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How reliable are crystalline silica dust concentration measurements?
Cox, L A; Van Orden, D R; Lee, R J; Arlauckas, S M; Kautz, R A; Warzel, A L; Bailey, K F; Ranpuria, A K.
Afiliación
  • Cox LA; Cox Associates and University of Colorado, 503 Franklin St, Denver, CO 80218, USA.
  • Van Orden DR; RJ Lee Group, Inc., 350 Hochberg Road, Monroeville, PA 15146, USA. Electronic address: drew@rjlg.com.
  • Lee RJ; RJ Lee Group, Inc., 350 Hochberg Road, Monroeville, PA 15146, USA.
  • Arlauckas SM; RJ Lee Group, Inc., 350 Hochberg Road, Monroeville, PA 15146, USA.
  • Kautz RA; RJ Lee Group, Inc., 350 Hochberg Road, Monroeville, PA 15146, USA.
  • Warzel AL; RJ Lee Group, Inc., 350 Hochberg Road, Monroeville, PA 15146, USA.
  • Bailey KF; Vulcan Materials Company, 1200 Urban Center Drive, Birmingham, AL 35242, USA.
  • Ranpuria AK; Sandler Occupational Medicine Associates, Inc., 12700 Sunrise Valley Dr, Suite 405, Reston, VA 20191, USA.
Regul Toxicol Pharmacol ; 73(1): 126-36, 2015 Oct.
Article en En | MEDLINE | ID: mdl-26160597
ABSTRACT
To determine how reliably commercial laboratories measure crystalline silica concentrations corresponding to OSHA's proposed limits, 105 filters were prepared with known masses of 20, 40, and 80 µg of respirable quartz corresponding to airborne silica concentrations of 25, 50, and 100 µg/m(3) and were submitted, in a blind test, to qualified commercial laboratories over a nine month period. Under these test conditions, the reported results indicated a lack of accuracy and precision needed to reliably inform regulatory compliance decisions. This was true even for filters containing only silica, without an interfering matrix. For 36 filters loaded with 20 or more micrograms of silica, the laboratories reported non-detected levels of silica. Inter-laboratory variability in this performance test program was so high that the reported results could not be used to reliably discriminate among filters prepared to reflect 8-h exposures to respirable quartz concentrations of 25, 50 and 100 µg/m(3). Moreover, even in intra-laboratory performance, there was so much variability in the reported results that 2-fold variations in exposure concentrations could not be reliably distinguished. Part of the variability and underreporting may result from the sample preparation process. The results of this study suggest that current laboratory methods and practices cannot necessarily be depended on, with high confidence, to support proposed regulatory standards with reliable data.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Dióxido de Silicio / Polvo Tipo de estudio: Guideline Idioma: En Revista: Regul Toxicol Pharmacol Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Dióxido de Silicio / Polvo Tipo de estudio: Guideline Idioma: En Revista: Regul Toxicol Pharmacol Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos