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M. E. Miller and J. D. Stuart, “Comparison of Gas-Sampled and SPME-Sampled Static Headspace for the Determination of Volatile Flavor Components,” Analytical Chemistry, Vol. 71, No. 1, 1999, pp. 23-27.
http://dx.doi.org/10.1021/ac980576v

has been cited by the following article:

• TITLE: A New SPME Thermal Desorption Interface for HPLC

  AUTHORS: John Jairo Ríos Acevedo, Mohamed Nour Kayali Sayadi, Luis María Polo Díez

  KEYWORDS: SPME-HPLC-FLD; SPME-HPLC Interface; Polynuclear Aromatic Hydrocarbons

  JOURNAL NAME: Journal of Analytical Sciences, Methods and Instrumentation, Vol.3 No.4, October 22, 2013

  ABSTRACT: A new SPME/HPLC interface is developed. It is based on thermal desorption from the SPME fiber and organic solvent collection of the desorbed analytes by sweeping them with an argon flow into a small organic solvent volume which is further injected into the HPLC chromatograph. Extraction and desorption parameters were investigated using five PAHs of different volatilities (naphthalene, acenaphthalene, fluorene, phenanthrene and anthracene) as test compounds and fluorimetric detection. Regression coefficients closed to 0.99 with RDS = 3) and detection limits in the range 0.07 - 0.99 μg.L-1 were found. A method was applied to determine the above PAHs in water samples. The results were compared with those supplied by the 550.1 EPA method showing the agreement of both methods at the 0.05 significance level.