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Human Paxillin

Updated: 2026-07-24

Overview

Human Serum Albumin (HSA) is the most abundant protein in blood plasma, synthesized by the liver. It consists of 585 amino acids with a heart-shaped molecular structure. HSA’s primary biological functions include maintaining colloid osmotic pressure (contributing 75-80% of plasma’s osmotic activity) and serving as a transport carrier for hydrophobic molecules like bilirubin, fatty acids, and medications such as warfarin. The global HSA market is valued at approximately $4 billion annually, driven by clinical applications and biopharmaceutical demand. Pharmaceutical-grade HSA is strictly regulated, with production requiring compliance with WHO and regional pharmacopeia standards (e.g., USP, EP). Recombinant HSA, produced via yeast or rice platforms, is gaining traction as an animal-free alternative.

Physical and Chemical Properties

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HSA exhibits remarkable stability across a wide pH range (4-9) and can reversibly bind diverse ligands at multiple sites, notably Sudlow Sites I and II. Its isoelectric point is ~4.7, and it shows intrinsic fluorescence due to tryptophan residues. The protein’s tertiary structure is maintained by 17 disulfide bonds, conferring resistance to thermal denaturation below 60°C. In solution, HSA forms a slightly viscous, clear fluid with typical concentrations of 5-25% w/v. Lyophilized formulations retain activity for years when stored properly. Analytical techniques like HPLC and electrophoresis are used to confirm purity, while dynamic light scattering assesses aggregation.

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Main Applications

Clinically, HSA solutions (5-20%) treat hypovolemia, burns, and hypoalbuminemia (e.g., in liver cirrhosis). In biopharmaceuticals, it serves as a stabilizer in vaccines (e.g., MMR) and biologics formulations. Research applications include cell culture media supplementation (typically at 0.1-1% concentration) and as a blocking agent in immunoassays. Emerging uses include nanoparticle drug delivery systems leveraging HSA’s binding properties (e.g., Abraxane® paclitaxel-albumin nanoparticles). Diagnostic applications involve calibrators for lab tests measuring osmotic pressure or liver function. The cosmetic industry employs HSA in anti-aging formulations for its moisture-retention properties.

Safety and Storage

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Pharmaceutical HSA undergoes viral inactivation (e.g., pasteurization at 60°C for 10 hours) and rigorous screening for pathogens. Allergenic reactions are rare (<0.1% incidence) but require monitoring during IV administration. Lyophilized powder should be reconstituted with sterile water or saline to avoid foaming. Long-term storage requires protection from light and excessive heat. Opened vials should be used immediately or refrigerated for ≤24 hours. Transport mandates temperature-controlled packaging (2-8°C) with temperature indicators. Occupational exposure limits follow general protein handling guidelines—avoid inhalation of powdered forms.

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B2B Procurement Guide

For therapeutic use, prioritize suppliers compliant with cGMP and holding relevant certifications (e.g., FDA, EMA approval). Key specifications include: purity (≥96% by SEC-HPLC), aluminum content (<200 μg/L), and residual host cell proteins (<50 ppm for recombinant). Batch-to-batch consistency is critical for industrial applications. Bulk purchasers (e.g., hospitals, manufacturers) should negotiate contracts with guaranteed supply continuity. Consider regional regulations—some countries restrict plasma-derived HSA imports. For research-grade purchases, validate endotoxin levels match experimental needs (typically <1 EU/mg for cell culture). Sample testing for osmolality and sterility is recommended before large orders.

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