Glycated Hemoglobin Analysis Filters
The use of ion exchange high-pressure liquid chromatography (HPLC) to determine the percentage content of HbA1c is currently considered the gold standard for analyzing HbA1c.
Glycosylated hemoglobin instruments have three mainstream detection principles, corresponding to completely two wavelength schemes, and the filter cannot be used interchangeably; All belong to the narrow band bandpass BP filter of transmittance colorimetry, with a specification system similar to that of biochemical filters, but there are significant differences in wavelength combination and general biochemical analyzer.
Standard size: Φ 8/Φ 10mm, universal thickness for mass production 2.0 mm.
Three major detection schemes&standard wavelength combinations
Scheme 1 | Latex enhanced immune turbidity method (fully automated biochemical matching, desktop HbA1c equipment)
Principle: Agglomeration turbidity detection, dual wavelength deduction of sample turbidity and bubble interference
Scheme 2 | Boric Acid Affinity/HPLC Ion Exchange Chromatography (Independent Saccharification Analyzer)
Scheme 3 | Fluorescence quenching method (small portable POCT saccharification equipment)
Two Mainstream Complete Sets of Filters
Group A | Immunoturbidimetric type (universal biochemical module, desktop HbA1c)
BP660 nm (main measurement), BP800 nm (reference)
Group B | Chromatography/HPLC ion exchange saccharification analyzer
BP415 nm (single wavelength)/BP420+BP500 (dual wavelength version)







