LM1010高速液体クロマトグラフィ法と化学発光免疫測定法によるバンコマイシン血中濃度測定値の比較

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Published in医療薬学 Vol. 51; no. 4; pp. 187 - 195
Main Authors 森川, 悟, 松下, 美由紀, 三浦, 昌朋, 赤嶺, 由美子
Format Journal Article
LanguageJapanese
Published 一般社団法人日本医療薬学会 10.04.2025
Subjects
Online AccessGet full text
ISSN1346-342X
1882-1499
DOI10.5649/jjphcs.51.187

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Author 赤嶺, 由美子
松下, 美由紀
三浦, 昌朋
森川, 悟
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  organization: 株式会社日立ハイテクサイエンス
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  fullname: 三浦, 昌朋
  organization: 秋田大学大学院医学系研究科薬物動態学講座
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  fullname: 赤嶺, 由美子
  organization: 秋田大学医学部附属病院薬剤部
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Copyright 日本医療薬学会
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References 1)Somerville AL, Wright DH, Rotschafer JC, Implications of vancomycin degradation products on therapeutic drug monitoring in patients with end-stage renal disease, Pharmacotherapy, 1999, 19, 702-707.
2)Morse GD, Nairn DK, Bertino JS Jr, Walshe JJ, Overestimation of vancomycin concentrations utilizing fluorescence polarization immunoassay in patients on peritoneal dialysis, Ther Drug Monit, 1987, 9, 212-215.
7)Hu MW, Anne L, Forni T, Gottwald K, Measurement of vancomycin in renally impaired patient samples using a new high-performance liquid chromatography method with vitamin B12 internal standard: comparison of high-performance liquid chromatography, emit, and fluorescence polarization immunoassay methods, Ther Drug Monit, 1990, 12, 562-569.
8)Backes DW, Aboleneen HI, Simpson JA, Quantitation of vancomycin and its crystalline degradation product (CDP-1) in human serum by high performance liquid chromatography, J Pharm Biomed Anal, 1998, 16, 1281-1287.
4)Chen CY, Li MY, Ma LY, Zhai XY, Luo DH, Zhou Y, Liu ZM, Cui YM, Precision and accuracy of commercial assays for vancomycin therapeutic drug monitoring: evaluation based on external quality assessment scheme, J Antimicrob Chemother, 2020, 75, 2110-2119.
3)Hortin GL, Landt M, Wilhite T, Smith CH, Cross-reactivity of a vancomycin degradation product in three immunoassays of vancomycin, Clin Chem, 1991, 37, 2009. doi: 10.1093/clinchem/37.11.2009a.
5)Fan Y, Peng X, Wu H, Liang X, Chen Y, Guo B, Zhang J, Simultaneous separation and determination of vancomycin and its crystalline degradation products in human serum by ultra high performance liquid chromatography tandem mass spectrometry method and its application in therapeutic drug monitoring, J Sep Sci, 2020, 43, 3987-3994.
6)Bland JM, Altman DG, Statistical methods for assessing agreement between two methods of clinical measurement, Lancet, 1986, 1, 307-310.
9)Committee of Practice Guidelines for TDM of Antimicrobial Agents, Japanese Society of Chemotherapy, Sectional Committee of Practice Guidelines for TDM, Antimicrobial Agents, The Japanese Society of Therapeutic Drug Monitoring, 抗菌薬TDM臨床実践ガイドライン2022, Jpn J Chemother, 2022, 70, 1-72.
References_xml – reference: 5)Fan Y, Peng X, Wu H, Liang X, Chen Y, Guo B, Zhang J, Simultaneous separation and determination of vancomycin and its crystalline degradation products in human serum by ultra high performance liquid chromatography tandem mass spectrometry method and its application in therapeutic drug monitoring, J Sep Sci, 2020, 43, 3987-3994.
– reference: 1)Somerville AL, Wright DH, Rotschafer JC, Implications of vancomycin degradation products on therapeutic drug monitoring in patients with end-stage renal disease, Pharmacotherapy, 1999, 19, 702-707.
– reference: 3)Hortin GL, Landt M, Wilhite T, Smith CH, Cross-reactivity of a vancomycin degradation product in three immunoassays of vancomycin, Clin Chem, 1991, 37, 2009. doi: 10.1093/clinchem/37.11.2009a.
– reference: 8)Backes DW, Aboleneen HI, Simpson JA, Quantitation of vancomycin and its crystalline degradation product (CDP-1) in human serum by high performance liquid chromatography, J Pharm Biomed Anal, 1998, 16, 1281-1287.
– reference: 9)Committee of Practice Guidelines for TDM of Antimicrobial Agents, Japanese Society of Chemotherapy, Sectional Committee of Practice Guidelines for TDM, Antimicrobial Agents, The Japanese Society of Therapeutic Drug Monitoring, 抗菌薬TDM臨床実践ガイドライン2022, Jpn J Chemother, 2022, 70, 1-72.
– reference: 6)Bland JM, Altman DG, Statistical methods for assessing agreement between two methods of clinical measurement, Lancet, 1986, 1, 307-310.
– reference: 7)Hu MW, Anne L, Forni T, Gottwald K, Measurement of vancomycin in renally impaired patient samples using a new high-performance liquid chromatography method with vitamin B12 internal standard: comparison of high-performance liquid chromatography, emit, and fluorescence polarization immunoassay methods, Ther Drug Monit, 1990, 12, 562-569.
– reference: 4)Chen CY, Li MY, Ma LY, Zhai XY, Luo DH, Zhou Y, Liu ZM, Cui YM, Precision and accuracy of commercial assays for vancomycin therapeutic drug monitoring: evaluation based on external quality assessment scheme, J Antimicrob Chemother, 2020, 75, 2110-2119.
– reference: 2)Morse GD, Nairn DK, Bertino JS Jr, Walshe JJ, Overestimation of vancomycin concentrations utilizing fluorescence polarization immunoassay in patients on peritoneal dialysis, Ther Drug Monit, 1987, 9, 212-215.
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SubjectTerms chemiluminescent immunoassay
high-performance liquid chromatography
method evaluation
vancomycin
Title LM1010高速液体クロマトグラフィ法と化学発光免疫測定法によるバンコマイシン血中濃度測定値の比較
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