References
- Graeme T , ClarkGT, HaynesJJ, BaylissMA, BurrowsL. Utilization of DBS within drug discovery: development of a serial microsampling pharmacokinetic study in mice. Bioanalysis2 (8), 1477–1488 (2010).
- Arienzo CJD , JiQC, DiscenzaLet al. DBS sampling can be used to stabilize prodrugs in drug discovery rodent studies without the addition of esterase inhibitors. Bioanalysis2 (8), 1415–1422 (2010).
- Rahavendran SV , VekichS, SkorHet al. Discovery pharmacokinetic studies in mice using serial microsampling; dried blood spots and microbore LC–MS/MS. Bioanalysis4 (9), 1077–1095 (2012).
- Nilsson LB , AhnoffM, JonssonO. Capillary microsampling in the regulatory environment: validation and use of bioanalytical capillary microsampling methods. Bioanalysis5 (6), 731–738 (2013).
- Baietto L , SimieleM, D’AvolioA. How effective is the use of DBS and DPS as tools to encourage widespread therapeutic drug monitoring?Bioanalysis6 (4), 425–427 (2014).
- Timmerman P , WhiteS, CobbZet al. Updates from the EBF DBS–microsampling consortium. Bioanalysis4 (16), 1969–1970 (2012).
- Meesters RJW , HooffGP. State-of-the-art dried blood spot analysis:an overview of recent advances and future trends. Bioanalysis5 (17), 2187–2208 (2013).
- Spooner N . A dried blood spot update: still an important bioanalytical technique?Bioanalysis5 (8), 879–883 (2013).
- White S , HawthorneG, DillenLet al. EBF: reflection on bioanalytical assay requirements used to support liquid microsampling. Bioanalysis6 (19), 2581–2586 (2014).
- Linder C , AnderssonM, WideK, BeckO, PohankaA. A LC–MS/MS method for therapeutic drug monitoring of carbamazepine; lamotrigine and valproic acid in DBS. Bioanalysis7 (16), 2031–2039 (2015).
- Abu-Rabie P , DenniffP, SpoonerN, ChowdhryBZ, PullenFS. Investigation of different approaches to incorporating internal standard in dbs quantitative bioanalytical workflows and their effect on nullifying hematocrit-based assay bias. Anal. Chem. 87, 4996–5003 (2015).
- Abu-Rabie P , DenniffP, SpoonerN, BrynjolffssenJ, GalluzzoP, SandersG. Method of applying internal standard to dried matrix spot samples for use in quantitative bioanalysis. Anal. Chem. 83, 8779–8786 (2011).
- Mano Y , KitaK, KusanoK. Hematocrit-independent recovery is a key for bioanalysis using volumetric absorptive microsampling devices; Mitra™. Bioanalysis7 (15), 1821–1829 (2015).
- Hempen CM , KosterEHM, OomsJA. Hematocrit-independent recovery of immunosuppressants from DBS using heated flow-through desorption. Bioanalysis7 (16), 2019–2029 (2015).
- Koster RA , AlffenaarJWC, BotmaRet al. What is the right blood hematocrit preparation procedure for standards and quality control samples for dried blood spot analysis? Bioanalysis 7 (3), 345–351 (2015).
- Lenk G , HanssonJ, BeckO, RoxhedN. The effect of drying on the homogeneity of DBS. Bioanalysis7 (16), 1977–1985 (2015).
- Vries RD , BarfieldM, van de MerbelNet al. The effect of hematocrit on bioanalysis of DBS: results from the EBF DBS-microsampling consortium. Bioanalysis5 (17), 2147–2160 (2013).
- Youhnovski N , BergeronA, FurtadoM, GarofoloF. Pre-cut dried blood spot (PCDBS): an alternative to dried blood spot (DBS) technique to overcome hematocrit impact. Rapid Commun. Mass Spectrom. 25, 2951–2958 (2011).
- Spooner N , Denniff1P, MichielsenLet al. A device for dried blood microsampling in quantitative bioanalysis: overcoming the issues associated with blood hematocrit. Bioanalysis7 (6), 653–659 (2015).
- Mengerink Y , MommersJ, QiuJ, MengerinkJ, SteijgerO, HoningM. A new DBS card with spot sizes independent of the hematocrit value of blood. Bioanalysis7 (16), 2095–2104 (2015).
- Lenk G , SandkvistS, PohankaA, StemmeG, BeckO, RoxhedN. A disposable sampling device to collect volume-measured DBS directly from a fingerprick onto DBS paper. Bioanalysis7 (16), 2085–2094 (2015).
- Barfield M , WhellerR. Use of dried plasma spots in the determination of pharmacokinetics in clinical studies: validation of a quantitative bioanalytical method. Anal. Chem. 83, 118–124 (2011).
- Kolocouri F , DotsikasY, LoukasYL. Dried plasma spots as an alternative sample collection technique for the quantitative LC–MS/MS determination of gabapentin. Anal. Bioanal. Chem. 398 (3), 1339–1347 (2010).
- Li Y , HenionJ, AbbottR, WangP. The use of a membrane filtration device to form dried plasma spots for the quantitative determination of guanfacine in whole blood. Rapid Commun. Mass Spectrom. 26, 1208–1212 (2012).
- Jonsson O , VillarRP, NilssonLBet al. Validation of a bioanalytical method using capillary microsampling of 8 μl plasma samples: application to a toxicokinetic study in mice. Bioanalysis4 (16), 1989 – (2012).
- Spreadborough M , DayJ, Jackson-AddieKet al. Bioanalytical implementation of plasma capillary microsampling: small hurdles: large gains. Bioanalysis5 (12), 1485–1489 (2013).
- Bowen CL , Licea-PerezH, KarlinseyMZet al. A novel approach to capillary plasma microsampling for quantitative bioanalysis. Bioanalysis5 (9), 1131–1135 (2013).
- Li F , FastMF, PlochAP. Accurate weighing and dilution-assisted plasma microsampling (AWADA-PM): an easy-to-implement and rugged strategy. Bioanalysis6 (6), 805–817 (2014).
- Hui YH , HuangNH, EbbertLet al. Pharmacokinetic comparisons of tail-bleeding with cannula- or retro-orbital bleeding techniques in rats using six marketed drugs. J. Pharmacol. Toxicol. Methods56 (2), 256–264 (2007).
- Rangaraj N , VaghasiyaK, JaiswalS, SharmaA, ShuklaM, LalJ. Do blood sampling sites affect pharmacokinetics?Chemistry & Biology Interface4 (3), 176–191 (2014).