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In clinical laboratories, precision and efficiency are critical when processing blood samples. One of the essential tools for laboratory work is the blood centrifuge machine, a device used to separate various components of blood, such as plasma, serum, and hematocrit (HCT), by utilizing centrifugal force. This article explores the different aspects of blood centrifugation, including separation principles, recommended settings, and common mistakes, along with practical guidance to help clinical labs choose the right centrifuge model based on their specific needs. As a trusted supplier, GlanLab offers a wide range of customizable blood centrifuge machines to meet the needs of diverse clinical environments.
Effective separation of blood components is key to obtaining accurate test results. A blood centrifuge machine is designed to separate blood into its different components, such as plasma, serum, and HCT, with the goal of achieving clear separation layers. In an ideal separation, plasma or serum should form a distinct upper layer, and the red blood cells (RBCs) should settle at the bottom, with minimal disturbance to the buffy coat.
Proper separation is crucial for ensuring that downstream tests—such as those for chemistry, coagulation, and hematology—are reliable. If blood samples are not properly separated, it can lead to contamination, skewed results, and delays in diagnosis.
To clarify, serum is obtained after the blood has clotted, while plasma is collected from blood that is anticoagulated and has not undergone clotting. Hematocrit (HCT) is a specific measurement that indicates the volume percentage of RBCs in blood and typically requires a specialized setup like a microhematocrit centrifuge.
Blood separation in a blood centrifuge machine occurs due to differences in the density of the blood components. Here’s what happens at each stage of the process:
When the sample is spun, the heavier components, such as the red blood cells (RBCs), move to the bottom of the tube, followed by the buffy coat, which contains white blood cells (WBCs) and platelets. The lighter components, such as plasma or serum, remain at the top.
Plasma: When using an anticoagulant tube, blood is spun promptly without allowing clotting to occur. This results in plasma as the upper layer.
Serum: After blood has been allowed to clot, it is then spun, and the resulting serum forms the top layer. Timing is essential; spinning too early or too late can lead to inaccurate results, as premature spinning may interfere with clot formation.
Component | What Happens |
Plasma | Forms from anticoagulated blood, remains at the top. |
Serum | Forms from clotted blood, stays at the top after spinning. |
Hematocrit (HCT) | RBCs settle at the bottom; typically measured with specialized centrifuges. |
HCT separation typically requires a microhematocrit-capillary centrifuge setup, differing from the usual plasma/serum spins due to the specific needs of hematocrit measurements.

In centrifugation, RCF (relative centrifugal force) is the primary factor that determines the efficiency of separation. Unlike RPM (revolutions per minute), which varies with rotor size, RCF is directly related to the force acting on the blood sample and is a more accurate measure of separation strength.
RCF is specified in terms of “×g,” which accounts for the rotor radius and speed. Different rotor designs require different RPMs to achieve the same RCF, making it important to follow protocol recommendations to avoid errors.
Many labs follow standard guidelines for time and RCF. For example, serum separation typically requires around 3000 ×g for 10 minutes, while HCT measurements may require higher speeds or different times based on the sample type and equipment used.
In some cases, adjusting the time or speed may yield better results, depending on the sample. Increasing speed is useful when the sample needs quick separation, while extended time can allow for more thorough separation without exceeding the limits of the blood cells. Rotor acceleration and braking settings also play a role in controlling gel barriers and reducing platelet contamination.
Choosing the right rotor is crucial for achieving optimal blood separation in a blood centrifuge machine.
A fixed-angle rotor positions tubes at a set angle, which helps achieve sharp sediment layers and is ideal for smaller sample volumes. On the other hand, a swing-bucket rotor allows the tubes to swing out during centrifugation, providing better separation for larger samples or more complex workflows.
| Rotor Type | Best For | Effect |
|---|---|---|
| Fixed-Angle | Routine Vacutainer Serum/Plasma | Sharp separation of small sample volumes |
| Swing-Bucket | Blood Banks, Larger Clinical Volumes | Better separation of larger tubes |
Routine Vacutainer Serum/Plasma: Fixed-angle rotors work best for standard serum and plasma separation.
Larger Volume Processing: For blood banks or larger clinical volumes, swing-bucket rotors provide the necessary space and balance for larger tubes or bags.
Multi-Tube Batches: Balancing practicality with capacity, multi-tube setups require rotors that offer efficient balancing and can handle multiple tubes simultaneously.

For smaller clinical environments, such as physician offices, the key is selecting a blood centrifuge machine that offers quick turnaround, ease of use, and compact design. Low-speed benchtop models are a perfect fit, providing flexibility and consistent results.
Mid-size hospitals require centrifuges with a wider range of rotor options, higher capacity, and enhanced repeatability. These models support varied workflows and accommodate multiple departments, offering flexibility with higher throughput and program memory features.
For blood banks or large clinical labs handling substantial volumes of blood, choosing a refrigerated blood centrifuge machine with specialized rotors is essential. These centrifuges offer safety features such as imbalance protection and are designed to maintain temperature stability during the process.
Despite the precision of modern centrifuges, mistakes in blood separation still occur.
Common errors include delayed processing, incorrect clotting time, improper tube selection, and mishandling leading to hemolysis.
Missteps during centrifugation, such as incorrect force or time settings, mismatched rotors, or aggressive braking, can lead to compromised separation quality.
Disturbing the layers when decanting or failing to aliquot promptly can cause separation to break down, affecting the quality of results.
Achieving consistent results in blood separation requires regular checks and good laboratory practices.
These include checking the rotor for cleanliness, verifying lid locks, and ensuring proper noise/vibration levels to prevent equipment failure.
Proper balancing is crucial for preventing vibration and breakage. Labs should adopt counterbalance logic when loading samples.
Recording key parameters like RCF, time, rotor settings, and brake speed ensures reproducibility and minimizes errors.
In conclusion, optimizing centrifugation protocols by focusing on sample handling, RCF/time settings, and rotor selection can significantly enhance the efficiency and reliability of blood processing. At GlanLab, we are dedicated to providing high-quality, customizable blood centrifuge machines that meet the specific needs of clinical labs and blood banks worldwide.
For more information on how to match your laboratory workflow with the right centrifuge configuration, contact us today!
What is the difference between plasma and serum?
Plasma is obtained from blood that has not clotted, while serum comes from blood that has undergone clotting.
How do I select the right rotor for my blood centrifuge?
The choice of rotor depends on the type and volume of the samples being processed, with fixed-angle rotors for small samples and swing-bucket rotors for larger volumes.
What are the common mistakes in centrifugation?
Common mistakes include delayed processing, improper tube types, incorrect speed/time settings, and mishandling during decanting.
Why is RCF preferred over RPM in centrifugation?
RCF provides a more accurate measure of the centrifugal force applied to the sample, making it a better indicator of separation efficiency.