Labeling
Label it to include the following, in addition to the information specified for
Labeling under
Injections 1: the time and date of constitution; the volume of constitution; the amount of
99mTc as labeled sestamibi expressed as total megabecquerels (or millicuries) per mL at the time of constitution; the expiration date and time; the lot number; and the statement CautionRadioactive Material. The labeling indicates that in making dosage calculations, correction is to be made for radioactive decay, and also indicates that the radioactive half-life of
99mTc is 6.0 hours.
Bacterial endotoxins 85
It contains not more than 175/
V USP Endotoxin Units per mL, in which
V is the maximum recommended total dose, in mL, at the expiration date or time.
Radiochemical purity
Preparation of the test vials
Constitute each of 4 vials with 1 mL (1875 ± 187.5 MBq, or 50 ± 5 mCi) of Sodium Pertechnetate Tc 99m Injection. Heat the vials in boiling water for 10 minutes. After heating, allow the vials to cool to room temperature for 15 minutes.
Method 1
(Thin-layer chromatography)Apply 1 to 2 µL of Injection about 1 cm from the bottom of a 25-mm × 7.75-cm reverse-phase chromatographic plate, and allow to dry (see
Chromatography 621). Position the plate in a chromatographic chamber and develop the chromatograms in a freshly prepared (not more than 4 hours) solvent system consisting of a mixture of acetonitrile, methanol, 3.85% ammonium acetate, and tetrahydrofuran (4:3:2:1) until the solvent front has moved about 6 cm from the origin. Remove the plate and allow it to air-dry. Determine the radioactivity distribution by scanning the chromatogram with a suitable radiation detector. A mean of not less than 90% (area %) of the radioactivity is found at an
RF value between 0.3 and 0.6. Free pertechnetate is located at about the
RF 0.8 to 1.0, and radiocolloid is located at about
RF 0 to 0.1. The sum of the mean percentages of free pertechnetate and colloid does not exceed 10%.
Method 2
(High-pressure liquid chromatography)
MOBILE PHASE
Prepare a filtered and degassed mixture of methanol, 0.05
M ammonium sulfate solution, and acetonitrile (45:35:20). Make adjustments if necessary (see
System Suitablity under
Chromatography 621).
CHROMATOGRAPHIC SYSTEM (see Chromatography 621)
The liquid chromatograph is equipped with a 3.9-mm × 30-cm column that contains 10-µm packing L1. It is also equipped with a flow-through gamma-ray detector. The flow rate is about 2 mL per minute. If
99mTc pentamibi dimethylvinyl isonitrile is present, the relative retention between the
99mTc sestamibi peak and the
99mTc pentamibi dimethylvinyl isonitrile peak is 1.3 to 1.5.
PROCEDURE
Inject about 5 µL (9.375 MBq or 250 µCi) of
Sodium Pertechnetate Tc 99m Injection into the chromatograph, and adjust the integrator/recording device so that the peak is 25% to 100% of full scale. Separately inject equal volumes (about 5 µL, 9.375 MBq, or 250 µCi) of the injection under test into the chromatograph, record the chromatograms, and measure the area percentage for all of the peaks present. The retention time for
99mTc sestamibi is about 5 to 10 minutes. The retention time for
99mTc pentamibi dimethylvinyl isonitrile is about 6 to 13 minutes. Correct for the presence of colloid, which is not measured by this method, taken by the equation:
Cf = [(100%)
(
Ac)] / 100,
in which
Cf is the correction factor, and
Ac is the mean area percentage for the colloid obtained from
Method 1. Obtain corrected area percentage by multiplying the correction factor (
Cf) by the area percentage of the peaks present in the chromatogram. A mean of not less than 90% (corrected area percentage) of the total radioactivity is represented by
99mTc sestamibi, and a mean of not more than 5% (corrected area percentage) of the total radioactivity is present as
99mTc pentamibi dimethylvinyl isonitrile.
Other requirements
It meets the requirements of the tests for
Radionuclide identification and
Radionuclidic purity under
Sodium Pertechnetate Tc 99m Injection. It meets also the requirements for
Injections 1, except that it may be distributed and dispensed prior to the completion of the test for
Sterility, the latter being started on the day of manufacture, and except that it is not subject to the recommendation on
Volume in Container.
Assay for radioactivity 821
Using a suitable counting assembly (see
Selection of a Counting Assembly), determine the radioactivity, in MBq (or in mCi) per mL, of the Injection by use of a calibrated system.