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Molecules
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Exploring Analytical Techniques in Pharmaceutical and Biomedical Analysis
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Exploring Analytical Techniques in Pharmaceutical and Biomedical Analysis

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Medicinal Chemistry".

Deadline for manuscript submissions: 30 September 2025 | Viewed by 1415

Special Issue Editors

Prof. Dr. Fengqing Yang

E-Mail Website
Guest Editor
School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China
Interests: chromatographic analysis; spectroscopic analysis; enzyme immobilizations and applications; preparation and applications of materials with enzyme-like activity
Special Issues, Collections and Topics in MDPI journals
Dr. Yuelin Song

E-Mail Website
Guest Editor
Modern Research Center for Traditional Chinese Medicine, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 100029, China
Interests: multi-dimensional liquid chromatography; mass spectrometry; traditional Chinese medicine
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Pharmaceutical and biomedical analysis is of great significance for the quality control of drugs, pharmacodynamic study, pharmacokinetic study, and metabolic profiling, etc. Analytical techniques have a decisive effect on the accuracy and precision of analysis results. Currently, there are lots of analytical techniques, such as chromatographic and spectroscopic methods, mass spectrometry, capillary electrophoresis and electrochemical methods, that have been widely applied in pharmaceutical and biomedical analysis. In practice, further exploring the analytical techniques in pharmaceutical and biomedical analysis is beneficial for drug research.

We would like to invite authors to contribute original research and review articles that will stimulate basic research on advanced analytical techniques for pharmaceutical and biomedical analysis. In this Special Issue, we will pay special attention to the manuscripts that evaluate and discuss analytical methods and their applications in pharmaceutical and biomedical analysis. Potential topics suitable for this Special Issue include, but are not limited to, the following: (1) recent advances in analytical methods for pharmaceutical and biomedical analysis; (2) applications of advanced analytical techniques in analyzing pharmaceuticals and their metabolites in different samples, such as pharmaceutical preparations and biological samples; (3) the use of state-of-the-art technology to improve the efficiency of traditional analytical methods for pharmaceutical and biomedical analysis.

Prof. Dr. Fengqing Yang
Dr. Yuelin Song
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Molecules is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • pharmaceutical analysis
  • biomedical analysis
  • chromatographic analysis
  • spectroscopic analysis
  • mass spectrometry analysis
  • capillary electrophoresis
  • electrochemical analysis

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Further information on MDPI's Special Issue policies can be found here.

Published Papers (2 papers)

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Research

15 pages, 3617 KiB  
Article
The Molecular Recognition of Lurasidone by Human Serum Albumin: A Combined Experimental and Computational Approach
by Nevena Živković, Emina Mrkalić, Ratomir Jelić, Jovica Tomović, Jadranka Odović, Marina Ćendić Serafinović and Miroslav Sovrlić
Molecules 2025, 30(7), 1420; https://doi.org/10.3390/molecules30071420 - 22 Mar 2025
Viewed by 274
Abstract
Lurasidone (LUR) is an antipsychotic drug whose interaction with human serum albumin (HSA) plays a crucial role in its pharmacokinetic and pharmacodynamic properties. A thorough understanding of LUR’s binding mechanism to HSA is crucial for predicting its transport, distribution, and potential drug interactions. [...] Read more.
Lurasidone (LUR) is an antipsychotic drug whose interaction with human serum albumin (HSA) plays a crucial role in its pharmacokinetic and pharmacodynamic properties. A thorough understanding of LUR’s binding mechanism to HSA is crucial for predicting its transport, distribution, and potential drug interactions. Methods: The interaction between LUR and HSA was investigated using fluorescence and circular dichroism (CD) spectroscopy, followed by molecular docking simulations. Binding characteristics were analyzed through quenching mechanisms, thermodynamic parameters, and competitive site marker experiments. Results: This study revealed a systematic decrease in HSA fluorescence intensity with increasing LUR concentration, indicating a static quenching mechanism driven by non-fluorescent complex formation. Binding constants suggest enhanced complex stability at higher temperatures, with thermodynamic analysis confirming an endothermic, hydrophobic interaction. Competitive site marker assays and synchronous fluorescence spectra confirmed that LUR primarily binds to site I (subdomain IIA) near tryptophan residues. Conformational changes in HSA, observed as a decrease in α-helix content, further demonstrate the structural impact of LUR binding. Conclusions: These findings offer key insights into the molecular interactions between LUR and HSA, enhancing our understanding of LUR’s pharmacokinetics and its potential interactions with other drugs. Understanding these binding characteristics can aid in optimizing LUR’s clinical application and predicting possible interactions with other biomolecules. Full article
(This article belongs to the Special Issue Exploring Analytical Techniques in Pharmaceutical and Biomedical Analysis)
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11 pages, 946 KiB  
Communication
The Development and Validation of a Simple HPLC-UV Method for the Determination of Vancomycin Concentration in Human Plasma and Application in Critically Ill Patients
by Asma Aboelezz, Novel Solomon Tesfamariam, Maged Kharouba, Tamara Gligoric and Sherif Hanafy Mahmoud
Molecules 2025, 30(5), 1062; https://doi.org/10.3390/molecules30051062 - 26 Feb 2025
Viewed by 691
Abstract
Vancomycin is an antimicrobial agent that exhibits high efficacy against Gram-positive bacteria. The importance of therapeutic drug monitoring (TDM) for vancomycin has been substantiated in specific patient cohorts, underscoring the significance of determining vancomycin plasma levels. This study presents the development and validation [...] Read more.
Vancomycin is an antimicrobial agent that exhibits high efficacy against Gram-positive bacteria. The importance of therapeutic drug monitoring (TDM) for vancomycin has been substantiated in specific patient cohorts, underscoring the significance of determining vancomycin plasma levels. This study presents the development and validation of a simple, reproducible, and practical approach for quantifying vancomycin levels in human plasma samples through high-performance liquid chromatography (HPLC). Deproteinization of plasma samples (0.3 mL) was achieved using 10% perchloric acid. The chromatographic separation was achieved using a C18 column. The mobile phase, consisting of phosphate buffer and acetonitrile (90:10, v/v), was run at a flow rate of 1 mL/min. Ultraviolet detection was conducted at a wavelength of 192 nm and the method was linear in the range of 4.5–80 mg/L (r2 > 0.99). Inter- and intra-day assay precision and accuracy were determined to be within the acceptable range. The run time was noted to be 10 min. This method was evaluated using different greenness tools, which indicated that the method is environmentally friendly. Our method was effectively applied to analyze vancomycin concentrations in critically ill patients. Thus, our approach has the potential for practical implementation in routine TDM procedures. Full article
(This article belongs to the Special Issue Exploring Analytical Techniques in Pharmaceutical and Biomedical Analysis)
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