Agilent Cary 60 UV-Vis Application Note for Drug Tablet Concentration Determination

This document highlights the method and advantages of using the Agilent Cary 60 UV-Vis spectrophotometer for determining drug tablet concentration in pharmaceutical applications.


Agilent Cary 60 UV-Vis Application Note for Drug Tablet Concentration Determination - cover page
Brand
Agilent
Category
Other
Document type
Application Note
Language
English
Pages
4
File format
PDF
File size
129 KB
Published
11 June, 2012
Updated
28 September, 2023
Model
Cary 60
MD5 checksum
2C3F0643477BED0B53F79704B9AFC8F2

About this manual

This document details the use of the Agilent Cary 60 UV-Vis spectrophotometer equipped with fiber optic probes for determining the concentration of active pharmaceutical ingredients (API) in drug tablets. It highlights the benefits of in situ measurements for drug development and production, offering time and cost savings compared to conventional sample transfer systems.

The note presents a case study involving the analysis of an anti-malarial API. Using the WinUV software's Concentration module, the document demonstrates the instrument's ability to generate linear concentration curves with high reproducibility. It concludes that this approach is critical for determining precise drug concentrations and supports regulatory compliance through 21 CFR part 11 capable software.

What's inside

  • Summary
  • Introduction
  • Apparatus and materials
  • Methods and results
  • Analysis
  • Discussion
  • Conclusions

Specifications

Instrument ModelCary 60 UV-VIS Spectrophotometer
Probe TypeTorlon fiber optic probe
Probe CouplerTorlon fiber optic probe coupler
Correlation Coefficient0.99976
Absorbance Range0-2 Absorbance units

Frequently asked questions

What software module assists with regulatory requirements?

The WinUV software contains the 21 CFR part 11 module that assists with meeting regulatory requirements.

What is the calibration equation for the anti-malarial API standards?

The calibration equation is Abs = 0.00688*Conc -0.01056.

What methods were adapted for the concentration measurements?

Methods were adapted in-house from those described in British Pharmacopoeia 2011.

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