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The long-term stability of drug products is critical to ensuring their quality, safety, and effectiveness over time. Stability directly influences a product's ability to maintain its intended characteristics, ensuring it performs as expected during its intended shelf life. Key attributes such as drug potency, impurities, dissolution, and other physicochemical measures of performance are tested to assess stability. These parameters indicate how well the product retains its quality over time and...
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Age-related pharmacokinetic changes are extensively documented, but understanding age-related pharmacodynamic alterations is relatively limited. This knowledge gap can be partly attributed to the complexity of developing appropriate measures of drug responses compared to bioanalytical methods for determining drug concentrations.Most information regarding age-related differences in human pharmacodynamics originates from cross-sectional studies. However, these studies assume that observed mean...
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Differential Scanning Calorimetry — A Method for Assessing the Thermal Stability and Conformation of Protein Antigen
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Differential Scanning Calorimetry — A Method for Assessing the Thermal Stability and Conformation of Protein Antigen

Published on: March 4, 2017

Benzodiazepine stability in postmortem samples stored at different temperatures.

Paula Melo1, M Lourdes Bastos, Helena M Teixeira

  • 1National Institute of Legal Medicine, North Branch, Porto, Portugal. paula.melo@dpinml.mj.pt

Journal of Analytical Toxicology
|February 1, 2012
PubMed
Summary
This summary is machine-generated.

Benzodiazepine stability in postmortem samples varied by drug and storage temperature. Ketazolam and chlordiazepoxide showed significant degradation, especially at room temperature, while estazolam remained stable.

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Published on: November 8, 2015

Area of Science:

  • Forensic Toxicology
  • Analytical Chemistry
  • Pharmacology

Background:

  • Benzodiazepines are commonly prescribed and frequently detected in postmortem toxicology.
  • Understanding the stability of these compounds in biological matrices is crucial for accurate interpretation of toxicological results.
  • Factors such as storage temperature and sample type can influence drug degradation.

Purpose of the Study:

  • To evaluate the stability of four benzodiazepines (lorazepam, estazolam, chlordiazepoxide, ketazolam) in postmortem blood, bile, and vitreous humor.
  • To assess the impact of different storage temperatures (-20°C, -80°C, 4°C, room temperature) over six months.
  • To investigate the influence of sodium fluoride (NaF) as a preservative.

Main Methods:

  • Solid-phase extraction (SPE) was employed for sample preparation.
  • High-performance liquid chromatography with diode-array detection (HPLC-DAD) was used for benzodiazepine quantification.
  • Samples were stored for six months under various conditions.

Main Results:

  • Benzodiazepine concentrations remained largely stable in samples stored at -20°C and -80°C.
  • Estazolam demonstrated high stability throughout the study period.
  • Ketazolam was the most unstable, with complete degradation at room temperature within weeks and at 4°C within months. Diazepam was detected upon ketazolam degradation.
  • Chlordiazepoxide degraded significantly, especially at room temperature and 4°C, with bile showing some preservation.

Conclusions:

  • Long-term storage of samples containing these benzodiazepines requires cautious interpretation of results due to potential degradation.
  • Bile and vitreous humor appear to be more advantageous matrices than blood for preserving benzodiazepines, particularly when microbial degradation is a concern.
  • Optimal storage at freezing temperatures (-20°C or -80°C) is recommended for maintaining benzodiazepine integrity in postmortem samples.