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Updated: May 28, 2026

Biomolecular Detection employing the Interferometric Reflectance Imaging Sensor (IRIS)
Published on: May 3, 2011
Reflectometric interference spectroscopy (RIfS) as a new tool to measure in the complex matrix milk at low analyte
1Institute of Physical and Theoretical Chemistry (IPTC), Eberhard Karls University of Tübingen, Tübingen, Germany. sabrina.rau@uni-tuebingen.de
Insights
This study optimized reflectometric interference spectroscopy (RIfS) for testosterone detection in milk. The improved biosensor assay minimizes matrix effects, enabling reliable, label-free quantification of low analyte concentrations without sample pretreatment.
Area of Science:
- Biosensor development
- Analytical chemistry
- Biotechnology
Background:
- Measuring low analyte concentrations in complex matrices like milk is challenging for biosensors.
- Label-free detection methods are particularly susceptible to matrix effects.
- Testosterone immunoassay in buffer is well-established, serving as a model system.
Purpose of the Study:
- To investigate and reduce matrix effects in testosterone immunoassays using reflectometric interference spectroscopy (RIfS).
- To develop a robust, label-free biosensor for quantifying testosterone in whole milk.
- To improve assay performance, including limit of detection and assay time.
Main Methods:
- Optimization of sensor surface chemistry for enhanced testosterone detection in buffer.
- Adaptation of surface chemistry and evaluation methods to mitigate matrix effects in milk.
- Utilized reflectometric interference spectroscopy (RIfS) for direct optical detection.
Main Results:
- Achieved a fivefold lower limit of detection (70.2 ng L(-1)) and quantification (130.0 ng L(-1)) for testosterone in buffer.
- Reduced assay time to 15 minutes.
- Established a reliable method for testosterone quantification in milk with a limit of detection of 94.4 ng L(-1) and recovery rates of 70-120%.
Conclusions:
- Successfully minimized matrix effects in whole milk using adapted RIfS surface chemistry and evaluation methods.
- Developed a label-free immunoassay for testosterone in milk requiring no sample pretreatment and allowing sensor regeneration.
- Demonstrated the first successful quantification of an analyte in milk at low concentrations using RIfS.
Abstract:
Measurements in complex matrices like milk still present a challenge in biosensor development. This is especially important when using a label-free detection method or when measuring low analyte concentrations. The direct optical method reflectometric interference spectroscopy (RIfS) was used for investigating matrix effects in immunoassay development. Furthermore, approaches to reduce these effects have been established. As a model system, the hormone testosterone has been chosen because this immunoassay has been well characterized in buffer. In a first step, the immunoassay for the detection of testosterone in buffer was improved beyond former published results. Therefore, the sensor surface was optimized, resulting in a fivefold lower limit of detection (70.2 ng L(-1)) and limit of quantification (130.0 ng L(-1)). Additionally, the assay time could be reduced to 15 min. Consequently, we used this improved assay to investigate matrix effects of whole pasteurized bovine milk. To minimize these effects, the surface chemistry was adapted and a suitable evaluation method was established, reducing the effects of Tyndall scattering and nonspecific binding to the sensor surface. These improvements allow for very reliable quantitative measurements in milk. The assay developed required no sample pretreatment and allowed for the regeneration of the sensor surface so that calibration could be performed on one chip. The calibration in milk (3.5% fat) resulted in a limit of detection of 94.4 ng L(-1) and a limit of quantification of 229.3 ng L(-1). Furthermore, recovery rates between 70% and 120% could be obtained. Thus, for the first time, an analyte in the matrix milk was successfully quantified with RIfS at low concentrations.
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