Last update Nov. 22, 2024

Indium-111; 111-In

Limited compatibility

Unsafe. Moderate/severe adverse effects. Compatible under certain circumstances. Follow-up recommended. Use safer alternative or discontinue breastfeeding from 5 to 7 T ½ . Read Commentary.

Indium-111 (111In) is a radioactive isotope of indium that emits X-rays. Its radiological elimination half-life is 67.2 hours (2.8 days). Various substrates can be labeled with Indium-111 for different diagnostic studies: 

  • It is combined with pentetic acid (pentetate) is used intrathecally in diagnostic studies of the Cerebrospinal Fluid.
  • Leukocytes labeled with Indium-111-hydroxyquinoline, Indium-111-oxyquinoline or Indium-11-oxine are used for localization of inflammatory lesions: abscesses, infections and inflammatory bowel disease. Platelets are similarly labeled.
  • Indium-111 bleomycin has been administered by intravenous injection for tumor detection. 
  • Indium-111 pentetreotide and the combination with octreotide is used for the detection and localization of tumors of neuroendocrine origin.
  • Monoclonal antibodies such as capromab pendetide, ibritumomab tiuxetan, altumomab pentetide, imciromab pendetide and satumomab pendetide have been labeled with indium-111 for detection of malignancies and localization of myocardial infarction.

Some indium-111 compounds such as octreotide are not absorbed by the gastrointestinal tract, so even if they reach breast milk they would not be absorbed by the infant.

Note: 1 mCi (millicurie) = 37 Mbq (megabecquerel)

Waiting times for breastfeeding after radionuclide administration to limit exposure to a maximum of 1 mSv (the average natural radiation received is 6.2 mSv each year.): (Hale, ARSAC 2024, IAEA 2018) 

  • Indium-111-CYT-356 (ProstaScint), dose of 5-17 mCi: 14 days.
  • Indium-111-DTPA (Cisternogram), 0.5-1.5 mCi dose: 14 days
  • Indium-111-DTPA (CSF-cisternogram, shunt patency) dose up to 0.5 mCi: 1 week
  • Indium-111-leukocytes, dose from 10 to 18 Mbq: 0 hours (Hale, ARSAC 2024, Mattsson 2021, ICRP 2008) or 6 - 7 days (ACMUI 2019, US.NCR 2016)
  • Indium-111-octreotide, 0 horas (Mattsson 2021, ICRP 2008), 100–200 MBq dose : 60 h (ARSAC 2024, IAEA  2018) or 6 days (ACMUI 2019)  
  • Indium-111-pentetriotide (OctreoScan), dose 6 mCi: 72 h (3 days)
  • Indium-111-santumomab pendetide (OncoScint), dose 4-6 mCi: 14 days

In case of doubt, milk radioactivity can be measured at a nuclear medicine center until measurements on milk samples demonstrate that it is safe to restart feeding. (ARSAC 2024, Stabin 2000)

If it is desired to completely limit (to 0 mSv) infant exposure, the passage of 5 radioactive half-lives (14 days) will have to be awaited. For leukocyte-labeled Indium-111, 1 day is sufficient.

If the mother has expressed and stored milk prior to the test, she may give it to the infant during the lactation break period. During the interruption period, the milk should be regularly expressed as completely as possible and either discarded or frozen and stored appropriately (ARSAC 2024). This stored milk will be fit for consumption after 10 T ½ (30 days) when the radioactivity will have completely disappeared.

Suggestions made at e-lactancia are done by APILAM team of health professionals, and are based on updated scientific publications. It is not intended to replace the relationship you have with your doctor but to compound it. The pharmaceutical industry contraindicates breastfeeding, mistakenly and without scientific reasons, in most of the drug data sheets.

Jose Maria Paricio, Founder & President of APILAM/e-Lactancia

Your contribution is essential for this service to continue to exist. We need the generosity of people like you who believe in the benefits of breastfeeding.

Thank you for helping to protect and promote breastfeeding.

José María Paricio, founder of e-lactancia.

Tradenames

Main tradenames from several countries containing Indium-111; 111-In in its composition:

Pharmacokinetics

Variable Value Unit
67 hours

References

  1. ARSAC. Administration of Radioactive Substances Advisory Committee. Notes for Guidance on the Clinical Administration of Radiopharmaceuticals and Use of Sealed Radioactive Sources. Section 7 Conception, Pregnancy and Breastfeeding, p. 51-58. ARSAC Support Unit. Centre for Radiation, Chemical and Environmental Hazards. Public Health England. 2024 Consulted on Nov. 19, 2024 Abstract Full text (link to original source) Full text (in our servers)
  2. Mattsson S, Leide-Svegborn S, Andersson M. X-RAY AND MOLECULAR IMAGING DURING PREGNANCY AND BREASTFEEDING-WHEN SHOULD WE BE WORRIED? Radiat Prot Dosimetry. 2021 Oct 12;195(3-4):339-348. Abstract Full text (link to original source)
  3. ACMUI: Advisory Committee on Medical Uses of Isotopes. Sub-Committee on Nursing Mother Guidelines for the Medical Administration of Radioactive Materials. Final Report Submitted: January 31, 2019 Full text (link to original source)
  4. IAEA - International Atomic Energy Agency. Radiation Protection and Safety in Medical Uses of Ionizing Radiation IAEA Safety Standards Series No. SSG-46, 2018 Abstract Full text (link to original source)
  5. US.NRC - Nuclear Regulatory Commission Office of Nuclear Material Safety and Safeguards. Apéndice U, Tabla U.3. Consolidated guidance about materials licenses. Program-specific guidance about medical use licenses. Draft Report for Comment. Appendix U, Table U.3. NUREG-1556. Vol.9, Rev 3. 2016 Full text (link to original source) Full text (in our servers)
  6. ICRP. Radiation dose to patients from radiopharmaceuticals. Addendum 3 to ICRP Publication 53. ICRP Publication 106. Annex D. Recommendations on breast-feeding interruptions, p. 163-165. Ann ICRP. 2008 Abstract Full text (link to original source) Full text (in our servers)

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