Dried blood spot sampling in combination with LC-MS/MS for quantitative analysis of small molecules
The collection of whole blood samples on paper, known as dried blood spot (DBS), dates back to the early 1960s in newborn screening for inherited metabolic disorders. DBS offers a number of advantages over conventional blood collection. As a less invasive sampling method, DBS offers simpler sample c...
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| Published in | Biomedical chromatography Vol. 24; no. 1; pp. 49 - 65 |
|---|---|
| Main Authors | , |
| Format | Journal Article |
| Language | English |
| Published |
Chichester, UK
John Wiley & Sons, Ltd
01.01.2010
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| Subjects | |
| Online Access | Get full text |
| ISSN | 0269-3879 1099-0801 1099-0801 |
| DOI | 10.1002/bmc.1367 |
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| Abstract | The collection of whole blood samples on paper, known as dried blood spot (DBS), dates back to the early 1960s in newborn screening for inherited metabolic disorders. DBS offers a number of advantages over conventional blood collection. As a less invasive sampling method, DBS offers simpler sample collection and storage and easier transfer, with reduced infection risk of various pathogens, and requires a smaller blood volume. To date, DBS‐LC‐MS/MS has emerged as an important method for quantitative analysis of small molecules. Despite the increasing popularity of DBS‐LC‐MS/MS, the method has its limitations in assay sensitivity due to the small sample size. Sample quality is often a concern. Systematic assessment on the potential impact of various blood sample properties on accurate quantification of analyte of interest is necessary. Whereas most analytes may be stable on DBS, unstable compounds present another challenge for DBS as enzyme inhibitors cannot be conveniently mixed during sample collection. Improvements on the chemistry of DBS card are desirable. In addition to capturing many representative DBS‐LS‐MS/MS applications, this review highlights some important aspects of developing and validating a rugged DBS‐LC‐MS/MS method for quantitative analysis of small molecules along with DBS sample collection, processing and storage. Copyright © 2009 John Wiley & Sons, Ltd. |
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| AbstractList | The collection of whole blood samples on paper, known as dried blood spot (DBS), dates back to the early 1960s in newborn screening for inherited metabolic disorders. DBS offers a number of advantages over conventional blood collection. As a less invasive sampling method, DBS offers simpler sample collection and storage and easier transfer, with reduced infection risk of various pathogens, and requires a smaller blood volume. To date, DBS-LC-MS/MS has emerged as an important method for quantitative analysis of small molecules. Despite the increasing popularity of DBS-LC-MS/MS, the method has its limitations in assay sensitivity due to the small sample size. Sample quality is often a concern. Systematic assessment on the potential impact of various blood sample properties on accurate quantification of analyte of interest is necessary. Whereas most analytes may be stable on DBS, unstable compounds present another challenge for DBS as enzyme inhibitors cannot be conveniently mixed during sample collection. Improvements on the chemistry of DBS card are desirable. In addition to capturing many representative DBS-LS-MS/MS applications, this review highlights some important aspects of developing and validating a rugged DBS-LC-MS/MS method for quantitative analysis of small molecules along with DBS sample collection, processing and storage. The collection of whole blood samples on paper, known as dried blood spot (DBS), dates back to the early 1960s in newborn screening for inherited metabolic disorders. DBS offers a number of advantages over conventional blood collection. As a less invasive sampling method, DBS offers simpler sample collection and storage and easier transfer, with reduced infection risk of various pathogens, and requires a smaller blood volume. To date, DBS‐LC‐MS/MS has emerged as an important method for quantitative analysis of small molecules. Despite the increasing popularity of DBS‐LC‐MS/MS, the method has its limitations in assay sensitivity due to the small sample size. Sample quality is often a concern. Systematic assessment on the potential impact of various blood sample properties on accurate quantification of analyte of interest is necessary. Whereas most analytes may be stable on DBS, unstable compounds present another challenge for DBS as enzyme inhibitors cannot be conveniently mixed during sample collection. Improvements on the chemistry of DBS card are desirable. In addition to capturing many representative DBS‐LS‐MS/MS applications, this review highlights some important aspects of developing and validating a rugged DBS‐LC‐MS/MS method for quantitative analysis of small molecules along with DBS sample collection, processing and storage. Copyright © 2009 John Wiley & Sons, Ltd. The collection of whole blood samples on paper, known as dried blood spot (DBS), dates back to the early 1960s in newborn screening for inherited metabolic disorders. DBS offers a number of advantages over conventional blood collection. As a less invasive sampling method, DBS offers simpler sample collection and storage and easier transfer, with reduced infection risk of various pathogens, and requires a smaller blood volume. To date, DBS-LC-MS/MS has emerged as an important method for quantitative analysis of small molecules. Despite the increasing popularity of DBS-LC-MS/MS, the method has its limitations in assay sensitivity due to the small sample size. Sample quality is often a concern. Systematic assessment on the potential impact of various blood sample properties on accurate quantification of analyte of interest is necessary. Whereas most analytes may be stable on DBS, unstable compounds present another challenge for DBS as enzyme inhibitors cannot be conveniently mixed during sample collection. Improvements on the chemistry of DBS card are desirable. In addition to capturing many representative DBS-LS-MS/MS applications, this review highlights some important aspects of developing and validating a rugged DBS-LC-MS/MS method for quantitative analysis of small molecules along with DBS sample collection, processing and storage.The collection of whole blood samples on paper, known as dried blood spot (DBS), dates back to the early 1960s in newborn screening for inherited metabolic disorders. DBS offers a number of advantages over conventional blood collection. As a less invasive sampling method, DBS offers simpler sample collection and storage and easier transfer, with reduced infection risk of various pathogens, and requires a smaller blood volume. To date, DBS-LC-MS/MS has emerged as an important method for quantitative analysis of small molecules. Despite the increasing popularity of DBS-LC-MS/MS, the method has its limitations in assay sensitivity due to the small sample size. Sample quality is often a concern. Systematic assessment on the potential impact of various blood sample properties on accurate quantification of analyte of interest is necessary. Whereas most analytes may be stable on DBS, unstable compounds present another challenge for DBS as enzyme inhibitors cannot be conveniently mixed during sample collection. Improvements on the chemistry of DBS card are desirable. In addition to capturing many representative DBS-LS-MS/MS applications, this review highlights some important aspects of developing and validating a rugged DBS-LC-MS/MS method for quantitative analysis of small molecules along with DBS sample collection, processing and storage. |
| Author | Li, Wenkui Tse, Francis L. S. |
| Author_xml | – sequence: 1 givenname: Wenkui surname: Li fullname: Li, Wenkui email: wenkui.li@novartis.com organization: Drug Metabolism and Pharmacokinetics, Novartis Institutes for Biomedical Research, One Health Plaza, East Hanover, NJ 07936, USA – sequence: 2 givenname: Francis L. S. surname: Tse fullname: Tse, Francis L. S. organization: Drug Metabolism and Pharmacokinetics, Novartis Institutes for Biomedical Research, One Health Plaza, East Hanover, NJ 07936, USA |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/20017122$$D View this record in MEDLINE/PubMed |
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Therapeutic drug monitoring of tacrolimus with the dried blood spot method. 2002; 16 2009b; 49 1990; 13 2009; 81 2004; 27 2000; 46 2008a 2006; 39 2007; 386 2008; 867 2006; 373 2008; 32 2003; 17 2008; 863 2009; 393 2004; 809 2009; 394 2008; 30 2008; 861 2007; 30 2009; 877 2005; 27 2009; 49 2002; 48 1963; 32 1993; 39 2001; 131 2009; 97 2001 2009; 50 2005; 823 2003; 49 2008; 21 2001; 15 2008; 22 2008b; 48 1999; 52 2008; 870 2003; 40 1999; 731 1996; 20 2009; 403 1997; 61 1995; 17 2004; 89 2009 2008 1997 2002; 3 2007; 92 2008; 54 2005; 80 1977; 45 1992; 38 2006; 831 2007; 53 2003; 335 1998; 21 1995; 41 2005; 19 2009; 74 2004; 50 2009; 31 2004; 18 2006; 89 2004; 16 2006; 88 2002; 322 2008; 48 2003; 25 2009a; 49 2009; 3 2008; 40 2007; 44 2008c; 22 e_1_2_1_60_1 e_1_2_1_81_1 e_1_2_1_20_1 e_1_2_1_41_1 e_1_2_1_66_1 e_1_2_1_68_1 e_1_2_1_24_1 e_1_2_1_45_1 e_1_2_1_62_1 e_1_2_1_22_1 e_1_2_1_43_1 e_1_2_1_64_1 e_1_2_1_85_1 e_1_2_1_28_1 e_1_2_1_49_1 e_1_2_1_26_1 e_1_2_1_47_1 Török D (e_1_2_1_77_1) 2002; 48 Adam BW (e_1_2_1_3_1) 2000; 46 e_1_2_1_71_1 e_1_2_1_31_1 e_1_2_1_54_1 e_1_2_1_8_1 e_1_2_1_56_1 e_1_2_1_79_1 e_1_2_1_6_1 Guthrie R (e_1_2_1_30_1) 1963; 32 e_1_2_1_35_1 e_1_2_1_50_1 e_1_2_1_73_1 e_1_2_1_4_1 e_1_2_1_10_1 e_1_2_1_33_1 e_1_2_1_52_1 e_1_2_1_75_1 e_1_2_1_2_1 e_1_2_1_16_1 e_1_2_1_39_1 e_1_2_1_14_1 e_1_2_1_37_1 Gempel K (e_1_2_1_29_1) 2000; 46 e_1_2_1_58_1 e_1_2_1_18_1 e_1_2_1_80_1 e_1_2_1_82_1 Chace DH (e_1_2_1_13_1) 1995; 41 e_1_2_1_42_1 e_1_2_1_65_1 Wong T (e_1_2_1_83_1) 1992; 38 e_1_2_1_40_1 e_1_2_1_67_1 e_1_2_1_23_1 e_1_2_1_46_1 e_1_2_1_84_1 e_1_2_1_21_1 e_1_2_1_44_1 e_1_2_1_63_1 e_1_2_1_86_1 O'Broin SD. (e_1_2_1_61_1) 1993; 39 e_1_2_1_27_1 Chace DH (e_1_2_1_12_1) 1993; 39 e_1_2_1_25_1 e_1_2_1_48_1 e_1_2_1_69_1 e_1_2_1_70_1 e_1_2_1_7_1 e_1_2_1_55_1 e_1_2_1_76_1 e_1_2_1_5_1 e_1_2_1_57_1 e_1_2_1_78_1 e_1_2_1_34_1 e_1_2_1_51_1 e_1_2_1_72_1 e_1_2_1_11_1 e_1_2_1_32_1 e_1_2_1_53_1 e_1_2_1_74_1 e_1_2_1_17_1 e_1_2_1_38_1 e_1_2_1_15_1 e_1_2_1_36_1 e_1_2_1_59_1 e_1_2_1_9_1 e_1_2_1_19_1 |
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| Snippet | The collection of whole blood samples on paper, known as dried blood spot (DBS), dates back to the early 1960s in newborn screening for inherited metabolic... |
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| SubjectTerms | Analytic Sample Preparation Methods Blood Chemical Analysis - methods Blood Specimen Collection Chromatography, Liquid - methods DBS dried blood spot(s) Drug Monitoring Humans LC-MS/MS newborn screening pharmacokinetics quantitative analysis Sensitivity and Specificity small molecules Tandem Mass Spectrometry - methods therapeutic drug monitoring toxicokinetics |
| Title | Dried blood spot sampling in combination with LC-MS/MS for quantitative analysis of small molecules |
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