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A practical workflow for capillary microsampling in nonclinical studies

    Linna Wang

    Bioanalytical Science, Bristol-Myers Squibb, Princeton, NJ 08543, USA

    ,
    Bonnie Wang

    Drug Safety Evaluation, Bristol-Myers Squibb, New Brunswick, NJ 08903, USA

    ,
    Kristina D Chadwick

    Drug Safety Evaluation, Bristol-Myers Squibb, New Brunswick, NJ 08903, USA

    ,
    Ting Su

    Drug Safety Evaluation, Bristol-Myers Squibb, New Brunswick, NJ 08903, USA

    ,
    Raja Mangipudy

    Drug Safety Evaluation, Bristol-Myers Squibb, New Brunswick, NJ 08903, USA

    ,
    Renuka C Pillutla

    Bioanalytical Science, Bristol-Myers Squibb, Princeton, NJ 08543, USA

    &
    Qin C Ji

    *Author for correspondence: Tel.: +1 609 252 5560;

    E-mail Address: qin.ji@bms.com

    Bioanalytical Science, Bristol-Myers Squibb, Princeton, NJ 08543, USA

    Published Online:https://doi.org/10.4155/bio-2018-0224

    Aim: The result of investigation on the procedure of sample handling and bioanalysis of small volume of plasma sample for nonclinical studies stored in 0.5-ml micronic tubes was reported. Results/methodology: Sample integrity of the small volume (25 μl) during long-term storage and the feasibility and data reliability of performing multiple re-assays on the small volume sample using 5 μl aliquot per analysis was evaluated. Conclusion: Integrity was maintained in samples (25 μl) stored for up to 1 month in 0.5-ml micronic tubes at -20°C. A 25 μl sample is sufficient for four-times of re-assays. This evaluation demonstrated the feasibility of this workflow of handling and bioanalysis on small volume plasma sample for GLP studies under the US FDA guidance.

    Papers of special note have been highlighted as: • of interest; •• of considerable interest

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