Vi–CELL BLU FAST Mode Option

The Vi–CELL BLU instrument introduced a new plate reader capability to the Vi–CELL family of cell analyzers. The plate option gives the user the ability to load up to 96 samples or a combination of samples and controls onto the instrument for continuous operation.

However running so many samples will result in a significantly long run time, approximately 3 hrs total for a full 96 well plate. This may raise some concerns about occupying an instrument for such a long time or viability drift in cells that are not particularly stable outside the incubator environment. To help mitigate these concerns we have equipped the Vi–CELL BLU with an optional FAST Mode of operation which can be used in either plate or carousel configuration to significantly reduce sample to sample operation times.


Wash Mode Volume Needed Sample Run Time Interval 100 Images, ~2x10^ cells/ml (mm:ss) Full Plate Time 96 Samples 100 Images, ~2x10^ cells/ml (h:mm:ss)
Normal Wash 200 µL  <130 seconds typical analysis time: normal mode 110 seconds Estimated 3:28:00 Typical 2:56:00
Fast Wash  170 µL   <90 seconds typical analysis time:80 seconds Estimated 2;24:00 Typical 2:08:00

The FAST Mode shortens the wash cycle duration saving approximately 30% on sample run time. The tradeoff is a potential increased risk of carry over between samples since the washing is less thorough than normal mode. This tradeoff may be acceptable depending on sample type and desired run time. Please note also that prolonged use of Fast Mode may result in increased build–up of trypan blue and proteinaceous material in the fluidics path of the instrument, so regular decontamination runs are recommended.

Setting Up Fast Mode

Wash mode is a configurable option during sample logging or set as the default in the Run Setting preferences screen. It can either be chosen in the sample setup bar which would allow multiple samples to be logged using the same settings, or it can be changed once the sample is in the queue list. For more instructions please consult the user manual.


The option to select either Normal or FAST mode during queue creation

Assessing Run–Run Carry Over

The basic scheme for assessing carryover is to alternate a cell or bead sample with blank buffer samples, in either a plate or carousel and to run either in Normal or Fast Wash mode. An example
of such a run is shown below.

Sample ID Wash Sample Type Cell Count
Beads–L07–norm.015   Normal Wash  L5 Bead 11903
Blanks–L07–norm.016   Normal Wash Blank 21
Beads–L07–norm.017   Normal Wash L5 Bead 12061
Blanks–L07–norm.018  Normal Wash Blank 5
Beads–L07–norm.019   Normal Wash L5 Bead 11444
Blanks–L07–norm.020   Normal Wash Blank 26
Beads–L07–fast.001   Fast Wash L5 Bead 11717
Blanks–L07–fast.002   Fast Wash Blank 24
Beads–L07–fast.003   Fast Wash L5 Bead 11368
Blanks–L07–fast.004   Fast Wash Blank 28

L5 size standard beads (6602794 lot 9012057F) were used as a general control due to their nominal size and approximate particle density of ~4 x 106 beads/mL. The instrument was run using a cell profile set up for L5 beads based on the default L10 bead profile.

CHO cells are a standard cell type that was used to determine carryover when using a biological sample. Absolute concentration was approximately 3 x 106 cells/mL but this is not a critical parameter as the main investigation is the relative number of cells between the normal and blank samples. Cells were analyzed using standard Mammalian cell type profile.

Particle concentration was not critical here but was used an indicator of expected performance. Particle counts between sample and blank were recorded. Residual carry over was determined by the number of beads appearing in the blank samples. Random analysis of captured images was also conducted to verify particles scored in blanks were bead and not some other debris.

Blank samples have highly variable count numbers as expected when running a sample with no particles. This causes some issues with the internal calculations so average particle counts are the most consistent parameter to use.


Instrument Settings for Analysis

Cell Type BCI L5 Beads Mammalian
Minimum diameter (μm) 2 6
Maximum diameter (μm) 10 30
Images 100 100
Cell sharpness 22 7
Minimum circularity   0.75 0.1
Decluster degree medium medium
Aspiration cycles 3 3
Viable spot brightness (%)  50 55
Viable spot area (%) 1 5
Mixing cycles 3 3

The results below show multiple runs on both carousel and plate sample loading. The data are presented as paired results showing the average of the sample count and the average of the carry over
count recorded between samples.

L5 Beads

Run Wash Mode L5 Bead Count Carryover Bead Count % Carryover # Sample Pairs
1 Normal Wash 10629 108 1.01% 20
2 Normal Wash 11784 11 0.10% 26
Normal Wash 11414 164 1.44% 60
Normal Wash 11862 236 1.99% 60
Normal Wash 11326 161 1.42% 40
1 Fast Wash 9392 226 2.40% 20
2 Fast Wash 11147 38 0.34% 54


CHO Cells

Run Wash Mode CHO Cell Count Carryover Cell Count % Carryover # Sample Pairs
1 Normal Wash 3939 3 0.07% 38
2 Normal Wash 5546 9 0.16% 48
3 Normal Wash 7986 3 0.04% 26
4 Normal Wash 5310 27 0.51% 24
1 Fast Wash 3952 5 0.13% 38
2 Fast Wash 5281 23 0.44% 36
3 Fast Wash 8595 21 0.24% 24



A T–test analysis between normal and fast wash residual bead counts in the blank samples gives a p value of 0.986 indicating no statistical difference between operation modes in terms of carry over
between samples. It is therefore possible operate the instrument in either mode and have confidence that the sample to sample carryover will be negligible. It should be noted that the degree of variability in the blank samples can be extremely high due to so few particles being counted but in all test cases the percentage carry over was always well below 1%.

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