The Experts below are selected from a list of 57 Experts worldwide ranked by ideXlab platform
W H Hannon - One of the best experts on this subject based on the ideXlab platform.
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The preparation and storage of dried-blood spot quality control materials for lysosomal storage disease screening tests
Clinical Biochemistry, 2011Co-Authors: B W Adam, J J Orsini, M Martin, E M Hall, S D Zobel, M Caggana, W H HannonAbstract:Abstract Objective We aimed to prepare dried-blood spot (DBS) quality control (QC) materials for lysosomal storage disease (LSD) screening tests and to determine optimum blood and DBS storage conditions. Methods We compared enzyme activities of five LSD markers in adult blood, umbilical-cord blood, and leukocyte-reduced blood. We measured activities in Liquid blood and DBSs after predetermined intervals at controlled temperatures and humidities. Results Lysosomal-enzyme activity levels in umbilical-cord blood mimicked those in newborn screening samples. Lysosomal-enzyme activities in leukocyte-reduced blood were lower than in LSD-positive patient samples. Enzyme activities were stable in Refrigerated Liquid blood for 32 days and in frozen DBSs stored at low humidity for a year. Activity losses from DBSs after 34 days at 37 ± 1 °C were 35%–66% in low humidity and 61%–100% in high humidity. Conclusions Umbilical-cord blood is the preferred matrix for LSD-normal DBS QC materials. Leukocyte-reduced blood is lysosomal enzyme-deficient. Failure to control humidity during DBS storage results in loss of lysosomal-enzyme activities.
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The preparation and storage of dried-blood spot quality control materials for lysosomal storage disease screening tests.
Clinical biochemistry, 2011Co-Authors: B W Adam, J J Orsini, M Martin, E M Hall, S D Zobel, M Caggana, W H HannonAbstract:We aimed to prepare dried-blood spot (DBS) quality control (QC) materials for lysosomal storage disease (LSD) screening tests and to determine optimum blood and DBS storage conditions. We compared enzyme activities of five LSD markers in adult blood, umbilical-cord blood, and leukocyte-reduced blood. We measured activities in Liquid blood and DBSs after predetermined intervals at controlled temperatures and humidities. Lysosomal-enzyme activity levels in umbilical-cord blood mimicked those in newborn screening samples. Lysosomal-enzyme activities in leukocyte-reduced blood were lower than in LSD-positive patient samples. Enzyme activities were stable in Refrigerated Liquid blood for 32 days and in frozen DBSs stored at low humidity for a year. Activity losses from DBSs after 34 days at 37±1°C were 35%-66% in low humidity and 61%-100% in high humidity. Umbilical-cord blood is the preferred matrix for LSD-normal DBS QC materials. Leukocyte-reduced blood is lysosomal enzyme-deficient. Failure to control humidity during DBS storage results in loss of lysosomal-enzyme activities. Published by Elsevier Inc.
B W Adam - One of the best experts on this subject based on the ideXlab platform.
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The preparation and storage of dried-blood spot quality control materials for lysosomal storage disease screening tests
Clinical Biochemistry, 2011Co-Authors: B W Adam, J J Orsini, M Martin, E M Hall, S D Zobel, M Caggana, W H HannonAbstract:Abstract Objective We aimed to prepare dried-blood spot (DBS) quality control (QC) materials for lysosomal storage disease (LSD) screening tests and to determine optimum blood and DBS storage conditions. Methods We compared enzyme activities of five LSD markers in adult blood, umbilical-cord blood, and leukocyte-reduced blood. We measured activities in Liquid blood and DBSs after predetermined intervals at controlled temperatures and humidities. Results Lysosomal-enzyme activity levels in umbilical-cord blood mimicked those in newborn screening samples. Lysosomal-enzyme activities in leukocyte-reduced blood were lower than in LSD-positive patient samples. Enzyme activities were stable in Refrigerated Liquid blood for 32 days and in frozen DBSs stored at low humidity for a year. Activity losses from DBSs after 34 days at 37 ± 1 °C were 35%–66% in low humidity and 61%–100% in high humidity. Conclusions Umbilical-cord blood is the preferred matrix for LSD-normal DBS QC materials. Leukocyte-reduced blood is lysosomal enzyme-deficient. Failure to control humidity during DBS storage results in loss of lysosomal-enzyme activities.
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The preparation and storage of dried-blood spot quality control materials for lysosomal storage disease screening tests.
Clinical biochemistry, 2011Co-Authors: B W Adam, J J Orsini, M Martin, E M Hall, S D Zobel, M Caggana, W H HannonAbstract:We aimed to prepare dried-blood spot (DBS) quality control (QC) materials for lysosomal storage disease (LSD) screening tests and to determine optimum blood and DBS storage conditions. We compared enzyme activities of five LSD markers in adult blood, umbilical-cord blood, and leukocyte-reduced blood. We measured activities in Liquid blood and DBSs after predetermined intervals at controlled temperatures and humidities. Lysosomal-enzyme activity levels in umbilical-cord blood mimicked those in newborn screening samples. Lysosomal-enzyme activities in leukocyte-reduced blood were lower than in LSD-positive patient samples. Enzyme activities were stable in Refrigerated Liquid blood for 32 days and in frozen DBSs stored at low humidity for a year. Activity losses from DBSs after 34 days at 37±1°C were 35%-66% in low humidity and 61%-100% in high humidity. Umbilical-cord blood is the preferred matrix for LSD-normal DBS QC materials. Leukocyte-reduced blood is lysosomal enzyme-deficient. Failure to control humidity during DBS storage results in loss of lysosomal-enzyme activities. Published by Elsevier Inc.
E M Hall - One of the best experts on this subject based on the ideXlab platform.
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The preparation and storage of dried-blood spot quality control materials for lysosomal storage disease screening tests
Clinical Biochemistry, 2011Co-Authors: B W Adam, J J Orsini, M Martin, E M Hall, S D Zobel, M Caggana, W H HannonAbstract:Abstract Objective We aimed to prepare dried-blood spot (DBS) quality control (QC) materials for lysosomal storage disease (LSD) screening tests and to determine optimum blood and DBS storage conditions. Methods We compared enzyme activities of five LSD markers in adult blood, umbilical-cord blood, and leukocyte-reduced blood. We measured activities in Liquid blood and DBSs after predetermined intervals at controlled temperatures and humidities. Results Lysosomal-enzyme activity levels in umbilical-cord blood mimicked those in newborn screening samples. Lysosomal-enzyme activities in leukocyte-reduced blood were lower than in LSD-positive patient samples. Enzyme activities were stable in Refrigerated Liquid blood for 32 days and in frozen DBSs stored at low humidity for a year. Activity losses from DBSs after 34 days at 37 ± 1 °C were 35%–66% in low humidity and 61%–100% in high humidity. Conclusions Umbilical-cord blood is the preferred matrix for LSD-normal DBS QC materials. Leukocyte-reduced blood is lysosomal enzyme-deficient. Failure to control humidity during DBS storage results in loss of lysosomal-enzyme activities.
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The preparation and storage of dried-blood spot quality control materials for lysosomal storage disease screening tests.
Clinical biochemistry, 2011Co-Authors: B W Adam, J J Orsini, M Martin, E M Hall, S D Zobel, M Caggana, W H HannonAbstract:We aimed to prepare dried-blood spot (DBS) quality control (QC) materials for lysosomal storage disease (LSD) screening tests and to determine optimum blood and DBS storage conditions. We compared enzyme activities of five LSD markers in adult blood, umbilical-cord blood, and leukocyte-reduced blood. We measured activities in Liquid blood and DBSs after predetermined intervals at controlled temperatures and humidities. Lysosomal-enzyme activity levels in umbilical-cord blood mimicked those in newborn screening samples. Lysosomal-enzyme activities in leukocyte-reduced blood were lower than in LSD-positive patient samples. Enzyme activities were stable in Refrigerated Liquid blood for 32 days and in frozen DBSs stored at low humidity for a year. Activity losses from DBSs after 34 days at 37±1°C were 35%-66% in low humidity and 61%-100% in high humidity. Umbilical-cord blood is the preferred matrix for LSD-normal DBS QC materials. Leukocyte-reduced blood is lysosomal enzyme-deficient. Failure to control humidity during DBS storage results in loss of lysosomal-enzyme activities. Published by Elsevier Inc.
M Caggana - One of the best experts on this subject based on the ideXlab platform.
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The preparation and storage of dried-blood spot quality control materials for lysosomal storage disease screening tests
Clinical Biochemistry, 2011Co-Authors: B W Adam, J J Orsini, M Martin, E M Hall, S D Zobel, M Caggana, W H HannonAbstract:Abstract Objective We aimed to prepare dried-blood spot (DBS) quality control (QC) materials for lysosomal storage disease (LSD) screening tests and to determine optimum blood and DBS storage conditions. Methods We compared enzyme activities of five LSD markers in adult blood, umbilical-cord blood, and leukocyte-reduced blood. We measured activities in Liquid blood and DBSs after predetermined intervals at controlled temperatures and humidities. Results Lysosomal-enzyme activity levels in umbilical-cord blood mimicked those in newborn screening samples. Lysosomal-enzyme activities in leukocyte-reduced blood were lower than in LSD-positive patient samples. Enzyme activities were stable in Refrigerated Liquid blood for 32 days and in frozen DBSs stored at low humidity for a year. Activity losses from DBSs after 34 days at 37 ± 1 °C were 35%–66% in low humidity and 61%–100% in high humidity. Conclusions Umbilical-cord blood is the preferred matrix for LSD-normal DBS QC materials. Leukocyte-reduced blood is lysosomal enzyme-deficient. Failure to control humidity during DBS storage results in loss of lysosomal-enzyme activities.
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The preparation and storage of dried-blood spot quality control materials for lysosomal storage disease screening tests.
Clinical biochemistry, 2011Co-Authors: B W Adam, J J Orsini, M Martin, E M Hall, S D Zobel, M Caggana, W H HannonAbstract:We aimed to prepare dried-blood spot (DBS) quality control (QC) materials for lysosomal storage disease (LSD) screening tests and to determine optimum blood and DBS storage conditions. We compared enzyme activities of five LSD markers in adult blood, umbilical-cord blood, and leukocyte-reduced blood. We measured activities in Liquid blood and DBSs after predetermined intervals at controlled temperatures and humidities. Lysosomal-enzyme activity levels in umbilical-cord blood mimicked those in newborn screening samples. Lysosomal-enzyme activities in leukocyte-reduced blood were lower than in LSD-positive patient samples. Enzyme activities were stable in Refrigerated Liquid blood for 32 days and in frozen DBSs stored at low humidity for a year. Activity losses from DBSs after 34 days at 37±1°C were 35%-66% in low humidity and 61%-100% in high humidity. Umbilical-cord blood is the preferred matrix for LSD-normal DBS QC materials. Leukocyte-reduced blood is lysosomal enzyme-deficient. Failure to control humidity during DBS storage results in loss of lysosomal-enzyme activities. Published by Elsevier Inc.
S D Zobel - One of the best experts on this subject based on the ideXlab platform.
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The preparation and storage of dried-blood spot quality control materials for lysosomal storage disease screening tests
Clinical Biochemistry, 2011Co-Authors: B W Adam, J J Orsini, M Martin, E M Hall, S D Zobel, M Caggana, W H HannonAbstract:Abstract Objective We aimed to prepare dried-blood spot (DBS) quality control (QC) materials for lysosomal storage disease (LSD) screening tests and to determine optimum blood and DBS storage conditions. Methods We compared enzyme activities of five LSD markers in adult blood, umbilical-cord blood, and leukocyte-reduced blood. We measured activities in Liquid blood and DBSs after predetermined intervals at controlled temperatures and humidities. Results Lysosomal-enzyme activity levels in umbilical-cord blood mimicked those in newborn screening samples. Lysosomal-enzyme activities in leukocyte-reduced blood were lower than in LSD-positive patient samples. Enzyme activities were stable in Refrigerated Liquid blood for 32 days and in frozen DBSs stored at low humidity for a year. Activity losses from DBSs after 34 days at 37 ± 1 °C were 35%–66% in low humidity and 61%–100% in high humidity. Conclusions Umbilical-cord blood is the preferred matrix for LSD-normal DBS QC materials. Leukocyte-reduced blood is lysosomal enzyme-deficient. Failure to control humidity during DBS storage results in loss of lysosomal-enzyme activities.
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The preparation and storage of dried-blood spot quality control materials for lysosomal storage disease screening tests.
Clinical biochemistry, 2011Co-Authors: B W Adam, J J Orsini, M Martin, E M Hall, S D Zobel, M Caggana, W H HannonAbstract:We aimed to prepare dried-blood spot (DBS) quality control (QC) materials for lysosomal storage disease (LSD) screening tests and to determine optimum blood and DBS storage conditions. We compared enzyme activities of five LSD markers in adult blood, umbilical-cord blood, and leukocyte-reduced blood. We measured activities in Liquid blood and DBSs after predetermined intervals at controlled temperatures and humidities. Lysosomal-enzyme activity levels in umbilical-cord blood mimicked those in newborn screening samples. Lysosomal-enzyme activities in leukocyte-reduced blood were lower than in LSD-positive patient samples. Enzyme activities were stable in Refrigerated Liquid blood for 32 days and in frozen DBSs stored at low humidity for a year. Activity losses from DBSs after 34 days at 37±1°C were 35%-66% in low humidity and 61%-100% in high humidity. Umbilical-cord blood is the preferred matrix for LSD-normal DBS QC materials. Leukocyte-reduced blood is lysosomal enzyme-deficient. Failure to control humidity during DBS storage results in loss of lysosomal-enzyme activities. Published by Elsevier Inc.
