High-throughput laboratories often face the challenge of reagent loss, due to dead volume in sample storage tubes. This issue not only increases waste but also affects the precision and efficiency of automated liquid handling processes.
To minimize sample loss, labs must adopt innovative solutions that address tube design, labware material and handling parameters. Optimized storage tube designs can significantly reduce residual volume, saving valuable reagents and improving workflow accuracy.
This application note explores key factors impacting dead volume and provides insights into how advanced tube designs enable maximum recovery for precious samples.
Download this application note to discover:
- Proven strategies to reduce reagent waste and residual volumes
- The science behind storage tube design and its impact on automation
- Practical tips for optimizing labware in automated workflows
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CONSUMABLES & INSTRUMENTS
Understanding the Importance
of Reagent “Dead Volume”
in Selecting Labware for
Automated Workflows
TECH NOTE
KobeBioRobotiX, Azenta Life Sciences
Azenta Life Sciences 2
CONSUMABLES & INSTRUMENTS TECH NOTE
The “Dead Volume” Dilemma
It is common knowledge that as the throughput of a life science lab increases then so does the potential for manual
sample handling errors which can risk cross contamination and experimental inconsistencies negatively impacting
important research.1
The solution is often considered to be extensive automation of liquid transfer processes to help with timesaving,
reduce labour costs, improve efficiency, and prevent poor sample handling that could result in cross-contamination.
However, the reality is that without accurately planning and defining the possible outcomes of investing in automation,
the best long-term value may not be achieved.
It has been found that the residual, or dead, volume of certain key items of labware can often affect both the
efficiency and cost per sample in an automated workflow. Nowhere is this more obvious than in sample storage tubes.
Whereas microplate manufacturers have long ago realized the importance of minimizing dead volume – especially
in reagent reservoirs - sample storage tube producers are only now reaching the same conclusion. Calculating the
amount of residual volume present in high-throughput automated laboratories is a key component that is integral to
understanding the total amount of loss occurring over the lifecycle of a precious sample or expensive reagent.2
Large dead volumes are particularly concerning for users handling valuable samples, such as stem cells, enzymes,
antibody solutions and difficult-to-make compounds. Although there is greater flexibility to reduce dead volume using
careful and practiced manual pipetting techniques, high-throughput labs need to use automated liquid handling
systems that have, by definition, only a limited range of motions.
Understanding and Avoiding Sample Loss
Automation engineers can undertake several methods to calculate the precise dead volume for each component used
and thus the overall sample loss in the automated workflow. Usefully, sample storage tube manufacturers can also
play a key role in reducing these losses and increasing the likelihood of maximum sample recovery.
To optimize sample recovery, it is necessary to consider which factors contribute to the scale of the dead volume in
sample storage tubes. Residual volume requirements vary based on several factors:
• Automated liquid handling parameters (pipette tips used, surface dispensing and submerged tip depth)
• Reagent properties (viscosity and surface tension)
• Labware (geometry and surface treatments)
• Environmental conditions (air temperature and humidity)
• Properly defined labware in the automated platform settings
Even the same combination of labware and reagent can have different residual volumes when changing the automated
liquid handler type or settings being used. Dead volume can be represented in two ways during automated processes.
Firstly, residual volume can be defined by the minimum amount of liquid required to be in the tube to prevent an
“insufficient liquid error” being triggered by the system. The second definition would be the minimum volume that
allows for complete aspiration from a point at a minimum height above the bottom of a tube.
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CONSUMABLES & INSTRUMENTS TECH NOTE
A specified liquid aspiration with varying liquid level detection, surface dispensing, tip submergence depth and
error handling approaches could yield different residual volume requirements that must be accounted for when
programming the liquid handler. For different labware and reagent combinations, the reagent may tend to “wick,”
coalesce or bead up into discrete regions, resulting in a non-uniform liquid level as the volume approaches lower
limits. This is often seen with natural hydrophobic materials for labware such as polypropylene. Any surface treatment
applied to the tube material can modify it further – plasma treatment tends to make the surface more hydrophilic and
increases dead volume by spreading residual liquid more thinly across the tube walls; low-binding treatment has the
opposite effect, increasing surface energy and repelling water thus causing droplets and beading to form which can
actually aid recovery of the “final drop” from a tube.
Additional Impacts on Residual Volume
The geometry of the bottom of the labware, as well as its surface properties, is thought to have the greatest impact on
residual volume, but workflow dependent factors like evaporation should also be kept in mind. Evaporation can easily
be controlled by re-capping the tubes or using a temporary push-cap or seal of such as the type supplied by Azenta
Life Sciences for just such a purpose.
Additionally, it is important to ensure your labware definition in the set up program of the robot matches your tube or
well geometry, and that the deck Z home point coordinate is accurately calibrated so that the liquid handling system
can calculate the correct rate of descent for the tip as liquid is removed from the tube if using surface dispensing.
When observing the tip move down the Z axis as it aspirates, it should keep a consistent distance between the bottom
of the tip and the liquid surface. If this is not observed, the container definition may need to be adjusted. It is good
practice for an automation engineer to test using material representative of their intended reagents (if possible) and
liquid handling parameters which will be used in the method, to ensure everything is optimized.
Checking for Sample Loss
It is possible to aspirate set amounts of a known volume and re-dispense back into the container to characterize
a robust residual volume limit. Checking by weight before and after aspiration from a previously dispensed known
volume is a widely used method for calculating dead volume in addition.
The design of storage tubes can significantly impact residual volume. For optimal sample aspiration, a design-change
opportunity was identified to incorporate internal compound curve tapers near the bottom of the tube. This new design
reduces the total volume retained in this area while still permitting industry-standard pipette tips to reach as close to
the bottom of the tube as possible.
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CONSUMABLES & INSTRUMENTS TECH NOTE
In the comparison above, it can be seen that by creating a tapered internal wall at the bottom of the tube the total
working volume is reduced for the same height (i.e. 15.8 mm for 1.0 mL volume vs. 20.1 mm for 1.0 mL volume) and at
the same time this improves the shape for maximum sample recovery with a standard
pipette tip.
In this example, the total amount of residual sample volume left in the 1.6 mL Tri-coded tube would be as low as 50 µl
(3% of working volume) compared to 210 µl (12% of working volume) with the standard 1.9 mL Tri-coded tube when
pipetting with an automated liquid handler that can go as low as 4 mm above the bottom of the inner well, but requires
a minimum of 4 mm internal diameter of the tube at that point.
Given most standard pipette tips for 10-1,000 µl dispensing have less than a 2 mm outer diameter at this point, it
is self-evident that even with the tapered design of the new 1.6 mL Tri-coded Maximum Recovery Tube there will
be no issues with automated liquid handling at 4 mm above the bottom of the inner tube. There are clear benefits
to the Maximum Recovery design. If the expected residual volume of the 1.6 mL Tri-coded tube is 50 µl and the 1.9
mL Tri-coded tube is 210 µl at the same Z-axis position in the liquid handler, one can compare the total amount of
unrecoverable sample over a set number of storage tubes used.
1.9 mL Tri-coded tube
(height in mm vs. volume in mL)
1.6 mL Tri-coded tube
(height in mm vs. volume in mL)
Customer Friendly Drawing
Dimensions are in mm
Rev. B
1.9ml Tri-coded Tube, 48-format,
External Thread, Capped
Base part number: 65-7641
Customer Friendly Drawing
Dimensions are in mm
Rev. A
1.6ml Tri-coded Tube, 48-format,
External Thread, Capped
Base part number: 65-7651
DESIGN COMPARISON BETWEEN 1.9 ML W.V ROUNDED BOTTOM TUBE & 1.6 ML
W.V. V-SHAPED BOTTOM TUBE.
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Azenta US, Inc. unless otherwise specified. 42031-ATN 0724
CONSUMABLES & INSTRUMENTS TECH NOTE
Conclusion
We may conclude that it is imperative that lab managers considering a switch to automated liquid handling
workflows should study the common variables and how to accurately measure the exact residual volume in
their sample storage tubes using an automated liquid handler in advance, using their own experimentation
and data from the robot and tube manufacturers. Producers are now starting to take into consideration design
aspects that allow users to benefit from reduced waste, not only to maximize the
recovery of precious samples, but to save on reagent purchasing costs with a
mind towards sustainable practices along the entire supply chain.
While the 1.6 mL Maximum Recovery Tube from Azenta Life Sciences
is the first uniquely designed sample storage tube designed
specifically for automated liquid handling, it is predicted that
this will become one of a family of tubes manufactured to
reduce dead volume and improve sample utilization.
Table 1 on the right shows the calculated amount of
sample loss for the 1.9 mL tubes over one hundred runs
is equivalent to 21,000 µl (21 mL) compared to 5,000
µl (5 mL) with the 1.6 mL tubes, resulting in a saving of
16 mL over the same number of tubes. With expensive
reagents, this can quickly accumulate into
substantial savings.
Table 1. Volume (μl) of Sample Lost per tube over one
hundred cycles
1.9 mL 1.6 mL
Volume (µl) of Sample Lost per tube over one hundred cycles
25000
20000
15000
10000
5000
0 5 10 15 20 25 30 35 40 45 50 55 60 65 70 75 80 85 90 95 100
30000
References
1 (2023) “What are dead volumes, and how do I reduce them?”, Opentrons, https://support.opentrons.com/s/article/What-are-dead-volumesand-how-do-I-reduce-them.
2 Reynolds, T. (2019) “What is automation in high-throughput science?” BIT 479/579 High-Throughput Discovery, https://htds.wordpress.
ncsu.edu/topics/what-is-automation-in-high-throughput-science-what-can-be-automated-and-how-is-automation-useful-in-comparisonto-manual-labor-i-e-automated-pipetting-vs-human-pipetting/.