Spectinomycin for Injectable Suspension
» Spectinomycin for Injectable Suspension contains an amount of Spectinomycin Hydrochloride equivalent to not less than 90.0 percent and not more than 120.0 percent of the labeled amount of spectinomycin (C14H24N2O7).
Packaging and storage— Preserve in Containers for Sterile Solids as described under Injections 1.
pH 791: between 4.0 and 7.0, in the suspension constituted as directed in the labeling.
Other requirements— It conforms to the Definition, responds to the Identification test, and meets the requirements for Crystallinity, Bacterial endotoxins, Sterility, Water, and Residue on ignition under Spectinomycin Hydrochloride. It meets also the requirements for Uniformity of Dosage Units 905 and Labeling under Injections 1.
Assay—
Internal standard solution , Standard preparation, and Chromatographic system—Prepare as directed in the Assay under Spectinomycin Hydrochloride.
Assay preparation 1— Suspend the contents of 1 container of Spectinomycin for Injectable Suspension in water, and dilute quantitatively with water to obtain a stock solution containing about 20 mg of spectinomycin per mL. Transfer 1.0 mL of this solution to a glass-stoppered, 25-mL conical flask, and freeze-dry. Add 10.0 mL of Internal standard solution and 1.0 mL of hexamethyldisilazane, and shake intermittently for 1 hour.
Assay preparation 2 (where the label states the quantity of spectinomycin in a given volume of constituted suspension)—Constitute 1 container of Spectinomycin for Injectable Suspension in a volume of water, accurately measured, corresponding to the volume of diluent specified in the labeling. Dilute an accurately measured portion of the constituted suspension quantitatively with water to obtain a stock solution containing about 20 mg of spectinomycin per mL. Transfer 1.0 mL of this solution to a glass-stoppered, 25-mL conical flask, and freeze-dry. Add 10.0 mL of Internal standard solution and 1.0 mL of hexamethyldisilazane, and shake intermittently for 1 hour.
Procedure— Proceed as directed in the Assay under Spectinomycin Hydrochloride. Calculate the quantity, in g, of C14H24N2O7 in the container of Spectinomycin for Injectable Suspension taken to prepare Assay preparation 1 taken by the formula:
(L1 / D1)(P / 1000)(WS)(RU / RS)
in which L1 is the labeled quantity, in g, of C14H24N2O7 in the container, and D1 is the concentration, in mg per mL, of spectinomycin in the stock solution used to prepare Assay preparation 1, on the basis of the labeled quantity in the container and the extent of dilution, and the other terms are as defined therein. Calculate the quantity, in mg, of C14H24N2O7 in each mL of constituted Injectable Suspension taken to prepare Assay preparation 2 taken by the formula:
(L2 / D2)(P / 1000)(WS)(RU / RS)
in which L2 is the labeled quantity, in mg, of C14H24N2O7 in each mL of constituted suspension of Spectinomycin for Injectable Suspension, and D2 is the concentration, in mg per mL, of spectinomycin in the stock solution used to prepare Assay preparation 2, on the basis of the labeled quantity in each mL of constituted suspension and the extent of dilution.
Auxiliary Information— Please check for your question in the FAQs before contacting USP.
Topic/Question Contact Expert Committee
Monograph Ahalya Wise, M.S.
Scientist
1-301-816-8161
(MDANT05) Monograph Development-Antibiotics
Reference Standards Lili Wang, Technical Services Scientist
1-301-816-8129
RSTech@usp.org
USP32–NF27 Page 3592
Pharmacopeial Forum: Volume No. 34(5) Page 1193
Chromatographic Column—
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.