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  • ContentsContents
  • Article InfoArticle Info
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  • Article title
  • Keywords
  • Introduction
  • Aim
  • Materials and methods
    • Instruments
    • Chemicals and pharmaceutical dosage forms
    • Solvents: Preparation of two different dissolution media
    • Development and validation of the UV-spectrophotometric method
    • Standard solutions preparation
    • Specificity
    • Linearity
    • Limit of detection (LOD) and limit of quantification (LOQ)
    • Analytical range
    • Stability
    • Repeatability and precision
    • Accuracy
    • Determination of FOS in commercial tablets
    • Results and discussion
    • LOQ and LOD
    • Analytical range
    • Stability
    • Repeatability and precision
    • Accuracy
    • Determination of FOS in pharmaceutical formulations
  • Conclusions
  • Ethical approval
  • Ethical statements
  • Conflict of interest
  • Use of AI
  • Funding
  • Data availability
  • Author contributions
  • Acknowledgments
  • References
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