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Sufentanil Citrate Injection
» Sufentanil Citrate Injection is a sterile solution of Sufentanil Citrate in Water for Injection. It contains the equivalent of not less than 90.0 percent and not more than 110.0 percent of the labeled amount of sufentanil citrate (C22H30N2O2S·C6H8O7).
CautionHandle Sufentanil Citrate Injection with great care, as it is a potent opioid analgesic.
Packaging and storage
Preserve in single-dose or multiple-dose containers, preferably of Type I glass.
Identification
A:
Ultraviolet Absorption
Solution:
50 µg per mL.
Medium:
Use Mobile phase prepared as directed in the Assay. [noteFor samples that do not require dilution to achieve 50 µg per mL, use Water for Injection as the medium for the Standard solution.]
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.
Bacterial endotoxins
pH
Particulate matter
Other requirements
It meets the requirements under Injections
Assay
Mobile phase and Chromatographic system
Prepare as directed in the test for Chromatographic purity under Sufentanil Citrate.
Standard preparation
Dissolve an accurately weighed quantity of USP Sufentanil Citrate RS in water, and dilute quantitatively, and stepwise if necessary, with water to obtain a solution having a known concentration of about 0.075 mg per mL.
Assay preparation
Use Sufentanil Citrate Injection.
Procedure
Separately inject equal volumes (about 100 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 sufentanil (C22H30N2O2S) in each mL of the Injection taken by the formula:
386.56 / 578.69C(rU / rS)
in which 386.56 and 578.69 are the molecular weights of sufentanil and sufentanil citrate, respectively; C is the concentration, in mg per mL, of USP Sufentanil Citrate RS in the Standard preparation; and rU and rS are the 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 3609
Pharmacopeial Forum: Volume No. 30(6) Page 2045
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.
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