Capillary microsampling in mice: effective way to move from sparse sampling to serial sampling in pharmacokinetics profiling

References

• Avery LB, Wang M, Kavosi MS, et al. (2016). Utility of a human FcRn transgenic mouse model in drug discovery for early assessment and prediction of human pharmacokinetics of monoclonal antibodies. MAbs 8:1064–78.
   PubMed Web of Science ®Google Scholar
• Barfield M, Wheller R. (2011). Use of dried plasma spots in the determination of pharmacokinetics in clinical studies: validation of a quantitative bioanalytical method. Anal Chem 83:118–24.
   PubMed Web of Science ®Google Scholar
• Bateman KP, Castonguay G, Xu L, et al. (2001). Reduction of animal usage by serial bleeding of mice for pharmacokinetic studies: application of robotic sample preparation and fast liquid chromatography mass spectrometry. J Chromatogr B 754:245–51.
   PubMedGoogle Scholar
• Beaudette P, Bateman KP. (2004). Discovery stage pharmacokinetics using dried blood spots. J Chromatogr B 809:153–8.
   PubMed Web of Science ®Google Scholar
• Bowen CL, Licea-Perez H, Karlinsey MZ, et al. (2013). A novel approach to capillary plasma microsampling for quantitative bioanalysis. Bioanalysis 5:1131–5.
   PubMed Web of Science ®Google Scholar
• Dainty TC, Richmond ES, Davies I, Blackwell MP. (2012). Dried blood spot bioanalysis: an evaluation of techniques and opportunities for reduction and refinement in mouse and juvenile rat toxicokinetic studies. Int J Toxicol 31:4–13.
   PubMed Web of Science ®Google Scholar
• Diehl KH, Hull R, Morton D, European Federation of Pharmaceutical Industries Association and European Centre for the Validation of Alternative Methods, et al. (2001). A good practice guide to the administration of substances and removal of blood, including routes and volumes. J Appl Toxicol 21:15–23.
   PubMed Web of Science ®Google Scholar
• Dillen L, Loomans T, Van de Perre G, et al. (2014). Blood microsampling using capillaries for drug-exposure determination in early preclinical studies: a beneficial strategy to reduce blood sample volumes. Bioanalysis 6:293–306.
   PubMed Web of Science ®Google Scholar
• Foundation for Biomedical Research. [Internet]. Rats and mice: the essential need for animals in medical research. [cited 04 February 2014]. Available from: http://www.fbresearch.org/wp-content/uploads/2013/2007/Rodents.pdf.
   Google Scholar
• Golde WT, Gollobin P, Rodriguez LL. (2005). A rapid, simple, and humane method for submandibular bleeding of mice using a lancet. Lab Anim (NY) 34:39–43.
   PubMed Web of Science ®Google Scholar
• Guhad F. (2005). Introduction to the 3Rs (Refinement, Reduction and Replacement). Contemp Top Lab Anim Sci 44:58–9.
   PubMedGoogle Scholar
• Heimann M, Käsermann HP, Pfister R, et al. (2009). Blood collection from the sublingual vein in mice and hamsters: a suitable alternative to retrobulbar technique that provides large volumes and minimizes tissue damage. Lab Anim 43:255–60.
   PubMedGoogle Scholar
• Hem A, Smith AJ, Solberg P. (1998). Saphenous vein puncture for blood sampling of the mouse, rat, hamster, gerbil, guinea pig, ferret and mink. Lab Anim 32:364–8.
   PubMedGoogle Scholar
• Herwaarden AE, Wagenaar E, Cornelia MM, et al. (2007). Knockout of cytochrome P450 3 yields new mouse models for understanding xenobiotic metabolism. J Clin Invest 117:3583–92.
   PubMed Web of Science ®Google Scholar
• Jonsson O, Palma Villar R, Nilsson LB, et al. (2012a). Capillary microsampling of 25 microl blood for the determination of toxicokinetic parameters in regulatory studies in animals. Bioanalysis 4:661–74.
   PubMed Web of Science ®Google Scholar
• Jonsson O, Villar RP, Nilsson LB, et al. (2012b). Validation of a bioanalytical method using capillary microsampling of 8 µl plasma samples: application to a toxicokinetic study in mice. Bioanalysis 4:1989–98.
   PubMed Web of Science ®Google Scholar
• Kim RB. (2006). Transporters and drug discovery: why, when, and how. Mol Pharm 3:26–32.
   PubMed Web of Science ®Google Scholar
• Kurawattimath V, Pocha K, Mariappan TT, Trivedi RK, et al. (2012). A modified serial blood sampling technique and utility of dried-blood spot technique in estimation of blood concentration: application in mouse pharmacokinetics. Eur J Drug Metab Pharmacokinet 37:23–30.
   PubMed Web of Science ®Google Scholar
• Long JM, James CA, Clark BJ, et al. (2002). Serial sampling in the mouse in support of pharmacokinetic studies with turbulent flow chromatography and tandem mass spectrometry. Chromatogr Suppl 55:S31–S34.
   Web of Science ®Google Scholar
• Patel NJ, Wickremsinhe E, Hui YH, et al. (2016). Evaluation and optimization of blood micro-sampling methods: serial sampling in a cross-over design from an individual mouse. J Pharm Pharm Sci 19:496–510.
   PubMed Web of Science ®Google Scholar
• Peng SX, Rockafellow BA, Skedzielewski TM, et al. (2009). Improved pharmacokinetic and bioavailability support of drug discovery using serial blood sampling in mice. J Pharm Sci 98:1877–84.
   PubMed Web of Science ®Google Scholar
• Rahavendran SV, Vekich S, Skor H, et al. (2012). Discovery pharmacokinetic studies in mice using serial microsampling, dried blood spots and microbore LC-MS/MS. Bioanalysis 4:1077–95.
   PubMed Web of Science ®Google Scholar
• Watanabe A, Watari R, Ogawa K, et al. (2015). Using improved serial blood sampling method of mice to study pharmacokinetics and drug-drug interaction. J Pharm Sci 104:955–61.
   Web of Science ®Google Scholar
• Wickremsinhe ER, Abdul BG, Huang NH, et al. (2011). Dried blood spot sampling: coupling bioanalytical feasibility, blood-plasma partitioning and transferability to in vivo preclinical studies. Bioanalysis 3:1635–46.
   PubMed Web of Science ®Google Scholar
• Xu RN, Fan L, Rieser MJ, El-Shourbagy TA. (2007). Recent advances in high-throughput quantitative bioanalysis by LC–MS/MS. J Pharm Biomed Anal 44:342–55.
   PubMed Web of Science ®Google Scholar