Packaging and storage
Preserve in tight, light-resistant containers.
Identification
A:
Place about 50 mg of Fluphenazine Decanoate and about 50 mg of
USP Fluphenazine Decanoate Dihydrochloride RS in separate, glass-stoppered, small centrifuge tubes, and treat each tube as follows. Add 1.5 mL of sodium hydroxide solution (1 in 250), and mix. Add 2 mL of carbon disulfide, shake vigorously for 2 minutes, and centrifuge. Dry the lower, clear layer by filtering through 2 g of anhydrous sodium sulfate: the IR absorption spectrum of the test preparation, determined in a 0.1-mm cell, exhibits maxima only at the same wavelengths as that of the Standard preparation, similarly measured.
B:
Use a suitable thin-layer chromatographic plate (see
Chromatography
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) coated with a 0.25-mm layer of chromatographic silica gel mixture. Impregnate the plate with a 1 in 20 solution of tetradecane in hexane, and allow to air-dry. Prepare a test solution in alcohol containing 20 mg per mL. Apply 1 µL each of the test solution and of a Standard solution of
USP Fluphenazine Decanoate Dihydrochloride RS in alcohol, similarly prepared. Allow the spots to dry. Apply to the spot from the Standard solution, 1.0 µL of 0.1 N sodium hydroxide and allow it to dry. Develop the plate in an equilibrated chamber using a mixture of methanol and water (9:1) as the mobile phase. Examine the plate under short-wavelength UV light at 254 nm: the
RF value of the principal spot obtained from the test solution corresponds to that obtained from the Standard solution.
Loss on drying
731
Dry it in vacuum at 60
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for 3 hours: it loses not more than 1.0% of its weight.
Ordinary impurities
466
Test solution:
methanol.
Standard solution:
methanol.
Eluant
: a mixture of acetone, cyclohexane, and ammonium hydroxide (16:6:1).
Visualization:
1; then spray the plate with 50% sulfuric acid.
Interpretation:
no individual ordinary impurity observed exceeds 1.0% and the total of any ordinary impurities observed does not exceed 2.0%.
Assay
Dissolve about 500 mg of Fluphenazine Decanoate, accurately weighed, in 50 mL of glacial acetic acid, add one drop of
crystal violet TS, and titrate with 0.1 N perchloric acid VS to a blue-green endpoint. Perform a blank determination, and make any necessary correction. Each mL of 0.1 N perchloric acid is equivalent to 29.59 mg of C
32H
44F
3N
3O
2S.
Auxiliary Information
Staff Liaison :
Ravi Ravichandran, Ph.D., Senior Scientist
Expert Committee : (MDPP05) Monograph Development-Psychiatrics and Psychoactives
USP29NF24 Page 947
Pharmacopeial Forum : Volume No. 29(6) Page 1887
Phone Number : 1-301-816-8330