Assay
Mobile phase
Prepare a suitable filtered and degassed mixture of water and acetonitrile (9:1).Make adjustments if necessary (see
System Suitabilityunder
Chromatography á621ñ).
Standard preparation
Dissolve an accurately weighed quantity of
USP Thiotepa RSin
Mobile phaseto obtain a solution having a known concentration of about 1.5mg per mL.
Assay preparation
Transfer about 75mg of Thiotepa,accurately weighed,to a 50-mLvolumetric flask,dissolve in Mobile phase,dilute with Mobile phaseto volume,and mix.
Resolution solution
Transfer about 10mg of
USP Thiotepa RSto a 4-mLvial,add 2mLof methanol,and mix.Add 50µLof 0.1%phosphoric acid solution.Place a cap on the vial,and heat at 65

for 50seconds.Cool the solution,add 1mLof methanol,and mix.
Chromatographic system
(see
Chromatography á621ñ)The liquid chromatograph is equipped with a 215-nm detector and a 4-mm ×15-cm column that contains packing L1.The flow rate is about 0.8mLper minute.Chromatograph the
Resolution solution,and record the peak responses as directed for
Procedure:the relative retention times are about 1.25for methoxythiotepa and 1.0for thiotepa,and the resolution,
R,between the methoxythiotepa peak and the thiotepa peak is not less than 3.0.Chromatograph the
Standard preparation,and record the responses as directed for
Procedure:the tailing factor for the thiotepa peak is not more than 1.8,the column efficiency is not less than 2600theoretical plates,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 C
6H
12N
3PSin the portion of Thiotepa taken by the formula:
50C(rU/rS),
in which
Cis the concentration,in mg per mL,of
USP Thiotepa RSin the
Standard preparation,and
rUand
rSare the thiotepa peak responses obtained from the
Assay preparationand the
Standard preparation,respectively.