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.
]