter, discarding the first 5 mL of the filtrate.
Procedure Separately inject equal volumes (about 25 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 isradipine (C19H21N3O5) in the portion of Capsules taken by the formula:
100C(rU / rS)in which C is the concentration, in mg per mL, of USP Isradipine RS in the Standard preparation; and rU and rS are the isradipine peak responses 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 2726Pharmacopeial Forum: Volume No. 30(2) Page 510
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.