Knowledge Center

Bilirubin Testing Equipment

Neonatal bilirubin is a yellow breakdown product of normal heme catabolism in newborns. Its levels are elevated in certain diseases and responsible for the yellow color of bruises.

Risk to Newborns

Hyperbilirubinemia is one of the most common problems encountered in term newborns. Up to 60% of term newborns have clinical jaundice in the first week of life.

High Bilirubin Levels are Common in Newborns

High bilirubin levels in newborns are relatively common, especially within three days of birth. This is sometimes called physiologic jaundice of the newborn. Within the first 24 hours of life, up to 50% of full-term newborns, and an even greater percentage of pre-term babies, may have a high bilirubin level. After birth, newborns begin breaking down the excess red blood cells (RBCs) they are born with and, since the newborn’s liver is not fully mature, it is unable to process the extra bilirubin, causing levels to rise in the blood and other body tissues. This situation usually resolves itself within a few days.

Principle of Operation

Total Bilirubin – The maximum light absorption of bilirubin occurs at a wavelength of 454 nm. Oxyhemoglobin (HbO2) has nearly equal absorbance at 454 and 540 nm. In the BR2, the absorbance at 540 nm (HbO2) is subtracted from the absorbance at 454 nm (TBR + HbO2). The remainder corresponds to TBR concentration corrected for oxyhemoglobin up to 600 mg/dL. Light from an incandescent source is collimated and directed through a cuvette containing the diluted sample. A fiber optic beam splitter with 454-nm and 540-nm channels splits the transmitted light, each made monochromatic by a narrow-bandpass interference filter. Matched solid-state photo-detectors and signal processing electronics measure the transmittances at 454 and 540 nm and display the TBR concentration digitally.

Direct Bilirubin – Direct Bilirubin is measured as the change in absorbance at 540 nm due to the formation of azobilirubin, using a two-minute, timed-endpoint modification to the Malloy and Evelyn method. After TBR has been measured on a sample, that same sample is acidified with HCl, establishing an absorbance baseline. Next, diazotized sulfanilic acid is added. Under these conditions, the conjugated (Direct) bilirubin fraction will react to form azobilirubin, which has maximum light absorption at 540 nm. At the end of the two-minute reaction period, the digital display locks in to hold the DBR readout until the next test is initiated.

Related Resources

Learn more by checking out our additional educational resources below.

Clinical Case Study

Improving cell count turnaround times with the GloCyte Automated Cell Counter

View

Clinical App Note

Reducing Error Associated with Manual Chamber Counts with the GloCyte® Automated Cell Counter for CSF

View

Clinical App Note

Clinical Osmometer Applications

View

Clinical App Note

The Importance of Measured Osmolality Testing With an In-house Osmometer

View

Clinical Webinar

Virtual Demo | GloCyte® Automated Cell Counter for CSF

View

Clinical Webinar

Virtual Demo | Artel PCS® Pipette Calibration System

View

Clinical Webinar

Virtual Demo | Anoxomat® III Anaerobic Jar System

View

Clinical Posters

Reducing Cell Count Bias with the GloCyte® Automated Cell Counter for CSF

View

Clinical Posters

Improving cell count turnaround times with the GloCyte® Automated Cell Counter for CSF

View

Clinical Posters

Shining Renewed Light on a Tried-and-True Test: The Critical Role of Osmolality Testing in Improving Health and Economic Outcomes in Patients with Hyponatremia

View

Clinical Knowledge Center

The Value of Our Clinical Osmometers

View

Clinical Knowledge Center

Measuring the Impact of Common Environmental Conditions on Laboratory Data Integrity

View

Clinical Knowledge Center

Freezing Point Depression Theory

View