PVP K-30 can serve as an enzyme stabilizer, encapsulation-sustained release agent, adhesive, stabilizer, protective colloid, and film-forming agent.PVP is readily soluble in water, alcohols, amines, and halogenated hydrocarbons, but insoluble in acetone, ether, etc. It exhibits excellent solubility, biocompatibility, physiological inertness, film-forming ability, film protection capacity, and the ability to complex with various organic and inorganic compounds. It is relatively stable to acids, salts, and heat, making it widely applicable. It is used to absorb phenols and tannins from aqueous extracts to purify plant enzymes, as a chromatographic adsorbent for separating aromatic acids, aldehydes, and phenols, and for clarifying beer and wine.
•Stabilization and Protection:
•Enzyme/Antibody Stabilizer: Encapsulates macromolecules (e.g., enzymes, antibodies) via hydrogen bonding and hydrophobic interactions, preventing denaturation or aggregation and extending active preservation time.
•Protective Colloid: Inhibits aggregation and sedimentation of particles (e.g., latex microspheres, nanogold particles), maintaining the homogeneity of the detection system.
• Dispersion and Solubilization Functions:
•Dispersant: Prevents aggregation of hydrophobic particles (e.g., lipids, insoluble substrates) through steric hindrance, improving reaction efficiency.
•Solubilizer: Increases the solubility of hydrophobic substances (e.g., certain chemiluminescent substrates) in aqueous phases.
•Film-Forming and Sustained Release:
•Film-Forming Ability: Forms a uniform film on the surface of microplates or test strips, protecting active ingredients from environmental interference (e.g., oxidation).
•Sustained-Release Carrier: Controls the release rate of detection reagents (e.g., color development time regulation in POCT test strips) through physical embedding or adsorption.
•Immunoassays:
•ELISA/Chemiluminescence: Used as a component of blocking or dilution buffers to reduce non-specific adsorption (e.g., blocking unbound sites on microplate surfaces).
•Latex-Enhanced Immunoturbidimetry: Stabilizes latex particle-antibody complexes, preventing false positives/negatives caused by aggregation.
•Molecular Diagnostics:
•PCR/qPCR: Inhibits non-specific binding of DNA polymerase, improving amplification specificity.
•Nucleic Acid Extraction: Adsorbs interferents (e.g., phenols, tannins) from samples to purify DNA/RNA (similar to the principle of plant enzyme purification).
•Biochemical Detection:
•Enzymatic Reaction Systems: Stabilizes enzyme activity (e.g., horseradish peroxidase HRP) and prevents substrate auto-oxidation.
•Chromogenic Substrate Preparation: Disperses insoluble chromogenic agents (e.g., TMB) to ensure uniform color development.
•Point-of-Care Testing (POCT):
•Test Strip Coating: Improves the hydrophilicity of nitrocellulose membranes, accelerates sample diffusion, and shortens detection time.
Luvitec is a trademark of BASF