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Automated Glucose Control in Ambr ® Bioreactors Using Raman Spectroscopy Michael Sibley 1 , Angus Woodhams 1 , Marek Hoehse 2 , Barney Zoro 1 * 1 Sartorius Royston, UK. 2 Sartorius Göttingen, Germany. *[email protected] Aims - Demonstrate physical integration of and automated data integration for Raman spectroscopy with Ambr ® bioreactors - Generate data to build a Raman model for glucose concentration in a typical cell culture - Build a Raman model for glucose concentration using SIMCA 16 software - Demonstrate real-time feedback control of glucose in culture based on the Ambr ® derived SIMCA 16 Raman model 1. BioPAT ® Spectro in Ambr ® Overview Figure 1. Schematic diagram of Ambr ® Analysis Module with BioPAT ® Spectro, fitted to an Ambr ® 250 High Throughput bioreactor system 2. BioPAT ® Spectro in Ambr ® Key Features - A user-replaceable Raman flow cell is integrated in the Ambr ® Analysis Module, compatible with both Ambr ® 15 Cell Culture and Ambr ® 250 High Throughput - Compatible with Raman Spectrometers and BioPAT ® Spectro Raman probes from Kaiser Optical Systems and Tornado Spectral Systems - Small sample volumes: 160 µL for Ambr ® 15, 200 µL for Ambr ® 250 High Throughput - Fast cycle time: ~10-15 min per sample - Samples can be automatically spiked with a concentrated analyte stock solution prior to Raman analysis - All key data from the Ambr ® process, Raman and other integrated analyzers are automatically collated by the Ambr ® Software - Identical Raman probes and flow cell optical paths support direct model transfer to Biostat STR ® - Requires compatible Ambr ® Analysis Module, Win10 Ambr ® Control PC, separate SIMCA 16 license for creating models - Suitable for typical mammalian fed-batch cell densities; microbial applications are not supported Figure 2. Ambr ® Analysis Module with BIOPAT ® Spectro fitted to an Ambr ® 15 system. Inset box: User replaceable BioPAT ® Spectro flow cell. 3. Model Building Ambr ® Run - N = 16 Ambr ® 250 High Throughput bioreactors - Sartorius’ Cellca2 Process CHO producing mAb (includes glucose-containing feeds) - Integrated Raman and Nova FLEX2 analyzers - If daily integrated Nova FLEX2 glucose <5 g/L, automated glucose feed to 5 g/L - >200 data points assayed by Flex2 then Raman, of which ~35 were spiked with 7.1 or 33.3 g/L glucose - Data was automatically collated in the Ambr ® software and one file exported by the operator - A separate copy of SIMCA 16 software was used for model building 4. Model Building Results - A good Raman model was generated for glucose using only non-spiked samples (Fig. 4) - Glucose model quality parameters are consistent with the best models in the literature - Glucose model range was suitable for feedback control in the cell culture process investigated - Spiking was not required to generate a good glucose model but spiking can increase model range (Fig. 5) - Spiking has been shown to improve range and model quality for other analytes e.g. lactate (data not shown) 5. Raman Based Ambr ® Process Control - Prior to the run, a glucose model previously built in SIMCA ® was loaded to the Ambr ® software - Sartorius’ Cellca2 Process CHO producing mAb - Integrated Raman and Nova FLEX2 analyzers - If daily integrated Raman or FLEX2 glucose <5 g/L, automated glucose feed to 5 g/L - N = 4 bioreactors were automatically fed glucose based on integrated Raman predictions - N = 4 bioreactors were automatically fed glucose based on integrated Nova FLEX2 analysis ambr® controller Ambr ® Analysis Module Ambr ® 250 High Throughput Raman spectrometer and controller Ambr ® computer BioPAT ® Spectro in Ambr ® Laser Raman spectroscopy Figure 6. Glucose concentrations in a fed-batch culture, measured by both integrated FLEX2 and Raman prediction. N=1 bioreactor shown for clarity. Figure 7. Cell culture VCD profiles. Glucose feeding controlled by either integrated Raman predictions (N=4) or Integrated FLEX2 assay (N=4). 9 8 7 6 5 4 3 2 1 0 0 2 4 6 8 10 12 14 Glucose [g/L] Time in culture (days) Integrated FLEX2 Integrated Raman 9 8 7 6 5 4 3 2 1 10 1 2 3 4 5 6 7 8 9 10 Nova FLEX2 glucose [g/L] y = x-3.168e-09 R 2 = 0.9788 Raman predicted glucose [g/L] RMSEE = 0.259042. RMSECV = 0.275695 6. Glucose Control Results - Glucose was maintained in culture in the range of 1-8 g/L (glucose readings >5 g/L were due to glucose in feeds) (Fig. 6) - Integrated Raman and Nova FLEX2 glucose assays were in very close agreement throughout (Fig. 6). - Cell culture profiles (Fig. 7) were very similar for glucose control based on Raman or Nova FLEX2 assays - BioPAT ® Spectro in Ambr ® enables fully automated glucose control capabilities similar to other analytical techniques (Fig. 7) - Further work will include confirmation of the Ambr glucose model performance in Sartorius’ Biostat ® STR bioreactors (50-2000 L scale) 7. Conclusion - Automated integration of Raman spectroscopy to Ambr ® is now possible - Fully automated data acquisition and alignment saves a significant amount of user time - A high quality glucose model was generated covering a wide concentration range (up to 15 g/L) - Ambr ® systems enable robust model building due to a range of setpoints and spiking of samples - Cell cultures controlled by integrated Raman or Nova FLEX2 analyzers showed very comparable glucose and VCD profiles 16 14 12 10 8 6 4 2 0 0 2 4 6 8 10 12 14 16 Nova FLEX2 glucose [g/L] y = x-6.777e-08 R 2 = 0.9786 Not spiked 33.3 g/L glucose 7.1 g/L glucose Raman predicted glucose [g/L] RMSEE = 0.331208. RMSECV = 0.346923 0 2 4 6 8 10 12 25 20 15 10 5 0 Time in culture (days) VCD (Million cells/mL) FLEX2 glucose control Raman glucose control Figure 4. Glucose model excluding spiked samples (N ~ 250 total) Figure 5. Glucose model, including spiked samples (N ~ 280 total) Design Ambr experiment: Range of setpoints; sample spiking Export Raman model(s) from SIMCA 16 (.USP files) and import to ambr Software Run Ambr experiment: including non-Raman reference assay(s) Configure Ambr experiment including Raman-based feedback control loops Automated data collection and collation: ambr process; integrated analyser; Spectra Run Ambr experiment: with or without non-Raman reference assay(s) Export a single data file (.csv) to SIMCA 16; use SIMCA ® to build Raman model(s) Fully automated real-time ambr system control based on integrated Raman assay Model Building Ambr ® Run Workflow diagram for BioPAT ® Spectro in Ambr ® Raman Based Ambr ® Process Control

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Page 1: Automated Glucose Control in Ambr Bioreactors Using …

Automated Glucose Control in Ambr® Bioreactors Using Raman Spectroscopy Michael Sibley1, Angus Woodhams1, Marek Hoehse2, Barney Zoro1*

1 Sartorius Royston, UK. 2 Sartorius Göttingen, Germany. *[email protected]

Aims- Demonstrate physical integration of and automated data integration for Raman spectroscopy with Ambr® bioreactors- Generate data to build a Raman model for glucose concentration in a typical cell culture- Build a Raman model for glucose concentration using SIMCA 16 software- Demonstrate real-time feedback control of glucose in culture based on the Ambr® derived SIMCA 16 Raman model

1. BioPAT® Spectro in Ambr® Overview

Figure 1. Schematic diagram of Ambr® Analysis Module with BioPAT® Spectro, fitted to an Ambr® 250 High Throughput bioreactor system

2. BioPAT® Spectro in Ambr® Key Features- A user-replaceable Raman flow cell is integrated in the Ambr® Analysis Module, compatible with both Ambr® 15 Cell Culture and Ambr® 250 High Throughput- Compatible with Raman Spectrometers and BioPAT® Spectro Raman probes from Kaiser Optical Systems and Tornado Spectral Systems- Small sample volumes: 160 µL for Ambr® 15, 200 µL for Ambr® 250 High Throughput - Fast cycle time: ~10-15 min per sample- Samples can be automatically spiked with a concentrated analyte stock solution prior to Raman analysis- All key data from the Ambr® process, Raman and other integrated analyzers are automatically collated by the Ambr® Software- Identical Raman probes and flow cell optical paths support direct model transfer to Biostat STR®- Requires compatible Ambr® Analysis Module, Win10 Ambr® Control PC, separate SIMCA 16 license for creating models- Suitable for typical mammalian fed-batch cell densities; microbial applications are not supported

Figure 2. Ambr® Analysis Module with BIOPAT® Spectro fitted to an Ambr ® 15 system. Inset box: User replaceable BioPAT® Spectro flow cell.

3. Model Building Ambr® Run- N = 16 Ambr® 250 High Throughput bioreactors- Sartorius’ Cellca2 Process CHO producing mAb (includes glucose-containing feeds)- Integrated Raman and Nova FLEX2 analyzers- If daily integrated Nova FLEX2 glucose <5 g/L, automated glucose feed to 5 g/L- >200 data points assayed by Flex2 then Raman, of which ~35 were spiked with 7.1 or 33.3 g/L glucose- Data was automatically collated in the Ambr® software and one file exported by the operator- A separate copy of SIMCA 16 software was used for model building

4. Model Building Results- A good Raman model was generated for glucose using only non-spiked samples (Fig. 4)- Glucose model quality parameters are consistent with the best models in the literature- Glucose model range was suitable for feedback control in the cell culture process investigated- Spiking was not required to generate a good glucose model but spiking can increase model range (Fig. 5)- Spiking has been shown to improve range and model quality for other analytes e.g. lactate (data not shown)

5. Raman Based Ambr® Process Control- Prior to the run, a glucose model previously built in SIMCA® was loaded to the Ambr® software- Sartorius’ Cellca2 Process CHO producing mAb- Integrated Raman and Nova FLEX2 analyzers- If daily integrated Raman or FLEX2 glucose <5 g/L, automated glucose feed to 5 g/L- N = 4 bioreactors were automatically fed glucose based on integrated Raman predictions- N = 4 bioreactors were automatically fed glucose based on integrated Nova FLEX2 analysis

ambr® controller

Ambr®

Analysis Module

Ambr® 250 High Throughput

Raman spectrometer and controller

Ambr® computer

BioPAT® Spectroin Ambr®

Laser

Raman spectroscopy

Figure 6. Glucose concentrations in a fed-batch culture, measured by both integrated FLEX2 and Raman prediction. N=1 bioreactor shown for clarity.

Figure 7. Cell culture VCD profiles. Glucose feeding controlled by either integrated Raman predictions (N=4) or Integrated FLEX2 assay (N=4).

0 2 4 6 8 10 12

25

20

15

10

5

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B. Glucose control using Raman Prediction vs integrated Flex2

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Time in culture (days)

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D (M

illio

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lls/m

L)

Glu

cose

[g/L

]

FLEX2 glucose control

Raman glucose control

A. Glucose measurement usingRaman Prediciton vs integrated Flex2

Time in culture (days)

Integrated FLEX2Integrated Raman

987654321

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1 2 3 4 5 6 7 8 9 10

Nov

a FL

EX

2 gl

ucos

e [g

/L] y = x-3.168e-09

R2 = 0.9788

Raman predicted glucose [g/L]RMSEE = 0.259042. RMSECV = 0.275695

16

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00 2 4 6 8 10 12 14 16

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R2 = 0.9786

Not spiked

33.3 g/L glucose

7.1 g/L glucose

Raman predicted glucose [g/L]RMSEE = 0.331208. RMSECV = 0.346923

6. Glucose Control Results- Glucose was maintained in culture in the range of 1-8 g/L (glucose readings >5 g/L were due to glucose in feeds) (Fig. 6)- Integrated Raman and Nova FLEX2 glucose assays were in very close agreement throughout (Fig. 6).- Cell culture profiles (Fig. 7) were very similar for glucose control based on Raman or Nova FLEX2 assays- BioPAT® Spectro in Ambr® enables fully automated glucose control capabilities similar to other analytical techniques (Fig. 7)- Further work will include confirmation of the Ambr glucose model performance in Sartorius’ Biostat® STR bioreactors (50-2000 L scale)

7. Conclusion- Automated integration of Raman spectroscopy to Ambr® is now possible- Fully automated data acquisition and alignment saves a significant amount of user time- A high quality glucose model was generated covering a wide concentration range (up to 15 g/L)- Ambr® systems enable robust model building due to a range of setpoints and spiking of samples- Cell cultures controlled by integrated Raman or Nova FLEX2 analyzers showed very comparable glucose and VCD profiles

987654321

10

1 2 3 4 5 6 7 8 9 10

Nov

a FL

EX

2 gl

ucos

e [g

/L] y = x-3.168e-09

R2 = 0.9788

Raman predicted glucose [g/L]RMSEE = 0.259042. RMSECV = 0.275695

16

14

12

10

8

6

4

2

00 2 4 6 8 10 12 14 16

Nov

a FL

EX

2 gl

ucos

e [g

/L] y = x-6.777e-08

R2 = 0.9786

Not spiked

33.3 g/L glucose

7.1 g/L glucose

Raman predicted glucose [g/L]RMSEE = 0.331208. RMSECV = 0.346923

0 2 4 6 8 10 12

25

20

15

10

5

0

B. Glucose control using Raman Prediction vs integrated Flex2

987654321

00 2 4 6 8 10 12 14

Time in culture (days)

VC

D (M

illio

n ce

lls/m

L)

Glu

cose

[g/L

]

FLEX2 glucose control

Raman glucose control

A. Glucose measurement usingRaman Prediciton vs integrated Flex2

Time in culture (days)

Integrated FLEX2Integrated Raman

Figure 4. Glucose model excluding spiked samples (N ~ 250 total) Figure 5. Glucose model, including spiked samples (N ~ 280 total)

Design Ambr experiment:Range of setpoints; sample spiking

Export Raman model(s) from SIMCA 16 (.USP files) and import to ambr Software

Run Ambr experiment:including non-Raman reference assay(s)

Configure Ambr experiment including Raman-based feedback control loops

Automated data collection and collation: ambr process; integrated analyser; Spectra

Run Ambr experiment: with or without non-Raman reference assay(s)

Export a single data file (.csv) to SIMCA 16; use SIMCA® to build Raman model(s)

Fully automated real-time ambr system control based on integrated Raman assay

Model Building Ambr® Run

Workflow diagram for BioPAT® Spectro in Ambr®

Raman Based Ambr® Process Control