Technetium (99mTc) albumin aggregated

Technetium Tc 99m albumin aggregated

Clinical data
Trade names	Pulmotech MAA
Other names	MP-4006
AHFS/Drugs.com	Micromedex Detailed Consumer Information
License data	US DailyMed: Technetium_Tc_99m_albumin
Routes of administration	Intravenous
ATC code	V09GA04 (WHO)
Legal status
Legal status	AU: Unscheduled US: ℞-only
Identifiers
DrugBank	DB14230 N
ChemSpider	none
UNII	799C8VF17R
KEGG	D06023
NY (what is this?)  (verify)

Technetium ^99mTc albumin aggregated (^99mTc-MAA) is an injectable radiopharmaceutical used in nuclear medicine. It consists of a sterile aqueous suspension of Technetium-99m (^99mTc) labeled to human albumin aggregate particles. It is commonly used for lung perfusion scanning. It is also less commonly used to visualise a peritoneovenous shunt and for isotope venography.

Preparation

DraxImage MAA kits for preparing ^99mTc-MAA are available in the United States from only a single manufacturer; Jubilant DraxImage Inc. The kits are delivered to nuclear pharmacies as lyophilized powders of non-radioactive ingredients sealed under nitrogen. A nuclear pharmacist adds anywhere from 50 - 100 mCi of Na[^99mTcO₄] to the reaction vial to make the final product, in the pH range of 3.8 to 8.0. After being allowed to react at room temperature for 15 minutes to ensure maximum labeling of the human albumin with ^99mTc, the kit can then be diluted with sterile normal saline as needed.

Once prepared the product will have a turbid white appearance.

Quality control

No less than 90% of MAA particles can be between 10 - 90 micrometres in size and no particles may exceed 150 micrometres due to the risk of pulmonary artery blockade. No less than 90% of the radioactivity present in the product must be tagged to albumin particles. Thus, no more than 10% soluble impurities may be present.

Dosage and imaging

The typical adult dose for a lung imaging study is 40-150 Megabecquerels (1-4 mCi) (containing between 100,000 - 200,000 albumin particles). The particle burden should be lowered for most pediatric patients and lowered to 50,000 for infants. The use of more than 250,000 particles in a dose is controversial as little extra data is acquired from such scans while there is an increased risk of toxicity. Patients with pulmonary hypertension should be administered a minimum number of particles to achieve a lung scan (i.e. 60,000). In any patient by administering a greater quantity of particles than necessary for the diagnostic procedure increases the risks of toxicity.

Because of gravity effects, people administered ^99mTc MAA should be in the supine position to ensure as even a distribution of particles throughout the lungs as possible.

The total percentage of particles trapped in the lungs can be determined through a whole body scan after the administration of ^99mTc MAA through the equation:

${\displaystyle \%\ {\text{Right-to-left shunt}}=\left({\frac {({\text{Total body counts}})-({\text{Total lung counts}})}{({\text{Total body counts}})}}\right)\times 100\%}$.

History

The technetium tc 99m aggregated albumin kit was approved for use in the United States in December 1987.

Further reading

External links

• "Technetium Tc 99m aggregated albumin". Drug Information Portal. U.S. National Library of Medicine.