Product image of Indium (111in) Oxinate Curium Netherlands (Indium (111in) Oxine) supplied by GNH India

Indium (111in) Oxinate Curium Netherlands

Active Ingredient:
Indium (111in) Oxine
Origin:
EU

Indium (111in) Oxinate Curium Netherlands (Indium (111in) Oxine)

Indium-111 oxine, the active ingredient in Indium (111in) Oxinate Curium Netherlands, is a radiopharmaceutical presented as a solution for injection for intravenous use. It is employed to label leukocytes and other cells, enabling visualization of infection, inflammation, and selected tumors in patients undergoing diagnostic imaging.

GNH India supplies Indium (111in) Oxinate Curium Netherlands as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company ensures quality and regulatory compliance throughout the supply chain.

Manufacturer / TM Owner

Curium Netherlands B.V.

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Indications & Clinical Uses

Indium-111 oxine is used in nuclear medicine for cell labeling and imaging of infectious, inflammatory, and neoplastic processes.

  • Infection detection: enables visualization of sites of bacterial or fungal infection by labeling patient leukocytes.
  • Inflammation assessment: facilitates imaging of inflammatory disorders such as vasculitis or sarcoidosis.
  • Tumor imaging: allows targeted imaging of certain tumors when appropriate cell labeling is performed.

How It Works

  • Indium-111 oxine penetrates cell membranes by passive diffusion, where the oxine ligand releases the radionuclide intracellularly. The indium-111 ion binds to cytoplasmic proteins and becomes trapped inside the labeled cell. Gamma photons emitted by indium-111 are then detected by a gamma camera, providing high‑resolution images of the distribution of labeled leukocytes or other cells within the body.

Side Effects

Adverse reactions are generally related to the injection procedure and radiation exposure.

Common Side Effects

  • Injection site pain: mild discomfort at the venipuncture site.
  • Transient flushing or warmth: brief sensation of heat following administration.
  • Nausea or mild headache: occasional short‑lived symptoms.

Serious or Rare Side Effects

  • Severe allergic reaction (anaphylaxis): rare but requires immediate medical attention.
  • Radiation‑induced tissue injury: high localized doses may cause tissue damage.
  • Hemodynamic instability: hypotension or arrhythmia in susceptible patients.

Precautions & Warnings

Use of Indium-111 oxine requires careful consideration of radiation safety and patient condition.

  • Pregnancy: avoid unless benefits outweigh potential fetal radiation risk.
  • Breastfeeding: discontinue nursing for an appropriate period after administration.
  • Renal impairment: monitor renal function as excretion is primarily renal.
  • Concomitant immunosuppressive therapy: may alter leukocyte labeling efficiency.
  • Storage: Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Radiopharmaceuticals can interact with other agents that affect cell labeling or radiation exposure.

Major Interactions (Avoid)

  • Concurrent administration of other gamma‑emitting radiotracers: may interfere with image interpretation.
  • High‑dose chelating agents (e.g., EDTA): can strip indium from labeled cells.
  • Therapeutic radiation therapy performed within 24 hours: increases cumulative radiation dose.

Moderate Interactions (Monitor Closely)

  • Corticosteroids or immunosuppressants: may reduce leukocyte labeling efficiency.
  • Anticoagulants: monitor for bleeding at injection site.
  • Contrast agents used in CT/MRI: schedule imaging to avoid overlap with scintigraphy.

Frequently Asked Questions

Indium-111 oxine is a diagnostic radiopharmaceutical used to label leukocytes or other cells so that infection, inflammation, and certain tumors can be visualized with gamma‑camera imaging. It helps clinicians locate sites of disease that are not easily seen with conventional imaging.

The oxine ligand carries the indium‑111 radionuclide across cell membranes. Once inside, the indium binds intracellular proteins and remains trapped, allowing the labeled cells to emit gamma photons that are captured by a gamma camera, producing detailed images of their distribution.

The administered activity is determined by the prescribing physician based on the specific diagnostic protocol, patient weight, and the intended imaging study. Dosing is individualized and should follow the radiopharmacy’s preparation guidelines.

Indium-111 oxine is classified as a radiopharmaceutical with potential fetal radiation exposure. It should be avoided in pregnancy unless the diagnostic benefit outweighs the risk. Breastfeeding mothers should discontinue nursing for a period recommended by the radiology team to prevent infant exposure.

Submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and necessary import documentation.

Compared with agents such as technetium‑99m‑labeled white blood cells, Indium-111 oxine offers a longer half‑life, allowing delayed imaging and better lesion-to‑background contrast for certain deep‑seated infections. However, it delivers a higher radiation dose, so the choice depends on clinical need and patient factors.

The product must be stored refrigerated at 2‑8 °C, protected from light, and never frozen or shaken. It should be handled in a radiopharmacy with appropriate shielding and contamination controls, and prepared immediately before administration.

Indium-111 oxine is supplied as a sterile solution for injection and is administered intravenously by a qualified healthcare professional. After labeling the patient’s leukocytes ex vivo, the labeled cells are reinfused, and imaging is performed at prescribed time points.

Serious risks include severe allergic reactions (anaphylaxis), radiation‑induced tissue injury, and hemodynamic instability such as hypotension. Patients should be monitored during and after administration, and emergency measures must be readily available.

Patients with known hypersensitivity to indium‑111 oxine or its excipients, pregnant women unless essential, and individuals who have received other gamma‑emitting radiotracers within the past 24 hours should avoid this agent. Clinical judgment is required for patients with severe renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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