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. 2014 Nov;16(6):1366-71.
doi: 10.1208/s12248-014-9659-7. Epub 2014 Sep 23.

Evaluation of acoustic membrane microparticle (AMMP) technology for a sensitive ligand binding assay to support pharmacokinetic determinations of a biotherapeutic

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Evaluation of acoustic membrane microparticle (AMMP) technology for a sensitive ligand binding assay to support pharmacokinetic determinations of a biotherapeutic

Shannon D Chilewski et al. AAPS J. 2014 Nov.

Abstract

Achieving the required sensitivity can be a challenge in the development of ligand binding assays for pharmacokinetic (PK) determinations of biotherapeutics. To address this need, BioScale's Acoustic Membrane Microparticle (AMMP) technology was evaluated for the quantification of a PEGylated domain antibody (dAb) biotherapeutic. Previous uses of this technology had shown utility in biomarker and process development applications and this is the first application, to our knowledge, for PK determinations. In this evaluation, AMMP was capable of delivering a sensitivity of 0.750 ng/mL, which surpasses the sensitivity requirements for the majority of assays to support PK determinations. This evaluation demonstrates that this emerging technology has the ability to produce the required sensitivity, reproducibility, and selectivity needed to meet the industry's standards for PK analysis.

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Figures

Fig. 1
Fig. 1
a Schematic representation of how the AMMP platform works. b Sandwich format: drug detection with polyclonal anti-drug antibody immobilized on the magnetic bead and the same polyclonal anti-drug antibody, fluorescein labeled, for detection of the complex on the sensor. Competition format: drug detection with the drug immobilized on the magnetic bead and the polyclonal rabbit anti-drug antibody, fluorescein labeled, competing for detection of the complex on the sensor
Fig. 2
Fig. 2
Competition format standard curves

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References

    1. Rhyne PW, Wong OT, Zhang YJ, Weiner RS. Electrochemiluminescence in bioanalysis. Bioanalysis. 2009;1(5):919–35. doi: 10.4155/bio.09.80. - DOI - PubMed
    1. Morgan E, Varro R, Sepulveda H, Ember JA, Apgar J, Wilson J, et al. Cytometric bead array: a multiplexed assay platform with applications in various areas of biology. Clin Immunol. 2004;110(3):252–66. doi: 10.1016/j.clim.2003.11.017. - DOI - PubMed
    1. Verch T, Bakhtiar R. Miniaturized immunoassays: moving beyond the microplate. Bioanalysis. 2012;4(2):177–88. doi: 10.4155/bio.11.301. - DOI - PubMed
    1. Soderstrom CI, Spriggs FP, Song W, Burrell S. Comparison of four distinct detection platforms using multiple ligand binding assay formats. J Immunol Methods. 2011;371(1–2):106–13. doi: 10.1016/j.jim.2011.06.020. - DOI - PubMed
    1. Zambito F KA, Zhang Y, DeSilva B. Development of a PK immunoassay for a therapeutic monoclonal antibody using optimiser technology. Poster presented at: National Biotechnology Conference. 2013 May 22–23; San Diego CA.

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