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68 Ga-labeled, imatinib encapsulated, theranostic liposomes: Formulation, characterization, and in vitro evaluation of anticancer activity
Cancer is still a global health problem. Among cancer types, breast cancer is the most frequently diagnosed one, and it causes a high mortality rate if not diagnosed in the early stages. In our study, imatinib encapsulated, nanosized, neutral/cationic liposome formulations were prepared as theranost...
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Published in: | Drug development research 2024-02, Vol.85 (1), p.e22136-e22136 |
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creator | Karpuz, Merve Ozgenc, Emre Oner, Ezgi Atlihan-Gundogdu, Evren Burak, Zeynep |
description | Cancer is still a global health problem. Among cancer types, breast cancer is the most frequently diagnosed one, and it causes a high mortality rate if not diagnosed in the early stages. In our study, imatinib encapsulated, nanosized, neutral/cationic liposome formulations were prepared as theranostic agents for breast cancer. After the characterization studies in which all liposomes exhibited proper profile owing to their particle size between 133 and 250 nm, polydispersity index values lower than 0.4, neutral and cationic zeta potential values, and high drug encapsulation efficiency, controlled drug release behaviors with zero-order kinetic were obtained. The higher than 90% radiolabeling efficiency values were obtained thanks to the determination of optimum radiolabeling condition (80°C temperature, 5 mCi radioactivity, and 10 min incubation period). According to the resazurin assay evaluating the cytotoxic profile of liposomes on MCF7 cells, neutral empty liposome was found as biocompatible, while both cationic liposomes (empty and drug-loaded ones) exhibited high nonspecific cytotoxicity at even low drug concentration due to the existence of stearyl amine in the formulations. However, dose-dependent cytotoxic effect and the highest cellular binding capacity were obtained by imatinib loaded neutral liposomes. In conclusion,
Ga-radiolabeled, imatinib-loaded, neutral, nanosized liposome formulation is the most promising one as a theranostic agent among all formulations. |
doi_str_mv | 10.1002/ddr.22136 |
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Ga-radiolabeled, imatinib-loaded, neutral, nanosized liposome formulation is the most promising one as a theranostic agent among all formulations.</description><identifier>ISSN: 0272-4391</identifier><identifier>EISSN: 1098-2299</identifier><identifier>DOI: 10.1002/ddr.22136</identifier><identifier>PMID: 38009423</identifier><language>eng</language><publisher>United States</publisher><subject>Antineoplastic Agents - chemistry ; Breast Neoplasms - drug therapy ; Female ; Humans ; Imatinib Mesylate - pharmacology ; Liposomes - chemistry ; Liposomes - therapeutic use ; Particle Size ; Precision Medicine</subject><ispartof>Drug development research, 2024-02, Vol.85 (1), p.e22136-e22136</ispartof><rights>2023 The Authors. Drug Development Research published by Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c903-d523e01598bafed44d9e9dbe1fb2c5d1f310ea1246ccea8a849922edb08298f3</cites><orcidid>0000-0001-6681-2448</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38009423$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Karpuz, Merve</creatorcontrib><creatorcontrib>Ozgenc, Emre</creatorcontrib><creatorcontrib>Oner, Ezgi</creatorcontrib><creatorcontrib>Atlihan-Gundogdu, Evren</creatorcontrib><creatorcontrib>Burak, Zeynep</creatorcontrib><title>68 Ga-labeled, imatinib encapsulated, theranostic liposomes: Formulation, characterization, and in vitro evaluation of anticancer activity</title><title>Drug development research</title><addtitle>Drug Dev Res</addtitle><description>Cancer is still a global health problem. Among cancer types, breast cancer is the most frequently diagnosed one, and it causes a high mortality rate if not diagnosed in the early stages. In our study, imatinib encapsulated, nanosized, neutral/cationic liposome formulations were prepared as theranostic agents for breast cancer. After the characterization studies in which all liposomes exhibited proper profile owing to their particle size between 133 and 250 nm, polydispersity index values lower than 0.4, neutral and cationic zeta potential values, and high drug encapsulation efficiency, controlled drug release behaviors with zero-order kinetic were obtained. The higher than 90% radiolabeling efficiency values were obtained thanks to the determination of optimum radiolabeling condition (80°C temperature, 5 mCi radioactivity, and 10 min incubation period). According to the resazurin assay evaluating the cytotoxic profile of liposomes on MCF7 cells, neutral empty liposome was found as biocompatible, while both cationic liposomes (empty and drug-loaded ones) exhibited high nonspecific cytotoxicity at even low drug concentration due to the existence of stearyl amine in the formulations. However, dose-dependent cytotoxic effect and the highest cellular binding capacity were obtained by imatinib loaded neutral liposomes. In conclusion,
Ga-radiolabeled, imatinib-loaded, neutral, nanosized liposome formulation is the most promising one as a theranostic agent among all formulations.</description><subject>Antineoplastic Agents - chemistry</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Imatinib Mesylate - pharmacology</subject><subject>Liposomes - chemistry</subject><subject>Liposomes - therapeutic use</subject><subject>Particle Size</subject><subject>Precision Medicine</subject><issn>0272-4391</issn><issn>1098-2299</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kMtOwzAQRS0EoqWw4AeQlyA1xY80tdmhihakSixgH03siWqUxMVOkMon8NWkD1iNdO-ZuziEXHM24YyJe2vDRAgusxMy5EyrRAitT8mQiZlIUqn5gFzE-MEY56lS52QgFWM6FXJIfjJFl5BUUGCFdkxdDa1rXEGxMbCJXQXtLm7XGKDxsXWGVm7jo68xPtCFD_UOcb4ZU7OGAKbF4L6PCTSWuoZ-uTZ4il9QdfuC-rKv-iloDAba_7ge2V6SsxKqiFfHOyJvi6f3-XOyel2-zB9XidFMJnYqJDI-1aqAEm2aWo3aFsjLQpip5aXkDIGLNDMGQYFKtRYCbcGU0KqUI3J7WN0E_9lhbPPaRYNVBQ36LuZC6VRmfCZkj94dUBN8jAHLfBN6P2Gbc5bvxOe9-HwvvmdvjrNdUaP9J_9My19u8IEx</recordid><startdate>202402</startdate><enddate>202402</enddate><creator>Karpuz, Merve</creator><creator>Ozgenc, Emre</creator><creator>Oner, Ezgi</creator><creator>Atlihan-Gundogdu, Evren</creator><creator>Burak, Zeynep</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6681-2448</orcidid></search><sort><creationdate>202402</creationdate><title>68 Ga-labeled, imatinib encapsulated, theranostic liposomes: Formulation, characterization, and in vitro evaluation of anticancer activity</title><author>Karpuz, Merve ; Ozgenc, Emre ; Oner, Ezgi ; Atlihan-Gundogdu, Evren ; Burak, Zeynep</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c903-d523e01598bafed44d9e9dbe1fb2c5d1f310ea1246ccea8a849922edb08298f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antineoplastic Agents - chemistry</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Imatinib Mesylate - pharmacology</topic><topic>Liposomes - chemistry</topic><topic>Liposomes - therapeutic use</topic><topic>Particle Size</topic><topic>Precision Medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karpuz, Merve</creatorcontrib><creatorcontrib>Ozgenc, Emre</creatorcontrib><creatorcontrib>Oner, Ezgi</creatorcontrib><creatorcontrib>Atlihan-Gundogdu, Evren</creatorcontrib><creatorcontrib>Burak, Zeynep</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Drug development research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karpuz, Merve</au><au>Ozgenc, Emre</au><au>Oner, Ezgi</au><au>Atlihan-Gundogdu, Evren</au><au>Burak, Zeynep</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>68 Ga-labeled, imatinib encapsulated, theranostic liposomes: Formulation, characterization, and in vitro evaluation of anticancer activity</atitle><jtitle>Drug development research</jtitle><addtitle>Drug Dev Res</addtitle><date>2024-02</date><risdate>2024</risdate><volume>85</volume><issue>1</issue><spage>e22136</spage><epage>e22136</epage><pages>e22136-e22136</pages><issn>0272-4391</issn><eissn>1098-2299</eissn><abstract>Cancer is still a global health problem. Among cancer types, breast cancer is the most frequently diagnosed one, and it causes a high mortality rate if not diagnosed in the early stages. In our study, imatinib encapsulated, nanosized, neutral/cationic liposome formulations were prepared as theranostic agents for breast cancer. After the characterization studies in which all liposomes exhibited proper profile owing to their particle size between 133 and 250 nm, polydispersity index values lower than 0.4, neutral and cationic zeta potential values, and high drug encapsulation efficiency, controlled drug release behaviors with zero-order kinetic were obtained. The higher than 90% radiolabeling efficiency values were obtained thanks to the determination of optimum radiolabeling condition (80°C temperature, 5 mCi radioactivity, and 10 min incubation period). According to the resazurin assay evaluating the cytotoxic profile of liposomes on MCF7 cells, neutral empty liposome was found as biocompatible, while both cationic liposomes (empty and drug-loaded ones) exhibited high nonspecific cytotoxicity at even low drug concentration due to the existence of stearyl amine in the formulations. However, dose-dependent cytotoxic effect and the highest cellular binding capacity were obtained by imatinib loaded neutral liposomes. In conclusion,
Ga-radiolabeled, imatinib-loaded, neutral, nanosized liposome formulation is the most promising one as a theranostic agent among all formulations.</abstract><cop>United States</cop><pmid>38009423</pmid><doi>10.1002/ddr.22136</doi><orcidid>https://orcid.org/0000-0001-6681-2448</orcidid></addata></record> |
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subjects | Antineoplastic Agents - chemistry Breast Neoplasms - drug therapy Female Humans Imatinib Mesylate - pharmacology Liposomes - chemistry Liposomes - therapeutic use Particle Size Precision Medicine |
title | 68 Ga-labeled, imatinib encapsulated, theranostic liposomes: Formulation, characterization, and in vitro evaluation of anticancer activity |
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