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Biomedical subjects

Stephanie M Pendergrass

Publications and source records attributed to Stephanie M Pendergrass.

3 recordsLinked to original sources

NMAM methods update: a laboratory response to concerns about technologically outdated and problematic methods.

The National Institute for Occupational Safety Health (NIOSH) publishes the NIOSH Manual of Analytical Methods (NMAM). The NMAM, although subject to various revisions and the incorporation of supplemental editions over the years, still contains many methods that are technologically outdated or problematic, as identified in a recent survey of the various users of the NMAM. Whereas the survey identified a number of problematic methods based on various chromatographic techniques, those selected for inclusion in this project employed analysis by gas chromatography (GC). The GC methods selected for evaluation were categorized as Phases 1, 2, 3, and 4 based on necessity as determined by the results of the client survey or internal assessment. The Phase 1 methods included: NMAM 1606 (Acetonitrile), NMAM 2005 (Nitroaromatic Compounds), and NMAM 1453 (Vinyl Acetate); the Phase 2 methods: NMAM 1003 (Halogenated Hydrocarbons), NMAM 1501 (Aromatic Hydrocarbons), NMAM 2555 (Ketones I), and NMAM 1403 (Alcohols IV); the Phase 3 methods: NMAM 2552 (Methyl Acrylate), NMAM 2537 (Methyl and Ethyl Methacrylate), and NMAM 2553 (Ketones II), and the Phase 4 methods: NMAM 2556 (Isophorone), NMAM 1460 (Isopropyl Acetate), and NMAM 1618 (Isopropyl Ether). All methods previously specifying packed column chromatography have been evaluated using the appropriate fused silica capillary column. Improvements in individual analyte desorption efficiencies were achieved at concentrations substantially lower than those used in the previous methods. Most analytes evaluated had their respective limit of detection lowered by a factor of ten-to twentyfold. Thirty-day storage stability studies, previously lacking in a number of methods or for new analytes, were successfully completed to meet current method development criteria. Additional benefits resulting from this effort included the incorporation of single analyte methods into chemically related multianalyte methods and the evaluation of certain isomers, such as the methylstyrenes and xylenes, which previously could not be separated.

Air Pollution, Indoor↗

Method development for the determination of diacetyl and acetoin at a microwave popcorn plant.

Separate sampling and analytical methods for the determination of diacetyl and acetoin have been developed to assess workplace exposures at a popcorn processing facility have been described. Diacetyl (NMAM 2557) is efficiently recovered from an Anasorb CMS sampler tube when the composition of methanol in the desorption solvent is 1%, and acetoin (NMAM 2558) is efficiently recovered when the concentration of methanol is increased to 5%. Desorption efficiencies for diacetyl and acetoin were acceptable, 89.9% (RSD = 0.018) and 94.9% (RSD = 0.019), respectively. Recoveries for nonanone, methyl ethyl ketone, and ethyl acetate were not optimized because they were present in very low concentrations in the popcorn processing facility and not considered to be major occupational health hazards. Samples were collected on Anasorb CMS solid sorbent tubes. All analytes were separated using a 30-m Stabilwax-DA fused silica capillary column, followed by analysis using gas chromatography with flame ionization detection. These methods were acceptable for monitoring and identifying exposures to diacetyl and acetoin present in the butter flavoring mixture used at popcorn processing facilities. For example, in the initial site visit the method was used to determine that maximum workers exposures to diacetyl (462.6 mg/m3), acetoin (59.1 mg/m3), and nonanone (0.45 mg/m3) occurred as the butter flavoring was added to the mixing kettle. When protective measures were recommended by NIOSH personnel and implemented bythe popcorn processing facility, the methods were then used to determine the effectiveness of these changes, which showed that diacetyl and acetoin concentrations had been reduced significantly to 0.97 and 2.3 mg/m3, respectively, while the concentration of nonanone fell to levels below the detection limit (LOD).

Acetoin↗