Investigating surrogate cerebrospinal fluid matrix compositions for use in quantitative LC-MS analysis of therapeutic antibodies in the cerebrospinal fluid

• Published in: Analytical and bioanalytical chemistry 2020-03, Vol.412 (7), p.1653-1661
• Main Authors: Fogh, Jens Rose, Jacobsen, Anne-Marie, Nguyen, Tam T. T. N., Rand, Kasper D., Olsen, Line Rørbæk
• Format: Article
• Language: English
• Subjects: Albumin; Amino Acid Sequence; Analysis; Analytical Chemistry; Animals; Antibodies - cerebrospinal fluid; Antibodies - chemistry; Biochemistry; Biopharmaceutics; Bovine serum albumin; Calibration; Cerebrospinal fluid; Characterization and Evaluation of Materials; Chemical compounds; Chemistry; Chemistry and Materials Science; Chromatography, Liquid - methods; Composition; Dilution; Dogs; Food Science; Haplorhini; Health aspects; Humans; Investigations; Laboratory Medicine; Monitoring/Environmental Analysis; Monoclonal antibodies; Pharmaceuticals; Quantitative analysis; Rats; Reference Standards; Research Paper; Sample preparation; Serum albumin; Tandem Mass Spectrometry - methods
• ISSN: 1618-2642; 1618-2650
• DOI: 10.1007/s00216-020-02403-3

As quantitative analysis of biotherapeutics in cerebrospinal fluid (CSF) with LC-MS becomes increasingly widespread, there is a need for method developments towards higher sensitivity. By using artificial CSF (aCSF) in the development phase, the consumption of costly and sparsely available CSF can be limited. The aCSF compositions tested here were made from various dilutions of bovine serum albumin (BSA) or rat plasma to mimic the total protein concentration found in CSF. Focusing on monoclonal antibodies, the aCSF was spiked with human immunoglobulin (hIgG) and prepared with the bottom-up analysis technique using LC-MS. Assuming that the composition of the aCSF would affect the digest, the response from aCSF matrices was compared with CSF from rat, monkey, and dog in terms of estimated sample concentration and matrix effects. The samples were spiked with hIgG in the range of 10 to 1000 ng/mL and volumes of 10 μL were transferred to sample preparation. The results indicate that BSA dilutions from 300 to 2000 μg/mL and rat plasma dilutions of 0.5–2% provide the most accurate concentration estimates when compared with rat CSF. 1000 μg/mL BSA did not produce significantly different concentration estimates for 500 ng/mL samples when compared with CSF from rat, monkey, and dog, and can therefore be used as aCSF for several different species.