(e rith'' roe mye' sin es' toe late).
Erythromycin, 2¢-propanoate, dodecyl sulfate (salt).
Erythromycin 2¢-propionate dodecyl sulfate (salt) [3521-62-8].
» Erythromycin Estolate has a potency equivalent to not less than 600 µg of erythromycin (C37H67NO13) per mg, calculated on the anhydrous basis.
Packaging and storage Preserve in tight containers.
USP Reference standards 11
Identification, Infrared Absorption 197K.
Crystallinity 695: meets the requirements.
Water, Method I 921: not more than 4.0%, 20 mL of methanol containing 10% of imidazole being used in place of methanol in the titration vessel.
Free erythromycin Prepare a test solution of it in methanol containing 10.0 mg per mL. Prepare a Standard solution of USP Erythromycin RS in methanol containing 0.3 mg per mL. [notePrepare these solutions immediately before use. ] Prepare a suitable thin-layer chromatographic plate (see Chromatography 621) coated with a 0.25-mm layer of chromatographic silica gel mixture. Before using, place the plate in an unlined developing chamber containing about 100 mL of methanol, and allow the solvent front to move to the top of the plate, marking the direction of travel. Remove the plate, and allow to dry. Apply separate 1-µL volumes of the test solution and the Standard solution on the plate, allow the spots to dry, and develop the chromatograms in a freshly prepared solvent system consisting of a mixture of methanol and chloroform (85:15) until the solvent front has moved about one-half of the length of the plate. Remove the plate from the developing chamber, mark the solvent front, and allow the plate to dry. Place the plate under a hood, and spray uniformly with a solution consisting of 150 mg of xanthydrol dissolved in a mixture of hydrochloric acid and glacial acetic acid (92.5:7.5). Heat the sprayed plate in an oven at 100 for 5 minutes. [CautionAvoid exposure to acid fumes when removing the plate from the oven. ] Examine the plate for reddish violet spots: free erythromycin has an RF value of about 0.3, and erythromycin estolate has an RF value of about 0.7. Any spot corresponding to free erythromycin obtained from the test solution does not exceed in size or intensity that of the principal spot obtained from the Standard solution (3.0%).
Assay Proceed with Erythromycin Estolate as directed for erythromycin under AntibioticsMicrobial Assays 81, using an accurately weighed quantity of Erythromycin Estolate dissolved in methanol to obtain a solution containing the equivalent of 1.0 mg of erythromycin per mL. Immediately dilute quantitatively with 9 volumes of Buffer No. 3, and allow to stand at room temperature for 18 hours. Dilute a portion of this solution quantitatively with Buffer No. 3 to obtain a Test Dilution having a concentration assumed to be equal to the median dose level of the Standard.
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USP35NF30 Page 3084