Cápka Vladimír, Bowers Christopher P, Narvesen Joan N, Rossi Richard F
Haskell Laboratory for Health and Environmental Sciences, E.I. du Pont de Nemours and Company, P.O. Box 50, Newark, DE 19714, USA.
Talanta. 2004 Nov 15;64(4):869-78. doi: 10.1016/j.talanta.2004.03.066.
The Wickbold decomposition method in combination with differential potentiometric detection via fluoride ion-selective electrode has been applied to analysis of total fluorine in biological matrices. The performance of the method has been evaluated for determination of total fluorine in rat blood. Total mineralization of the biological sample is achieved by combustion of the sample in oxygen/hydrogen flame and subsequent absorption of the resulting fluoride in aqueous absorption medium. The fluoride is then quantified by highly selective automated differential static potentiometry with fluoride ion-selective electrode. Total fluorine determination has been evaluated in terms of sample carryover, reproducibility, precision, as well as feasibility to routine analysis of alternative biological matrices. Our results indicate that, up to 100ppm fluorine in blood, the method does not suffer from sample carryover. Limits of quantitation of 0.5ppm and limits of detection of 0.24ppm fluorine in 0.5g blood samples were achieved by elimination of inherent limitations of fluoride ion-selective electrode detection via automated differential static potentiometric measurements. The Wickbold decomposition method was found to be suitable for routine total fluorine determination in blood samples despite its relatively low throughput and high operator skill requirements.
威克博尔德分解法结合氟离子选择性电极的差分电位检测已应用于生物基质中总氟的分析。该方法的性能已针对大鼠血液中总氟的测定进行了评估。生物样品的完全矿化是通过在氧/氢火焰中燃烧样品并随后将生成的氟化物吸收到水性吸收介质中来实现的。然后用氟离子选择性电极通过高选择性自动差分静态电位法对氟化物进行定量。已从样品残留、重现性、精密度以及对替代生物基质进行常规分析的可行性方面对总氟测定进行了评估。我们的结果表明,对于血液中高达100ppm的氟,该方法不存在样品残留问题。通过自动差分静态电位测量消除了氟离子选择性电极检测的固有局限性,在0.5g血液样品中实现了0.5ppm的定量限和0.24ppm的氟检测限。尽管威克博尔德分解法通量相对较低且对操作人员技能要求较高,但它被发现适用于血液样品中总氟的常规测定。