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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Current Protein &amp; Peptide Science</journal-id><journal-title-group><journal-title xml:lang="en">Current Protein &amp; Peptide Science</journal-title><trans-title-group xml:lang="ru"><trans-title>Current Protein &amp; Peptide Science</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1389-2037</issn><issn publication-format="electronic">1875-5550</issn><publisher><publisher-name xml:lang="en">Bentham Science</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">645661</article-id><article-id pub-id-type="doi">10.2174/0113892037284277240126094716</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Life Sciences</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Spectroscopic Analysis of the Effect of Ibuprofen Degradation Products on the Interaction between Ibuprofen and Human Serum Albumin</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Ploch-Jankowska</surname><given-names>Anna</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff id="aff1"><institution>Department of Pharmacy and Ecological Chemistry, Institute of Chemistry, University of Opole</institution></aff><pub-date date-type="pub" iso-8601-date="2024-06-01" publication-format="electronic"><day>01</day><month>06</month><year>2024</year></pub-date><volume>25</volume><issue>6</issue><issue-title xml:lang="ru"/><fpage>492</fpage><lpage>506</lpage><history><date date-type="received" iso-8601-date="2025-01-11"><day>11</day><month>01</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Bentham Science Publishers</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Bentham Science Publishers</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://journals.eco-vector.com/1389-2037/article/view/645661">https://journals.eco-vector.com/1389-2037/article/view/645661</self-uri><abstract xml:lang="en"><p id="idm46466589598080">Background:Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) are one of the most commonly used groups of medicinal compounds in the world. The wide access to NSAIDs and the various ways of storing them due to their easy accessibility often entail the problem with the stability and durability resulting from the exposure of drugs to external factors. The aim of the research was to evaluate in vitro the mechanism of competition between ibuprofen (IBU) and its degradation products, i.e., 4'-isobutylacetophenone (IBAP) and (2RS)-2-(4- formylphenyl)propionic acid (FPPA) during transport in a complex with fatted (HSA) and defatted (dHSA) human serum albumin.</p><p id="idm46466589602080">Methods:The research was carried out using spectroscopic techniques, such as spectrophotometry, infrared spectroscopy and nuclear magnetic resonance spectroscopy</p><p id="idm46466589606048">Results:The comprehensive application of spectroscopic techniques allowed, among others, for the determination of the binding constant, the number of classes of binding sites and the cooperativeness constant of the analyzed systems IBU-(d)HSA, IBU-(d)HSA-FPPA, IBU-(d)HSA-IBAP; the determination of the effect of ibuprofen and its degradation products on the secondary structure of albumin; identification and assessment of interactions between ligand and albumin; assessment of the impact of the presence of fatty acids in the structure of albumin and the measurement temperature on the binding of IBU, IBAP and FPPA to (d)HSA.</p><p id="idm46466589611104">Conclusion:The conducted research allowed us to conclude that the presence of ibuprofen degradation products and the increase in their concentration significantly affect the formation of the IBU-albumin complex and thus, the value of the association constant of the drug, changing the concentration of its free fraction in the blood plasma. It was also found that the presence of an ibuprofen degradation product in a complex with albumin affects its secondary structure.</p></abstract><kwd-group xml:lang="en"><kwd>Ibuprofen</kwd><kwd>4'-isobutylacetophenone</kwd><kwd>(2RS)-2-(4-formylphenyl)propionic acid</kwd><kwd>spectroscopic analysis</kwd><kwd>Ibuprofen degradation</kwd><kwd>human serum albumin.</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Kostowski, W.; Herman, Z.S. Farmakologia; Wydawnictwo Lekarskie PZWL: Warszawa, 2008.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Czyrski, A.; Kazińska, I. Nonsteroidal anti-inflammatory drugs derived from 2-arylpropionic acid. Gazeta Farmaceutyczna, 2013, 22(4), 28-30.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Paulose-Ram, R.; Hirsch, R.; Dillon, C.; Gu, Q. Frequent monthly use of selected non-prescription and prescription non-narcotic analgesics among U.S. adults. 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