Calibration and validation of confocal spectral imaging systems
- 5 October 2004
- journal article
- review article
- Published by Wiley in Cytometry Part A
- Vol. 62A (1) , 8-34
- https://doi.org/10.1002/cyto.a.20087
Abstract
Background Confocal spectral imaging (CSI) microscopic systems currently on the market delineate multiple fluorescent proteins, labels, or dyes within biological specimens by performing spectral characterizations. However, some CSI systems have been found to present inconsistent spectral profiles of reference spectra within a particular system and between related and unrelated instruments. This variability confirms that there is a need for a standardized, objective calibration and validation protocol. Methods Our protocol uses an inexpensive multi‐ion discharge lamp (MIDL) that contains Hg+, Ar+, and inorganic fluorophores that emit distinct, stable, spectral features in place of a sample. We derived reference spectra from the MIDL data to accurately predict the spectral resolution, ratio of wavelength to wavelength, contrast, and aliasing parameters of any CSI system. We were also able to predict and confirm the influence of pinhole diameter on spectral profiles. Results Using this simulation, we determined that there was good agreement between observed and theoretical expectations, thus enabling us to identify malfunctioning subsystems. We examined eight CSI systems and one nonconfocal spectral system, all of which displayed spectral inconsistencies. No instrument met its optimal performance expectations. In two systems, we established the need for factory realignment that had not been otherwise recognized. Conclusions We found that using a primary light source that emits an absolute standard “reference spectrum” enabled us to diagnose instrumental errors and measure accuracy and reproducibility under normalized conditions. With this information, a CSI operator can determine whether a CSI system is working optimally and make objective comparisons with the performance of other CSI systems. We determined that, if CSI systems were standardized to produce the same spectral profile of a MIDL lamp, researchers could be confident that the same experimental findings would be obtained on any CSI system.Keywords
This publication has 11 references indexed in Scilit:
- Selection of Quantum Dot Wavelengths for Biomedical Assays and ImagingMolecular Imaging, 2003
- Multi-Spectral Imaging and Linear Unmixing Add a Whole New Dimension to Laser Scanning Fluorescence MicroscopyBioTechniques, 2001
- Evaluation of confocal microscopy system performanceCytometry, 2001
- Practical Confocal Microscopy and the Evaluation of System PerformanceMethods, 1999
- The Specimen Illumination Path and Its Effect on Image QualityPublished by Springer Nature ,1995
- Tutorial on Practical Confocal Microscopy and Use of the Confocal Test SpecimenPublished by Springer Nature ,1995
- Fundamental Limits in Confocal MicroscopyPublished by Springer Nature ,1995
- The Role of the Pinhole in Confocal Imaging SystemPublished by Springer Nature ,1995
- Confocal-line microscopyJournal of Microscopy, 1992
- Increasing sensitivity of the Ortho analytical cytofluorograph by modifying the fluid systemCytometry, 1990