Loading…
Tripodal amphiphilic pseudopeptidic nanovesicles as p-coumaric acid delivery systems for brain cancer cells
Nanovesicles based on tripodal amphiphilic pseudopeptides are prepared as carriers for p-coumaric acid (p-CA) delivery. Loaded nanovesicles are obtained by both thin film hydration and ethanol injection methods with positive Z-potential values. The last technique renders lower particle sizes and exc...
Saved in:
Published in: | Materials today chemistry 2023-01, Vol.27, p.101266, Article 101266 |
---|---|
Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c306t-e44833c9e12a102a5377964cca0b08a174f13a4e6cf41292288abae25ff7808d3 |
---|---|
cites | cdi_FETCH-LOGICAL-c306t-e44833c9e12a102a5377964cca0b08a174f13a4e6cf41292288abae25ff7808d3 |
container_end_page | |
container_issue | |
container_start_page | 101266 |
container_title | Materials today chemistry |
container_volume | 27 |
creator | Lotfallah, A.H. Andreu, J.J. Hathout, R.M. Kassem, D.H. Ibrahim, S.S. Altava, B. García-Verdugo, E. Luis, S.V. |
description | Nanovesicles based on tripodal amphiphilic pseudopeptides are prepared as carriers for p-coumaric acid (p-CA) delivery. Loaded nanovesicles are obtained by both thin film hydration and ethanol injection methods with positive Z-potential values. The last technique renders lower particle sizes and excellent polydispersity index, with average values of 130 nm and 0.123, respectively, although the drug loading obtained after ultracentrifugation is lower. In vitro release experiments, including the use of different external stimuli such as pH and proteolytic enzymes, provide interesting results. The prepared nanovesicles are tested on normal cells (VERO), displaying a high safety profile scoring with a 50% inhibitory concentration (IC50) of 1,822 μg/mL. A 40-times increase in the in vitro cytotoxic effect of p-CA on Glioma GL261 brain cancer cells, from IC50 1,082 μg/mL to 29 μg/mL, is observed using the loaded pseudopeptide nanovesicles. 1H NMR studies reveal that the drug is mainly located inside the nanoparticle bilayer. Transmembrane carboxyfluorescein studies reveal that the amphiphilic compound does not provide a significant membrane fluidification. Experimental data suggest that the observed biological activity can be associated to an enhanced permeability and retention effect. The present results highlight the potential of such nanovesicles as potent p-CA carriers for brain cancer therapy.
[Display omitted]
•Nanovesicles based on tripodal amphiphilic pseudopeptide are prepared as carriers for p-coumaric acid delivery.•Nanovesicles with average values of particle sizes of 130 nm and polydispersity index of 0.123 are obtained.•A high safety profile on normal cells of tripodal amphiphilic pseudopeptide nanovesicles is observed.•In vitro cytotoxic effect of p-coumaric acid increases 40 times when loaded on nanovesicles.•In vitro release studies in the presence of thermolysin facilitated a faster drug release. |
doi_str_mv | 10.1016/j.mtchem.2022.101266 |
format | article |
fullrecord | <record><control><sourceid>elsevier_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1016_j_mtchem_2022_101266</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S2468519422004955</els_id><sourcerecordid>S2468519422004955</sourcerecordid><originalsourceid>FETCH-LOGICAL-c306t-e44833c9e12a102a5377964cca0b08a174f13a4e6cf41292288abae25ff7808d3</originalsourceid><addsrcrecordid>eNp9kMtqwzAQRUVpoaHNH3ShH3AqybJsbwol9AWBbtK1mIzGRKn8QHIC-fs6uIuuCgPz4l4uh7EHKVZSSPN4WLUj7qldKaHU5aSMuWILpU2VFbLW13_mW7ZM6SCEUELmujAL9r2NfugdBA7tsPdTBY98SHR0_UDD6N20dtD1J0oeAyUOiQ8Z9scW4vQC9I47Cv5E8czTOY3UJt70ke8i-I4jdEiRI4WQ7tlNAyHR8rffsa_Xl-36Pdt8vn2snzcZ5sKMGWld5TnWJBVIoaDIy7I2GhHETlQgS93IHDQZbLRUtVJVBTsgVTRNWYnK5XdMz74Y-5QiNXaIfop7tlLYCzN7sDMze2FmZ2aT7GmW0ZTt5CnahJ6m-M5HwtG63v9v8APRH3jG</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Tripodal amphiphilic pseudopeptidic nanovesicles as p-coumaric acid delivery systems for brain cancer cells</title><source>ScienceDirect Freedom Collection 2022-2024</source><creator>Lotfallah, A.H. ; Andreu, J.J. ; Hathout, R.M. ; Kassem, D.H. ; Ibrahim, S.S. ; Altava, B. ; García-Verdugo, E. ; Luis, S.V.</creator><creatorcontrib>Lotfallah, A.H. ; Andreu, J.J. ; Hathout, R.M. ; Kassem, D.H. ; Ibrahim, S.S. ; Altava, B. ; García-Verdugo, E. ; Luis, S.V.</creatorcontrib><description>Nanovesicles based on tripodal amphiphilic pseudopeptides are prepared as carriers for p-coumaric acid (p-CA) delivery. Loaded nanovesicles are obtained by both thin film hydration and ethanol injection methods with positive Z-potential values. The last technique renders lower particle sizes and excellent polydispersity index, with average values of 130 nm and 0.123, respectively, although the drug loading obtained after ultracentrifugation is lower. In vitro release experiments, including the use of different external stimuli such as pH and proteolytic enzymes, provide interesting results. The prepared nanovesicles are tested on normal cells (VERO), displaying a high safety profile scoring with a 50% inhibitory concentration (IC50) of 1,822 μg/mL. A 40-times increase in the in vitro cytotoxic effect of p-CA on Glioma GL261 brain cancer cells, from IC50 1,082 μg/mL to 29 μg/mL, is observed using the loaded pseudopeptide nanovesicles. 1H NMR studies reveal that the drug is mainly located inside the nanoparticle bilayer. Transmembrane carboxyfluorescein studies reveal that the amphiphilic compound does not provide a significant membrane fluidification. Experimental data suggest that the observed biological activity can be associated to an enhanced permeability and retention effect. The present results highlight the potential of such nanovesicles as potent p-CA carriers for brain cancer therapy.
[Display omitted]
•Nanovesicles based on tripodal amphiphilic pseudopeptide are prepared as carriers for p-coumaric acid delivery.•Nanovesicles with average values of particle sizes of 130 nm and polydispersity index of 0.123 are obtained.•A high safety profile on normal cells of tripodal amphiphilic pseudopeptide nanovesicles is observed.•In vitro cytotoxic effect of p-coumaric acid increases 40 times when loaded on nanovesicles.•In vitro release studies in the presence of thermolysin facilitated a faster drug release.</description><identifier>ISSN: 2468-5194</identifier><identifier>EISSN: 2468-5194</identifier><identifier>DOI: 10.1016/j.mtchem.2022.101266</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Brain cancer ; Drug delivery ; Nanovesicles ; Pseudopeptide ; Self-assembly</subject><ispartof>Materials today chemistry, 2023-01, Vol.27, p.101266, Article 101266</ispartof><rights>2022 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c306t-e44833c9e12a102a5377964cca0b08a174f13a4e6cf41292288abae25ff7808d3</citedby><cites>FETCH-LOGICAL-c306t-e44833c9e12a102a5377964cca0b08a174f13a4e6cf41292288abae25ff7808d3</cites><orcidid>0000-0001-5102-3235 ; 0000-0001-5160-5542 ; 0000-0002-8839-3819 ; 0000-0001-9153-4355 ; 0000-0002-8159-3447</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></links><search><creatorcontrib>Lotfallah, A.H.</creatorcontrib><creatorcontrib>Andreu, J.J.</creatorcontrib><creatorcontrib>Hathout, R.M.</creatorcontrib><creatorcontrib>Kassem, D.H.</creatorcontrib><creatorcontrib>Ibrahim, S.S.</creatorcontrib><creatorcontrib>Altava, B.</creatorcontrib><creatorcontrib>García-Verdugo, E.</creatorcontrib><creatorcontrib>Luis, S.V.</creatorcontrib><title>Tripodal amphiphilic pseudopeptidic nanovesicles as p-coumaric acid delivery systems for brain cancer cells</title><title>Materials today chemistry</title><description>Nanovesicles based on tripodal amphiphilic pseudopeptides are prepared as carriers for p-coumaric acid (p-CA) delivery. Loaded nanovesicles are obtained by both thin film hydration and ethanol injection methods with positive Z-potential values. The last technique renders lower particle sizes and excellent polydispersity index, with average values of 130 nm and 0.123, respectively, although the drug loading obtained after ultracentrifugation is lower. In vitro release experiments, including the use of different external stimuli such as pH and proteolytic enzymes, provide interesting results. The prepared nanovesicles are tested on normal cells (VERO), displaying a high safety profile scoring with a 50% inhibitory concentration (IC50) of 1,822 μg/mL. A 40-times increase in the in vitro cytotoxic effect of p-CA on Glioma GL261 brain cancer cells, from IC50 1,082 μg/mL to 29 μg/mL, is observed using the loaded pseudopeptide nanovesicles. 1H NMR studies reveal that the drug is mainly located inside the nanoparticle bilayer. Transmembrane carboxyfluorescein studies reveal that the amphiphilic compound does not provide a significant membrane fluidification. Experimental data suggest that the observed biological activity can be associated to an enhanced permeability and retention effect. The present results highlight the potential of such nanovesicles as potent p-CA carriers for brain cancer therapy.
[Display omitted]
•Nanovesicles based on tripodal amphiphilic pseudopeptide are prepared as carriers for p-coumaric acid delivery.•Nanovesicles with average values of particle sizes of 130 nm and polydispersity index of 0.123 are obtained.•A high safety profile on normal cells of tripodal amphiphilic pseudopeptide nanovesicles is observed.•In vitro cytotoxic effect of p-coumaric acid increases 40 times when loaded on nanovesicles.•In vitro release studies in the presence of thermolysin facilitated a faster drug release.</description><subject>Brain cancer</subject><subject>Drug delivery</subject><subject>Nanovesicles</subject><subject>Pseudopeptide</subject><subject>Self-assembly</subject><issn>2468-5194</issn><issn>2468-5194</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kMtqwzAQRUVpoaHNH3ShH3AqybJsbwol9AWBbtK1mIzGRKn8QHIC-fs6uIuuCgPz4l4uh7EHKVZSSPN4WLUj7qldKaHU5aSMuWILpU2VFbLW13_mW7ZM6SCEUELmujAL9r2NfugdBA7tsPdTBY98SHR0_UDD6N20dtD1J0oeAyUOiQ8Z9scW4vQC9I47Cv5E8czTOY3UJt70ke8i-I4jdEiRI4WQ7tlNAyHR8rffsa_Xl-36Pdt8vn2snzcZ5sKMGWld5TnWJBVIoaDIy7I2GhHETlQgS93IHDQZbLRUtVJVBTsgVTRNWYnK5XdMz74Y-5QiNXaIfop7tlLYCzN7sDMze2FmZ2aT7GmW0ZTt5CnahJ6m-M5HwtG63v9v8APRH3jG</recordid><startdate>202301</startdate><enddate>202301</enddate><creator>Lotfallah, A.H.</creator><creator>Andreu, J.J.</creator><creator>Hathout, R.M.</creator><creator>Kassem, D.H.</creator><creator>Ibrahim, S.S.</creator><creator>Altava, B.</creator><creator>García-Verdugo, E.</creator><creator>Luis, S.V.</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-5102-3235</orcidid><orcidid>https://orcid.org/0000-0001-5160-5542</orcidid><orcidid>https://orcid.org/0000-0002-8839-3819</orcidid><orcidid>https://orcid.org/0000-0001-9153-4355</orcidid><orcidid>https://orcid.org/0000-0002-8159-3447</orcidid></search><sort><creationdate>202301</creationdate><title>Tripodal amphiphilic pseudopeptidic nanovesicles as p-coumaric acid delivery systems for brain cancer cells</title><author>Lotfallah, A.H. ; Andreu, J.J. ; Hathout, R.M. ; Kassem, D.H. ; Ibrahim, S.S. ; Altava, B. ; García-Verdugo, E. ; Luis, S.V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c306t-e44833c9e12a102a5377964cca0b08a174f13a4e6cf41292288abae25ff7808d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Brain cancer</topic><topic>Drug delivery</topic><topic>Nanovesicles</topic><topic>Pseudopeptide</topic><topic>Self-assembly</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lotfallah, A.H.</creatorcontrib><creatorcontrib>Andreu, J.J.</creatorcontrib><creatorcontrib>Hathout, R.M.</creatorcontrib><creatorcontrib>Kassem, D.H.</creatorcontrib><creatorcontrib>Ibrahim, S.S.</creatorcontrib><creatorcontrib>Altava, B.</creatorcontrib><creatorcontrib>García-Verdugo, E.</creatorcontrib><creatorcontrib>Luis, S.V.</creatorcontrib><collection>CrossRef</collection><jtitle>Materials today chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lotfallah, A.H.</au><au>Andreu, J.J.</au><au>Hathout, R.M.</au><au>Kassem, D.H.</au><au>Ibrahim, S.S.</au><au>Altava, B.</au><au>García-Verdugo, E.</au><au>Luis, S.V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tripodal amphiphilic pseudopeptidic nanovesicles as p-coumaric acid delivery systems for brain cancer cells</atitle><jtitle>Materials today chemistry</jtitle><date>2023-01</date><risdate>2023</risdate><volume>27</volume><spage>101266</spage><pages>101266-</pages><artnum>101266</artnum><issn>2468-5194</issn><eissn>2468-5194</eissn><abstract>Nanovesicles based on tripodal amphiphilic pseudopeptides are prepared as carriers for p-coumaric acid (p-CA) delivery. Loaded nanovesicles are obtained by both thin film hydration and ethanol injection methods with positive Z-potential values. The last technique renders lower particle sizes and excellent polydispersity index, with average values of 130 nm and 0.123, respectively, although the drug loading obtained after ultracentrifugation is lower. In vitro release experiments, including the use of different external stimuli such as pH and proteolytic enzymes, provide interesting results. The prepared nanovesicles are tested on normal cells (VERO), displaying a high safety profile scoring with a 50% inhibitory concentration (IC50) of 1,822 μg/mL. A 40-times increase in the in vitro cytotoxic effect of p-CA on Glioma GL261 brain cancer cells, from IC50 1,082 μg/mL to 29 μg/mL, is observed using the loaded pseudopeptide nanovesicles. 1H NMR studies reveal that the drug is mainly located inside the nanoparticle bilayer. Transmembrane carboxyfluorescein studies reveal that the amphiphilic compound does not provide a significant membrane fluidification. Experimental data suggest that the observed biological activity can be associated to an enhanced permeability and retention effect. The present results highlight the potential of such nanovesicles as potent p-CA carriers for brain cancer therapy.
[Display omitted]
•Nanovesicles based on tripodal amphiphilic pseudopeptide are prepared as carriers for p-coumaric acid delivery.•Nanovesicles with average values of particle sizes of 130 nm and polydispersity index of 0.123 are obtained.•A high safety profile on normal cells of tripodal amphiphilic pseudopeptide nanovesicles is observed.•In vitro cytotoxic effect of p-coumaric acid increases 40 times when loaded on nanovesicles.•In vitro release studies in the presence of thermolysin facilitated a faster drug release.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.mtchem.2022.101266</doi><orcidid>https://orcid.org/0000-0001-5102-3235</orcidid><orcidid>https://orcid.org/0000-0001-5160-5542</orcidid><orcidid>https://orcid.org/0000-0002-8839-3819</orcidid><orcidid>https://orcid.org/0000-0001-9153-4355</orcidid><orcidid>https://orcid.org/0000-0002-8159-3447</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2468-5194 |
ispartof | Materials today chemistry, 2023-01, Vol.27, p.101266, Article 101266 |
issn | 2468-5194 2468-5194 |
language | eng |
recordid | cdi_crossref_primary_10_1016_j_mtchem_2022_101266 |
source | ScienceDirect Freedom Collection 2022-2024 |
subjects | Brain cancer Drug delivery Nanovesicles Pseudopeptide Self-assembly |
title | Tripodal amphiphilic pseudopeptidic nanovesicles as p-coumaric acid delivery systems for brain cancer cells |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T01%3A46%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Tripodal%20amphiphilic%20pseudopeptidic%20nanovesicles%20as%20p-coumaric%20acid%20delivery%20systems%20for%20brain%20cancer%20cells&rft.jtitle=Materials%20today%20chemistry&rft.au=Lotfallah,%20A.H.&rft.date=2023-01&rft.volume=27&rft.spage=101266&rft.pages=101266-&rft.artnum=101266&rft.issn=2468-5194&rft.eissn=2468-5194&rft_id=info:doi/10.1016/j.mtchem.2022.101266&rft_dat=%3Celsevier_cross%3ES2468519422004955%3C/elsevier_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c306t-e44833c9e12a102a5377964cca0b08a174f13a4e6cf41292288abae25ff7808d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |