Technetium Tc 99m Pyrophosphate Injection »Technetium Tc 99m Pyrophosphate Injection is a sterile,aqueous solution,suitable for intravenous administration,of pyrophosphate that is labeled with 99mTc.It contains not less than 90.0percent and not more than 110.0percent of the labeled amount of 99mTc as pyrophosphate expressed in megabecquerels (microcuries or millicuries)per mLat the time indicated in the labeling.It may contain antimicrobial agents,buffers,reducing agents,and stabilizers.Other chemical forms of radioactivity do not exceed 10.0percent of the total radioactivity. Packaging and storage— Preserve in single-dose or multiple-dose containers,at a temperature between 2and 8. Labeling— Label it to include the following,in addition to the information specified for Labelingunder Injections á1ñ:the time and date of calibration;the amount of 99mTc as labeled tetrasodium pyrophosphate expressed as total megabecquerels (microcuries or millicuries)and concentration as megabecquerels (microcuries or millicuries)per mLat the time of calibration;the expiration date and time;and the statement “Caution—Radioactive 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 6.0hours. USP Reference standards á11ñ USP Endotoxin RS. Bacterial endotoxins á85ñ The limit of endotoxin content is not more than 175/VUSP Endotoxin Unit per mLof the Injection,when compared with the USP Endotoxin RS,in which Vis the maximum recommended total dose,in mL,at the expiration date or time. pHá791ñ: between 4.0and 7.5. Radiochemical purity— The determination of radiochemical purity for this product requires the use of two separate chromatography systems. System A— Under an atmosphere of nitrogen,place a measured volume of Injection,appropriately diluted,such that it provides a count rate of about 20,000counts per minute,about 20mm from one end of a thin-layer chromatographic strip impregnated with silica gel (see Chromatography á621ñ),and allow to dry.Develop the chromatogram over a suitable period by ascending chromatography,using saline TS,and dry it under nitrogen.Determine the radioactivity distribution by scanning the chromatogram with a suitable collimated radiation detector.Hydrolyzed Tc 99m and technetium-tin colloid are located at the origin (RF0to 0.1). System B— Proceed as directed for System A,except to develop the chromatogram in a mixture of methanol and acetone (1:1).Free pertechnetate is located at the solvent front.The sum of the percentage of radioactivity at the origin in System Aplus the percentage of radioactivity at the solvent front in System Bis not greater than 10.0%. Biological distribution— Inject intravenously between 0.075MBq and 75MBq (2µCi and 2mCi)of Injection,in a volume not exceeding 0.2mL,into the caudal or external jugular vein of each of three 175-to 250-g rats.Approximately 1hour after the injection,sacrifice the animals,and carefully remove the liver,both kidneys,and one femur of each by dissection,freeing the femur from soft tissue.Remove the tail 20to 30mm above the injection site,and discard.Place each organ,both kidneys,and the remaining carcass in separate,suitable counting containers,and determine the radioactivity,in counts per minute,in each container with an appropriate detector,using the same counting geometry.Determine the percentage of radioactivity in the liver,kidneys,and femur taken by the formula: 100(A/B), in which Ais the net radioactivity,in counts per minute,in the organ,and Bis the total radioactivity,in counts per minute,in the liver,kidneys,femur,and carcass.Not more than 5.0%of the total radioactivity is found in the liver or in the kidneys,and not less than 1.0%of the total radioactivity is found in the femur,in not fewer than 2of the rats. Other requirements— It meets the requirements of the tests for Radionuclide identificationand Radionuclidic purityunder Sodium Pertechnetate Tc 99m Injection.It meets also the requirements under Injections á1ñ,except that it may be distributed or dispensed prior to completion of the test for Sterility,the latter test being started on the day of final manufacture,and except that it is not subject to the recommendation on Volume in Container. Assay for radioactivity á821ñ Using a suitable counting assembly (see Selection of a Counting Assembly),determine the radioactivity,in MBq (µCi)per mL,of the Injection by use of a calibrated system. Auxiliary Information— Staff Liaison:Andrzej Wilk,Ph.D.,Senior Scientific Associate Expert Committee:(RMI)Radiopharmaceuticals and Medical Imaging Agents USP28–NF23Page 1862 Phone Number:1-301-816-8305