A histomorphometric study to evaluate the therapeutic effects of biosynthesized silver nanoparticles on the kidneys infected with Plasmodium chabaudi

The study aimed to verify the pathogenic malarial kidney infections and histopathological pictures in mice infected with using leaf extract silver nanoparticles (IOLEAgNPs). Fifty healthy adult female mice C57BL/6 were used. Animals were divided into five groups, with each group of ten mice. The fir...

Full description

Saved in:
Bibliographic Details
Published inOpen life sciences Vol. 19; no. 1; pp. 20220968 - 34
Main Authors Murshed, Mutee, Al-Tamimi, Jameel, Ibrahim, Khalid Elfaki, Al-Quraishy, Saleh
Format Journal Article
LanguageEnglish
Published Poland De Gruyter 01.01.2024
Subjects
Online AccessGet full text
ISSN2391-5412
2391-5412
DOI10.1515/biol-2022-0968

Cover

Abstract The study aimed to verify the pathogenic malarial kidney infections and histopathological pictures in mice infected with using leaf extract silver nanoparticles (IOLEAgNPs). Fifty healthy adult female mice C57BL/6 were used. Animals were divided into five groups, with each group of ten mice. The first control non-infected group was given distilled water for 7 days. The second group was orally given 50 mg/kg of IOLEAgNPs. The third, fourth, and fifth groups were injected intraperitoneally with 10 parasitized erythrocytes of . After 1 h, the fourth group received 50 mg/kg of IOLEAgNPs, while the fifth group orally received 10 mg/kg chloroquine phosphate. The histopathology of the kidney was studied by routine histology method with hematoxylin–eosin staining. The kidney revealed cerebral microvessel congestion, hemorrhages, and necrosis. Cast formation, glomerulonephritis, tubular necrosis, and congestion were observed in the kidney cortex. Consequently, the targeted medical IOLEAgNPs reduced this degeneration impact on renal tissue. Proven that plant-source synthesized IOLEAgNPs play a preventive role as antimalarial agents in female mice infected with
AbstractList The study aimed to verify the pathogenic malarial kidney infections and histopathological pictures in mice infected with Plasmodium chabaudi using Indigofera oblongifolia leaf extract silver nanoparticles (IOLEAgNPs). Fifty healthy adult female mice C57BL/6 were used. Animals were divided into five groups, with each group of ten mice. The first control non-infected group was given distilled water for 7 days. The second group was orally given 50 mg/kg of IOLEAgNPs. The third, fourth, and fifth groups were injected intraperitoneally with 10 5 parasitized erythrocytes of P. chabaudi . After 1 h, the fourth group received 50 mg/kg of IOLEAgNPs, while the fifth group orally received 10 mg/kg chloroquine phosphate. The histopathology of the kidney was studied by routine histology method with hematoxylin–eosin staining. The kidney revealed cerebral microvessel congestion, hemorrhages, and necrosis. Cast formation, glomerulonephritis, tubular necrosis, and congestion were observed in the kidney cortex. Consequently, the targeted medical IOLEAgNPs reduced this degeneration impact on renal tissue. Proven that plant-source synthesized IOLEAgNPs play a preventive role as antimalarial agents in female mice infected with P. chabaudi.
The study aimed to verify the pathogenic malarial kidney infections and histopathological pictures in mice infected with Plasmodium chabaudi using Indigofera oblongifolia leaf extract silver nanoparticles (IOLEAgNPs). Fifty healthy adult female mice C57BL/6 were used. Animals were divided into five groups, with each group of ten mice. The first control non-infected group was given distilled water for 7 days. The second group was orally given 50 mg/kg of IOLEAgNPs. The third, fourth, and fifth groups were injected intraperitoneally with 105 parasitized erythrocytes of P. chabaudi. After 1 h, the fourth group received 50 mg/kg of IOLEAgNPs, while the fifth group orally received 10 mg/kg chloroquine phosphate. The histopathology of the kidney was studied by routine histology method with hematoxylin–eosin staining. The kidney revealed cerebral microvessel congestion, hemorrhages, and necrosis. Cast formation, glomerulonephritis, tubular necrosis, and congestion were observed in the kidney cortex. Consequently, the targeted medical IOLEAgNPs reduced this degeneration impact on renal tissue. Proven that plant-source synthesized IOLEAgNPs play a preventive role as antimalarial agents in female mice infected with P. chabaudi.
The study aimed to verify the pathogenic malarial kidney infections and histopathological pictures in mice infected with using leaf extract silver nanoparticles (IOLEAgNPs). Fifty healthy adult female mice C57BL/6 were used. Animals were divided into five groups, with each group of ten mice. The first control non-infected group was given distilled water for 7 days. The second group was orally given 50 mg/kg of IOLEAgNPs. The third, fourth, and fifth groups were injected intraperitoneally with 10 parasitized erythrocytes of . After 1 h, the fourth group received 50 mg/kg of IOLEAgNPs, while the fifth group orally received 10 mg/kg chloroquine phosphate. The histopathology of the kidney was studied by routine histology method with hematoxylin-eosin staining. The kidney revealed cerebral microvessel congestion, hemorrhages, and necrosis. Cast formation, glomerulonephritis, tubular necrosis, and congestion were observed in the kidney cortex. Consequently, the targeted medical IOLEAgNPs reduced this degeneration impact on renal tissue. Proven that plant-source synthesized IOLEAgNPs play a preventive role as antimalarial agents in female mice infected with
The study aimed to verify the pathogenic malarial kidney infections and histopathological pictures in mice infected with Plasmodium chabaudi using Indigofera oblongifolia leaf extract silver nanoparticles (IOLEAgNPs). Fifty healthy adult female mice C57BL/6 were used. Animals were divided into five groups, with each group of ten mice. The first control non-infected group was given distilled water for 7 days. The second group was orally given 50 mg/kg of IOLEAgNPs. The third, fourth, and fifth groups were injected intraperitoneally with 105 parasitized erythrocytes of P. chabaudi. After 1 h, the fourth group received 50 mg/kg of IOLEAgNPs, while the fifth group orally received 10 mg/kg chloroquine phosphate. The histopathology of the kidney was studied by routine histology method with hematoxylin-eosin staining. The kidney revealed cerebral microvessel congestion, hemorrhages, and necrosis. Cast formation, glomerulonephritis, tubular necrosis, and congestion were observed in the kidney cortex. Consequently, the targeted medical IOLEAgNPs reduced this degeneration impact on renal tissue. Proven that plant-source synthesized IOLEAgNPs play a preventive role as antimalarial agents in female mice infected with P. chabaudi.The study aimed to verify the pathogenic malarial kidney infections and histopathological pictures in mice infected with Plasmodium chabaudi using Indigofera oblongifolia leaf extract silver nanoparticles (IOLEAgNPs). Fifty healthy adult female mice C57BL/6 were used. Animals were divided into five groups, with each group of ten mice. The first control non-infected group was given distilled water for 7 days. The second group was orally given 50 mg/kg of IOLEAgNPs. The third, fourth, and fifth groups were injected intraperitoneally with 105 parasitized erythrocytes of P. chabaudi. After 1 h, the fourth group received 50 mg/kg of IOLEAgNPs, while the fifth group orally received 10 mg/kg chloroquine phosphate. The histopathology of the kidney was studied by routine histology method with hematoxylin-eosin staining. The kidney revealed cerebral microvessel congestion, hemorrhages, and necrosis. Cast formation, glomerulonephritis, tubular necrosis, and congestion were observed in the kidney cortex. Consequently, the targeted medical IOLEAgNPs reduced this degeneration impact on renal tissue. Proven that plant-source synthesized IOLEAgNPs play a preventive role as antimalarial agents in female mice infected with P. chabaudi.
Author Al-Quraishy, Saleh
Al-Tamimi, Jameel
Murshed, Mutee
Ibrahim, Khalid Elfaki
Author_xml – sequence: 1
  givenname: Mutee
  orcidid: 0000-0003-3717-6424
  surname: Murshed
  fullname: Murshed, Mutee
  email: mmurshed@ksu.edu.sa
  organization: Department of Zoology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia
– sequence: 2
  givenname: Jameel
  orcidid: 0000-0001-9022-2448
  surname: Al-Tamimi
  fullname: Al-Tamimi, Jameel
  email: jtamimi@ksu.edu.sa
  organization: Department of Zoology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia
– sequence: 3
  givenname: Khalid Elfaki
  orcidid: 0000-0002-3617-4876
  surname: Ibrahim
  fullname: Ibrahim, Khalid Elfaki
  email: kibrahim@ksu.edu.sa
  organization: Department of Zoology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia
– sequence: 4
  givenname: Saleh
  orcidid: 0000-0003-4204-3124
  surname: Al-Quraishy
  fullname: Al-Quraishy, Saleh
  email: squrishi@ksu.edu.sa
  organization: Department of Zoology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia
BackLink https://www.ncbi.nlm.nih.gov/pubmed/39450309$$D View this record in MEDLINE/PubMed
BookMark eNp1ks1u1DAUhSNUREvpliXykk2KfzPxClVVgUqVYAFry7GvJx6SeLCdVsN78L44M0PVLlhYtny_c66te15XJ1OYoKreEnxJBBEfOh-GmmJKayyb9kV1RpkkteCEnjw5n1YXKW0wxkRwKnDzqjplkgvMsDyr_lyh3qccxhC3fRghR29QyrPdoRwQ3Oth1hlQ7vcr6i3MuRDgHJicUHCoPCLtplJM_jdYlPxwDxFNegpbHQs7QMGmvcNPbyfYJeSnRV3gB5979G3QaQzWzyMyve70bP2b6qXTQ4KL435e_fh08_36S3339fPt9dVdbXhDc02ZaTBwLAwYK51hxHYrZzCsOgoNuA5L1hgtZLuylBqQwlLJqCANF67pGDuvbg--NuiN2kY_6rhTQXu1vwhxrY5_UIw7xpkDDm3LmSbS4tKtNc5y56zhxevjwWs7dyNYA1OOenhm-rwy-V6tw70iRGAs6Ko4vD86xPBrhpTV6JOBYdAThDkpRigWckXbBX33tNljl3-DLcDlATAxpBTBPSIEqyU8agmPWsKjlvAUgTwIHvSQIVpYx3lXDmoT5jiVIfxHSCRhfwE1edAm
Cites_doi 10.1007/978-3-030-74786-2_27-1
10.1016/j.colsurfb.2013.06.036
10.1016/j.pt.2011.01.002
10.1021/acsbiomaterials.0c01420
10.1016/j.phyplu.2022.100361
10.1007/978-1-4939-9777-0_6
10.1016/B978-0-7020-4226-3.00010-X
10.3390/molecules27051484
10.1186/s12882-021-02428-5
10.14202/vetworld.2017.790-797
10.1007/s00424-022-02696-6
10.5455/ijlr.20201105055839
10.1186/s12989-016-0124-x
10.21608/eajbsd.2021.185127
10.1007/s12668-019-00612-4
10.1016/j.sjbs.2020.12.014
10.21608/ejfsat.2019.12218.1070
10.1016/S0140-6736(16)32064-5
10.1080/01926230252824761
10.1371/journal.pone.0293037
10.1016/j.jep.2020.112608
10.1016/j.micpath.2020.104590
10.1136/bmjopen-2019-029053
10.1186/s12936-017-1775-2
10.1371/journal.ppat.1004558
10.1007/s11356-020-10027-4
10.1186/s12936-015-0812-2
10.1016/j.phymed.2008.06.008
10.1186/s12906-017-1841-x
ContentType Journal Article
Copyright 2024 the author(s), published by De Gruyter.
2024 the author(s), published by De Gruyter 2024 the author(s), published by De Gruyter
Copyright_xml – notice: 2024 the author(s), published by De Gruyter.
– notice: 2024 the author(s), published by De Gruyter 2024 the author(s), published by De Gruyter
DBID AAYXX
CITATION
NPM
7X8
5PM
DOA
DOI 10.1515/biol-2022-0968
DatabaseName CrossRef
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList

PubMed

CrossRef
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  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 Biology
EISSN 2391-5412
EndPage 34
ExternalDocumentID oai_doaj_org_article_34f343fe4e8843a19d01db8cfd4ffdc4
PMC11500527
39450309
10_1515_biol_2022_0968
10_1515_biol_2022_0968191
Genre Journal Article
GroupedDBID 5VS
AAFWJ
ABFKT
ACGFS
ADBBV
AENEX
AFBDD
AFPKN
AHGSO
ALMA_UNASSIGNED_HOLDINGS
BCNDV
EBS
ECGQY
GROUPED_DOAJ
KQ8
M~E
PGMZT
QD8
RPM
Y2W
AAYXX
CITATION
M48
SLJYH
AIKXB
EJD
IPNFZ
NPM
RIG
7X8
5PM
ID FETCH-LOGICAL-c462t-23c60e405cecd9fc31db7fc0e7b2e6efb0936ca5987d22ce95d293251645f6b33
IEDL.DBID DOA
ISSN 2391-5412
IngestDate Wed Aug 27 01:30:21 EDT 2025
Thu Aug 21 18:30:51 EDT 2025
Thu Jul 10 17:31:58 EDT 2025
Thu Apr 03 07:02:41 EDT 2025
Tue Aug 19 06:03:31 EDT 2025
Sat Sep 06 16:59:13 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords biosynthesized
glomerulonephritis
tubular necrosis
kidney cortex
Language English
License This work is licensed under the Creative Commons Attribution 4.0 International License.
http://creativecommons.org/licenses/by/4.0
2024 the author(s), published by De Gruyter.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c462t-23c60e405cecd9fc31db7fc0e7b2e6efb0936ca5987d22ce95d293251645f6b33
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0003-3717-6424
0000-0001-9022-2448
0000-0002-3617-4876
0000-0003-4204-3124
OpenAccessLink https://doaj.org/article/34f343fe4e8843a19d01db8cfd4ffdc4
PMID 39450309
PQID 3120597287
PQPubID 23479
PageCount 10
ParticipantIDs doaj_primary_oai_doaj_org_article_34f343fe4e8843a19d01db8cfd4ffdc4
pubmedcentral_primary_oai_pubmedcentral_nih_gov_11500527
proquest_miscellaneous_3120597287
pubmed_primary_39450309
crossref_primary_10_1515_biol_2022_0968
walterdegruyter_journals_10_1515_biol_2022_0968191
PublicationCentury 2000
PublicationDate 2024-01-01
PublicationDateYYYYMMDD 2024-01-01
PublicationDate_xml – month: 01
  year: 2024
  text: 2024-01-01
  day: 01
PublicationDecade 2020
PublicationPlace Poland
PublicationPlace_xml – name: Poland
PublicationTitle Open life sciences
PublicationTitleAlternate Open Life Sci
PublicationYear 2024
Publisher De Gruyter
Publisher_xml – name: De Gruyter
References 2024102314180588168_j_biol-2022-0968_ref_021
2024102314180588168_j_biol-2022-0968_ref_020
2024102314180588168_j_biol-2022-0968_ref_001
2024102314180588168_j_biol-2022-0968_ref_023
2024102314180588168_j_biol-2022-0968_ref_022
2024102314180588168_j_biol-2022-0968_ref_003
2024102314180588168_j_biol-2022-0968_ref_025
2024102314180588168_j_biol-2022-0968_ref_002
2024102314180588168_j_biol-2022-0968_ref_024
2024102314180588168_j_biol-2022-0968_ref_005
2024102314180588168_j_biol-2022-0968_ref_027
2024102314180588168_j_biol-2022-0968_ref_004
2024102314180588168_j_biol-2022-0968_ref_026
2024102314180588168_j_biol-2022-0968_ref_007
2024102314180588168_j_biol-2022-0968_ref_029
2024102314180588168_j_biol-2022-0968_ref_006
2024102314180588168_j_biol-2022-0968_ref_028
2024102314180588168_j_biol-2022-0968_ref_009
2024102314180588168_j_biol-2022-0968_ref_008
2024102314180588168_j_biol-2022-0968_ref_030
2024102314180588168_j_biol-2022-0968_ref_010
2024102314180588168_j_biol-2022-0968_ref_032
2024102314180588168_j_biol-2022-0968_ref_031
2024102314180588168_j_biol-2022-0968_ref_012
2024102314180588168_j_biol-2022-0968_ref_034
2024102314180588168_j_biol-2022-0968_ref_011
2024102314180588168_j_biol-2022-0968_ref_033
2024102314180588168_j_biol-2022-0968_ref_014
2024102314180588168_j_biol-2022-0968_ref_013
2024102314180588168_j_biol-2022-0968_ref_016
2024102314180588168_j_biol-2022-0968_ref_015
2024102314180588168_j_biol-2022-0968_ref_018
2024102314180588168_j_biol-2022-0968_ref_017
2024102314180588168_j_biol-2022-0968_ref_019
References_xml – ident: 2024102314180588168_j_biol-2022-0968_ref_006
  doi: 10.1007/978-3-030-74786-2_27-1
– ident: 2024102314180588168_j_biol-2022-0968_ref_016
  doi: 10.1016/j.colsurfb.2013.06.036
– ident: 2024102314180588168_j_biol-2022-0968_ref_026
– ident: 2024102314180588168_j_biol-2022-0968_ref_001
– ident: 2024102314180588168_j_biol-2022-0968_ref_002
  doi: 10.1016/j.pt.2011.01.002
– ident: 2024102314180588168_j_biol-2022-0968_ref_019
  doi: 10.1021/acsbiomaterials.0c01420
– ident: 2024102314180588168_j_biol-2022-0968_ref_012
  doi: 10.1016/j.phyplu.2022.100361
– ident: 2024102314180588168_j_biol-2022-0968_ref_007
  doi: 10.1007/978-1-4939-9777-0_6
– ident: 2024102314180588168_j_biol-2022-0968_ref_024
  doi: 10.1016/B978-0-7020-4226-3.00010-X
– ident: 2024102314180588168_j_biol-2022-0968_ref_014
  doi: 10.3390/molecules27051484
– ident: 2024102314180588168_j_biol-2022-0968_ref_028
  doi: 10.1186/s12882-021-02428-5
– ident: 2024102314180588168_j_biol-2022-0968_ref_004
  doi: 10.14202/vetworld.2017.790-797
– ident: 2024102314180588168_j_biol-2022-0968_ref_008
  doi: 10.1007/s00424-022-02696-6
– ident: 2024102314180588168_j_biol-2022-0968_ref_011
– ident: 2024102314180588168_j_biol-2022-0968_ref_025
  doi: 10.5455/ijlr.20201105055839
– ident: 2024102314180588168_j_biol-2022-0968_ref_009
  doi: 10.1186/s12989-016-0124-x
– ident: 2024102314180588168_j_biol-2022-0968_ref_010
  doi: 10.21608/eajbsd.2021.185127
– ident: 2024102314180588168_j_biol-2022-0968_ref_021
  doi: 10.1007/s12668-019-00612-4
– ident: 2024102314180588168_j_biol-2022-0968_ref_030
  doi: 10.1016/j.sjbs.2020.12.014
– ident: 2024102314180588168_j_biol-2022-0968_ref_033
  doi: 10.21608/ejfsat.2019.12218.1070
– ident: 2024102314180588168_j_biol-2022-0968_ref_027
– ident: 2024102314180588168_j_biol-2022-0968_ref_031
– ident: 2024102314180588168_j_biol-2022-0968_ref_015
  doi: 10.1016/S0140-6736(16)32064-5
– ident: 2024102314180588168_j_biol-2022-0968_ref_023
  doi: 10.1080/01926230252824761
– ident: 2024102314180588168_j_biol-2022-0968_ref_032
  doi: 10.1371/journal.pone.0293037
– ident: 2024102314180588168_j_biol-2022-0968_ref_029
  doi: 10.1016/j.jep.2020.112608
– ident: 2024102314180588168_j_biol-2022-0968_ref_018
  doi: 10.1016/j.micpath.2020.104590
– ident: 2024102314180588168_j_biol-2022-0968_ref_034
  doi: 10.1136/bmjopen-2019-029053
– ident: 2024102314180588168_j_biol-2022-0968_ref_003
  doi: 10.1186/s12936-017-1775-2
– ident: 2024102314180588168_j_biol-2022-0968_ref_005
  doi: 10.1371/journal.ppat.1004558
– ident: 2024102314180588168_j_biol-2022-0968_ref_017
  doi: 10.1007/s11356-020-10027-4
– ident: 2024102314180588168_j_biol-2022-0968_ref_022
  doi: 10.1186/s12936-015-0812-2
– ident: 2024102314180588168_j_biol-2022-0968_ref_013
  doi: 10.1016/j.phymed.2008.06.008
– ident: 2024102314180588168_j_biol-2022-0968_ref_020
  doi: 10.1186/s12906-017-1841-x
SSID ssj0001542506
Score 2.308113
Snippet The study aimed to verify the pathogenic malarial kidney infections and histopathological pictures in mice infected with using leaf extract silver...
The study aimed to verify the pathogenic malarial kidney infections and histopathological pictures in mice infected with Plasmodium chabaudi using Indigofera...
The study aimed to verify the pathogenic malarial kidney infections and histopathological pictures in mice infected with Plasmodium chabaudi using Indigofera...
SourceID doaj
pubmedcentral
proquest
pubmed
crossref
walterdegruyter
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Publisher
StartPage 20220968
SubjectTerms biosynthesized
glomerulonephritis
kidney cortex
tubular necrosis
Title A histomorphometric study to evaluate the therapeutic effects of biosynthesized silver nanoparticles on the kidneys infected with Plasmodium chabaudi
URI https://www.degruyter.com/doi/10.1515/biol-2022-0968
https://www.ncbi.nlm.nih.gov/pubmed/39450309
https://www.proquest.com/docview/3120597287
https://pubmed.ncbi.nlm.nih.gov/PMC11500527
https://doaj.org/article/34f343fe4e8843a19d01db8cfd4ffdc4
Volume 19
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Li9UwFA4yILgZfNsZlQiCqzK5SZo2y1EcBhfiwoHZhTydIjeVaYtc_8f8X0-S3uFeH7hx25Q0Od9J853k5AtCrzvrLXC2UBvLZc0b3dYwCZLaOukk01KEkLN8P4rzC_7hsrncueor5YQVeeBiuBPGA-MseO67jjO9ko6snOlscDwEZ7MSKJFkJ5gq54PBF4lYVBphzj5JmkbgEhB6AWnv9mahLNb_J4b5e6Lk4fe8ie38l-t5M203TfNcdHYfHS4kEp-Wxj9Ad3x8iO6WayU3j9DNKc4ywusBjDis051ZFmcdWTwNeNH39hioH945foWX1A48BAzdGDcRCsf-h3d47FP-NI46Qoi9ZNLhIeYavvYugjfgktUFL6eVXfwJSPl6cP28xvZKGz27_jG6OHv_-d15vVy_UFsu6FRTZgXxQOgATieDZWD3NljiW0O98MEQyYTVjexaR6n1snHAHYAvCd4EYRh7gg7iEP0zhEVrIC4SreuM5iyd2pRNa7XkUlNnjazQmy0c6ltR2VApOgHgVAJOJeBUAq5CbxNat28ldez8AHxGLRZQ__KZCr3aYq1gNKUtEh39MI-KrSjwzRbCyAo9LdjffopJ3qQNqQp1e16x15b9kthfZcXuRLtJQ6FS-osDqeWXMf6lvxBOH_2PLh-je1AnL4tHz9HBdD37F0CnJvMyj5yfIGUlxw
linkProvider Directory of Open Access Journals
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3LbtQwFLWgFaKbimcbnkZCYhVNJnaceDkgygClINFK3Vl-diKIgyaJ0PAf_C_XSTrMUNiwjWPH9rmOz7WvjxF6XmirgbO5WGnKY5rJPIZJMIm14YYTyZlzfZTvCZuf0Xfn2fnGWZgQVmnsxbJbtYNC6sTUugsLZWutAZiBJ0GhCAAGRwooeDFZtNXX62iXFYyCA7Y7m7_5_PH3SksGdpmwUbHxau6tGakX7v8b27waNLn_vd_QXtd2Y146uoX2R0KJZ4MF3EbXrL-DbgxXTK7uop8z3EsKVzV0aF2F-7M07jVlcVvjUevbYqCBeOMoFh7DPHDtMDSjWXlIbMof1uCmDLHU2EsP7vYYVYdr35fwpTQeLAMPEV7wcljlxZ-AoFe1KbsK64VUsjPlPXR29Pr01Twer2KINWVpG6dEs8QCuQNoDXeaTI3KnU5srlLLrFMJJ0zLjBe5SVNteWaARwB3YjRzTBFyH-342ttDhFmuwEdiuSmUpCSc4ORZriWnXKZGKx6hF5dwiG-D4oYIngoAJwJwIgAnAnARehnQWr8VlLL7B_XyQow9IAh1hBJnqS0KSuSUmwTqXmhnqHNG0wg9u8RawMgK2yXS27prBJmmwD1zcCkjdDBgv_4U4TQLm1MRKrasYqsu2ym-XPTq3YGCJ1kKhaZ_GJAYfx_NP9oLrvWD_8n0FN2cn344FsdvT94_RHuQRIdFpEdop1129jHQqlY9GcfNLzhuJ3U
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3LbtQwFLWgFYhNxbOEp5GQWEWTiR0nXg6PYXioVIJK7Cw_2wiNU00SoeE_-F-uE8_QobBhG8eO7XMdn2tfHyP0vNJWA2dzqdKUp7SQZQqTYJZqww0nkjPnhijfI7Y4oe-_FptowjaGVRp7uurX3aiQOjGN7sNC2VZrAGbgSVAoAoDBkQIKXk3OjbuK9hmrGJj6_mzx9vOn3wstBZhlxqJg4-XMOxPSoNv_N7J5OWby4Puwn72t7IVpaX4THUQ-iWejAdxCV6y_ja6NN0yu76CfMzwoCi8b6M9mGa7P0niQlMVdg6PUt8XAAvGFk1g4RnngxmFoRrv2kNjWP6zBbR1CqbGXHrztGFSHGz-U8K02HgwDjwFe8HJY5MXHwM-Xjan7JdZnUsne1HfRyfzNl1eLNN7EkGrK8i7NiWaZBW4HyBruNJkaVTqd2VLlllmnMk6YlgWvSpPn2vLCAI0A6sRo4Zgi5B7a84239xFmpQIXiZWmUpKScICTF6WWnHKZG614gl5s4BDno-CGCI4KACcCcCIAJwJwCXoZ0Nq-FYSyhwfN6lTEHhCEOkKJs9RWFSVyyk0Gda-0M9Q5o2mCnm2wFjCwwm6J9LbpW0GmOVDPEjzKBB2O2G8_RTgtwt5Ugqodq9ipy26Kr88G8e7AwLMih0LzPwxIxL9H-4_2gmf94H8yPUXXj1_Pxcd3Rx8eohuQQsclpEdor1v19jGQqk49icPmF0shJps
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=A+histomorphometric+study+to+evaluate+the+therapeutic+effects+of+biosynthesized+silver+nanoparticles+on+the+kidneys+infected+with+Plasmodium+chabaudi&rft.jtitle=Open+life+sciences&rft.au=Murshed%2C+Mutee&rft.au=Al-Tamimi%2C+Jameel&rft.au=Ibrahim%2C+Khalid+Elfaki&rft.au=Al-Quraishy%2C+Saleh&rft.date=2024-01-01&rft.pub=De+Gruyter&rft.eissn=2391-5412&rft.volume=19&rft.issue=1&rft_id=info:doi/10.1515%2Fbiol-2022-0968&rft.externalDocID=PMC11500527
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2391-5412&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2391-5412&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2391-5412&client=summon