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Development and multicenter validation of an LC-MS-based bioanalytical method for antisense therapeutics.
Sun, Yuchen; Nitta, Shin-Ichiro; Saito, Kosuke; Hosogai, Ryuta; Nakai, Keiko; Goda, Ryoya; Shimizu, Hisao; Fujita, Hisashi; Kakehi, Masaaki; Murata, Kazuyuki; Yamaguchi, Takeru; Okuzono, Takeshi; Yamane, Shinichi; Kawabata, Mitsuhiko; Matsunuma, Takayuki; Takahara, Kentaro; Kato, Noriko; Yamada, Masaki; Yoshida, Tokuyuki; Inoue, Takao; Saito, Yoshiro.
Afiliação
  • Sun Y; Division of Medicinal Safety Science, National Institute of Health Sciences, Kanagawa, 210-9501, Japan.
  • Nitta SI; LSI Medience Corporation, Tokyo, 105-0023, Japan.
  • Saito K; Division of Medicinal Safety Science, National Institute of Health Sciences, Kanagawa, 210-9501, Japan.
  • Hosogai R; LSI Medience Corporation, Tokyo, 105-0023, Japan.
  • Nakai K; LSI Medience Corporation, Tokyo, 105-0023, Japan.
  • Goda R; Daiichi Sankyo Company Ltd, Tokyo, 140-8710, Japan.
  • Shimizu H; Takeda Pharmaceutical Company Ltd, Kanagawa, 251-8555, Japan.
  • Fujita H; Takeda Pharmaceutical Company Ltd, Kanagawa, 251-8555, Japan.
  • Kakehi M; Takeda Pharmaceutical Company Ltd, Kanagawa, 251-8555, Japan.
  • Murata K; Sumika Chemical Analysis Service Ltd, Osaka, 554-0022, Japan.
  • Yamaguchi T; Sumika Chemical Analysis Service Ltd, Osaka, 554-0022, Japan.
  • Okuzono T; Sekisui Medical Co. Ltd, Tokyo, 103-0027, Japan.
  • Yamane S; Sekisui Medical Co. Ltd, Tokyo, 103-0027, Japan.
  • Kawabata M; Shin Nippon Biomedical Laboratories Ltd, Tokyo, 104-0044, Japan.
  • Matsunuma T; Thermo Fisher Scientific KK, Kanagawa, 221-0022, Japan.
  • Takahara K; Thermo Fisher Scientific KK, Kanagawa, 221-0022, Japan.
  • Kato N; Shimadzu Corporation, Kyoto, 140-8710, Japan.
  • Yamada M; Shimadzu Corporation, Kyoto, 140-8710, Japan.
  • Yoshida T; Division of Molecular Target & Gene Therapy Products, National Institute of Health Sciences, Kanagawa, 210-9501, Japan.
  • Inoue T; Division of Molecular Target & Gene Therapy Products, National Institute of Health Sciences, Kanagawa, 210-9501, Japan.
  • Saito Y; Division of Medicinal Safety Science, National Institute of Health Sciences, Kanagawa, 210-9501, Japan.
Bioanalysis ; 14(18): 1213-1227, 2022 Sep.
Article em En | MEDLINE | ID: mdl-36408704
ABSTRACT

Background:

Many bioanalytical methods for antisense oligonucleotides (ASOs) using LC-MS have been reported. However, no data have been available on the reproducibility and robustness of a single bioanalytical method for ASOs. As such, in the current study, we evaluated the reproducibility and robustness of LC-MS-based bioanalytical methods for ASOs in multiple laboratories. Methods/

Results:

Seven independent laboratories were included in this study. Mipomersen was measured by ion-pairing LC-MS (IP-LC-MS) as a model ASO using different LC-MS. The validation results of calibration curve, accuracy, precision and selectivity met the criteria of conventional bioanalytical method validation guidelines using LC/GC-MS for drugs in all laboratories. Meanwhile, carryover (>20%) was detected in three laboratories.

Conclusion:

We first demonstrated the multicenter-validated IP-LC-MS bioanalytical method for ASOs. Our data showed that the method was sensitive, robust and reproducible. However, the occurrence of carryover should be carefully monitored in its future application.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Terapia Biológica / Espectrometria de Massas em Tandem Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Terapia Biológica / Espectrometria de Massas em Tandem Idioma: En Ano de publicação: 2022 Tipo de documento: Article