Chemotherapy is a key element in cancer treatment. The first drugs to be clinically used for this purpose were platinum(ii) complexes and even today they are highly effective in the treatment of the disease. However, side effects, resulting from their use, limit their clinical usefulness. Furthermore, if administered intravenously into the circulation, platinum(ii)-based anticancer medications may cause adverse effects due to interactions with molecules found in human bodies, thus preventing them to reach the final target. Stomach secretions can also destroy them. As a result, their absorption might be restricted, rendering oral delivery ineffective. Over the years, several methodologies were developed to overcome the limits associated with the use of the platinum(ii) drugs, including their targeted delivery. In this context, our study proposes copper(ii) oxide nanoparticles (CuO NPS) as a promising and excellent carrier of platinum(ii)-based anticancer drugs. In this work, we examined the loading efficiency of cisplatin, oxaliplatin and nedaplatin on the surface of CuO nanoparticles by using experimental techniques such as UV-visible spectroscopy, FTIR spectroscopy, the BET method, and XRD, and theoretical ones based on DFT calculations under periodic boundary conditions (PBC). UV-vis spectroscopy determined that cisplatin had the highest entrapment efficiency and loading capacity compared to the other drugs, with 52% entrapment efficacy and an adsorption capacity of 949 mg g−1, indicating a stronger binding with CuO nanoparticles. The experimental results are consistent with DFT simulations indicating that Pt(ii)-drugs exhibit favorable adsorption on CuO (111) surfaces, particularly when the Pt(ii)-drug is cisplatin. The most stable configurations indicate that cisplatin, nedaplatin, and oxaliplatin prefer to coordinate with the surface tri-coordinated Cu. However, cisplatin has the most intense contact with the copper oxide surface, with an adsorption energy (Eads) of −3.0 eV. Both experimental and theoretical results highlight that CuO nanoparticles are excellent Pt(ii) anticancer drug carriers, especially in the case of cisplatin, which undergoes strong interactions with the support, necessary for the delivery phase, and easy desorption, important in the antitumor action phase of the drug.

Copper oxide nanoparticles as delivery vehicles for different Pt(ii)-drugs: experimental and theoretical evaluation

Camellone, Matteo Farnesi;Ritacco, Ida;
2025

Abstract

Chemotherapy is a key element in cancer treatment. The first drugs to be clinically used for this purpose were platinum(ii) complexes and even today they are highly effective in the treatment of the disease. However, side effects, resulting from their use, limit their clinical usefulness. Furthermore, if administered intravenously into the circulation, platinum(ii)-based anticancer medications may cause adverse effects due to interactions with molecules found in human bodies, thus preventing them to reach the final target. Stomach secretions can also destroy them. As a result, their absorption might be restricted, rendering oral delivery ineffective. Over the years, several methodologies were developed to overcome the limits associated with the use of the platinum(ii) drugs, including their targeted delivery. In this context, our study proposes copper(ii) oxide nanoparticles (CuO NPS) as a promising and excellent carrier of platinum(ii)-based anticancer drugs. In this work, we examined the loading efficiency of cisplatin, oxaliplatin and nedaplatin on the surface of CuO nanoparticles by using experimental techniques such as UV-visible spectroscopy, FTIR spectroscopy, the BET method, and XRD, and theoretical ones based on DFT calculations under periodic boundary conditions (PBC). UV-vis spectroscopy determined that cisplatin had the highest entrapment efficiency and loading capacity compared to the other drugs, with 52% entrapment efficacy and an adsorption capacity of 949 mg g−1, indicating a stronger binding with CuO nanoparticles. The experimental results are consistent with DFT simulations indicating that Pt(ii)-drugs exhibit favorable adsorption on CuO (111) surfaces, particularly when the Pt(ii)-drug is cisplatin. The most stable configurations indicate that cisplatin, nedaplatin, and oxaliplatin prefer to coordinate with the surface tri-coordinated Cu. However, cisplatin has the most intense contact with the copper oxide surface, with an adsorption energy (Eads) of −3.0 eV. Both experimental and theoretical results highlight that CuO nanoparticles are excellent Pt(ii) anticancer drug carriers, especially in the case of cisplatin, which undergoes strong interactions with the support, necessary for the delivery phase, and easy desorption, important in the antitumor action phase of the drug.
Campo DC Valore Lingua
dc.authority.ancejournal JOURNAL OF MATERIALS CHEMISTRY. B en
dc.authority.orgunit Istituto Officina dei Materiali - IOM - en
dc.authority.people Abdelkareem, Shahdan en
dc.authority.people El-Sayed, Mayyada M. H. en
dc.authority.people Yacoub, Nahed en
dc.authority.people Reda, Aly en
dc.authority.people Butera, Valeria en
dc.authority.people Camellone, Matteo Farnesi en
dc.authority.people Ritacco, Ida en
dc.authority.people Shoeib, Tamer en
dc.collection.id.s b3f88f24-048a-4e43-8ab1-6697b90e068e *
dc.collection.name 01.01 Articolo in rivista *
dc.contributor.appartenenza Istituto Officina dei Materiali - IOM - *
dc.contributor.appartenenza.mi 1051 *
dc.contributor.area Non assegn *
dc.date.accessioned 2026/03/04 17:32:29 -
dc.date.available 2026/03/04 17:32:29 -
dc.date.firstsubmission 2025/12/16 15:24:34 *
dc.date.issued 2025 -
dc.date.submission 2025/12/16 15:24:34 *
dc.description.abstracteng Chemotherapy is a key element in cancer treatment. The first drugs to be clinically used for this purpose were platinum(ii) complexes and even today they are highly effective in the treatment of the disease. However, side effects, resulting from their use, limit their clinical usefulness. Furthermore, if administered intravenously into the circulation, platinum(ii)-based anticancer medications may cause adverse effects due to interactions with molecules found in human bodies, thus preventing them to reach the final target. Stomach secretions can also destroy them. As a result, their absorption might be restricted, rendering oral delivery ineffective. Over the years, several methodologies were developed to overcome the limits associated with the use of the platinum(ii) drugs, including their targeted delivery. In this context, our study proposes copper(ii) oxide nanoparticles (CuO NPS) as a promising and excellent carrier of platinum(ii)-based anticancer drugs. In this work, we examined the loading efficiency of cisplatin, oxaliplatin and nedaplatin on the surface of CuO nanoparticles by using experimental techniques such as UV-visible spectroscopy, FTIR spectroscopy, the BET method, and XRD, and theoretical ones based on DFT calculations under periodic boundary conditions (PBC). UV-vis spectroscopy determined that cisplatin had the highest entrapment efficiency and loading capacity compared to the other drugs, with 52% entrapment efficacy and an adsorption capacity of 949 mg g−1, indicating a stronger binding with CuO nanoparticles. The experimental results are consistent with DFT simulations indicating that Pt(ii)-drugs exhibit favorable adsorption on CuO (111) surfaces, particularly when the Pt(ii)-drug is cisplatin. The most stable configurations indicate that cisplatin, nedaplatin, and oxaliplatin prefer to coordinate with the surface tri-coordinated Cu. However, cisplatin has the most intense contact with the copper oxide surface, with an adsorption energy (Eads) of −3.0 eV. Both experimental and theoretical results highlight that CuO nanoparticles are excellent Pt(ii) anticancer drug carriers, especially in the case of cisplatin, which undergoes strong interactions with the support, necessary for the delivery phase, and easy desorption, important in the antitumor action phase of the drug. -
dc.description.allpeople Abdelkareem, Shahdan; El-Sayed, Mayyada M. H.; Yacoub, Nahed; Reda, Aly; Butera, Valeria; Camellone, Matteo Farnesi; Ritacco, Ida; Shoeib, Tamer -
dc.description.allpeopleoriginal Abdelkareem, Shahdan; El-Sayed, Mayyada M.H.; Yacoub, Nahed; Reda, Aly; Butera, Valeria; Camellone, Matteo Farnesi; Ritacco, Ida; Shoeib, Tamer en
dc.description.fulltext open en
dc.description.numberofauthors 8 -
dc.identifier.doi 10.1039/d4tb02636e en
dc.identifier.isi WOS:001538361300001 en
dc.identifier.scopus 2-s2.0-105013294673 en
dc.identifier.source crossref *
dc.identifier.uri https://hdl.handle.net/20.500.14243/560630 -
dc.language.iso eng en
dc.relation.firstpage 10027 en
dc.relation.issue 32 en
dc.relation.lastpage 10042 en
dc.relation.numberofpages 16 en
dc.relation.volume 13 en
dc.subject.keywords chemotherapy -
dc.subject.singlekeyword chemotherapy *
dc.title Copper oxide nanoparticles as delivery vehicles for different Pt(ii)-drugs: experimental and theoretical evaluation en
dc.type.driver info:eu-repo/semantics/article -
dc.type.full 01 Contributo su Rivista::01.01 Articolo in rivista it
dc.type.miur 262 -
iris.isi.extIssued 2025 -
iris.isi.extTitle Copper oxide nanoparticles as delivery vehicles for different Pt(ii)-drugs: experimental and theoretical evaluation -
iris.mediafilter.data 2026/03/05 03:25:43 *
iris.orcid.lastModifiedDate 2026/03/04 17:32:29 *
iris.orcid.lastModifiedMillisecond 1772641949113 *
iris.scopus.extIssued 2025 -
iris.scopus.extTitle Copper oxide nanoparticles as delivery vehicles for different Pt(ii)-drugs: experimental and theoretical evaluation -
iris.sitodocente.maxattempts 1 -
iris.unpaywall.bestoahost publisher *
iris.unpaywall.bestoaversion publishedVersion *
iris.unpaywall.doi 10.1039/d4tb02636e *
iris.unpaywall.hosttype publisher *
iris.unpaywall.isoa true *
iris.unpaywall.journalisindoaj false *
iris.unpaywall.landingpage https://doi.org/10.1039/d4tb02636e *
iris.unpaywall.license cc-by *
iris.unpaywall.metadataCallLastModified 05/03/2026 04:57:47 -
iris.unpaywall.metadataCallLastModifiedMillisecond 1772683067591 -
iris.unpaywall.oastatus hybrid *
iris.unpaywall.pdfurl https://pubs.rsc.org/en/content/articlepdf/2025/tb/d4tb02636e *
isi.authority.ancejournal JOURNAL OF MATERIALS CHEMISTRY. B###2050-750X *
isi.category QE *
isi.contributor.affiliation Egyptian Knowledge Bank (EKB) -
isi.contributor.affiliation Egyptian Knowledge Bank (EKB) -
isi.contributor.affiliation Egyptian Knowledge Bank (EKB) -
isi.contributor.affiliation Egyptian Knowledge Bank (EKB) -
isi.contributor.affiliation University of Palermo -
isi.contributor.affiliation Consiglio Nazionale delle Ricerche (CNR) -
isi.contributor.affiliation University of Salerno -
isi.contributor.affiliation Egyptian Knowledge Bank (EKB) -
isi.contributor.country Egypt -
isi.contributor.country Egypt -
isi.contributor.country Egypt -
isi.contributor.country Egypt -
isi.contributor.country Italy -
isi.contributor.country Italy -
isi.contributor.country Italy -
isi.contributor.country Egypt -
isi.contributor.name Shahdan -
isi.contributor.name Mayyada M. H. -
isi.contributor.name Nahed -
isi.contributor.name Aly -
isi.contributor.name Valeria -
isi.contributor.name Matteo Farnesi -
isi.contributor.name Ida -
isi.contributor.name Tamer -
isi.contributor.researcherId OAC-7582-2025 -
isi.contributor.researcherId W-6741-2019 -
isi.contributor.researcherId GHT-4726-2022 -
isi.contributor.researcherId JBS-7503-2023 -
isi.contributor.researcherId JCE-4132-2023 -
isi.contributor.researcherId C-4574-2011 -
isi.contributor.researcherId FWT-1724-2022 -
isi.contributor.researcherId M-5044-2019 -
isi.contributor.subaffiliation Sch Sci & Engn -
isi.contributor.subaffiliation Sch Sci & Engn -
isi.contributor.subaffiliation Sch Sci & Engn -
isi.contributor.subaffiliation Sch Sci & Engn -
isi.contributor.subaffiliation Dipartimento Sci & Tecnol Biol Chim & Farmaceut -
isi.contributor.subaffiliation -
isi.contributor.subaffiliation Dipartimento Chim & Biol -
isi.contributor.subaffiliation Sch Sci & Engn -
isi.contributor.surname Abdelkareem -
isi.contributor.surname El-Sayed -
isi.contributor.surname Yacoub -
isi.contributor.surname Reda -
isi.contributor.surname Butera -
isi.contributor.surname Camellone -
isi.contributor.surname Ritacco -
isi.contributor.surname Shoeib -
isi.date.issued 2025 *
isi.description.abstracteng Chemotherapy is a key element in cancer treatment. The first drugs to be clinically used for this purpose were platinum(ii) complexes and even today they are highly effective in the treatment of the disease. However, side effects, resulting from their use, limit their clinical usefulness. Furthermore, if administered intravenously into the circulation, platinum(ii)-based anticancer medications may cause adverse effects due to interactions with molecules found in human bodies, thus preventing them to reach the final target. Stomach secretions can also destroy them. As a result, their absorption might be restricted, rendering oral delivery ineffective. Over the years, several methodologies were developed to overcome the limits associated with the use of the platinum(ii) drugs, including their targeted delivery. In this context, our study proposes copper(ii) oxide nanoparticles (CuO NPS) as a promising and excellent carrier of platinum(ii)-based anticancer drugs. In this work, we examined the loading efficiency of cisplatin, oxaliplatin and nedaplatin on the surface of CuO nanoparticles by using experimental techniques such as UV-visible spectroscopy, FTIR spectroscopy, the BET method, and XRD, and theoretical ones based on DFT calculations under periodic boundary conditions (PBC). UV-vis spectroscopy determined that cisplatin had the highest entrapment efficiency and loading capacity compared to the other drugs, with 52% entrapment efficacy and an adsorption capacity of 949 mg g-1, indicating a stronger binding with CuO nanoparticles. The experimental results are consistent with DFT simulations indicating that Pt(ii)-drugs exhibit favorable adsorption on CuO (111) surfaces, particularly when the Pt(ii)-drug is cisplatin. The most stable configurations indicate that cisplatin, nedaplatin, and oxaliplatin prefer to coordinate with the surface tri-coordinated Cu. However, cisplatin has the most intense contact with the copper oxide surface, with an adsorption energy (Eads) of -3.0 eV. Both experimental and theoretical results highlight that CuO nanoparticles are excellent Pt(ii) anticancer drug carriers, especially in the case of cisplatin, which undergoes strong interactions with the support, necessary for the delivery phase, and easy desorption, important in the antitumor action phase of the drug. *
isi.description.allpeopleoriginal Abdelkareem, S; El-Sayed, MMH; Yacoub, N; Reda, A; Butera, V; Camellone, MF; Ritacco, I; Shoeib, T; *
isi.document.sourcetype WOS.SCI *
isi.document.type Article *
isi.document.types Article *
isi.identifier.doi 10.1039/d4tb02636e *
isi.identifier.eissn 2050-7518 *
isi.identifier.isi WOS:001538361300001 *
isi.journal.journaltitle JOURNAL OF MATERIALS CHEMISTRY B *
isi.journal.journaltitleabbrev J MATER CHEM B *
isi.language.original English *
isi.publisher.place THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND *
isi.relation.firstpage 10027 *
isi.relation.issue 32 *
isi.relation.lastpage 10042 *
isi.relation.volume 13 *
isi.title Copper oxide nanoparticles as delivery vehicles for different Pt(ii)-drugs: experimental and theoretical evaluation *
scopus.authority.ancejournal JOURNAL OF MATERIALS CHEMISTRY. B###2050-750X *
scopus.category 2700 *
scopus.category 1600 *
scopus.category 2204 *
scopus.category 2500 *
scopus.contributor.affiliation The American University in Cairo -
scopus.contributor.affiliation The American University in Cairo -
scopus.contributor.affiliation The American University in Cairo -
scopus.contributor.affiliation The American University in Cairo -
scopus.contributor.affiliation Università di Palermo -
scopus.contributor.affiliation Consiglio Nazionale delle Ricerche-Istituto Officina dei Materiali (CNR-IOM) -
scopus.contributor.affiliation Università degli Studi di Salerno -
scopus.contributor.affiliation The American University in Cairo -
scopus.contributor.afid 60218045 -
scopus.contributor.afid 60218045 -
scopus.contributor.afid 60218045 -
scopus.contributor.afid 60218045 -
scopus.contributor.afid 60017697 -
scopus.contributor.afid 60116558 -
scopus.contributor.afid 60007061 -
scopus.contributor.afid 60218045 -
scopus.contributor.auid 60013099100 -
scopus.contributor.auid 57190859696 -
scopus.contributor.auid 8594326700 -
scopus.contributor.auid 57195415497 -
scopus.contributor.auid 44461053900 -
scopus.contributor.auid 59712799400 -
scopus.contributor.auid 56641682500 -
scopus.contributor.auid 6603516521 -
scopus.contributor.country Egypt -
scopus.contributor.country Egypt -
scopus.contributor.country Egypt -
scopus.contributor.country Egypt -
scopus.contributor.country Italy -
scopus.contributor.country Italy -
scopus.contributor.country Italy -
scopus.contributor.country Egypt -
scopus.contributor.dptid -
scopus.contributor.dptid -
scopus.contributor.dptid -
scopus.contributor.dptid -
scopus.contributor.dptid 113469372 -
scopus.contributor.dptid -
scopus.contributor.dptid 118325042 -
scopus.contributor.dptid -
scopus.contributor.name Shahdan -
scopus.contributor.name Mayyada M.H. -
scopus.contributor.name Nahed -
scopus.contributor.name Aly -
scopus.contributor.name Valeria -
scopus.contributor.name Matteo Farnesi -
scopus.contributor.name Ida -
scopus.contributor.name Tamer -
scopus.contributor.subaffiliation Department of Chemistry;School of Sciences & Engineering; -
scopus.contributor.subaffiliation Department of Chemistry;School of Sciences & Engineering; -
scopus.contributor.subaffiliation Department of Chemistry;School of Sciences & Engineering; -
scopus.contributor.subaffiliation Department of Chemistry;School of Sciences & Engineering; -
scopus.contributor.subaffiliation Dipartimento di Scienze e Tecnologie Biologiche;Chimiche e Farmaceutiche; -
scopus.contributor.subaffiliation -
scopus.contributor.subaffiliation Dipartimento di Chimica e Biologia; -
scopus.contributor.subaffiliation Department of Chemistry;School of Sciences & Engineering; -
scopus.contributor.surname Abdelkareem -
scopus.contributor.surname El-Sayed -
scopus.contributor.surname Yacoub -
scopus.contributor.surname Reda -
scopus.contributor.surname Butera -
scopus.contributor.surname Camellone -
scopus.contributor.surname Ritacco -
scopus.contributor.surname Shoeib -
scopus.date.issued 2025 *
scopus.description.abstracteng Chemotherapy is a key element in cancer treatment. The first drugs to be clinically used for this purpose were platinum(ii) complexes and even today they are highly effective in the treatment of the disease. However, side effects, resulting from their use, limit their clinical usefulness. Furthermore, if administered intravenously into the circulation, platinum(ii)-based anticancer medications may cause adverse effects due to interactions with molecules found in human bodies, thus preventing them to reach the final target. Stomach secretions can also destroy them. As a result, their absorption might be restricted, rendering oral delivery ineffective. Over the years, several methodologies were developed to overcome the limits associated with the use of the platinum(ii) drugs, including their targeted delivery. In this context, our study proposes copper(ii) oxide nanoparticles (CuO NPS) as a promising and excellent carrier of platinum(ii)-based anticancer drugs. In this work, we examined the loading efficiency of cisplatin, oxaliplatin and nedaplatin on the surface of CuO nanoparticles by using experimental techniques such as UV-visible spectroscopy, FTIR spectroscopy, the BET method, and XRD, and theoretical ones based on DFT calculations under periodic boundary conditions (PBC). UV-vis spectroscopy determined that cisplatin had the highest entrapment efficiency and loading capacity compared to the other drugs, with 52% entrapment efficacy and an adsorption capacity of 949 mg g−1, indicating a stronger binding with CuO nanoparticles. The experimental results are consistent with DFT simulations indicating that Pt(ii)-drugs exhibit favorable adsorption on CuO (111) surfaces, particularly when the Pt(ii)-drug is cisplatin. The most stable configurations indicate that cisplatin, nedaplatin, and oxaliplatin prefer to coordinate with the surface tri-coordinated Cu. However, cisplatin has the most intense contact with the copper oxide surface, with an adsorption energy (Eads) of −3.0 eV. Both experimental and theoretical results highlight that CuO nanoparticles are excellent Pt(ii) anticancer drug carriers, especially in the case of cisplatin, which undergoes strong interactions with the support, necessary for the delivery phase, and easy desorption, important in the antitumor action phase of the drug. *
scopus.description.allpeopleoriginal Abdelkareem S.; El-Sayed M.M.; Yacoub N.; Reda A.; Butera V.; Camellone M.F.; Ritacco I.; Shoeib T. *
scopus.differences scopus.description.allpeopleoriginal *
scopus.document.type ar *
scopus.document.types ar *
scopus.identifier.doi 10.1039/d4tb02636e *
scopus.identifier.eissn 2050-7518 *
scopus.identifier.pmid 40726471 *
scopus.identifier.pui 2040030379 *
scopus.identifier.scopus 2-s2.0-105013294673 *
scopus.journal.sourceid 21100229202 *
scopus.language.iso eng *
scopus.publisher.name Royal Society of Chemistry *
scopus.relation.firstpage 10027 *
scopus.relation.issue 32 *
scopus.relation.lastpage 10042 *
scopus.relation.volume 13 *
scopus.title Copper oxide nanoparticles as delivery vehicles for different Pt(ii)-drugs: experimental and theoretical evaluation *
scopus.titleeng Copper oxide nanoparticles as delivery vehicles for different Pt(ii)-drugs: experimental and theoretical evaluation *
Appare nelle tipologie: 01.01 Articolo in rivista
File in questo prodotto:
File Dimensione Formato  
d4tb02636e.pdf

accesso aperto

Tipologia: Versione Editoriale (PDF)
Licenza: Creative commons
Dimensione 5.42 MB
Formato Adobe PDF
5.42 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/560630
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 2
  • ???jsp.display-item.citation.isi??? 2
social impact