Quantitation of Conjugation-related Residual Solvents in Antibody Drug Conjugates using Headspace Gas Chromatography

Page: [829 - 837] Pages: 9

  • * (Excluding Mailing and Handling)

Abstract

Background: Antibody Drug Conjugates (ADCs) are complex hybrid molecules comprised of a monoclonal antibody (mAb) connected to a small molecule drug through a linker. The key step in the production of ADCs is bringing together the protein in an aqueous buffer with a hydrophobic small molecule in order to achieve conjugation of the molecules. This step involves dissolving the small molecule portion of the compound in an aqueous miscible organic solvent. These solvents and unconjugated small molecules are ideally cleared by downstream processing in order to achieve the desired product quality. As part of the control system to ensure product quality, the determination of residual solvents in pharmaceuticals is of significant importance in order to protect patient safety and ensure an efficacious drug.

Objective: Headspace gas chromatography (HS-GC) is the most widely used tool for quantification of residual solvents for small molecule active pharmaceutical ingredients (APIs) but is not widely used for the analysis of protein-containing samples. In this study, the detection of residual solvents in headspace injections was explored using various conditions in order to detect commonly used conjugation solvents including N,N-dimethylacetamide (DMA), N,N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), Ethylene Glycol (EG), and Propylene Glycol (PG) in an ADC drug product sample.

Methods: Various organic solvents were explored to enhance the response observed with complex protein and residual solvent matrixes. As EG and PG do not partition into the headspace efficiently in the ADC drug product samples that contain large amounts of water, ionic liquids and other ionic compounds were screened with the ADC samples to see if they could improve the partitioning of the key solvents EG and PG.

Results: Following headspace and chromatographic optimization, we have developed an approach for the detection and quantification of several conjugation reaction solvents in ADC samples.

Conclusion: This new approach is an HS-GC method that simplifies Gas Chromatography (GC) analysis and sample preparation and can be readily implemented in quality control testing for bioconjugated products.

Keywords: Antibody drug conjugate, headspace gas chromatography, residual solvents, pharmaceutical analysis, biotherapeutics, cytotoxicity.

Graphical Abstract

[1]
Drake, P.M.; Rabuka, D. Recent developments in ADC technology: preclinical studies signal future clinical trends. BioDrugs, 2017, 31(6), 521-531.
[http://dx.doi.org/10.1007/s40259-017-0254-1] [PMID: 29119409]
[2]
de Goeij, B.E.; Lambert, J.M. New developments for antibody-drug conjugate-based therapeutic approaches. Curr. Opin. Immunol., 2016, 40, 14-23.
[http://dx.doi.org/10.1016/j.coi.2016.02.008] [PMID: 26963132]
[3]
Medley, C.D.; Kay, J.; Li, Y.; Gruenhagen, J.; Yehl, P.; Chetwyn, N.P. Quantification of residual solvents in antibody drug conjugates using gas chromatography. Anal. Chim. Acta, 2014, 850, 92-96.
[http://dx.doi.org/10.1016/j.aca.2014.09.003] [PMID: 25441165]
[4]
Jain, N.; Smith, S.W.; Ghone, S.; Tomczuk, B. Current ADC linker chemistry. Pharm. Res., 2015, 32(11), 3526-3540.
[http://dx.doi.org/10.1007/s11095-015-1657-7] [PMID: 25759187]
[5]
Chen, T.; Chen, Y.; Stella, C.; Medley, C.D.; Gruenhagen, J.A.; Zhang, K. Antibody-drug conjugate characterization by chromatographic and electrophoretic techniques. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci., 2016, 1032, 39-50.
[http://dx.doi.org/10.1016/j.jchromb.2016.07.023] [PMID: 27451254]
[6]
Avdovich, H.W.; Lebelle, M.J.; Savard, C.; Wilson, W.L. Nuclear magnetic resonance identification and estimation of solvent residues in cocaine. Forensic Sci. Int., 1991, 49, 225-235.
[http://dx.doi.org/10.1016/0379-0738(91)90083-U]
[7]
Dai, L.; Quiroga, A.C.; Zhang, K.; Runes, H.B.; Yazzie, D.T.; Mistry, K.; Chetwyn, N.P.; Dong, M.W. A generic headspace GC method for residual solvents in pharmaceuticals: benefits, rationale, and adaptations for new chemical entities. LC GC N. Am., 2010, 28, 54-66.
[8]
Muskegon, M.I. 2008 https://www.uvm.edu/~vgn/outreach/documents/acetonitrile.pdf [Accessed Jun 12, 2018]; 75% acetonitrile/25% water- 800; MSDS No.000000013225 Online; Honeywell International Inc:
[9]
Nacham, O.; Ho, T.D.; Anderson, J.L.; Webster, G.K. Use of ionic liquids as headspace gas chromatography diluents for the analysis of residual solvents in pharmaceuticals. J. Pharm. Biomed. Anal., 2017, 145, 879-886.
[http://dx.doi.org/10.1016/j.jpba.2017.05.033] [PMID: 29843206]
[10]
Penton, Z. Optimization of conditions in static headspace GC. J. Sep. Sci., 1992, 15, 834-836.
[11]
Es’haghi, Z.; Ebrahimi, M.; Hosseini, M.S. Optimization of a novel method for determination of benzene, toluene, ethylbenzene, and xylenes in hair and waste water samples by carbon nanotubes reinforced sol-gel based hollow fiber solid phase microextraction and gas chromatography using factorial experimental design. J. Chromatogr. A, 2011, 1218(21), 3400-3406.
[http://dx.doi.org/10.1016/j.chroma.2011.03.043] [PMID: 21489540]