UHPLC–MS/MS Method for the Simultaneous Quantification of 12 Antiretroviral Drugs in Human Plasma Using Dried Sample Spot Devices: Development, Validation, and Stability Evaluation

: The method demonstrated robustness and reproducibility in accordance with FDA and EMA guidelines. It ensures satisfactory accuracy and rapid analysis, supporting its application in clinical practice, including for monitoring the newest long-acting drugs.

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Publication Details

Journal
Pharmaceutics
Published
2026-04-21
DOI
https://doi.org/10.3390/pharmaceutics18040513
Primary Topic
Pharmaceutical Quality and Counterfeiting
Type
article
Field-Weighted Citation Impact
0.00

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article

UHPLC–MS/MS Method for the Simultaneous Quantification of 12 Antiretroviral Drugs in Human Plasma Using Dried Sample Spot Devices: Development, Validation, and Stability Evaluation

Marco Simiele, Amedeo De Nicolò, Alice Palermiti, A D'Avolio et al.
Pharmaceutics
Pharmaceutical Quality and Counterfeiting
article

UHPLC–MS/MS Method for the Simultaneous Quantification of 12 Antiretroviral Drugs in Human Plasma Using Dried Sample Spot Devices: Development, Validation, and Stability Evaluation

Marco Simiele, Amedeo De Nicolò, Alice Palermiti, A D'Avolio, Jessica Cusato, Greta Sabbia, Alessandra Manca, Sara Soloperto, Martina Billi, Elisa Barnini, Camilla Martino, Gianluca Bianco, Elisa Martina
article en

Abstract

: The method demonstrated robustness and reproducibility in accordance with FDA and EMA guidelines. It ensures satisfactory accuracy and rapid analysis, supporting its application in clinical practice, including for monitoring the newest long-acting drugs.

PharmaceuticsVol. 18(4)
University of Turin (IT)
European Commission
Good health and well-being
Openalex Percentile: Top 15%
Pharmaceutical Quality and Counterfeiting
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