Clogging of microfluidic constrictions by monoclonal antibody aggregates: role of aggregate shape and deformability. Issue 4 (9th December 2019)
- Record Type:
- Journal Article
- Title:
- Clogging of microfluidic constrictions by monoclonal antibody aggregates: role of aggregate shape and deformability. Issue 4 (9th December 2019)
- Main Title:
- Clogging of microfluidic constrictions by monoclonal antibody aggregates: role of aggregate shape and deformability
- Authors:
- Duchêne, Charles
Filipe, Vasco
Huille, Sylvain
Lindner, Anke - Abstract:
- Abstract : Using a microfluidic model system, we demonstrate that aggregates formed in solutions of monoclonal antibodies geometrically clog constrictions and that unclogging can be obtained by increasing the applied pressure through aggregate deformability. Abstract : The formation of aggregates in solutions of monoclonal antibodies is difficult to prevent. Even if the occurrence of large aggregates is rare, their existence can lead to partial or total clogging of constrictions in injection devices, with drastic effects on drug delivery. Little is known on the origin and characteristics of such clogging events. Here we investigate a microfluidic model system to gain fundamental understanding of the clogging of constrictions by monoclonal antibody aggregates. Highly concentrated solutions of monoclonal antibodies were used to create protein aggregates (larger than 50 microns) using mechanical or heat stress. We show that clogging occurs when aggregates reach the size of the constriction and that clogs can in some cases be released by increasing the applied pressure. This indicates the important role of protein aggregate deformability. We perform systematic experiments for different relative aggregate sizes and applied pressures, and measure the resulting flow-rate. This allows us to present first in situ estimates of an effective Young's modulus. Despite their different shapes and densities, we can predict the number of clogging events for a given constriction size from theAbstract : Using a microfluidic model system, we demonstrate that aggregates formed in solutions of monoclonal antibodies geometrically clog constrictions and that unclogging can be obtained by increasing the applied pressure through aggregate deformability. Abstract : The formation of aggregates in solutions of monoclonal antibodies is difficult to prevent. Even if the occurrence of large aggregates is rare, their existence can lead to partial or total clogging of constrictions in injection devices, with drastic effects on drug delivery. Little is known on the origin and characteristics of such clogging events. Here we investigate a microfluidic model system to gain fundamental understanding of the clogging of constrictions by monoclonal antibody aggregates. Highly concentrated solutions of monoclonal antibodies were used to create protein aggregates (larger than 50 microns) using mechanical or heat stress. We show that clogging occurs when aggregates reach the size of the constriction and that clogs can in some cases be released by increasing the applied pressure. This indicates the important role of protein aggregate deformability. We perform systematic experiments for different relative aggregate sizes and applied pressures, and measure the resulting flow-rate. This allows us to present first in situ estimates of an effective Young's modulus. Despite their different shapes and densities, we can predict the number of clogging events for a given constriction size from the aggregate size distribution measured by Flow Imaging Microscopy (MFI). In addition our device can detect the occurrence of very rare big aggregates often overlooked by other detection methods. … (more)
- Is Part Of:
- Soft matter. Volume 16:Issue 4(2019)
- Journal:
- Soft matter
- Issue:
- Volume 16:Issue 4(2019)
- Issue Display:
- Volume 16, Issue 4 (2019)
- Year:
- 2019
- Volume:
- 16
- Issue:
- 4
- Issue Sort Value:
- 2019-0016-0004-0000
- Page Start:
- 921
- Page End:
- 928
- Publication Date:
- 2019-12-09
- Subjects:
- Soft condensed matter -- Periodicals
530.413 - Journal URLs:
- http://www.rsc.org/Publishing/Journals/sm/index.asp ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9sm01583c ↗
- Languages:
- English
- ISSNs:
- 1744-683X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8321.419000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12674.xml