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Journal articles on the topic 'Bioanalytical methods'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Woltman, Steven J. "Bioanalytical methods." TrAC Trends in Analytical Chemistry 15, no. 5 (1996): VI. http://dx.doi.org/10.1016/0165-9936(96)80634-0.

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2

Anjani, M. Nikhare* R. T. Lohiya S. W. Rangari M. J. Umekar. "An Overview of the Development and Validation of Bioanalytical Methods using HPLC." International Journal of Pharmaceutical Sciences 2, no. 11 (2024): 319–25. https://doi.org/10.5281/zenodo.14045042.

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A key component of successful drug development is the creation of sensitive, dependable, and selective bioanalytical techniques for the quantitative assessment of medications and their metabolites in biological matrices. The pharmacokinetic and toxicokinetic analyses of investigational new drug applications (INDs), new drug applications (NDAs), and abbreviated new drug applications (ANDAs) all require the data gathered from these techniques. Critical judgments supporting a drug's safety and efficacy are based on the findings of human clinical trials, including bioavailability and bioequivalenc

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3

Skrzydlewska, Elżbieta. "Bioanalytical Methods in Toxicology." Toxicology Mechanisms and Methods 18, no. 6 (2008): 453. http://dx.doi.org/10.1080/15376510802156655.

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4

Hartmann, C., J. Smeyers-Verbeke, D. L. Massart, and R. D. McDowall. "Validation of bioanalytical chromatographic methods." Journal of Pharmaceutical and Biomedical Analysis 17, no. 2 (1998): 193–218. http://dx.doi.org/10.1016/s0731-7085(97)00198-2.

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5

Labuda, Ján, Richard P. Bowater, Miroslav Fojta, et al. "Terminology of bioanalytical methods (IUPAC Recommendations 2018)." Pure and Applied Chemistry 90, no. 7 (2018): 1121–98. http://dx.doi.org/10.1515/pac-2016-1120.

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AbstractRecommendations are given concerning the terminology of methods of bioanalytical chemistry. With respect to dynamic development particularly in the analysis and investigation of biomacromolecules, terms related to bioanalytical samples, enzymatic methods, immunoanalytical methods, methods used in genomics and nucleic acid analysis, proteomics, metabolomics, glycomics, lipidomics, and biomolecules interaction studies are introduced.

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6

Van Emon, Jeanette M. "Bioanalytical Methods for Food Contaminant Analysis." Journal of AOAC INTERNATIONAL 93, no. 6 (2010): 1681–91. http://dx.doi.org/10.1093/jaoac/93.6.1681.

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Abstract Foods are complex mixtures of lipids, carbohydrates, proteins, vitamins, organic compounds, and other naturally occurring substances. Sometimes added to this mixture are residues of pesticides, veterinary and human drugs, microbial toxins, preservatives, contaminants from food processing and packaging, and other residues. This milieu of compounds can pose difficulties in the analysis of food contaminants. There is an expanding need for rapid and cost-effective residue methods for difficult food matrixes to safeguard our food supply. Bioanalytical methods are established for many food

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7

Gleason, Carol R., Qin C. Ji, and Enaksha R. Wickremsinhe. "Evaluation of correlation between bioanalytical methods." Bioanalysis 12, no. 6 (2020): 419–26. http://dx.doi.org/10.4155/bio-2020-0019.

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Bioanalytical methods evolve throughout clinical development timelines, resulting in the need for establishing equivalency or correlation between different methods to enable comparison of data across different studies. This is accomplished by the conduct of cross validations and correlative studies to compare and describe the relationship. The incurred sample reanalysis acceptance criterion seems to be adopted universally for cross validations and correlative studies; however, this does not identify any trends or biases between the two methods (datasets) being compared. Presented here are grap

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8

Singh, Anamika, and Tamanna Narsinghan. "BIOANALYTICAL METHOD VALIDATION: A COMPREHENSIVE ASSESSMENT OF VARIOUS REGULATORY GUIDELINES." Indian Drugs 60, no. 06 (2023): 7–25. http://dx.doi.org/10.53879/id.60.06.12583.

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Bioanalytical methods are used to analyse an analyte in a biological matrix. Bioanalytical method validation is the process of determining the suitability of the given bioanalytical methodology for providing the required analytical data. Validation of the bioanalytical methods demonstrates and ensures that the methods used for the quantification of analyte in biological fluids are reliable, reproducible and suitable for its intended application. Different regulatory agencies like Food and Drug administration (FDA), The National Health Surveillance Agency or Agência Nacional de Vigilância Sanit

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9

Jordan, Gregor, and Roland F. Staack. "Toward comparability of anti-drug antibody assays: is the amount of anti-drug antibody–reagent complexes at cut-point (CP-ARC) the missing piece?" Bioanalysis 12, no. 14 (2020): 1021–31. http://dx.doi.org/10.4155/bio-2020-0143.

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Immunogenicity testing is a mandatory and critical activity during the development of therapeutic proteins. Multiple regulatory guidelines provide clear recommendations on appropriate immunogenicity testing strategies and required bioanalytical assay performances. Unfortunately, it is still generally accepted that a comparison of the immunogenicity of different compounds is not possible due to apparent performance differences of the used bioanalytical methods. In this perspective, we propose the ‘cut-point anti-drug antibody–reagents complex’ (CP-ARC) concept for technical comparability of the

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10

Waikar, Sakshi S., Manisha Raut, Tejashree Dugaje, Vasim T. Pathan, Atul R. Bendale, and Anil G. Jadhav. "Extensive assessment of fundamental factors in the development and validation of bioanalytical methods: Highlighting accuracy and reliability." International Journal of Pharmaceutical Chemistry and Analysis 11, no. 4 (2024): 274–80. https://doi.org/10.18231/j.ijpca.2024.040.

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Bioanalysis is a pivotal method employed in the pharmaceutical industry for the quantitative analysis of drugs and their metabolites within biological samples. It plays a crucial role in various aspects of pharmaceutical research, including bioequivalence, pharmacokinetic, and toxicokinetic studies. Method development, validation, and sample analysis are integral components of bioanalytical processes, ensuring the accuracy and reliability of results. Throughout each stage of analysis, careful evaluation is required to identify and mitigate any potential sources of interference, such as environ

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11

TSUYAMA, Naohiro. "Visualization of Radiation Dose by Bioanalytical Methods." BUNSEKI KAGAKU 63, no. 6 (2014): 445–53. http://dx.doi.org/10.2116/bunsekikagaku.63.445.

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12

Heudi, Olivier. "Green bioanalytical methods are now a reality." Bioanalysis 4, no. 11 (2012): 1257. http://dx.doi.org/10.4155/bio.12.112.

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13

Wong, Yong Foo, Constanze Hartmann, and Philip J Marriott. "Multidimensional gas chromatography methods for bioanalytical research." Bioanalysis 6, no. 18 (2014): 2461–79. http://dx.doi.org/10.4155/bio.14.186.

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14

Gilbert, Mary T., Irina Barinov-Colligon, and Joy R. Miksic. "Cross-validation of bioanalytical methods between laboratories." Journal of Pharmaceutical and Biomedical Analysis 13, no. 4-5 (1995): 385–94. http://dx.doi.org/10.1016/0731-7085(95)01310-h.

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15

Braggio, S., R. J. Barnaby, P. Grossi, and M. Cugola. "A strategy for validation of bioanalytical methods." Journal of Pharmaceutical and Biomedical Analysis 14, no. 4 (1996): 375–88. http://dx.doi.org/10.1016/0731-7085(95)01644-9.

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16

Jaiswal, Y. S., N. D. Grampurohit, and S. B. Bari. "Recent Trends in Validation of Bioanalytical Methods." Analytical Letters 40, no. 13 (2007): 2497–505. http://dx.doi.org/10.1080/00032710701585628.

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17

Babington, Ruth, Sonia Matas, M. Pilar Marco, and Roger Galve. "Current bioanalytical methods for detection of penicillins." Analytical and Bioanalytical Chemistry 403, no. 6 (2012): 1549–66. http://dx.doi.org/10.1007/s00216-012-5960-4.

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18

Sun, Yuchen, Shin-ichiro Nitta, Kosuke Saito, et al. "Development and multicenter validation of an LC–MS-based bioanalytical method for antisense therapeutics." Bioanalysis 14, no. 18 (2022): 1213–27. http://dx.doi.org/10.4155/bio-2022-0126.

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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, accura

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19

Blaškovičová, Jana, and Ján Labuda. "Analytical methods in herpesvirus genomics." Acta Chimica Slovaca 7, no. 2 (2014): 109–18. http://dx.doi.org/10.2478/acs-2014-0019.

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Abstract Genomics is a branch of bioanalytical chemistry characterized as the study of the genome structure and function. Genome represents the complete set of chromosomal and extrachromosomal genes of an organism, a cell, an organelle or a virus. There are at least five from eight species of herpesviruses commonly widespread among humans, Herpes simplex virus type 1 and 2, Varicella zoster virus, Epstein-Barr virus and Cytomegalovirus. Human gammaherpesviruses can cause serious diseases including B-cell lymphoma and Kaposi’s sarcoma. Diagnostics and study of the herpesviruses is directly depe

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20

Bairagee, Deepika. "Liquid Chromatographic Methods for Anti-tubercular Agents: An Overview." International Journal of PharmTech Research 13, no. 1 (2020): 26–36. http://dx.doi.org/10.20902/ijptr.2019.130104.

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The aim of this review is to summarise the different analytical and bioanalytical methods used to determine the concentration of anti-tubercular agents from last few years. As we know that tuberculosis is a life threatening disease and second to HIV in terms of deaths due to infectious diseases. Drug resistance development of the first-line drugs is a most important concern in the cure of this disease. There is no comprehensive and critical review in the literature for the analytical and bioanalytical methods for the determination of ant-tubercular agents from last few years. So this work prov

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21

Reddy, Konatham Teja Kumar, Sudha Divya Madhuri Kallam, Anoop Bodapati, and Alapati Sahithi. "Review on Green Bioanalytical Chemistry with Sustainable Approaches in Method Development: Unveiling the Crucial Role of Sustainable Bioanalysis in the Future of Chemistry." INTERNATIONAL JOURNAL OF PHARMACEUTICAL QUALITY ASSURANCE 15, no. 03 (2024): 1827–32. http://dx.doi.org/10.25258/ijpqa.15.3.110.

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Green bioanalytical chemistry, with its focus on incorporating sustainable practices into developing bioanalytical methods, has the potential to significantly reduce the environmental impact of laboratory activities. This approach, while maintaining the high standards required for analytical precision and accuracy, includes key strategies such as reducing hazardous chemicals, optimizing energy use, and implementing waste-reduction practices. This review highlights recent advancements in green bioanalytical chemistry, including green solvent systems, miniaturized techniques, and eco-friendly an

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22

Rebe Raz, Sabina, and Willem Haasnoot. "Multiplex bioanalytical methods for food and environmental monitoring." TrAC Trends in Analytical Chemistry 30, no. 9 (2011): 1526–37. http://dx.doi.org/10.1016/j.trac.2011.04.016.

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23

Dell, D., B. Lausecker, G. Hopfgartner, P. L. M. van Giersbergen, and J. Dingemanse. "Evolving bioanalytical methods for the cardiovascular drug bosentan." Chromatographia 55, S1 (2002): S115—S119. http://dx.doi.org/10.1007/bf02493366.

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24

Zhang, Guodong, Alvin V. Terry Jr, and Michael G. Bartlett. "Bioanalytical methods for the determination of antipsychotic drugs." Biomedical Chromatography 22, no. 7 (2008): 671–87. http://dx.doi.org/10.1002/bmc.997.

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25

Zhang, Shouxiang, David W. Greening, and Yuning Hong. "Correction: Recent advances in bioanalytical methods to measure proteome stability in cells." Analyst 146, no. 7 (2021): 2400. http://dx.doi.org/10.1039/d1an90022f.

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26

Ali, Mohsin, Muhammad Usman, Huma Rasheed, et al. "A systematic review on chromatography-based method validation for quantification of vancomycin in biological matrices." Bioanalysis 12, no. 24 (2020): 1767–86. http://dx.doi.org/10.4155/bio-2020-0230.

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A fully validated bioanalytical methods are prerequisite for pharmacokinetic and bioequivalence studies as well as for therapeutic drug monitoring. Due to high pharmacokinetic variability and narrow therapeutic index, vancomycin requires reliable quantification methods for therapeutic drug monitoring. To identify published chromatographic based bioanalytical methods for vancomycin in current systematic review, PubMed and ScienceDirect databases were searched. The selected records were evaluated against the method validation criteria derived from international guidelines for critical assessment

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27

Zhang, Shouxiang, David W. Greening, and Yuning Hong. "Recent advances in bioanalytical methods to measure proteome stability in cells." Analyst 146, no. 7 (2021): 2097–109. http://dx.doi.org/10.1039/d0an01547d.

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This review summarizes recent bioanalytical methods for measuring and profiling protein stability in cells on a proteome-wide scale, which can provide insights for proteostasis and associated diseases.

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28

Al, Selen, and Olcay Sagirli. "Application of salt-assisted liquid extraction in bioanalytical methods." Euchembioj Reviews, no. 1 (October 15, 2024): 70–80. http://dx.doi.org/10.62063/rev-13.

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This review provides a comprehensive analysis of bioanalytical methods employed for the quantification of drug molecules in various biological matrices, including human plasma, urine, breast milk, and mouse plasma. The study not only examines traditional sample preparation techniques such as protein precipitation (PP), liquid-liquid extraction (LLE), and solid-phase extraction (SPE), but also delves into the relatively new and innovative salting-assisted liquid-liquid extraction (SALLE). It offers a thorough comparison of analytical methods utilizing SALLE, focusing on key parameters such as a

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29

Gniazdowska, Elżbieta, Edyta Gilant, and Katarzyna Buś-Kwaśnik. "ICH M10 guideline - a harmonized global approach to bioanalysis." Prospects in Pharmaceutical Sciences 21, no. 3 (2023): 57–63. http://dx.doi.org/10.56782/pps.152.

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Bioanalytical methods are used in research on small-molecule and large-molecule drug products to determine analytes and their metabolites in biological matrices such as blood, plasma, serum, urine, feces, saliva, other biological fluids, or tissues. Validation of a bioanalytical method is the essential step before the implementation of the method into routine use in toxicokinetic or pharmacokinetic studies. Harmonization of recommendations for the validation of bioanalytical methods has been advocated for many years. In 2022, The International Council for Harmonisation of Technical Requirement

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30

Bouchafra, Houda, Aimen El Orche, Choukri El Khabbaz, et al. "Determination and validation of tiaprofenic acid in human plasma: A detailed LC-MS/MS-based analysis following ICH M10 guidelines and the accuracy profile approach." Current Chemistry Letters 13, no. 4 (2024): 707–16. http://dx.doi.org/10.5267/j.ccl.2024.4.003.

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The validation of bioanalytical methods holds critical importance for regulatory agencies and organizations dedicated to ensuring the safety, efficacy, and quality of pharmaceuticals. In this context, the recent release of the ICH M10 guideline in May 2022 represents a significant milestone in standardizing bioanalytical method validation globally. However, this guideline lacks explicit experimental protocols for implementation. In this study, we address the practical implementation of the newly released ICH M10 guideline by providing a detailed validation protocol for a bioanalytical method.

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31

Wieling, J., J. Hempenius, H. J. Jeuring, J. H. G. Jonkman, P. M. J. Coenegracht, and D. A. Doornbos. "Development of a laboratory robotic system for automated bioanalytical methods — II. A robot computer program for guarding totally automated bioanalytical methods." Journal of Pharmaceutical and Biomedical Analysis 8, no. 7 (1990): 577–82. http://dx.doi.org/10.1016/0731-7085(90)80083-2.

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32

Takahashi, Hiromi, Yoshinobu Baba, and Takao Yasui. "Oxide nanowire microfluidics addressing previously-unattainable analytical methods for biomolecules towards liquid biopsy." Chemical Communications 57, no. 98 (2021): 13234–45. http://dx.doi.org/10.1039/d1cc05096f.

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Nanowire microfluidics using a combination of self-assembly and nanofabrication technologies is expected to provide bioanalytical methods for liquid biopsy, which are impossible to achieve with conventional technologies.

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33

Jabeen, Nameera, and M. Akiful Haque. "A Review on Bioanalytical Method Development and Validation for Estimation of Drugs by Using Hyphenated Techniques and its Applications on Routine Analysis." Archives of Current Research International 23, no. 2 (2023): 18–35. http://dx.doi.org/10.9734/acri/2023/v23i2556.

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Bioanalytical methods are used to create a protocol that can identify and quantify bioactive molecules and their metabolites in human and animal samples. For determining the medication and its metabolites present in human/animal body, the bioanalytical method is efficient. One of the prominent bioanalytical roles is creating new techniques, validating existing processes, and analyzing samples. Most importantly, a compound can be calculated using many methods and can also be detected using various analytical methods. In specific biological samples, the drugs can be evaluated by different extrac

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34

Rahimpour, Elaheh, Sima Alvani-Alamdari, and Abolghasem Jouyban. "A Comprehensive Review on Developed Pharmaceutical Analysis Methods by Iranian Analysts in 2018." Pharmaceutical Sciences 26, no. 2 (2020): 107–32. http://dx.doi.org/10.34172/ps.2020.10.

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This article summarizes the publishing activities including bioanalytical and pharmaceutical analyses researches carried out in Iran in 2018 in order to connect academic researchers to those in industry, medical care units and hospitals. A wide spectrum of analytical methods has been used to determine and/or evaluate drug levels in the biological samples, based on physical, chemical and biochemical principles. We have compiled a concise survey of the literature covering 125 reports and tabulated the relevant analytical parameters. Chromatographic and electrochemical methods were found to be th

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35

Mujewar, Imran N., Omprakash G. Bhusnure, Sneha R. Jagtap, Sachin B. Gholve, Padmaja S. Giram, and Atul B. Savangikar. "A Review on Bioanalytical Method Development and Various Validation Stages Involved In Method Development Using RP- HPLC." Journal of Drug Delivery and Therapeutics 9, no. 4-s (2019): 789–95. http://dx.doi.org/10.22270/jddt.v9i4-s.3422.

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Bioanalysis is an essential part in drug discovery and development. Bioanalysis is related to the analysis of analytes (drugs, metabolites, biomarkers) in biological samples and it involves several steps from sample collection to sample analysis and data reporting. The first step is sample collection from clinical or preclinical studies; then sending the samples to laboratory for analysis. Second step is sample preparation and it is very important step in bioanalysis. In order to reach reliable results, a robust and stable sample preparation method should be applied. The role of sample prepara

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36

Shah, Vinod P. "The history of bioanalytical method validation and regulation: Evolution of a guidance document on bioanalytical methods validation." AAPS Journal 9, no. 1 (2007): E43—E47. http://dx.doi.org/10.1208/aapsj0901005.

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37

Sherry, James. "Environmental immunoassays and other bioanalytical methods: overview and update." Chemosphere 34, no. 5-7 (1997): 1011–25. http://dx.doi.org/10.1016/s0045-6535(97)00403-7.

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38

Horvai, G. "Teaching bioanalytical methods in a BSc analytical chemistry course." Analytical and Bioanalytical Chemistry 404, no. 1 (2012): 1–3. http://dx.doi.org/10.1007/s00216-012-6081-9.

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39

Ramanathan, Lakshmi, and Helen Shen. "LC–TOF–MS methods to quantify siRNAs and major metabolite in plasma, urine and tissues." Bioanalysis 11, no. 21 (2019): 1983–92. http://dx.doi.org/10.4155/bio-2019-0134.

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There are a few different bioanalytical approaches that have been used for the quantification of siRNA in biological matrices, such as S1 nuclease protection ‘cutting ELISA’, fluorescent probe hybridization HPLC, HPLC UV, LC–MS/high-resolution accurate-mass (HRAM) and LC–MS/MS. We have developed and validated plasma assays for several oligonucleotides such as GalNAc-conjugated siRNA, using uHPLC and high-resolution mass spectrometer by TOF detection. Although the molecular weights are in the range of 7000–9000, we were able to meet the same assay acceptance criteria as for the small molecules

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40

Sravanthi Gandu, Kumaraswamy Gandla, and Lalitha Repudi. "Green metric tools and white assessment in bioanalytical method development and validation: A comprehensive review." World Journal of Advanced Research and Reviews 26, no. 3 (2025): 1674–80. https://doi.org/10.30574/wjarr.2025.26.3.2362.

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The increasing demand for sustainable and eco-friendly practices in pharmaceutical and bioanalytical research has prompted the integration of green chemistry principles into analytical method development. This review discusses the implementation of Green Analytical Chemistry (GAC) metrics, such as Analytical Eco-Scale, Green Analytical Procedure Index (GAPI), and Analytical Greenness (AGREE), as well as the emerging White Analytical Chemistry (WAC) concept, in the development and validation of bioanalytical methods. We highlight the significance, methodology, and applications of these tools in

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41

Makowski, Nina, Agnes M. Ciplea, Mohsin Ali, Ilja Burdman, Anke Bartel, and Bjoern B. Burckhardt. "A comprehensive quality control system suitable for academic research: application in a pediatric study." Bioanalysis 12, no. 5 (2020): 319–33. http://dx.doi.org/10.4155/bio-2019-0242.

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Aim: Clinical research in pediatrics is progressively initiated by academia. As the reliability of pharmacodynamic measures is closely linked to the quality of bioanalytical data, bioanalytical quality assurance is crucial. However, clear guidance on comprehensive bioanalytical quality monitoring in the academic environment is lacking. Methods & results: By applying regulatory guidelines, international recommendations and scientific discussions, a five-step quality control system for monitoring the bioanalysis of aldosterone by immunoassay was developed. It comprised performance qualificat

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42

Haulenbeek, Jonathan, and Christopher J. Beaver. "The impact of ligand binding based assays critical reagent characterization and storage." Bioanalysis 13, no. 10 (2021): 797–805. http://dx.doi.org/10.4155/bio-2020-0288.

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Biological critical reagents are the foundation of many bioanalytical methods and often chemically modified or conjugated with various chemical tags. As such, the quality and performance of these methods are inherently tied to the quality and stability of critical reagents. This article will outline recommendations for conjugated critical reagent development and characterization. Examples of the impact of regent quality will be discussed for the two common bioanalytical assays in support of drug development for biotherapeutics. Finally, a brief discussion of conjugated reagent stability and re

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43

Wickremsinhe, Enaksha R., and Lisa B. Lee. "Quantification of abemaciclib and metabolites: evolution of bioanalytical methods supporting a novel oncolytic agent." Bioanalysis 13, no. 9 (2021): 711–24. http://dx.doi.org/10.4155/bio-2021-0039.

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Aim: Bioanalytical methods undergo many revisions and modifications throughout drug development to meet the objectives of the study and development program. Results: Validated LC–MS/MS methodology used to quantify abemaciclib and four metabolites in human plasma is described. The method, initially validated to support the first-in-human study, was successfully modified to include additional metabolites as in vitro and in vivo information about the activity and abundance of human metabolites became available. Consistent performance of the method over time was demonstrated by an incurred sample

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44

Hackel, Dana T., Theingi M. Thway, Shiew Mei Huang, and Yow-Ming C. Wang. "A survey of pharmacokinetic bioanalytical methods in biosimilar biological license applications for the assessment of target and antidrug antibody effects." Bioanalysis 13, no. 17 (2021): 1323–32. http://dx.doi.org/10.4155/bio-2021-0116.

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The presence of circulating targets and antidrug antibodies can influence the ability of a bioanalytical method to measure therapeutic protein (TP) concentration relevant to exposure-response evaluations. This project surveyed biosimilar submissions for their bioanalytical methods. Survey results revealed that 97% of pharmacokinetic methods designed to measure theoretically free or partial-free TPs with respect to target indeed measured free or partial-free TPs when considering experimental testing results for target effects. Antidrug antibody effect is less often evaluated. The observed trend

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45

Vazvaei, Faye, and Jeffrey X. Duggan. "Validation of LC–MS/MS bioanalytical methods for protein therapeutics." Bioanalysis 6, no. 13 (2014): 1739–42. http://dx.doi.org/10.4155/bio.14.125.

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46

Giorgianni, Francesco, Diwa Koirala, and Sarka Beranova-Giorgianni. "Proteomics of the human pituitary tissue: bioanalytical methods and applications." Bioanalysis 6, no. 14 (2014): 1989–2003. http://dx.doi.org/10.4155/bio.14.132.

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47

Fachi, Mariana Millan, Letícia Paula Leonart, Flávia Lada Degaut Pontes, Raquel de Oliveira Vilhena, Letícia Bonancio Cerqueira, and Roberto Pontarolo. "Bioanalytical methods for the detection of antidiabetic drugs: a review." Bioanalysis 9, no. 24 (2017): 2015–25. http://dx.doi.org/10.4155/bio-2017-0182.

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48

Nijem, I., R. Elliott, J. Brumm, et al. "Cross validation of pharmacokinetic bioanalytical methods: Experimental and statistical design." Journal of Pharmaceutical and Biomedical Analysis 252 (January 2025): 116485. http://dx.doi.org/10.1016/j.jpba.2024.116485.

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49

Rozet, E., R. D. Marini, E. Ziemons, B. Boulanger, and Ph Hubert. "Advances in validation, risk and uncertainty assessment of bioanalytical methods." Journal of Pharmaceutical and Biomedical Analysis 55, no. 4 (2011): 848–58. http://dx.doi.org/10.1016/j.jpba.2010.12.018.

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50

Zhang, Run, Bo Song, and Jingli Yuan. "Bioanalytical methods for hypochlorous acid detection: Recent advances and challenges." TrAC Trends in Analytical Chemistry 99 (February 2018): 1–33. http://dx.doi.org/10.1016/j.trac.2017.11.015.

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