Features of Sample Preparation of Cell Culture Samples for Metabolomic Screening by LC-MS/MS Научная публикация
Журнал |
Journal of Pharmaceutical and Biomedical Analysis
ISSN: 2095-1779 |
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Вых. Данные | Год: 2026, Том: 267, Номер статьи : 117146, Страниц : 12 DOI: 10.1016/j.jpba.2025.117146 | ||||||||||||
Ключевые слова | Cell culture metabolomics; HPLC-MS/MS standardization; Cell number optimization; Targeted metabolomics; HILIC; RP LC | ||||||||||||
Авторы |
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Организации |
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Информация о финансировании (5)
1 | Министерство науки и высшего образования Российской Федерации (с 15 мая 2018) | FWNR-2022-0023 |
2 | Министерство науки и высшего образования Российской Федерации (с 15 мая 2018) | FWUR-2024-0032 |
3 | Министерство науки и высшего образования Российской Федерации (с 15 мая 2018) | 075-00365-25-00 |
4 | Министерство науки и высшего образования Российской Федерации (с 15 мая 2018) | FSUS-2025-0012 |
5 | Министерство науки и высшего образования Российской Федерации (с 15 мая 2018) | FWNR-2025-0016 (125031103454-7)(075-03-2025-636) |
Реферат:
Metabolomic analysis has become an essential tool in the life sciences, providing insights into cellular metabolism. However, preparing cell cultures for metabolomic screening remains challenging, especially with samples containing variable cell numbers. Standardized and reproducible protocols are required to ensure reliable data while maintaining compatibility with high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). Using melanoma cell lines SK-MEL-28 (human) and B16 (mouse) as models, we developed and optimized a convenient sample preparation protocol for metabolomic screening by HPLC-MS/MS. The study is focused on optimizing key steps, including cell lysis, metabolite extraction, and normalization strategies for accurate semiquantitative analysis. The effects of cell count on metabolomic coverage and detection sensitivity were evaluated using hydrophilic interaction liquid chromatography (HILIC) and reversed-phase (RP) chromatography. The protocol enables efficient detection of several metabolite classes from samples containing as few as 10,000 cells. The optimal cell count for reliable analysis was found to be 400,000 – 500,000 cells, ensuring consistent and reproducible detection within the method’s analytical coverage. Our findings emphasize the importance of cell size and number in metabolomic studies, as larger cells provide improved metabolomic coverage. Moreover, metabolites exhibited varying detection limits, highlighting the need to adjust sample preparation strategies according to metabolite characteristics. The proposed protocol offers a robust and reproducible approach for the metabolomic screening of adherent melanoma cell cultures by HPLC-MS/MS and can be adapted for non-adherent and other cell types. Balancing sensitivity, reproducibility, and feasibility, this method provides a standardized solution for cell metabolomic studies in pharmacometabolomics, cancer research, and related fields.
Библиографическая ссылка:
Basov N.V.
, Butikova E.A.
, Sotnikova M.A.
, Razumov I.A.
, Sotnikova Y.S.
, Patrushev Y.V.
, Rogachev A.D.
, Salakhutdinov N.F.
, Pokrovsky A.G.
Features of Sample Preparation of Cell Culture Samples for Metabolomic Screening by LC-MS/MS
Journal of Pharmaceutical and Biomedical Analysis. 2026. V.267. 117146 :1-12. DOI: 10.1016/j.jpba.2025.117146 Scopus РИНЦ PMID OpenAlex
Features of Sample Preparation of Cell Culture Samples for Metabolomic Screening by LC-MS/MS
Journal of Pharmaceutical and Biomedical Analysis. 2026. V.267. 117146 :1-12. DOI: 10.1016/j.jpba.2025.117146 Scopus РИНЦ PMID OpenAlex
Даты:
Поступила в редакцию: | 11 июн. 2025 г. |
Принята к публикации: | 13 сент. 2025 г. |
Опубликована online: | 15 сент. 2025 г. |
Опубликована в печати: | 1 янв. 2026 г. |
Идентификаторы БД:
Scopus: | 2-s2.0-105016313330 |
РИНЦ: | 82893525 |
PMID (PubMed): | 40972480 |
OpenAlex: | W4414230274 |
Цитирование в БД:
Пока нет цитирований