Assay
Standard preparation
Dissolve an accurately weighed quantity of
USP Chloramphenicol RS in
Mobile phase, and dilute quantitatively, and stepwise if necessary, with
Mobile phase to obtain a solution having a known concentration of about 100 µg per mL. Filter a portion of this solution through a 0.5-µm or finer porosity filter, and use the clear filtrate as the
Standard preparation.
Assay preparation
Transfer the contents of 1 container of Chloramphenicol for Ophthalmic Solution to a suitable container with the aid of Mobile phase, and dilute quantitatively, and stepwise if necessary, with Mobile phase to obtain a solution having a concentration of about 100 µg of chloramphenicol per mL. Filter a portion of this solution through a 0.5-µm or finer porosity filter, and use the clear filtrate as the Assay preparation.
Procedure
Proceed as directed for
Procedure in the
Assay under
Chloramphenicol. Calculate the quantity, in mg, of C
11H
12Cl
2N
2O
5 in the container of Chloramphenicol for Ophthalmic Solution taken by the formula:
(L / D)C(rU / rS),
in which
L is the labeled quantity, in mg, of chloramphenicol in the container,
D is the concentration, in µg per mL, of chloramphenicol in the
Assay preparation, based on the labeled quantity and the extent of dilution, and the other terms are as defined therein.