Toxicological evaluation of copper oxide nanoparticles following their intraperitoneal injection to Wistar rats

Copper oxide (Cu O) nanoparticles (CO NPs) are in extensive use during our everyday life as antimicrobial agent, lubricant, in manufacturing electrodes of lithium ion batteries as well as for photo catalytic degradation of organic pollutants. Due to extensive and diverse use Cu O NPs, they are likel...

Full description

Saved in:
Bibliographic Details
Published inToxicology research (Cambridge) Vol. 13; no. 4; p. tfae125
Main Authors Shareef, Nisha, Abid, Shairyar, Amir, Aqsa, Ismail, Amir, Ullah, Abd, Ahmad, Adnan, Ibenmoussa, Samir, Bin Jardan, Yousef A, Bourhia, Mohammed, Ibrahim, Ather, Iqbal, Furhan
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.08.2024
Subjects
Online AccessGet full text
ISSN2045-4538
2045-452X
2045-4538
DOI10.1093/toxres/tfae125

Cover

Abstract Copper oxide (Cu O) nanoparticles (CO NPs) are in extensive use during our everyday life as antimicrobial agent, lubricant, in manufacturing electrodes of lithium ion batteries as well as for photo catalytic degradation of organic pollutants. Due to extensive and diverse use Cu O NPs, they are likely to accumulate in the environment and to affect the live forms. Present investigation was aimed to report the biocompatibility of CO NPs in Wistar rats in sex specific manner. CO NPs, having average diameter of 14.06 nm, were synthesized by co-precipitation method and scanning electron microscopy and X ray diffraction were used for their characterization. For 14 consecutive days, Wistar rats (6 weeks old) of both sexes were intraperitoneally injected with 10 mg/mL saline/Kg body weight of CO NPs, while the control groups intraperitoneally received saline solution for same duration. Behavioral tests (open field and novel object recognition), complete blood count, selected biomarkers of oxidative stress and Copper concentration in brain and liver were determined in all subjects. High mortality rates [male 40% and female 60%] were observed in rats exposed to CO NPs. A sever decrease in body weight was also observed in both male and female rats exposed to CO NPs. Female rats treated with CO NPs spent significantly more time with novel object as compared to control [  = 0.05] during second trial of novel object test. CO NPs treated female rats had higher mean corpuscular hemoglobin [  < 0.001] levels and Copper concentration in liver [  = 0.04] than control. Male rats exposed to CO NPs had significantly higher mean corpuscular volume [  = 0.02] and superoxide dismutase [SOD] [  = 0.04] in lungs than their control group. All other studied parameters non significantly varied upon comparison between CO NPs treated and untreated rats of both sex. In conclusion, we are reporting that intraperitoneal injections of CO NPs for 14 days can disturb complete blood count and biomarkers of oxidative stress in lungs of Wistar rats.
AbstractList Graphical Abstract
Copper oxide (Cu O) nanoparticles (CO NPs) are in extensive use during our everyday life as antimicrobial agent, lubricant, in manufacturing electrodes of lithium ion batteries as well as for photo catalytic degradation of organic pollutants. Due to extensive and diverse use Cu O NPs, they are likely to accumulate in the environment and to affect the live forms. Present investigation was aimed to report the biocompatibility of CO NPs in Wistar rats in sex specific manner. CO NPs, having average diameter of 14.06 nm, were synthesized by co-precipitation method and scanning electron microscopy and X ray diffraction were used for their characterization. For 14 consecutive days, Wistar rats (6 weeks old) of both sexes were intraperitoneally injected with 10 mg/mL saline/Kg body weight of CO NPs, while the control groups intraperitoneally received saline solution for same duration. Behavioral tests (open field and novel object recognition), complete blood count, selected biomarkers of oxidative stress and Copper concentration in brain and liver were determined in all subjects. High mortality rates [male 40% and female 60%] were observed in rats exposed to CO NPs. A sever decrease in body weight was also observed in both male and female rats exposed to CO NPs. Female rats treated with CO NPs spent significantly more time with novel object as compared to control [  = 0.05] during second trial of novel object test. CO NPs treated female rats had higher mean corpuscular hemoglobin [  < 0.001] levels and Copper concentration in liver [  = 0.04] than control. Male rats exposed to CO NPs had significantly higher mean corpuscular volume [  = 0.02] and superoxide dismutase [SOD] [  = 0.04] in lungs than their control group. All other studied parameters non significantly varied upon comparison between CO NPs treated and untreated rats of both sex. In conclusion, we are reporting that intraperitoneal injections of CO NPs for 14 days can disturb complete blood count and biomarkers of oxidative stress in lungs of Wistar rats.
Copper oxide (Cu2O) nanoparticles (CO NPs) are in extensive use during our everyday life as antimicrobial agent, lubricant, in manufacturing electrodes of lithium ion batteries as well as for photo catalytic degradation of organic pollutants. Due to extensive and diverse use Cu2O NPs, they are likely to accumulate in the environment and to affect the live forms. Present investigation was aimed to report the biocompatibility of CO NPs in Wistar rats in sex specific manner. CO NPs, having average diameter of 14.06 nm, were synthesized by co-precipitation method and scanning electron microscopy and X ray diffraction were used for their characterization.BackgroundCopper oxide (Cu2O) nanoparticles (CO NPs) are in extensive use during our everyday life as antimicrobial agent, lubricant, in manufacturing electrodes of lithium ion batteries as well as for photo catalytic degradation of organic pollutants. Due to extensive and diverse use Cu2O NPs, they are likely to accumulate in the environment and to affect the live forms. Present investigation was aimed to report the biocompatibility of CO NPs in Wistar rats in sex specific manner. CO NPs, having average diameter of 14.06 nm, were synthesized by co-precipitation method and scanning electron microscopy and X ray diffraction were used for their characterization.For 14 consecutive days, Wistar rats (6 weeks old) of both sexes were intraperitoneally injected with 10 mg/mL saline/Kg body weight of CO NPs, while the control groups intraperitoneally received saline solution for same duration. Behavioral tests (open field and novel object recognition), complete blood count, selected biomarkers of oxidative stress and Copper concentration in brain and liver were determined in all subjects.MethodsFor 14 consecutive days, Wistar rats (6 weeks old) of both sexes were intraperitoneally injected with 10 mg/mL saline/Kg body weight of CO NPs, while the control groups intraperitoneally received saline solution for same duration. Behavioral tests (open field and novel object recognition), complete blood count, selected biomarkers of oxidative stress and Copper concentration in brain and liver were determined in all subjects.High mortality rates [male 40% and female 60%] were observed in rats exposed to CO NPs. A sever decrease in body weight was also observed in both male and female rats exposed to CO NPs. Female rats treated with CO NPs spent significantly more time with novel object as compared to control [P = 0.05] during second trial of novel object test. CO NPs treated female rats had higher mean corpuscular hemoglobin [P < 0.001] levels and Copper concentration in liver [P = 0.04] than control. Male rats exposed to CO NPs had significantly higher mean corpuscular volume [P = 0.02] and superoxide dismutase [SOD] [P = 0.04] in lungs than their control group. All other studied parameters non significantly varied upon comparison between CO NPs treated and untreated rats of both sex.ResultsHigh mortality rates [male 40% and female 60%] were observed in rats exposed to CO NPs. A sever decrease in body weight was also observed in both male and female rats exposed to CO NPs. Female rats treated with CO NPs spent significantly more time with novel object as compared to control [P = 0.05] during second trial of novel object test. CO NPs treated female rats had higher mean corpuscular hemoglobin [P < 0.001] levels and Copper concentration in liver [P = 0.04] than control. Male rats exposed to CO NPs had significantly higher mean corpuscular volume [P = 0.02] and superoxide dismutase [SOD] [P = 0.04] in lungs than their control group. All other studied parameters non significantly varied upon comparison between CO NPs treated and untreated rats of both sex.In conclusion, we are reporting that intraperitoneal injections of CO NPs for 14 days can disturb complete blood count and biomarkers of oxidative stress in lungs of Wistar rats.ConclusionIn conclusion, we are reporting that intraperitoneal injections of CO NPs for 14 days can disturb complete blood count and biomarkers of oxidative stress in lungs of Wistar rats.
Author Abid, Shairyar
Ismail, Amir
Ibenmoussa, Samir
Iqbal, Furhan
Ullah, Abd
Ibrahim, Ather
Amir, Aqsa
Bin Jardan, Yousef A
Bourhia, Mohammed
Ahmad, Adnan
Shareef, Nisha
Author_xml – sequence: 1
  givenname: Nisha
  surname: Shareef
  fullname: Shareef, Nisha
– sequence: 2
  givenname: Shairyar
  surname: Abid
  fullname: Abid, Shairyar
– sequence: 3
  givenname: Aqsa
  surname: Amir
  fullname: Amir, Aqsa
– sequence: 4
  givenname: Amir
  surname: Ismail
  fullname: Ismail, Amir
– sequence: 5
  givenname: Abd
  surname: Ullah
  fullname: Ullah, Abd
– sequence: 6
  givenname: Adnan
  surname: Ahmad
  fullname: Ahmad, Adnan
– sequence: 7
  givenname: Samir
  surname: Ibenmoussa
  fullname: Ibenmoussa, Samir
– sequence: 8
  givenname: Yousef A
  surname: Bin Jardan
  fullname: Bin Jardan, Yousef A
– sequence: 9
  givenname: Mohammed
  surname: Bourhia
  fullname: Bourhia, Mohammed
– sequence: 10
  givenname: Ather
  surname: Ibrahim
  fullname: Ibrahim, Ather
– sequence: 11
  givenname: Furhan
  orcidid: 0000-0003-4996-0152
  surname: Iqbal
  fullname: Iqbal, Furhan
BackLink https://www.ncbi.nlm.nih.gov/pubmed/39132193$$D View this record in MEDLINE/PubMed
BookMark eNp1kc1LXDEUxYNY_N66LFl2M5qP9zLvraRIWwtCN4rLkJd3M0Yyuc8kY_W_N-NMxRaaTQL3d8495ByS3YgRCDnl7IyzXp4XfE6Qz4szwEW7Qw4Ea9pZ08pu98N7n5zk_MDqmTOhZLtH9mXPpeC9PCB4g8_eYsCFtyZQeDJhZYrHSNFRi9MEiVZiBBpNxMmk4m2ATB2GgL99XNByDz5RH0syFfalRqxGPj6AffMpSO98LibRZEo-Jp-cCRlOtvcRuf3-7ebyanb968fPy6_XM1uzlZnqbCP6XoyNM2psRzt2_dzxRnGYCwfMDIMxdmhGV4FBjd1cqJZVlWDd0KlBHpGLje-0GpYwWljnC3pKfmnSi0bj9d-T6O_1Ap8055IpyVV1-LJ1SPi4glz00mcLIZgIuMpasl4wzlm7Rj9_XPa-5c83V-BsA9iEOSdw7whnel2l3lSpt1VWQfOPwPry1ksN68P_ZK8W56s8
CitedBy_id crossref_primary_10_1007_s12011_025_04562_9
Cites_doi 10.2217/nnm.11.154
10.1177/0192623308318214
10.1007/s00210-020-01899-x
10.1016/j.jiec.2014.06.022
10.1002/jat.3548
10.1289/ehp.7339
10.30539/iraqijvm.v38i1.259
10.1155/2017/7056864
10.1186/s12989-016-0169-x
10.1080/17435390.2018.1530390
10.1016/j.toxlet.2005.10.003
10.1049/iet-nbt.2019.0176
10.1007/s11356-023-28437-5
10.1016/j.toxlet.2012.07.007
10.1007/s00253-023-12364-z
10.1016/j.ijantimicag.2008.12.004
10.1007/s00210-019-01787-z
10.1080/10611860400015936
10.14348/molcells.2016.2198
10.3906/zoo-1512-23
10.1080/19393210.2014.888783
10.1007/s11356-014-3734-6
10.4103/epj.epj_15_17
10.1080/08958370701493282
ContentType Journal Article
Copyright The Author(s) 2024. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.
The Author(s) 2024. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2024
Copyright_xml – notice: The Author(s) 2024. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.
– notice: The Author(s) 2024. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2024
DBID AAYXX
CITATION
NPM
7X8
5PM
DOI 10.1093/toxres/tfae125
DatabaseName CrossRef
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList
PubMed
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Public Health
EISSN 2045-4538
ExternalDocumentID PMC11306316
39132193
10_1093_toxres_tfae125
Genre Journal Article
GrantInformation_xml – fundername: ;
  grantid: RSP2024R457
GroupedDBID 0-7
0R~
4.4
53G
5WD
705
AABZA
AACZT
AAEMU
AAHBH
AAIWI
AAPQZ
AAPXW
AARHZ
AAUAY
AAVAP
AAWGC
AAYXX
ABDFA
ABEJV
ABEMK
ABGNP
ABJNI
ABMNT
ABNHQ
ABPQP
ABPTD
ABVGC
ABWST
ABXOH
ABXVV
ABXZS
ACGFS
ACLDK
ACPRK
ACUFI
ADBBV
ADGKP
ADGZP
ADIPN
ADMRA
ADNBA
ADQBN
ADSRN
ADVEK
AEFDR
AELWJ
AENEX
AESAV
AETBJ
AFFZL
AFGWE
AFLYV
AFRAH
AGINJ
AGORE
AGQXC
AHGBF
AHGCF
AHMMS
AJBYB
AJEEA
AJNCP
ALMA_UNASSIGNED_HOLDINGS
ALXQX
ANUXI
AOIJS
APEMP
ASKNT
ATGXG
AUDPV
BCRHZ
BEYMZ
BSQNT
C6K
CITATION
EBS
EE0
EF-
FHSFR
FLUFQ
FOEOM
FOTVD
FQBLK
GAUVT
HZ~
H~N
J3I
JXSIZ
KOP
KSI
KSN
NOMLY
NU-
O-G
O9-
OBOKY
OCZFY
OJZSN
OPAEJ
OWPYF
R7G
RCNCU
ROX
RPM
RPMJG
RSCEA
RUSNO
SKA
SLH
YXANX
AAJAE
ADIYS
AFVBQ
ANBJS
EJD
H13
HH5
HYE
J3G
J3H
KBUDW
ML0
NPM
7X8
5PM
ID FETCH-LOGICAL-c391t-68c42992d4fa6d5dcd897f1461e72fe0abbaacb4df4fab6d87265068c208b86b3
ISSN 2045-4538
2045-452X
IngestDate Thu Aug 21 18:28:59 EDT 2025
Tue Aug 05 10:54:32 EDT 2025
Sun Aug 10 01:31:43 EDT 2025
Tue Jul 01 02:09:50 EDT 2025
Thu Apr 24 23:07:54 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 4
Keywords blood chemistry
Cu2O NPs
Wistar rat
behavior
biomarkers of oxidative stress
Language English
License https://academic.oup.com/pages/standard-publication-reuse-rights
The Author(s) 2024. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.
This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/pages/standard-publication-reuse-rights)
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c391t-68c42992d4fa6d5dcd897f1461e72fe0abbaacb4df4fab6d87265068c208b86b3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Nisha Shareef and Shairyar Abid share the first authorship.
ORCID 0000-0003-4996-0152
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/11306316
PMID 39132193
PQID 3092011056
PQPubID 23479
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_11306316
proquest_miscellaneous_3092011056
pubmed_primary_39132193
crossref_primary_10_1093_toxres_tfae125
crossref_citationtrail_10_1093_toxres_tfae125
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2024-08-01
PublicationDateYYYYMMDD 2024-08-01
PublicationDate_xml – month: 08
  year: 2024
  text: 2024-08-01
  day: 01
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
PublicationTitle Toxicology research (Cambridge)
PublicationTitleAlternate Toxicol Res (Camb)
PublicationYear 2024
Publisher Oxford University Press
Publisher_xml – name: Oxford University Press
References Yokohira (2024080805281174500_ref16) 2008; 36
Canli (2024080805281174500_ref23) 2017; 41
Lockman (2024080805281174500_ref19) 2004; 12
Costa (2024080805281174500_ref2) 2018; 38
Al-Taae (2024080805281174500_ref22) 2014; 38
Ana (2024080805281174500_ref17) 2012; 213
Riaz (2024080805281174500_ref8) 2020; 393
Naz (2024080805281174500_ref6) 2020; 14
Oberdorster (2024080805281174500_ref7) 2005; 113
Chen (2024080805281174500_ref15) 2006; 163
Seo (2024080805281174500_ref25) 2016; 39
Rastabi (2024080805281174500_ref18) 2014; 22
Park (2024080805281174500_ref27) 2007; 19
Trickler (2024080805281174500_ref5) 2012; 7
Lee (2024080805281174500_ref21) 2016; 13
Ren (2024080805281174500_ref13) 2009; 33
Salim (2024080805281174500_ref11) 2022; 44
Yilmaz (2024080805281174500_ref24) 2015; 22
Arshadi-Rastabi (2024080805281174500_ref14) 2015; 22
De Jong (2024080805281174500_ref20) 2019; 13
Khosa (2024080805281174500_ref9) 2020; 393
Ismail (2024080805281174500_ref12) 2014; 7
Abdelbasir (2024080805281174500_ref4) 2023; 30
Naz (2024080805281174500_ref1) 2023; 107
Noureen (2024080805281174500_ref10) 2021; 43
Arafa (2024080805281174500_ref26) 2017; 16
Du (2024080805281174500_ref3) 2017; 2017
References_xml – volume: 7
  start-page: 835
  issue: 6
  year: 2012
  ident: 2024080805281174500_ref5
  article-title: Effects of copper nanoparticles on rat cerebral microvessel endothelial cells
  publication-title: Nanomedicine (Lond)
  doi: 10.2217/nnm.11.154
– volume: 36
  start-page: 620
  issue: 4
  year: 2008
  ident: 2024080805281174500_ref16
  article-title: Lung toxicity of fine particles on intratracheal instillation in a bioassay model using f344 male rats
  publication-title: Toxicol Pathol
  doi: 10.1177/0192623308318214
– volume: 393
  start-page: 2019
  issue: 11
  year: 2020
  ident: 2024080805281174500_ref8
  article-title: Intraperitoneal injections of copper ferrite nanoparticles disturb blood, plasma and antioxidant parameters of Wistar rats in a sex specific manner
  publication-title: Naunyn Schmiedebergs Arch Pharmacol
  doi: 10.1007/s00210-020-01899-x
– volume: 22
  start-page: 34
  year: 2014
  ident: 2024080805281174500_ref18
  article-title: Synthesis, characterization and stability of Cu2O nanoparticles produced via super-saturation method considering operational parameters effect
  publication-title: J Indus Engineer Chem
  doi: 10.1016/j.jiec.2014.06.022
– volume: 22
  start-page: 34
  year: 2015
  ident: 2024080805281174500_ref14
  article-title: Synthesis, characterization and stability of Cu2O nanoparticles produced via supersaturation method considering operational parameters effect
  publication-title: J Ind Eng Chem
  doi: 10.1016/j.jiec.2014.06.022
– volume: 38
  start-page: 385
  issue: 3
  year: 2018
  ident: 2024080805281174500_ref2
  article-title: Transcriptional profiling reveals gene expression changes associated with inflammation and cell proliferation following short-term inhalation exposure to copper oxide nanoparticles
  publication-title: J Appl Toxicol
  doi: 10.1002/jat.3548
– volume: 113
  start-page: 823
  issue: 7
  year: 2005
  ident: 2024080805281174500_ref7
  article-title: Nanotoxicology: an emerging discipline evolving from studies of ultrafine particles
  publication-title: Environ Health Perspect
  doi: 10.1289/ehp.7339
– volume: 38
  start-page: 83
  issue: 1
  year: 2014
  ident: 2024080805281174500_ref22
  article-title: Hematological and biochemical evaluation after different orally doses of copper sulfate in rats
  publication-title: Iraq J Vet Med
  doi: 10.30539/iraqijvm.v38i1.259
– volume: 2017
  start-page: 7056864
  year: 2017
  ident: 2024080805281174500_ref3
  article-title: Synthesis and investigation of antimicrobial activity of Cu2O nanoparticles/zeolite
  publication-title: J Nanoparticl
  doi: 10.1155/2017/7056864
– volume: 13
  start-page: 56
  issue: 1
  year: 2016
  ident: 2024080805281174500_ref21
  article-title: Comparative toxicity and biodistribution assessments in rats following subchronic oral exposure to copper nanoparticles and microparticles
  publication-title: Part Fibre Toxicol
  doi: 10.1186/s12989-016-0169-x
– volume: 13
  start-page: 50
  issue: 1
  year: 2019
  ident: 2024080805281174500_ref20
  article-title: Toxicity of copper oxide and basic copper carbonate nanoparticles after short-term oral exposure in rats
  publication-title: Nanotoxicology
  doi: 10.1080/17435390.2018.1530390
– volume: 44
  start-page: 59
  issue: 5
  year: 2022
  ident: 2024080805281174500_ref11
  article-title: Induction of selenium nanoparticles disturbs behavior, blood and serum biomarkers and oxidative stress markers from vital organs of male and female albino mice
  publication-title: J Chem Soc Pak
– volume: 43
  start-page: 46
  issue: 1
  year: 2021
  ident: 2024080805281174500_ref10
  article-title: Synthesis, characterization and biocompatibility of holmium Zirconate/zinc sulphide nanocomposite in albino mice in a gender specific manner
  publication-title: J Chem Soc Pak
– volume: 163
  start-page: 109
  issue: 2
  year: 2006
  ident: 2024080805281174500_ref15
  article-title: Acute toxicological effects of copper nanoparticles in vivo
  publication-title: Toxicol Lett
  doi: 10.1016/j.toxlet.2005.10.003
– volume: 14
  start-page: 1
  issue: 1
  year: 2020
  ident: 2024080805281174500_ref6
  article-title: Toxicity of copper oxide nanoparticles: a review study
  publication-title: IET Nanobiotechnol
  doi: 10.1049/iet-nbt.2019.0176
– volume: 30
  start-page: 89690
  issue: 38
  year: 2023
  ident: 2024080805281174500_ref4
  article-title: Synthesis of Cu and CuO nanoparticles from e-waste and evaluation of their antibacterial and photocatalytic properties
  publication-title: Environ Sci Pollut Res
  doi: 10.1007/s11356-023-28437-5
– volume: 213
  start-page: 220
  issue: 2
  year: 2012
  ident: 2024080805281174500_ref17
  article-title: Cognitive impairment in rats induced by nano-CuO and its possible mechanisms
  publication-title: Toxicol Lett
  doi: 10.1016/j.toxlet.2012.07.007
– volume: 107
  start-page: 1039
  issue: 4
  year: 2023
  ident: 2024080805281174500_ref1
  article-title: Synthesis, biomedical applications, and toxicity of CuO nanoparticles
  publication-title: Appl Microbiol Biotechnol
  doi: 10.1007/s00253-023-12364-z
– volume: 33
  start-page: 587
  issue: 6
  year: 2009
  ident: 2024080805281174500_ref13
  article-title: Characterisation of copper oxide nanoparticles for antimicrobial applications
  publication-title: Int J Antimicrob Agents
  doi: 10.1016/j.ijantimicag.2008.12.004
– volume: 393
  start-page: 717
  issue: 4
  year: 2020
  ident: 2024080805281174500_ref9
  article-title: Synthesis and characterization of newly synthesized neodymium Zirconate zinc Sulfide nano composite and its effect on selected aspects of albino mice behavior
  publication-title: Naunyn Schmiedeberg's Arch Pharmacol
  doi: 10.1007/s00210-019-01787-z
– volume: 12
  start-page: 635
  issue: 9–10
  year: 2004
  ident: 2024080805281174500_ref19
  article-title: Nanoparticle surface charges alter blood–brain barrier integrity and permeability
  publication-title: J Drug Target
  doi: 10.1080/10611860400015936
– volume: 39
  start-page: 195
  issue: 3
  year: 2016
  ident: 2024080805281174500_ref25
  article-title: Copper ion from Cu2O crystal induces AMPK-mediated autophagy via superoxide in endothelial cells
  publication-title: Mol Cell
  doi: 10.14348/molcells.2016.2198
– volume: 41
  start-page: 259
  year: 2017
  ident: 2024080805281174500_ref23
  article-title: Effects of aluminum, copper, and titanium nanoparticles on some blood parameters in Wistar rats
  publication-title: Turk J Zool
  doi: 10.3906/zoo-1512-23
– volume: 7
  start-page: 213
  issue: 30
  year: 2014
  ident: 2024080805281174500_ref12
  article-title: Heavy metals in vegetables and respective soils irrigated by canal, municipal waste and tube well waters
  publication-title: Food Addit Contaminat Part B
  doi: 10.1080/19393210.2014.888783
– volume: 22
  start-page: 4747
  issue: 6
  year: 2015
  ident: 2024080805281174500_ref24
  article-title: The effects of cyfluthrin on some biomarkers in the liver and kidney of Wistar rats
  publication-title: Environ Sci Pollut Res
  doi: 10.1007/s11356-014-3734-6
– volume: 16
  start-page: 78
  issue: 2
  year: 2017
  ident: 2024080805281174500_ref26
  article-title: Modulation effects of quercetin against copper oxide nanoparticles-induced liver toxicity in rats
  publication-title: Egypt Pharmaceut J
  doi: 10.4103/epj.epj_15_17
– volume: 19
  start-page: 59
  issue: Suppl 1
  year: 2007
  ident: 2024080805281174500_ref27
  article-title: Cellular toxicity of various inhalable metal nanoparticles on human alveolar epithelial cells
  publication-title: Inhal Toxicol
  doi: 10.1080/08958370701493282
SSID ssj0000702635
Score 2.3133893
Snippet Copper oxide (Cu O) nanoparticles (CO NPs) are in extensive use during our everyday life as antimicrobial agent, lubricant, in manufacturing electrodes of...
Copper oxide (Cu2O) nanoparticles (CO NPs) are in extensive use during our everyday life as antimicrobial agent, lubricant, in manufacturing electrodes of...
Graphical Abstract
SourceID pubmedcentral
proquest
pubmed
crossref
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage tfae125
Title Toxicological evaluation of copper oxide nanoparticles following their intraperitoneal injection to Wistar rats
URI https://www.ncbi.nlm.nih.gov/pubmed/39132193
https://www.proquest.com/docview/3092011056
https://pubmed.ncbi.nlm.nih.gov/PMC11306316
Volume 13
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3db9MwELfKeEFCiG86PmQkJB6qbE3sOM5jhZgmJHjaxN4i27HVIJaUNBXb_gH-bc5x4ialSIOXqEocJ-39enc-3_0OoXdgwgSPuQqYljSgiVIBJ-DImTxKQ26MMO1WzOcv7PScfrqILyaTX4OspU0jj9TN3rqS_5EqnAO52irZf5CsnxROwGeQLxxBwnC8nYyrq0J57bUl7na54quVrmcwItezUpSwOO5y4GYGZF_97OqkCpuP3tgarLqwxNwtCcc37TqIg2P61TqY9QyAsh46sv7R17OOL2jZbgj3JWCDCIPlhNbaONytl94OLGThgtJLUdTXwmcJLy4L12H7x1pskXspXLTaXh2GKiLqE-U6jWap7wMaOzqXI73nXK-SyQB6dK-mdyxYTXVVW3V60hihQ1dCPSbV3jF2PgXRbb6TzM2QdfffQXejBJywQdinNenJ3JL22EaF_et6AlBy7KY47qYYOzh_rFp2k28H3szZQ_SgW4bghYPEIzTR5WN038VwsStNe4KqEb7wFl-4MtjhC7f4wiN8YY8v3OIL7-ALe3zhpsIOX9ji6yk6P_l49uE06Bp0BIqkYRMwrqw7E-XUCJbHucp5mhjbKV4nkdFzIaUQStLcwADJcp5EsCCAu6I5l5xJ8gwdlPDkFwhTHc2VYFxLZaithpZEypCJkIL9TYWcoqD_VTPVsdfbJirfs_2CnKL3fvzK8bb8deTbXkgZqFa7XyZKXW3WGZmnrXscsyl67oTm54LvT8DYkyniI3H6AZa2fXylLJYtfXsIbiMjITu89Su-RPe2f6dX6KCpN_o1-MKNfNPi9DfWF8SI
linkProvider National Library of Medicine
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Toxicological+evaluation+of+copper+oxide+nanoparticles+following+their+intraperitoneal+injection+to+Wistar+rats&rft.jtitle=Toxicology+research+%28Cambridge%29&rft.au=Shareef%2C+Nisha&rft.au=Abid%2C+Shairyar&rft.au=Amir%2C+Aqsa&rft.au=Ismail%2C+Amir&rft.date=2024-08-01&rft.issn=2045-4538&rft.eissn=2045-4538&rft.volume=13&rft.issue=4&rft_id=info:doi/10.1093%2Ftoxres%2Ftfae125&rft.externalDBID=n%2Fa&rft.externalDocID=10_1093_toxres_tfae125
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2045-4538&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2045-4538&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2045-4538&client=summon