Nystatin standard preparation
Dissolve about 20 mg of
USP Nystatin RS, accurately weighed, in 40.0 mL of dimethyl sulfoxide in a 200-mL volumetric flask, dilute with methanol to volume, and mix. Transfer 4.0 mL of this solution to a 50-mL volumetric flask, dilute with methanol to volume, and mix.
Amphotericin B standard preparation
Dissolve about 50 mg of
USP Amphotericin B RS, accurately weighed, in 10.0 mL of dimethyl sulfoxide in a 50-mL volumetric flask, dilute with methanol to volume, and mix. Transfer 4.0 mL of this solution to a 50-mL volumetric flask, dilute with methanol to volume, and mix. Prepare this solution fresh daily.
Procedure
Concomitantly determine the absorbances of the
Nystatin and
Amphotericin B standard preparations and the
Test preparation in 1-cm cells at 304 nm and at 282 nm, with a suitable spectrophotometer, using a 1 in 62.5 solution of dimethyl sulfoxide in methanol as the blank. Calculate the percentage of amphotericin A taken by the formula:
in which
WN is the weight, in mg, of
USP Nystatin RS taken,
AB282 and
AB304 are the absorbances of the
Amphotericin B standard preparation at 282 nm and 304 nm, respectively,
AN282 and
AN304 are the absorbances of the
Nystatin standard preparation at 282 nm and 304 nm, respectively,
AU282 and
AU304 are the absorbances of the
Test preparation at 282 nm and 304 nm, respectively, and
WU is the weight, in mg, of the Amphotericin B taken: not more than 5%, calculated on the dried basis, is found.
[NOTEAmphotericin B intended for use in preparing dermatological creams, lotions, and ointments, and oral suspensions and capsules, contains not more than 15% of amphotericin A, calculated on the dried basis.
]