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Performance evaluation of the HPLC diode array and evaporative light scattering detection for the implementation of dose-banded gemcitabine infusion bags
  1. Thomas Stalder1,
  2. Claire Andre1,
  3. Maurad Ben Mahi2,
  4. Lydie Lethier1,
  5. Samuel Limat2,
  6. Christine Legat2,
  7. Yves Guillaume1
  1. 1Franche-Comte University Faculty of Medical and Pharmaceutical Sciences, Besançon, France
  2. 2Pôle pharmacie, CHU Besançon, Besançon, France
  1. Correspondence to Professor Yves Guillaume, Franche-Comte University Faculty of Medical and Pharmaceutical Sciences, Besançon, France; yves.guillaume{at}univ-fcomte.fr

Abstract

Background Dose banding (DB) was used to optimise the individualisation of patient treatments with gemcitabine (Gem) in order to improve workload planning at the pharmacy of the University Hospital Centre of Besançon (UHCB). A new simple and fast high-performance liquid chromatographic (HPLC) method was also developed for the quantification of Gem without dilution of the infusion bags.

Methods Individual doses of Gem preparations were retrospectively analysed over a 1-year period to determine the frequency of prepared doses. Using a maximum gap of 7.5% around the doses chosen, the selected Gem standard doses were 1400 mg, 1600 mg, 1800 mg and 2000 mg. Following the DB scheme, the frequency of prescription of standard and individualised Gem doses was analysed over a period of 10 months. The four selected Gem standard doses were aseptically prepared in polyolefin infusion bags. Each series of 20 bags was stocked under refrigerated storage conditions (4°C) for up to 84 days. The quantification of Gem without dilution of the infusion bags was obtained by the development of a HPLC method coupled to a diode array detector (DAD) or an evaporative light scattering detector (ELSD).

Results During the 10-month period following implementation of the DB, 75.6% of the 1266 prescribed doses were covered by the four standardised preparations. The number of different Gem doses was reduced from 183 to 55. Concerning the Gem quantification, both heteroscedasticity and non-linearity were observed with DAD. Using an ELSD, the trueness values were between 98.59% and 101.52% with excellent repeatability values between 0.66% and 1.42%.

Conclusion A new HPLC method has been developed for the quantification of Gem without dilution of the infusion bags prepared in advance as a result of a target DB scheme successfully implemented in our pharmacy department.

  • analytic sample preparation methods
  • chemistry, pharmaceutical
  • laboratories, hospital
  • pharmaceutical preparations
  • pharmacy service, hospital

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