Ecofriendly synthesis characterization and biological activities of Eruca sativa mediated silver oxide nanoparticles

One of the popular subjects of millennia is the synthesis of nanostructures, their applications in numerous fields, and their interaction with various biological systems, making them appealing for drug delivery systems, and diagnostic and therapeutic agents. In this study, silver oxide nanoparticles...

Full description

Saved in:
Bibliographic Details
Published inScientific reports Vol. 15; no. 1; pp. 13466 - 18
Main Authors Gul, Farhat, Ullah, Zakir, Iqbal, Javed, Abbasi, Banzeer Ahsan, Ali, Sarfaraz, Kanwal, Sobia, Uddin, Jamal, Kazi, Mohsin, Mahmood, Tariq
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 18.04.2025
Nature Publishing Group
Nature Portfolio
Subjects
Online AccessGet full text

Cover

Loading…
Abstract One of the popular subjects of millennia is the synthesis of nanostructures, their applications in numerous fields, and their interaction with various biological systems, making them appealing for drug delivery systems, and diagnostic and therapeutic agents. In this study, silver oxide nanoparticles were synthesized using E. sativa (ES) aqueous extract. The biosynthesis was followed via UV-vis spectroscopy by analysis, FTIR, XRD, TEM, and Zeta potential to further analyze the synthesized nanoparticles. Furthermore, the biosynthesized silver oxide nanoparticles (Ag 2 ONPs) were checked through various biological activities. The antioxidative potential was assessed by performing a DPPH radical scavenging assay, total reducing power assay, and total antioxidant capacity assay. Antimicrobial potential was observed against various bacterial and fungal strains. Likewise, Artemia salina (brine shrimps) was used to study cytotoxicity, while VERO and HEK-293 cell lines were applied to check the biocompatibility of synthesized NPs. Anticancer potential was evaluated against the Hep-2 cells by utilizing an MTT assay. A mean crystallite ~ 50 nm size is evidenced by TEM analysis. Notable antimicrobial activity was detected with various bacterial and fungal strains with maximum ZOI by B . subtilis was 18.5 ± 2.36 mm at 1000 µg/mL and A . niger reveals a minimum ZOP of 16 ± 1.7 mm at 1000 µg/mL respectively. A dose-dependent response was observed in biological evaluation against A . salina (LC 50 : 12.21 µg/mL), DPPH (IC 50 : 62.36 µg/mL), VERO cell line (IC 50 : 43.11 µg/mL), HEK-293 cell line (IC 50 : 26.56 µg/mL), and Hep-2 cell line (IC 50 : 9.97 µg/mL). The multifaceted attributes of ES-Ag 2 ONPs encompassing antimicrobial, antioxidant, cytotoxic, and anticancer properties render them a versatile platform in drug delivery and biomedical horizons. However, detailed investigation and clinical trials will undoubtedly provide translational applications in diverse fields.
AbstractList Abstract One of the popular subjects of millennia is the synthesis of nanostructures, their applications in numerous fields, and their interaction with various biological systems, making them appealing for drug delivery systems, and diagnostic and therapeutic agents. In this study, silver oxide nanoparticles were synthesized using E. sativa (ES) aqueous extract. The biosynthesis was followed via UV-vis spectroscopy by analysis, FTIR, XRD, TEM, and Zeta potential to further analyze the synthesized nanoparticles. Furthermore, the biosynthesized silver oxide nanoparticles (Ag2ONPs) were checked through various biological activities. The antioxidative potential was assessed by performing a DPPH radical scavenging assay, total reducing power assay, and total antioxidant capacity assay. Antimicrobial potential was observed against various bacterial and fungal strains. Likewise, Artemia salina (brine shrimps) was used to study cytotoxicity, while VERO and HEK-293 cell lines were applied to check the biocompatibility of synthesized NPs. Anticancer potential was evaluated against the Hep-2 cells by utilizing an MTT assay. A mean crystallite ~ 50 nm size is evidenced by TEM analysis. Notable antimicrobial activity was detected with various bacterial and fungal strains with maximum ZOI by B. subtilis was 18.5 ± 2.36 mm at 1000 µg/mL and A. niger reveals a minimum ZOP of 16 ± 1.7 mm at 1000 µg/mL respectively. A dose-dependent response was observed in biological evaluation against A. salina (LC50: 12.21 µg/mL), DPPH (IC50: 62.36 µg/mL), VERO cell line (IC50: 43.11 µg/mL), HEK-293 cell line (IC50: 26.56 µg/mL), and Hep-2 cell line (IC50: 9.97 µg/mL). The multifaceted attributes of ES-Ag2ONPs encompassing antimicrobial, antioxidant, cytotoxic, and anticancer properties render them a versatile platform in drug delivery and biomedical horizons. However, detailed investigation and clinical trials will undoubtedly provide translational applications in diverse fields.
One of the popular subjects of millennia is the synthesis of nanostructures, their applications in numerous fields, and their interaction with various biological systems, making them appealing for drug delivery systems, and diagnostic and therapeutic agents. In this study, silver oxide nanoparticles were synthesized using E. sativa (ES) aqueous extract. The biosynthesis was followed via UV-vis spectroscopy by analysis, FTIR, XRD, TEM, and Zeta potential to further analyze the synthesized nanoparticles. Furthermore, the biosynthesized silver oxide nanoparticles (Ag ONPs) were checked through various biological activities. The antioxidative potential was assessed by performing a DPPH radical scavenging assay, total reducing power assay, and total antioxidant capacity assay. Antimicrobial potential was observed against various bacterial and fungal strains. Likewise, Artemia salina (brine shrimps) was used to study cytotoxicity, while VERO and HEK-293 cell lines were applied to check the biocompatibility of synthesized NPs. Anticancer potential was evaluated against the Hep-2 cells by utilizing an MTT assay. A mean crystallite ~ 50 nm size is evidenced by TEM analysis. Notable antimicrobial activity was detected with various bacterial and fungal strains with maximum ZOI by B. subtilis was 18.5 ± 2.36 mm at 1000 µg/mL and A. niger reveals a minimum ZOP of 16 ± 1.7 mm at 1000 µg/mL respectively. A dose-dependent response was observed in biological evaluation against A. salina (LC : 12.21 µg/mL), DPPH (IC : 62.36 µg/mL), VERO cell line (IC : 43.11 µg/mL), HEK-293 cell line (IC : 26.56 µg/mL), and Hep-2 cell line (IC : 9.97 µg/mL). The multifaceted attributes of ES-Ag ONPs encompassing antimicrobial, antioxidant, cytotoxic, and anticancer properties render them a versatile platform in drug delivery and biomedical horizons. However, detailed investigation and clinical trials will undoubtedly provide translational applications in diverse fields.
One of the popular subjects of millennia is the synthesis of nanostructures, their applications in numerous fields, and their interaction with various biological systems, making them appealing for drug delivery systems, and diagnostic and therapeutic agents. In this study, silver oxide nanoparticles were synthesized using E. sativa (ES) aqueous extract. The biosynthesis was followed via UV-vis spectroscopy by analysis, FTIR, XRD, TEM, and Zeta potential to further analyze the synthesized nanoparticles. Furthermore, the biosynthesized silver oxide nanoparticles (Ag 2 ONPs) were checked through various biological activities. The antioxidative potential was assessed by performing a DPPH radical scavenging assay, total reducing power assay, and total antioxidant capacity assay. Antimicrobial potential was observed against various bacterial and fungal strains. Likewise, Artemia salina (brine shrimps) was used to study cytotoxicity, while VERO and HEK-293 cell lines were applied to check the biocompatibility of synthesized NPs. Anticancer potential was evaluated against the Hep-2 cells by utilizing an MTT assay. A mean crystallite ~ 50 nm size is evidenced by TEM analysis. Notable antimicrobial activity was detected with various bacterial and fungal strains with maximum ZOI by B . subtilis was 18.5 ± 2.36 mm at 1000 µg/mL and A . niger reveals a minimum ZOP of 16 ± 1.7 mm at 1000 µg/mL respectively. A dose-dependent response was observed in biological evaluation against A . salina (LC 50 : 12.21 µg/mL), DPPH (IC 50 : 62.36 µg/mL), VERO cell line (IC 50 : 43.11 µg/mL), HEK-293 cell line (IC 50 : 26.56 µg/mL), and Hep-2 cell line (IC 50 : 9.97 µg/mL). The multifaceted attributes of ES-Ag 2 ONPs encompassing antimicrobial, antioxidant, cytotoxic, and anticancer properties render them a versatile platform in drug delivery and biomedical horizons. However, detailed investigation and clinical trials will undoubtedly provide translational applications in diverse fields.
One of the popular subjects of millennia is the synthesis of nanostructures, their applications in numerous fields, and their interaction with various biological systems, making them appealing for drug delivery systems, and diagnostic and therapeutic agents. In this study, silver oxide nanoparticles were synthesized using E. sativa (ES) aqueous extract. The biosynthesis was followed via UV-vis spectroscopy by analysis, FTIR, XRD, TEM, and Zeta potential to further analyze the synthesized nanoparticles. Furthermore, the biosynthesized silver oxide nanoparticles (Ag2ONPs) were checked through various biological activities. The antioxidative potential was assessed by performing a DPPH radical scavenging assay, total reducing power assay, and total antioxidant capacity assay. Antimicrobial potential was observed against various bacterial and fungal strains. Likewise, Artemia salina (brine shrimps) was used to study cytotoxicity, while VERO and HEK-293 cell lines were applied to check the biocompatibility of synthesized NPs. Anticancer potential was evaluated against the Hep-2 cells by utilizing an MTT assay. A mean crystallite ~ 50 nm size is evidenced by TEM analysis. Notable antimicrobial activity was detected with various bacterial and fungal strains with maximum ZOI by B. subtilis was 18.5 ± 2.36 mm at 1000 µg/mL and A. niger reveals a minimum ZOP of 16 ± 1.7 mm at 1000 µg/mL respectively. A dose-dependent response was observed in biological evaluation against A. salina (LC50: 12.21 µg/mL), DPPH (IC50: 62.36 µg/mL), VERO cell line (IC50: 43.11 µg/mL), HEK-293 cell line (IC50: 26.56 µg/mL), and Hep-2 cell line (IC50: 9.97 µg/mL). The multifaceted attributes of ES-Ag2ONPs encompassing antimicrobial, antioxidant, cytotoxic, and anticancer properties render them a versatile platform in drug delivery and biomedical horizons. However, detailed investigation and clinical trials will undoubtedly provide translational applications in diverse fields.One of the popular subjects of millennia is the synthesis of nanostructures, their applications in numerous fields, and their interaction with various biological systems, making them appealing for drug delivery systems, and diagnostic and therapeutic agents. In this study, silver oxide nanoparticles were synthesized using E. sativa (ES) aqueous extract. The biosynthesis was followed via UV-vis spectroscopy by analysis, FTIR, XRD, TEM, and Zeta potential to further analyze the synthesized nanoparticles. Furthermore, the biosynthesized silver oxide nanoparticles (Ag2ONPs) were checked through various biological activities. The antioxidative potential was assessed by performing a DPPH radical scavenging assay, total reducing power assay, and total antioxidant capacity assay. Antimicrobial potential was observed against various bacterial and fungal strains. Likewise, Artemia salina (brine shrimps) was used to study cytotoxicity, while VERO and HEK-293 cell lines were applied to check the biocompatibility of synthesized NPs. Anticancer potential was evaluated against the Hep-2 cells by utilizing an MTT assay. A mean crystallite ~ 50 nm size is evidenced by TEM analysis. Notable antimicrobial activity was detected with various bacterial and fungal strains with maximum ZOI by B. subtilis was 18.5 ± 2.36 mm at 1000 µg/mL and A. niger reveals a minimum ZOP of 16 ± 1.7 mm at 1000 µg/mL respectively. A dose-dependent response was observed in biological evaluation against A. salina (LC50: 12.21 µg/mL), DPPH (IC50: 62.36 µg/mL), VERO cell line (IC50: 43.11 µg/mL), HEK-293 cell line (IC50: 26.56 µg/mL), and Hep-2 cell line (IC50: 9.97 µg/mL). The multifaceted attributes of ES-Ag2ONPs encompassing antimicrobial, antioxidant, cytotoxic, and anticancer properties render them a versatile platform in drug delivery and biomedical horizons. However, detailed investigation and clinical trials will undoubtedly provide translational applications in diverse fields.
One of the popular subjects of millennia is the synthesis of nanostructures, their applications in numerous fields, and their interaction with various biological systems, making them appealing for drug delivery systems, and diagnostic and therapeutic agents. In this study, silver oxide nanoparticles were synthesized using E. sativa (ES) aqueous extract. The biosynthesis was followed via UV-vis spectroscopy by analysis, FTIR, XRD, TEM, and Zeta potential to further analyze the synthesized nanoparticles. Furthermore, the biosynthesized silver oxide nanoparticles (Ag2ONPs) were checked through various biological activities. The antioxidative potential was assessed by performing a DPPH radical scavenging assay, total reducing power assay, and total antioxidant capacity assay. Antimicrobial potential was observed against various bacterial and fungal strains. Likewise, Artemia salina (brine shrimps) was used to study cytotoxicity, while VERO and HEK-293 cell lines were applied to check the biocompatibility of synthesized NPs. Anticancer potential was evaluated against the Hep-2 cells by utilizing an MTT assay. A mean crystallite ~ 50 nm size is evidenced by TEM analysis. Notable antimicrobial activity was detected with various bacterial and fungal strains with maximum ZOI by B. subtilis was 18.5 ± 2.36 mm at 1000 µg/mL and A. niger reveals a minimum ZOP of 16 ± 1.7 mm at 1000 µg/mL respectively. A dose-dependent response was observed in biological evaluation against A. salina (LC50: 12.21 µg/mL), DPPH (IC50: 62.36 µg/mL), VERO cell line (IC50: 43.11 µg/mL), HEK-293 cell line (IC50: 26.56 µg/mL), and Hep-2 cell line (IC50: 9.97 µg/mL). The multifaceted attributes of ES-Ag2ONPs encompassing antimicrobial, antioxidant, cytotoxic, and anticancer properties render them a versatile platform in drug delivery and biomedical horizons. However, detailed investigation and clinical trials will undoubtedly provide translational applications in diverse fields.
ArticleNumber 13466
Author Gul, Farhat
Uddin, Jamal
Abbasi, Banzeer Ahsan
Mahmood, Tariq
Iqbal, Javed
Ullah, Zakir
Kazi, Mohsin
Kanwal, Sobia
Ali, Sarfaraz
Author_xml – sequence: 1
  givenname: Farhat
  surname: Gul
  fullname: Gul, Farhat
  organization: Department of Plant Sciences, Faculty of Biological Sciences, Quaid-i-Azam University
– sequence: 2
  givenname: Zakir
  surname: Ullah
  fullname: Ullah, Zakir
  email: zakirullah@bs.qau.edu.pk
  organization: Department of Plant Sciences, Faculty of Biological Sciences, Quaid-i-Azam University
– sequence: 3
  givenname: Javed
  surname: Iqbal
  fullname: Iqbal, Javed
  organization: Department of Botany, Bacha Khan University
– sequence: 4
  givenname: Banzeer Ahsan
  surname: Abbasi
  fullname: Abbasi, Banzeer Ahsan
  organization: Department of Botany, Rawalpindi Women University
– sequence: 5
  givenname: Sarfaraz
  surname: Ali
  fullname: Ali, Sarfaraz
  organization: Quality Control laboratory (Biological), National Institute of Health
– sequence: 6
  givenname: Sobia
  surname: Kanwal
  fullname: Kanwal, Sobia
  organization: Department of Biology and Environmental Sciences, Allama Iqbal Open University
– sequence: 7
  givenname: Jamal
  surname: Uddin
  fullname: Uddin, Jamal
  email: JUddin@coppin.edu
  organization: Center for Nanotechnology, Department of Natural Sciences, Coppin State University
– sequence: 8
  givenname: Mohsin
  surname: Kazi
  fullname: Kazi, Mohsin
  email: mkazi@ksu.edu.sa
  organization: Department of Pharmaceutics, College of Pharmacy, King Saud University
– sequence: 9
  givenname: Tariq
  surname: Mahmood
  fullname: Mahmood, Tariq
  email: tmahmood@qau.edu.pk
  organization: Department of Plant Sciences, Faculty of Biological Sciences, Quaid-i-Azam University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/40251221$$D View this record in MEDLINE/PubMed
BookMark eNp9kk1vEzEQhi1UREvpH-CALHHhsuCvtb0nhKoAlSpxgbM1sb2Jo40d7N2o4dfjZkNpOeCLrZnnfWdsz0t0FlP0CL2m5D0lXH8ogradbghrG62kIk33DF0wItqGccbOHp3P0VUpG1JXyzpBuxfoXFQZZYxeoHFhU5-Dj2444HKI49qXULBdQwY7-hx-wRhSxBAdXoY0pFWwMOCaC_swBl9w6vEiTxZwqeQe8Na7AKN3uIRh7zNOd8F5HCGmHeQx2MGXV-h5D0PxV6f9Ev34vPh-_bW5_fbl5vrTbWNFJ8amJ1YqrqwUbSuJ1EyRrvfOLhVznetBO2qVsFoJIWXLvQMtuOsY0dK2AJZfopvZ1yXYmF0OW8gHkyCYYyDllTm1ZKwjmlCiWiW40IyA9XzJnVOU9boGqtfH2Ws3LesVrY9jhuGJ6dNMDGuzSntDGSFaUFod3p0ccvo5-TKabSjWDwNEn6ZiOO2opJrotqJv_0E3acqxvtWREppKeW_45nFLD738-d0KsBmwOZWSff-AUGLup8jMU2SqwBynyHRVxGdRqXBc-fy39n9UvwGHn8sE
Cites_doi 10.1016/j.jphotobiol.2017.03.023
10.1155/2014/256919
10.1021/acsomega.3c06233
10.1016/j.molstruc.2020.128490
10.1016/j.biopha.2016.09.016
10.1080/17460441.2022.2097659
10.1186/s12951-018-0408-4
10.1007/s11837-019-03784-2
10.3390/molecules21030365
10.1039/D0BM00029A
10.1038/s41598-024-60694-3
10.3390/biomedicines8050117
10.1016/j.msec.2015.08.022
10.3390/antibiotics11070853
10.1142/S0219581X21500605
10.1016/j.inoche.2021.109020
10.3390/ph15080968
10.1111/j.1365-2672.2012.05253.x
10.1016/j.biopha.2023.114687
10.1016/j.egypro.2017.03.035
10.22271/flora.2016.v4.i6c.03
10.1016/j.ultsonch.2017.11.001
10.1016/B978-0-323-95376-4.00012-5
10.1038/s41598-021-99839-z
10.1088/2053-1591/ab4f04
10.1002/aenm.202001119
10.1088/2053-1591/ab23e1
10.1016/j.apt.2022.103645
10.1002/jemt.23756
10.1016/j.jclepro.2019.05.157
10.2147/IJN.S122842
10.1093/mmy/myab028
10.1002/pi.5304
10.1021/acs.jafc.7b05830
10.2174/18756298MTA5jNzYp2
10.1016/j.colsurfa.2016.05.058
10.1093/cid/ciw691
10.3390/microorganisms11041069
10.1016/j.matchemphys.2019.121976
10.1021/acs.biomac.0c00726
10.1016/j.colsurfb.2020.111156
10.1155/2022/3863138
10.1016/j.molstruc.2023.136012
10.1016/j.ijid.2017.01.020
10.3390/su151612186
10.3390/molecules20058856
10.1039/C4AN00816B
10.3389/fmicb.2019.00008
10.1016/j.tiv.2011.01.004
10.1016/j.jphotobiol.2019.111650
10.1016/j.jphotobiol.2018.04.020
10.1016/j.talanta.2022.124026
10.3109/13880209.2014.986687
10.1016/j.jmii.2014.04.013
10.22159/ajpcr.2018.v11i1.21999
10.1002/jemt.23522
10.1007/s11356-023-25343-8
10.3389/fchem.2018.00360
10.1016/B978-0-443-15518-5.00024-0
10.1088/2043-6254/aaec0e
10.1002/jps.24001
10.1039/C4NR01405G
10.24966/NTMB-2044/100022
10.1007/s00775-019-01717-7
10.1021/acs.molpharmaceut.8b00640
10.1016/S1473-3099(16)00078-5
10.3389/fchem.2022.952006
10.1007/s11468-019-01101-w
10.3390/su151712783
10.22159/ajpcr.2018.v11i3.20858
10.1016/j.micres.2016.06.004
10.1016/j.apt.2018.03.025
10.4103/0250-474X.108420
10.3390/molecules28073240
10.1039/C7NJ02453C
10.1007/s13204-012-0125-5
10.1080/14787210.2019.1614914
10.1016/j.envpol.2019.113358
10.4172/0974-8369.1000363
10.1166/jnn.2017.12636
10.1016/j.heliyon.2021.e06923
10.1016/j.molstruc.2019.126979
10.22207/JPAM.14.3.48
10.1016/j.inoche.2020.108385
10.1016/B978-0-323-46139-9.00001-3
10.1016/j.bcab.2023.102870
ContentType Journal Article
Copyright The Author(s) 2025
2025. The Author(s).
Copyright Nature Publishing Group 2025
The Author(s) 2025 2025
Copyright_xml – notice: The Author(s) 2025
– notice: 2025. The Author(s).
– notice: Copyright Nature Publishing Group 2025
– notice: The Author(s) 2025 2025
DBID C6C
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7X7
7XB
88A
88E
88I
8FE
8FH
8FI
8FJ
8FK
ABUWG
AEUYN
AFKRA
AZQEC
BBNVY
BENPR
BHPHI
CCPQU
DWQXO
FYUFA
GHDGH
GNUQQ
HCIFZ
K9.
LK8
M0S
M1P
M2P
M7P
PHGZM
PHGZT
PIMPY
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
Q9U
7X8
5PM
DOA
DOI 10.1038/s41598-025-87670-9
DatabaseName Springer Nature OA Free Journals
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Central (Corporate)
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Biology Database (Alumni Edition)
Medical Database (Alumni Edition)
Science Database (Alumni Edition)
ProQuest SciTech Collection
ProQuest Natural Science Collection
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest One Sustainability
ProQuest Central UK/Ireland
ProQuest Central Essentials
Biological Science Collection
ProQuest Central
Natural Science Collection
ProQuest One
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
SciTech Premium Collection
ProQuest Health & Medical Complete (Alumni)
ProQuest Biological Science Collection
ProQuest Health & Medical Collection
Medical Database
Science Database
Biological Science Database
ProQuest Central Premium
ProQuest One Academic (New)
Publicly Available Content Database
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
ProQuest Central Basic
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Open Access Journals
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Publicly Available Content Database
ProQuest Central Student
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
SciTech Premium Collection
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Natural Science Collection
ProQuest Central China
ProQuest Biology Journals (Alumni Edition)
ProQuest Central
ProQuest One Applied & Life Sciences
ProQuest One Sustainability
ProQuest Health & Medical Research Collection
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
Natural Science Collection
ProQuest Central Korea
Health & Medical Research Collection
Biological Science Collection
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest Science Journals (Alumni Edition)
ProQuest Biological Science Collection
ProQuest Central Basic
ProQuest Science Journals
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
Biological Science Database
ProQuest SciTech Collection
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList
MEDLINE


MEDLINE - Academic
Publicly Available Content Database
Database_xml – sequence: 1
  dbid: C6C
  name: Springer Nature OA Free Journals
  url: http://www.springeropen.com/
  sourceTypes: Publisher
– sequence: 2
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 3
  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
– sequence: 4
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 5
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Biology
EISSN 2045-2322
EndPage 18
ExternalDocumentID oai_doaj_org_article_cd08010757434820ace3b3dd712f8482
PMC12008411
40251221
10_1038_s41598_025_87670_9
Genre Journal Article
GrantInformation_xml – fundername: Mohsin Kazi
  grantid: RSPD2024R994; RSPD2024R994; RSPD2024R994; RSPD2024R994; RSPD2024R994; RSPD2024R994; RSPD2024R994; RSPD2024R994
– fundername: Jamal Uddin
  grantid: RSPD2024R994; RSPD2024R994; RSPD2024R994; RSPD2024R994; RSPD2024R994; RSPD2024R994; RSPD2024R994; RSPD2024R994
– fundername: Mohsin Kazi
  grantid: RSPD2024R994
– fundername: Jamal Uddin
  grantid: RSPD2024R994
GroupedDBID 0R~
4.4
53G
5VS
7X7
88E
88I
8FE
8FH
8FI
8FJ
AAFWJ
AAJSJ
AAKDD
AASML
ABDBF
ABUWG
ACGFS
ACUHS
ADBBV
ADRAZ
AENEX
AEUYN
AFKRA
AFPKN
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AOIJS
AZQEC
BAWUL
BBNVY
BCNDV
BENPR
BHPHI
BPHCQ
BVXVI
C6C
CCPQU
DIK
DWQXO
EBD
EBLON
EBS
ESX
FYUFA
GNUQQ
GROUPED_DOAJ
GX1
HCIFZ
HH5
HMCUK
HYE
KQ8
LK8
M1P
M2P
M7P
M~E
NAO
OK1
PHGZT
PIMPY
PQQKQ
PROAC
PSQYO
RNT
RNTTT
RPM
SNYQT
UKHRP
AAYXX
CITATION
PHGZM
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7XB
88A
8FK
AARCD
K9.
M48
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQUKI
PRINS
Q9U
7X8
5PM
PUEGO
ID FETCH-LOGICAL-c494t-f0c6737c645560682709fedcb72d9dfa8d1c74c87446653eda843d92086c5aac3
IEDL.DBID 7X7
ISSN 2045-2322
IngestDate Wed Aug 27 01:23:09 EDT 2025
Thu Aug 21 18:28:09 EDT 2025
Fri Jul 11 18:36:02 EDT 2025
Wed Aug 13 04:11:41 EDT 2025
Tue Apr 22 01:20:47 EDT 2025
Sun Jul 06 05:03:09 EDT 2025
Sat Apr 19 01:10:46 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords Antimicrobial
Silver oxide nanoparticles
Cytotoxic
Anticancer
E. sativa
Language English
License 2025. The Author(s).
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c494t-f0c6737c645560682709fedcb72d9dfa8d1c74c87446653eda843d92086c5aac3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
OpenAccessLink https://www.proquest.com/docview/3191481661?pq-origsite=%requestingapplication%
PMID 40251221
PQID 3191481661
PQPubID 2041939
PageCount 18
ParticipantIDs doaj_primary_oai_doaj_org_article_cd08010757434820ace3b3dd712f8482
pubmedcentral_primary_oai_pubmedcentral_nih_gov_12008411
proquest_miscellaneous_3191618085
proquest_journals_3191481661
pubmed_primary_40251221
crossref_primary_10_1038_s41598_025_87670_9
springer_journals_10_1038_s41598_025_87670_9
PublicationCentury 2000
PublicationDate 2025-04-18
PublicationDateYYYYMMDD 2025-04-18
PublicationDate_xml – month: 04
  year: 2025
  text: 2025-04-18
  day: 18
PublicationDecade 2020
PublicationPlace London
PublicationPlace_xml – name: London
– name: England
PublicationTitle Scientific reports
PublicationTitleAbbrev Sci Rep
PublicationTitleAlternate Sci Rep
PublicationYear 2025
Publisher Nature Publishing Group UK
Nature Publishing Group
Nature Portfolio
Publisher_xml – name: Nature Publishing Group UK
– name: Nature Publishing Group
– name: Nature Portfolio
References N Liaqat (87670_CR49) 2022; 10
RRR Kannan (87670_CR42) 2013; 3
BA Abbasi (87670_CR48) 2020; 83
K Velsankar (87670_CR19) 2023; 53
J Iqbal (87670_CR38) 2021; 11
BA Abbasi (87670_CR30) 2019; 6
A Hussain (87670_CR89) 2019; 10
ER Swy (87670_CR2) 2014; 6
J Iqbal (87670_CR34) 2020; 1199
GA Rather (87670_CR25) 2021; 134
D Nayak (87670_CR85) 2016; 58
BR Sushobhan (87670_CR8) 2017; 109
H Houri (87670_CR56) 2017; 57
BA Abbasi (87670_CR35) 2020; 1218
P Balashanmugam (87670_CR78) 2016; 192
Z Ullah (87670_CR6) 2024; 14
A Benslama (87670_CR51) 2016; 4
AA El-Bassuony (87670_CR72) 2020; 72
J Singh (87670_CR40) 2018; 16
D Debnath (87670_CR92) 2017; 66
J Iqbal (87670_CR37) 2020; 8
T Khan (87670_CR61) 2020; 194
87670_CR44
R Ridolfo (87670_CR12) 2020; 22
I Hasan (87670_CR16) 2019; 230
H Vahidi (87670_CR28) 2020; 7
C Sharmila (87670_CR11) 2018; 11
87670_CR84
I Ullah (87670_CR93) 2020; 2020
K Velsankar (87670_CR41) 2023; 1291
D Zhang (87670_CR15) 2014; 139
87670_CR80
ZK Xia (87670_CR74) 2016; 49
JJ Artunduaga Bonilla (87670_CR76) 2021; 59
A Nasrollahi (87670_CR70) 2011; 5
AJ Adur (87670_CR64) 2018; 183
J Jampilek (87670_CR67) 2022; 17
JS Teodoro (87670_CR87) 2011; 25
NT Khan (87670_CR71) 2017; 9
RAD Lish (87670_CR81) 2019; 255
A Rónavári (87670_CR18) 2017; 12
S Majeed (87670_CR20) 2023; 253
S Francis (87670_CR23) 2017; 41
87670_CR32
V Castro-Aceituno (87670_CR90) 2016; 84
CA Dos Santos (87670_CR59) 2014; 103
A Behera (87670_CR91) 2021; 20
M Li (87670_CR14) 2020; 8
K Velsankar (87670_CR9) 2019; 200
S Bibi (87670_CR24) 2023; 8
HD Kabiru (87670_CR82) 2022; 8
A Zumla (87670_CR55) 2016; 16
A Zuhrotun (87670_CR46) 2023; 28
T Naseri (87670_CR7) 2020; 15
A Bouafia (87670_CR4) 2021; 18
S Ijaz (87670_CR86) 2023; 162
R Ullah (87670_CR31) 2023; 15
G Apsana (87670_CR10) 2018; 11
CS Yang (87670_CR47) 2018; 66
S Naraginti (87670_CR17) 2017; 170
ARG Ghomi (87670_CR26) 2019; 18
F Rodríguez-Félix (87670_CR65) 2021; 7
M Safarpoor (87670_CR73) 2018; 42
JS Eswari (87670_CR50) 2018; 9
S Shehensha (87670_CR79) 2020; 14
MK Rai (87670_CR60) 2012; 112
Z Ullah (87670_CR5) 2023; 15
P Dahiya (87670_CR53) 2012; 74
K Velsankar (87670_CR62) 2022; 33
87670_CR29
AM Awadelkareem (87670_CR88) 2022; 11
SV Gudkov (87670_CR39) 2022; 15
A Dziedzic (87670_CR83) 2016; 21
S Barua (87670_CR13) 2017; 17
87670_CR21
B Buszewski (87670_CR66) 2016; 506
Z Ullah (87670_CR43) 2023; 11
D Van Duin (87670_CR52) 2016; 30
K Velsankar (87670_CR45) 2020; 239
H Vahidi (87670_CR27) 2021; 124
D Dey (87670_CR54) 2015; 53
SR Lockhart (87670_CR69) 2017; 64
S Uddin (87670_CR33) 2021; 84
S Soares (87670_CR22) 2018; 6
M Wu (87670_CR3) 2020; 10
J Iqbal (87670_CR36) 2019; 6
B Ahmed (87670_CR68) 2018; 29
M Alavi (87670_CR57) 2019; 17
SA Akintelu (87670_CR63) 2019; 6
P Nisar (87670_CR75) 2019; 24
G Narasimha (87670_CR77) 2013; 7
G Franci (87670_CR58) 2015; 20
O Gotov (87670_CR1) 2018; 15
References_xml – volume: 170
  start-page: 225
  year: 2017
  ident: 87670_CR17
  publication-title: J. Photochem. Photobiol., B
  doi: 10.1016/j.jphotobiol.2017.03.023
– ident: 87670_CR80
  doi: 10.1155/2014/256919
– volume: 8
  start-page: 45750
  issue: 48
  year: 2023
  ident: 87670_CR24
  publication-title: ACS Omega
  doi: 10.1021/acsomega.3c06233
– volume: 1218
  start-page: 128490
  year: 2020
  ident: 87670_CR35
  publication-title: J. Mol. Struct.
  doi: 10.1016/j.molstruc.2020.128490
– volume: 84
  start-page: 158
  year: 2016
  ident: 87670_CR90
  publication-title: Biomed. Pharmacother.
  doi: 10.1016/j.biopha.2016.09.016
– volume: 17
  start-page: 949
  issue: 9
  year: 2022
  ident: 87670_CR67
  publication-title: Expert Opin. Drug Discov.
  doi: 10.1080/17460441.2022.2097659
– volume: 16
  start-page: 1
  year: 2018
  ident: 87670_CR40
  publication-title: J. Nanobiotechnol.
  doi: 10.1186/s12951-018-0408-4
– volume: 72
  start-page: 1154
  issue: 3
  year: 2020
  ident: 87670_CR72
  publication-title: JOM
  doi: 10.1007/s11837-019-03784-2
– volume: 21
  start-page: 365
  issue: 3
  year: 2016
  ident: 87670_CR83
  publication-title: Molecules
  doi: 10.3390/molecules21030365
– volume: 8
  start-page: 1802
  issue: 7
  year: 2020
  ident: 87670_CR14
  publication-title: Biomaterials Sci.
  doi: 10.1039/D0BM00029A
– volume: 14
  start-page: 10484
  issue: 1
  year: 2024
  ident: 87670_CR6
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-024-60694-3
– volume: 8
  start-page: 117
  issue: 5
  year: 2020
  ident: 87670_CR37
  publication-title: Biomedicines
  doi: 10.3390/biomedicines8050117
– volume: 58
  start-page: 44
  year: 2016
  ident: 87670_CR85
  publication-title: Mater. Sci. Engineering: C
  doi: 10.1016/j.msec.2015.08.022
– volume: 11
  start-page: 853
  issue: 7
  year: 2022
  ident: 87670_CR88
  publication-title: Antibiotics
  doi: 10.3390/antibiotics11070853
– volume: 20
  start-page: 2150060
  issue: 06
  year: 2021
  ident: 87670_CR91
  publication-title: Int. J. Nanosci.
  doi: 10.1142/S0219581X21500605
– volume: 134
  start-page: 109020
  year: 2021
  ident: 87670_CR25
  publication-title: Inorg. Chem. Commun.
  doi: 10.1016/j.inoche.2021.109020
– volume: 15
  start-page: 968
  issue: 8
  year: 2022
  ident: 87670_CR39
  publication-title: Pharmaceuticals
  doi: 10.3390/ph15080968
– volume: 112
  start-page: 841
  issue: 5
  year: 2012
  ident: 87670_CR60
  publication-title: J. Appl. Microbiol.
  doi: 10.1111/j.1365-2672.2012.05253.x
– volume: 162
  start-page: 114687
  year: 2023
  ident: 87670_CR86
  publication-title: Biomed. Pharmacother.
  doi: 10.1016/j.biopha.2023.114687
– volume: 109
  start-page: 385
  year: 2017
  ident: 87670_CR8
  publication-title: Energy Procedia
  doi: 10.1016/j.egypro.2017.03.035
– volume: 4
  start-page: 158
  issue: 6
  year: 2016
  ident: 87670_CR51
  publication-title: Int. J. Herb. Med.
  doi: 10.22271/flora.2016.v4.i6c.03
– volume: 42
  start-page: 76
  year: 2018
  ident: 87670_CR73
  publication-title: Ultrason. Sonochem.
  doi: 10.1016/j.ultsonch.2017.11.001
– ident: 87670_CR29
  doi: 10.1016/B978-0-323-95376-4.00012-5
– volume: 11
  start-page: 20988
  issue: 1
  year: 2021
  ident: 87670_CR38
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-021-99839-z
– volume: 6
  start-page: 115407
  issue: 11
  year: 2019
  ident: 87670_CR36
  publication-title: Mater. Res. Express
  doi: 10.1088/2053-1591/ab4f04
– volume: 5
  start-page: 523
  issue: 4
  year: 2011
  ident: 87670_CR70
  publication-title: Int. J. Appl. Sci. Biotechnol.
– volume: 10
  start-page: 2001119
  issue: 25
  year: 2020
  ident: 87670_CR3
  publication-title: Adv. Energy Mater.
  doi: 10.1002/aenm.202001119
– volume: 6
  start-page: 0850a7
  issue: 8
  year: 2019
  ident: 87670_CR30
  publication-title: Mater. Res. Express
  doi: 10.1088/2053-1591/ab23e1
– volume: 33
  start-page: 103645
  issue: 7
  year: 2022
  ident: 87670_CR62
  publication-title: Adv. Powder Technol.
  doi: 10.1016/j.apt.2022.103645
– volume: 84
  start-page: 2004
  issue: 9
  year: 2021
  ident: 87670_CR33
  publication-title: Microsc. Res. Tech.
  doi: 10.1002/jemt.23756
– volume: 230
  start-page: 1148
  year: 2019
  ident: 87670_CR16
  publication-title: J. Clean. Prod.
  doi: 10.1016/j.jclepro.2019.05.157
– volume: 12
  start-page: 871
  year: 2017
  ident: 87670_CR18
  publication-title: Int. J. Nanomed.
  doi: 10.2147/IJN.S122842
– volume: 59
  start-page: 993
  issue: 10
  year: 2021
  ident: 87670_CR76
  publication-title: Med. Mycol.
  doi: 10.1093/mmy/myab028
– volume: 66
  start-page: 512
  issue: 4
  year: 2017
  ident: 87670_CR92
  publication-title: Polym. Int.
  doi: 10.1002/pi.5304
– volume: 66
  start-page: 3063
  issue: 12
  year: 2018
  ident: 87670_CR47
  publication-title: J. Agric. Food Chem.
  doi: 10.1021/acs.jafc.7b05830
– volume: 7
  start-page: 315
  issue: 4
  year: 2020
  ident: 87670_CR28
  publication-title: Nanomed. J.
– volume: 18
  start-page: 725
  issue: 6
  year: 2021
  ident: 87670_CR4
  publication-title: Mini-Rev. Org. Chem.
  doi: 10.2174/18756298MTA5jNzYp2
– volume: 506
  start-page: 170
  year: 2016
  ident: 87670_CR66
  publication-title: Colloids Surf., a
  doi: 10.1016/j.colsurfa.2016.05.058
– volume: 64
  start-page: 134
  issue: 2
  year: 2017
  ident: 87670_CR69
  publication-title: Clin. Infecti. Dis.
  doi: 10.1093/cid/ciw691
– volume: 11
  start-page: 1069
  issue: 4
  year: 2023
  ident: 87670_CR43
  publication-title: Microorganisms
  doi: 10.3390/microorganisms11041069
– volume: 239
  start-page: 121976
  year: 2020
  ident: 87670_CR45
  publication-title: Mater. Chem. Phys.
  doi: 10.1016/j.matchemphys.2019.121976
– volume: 22
  start-page: 126
  issue: 1
  year: 2020
  ident: 87670_CR12
  publication-title: Biomacromolecules
  doi: 10.1021/acs.biomac.0c00726
– volume: 194
  start-page: 111156
  year: 2020
  ident: 87670_CR61
  publication-title: Colloids Surf. B
  doi: 10.1016/j.colsurfb.2020.111156
– ident: 87670_CR84
  doi: 10.1155/2022/3863138
– volume: 1291
  start-page: 136012
  year: 2023
  ident: 87670_CR41
  publication-title: J. Mol. Struct.
  doi: 10.1016/j.molstruc.2023.136012
– volume: 57
  start-page: 21
  year: 2017
  ident: 87670_CR56
  publication-title: Int. J. Infect. Dis.
  doi: 10.1016/j.ijid.2017.01.020
– volume: 7
  start-page: 114
  issue: 3
  year: 2013
  ident: 87670_CR77
  publication-title: J. Nanosci. Nanotechnol
– volume: 15
  start-page: 12186
  issue: 16
  year: 2023
  ident: 87670_CR31
  publication-title: Sustainability
  doi: 10.3390/su151612186
– volume: 20
  start-page: 8856
  issue: 5
  year: 2015
  ident: 87670_CR58
  publication-title: Molecules
  doi: 10.3390/molecules20058856
– volume: 139
  start-page: 4613
  issue: 18
  year: 2014
  ident: 87670_CR15
  publication-title: Analyst
  doi: 10.1039/C4AN00816B
– volume: 10
  start-page: 8
  year: 2019
  ident: 87670_CR89
  publication-title: Front. Microbiol.
  doi: 10.3389/fmicb.2019.00008
– volume: 25
  start-page: 664
  issue: 3
  year: 2011
  ident: 87670_CR87
  publication-title: Toxicol. In Vitro
  doi: 10.1016/j.tiv.2011.01.004
– volume: 200
  start-page: 111650
  year: 2019
  ident: 87670_CR9
  publication-title: J. Photochem. Photobiol., B
  doi: 10.1016/j.jphotobiol.2019.111650
– volume: 183
  start-page: 30
  year: 2018
  ident: 87670_CR64
  publication-title: J. Photochem. Photobiol., B
  doi: 10.1016/j.jphotobiol.2018.04.020
– volume: 253
  start-page: 124026
  year: 2023
  ident: 87670_CR20
  publication-title: Talanta
  doi: 10.1016/j.talanta.2022.124026
– volume: 30
  start-page: 377
  issue: 2
  year: 2016
  ident: 87670_CR52
  publication-title: Infect. Disease Clin.
– volume: 53
  start-page: 1474
  issue: 10
  year: 2015
  ident: 87670_CR54
  publication-title: Pharm. Biol.
  doi: 10.3109/13880209.2014.986687
– volume: 49
  start-page: 182
  issue: 2
  year: 2016
  ident: 87670_CR74
  publication-title: J. Microbiol. Immunol. Infect.
  doi: 10.1016/j.jmii.2014.04.013
– volume: 11
  start-page: 341
  issue: 1
  year: 2018
  ident: 87670_CR11
  publication-title: Asian J. Pharm. Clin. Res.
  doi: 10.22159/ajpcr.2018.v11i1.21999
– volume: 83
  start-page: 1308
  issue: 11
  year: 2020
  ident: 87670_CR48
  publication-title: Microsc. Res. Tech.
  doi: 10.1002/jemt.23522
– ident: 87670_CR44
  doi: 10.1007/s11356-023-25343-8
– volume: 6
  start-page: 360
  year: 2018
  ident: 87670_CR22
  publication-title: Front. Chem.
  doi: 10.3389/fchem.2018.00360
– volume: 2020
  start-page: 1215395
  issue: 1
  year: 2020
  ident: 87670_CR93
  publication-title: Oxidative Med. Cell. Longev.
– ident: 87670_CR21
  doi: 10.1016/B978-0-443-15518-5.00024-0
– volume: 9
  start-page: 045007
  issue: 4
  year: 2018
  ident: 87670_CR50
  publication-title: Adv. Nat. Sci. NanoSci. NanoTechnol.
  doi: 10.1088/2043-6254/aaec0e
– volume: 103
  start-page: 1931
  issue: 7
  year: 2014
  ident: 87670_CR59
  publication-title: J. Pharm. Sci.
  doi: 10.1002/jps.24001
– volume: 6
  start-page: 13104
  issue: 21
  year: 2014
  ident: 87670_CR2
  publication-title: Nanoscale
  doi: 10.1039/C4NR01405G
– volume: 6
  start-page: 1
  year: 2019
  ident: 87670_CR63
  publication-title: J. Nanotechnol Nanomed. Nanobiotechnol.
  doi: 10.24966/NTMB-2044/100022
– volume: 24
  start-page: 929
  year: 2019
  ident: 87670_CR75
  publication-title: J. Biol. Inorg. Chem.
  doi: 10.1007/s00775-019-01717-7
– volume: 15
  start-page: 4668
  issue: 10
  year: 2018
  ident: 87670_CR1
  publication-title: Mol. Pharm.
  doi: 10.1021/acs.molpharmaceut.8b00640
– volume: 16
  start-page: e47
  issue: 4
  year: 2016
  ident: 87670_CR55
  publication-title: Lancet. Infect. Dis
  doi: 10.1016/S1473-3099(16)00078-5
– volume: 10
  start-page: 952006
  year: 2022
  ident: 87670_CR49
  publication-title: Front. Chem.
  doi: 10.3389/fchem.2022.952006
– volume: 15
  start-page: 907
  issue: 4
  year: 2020
  ident: 87670_CR7
  publication-title: Plasmonics
  doi: 10.1007/s11468-019-01101-w
– volume: 15
  start-page: 12783
  issue: 17
  year: 2023
  ident: 87670_CR5
  publication-title: Sustainability
  doi: 10.3390/su151712783
– volume: 11
  start-page: 384
  year: 2018
  ident: 87670_CR10
  publication-title: Asian J. Pharm. Clin. Res.
  doi: 10.22159/ajpcr.2018.v11i3.20858
– volume: 192
  start-page: 52
  year: 2016
  ident: 87670_CR78
  publication-title: Microbiol. Res.
  doi: 10.1016/j.micres.2016.06.004
– volume: 29
  start-page: 1601
  issue: 7
  year: 2018
  ident: 87670_CR68
  publication-title: Adv. Powder Technol.
  doi: 10.1016/j.apt.2018.03.025
– volume: 74
  start-page: 443
  issue: 5
  year: 2012
  ident: 87670_CR53
  publication-title: Indian J. Pharm. Sci.
  doi: 10.4103/0250-474X.108420
– volume: 28
  start-page: 3240
  issue: 7
  year: 2023
  ident: 87670_CR46
  publication-title: Molecules
  doi: 10.3390/molecules28073240
– volume: 41
  start-page: 14288
  issue: 23
  year: 2017
  ident: 87670_CR23
  publication-title: New J. Chem.
  doi: 10.1039/C7NJ02453C
– volume: 3
  start-page: 229
  year: 2013
  ident: 87670_CR42
  publication-title: Appl. Nanosci.
  doi: 10.1007/s13204-012-0125-5
– volume: 17
  start-page: 419
  issue: 6
  year: 2019
  ident: 87670_CR57
  publication-title: Expert Rev. anti-infective Therapy
  doi: 10.1080/14787210.2019.1614914
– volume: 255
  start-page: 113358
  year: 2019
  ident: 87670_CR81
  publication-title: Environ. Pollut.
  doi: 10.1016/j.envpol.2019.113358
– volume: 9
  start-page: 1
  issue: 1
  year: 2017
  ident: 87670_CR71
  publication-title: Biology Med.
  doi: 10.4172/0974-8369.1000363
– volume: 8
  start-page: 9
  issue: 4
  year: 2022
  ident: 87670_CR82
  publication-title: Int. J. Sci. Global Sustain.
– volume: 17
  start-page: 968
  issue: 2
  year: 2017
  ident: 87670_CR13
  publication-title: J. Nanosci. Nanotechnol.
  doi: 10.1166/jnn.2017.12636
– volume: 7
  start-page: e06923
  issue: 4
  year: 2021
  ident: 87670_CR65
  publication-title: Heliyon
  doi: 10.1016/j.heliyon.2021.e06923
– volume: 1199
  start-page: 126979
  year: 2020
  ident: 87670_CR34
  publication-title: J. Mol. Struct.
  doi: 10.1016/j.molstruc.2019.126979
– volume: 14
  start-page: 2075
  issue: 3
  year: 2020
  ident: 87670_CR79
  publication-title: J. Pure Appl. Microbiol.
  doi: 10.22207/JPAM.14.3.48
– volume: 124
  start-page: 108385
  year: 2021
  ident: 87670_CR27
  publication-title: Inorg. Chem. Commun.
  doi: 10.1016/j.inoche.2020.108385
– ident: 87670_CR32
  doi: 10.1016/B978-0-323-46139-9.00001-3
– volume: 53
  start-page: 102870
  year: 2023
  ident: 87670_CR19
  publication-title: Biocatal. Agric. Biotechnol.
  doi: 10.1016/j.bcab.2023.102870
– volume: 18
  start-page: 2101
  issue: 4
  year: 2019
  ident: 87670_CR26
  publication-title: Iran. J. Pharm. Research: IJPR
SSID ssj0000529419
Score 2.4457402
Snippet One of the popular subjects of millennia is the synthesis of nanostructures, their applications in numerous fields, and their interaction with various...
Abstract One of the popular subjects of millennia is the synthesis of nanostructures, their applications in numerous fields, and their interaction with various...
SourceID doaj
pubmedcentral
proquest
pubmed
crossref
springer
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Publisher
StartPage 13466
SubjectTerms 631/449
631/45
Animals
Anti-Infective Agents - chemistry
Anti-Infective Agents - pharmacology
Anticancer
Antimicrobial
Antimicrobial activity
Antimicrobial agents
Antineoplastic Agents - chemistry
Antineoplastic Agents - pharmacology
Antioxidants
Antioxidants - chemistry
Antioxidants - pharmacology
Artemia - drug effects
Bacteria - drug effects
Biocompatibility
Biosynthesis
Cancer
Cell lines
Chlorocebus aethiops
Clinical trials
Crystals
Cytotoxic
Cytotoxicity
Drug delivery
Drug delivery systems
E. sativa
Green Chemistry Technology
HEK293 Cells
Humanities and Social Sciences
Humans
Metal Nanoparticles - chemistry
Microbial Sensitivity Tests
multidisciplinary
Nanoparticles
Oxides - chemistry
Oxides - pharmacology
Plant Extracts - chemistry
Plant Extracts - pharmacology
Science
Science (multidisciplinary)
Silver
Silver Compounds - chemistry
Silver Compounds - pharmacology
Silver oxide nanoparticles
Strains (organisms)
Ultraviolet spectroscopy
Vero Cells
Zeta potential
SummonAdditionalLinks – databaseName: DOAJ Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3daxQxEA9SEHwRv11bJYJvujSfu8mjypVSqE8W-hZySRYPJCvutXj_fWeSvbPnB774mmyWJDPJ_IbM_IaQN14zAV5AaC3zqVXR29bzAI5rSJaZJWhMqUVw_qk7vVBnl_ryVqkvjAmr9MB1445DBEwDPooGU6fAXPmQ5FLG2HMxGGjA2xds3i1nqrJ6C6u4nbNkmDTHE1gqzCYTGi-AnrV2zxIVwv4_oczfgyV_eTEthujkAbk_I0j6vs78IbmT8iNyt9aU3Dwm60UYByQvjl83dNpkAHjTaqJhR8xc8y6pz5FWBiYUE8X8huvCrkrHgS5A4p5ioM-1pyW5BIApnVYYRk3HH6uYaPYZ_O05rO4JuThZfP542s6lFdqgrFq3AwtYoCZ0SgPk6YzomR1gjcteRBsHbyIPvQrIjd91WqbojZLRCnCAgvY-yKfkII85PScUjnSw3ssO_qlYUsZqhCGG6yEJ1bGGvN1us_tWGTRcefmWxlWhOBCKK0JxtiEfUBK7L5H9ujSATrh5Ue5fOtGQo60c3XwkJyeRyQ5fSXlDXu-64TDhC4nPabyq33TcAAxtyLMq9t1MFHpjQsBos6cQe1Pd78mrL4Wwm2OQieIw9N1Wd37O6-978eJ_7MUhuSdQ6ZGe0hyRg_X3q_QScNR6-aocmRu9nhiU
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: Springer Nature OA Free Journals
  dbid: C6C
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1Lb9QwELZKERIX1PJMH8hI3CDCduzEPpbVVhUSnKjUm-W1HVgJOVWzrdh_z4zzQAvlwDW2I9szE3-TmflMyFunmAAvwJeGuVjK4EzpuAfH1UfD9Ao0Jt9F8PlLfXEpP12pqz0iplqYnLSfKS3zZ3rKDvvQw0GDxWBCof02rDQPyEOkbketXtSL-b8KRq4kN2N9DKv0PUN3zqBM1X8fvvw7TfKPWGk-gs4PyJMRO9KzYbaHZC-mp-TRcJvk9hnZLH3XIm1x-LGl_TYBtOvXPfUzJfNQcUldCnTgXkIBUaxsuMu8qrRr6RJk7Sim-Nw5mstKAJLSfo0J1LT7uQ6RJpfA0x637Dm5PF9-XVyU46UKpZdGbsqWebyaxtdSAdiptWiYaWGNq0YEE1qnA_eN9Hlra1XF4LSsghHg-njlnK9ekP3UpfiKUDBmb5yraninZFFqoxCAaK7aKGTNCvJu2mZ7PXBn2BzzrrQdhGJBKDYLxZqCfERJzD2R9zo_6G6-2XFR1gdAuOCxKgA-EsCL87FaVSE0XLQaHhTkZJKjHY2xtxVy2GF8lBfkzdwMZoSxEZdidzv0qbkGAFqQl4PY55lI9MOEgNF6RyF2prrbktbfM1U3x_QSyWHo-0l3fs_r33tx9H_dj8ljgeqNFJT6hOxvbm7jKWClzep1No5f0FIPIw
  priority: 102
  providerName: Springer Nature
Title Ecofriendly synthesis characterization and biological activities of Eruca sativa mediated silver oxide nanoparticles
URI https://link.springer.com/article/10.1038/s41598-025-87670-9
https://www.ncbi.nlm.nih.gov/pubmed/40251221
https://www.proquest.com/docview/3191481661
https://www.proquest.com/docview/3191618085
https://pubmed.ncbi.nlm.nih.gov/PMC12008411
https://doaj.org/article/cd08010757434820ace3b3dd712f8482
Volume 15
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3da9swEBdby2Avo92nuzZosLfN1JZlWXoqaUgpgZWxrZA3oUjyGhh2V6el-e93Jysu2deTQf5A8p2k3-nufkfIe1NmDKwAm6rM-JQ7o1KTWzBcrVeZXIDGhFoEny7E-SWfzct5PHDrYljlZk0MC7VrLZ6RHxdIRIZOrvzk-meKVaPQuxpLaDwmu0hdhiFd1bwazljQi8VzFXNlskIed7BfYU4ZK3EZqLJUbe1Hgbb_b1jzz5DJ3_ymYTs62yPPIo6k417w--SRb56TJ31lyfULspratkYKY_djTbt1AzCvW3bUDvTMffYlNY2jPQ8TCotilsNd4FilbU2nIHdDMdznztCQYgLwlHZLDKam7f3SedqYBqzuGFz3klyeTb9NztNYYCG1XPFVWmcWy9RYwUsAPkKyKlM1jHFRMadcbaTLbcUtMuQLURbeGckLpxiYQbY0xhavyE7TNv4NoTCxrTKmEPBNnnkuVYlgROZl7RkXWUI-bH6zvu55NHTwfxdS90LRIBQdhKJVQk5REsOTyIEdGtqb7zoOSlsHaBes1xJAEAcgY6wvFoVzVc5qCQ0JOdzIUceJ2ekHNUrIu-E2TCn0k5jGt7f9MyKXAEYT8roX-9ATjjYZY_C23FKIra5u32mWV4G2O8dQE57Dqx83uvPQr3__i4P_D-MtecpQnZF-Uh6SndXNrT8CnLRajMJkGJHd8Xj2dQbX0-nF5y_QOhGTUTh7-AU2iRYp
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwEB6VrRBcEG8CBYwEJ4iaOE5iHxCisNWWtiuEWqk312s7sBJKSrMt7J_iNzKTV7W8br3mJcczHn_jmfkG4LlJI45egA1VZHwonFGhiS06rtarSM5QY5peBPvTbHIoPhylR2vws6-FobTK3iY2htpVls7INxMiIqMgV_zm5FtIXaMoutq30GjVYtcvv6PLVr_eeY_yfcH59vjg3STsugqEViixCIvIUm8Wm4kUd_tM8jxShXd2lnOnXGGki20uLNHCZ1maeGekSJziiP1taoxN8LtXYF0k6MqMYH1rPP34aTjVobiZiFVXnRMlcrPGHZKq2HhKhiePQrWyAzaNAv6Gbv9M0vwtUttsgNs34UaHXNnbVtVuwZovb8PVtpfl8g4sxrYqiDTZfV2yelkisKznNbMDIXRb78lM6VjL_ETqwaiu4rxhdWVVwcaoaYZRgtG5YU1RCwJiVs8pfZtVP-bOs9KU6Od36Xx34fBSJv8ejMqq9A-AoSmxypgkw2-KyAupUoI_Mk4Lz0UWBfCyn2Z90jJ36CbinkjdCkWjUHQjFK0C2CJJDE8S63ZzoTr9rLuf0tYhvkZ_OUXYJRA6GeuTWeJcHvNC4oUANno56s4U1PpCcQN4NtzGRUyRGVP66qx9Joslwt8A7rdiH0YiyAvkHN-WKwqxMtTVO-X8S0MUHlNyi4jx1Ve97lyM699z8fD_v_EUrk0O9vf03s509xFc56TaRH4pN2C0OD3zjxGlLWZPuqXB4PiyV-MvunVPEg
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwELZKEagXxJtAASPBCaJN_EjsA0JAd9VSqDhQaW_GazuwUpWUZlvYv8avY8ZJtlpet17zkuOZsb_xzHxDyFMrMwZegEt1ZkMqvNWpzR04ri7oTM1AY2Ivgg8Hxe6heDeV0w3yc6iFwbTKYU2MC7VvHJ6RjzgSkWGQKx9VfVrEx53Jq-NvKXaQwkjr0E6jU5H9sPwO7lv7cm8HZP2Mscn409vdtO8wkDqhxSKtMod9WlwhJOz8hWJlpqvg3axkXvvKKp-7UjikiC8KyYO3SnCvGfgBTlrrOHz3ErlccpmjjZXTcnW-gxE0keu-TifjatTCXon1bEziElRmqV7bC2PLgL_h3D_TNX-L2catcHKdXOsxLH3dKd0NshHqm-RK19VyeYssxq6pkD7ZHy1pu6wBYrbzlroVNXRX-Ult7WnHAYWKQrHC4izyu9KmomPQOUsx1ejM0ljeAtCYtnNM5KbNj7kPtLY1ePx9Yt9tcnghU3-HbNZNHe4RCouK09byAr4psiCUlgiEVC6rwESRJeT5MM3muOPwMDH2zpXphGJAKCYKxeiEvEFJrJ5E_u14oTn5YvqfMs4D0gbPWQIAEwCirAt8xr0vc1YpuJCQ7UGOpl8UWnOuwgl5sroN5owxGluH5rR7psgVAOGE3O3EvhqJQH-QMXhbrSnE2lDX79Tzr5EyPMc0F5HDqy8G3Tkf17_n4v7_f-MxuQo2aN7vHew_IFsMNRtZMNU22VycnIaHANcWs0fRLij5fNGG-AucVVHi
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=Ecofriendly+synthesis+characterization+and+biological+activities+of+Eruca+sativa+mediated+silver+oxide+nanoparticles&rft.jtitle=Scientific+reports&rft.date=2025-04-18&rft.pub=Nature+Publishing+Group&rft.eissn=2045-2322&rft.volume=15&rft.issue=1&rft.spage=13466&rft_id=info:doi/10.1038%2Fs41598-025-87670-9&rft.externalDBID=HAS_PDF_LINK
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2045-2322&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2045-2322&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2045-2322&client=summon