ARMOBIOX Human Albumin

ARMOBIOX Human Albumin

Human albumin therapy for restoring blood volume, oncotic pressure, and treating albumin deficiency

ARMOBIOX Human Albumin Product

Pharmacokinetics

  • Under normal circumstances, the concentration of human albumin is 4 to 5 g/kg of body weight, with 40 to 45% intravascular and 55 to 60% extravascular.

  • Abnormal distribution may occur in cases of severe burns or septic shock.

  • The half-life of albumin averages approximately 19 days.

  • Elimination occurs predominantly intracellularly via lysosomal proteases.

  • Less than 10% of infused albumin leaves the intravascular compartment within the first 2 hours after infusion.

  • The circulating volume increases 1 to 3 hours after administration.

  • Balanced distribution between intravascular and interstitial spaces requires 48 hours.

  • Human albumin is osmotically active and regulates circulating blood volume.

  • When 50 mL of 20% human albumin is administered intravenously, approximately 175 mL of fluid is returned to circulation within 15 minutes.

  • The degree of plasma expansion depends on initial blood volume.

  • The risk of transmitting hepatitis is minimal with human albumin, and blood compatibility testing is not required.

Therapeutic Indications

  • Increasing oncotic pressure in cases of oncotic deficiency

  • Therapy for albumin deficiency

  • Emergency treatment of shock and similar states requiring rapid blood volume restoration

  • Treatment of burns

  • Hypoproteinemia with or without edema

Available Presentations

10 g HSA 50mL vial

Composition

Human albumin 10.0 g
Caprylic acid 2.12 mg
N-acetyl-DL-tryptophan 3.64 mg
Water for injection q.s. 50 mL

Electrolytes

Sodium Not more than 160 mmol/L