Product image of Intralipide (Soya Oil, Purified) supplied by GNH India

Intralipide

Active Ingredient:
Soya Oil, Purified
Origin:
EU

Intralipide (Soya Oil, Purified)

Soya Oil, Purified, the active ingredient in Intralipide, is an excipient presented as a solution for injection for intravenous use. It functions as a lipid solvent and carrier in parenteral drug formulations and nutrition support.

GNH India supplies Intralipide as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The product meets European Union pharmacopeial standards and is manufactured under GMP conditions. It is distributed in compliance with international regulatory requirements.

Manufacturer / TM Owner

Fresenius Kabi France S.A.S.

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Indications & Clinical Uses

Intralipide is used as a lipid solvent and carrier in intravenous drug delivery and parenteral nutrition.

  • Parenteral nutrition: provides essential fatty acids and calories for patients unable to receive enteral feeding.
  • Lipid-based drug formulations: solubilizes lipophilic medications for intravenous administration.
  • Drug dilution and reconstitution: serves as a diluent for certain injectable agents.

How It Works

  • Purified soy oil consists mainly of triglycerides rich in linoleic acid. After intravenous infusion it forms a stable oil‑in‑water emulsion that integrates into the plasma lipid pool, creating a hydrophobic environment that enhances the solubility of lipophilic compounds. The emulsion is metabolized by lipoprotein lipase, releasing free fatty acids that are taken up by tissues for energy and membrane synthesis.

Side Effects

Intravenous administration of Intralipide may be associated with the following adverse reactions.

Common Side Effects

  • Mild infusion site erythema: localized redness at the injection site.
  • Transient fever: low‑grade temperature rise during or shortly after infusion.
  • Nausea: occasional feeling of queasiness without vomiting.
  • Hypertriglyceridemia (mild): temporary increase in serum triglyceride levels.

Serious or Rare Side Effects

  • Fat overload syndrome: severe metabolic disturbance from excessive lipid load.
  • Pulmonary embolism: rare blockage of pulmonary vessels by lipid particles.
  • Anaphylactoid reaction: sudden systemic hypersensitivity with hypotension and rash.
  • Hepatic dysfunction: elevated liver enzymes in susceptible patients.

Precautions & Warnings

When using Intralipide, the following precautions should be observed.

  • Patient lipid status: assess baseline triglyceride levels before infusion.
  • Metabolic disorders: avoid in patients with severe hyperlipidaemia or lipid metabolism disorders.
  • Infusion rate: administer at recommended rate to reduce risk of fat overload.
  • Compatibility: verify compatibility with co‑administered drugs before mixing.
  • Monitoring: observe for signs of respiratory distress, allergic reaction, or sudden changes in vital signs.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Intralipide may interact with other agents administered intravenously.

Major Interactions (Avoid)

  • Concurrent lipid emulsions: co‑administration can precipitate fat overload syndrome.
  • Propofol infusion: additive lipid load may increase triglyceride levels excessively.
  • High‑dose heparin: may potentiate hypertriglyceridemia.

Moderate Interactions (Monitor Closely)

  • Lipophilic antibiotics (e.g., vancomycin): monitor for altered plasma concentrations.
  • Hormone therapies (e.g., estradiol): observe for changes in drug distribution.
  • Immunosuppressants (e.g., cyclosporine): assess for potential changes in blood levels.

Frequently Asked Questions

Intralipide is a sterile solution of purified soy oil that serves as an excipient solvent in intravenous drug formulations and as a lipid source in parenteral nutrition. It helps dissolve lipophilic medicines and provides essential fatty acids for patients who cannot receive nutrition orally.

Purified soy oil is composed mainly of triglycerides that form a stable oil‑in‑water emulsion after intravenous infusion. This emulsion creates a hydrophobic phase that increases the solubility of lipophilic drugs, while also delivering fatty acids that are metabolized for energy and cell‑membrane synthesis.

The dose of Intralipide is determined by the prescribing clinician based on the specific therapeutic context, such as the volume needed for drug dilution or the caloric requirement in parenteral nutrition. No fixed regimen is provided in public literature.

Safety data for Intralipide during pregnancy or lactation are limited. Because it is an oil‑based excipient, clinicians usually weigh potential benefits against unknown risks and may limit use to situations where alternative options are not available.

To order Intralipide, 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 required) and any necessary import documentation.

Intralipide is a purified soy‑oil emulsion specifically marketed as an excipient, whereas other lipid emulsions (e.g., Intralipid) are formulated as complete nutritional products. Both provide fatty acids, but Intralipide is typically used in smaller volumes for drug solubilisation rather than as a primary caloric source.

Intralipide should be stored at 2‑8 °C, protected from light, and kept in its original container. Do not freeze or vigorously shake the vial, as this can destabilise the emulsion. If the product reaches room temperature, it may be used within the time frame specified by the manufacturer.

Intralipide is administered intravenously, either as a standalone infusion or mixed with other injectable medicines according to the prescriber’s instructions. The solution is typically delivered through a sterile infusion set, and the infusion rate should follow the recommended guidelines to avoid lipid‑related complications.

The most serious risks include fat overload syndrome, pulmonary embolism from lipid particles, and severe anaphylactoid reactions. Clinicians should monitor triglyceride levels, respiratory status, and signs of hypersensitivity during and after infusion, especially in patients with pre‑existing metabolic or pulmonary conditions.

Intralipide should be avoided in patients with known severe hyperlipidaemia, disorders of lipid metabolism, or a history of allergic reactions to soy products. It is also contraindicated when co‑administration with other high‑lipid emulsions would exceed safe lipid load limits.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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