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[Stability of tetracycline during fermentation].

B C Cunha

    Revista De Farmacia E Bioquimica Da Universidade De Sao Paulo
    |July 1, 1976
    PubMed
    Summary

    Tetracycline stability significantly decreases at low pH (1.5), with thermal inactivation rates increasing sharply with temperature. A degradation mechanism involving entropy and steric factors was proposed for this antibiotic.

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    [Oxygen absorption of a biodynamic system in a transitional regimen. I. Determination of operational parameters].

    Revista de farmacia e bioquimica da Universidade de Sao Paulo·1976
    See all related articles

    Area of Science:

    • Pharmaceutical Chemistry
    • Chemical Kinetics
    • Drug Stability

    Context:

    • Understanding antibiotic degradation is crucial for effective drug formulation and storage.
    • Tetracycline is a widely used antibiotic whose stability can be affected by environmental factors.
    • Previous studies have investigated tetracycline degradation, but specific kinetic data at varying pH and temperatures are essential.

    Purpose:

    • To investigate the thermal stability of tetracycline at acidic pH values (6.0 and 1.5).
    • To determine the thermal inactivation kinetics of tetracycline at different temperatures (40-100°C) and pH 1.5.
    • To elucidate the degradation mechanism of tetracycline under acidic and thermal stress.

    Summary:

    • The study quantified tetracycline's thermal inactivation constant at pH 1.5, revealing rates from 1.62 min⁻¹ at 40°C to 65.83 min⁻¹ at 100°C.
    • Degradation rates were significantly higher at lower pH, indicating increased instability.
    • A proposed degradation mechanism considered variations in entropy and steric factors, offering insights into the molecular pathways.

    Impact:

    • Provides critical kinetic data for predicting tetracycline shelf-life under specific storage conditions.
    • Informs the development of more stable tetracycline formulations.
    • Contributes to a deeper understanding of antibiotic degradation mechanisms, aiding in the design of future antimicrobial agents.

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