Product image of Nanoscint (Human Serum Albumin) supplied by GNH India

Nanoscint

Active Ingredient:
Human Serum Albumin
Origin:
EU

Nanoscint (Human Serum Albumin)

Human Serum Albumin, the active ingredient in Nanoscint, is a plasma protein (albumin) presented as a sterile solution for injection for intravenous or subcutaneous use. It is employed to treat hypoalbuminemia and to expand intravascular volume in patients with burns, hypovolemic shock, or other conditions requiring restoration of plasma oncotic pressure.

GNH India supplies Nanoscint as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, with a focus on quality assurance and regulatory compliance.

Manufacturer / TM Owner

Radiopharmacy Laboratórium Kft.

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Indications & Clinical Uses

Nanoscint, a human serum albumin solution, is used in clinical situations that require plasma protein replacement or rapid intravascular volume expansion.

  • Hypoalbuminemia: restores plasma oncotic pressure and raises serum albumin levels.
  • Burn injuries: provides volume expansion and supports fluid resuscitation.
  • Hypovolemic shock: increases circulating volume to stabilize hemodynamics.
  • Surgical or trauma patients: maintains oncotic balance during peri‑operative fluid management.

How It Works

  • Human serum albumin administered intravenously or subcutaneously distributes within the vascular compartment, where it contributes to plasma colloid osmotic pressure. By increasing oncotic forces, it draws water from the interstitial space into the circulation, expanding intravascular volume. The exogenous albumin also replenishes depleted endogenous albumin, supporting transport of endogenous substances and maintaining vascular integrity.

Side Effects

Nanoscint may be associated with a range of adverse reactions, which are classified by frequency and severity.

Common Side Effects

  • Fever: transient elevation of body temperature.
  • Headache: mild to moderate intensity.
  • Nausea: occasional feeling of queasiness.
  • Injection site pain: localized discomfort at the administration site.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergic response requiring immediate intervention.
  • Fluid overload: signs of pulmonary edema or heart failure.
  • Hemolysis: destruction of red blood cells observed in rare cases.
  • Thromboembolic events: clot formation in veins or arteries.

Precautions & Warnings

When using Nanoscint, clinicians should observe specific precautions to ensure patient safety and product integrity.

  • Assess albumin levels: measure serum albumin before initiating therapy.
  • Monitor fluid balance: track input/output and signs of overload.
  • Evaluate cardiac function: consider underlying heart disease before volume expansion.
  • Use caution in renal impairment: adjust volume and monitor renal parameters.
  • Avoid concurrent use with other colloids unless clinically justified: may increase risk of volume overload.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Nanoscint can interact with other medicines, affecting safety or efficacy.

Major Interactions (Avoid)

  • Diuretics: may exacerbate hypovolemia when combined with aggressive volume expansion.
  • ACE inhibitors or ARBs: increased risk of hypotension and renal impairment.

Moderate Interactions (Monitor Closely)

  • Vasopressors: may require dose adjustments due to altered intravascular volume.
  • Anticoagulants: monitor coagulation parameters as volume changes can affect drug distribution.
  • Other plasma expanders: combined use can lead to fluid overload.

Frequently Asked Questions

Nanoscint is a sterile solution of human serum albumin indicated for the treatment of hypoalbuminemia and for rapid intravascular volume expansion in conditions such as severe burns, hypovolemic shock, and peri‑operative fluid management.

Human serum albumin increases plasma colloid osmotic pressure, drawing water from the interstitial space into the bloodstream. This expands circulating volume, restores oncotic balance, and supports transport of endogenous substances, helping to stabilize hemodynamics in patients with low albumin or fluid loss.

The dose of Nanoscint is individualized by the prescribing clinician based on the patient’s serum albumin level, weight, clinical condition, and desired volume expansion. No fixed regimen is provided; dosing is adjusted to achieve therapeutic goals while avoiding overload.

Safety data for Nanoscint in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made by the treating physician.

To order Nanoscint, submit an enquiry on the product page at gnhindia.com with 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 import documentation.

Nanoscint provides a purified human serum albumin solution comparable to other commercial albumin preparations. Unlike synthetic colloids, it carries a lower risk of coagulopathy and renal dysfunction, but it shares similar indications for volume expansion and hypoalbuminemia correction.

Nanoscint must be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. Before use, inspect for particulate matter and ensure the solution is clear; allow the product to reach room temperature if required for administration.

Nanoscint is administered by intravenous or subcutaneous injection under aseptic conditions. The rate of infusion is determined by the prescriber, typically given slowly to monitor tolerance and avoid rapid shifts in intravascular volume.

Serious risks include anaphylactic reactions, fluid overload leading to pulmonary edema or heart failure, hemolysis, and rare thromboembolic events. Prompt recognition and management of these events are essential during and after administration.

Nanoscint is contraindicated in patients with known hypersensitivity to human serum albumin or any component of the formulation. Caution is advised in individuals with severe heart failure, uncontrolled hypertension, or active pulmonary edema where additional volume could be harmful.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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