Product image of Metalcaptase (Penicillamine) supplied by GNH India

Metalcaptase

Active Ingredient:
Penicillamine
Origin:
EU

Metalcaptase (Penicillamine)

Penicillamine, the active ingredient in Metalcaptase, is a chelating agent presented as an oral tablet for oral use. It is employed to reduce copper accumulation in Wilson's disease, to modulate immune activity in rheumatoid arthritis, and to bind cystine in cystinuria.
GNH India supplies Metalcaptase as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution. Customers benefit from consistent product availability and regulatory compliance across EU and other markets.

Manufacturer / TM Owner

Heyl Chemisch-Pharmazeutische Fabrik Gmbh & Co. Kg

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Indications & Clinical Uses

Metalcaptase (penicillamine) is used in disorders where copper overload or abnormal amino‑acid metabolism requires chelation, as well as in autoimmune inflammation.

  • Wilson's disease: reduces hepatic and extra‑hepatic copper stores, helping to prevent organ damage.
  • Rheumatoid arthritis: decreases disease activity by modulating immune response and reducing joint inflammation.
  • Cystinuria: binds cystine in urine, forming soluble complexes that lower the risk of stone formation.

How It Works

  • Penicillamine is a low‑molecular‑weight thiol that chelates copper and other heavy metals by forming stable, water‑soluble complexes that are excreted in urine. In rheumatoid arthritis, the drug interferes with T‑cell activation and cytokine production, leading to immunomodulation and reduced inflammatory joint damage.

Side Effects

Penicillamine may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Taste alteration: metallic or sour taste in the mouth.
  • Gastrointestinal upset: nausea, vomiting, abdominal pain or diarrhoea.
  • Skin rash: mild erythema or pruritus.
  • Mild leukopenia: slight reduction in white‑blood‑cell count.
  • Joint stiffness: transient increase in arthralgia.

Serious or Rare Side Effects

  • Agranulocytosis: severe drop in neutrophils, increasing infection risk.
  • Hepatotoxicity: significant elevation of liver enzymes or liver failure.
  • Nephrotic syndrome: proteinuria with edema and hypoalbuminaemia.
  • Stevens‑Johnson syndrome: severe mucocutaneous reactions.
  • Aplastic anemia: pancytopenia requiring immediate medical attention.

Precautions & Warnings

Before initiating therapy, clinicians should assess baseline parameters and monitor patients regularly.

  • Monitor copper levels: periodic measurement to guide dosage adjustments.
  • Liver function tests: check baseline and repeat during treatment.
  • Complete blood count: regular monitoring for leukopenia or agranulocytosis.
  • Renal function: assess creatinine clearance in patients with kidney impairment.
  • Hypersensitivity: discontinue if signs of allergic reaction appear.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Penicillamine can affect the absorption or activity of several concomitant medicines.

Major Interactions (Avoid)

  • Zinc supplements: compete for intestinal absorption, reducing penicillamine efficacy.
  • Iron preparations: form insoluble complexes, markedly decreasing bioavailability.
  • Tetracycline antibiotics: chelation reduces antibiotic absorption.
  • Anticoagulants (e.g., warfarin): may enhance anticoagulant effect, increasing bleeding risk.
  • Sulfonamides: increased risk of severe skin reactions.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors: potential additive effect on renal function.
  • NSAIDs: may increase risk of nephrotoxicity.
  • Diuretics: monitor electrolyte balance, especially potassium.
  • Oral contraceptives: possible reduction in contraceptive effectiveness.
  • Immunosuppressants: watch for additive bone‑marrow suppression.

Frequently Asked Questions

Metalcaptase contains penicillamine, which is prescribed for Wilson's disease to lower copper accumulation, for rheumatoid arthritis to modulate immune activity, and for cystinuria to reduce cystine stone formation. These indications are based on its chelating and immunomodulatory properties.

Penicillamine binds copper and other heavy metals through its thiol group, creating soluble complexes that are eliminated in urine. In rheumatoid arthritis, it interferes with T‑cell activation and cytokine release, thereby dampening the inflammatory response.

The dosage of Metalcaptase is individualized by the prescribing clinician based on the specific indication, disease severity, patient age, renal function and laboratory monitoring. Patients should follow the dose and schedule provided by their healthcare professional.

Safety data for penicillamine in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies the possible risk to the fetus or infant, and this decision must be made by a qualified prescriber.

To request Metalcaptase, 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 and any necessary import documentation.

Penicillamine is a small‑molecule thiol chelator, distinct from agents such as trientine or dimercaprol. It offers oral administration and is effective for Wilson's disease and cystinuria, but may have a higher incidence of immune‑related side effects compared with some newer chelators.

Metalcaptase should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the product away from moisture, excessive heat and direct sunlight to maintain stability.

Metalcaptase is taken orally, usually with a full glass of water. It may be prescribed to be taken on an empty stomach or with food depending on the prescriber's guidance, and patients should follow the specific instructions given by their healthcare provider.

Serious adverse events include agranulocytosis, severe liver injury, nephrotic syndrome, Stevens‑Johnson syndrome and aplastic anemia. Patients should be monitored regularly for blood counts, liver and kidney function, and any signs of severe skin reactions or infection.

Metalcaptase is contraindicated in individuals with known hypersensitivity to penicillamine or any component of the formulation, and it should be avoided in patients with active peptic ulcer disease, severe renal impairment, or those who have experienced severe hematologic reactions to the drug.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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