Product image of Ioflupane (123i) Rotop (Ioflupane (123i)) supplied by GNH India

Ioflupane (123i) Rotop

Active Ingredient:
Ioflupane (123i)
Origin:
EU

Ioflupane (123i) Rotop (Ioflupane (123i))

Ioflupane, the active ingredient in Ioflupane (123i) Rotop, is a radiopharmaceutical presented as an injectable solution for intravenous use. It helps clinicians evaluate Parkinsonian syndromes, differentiate movement disorders, and assess dopaminergic deficits in neurodegenerative diseases.
GNH India supplies Ioflupane (123i) Rotop as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, diagnostic centres and nuclear medicine clinics worldwide.

Manufacturer / TM Owner

Rotop Radiopharmacy Gmbh

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Indications & Clinical Uses

Ioflupane is used in the diagnostic pathway that assesses dopaminergic neuronal integrity in movement‑disorder patients.

  • Parkinsonian syndromes: enables visualization of presynaptic dopamine transporter loss to support diagnosis.
  • Atypical parkinsonian disorders: assists in distinguishing Parkinson disease from other neurodegenerative movement disorders.
  • Neurodegenerative disease assessment: provides quantitative data on dopaminergic neuronal integrity for research and clinical monitoring.

How It Works

  • Ioflupane is a radiolabelled analogue that binds selectively to presynaptic dopamine transporters (DAT) in the striatum. After intravenous injection, the iodine‑123 isotope emits gamma photons that are captured by single‑photon emission computed tomography (SPECT), producing high‑resolution images of DAT density and thereby reflecting the functional status of dopaminergic neurons.

Side Effects

Adverse reactions to Ioflupane are generally related to its radiopharmaceutical nature and the injection procedure.

Common Side Effects

  • Headache: transient mild headache reported after injection.
  • Nausea: occasional upset stomach or nausea.
  • Injection site pain: mild discomfort at the venipuncture site.

Serious or Rare Side Effects

  • Allergic reaction: urticaria, bronchospasm, or anaphylaxis requiring immediate medical attention.
  • Severe hypotension: marked drop in blood pressure following administration.
  • Radiation‑induced thyroid dysfunction: rare alteration of thyroid function due to iodine‑123 exposure.

Precautions & Warnings

When using Ioflupane, consider the following safety measures.

  • Pregnancy: safety not established; avoid unless benefit outweighs risk.
  • Breastfeeding: unknown; consider discontinuing nursing during treatment.
  • Renal impairment: reduced clearance may affect image quality; evaluate renal function.
  • Thyroid disease: assess thyroid function before use because of iodine load.
  • Concomitant iodine‑containing drugs: may interfere with imaging; discontinue when feasible.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Ioflupane may interact with other substances that affect iodine handling or dopamine pathways.

Major Interactions (Avoid)

  • Iodine‑containing contrast agents: can block DAT binding and compromise imaging.
  • Amiodarone or other high‑iodine medications: may reduce tracer uptake.
  • Antipsychotics that block dopamine transporters: interfere with binding and image interpretation.

Moderate Interactions (Monitor Closely)

  • MAO‑B inhibitors: may modestly alter DAT availability.
  • Levodopa therapy: may affect background signal; timing of administration should be considered.

Frequently Asked Questions

Ioflupane (123i) Rotop is a radiopharmaceutical used to image presynaptic dopamine transporters with SPECT. It helps clinicians diagnose Parkinsonian syndromes, differentiate atypical movement disorders, and evaluate dopaminergic neuronal loss in neurodegenerative diseases.

After intravenous injection, Ioflupane binds selectively to dopamine transporters located on presynaptic nerve terminals in the striatum. The iodine‑123 label emits gamma photons that are detected by SPECT, producing a visual map of transporter density that reflects neuronal integrity.

The prescribed dose of Ioflupane is determined by the treating physician or nuclear medicine specialist based on the patient’s clinical context, imaging protocol, and regulatory guidelines. Specific dosing regimens are not disclosed here.

Safety of Ioflupane in pregnancy and lactation has not been established. It should be avoided unless the potential diagnostic benefit justifies the potential risk to the fetus or infant, and the decision must be made by the prescribing clinician.

To place an order, 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 if needed) and necessary import documentation.

Ioflupane is the most widely used iodine‑123 labelled DAT tracer for SPECT, offering high specificity for presynaptic dopamine transporters. Compared with alternatives such as fluorine‑18 labelled PET tracers, Ioflupane provides broader global availability and longer half‑life, but PET agents may deliver higher spatial resolution.

Ioflupane must be stored refrigerated at 2‑8 °C, protected from light, and should never be frozen or shaken. The product should be kept in its original container until use to maintain radiochemical stability.

Ioflupane is administered as a single intravenous injection under the supervision of a qualified healthcare professional. After injection, a waiting period (typically 3–6 hours) allows tracer distribution before SPECT imaging is performed.

Serious risks include allergic reactions that can progress to anaphylaxis, severe hypotension immediately after injection, and rare radiation‑induced thyroid dysfunction. Patients should be monitored closely for any signs of these events during and after the procedure.

Ioflupane is contraindicated in patients with known severe allergy to iodine‑123 or any component of the formulation, and in those who have recently received high‑iodine contrast agents that could interfere with imaging. Caution is also advised for individuals with uncontrolled thyroid disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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