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6141921 
Journal Article 
Titrimetric determination of Cremophor (R) EL in aqueous solutions and biofluids Part 2: Ruggedness of the method with respect to biofluids 
Kunkel, M; Meyer, T; Bohler, J; Keller, E; Frahm, AW 
1999 
Yes 
Journal of Pharmaceutical and Biomedical Analysis
ISSN: 0731-7085
EISSN: 1873-264X 
21 
911-922 
English 
A titration method for Cremophor EL, as a multicomponent mixture commonly used as non-ionic emulgent for manufacturing certain parenteralia, was developed for quantitative routine analysis in biofluids. A coated wire electrode is used as the end-point indicator in potentiometric titrations of Cremophor EL with sodium tetraphenylborate. The method tolerates a broad pH range, addition of alkanols and components of drug formulations and is sufficiently rugged. Reliable results are obtained at 20 degrees C. Disturbing ions from biofluid matrices can be masked or complexed by addition of formaldehyde, ethylenediaminetetraacetic acid and sodium fluoride. Sodium hydroxide is used for the required adjustment of the samples to pH 10. Cremophor EL spiked urine samples can be determined directly, whereas the true value of the emulgent content in the case of Cremophor EL spiked plasma samples is achieved by means of a conventional method. 
Cremophor (R) EL; potentiometry; NIO-tensid-electrode; biofluids 
PFAS
• PFAS 150
     Trifluoroacetic acid