Prednisolone Syrup
(Current title—not to change until June 1,2005)
Monograph title change—to become official June 1,2005
See Prednisolone Oral Solution
»Prednisolone Syrup contains not less than 90.0percent and not more than 110.0percent of the labeled amount of prednisolone (C21H28O5).It may contain alcohol.
Packaging and storage— Preserve in tight,light-resistant containers.
Identification— The retention time of the major peak in the chromatogram of the Assay preparationcorresponds to that in the chromatogram of the Standard preparation,as obtained in the Assay.
pHá791ñ: between 3.0and 4.5.
Alcohol content,Method IIá611ñ(if present): not less than 90.0%and not more than 115.0%of the labeled amount.
Assay—
Citrate buffer— Prepare a 0.0033Msolution of citric acid in water,adjust with 1Nsodium hydroxide to a pHof 6.2,and mix.
Diluting solution: a mixture of methanol and water (1:1).
Mobile phase— Prepare a filtered and degassed mixture of Citrate bufferand methanol (31:19).Make adjustments if necessary (see System Suitabilityunder Chromatography á621ñ).
System suitability solution— Dissolve suitable quantities of prednisolone and hydrocortisone in a mixture of methanol and water (1:1)to obtain a solution containing about 100µg per mLand 90µg per mL,respectively.
Standard preparation— Dissolve an accurately weighed quantity of USP Prednisolone RSin Diluting solution,and dilute quantitatively,and stepwise if necessary,with Diluting solutionto obtain a solution having a known concentration of about 0.1mg per mL.
Assay preparation— Transfer an accurately measured volume of Syrup,equivalent to about 5.0mg of prednisolone,to a 50-mLvolumetric flask,dissolve in Diluting solution,shake by mechanical means for 15minutes,dilute with Diluting solutionto volume,and mix.
Chromatographic system (see Chromatography á621ñ) The liquid chromatograph is equipped with a 254-nm detector and a 4.6-mm ×15-cm column that contains packing L10.The flow rate is about 1mLper minute.Chromatograph the System suitability solution,and record the peak responses as directed for Procedure:the relative retention times are about 0.8for hydrocortisone and 1.0for prednisolone;the resolution,R,between hydrocortisone and prednisolone is not less than 2.5;and the relative standard deviation for replicate injections is not more than 2.0%.
Procedure— Separately inject equal volumes (about 10µL)of the Standard preparationand the Assay preparationinto the chromatograph,record the chromatograms,and measure the responses for the major peaks.Calculate the quantity,in mg,of prednisolone (C21H28O5)in the volume of Syrup taken by the formula:
50C(rU/rS),
in which Cis the concentration,in mg per mL,of USP Prednisolone RSin the Standard preparation;and rUand rSare the peak responses obtained from the Assay preparationand the Standard preparation,respectively.
Auxiliary Information— Staff Liaison:Clydewyn M.Anthony,Ph.D.,Scientist
Expert Committee:(PA1)Pharmaceutical Analysis 1
USP28–NF23Page 1609
Pharmacopeial Forum:Volume No.28(2)Page 347
Phone Number:1-301-816-8139