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Complex-Forming Properties of the Anti-Inflammatory Sialorphin Derivative Palmitic Acid-Lysine-Lysine-Glutamine-Histidine-Asparagine-Proline-Arginine with Cu(II) Ions in an Aqueous Solution
The present work describes the complexation of the anti-inflammatory sialorphin derivative Pal-Lys-Lys-Gln-His-Asn-Pro-Arg (palmitic acid-lysine-lysine-glutamine-histidine-asparagine-proline-arginine) with Cu(II) ions in an aqueous solution, at a temperature of 25.0 ± 0.1 °C, over the whole pH range...
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Published in: | Molecules (Basel, Switzerland) Switzerland), 2023-12, Vol.29 (1), p.90 |
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description | The present work describes the complexation of the anti-inflammatory sialorphin derivative Pal-Lys-Lys-Gln-His-Asn-Pro-Arg (palmitic acid-lysine-lysine-glutamine-histidine-asparagine-proline-arginine) with Cu(II) ions in an aqueous solution, at a temperature of 25.0 ± 0.1 °C, over the whole pH range. The complexing properties were characterized by potentiometric and UV-Vis spectrophotometric methods. The potentiometric method was used to calculate the logarithms of the overall stability constants (log
) and the values of the stepwise dissociation constants (p
) of the studied complexes. The percentage of each species formed in an aqueous solution was estimated from the species distribution curve as a function of pH. The absorbance (
) and molar absorption coefficient (
) values for the Cu(II)-sialorphin derivative system were determined with UV-Vis spectroscopy. Our studies indicate that the sialorphin derivative forms stable complexes with Cu(II) ions, which may lead to future biological and therapeutic applications. |
doi_str_mv | 10.3390/molecules29010090 |
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) and the values of the stepwise dissociation constants (p
) of the studied complexes. The percentage of each species formed in an aqueous solution was estimated from the species distribution curve as a function of pH. The absorbance (
) and molar absorption coefficient (
) values for the Cu(II)-sialorphin derivative system were determined with UV-Vis spectroscopy. Our studies indicate that the sialorphin derivative forms stable complexes with Cu(II) ions, which may lead to future biological and therapeutic applications.</description><identifier>ISSN: 1420-3049</identifier><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules29010090</identifier><identifier>PMID: 38202673</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Amino acids ; Anti-inflammatory drugs ; Aqueous solutions ; Cholesterol ; Cu(II) complexes ; Edema ; Enkephalins ; Fatty acids ; High density lipoprotein ; Inflammation ; Ligands ; Narcotics ; Natriuretic peptides ; palmitic acid ; Peptides ; Physiology ; potentiometry ; protonation constant ; Saturated fatty acids ; sialorphin ; Spectrum analysis ; Triglycerides ; UV-Vis spectroscopy ; Vegetable oils</subject><ispartof>Molecules (Basel, Switzerland), 2023-12, Vol.29 (1), p.90</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c513t-7190618b0d9f05567a008d102884d83313ac693a8a47e19e6ce8a8cadf4a15df3</cites><orcidid>0000-0002-8443-4417 ; 0000-0003-0275-3017 ; 0000-0002-9741-4562 ; 0000-0001-7706-1993 ; 0000-0003-3194-834X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2912731137/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2912731137?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38202673$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pająk, Marek</creatorcontrib><creatorcontrib>Kamysz, Elżbieta</creatorcontrib><creatorcontrib>Sikora, Karol</creatorcontrib><creatorcontrib>Fichna, Jakub</creatorcontrib><creatorcontrib>Woźniczka, Magdalena</creatorcontrib><title>Complex-Forming Properties of the Anti-Inflammatory Sialorphin Derivative Palmitic Acid-Lysine-Lysine-Glutamine-Histidine-Asparagine-Proline-Arginine with Cu(II) Ions in an Aqueous Solution</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>The present work describes the complexation of the anti-inflammatory sialorphin derivative Pal-Lys-Lys-Gln-His-Asn-Pro-Arg (palmitic acid-lysine-lysine-glutamine-histidine-asparagine-proline-arginine) with Cu(II) ions in an aqueous solution, at a temperature of 25.0 ± 0.1 °C, over the whole pH range. The complexing properties were characterized by potentiometric and UV-Vis spectrophotometric methods. The potentiometric method was used to calculate the logarithms of the overall stability constants (log
) and the values of the stepwise dissociation constants (p
) of the studied complexes. The percentage of each species formed in an aqueous solution was estimated from the species distribution curve as a function of pH. The absorbance (
) and molar absorption coefficient (
) values for the Cu(II)-sialorphin derivative system were determined with UV-Vis spectroscopy. Our studies indicate that the sialorphin derivative forms stable complexes with Cu(II) ions, which may lead to future biological and therapeutic applications.</description><subject>Amino acids</subject><subject>Anti-inflammatory drugs</subject><subject>Aqueous solutions</subject><subject>Cholesterol</subject><subject>Cu(II) complexes</subject><subject>Edema</subject><subject>Enkephalins</subject><subject>Fatty acids</subject><subject>High density lipoprotein</subject><subject>Inflammation</subject><subject>Ligands</subject><subject>Narcotics</subject><subject>Natriuretic peptides</subject><subject>palmitic acid</subject><subject>Peptides</subject><subject>Physiology</subject><subject>potentiometry</subject><subject>protonation constant</subject><subject>Saturated fatty acids</subject><subject>sialorphin</subject><subject>Spectrum analysis</subject><subject>Triglycerides</subject><subject>UV-Vis spectroscopy</subject><subject>Vegetable oils</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUstu1DAUjRCIlsIHsEGW2JRFih3nYa9QNNA20khUKqyjO44z45FjB9uZMh_Hv-H0RQeQF_f4-pxz5aObJG8JPqOU44-D1VJMWvqMY4Ixx8-SY5JnOKU458-f4KPklfdbjDOSk-JlckRZhrOyosfJr4UdRi1_pufWDcqs0ZWzo3RBSY9sj8JGotoElTam1zAMEKzbo2sF2rpxowz6LJ3aQVA7ia5ADyoogWqhunS598rIh3KhpwDDjC6VD6qbUe1HcLCeYRyqb1suXiNANyps0GI6bZoPqLHGozgKDKp_TNJOHl3b6KeseZ286EF7-ea-niTfz798W1ymy68XzaJepqIgNKQV4bgkbIU73uOiKCvAmHUEZ4zlHaOUUBAlp8AgryThshSSARPQ9TmQouvpSdLc-XYWtu3o1ABu31pQ7W3DunULMTOhZUtoCYJUhcCszPOMrCopK8gLRjiDbMWj16c7r3FaDbIT0gQH-sD08MWoTbu2u5bgquJljqPD6b2DszEQH9pBeSG1BjOn02ac0LzAvCKR-v4v6tZOzsSsZlZWUUJo9Ye1hvgDZXobB4vZtK3jTJqXBSsi6-w_rHg6OShhjexV7B8IyJ1AOOu9k_3jJwlu5wVu_1ngqHn3NJ1HxcPG0t91zO-c</recordid><startdate>20231222</startdate><enddate>20231222</enddate><creator>Pająk, Marek</creator><creator>Kamysz, Elżbieta</creator><creator>Sikora, Karol</creator><creator>Fichna, Jakub</creator><creator>Woźniczka, Magdalena</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-8443-4417</orcidid><orcidid>https://orcid.org/0000-0003-0275-3017</orcidid><orcidid>https://orcid.org/0000-0002-9741-4562</orcidid><orcidid>https://orcid.org/0000-0001-7706-1993</orcidid><orcidid>https://orcid.org/0000-0003-3194-834X</orcidid></search><sort><creationdate>20231222</creationdate><title>Complex-Forming Properties of the Anti-Inflammatory Sialorphin Derivative Palmitic Acid-Lysine-Lysine-Glutamine-Histidine-Asparagine-Proline-Arginine with Cu(II) Ions in an Aqueous Solution</title><author>Pająk, Marek ; Kamysz, Elżbieta ; Sikora, Karol ; Fichna, Jakub ; Woźniczka, Magdalena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c513t-7190618b0d9f05567a008d102884d83313ac693a8a47e19e6ce8a8cadf4a15df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Amino acids</topic><topic>Anti-inflammatory drugs</topic><topic>Aqueous solutions</topic><topic>Cholesterol</topic><topic>Cu(II) complexes</topic><topic>Edema</topic><topic>Enkephalins</topic><topic>Fatty acids</topic><topic>High density lipoprotein</topic><topic>Inflammation</topic><topic>Ligands</topic><topic>Narcotics</topic><topic>Natriuretic peptides</topic><topic>palmitic acid</topic><topic>Peptides</topic><topic>Physiology</topic><topic>potentiometry</topic><topic>protonation constant</topic><topic>Saturated fatty acids</topic><topic>sialorphin</topic><topic>Spectrum analysis</topic><topic>Triglycerides</topic><topic>UV-Vis spectroscopy</topic><topic>Vegetable oils</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pająk, Marek</creatorcontrib><creatorcontrib>Kamysz, Elżbieta</creatorcontrib><creatorcontrib>Sikora, Karol</creatorcontrib><creatorcontrib>Fichna, Jakub</creatorcontrib><creatorcontrib>Woźniczka, Magdalena</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pająk, Marek</au><au>Kamysz, Elżbieta</au><au>Sikora, Karol</au><au>Fichna, Jakub</au><au>Woźniczka, Magdalena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Complex-Forming Properties of the Anti-Inflammatory Sialorphin Derivative Palmitic Acid-Lysine-Lysine-Glutamine-Histidine-Asparagine-Proline-Arginine with Cu(II) Ions in an Aqueous Solution</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><addtitle>Molecules</addtitle><date>2023-12-22</date><risdate>2023</risdate><volume>29</volume><issue>1</issue><spage>90</spage><pages>90-</pages><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>The present work describes the complexation of the anti-inflammatory sialorphin derivative Pal-Lys-Lys-Gln-His-Asn-Pro-Arg (palmitic acid-lysine-lysine-glutamine-histidine-asparagine-proline-arginine) with Cu(II) ions in an aqueous solution, at a temperature of 25.0 ± 0.1 °C, over the whole pH range. The complexing properties were characterized by potentiometric and UV-Vis spectrophotometric methods. The potentiometric method was used to calculate the logarithms of the overall stability constants (log
) and the values of the stepwise dissociation constants (p
) of the studied complexes. The percentage of each species formed in an aqueous solution was estimated from the species distribution curve as a function of pH. The absorbance (
) and molar absorption coefficient (
) values for the Cu(II)-sialorphin derivative system were determined with UV-Vis spectroscopy. Our studies indicate that the sialorphin derivative forms stable complexes with Cu(II) ions, which may lead to future biological and therapeutic applications.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>38202673</pmid><doi>10.3390/molecules29010090</doi><orcidid>https://orcid.org/0000-0002-8443-4417</orcidid><orcidid>https://orcid.org/0000-0003-0275-3017</orcidid><orcidid>https://orcid.org/0000-0002-9741-4562</orcidid><orcidid>https://orcid.org/0000-0001-7706-1993</orcidid><orcidid>https://orcid.org/0000-0003-3194-834X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amino acids Anti-inflammatory drugs Aqueous solutions Cholesterol Cu(II) complexes Edema Enkephalins Fatty acids High density lipoprotein Inflammation Ligands Narcotics Natriuretic peptides palmitic acid Peptides Physiology potentiometry protonation constant Saturated fatty acids sialorphin Spectrum analysis Triglycerides UV-Vis spectroscopy Vegetable oils |
title | Complex-Forming Properties of the Anti-Inflammatory Sialorphin Derivative Palmitic Acid-Lysine-Lysine-Glutamine-Histidine-Asparagine-Proline-Arginine with Cu(II) Ions in an Aqueous Solution |
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