Spectinomycin Hydrochloride
495.354H-Pyrano[2,3-b][1,4]benzodioxin-4-one, decahydro-4a,7,9-trihydroxy-2-methyl-6,8-bis(methylamino)-, dihydrochloride, pentahydrate, [2R-(2
,4a
,5a,6,7,8,9,9a,10a)]-.
(2R,4aR,5aR,6S,7S,8R,9S,9aR,10aS)-Decahydro-4a,7,9-trihydroxy-2-methyl-6,8-bis(methylamino)-4H-pyrano[2,3-b]1,4]benzodioxin-4-one dihydrochloride pentahydrate
[22189-32-8].Anhydrous 405.28
[21736-83-4].» Spectinomycin Hydrochloride has a potency equivalent to not less than 603 µg of spectinomycin (C14H24 N2O7) per mg.
Packaging and storage—
Preserve in tight containers.
Labeling—
Where it is intended for use in preparing injectable dosage forms, the label states that it is sterile or must be subjected to further processing during the preparation of injectable dosage forms.
Identification, Infrared Absorption 
197M
—
Do not dry specimen.
197M—
Do not dry specimen.
Crystallinity 695:
meets the requirements.
695:
meets the requirements.
Bacterial endotoxins 85—
Where the label states that Spectinomycin Hydrochloride is sterile or that it must be subjected to further processing during the preparation of injectable dosage forms, it contains not more than 0.09 USP Endotoxin Unit per mg of spectinomycin.
85—
Where the label states that Spectinomycin Hydrochloride is sterile or that it must be subjected to further processing during the preparation of injectable dosage forms, it contains not more than 0.09 USP Endotoxin Unit per mg of spectinomycin.
Sterility 71—
Where the label states that Spectinomycin Hydrochloride is sterile, it meets the requirements when tested as directed for Membrane Filtration under Test for Sterility of the Product to be Examined.
71—
Where the label states that Spectinomycin Hydrochloride is sterile, it meets the requirements when tested as directed for Membrane Filtration under Test for Sterility of the Product to be Examined.
pH 791:
between 3.8 and 5.6, in a solution containing 10 mg per mL.
791:
between 3.8 and 5.6, in a solution containing 10 mg per mL.
Water, Method I 921:
between 16.0% and 20.0%.
921:
between 16.0% and 20.0%.
Residue on ignition 281:
not more than 1.0%, the charred residue being moistened with 2 mL of nitric acid and 5 drops of sulfuric acid.
281:
not more than 1.0%, the charred residue being moistened with 2 mL of nitric acid and 5 drops of sulfuric acid.
Assay—
Internal standard solution—
Dissolve triphenylantimony in dimethylformamide to obtain a solution containing about 2 mg per mL.
Standard preparation—
Transfer about 30 mg of USP Spectinomycin Hydrochloride RS, accurately weighed, to a glass-stoppered, 25-mL conical flask. Add 10.0 mL of Internal standard solution and 1.0 mL of hexamethyldisilazane, and shake intermittently for 1 hour.
Assay preparation—
Proceed as directed under Standard preparation using Spectinomycin Hydrochloride.
Chromatographic system
(see Chromatography 621)—The gas chromatograph is equipped with a flame-ionization detector and contains a 3-mm × 60-cm glass column packed with 5 percent phase G27 on 80- to 100-mesh support S1AB. The column and detector are maintained at about 190
and 220, respectively, and the injection port at about 215, and dry helium is used as the carrier gas at a flow rate of about 45 mL per minute. Chromatograph the Standard preparation, and record the chromatogram as directed for Procedure: the resolution, R, between the major peaks is not less than 2.0; and the relative standard deviation of the peak response ratios, RS, from replicate injections of the Standard preparation is not more than 3.5%.
621)—The gas chromatograph is equipped with a flame-ionization detector and contains a 3-mm × 60-cm glass column packed with 5 percent phase G27 on 80- to 100-mesh support S1AB. The column and detector are maintained at about 190 and 220, respectively, and the injection port at about 215, and dry helium is used as the carrier gas at a flow rate of about 45 mL per minute. Chromatograph the Standard preparation, and record the chromatogram as directed for Procedure: the resolution, R, between the major peaks is not less than 2.0; and the relative standard deviation of the peak response ratios, RS, from replicate injections of the Standard preparation is not more than 3.5%.
Procedure—
Separately inject equal volumes (about 1 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 ratio, RU, of the response of the spectinomycin peak to the response of the internal standard peak in the chromatogram from the Assay preparation, and similarly calculate the ratio, RS, in the chromatogram from the Standard preparation. Calculate the quantity, in µg, of C14H24N2O7 in the portion of Spectinomycin Hydrochloride taken to prepare the Assay preparation by the formula:
P(WS)(RU / RS)
in which P is the potency of USP Spectinomycin Hydrochloride RS, in µg of spectinomycin per mg; and WS is the weight, in mg, of USP Spectinomycin Hydrochloride RS taken from the Standard preparation; and the other terms are as defined above.
Auxiliary Information—
Please check for your question in the FAQs before contacting USP.
Chromatographic Column—
| 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 |
|
| 85 |
Radhakrishna S Tirumalai, Ph.D.
Senior Scientist 1-301-816-8339 |
(MSA05) Microbiology and Sterility Assurance |
| 71 |
Radhakrishna S Tirumalai, Ph.D.
Senior Scientist 1-301-816-8339 |
(MSA05) Microbiology and Sterility Assurance |
USP32–NF27 Page 3592
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.