Your browser doesn't support javascript.
loading
Continuous Biosensor Based on Particle Motion: How Does the Concentration Measurement Precision Depend on Time Scale?
Lubken, Rafiq M; Lin, Yu-Ting; Haenen, Stijn R R; Bergkamp, Max H; Yan, Junhong; Nommensen, Paul A; Prins, Menno W J.
Afiliação
  • Lubken RM; Helia Biomonitoring, Eindhoven 5612 AR, The Netherlands.
  • Lin YT; Helia Biomonitoring, Eindhoven 5612 AR, The Netherlands.
  • Haenen SRR; Helia Biomonitoring, Eindhoven 5612 AR, The Netherlands.
  • Bergkamp MH; Helia Biomonitoring, Eindhoven 5612 AR, The Netherlands.
  • Yan J; Helia Biomonitoring, Eindhoven 5612 AR, The Netherlands.
  • Nommensen PA; Avebe Innovation Center, Groningen 9747 AA, The Netherlands.
  • Prins MWJ; Helia Biomonitoring, Eindhoven 5612 AR, The Netherlands.
ACS Sens ; 9(9): 4924-4933, 2024 Sep 27.
Article em En | MEDLINE | ID: mdl-39166946
ABSTRACT
Continuous biosensors measure concentration-time profiles of biomolecular substances in order to allow for comparisons of measurement data over long periods of time. To make meaningful comparisons of time-dependent data, it is essential to understand how measurement imprecision depends on the time interval between two evaluation points, as the applicable imprecision determines the significance of measured concentration differences. Here, we define a set of measurement imprecisions that relate to different sources of variation and different time scales, ranging from minutes to weeks, and study these using statistical analyses of measurement data. The methodology is exemplified for Biosensing by Particle Motion (BPM), a continuous, affinity-based sensing technology with single-particle and single-molecule resolution. The studied BPM sensor measures specific small molecules (glycoalkaloids) in an industrial food matrix (potato fruit juice). Measurements were performed over several months at two different locations, on nearly 50 sensor cartridges with in total more than 1000 fluid injections. Statistical analyses of the measured signals and concentrations show that the relative residuals are normally distributed, allowing extraction and comparisons of the proposed imprecision parameters. The results indicate that sensor noise is the most important source of variation followed by sample pretreatment. Variations caused by fluidic transport, changes of the sensor during use (drift), and variations due to different sensor cartridges and cartridge replacements appear to be small. The imprecision due to sensor noise is recorded over few-minute time scales and is attributed to stochastic fluctuations of the single-molecule measurement principle, false-positive signals in the signal processing, and nonspecific interactions. The developed methodology elucidates both time-dependent and time-independent factors in the measurement imprecision, providing essential knowledge for interpreting concentration-time profiles as well as for further development of continuous biosensing technologies.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnicas Biossensoriais Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnicas Biossensoriais Idioma: En Ano de publicação: 2024 Tipo de documento: Article