Identification and validation of Sertoli cell homing peptides as molecular steering for testis targeted drug delivery

The testicle, an organ privileged with immunity because of Blood-Testis Barrier (BTB), poses a major impediment to developing and delivering drugs to the testes. These problems can be prevented by targeting testicular cells using specific ligands, such as homing peptides. This is the first study to...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Journal of drug targeting Ročník 31; číslo 4; s. 390 - 401
Hlavní autoři: Jirwankar, Yugandhara, Dighe, Vikas
Médium: Journal Article
Jazyk:angličtina
Vydáno: England Taylor & Francis 21.04.2023
Témata:
ISSN:1061-186X, 1029-2330, 1029-2330
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Abstract The testicle, an organ privileged with immunity because of Blood-Testis Barrier (BTB), poses a major impediment to developing and delivering drugs to the testes. These problems can be prevented by targeting testicular cells using specific ligands, such as homing peptides. This is the first study to demonstrate the successful selection of Sertoli cell homing peptides using a phage display peptide library. The identification of peptides is performed with Sanger sequencing and high-throughput NGS. The Sertoli cell and testis targeting potential of the SCHP1 and SCHP2 was confirmed using confocal microscopy and flow cytometry of the FITC-labelled peptides and in vivo bio-distribution of the corresponding Cy5.5-tagged peptides. Secondary structures were predicted in the setting of different polarity by circular dichroism. The results suggest that SCHP1 and SCHP2 can effectively target Sertoli cells. In vivo bio-distribution in mouse models indicated significantly higher uptake of SCHP1 and SCHP2 by testes compared with the heart, brain, and spleen. SCHP1 and SCHP2 can be adopted as molecular steering for targeted male contraceptive delivery, treatment of testicular cancer, and male infertility. Further development of the peptides into peptidomimetics may increase their stability, and information on the molecular targets of these peptides may reveal their therapeutic potential.
AbstractList The testicle, an organ privileged with immunity because of Blood-Testis Barrier (BTB), poses a major impediment to developing and delivering drugs to the testes. These problems can be prevented by targeting testicular cells using specific ligands, such as homing peptides. This is the first study to demonstrate the successful selection of Sertoli cell homing peptides using a phage display peptide library. The identification of peptides is performed with Sanger sequencing and high-throughput NGS. The Sertoli cell and testis targeting potential of the SCHP1 and SCHP2 was confirmed using confocal microscopy and flow cytometry of the FITC-labelled peptides and bio-distribution of the corresponding Cy5.5-tagged peptides. Secondary structures were predicted in the setting of different polarity by circular dichroism. The results suggest that SCHP1 and SCHP2 can effectively target Sertoli cells. bio-distribution in mouse models indicated significantly higher uptake of SCHP1 and SCHP2 by testes compared with the heart, brain, and spleen. SCHP1 and SCHP2 can be adopted as molecular steering for targeted male contraceptive delivery, treatment of testicular cancer, and male infertility. Further development of the peptides into peptidomimetics may increase their stability, and information on the molecular targets of these peptides may reveal their therapeutic potential.
The testicle, an organ privileged with immunity because of Blood-Testis Barrier (BTB), poses a major impediment to developing and delivering drugs to the testes. These problems can be prevented by targeting testicular cells using specific ligands, such as homing peptides. This is the first study to demonstrate the successful selection of Sertoli cell homing peptides using a phage display peptide library. The identification of peptides is performed with Sanger sequencing and high-throughput NGS. The Sertoli cell and testis targeting potential of the SCHP1 and SCHP2 was confirmed using confocal microscopy and flow cytometry of the FITC-labelled peptides and in vivo bio-distribution of the corresponding Cy5.5-tagged peptides. Secondary structures were predicted in the setting of different polarity by circular dichroism. The results suggest that SCHP1 and SCHP2 can effectively target Sertoli cells. In vivo bio-distribution in mouse models indicated significantly higher uptake of SCHP1 and SCHP2 by testes compared with the heart, brain, and spleen. SCHP1 and SCHP2 can be adopted as molecular steering for targeted male contraceptive delivery, treatment of testicular cancer, and male infertility. Further development of the peptides into peptidomimetics may increase their stability, and information on the molecular targets of these peptides may reveal their therapeutic potential.
The testicle, an organ privileged with immunity because of Blood-Testis Barrier (BTB), poses a major impediment to developing and delivering drugs to the testes. These problems can be prevented by targeting testicular cells using specific ligands, such as homing peptides. This is the first study to demonstrate the successful selection of Sertoli cell homing peptides using a phage display peptide library. The identification of peptides is performed with Sanger sequencing and high-throughput NGS. The Sertoli cell and testis targeting potential of the SCHP1 and SCHP2 was confirmed using confocal microscopy and flow cytometry of the FITC-labelled peptides and in vivo bio-distribution of the corresponding Cy5.5-tagged peptides. Secondary structures were predicted in the setting of different polarity by circular dichroism. The results suggest that SCHP1 and SCHP2 can effectively target Sertoli cells. In vivo bio-distribution in mouse models indicated significantly higher uptake of SCHP1 and SCHP2 by testes compared with the heart, brain, and spleen. SCHP1 and SCHP2 can be adopted as molecular steering for targeted male contraceptive delivery, treatment of testicular cancer, and male infertility. Further development of the peptides into peptidomimetics may increase their stability, and information on the molecular targets of these peptides may reveal their therapeutic potential.The testicle, an organ privileged with immunity because of Blood-Testis Barrier (BTB), poses a major impediment to developing and delivering drugs to the testes. These problems can be prevented by targeting testicular cells using specific ligands, such as homing peptides. This is the first study to demonstrate the successful selection of Sertoli cell homing peptides using a phage display peptide library. The identification of peptides is performed with Sanger sequencing and high-throughput NGS. The Sertoli cell and testis targeting potential of the SCHP1 and SCHP2 was confirmed using confocal microscopy and flow cytometry of the FITC-labelled peptides and in vivo bio-distribution of the corresponding Cy5.5-tagged peptides. Secondary structures were predicted in the setting of different polarity by circular dichroism. The results suggest that SCHP1 and SCHP2 can effectively target Sertoli cells. In vivo bio-distribution in mouse models indicated significantly higher uptake of SCHP1 and SCHP2 by testes compared with the heart, brain, and spleen. SCHP1 and SCHP2 can be adopted as molecular steering for targeted male contraceptive delivery, treatment of testicular cancer, and male infertility. Further development of the peptides into peptidomimetics may increase their stability, and information on the molecular targets of these peptides may reveal their therapeutic potential.
Author Jirwankar, Yugandhara
Dighe, Vikas
Author_xml – sequence: 1
  givenname: Yugandhara
  orcidid: 0000-0002-6196-1687
  surname: Jirwankar
  fullname: Jirwankar, Yugandhara
  organization: National Centre for Preclinical Reproductive and Genetic Toxicology, ICMR - National Institute for Research in Reproductive and Child Health
– sequence: 2
  givenname: Vikas
  orcidid: 0000-0001-9718-7358
  surname: Dighe
  fullname: Dighe, Vikas
  organization: National Centre for Preclinical Reproductive and Genetic Toxicology, ICMR - National Institute for Research in Reproductive and Child Health
BackLink https://www.ncbi.nlm.nih.gov/pubmed/36604336$$D View this record in MEDLINE/PubMed
BookMark eNqFUU2PFCEQJWaN-6E_QcPRS48FdNPd8aLZ-LHJJh7UxBthoBgxNIxAr5l_b7czc_Ggp6oK772i3rsmFzFFJOQ5gw2DAV4xkIwN8tuGA-cbzmQL0D8iVwz42HAh4GLtJWtW0CW5LuUHABOSwRNyKaSEVgh5ReY7i7F6542uPkWqo6UPOnh7HJOjnzHXFDw1GAL9niYfd3SP--otFqoLnVJAMwedaamIeX12KdOKpfpCq847rGipzfOOWgz-AfPhKXnsdCj47FRvyNf3777cfmzuP324u31735iWidpY0WtpR8NxtA6Wq9G1gO3Ixt4OvLNslNgbMFxut8PY62WQrOvQQWe7cUBxQ14edfc5_ZyXH6nJl_UQHTHNRfFeLlqSi26BvjhB5-2EVu2zn3Q-qLNVC-D1EWByKiWjU8bXPy7VrH1QDNQajDoHo9Zg1CmYhd39xT4v-B_vzZHn4-LqpH-lHKyq-hBSdllH44sS_5b4Ddefpj4
CitedBy_id crossref_primary_10_1002_smll_202307111
crossref_primary_10_3389_fmicb_2025_1571679
Cites_doi 10.1016/j.urology.2006.02.045
10.1080/1061186031000086063
10.1038/380364a0
10.1007/s40005-017-0374-0
10.1016/S0066-4103(08)00201-9
10.1007/978-1-60327-569-9_18
10.1126/science.4001944
10.2174/0929867323666160112122724
10.1039/c0ib00013b
10.1021/acs.chemrev.9b00008
10.1161/CIRCULATIONAHA.104.529537
10.1056/NEJMra1407550
10.1093/nar/gkv1100
10.1016/j.chroma.2019.04.037
10.1016/j.jviromet.2017.11.012
10.1038/nm0202-121
10.7150/ijbs.31957
10.1007/978-1-4939-0659-8_18
10.1016/j.ucl.2013.08.012
10.1055/s-0036-1571435
10.1073/pnas.251687998
10.1055/s-0034-1375184
10.1002/j.1939-4640.2004.tb02780.x
10.1016/j.juro.2015.03.076
10.1101/pdb.prot093419
10.1186/gb-2007-8-2-r24
10.1002/med.20225
10.1074/jbc.274.17.11593
10.2174/1573413052953110
10.3109/1061186X.2011.572974
10.1007/s13346-011-0039-x
10.1080/1061186X.2018.1531419
10.1038/nm1048
10.1038/nrurol.2011.26
10.1371/journal.pone.0012252
10.1016/j.drudis.2014.10.003
10.1002/ijc.20931
10.1093/bioinformatics/btab203
10.1007/978-1-4939-2020-4_17
ContentType Journal Article
Copyright 2023 Informa UK Limited, trading as Taylor & Francis Group 2023
Copyright_xml – notice: 2023 Informa UK Limited, trading as Taylor & Francis Group 2023
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1080/1061186X.2022.2164007
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE

MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Pharmacy, Therapeutics, & Pharmacology
EISSN 1029-2330
EndPage 401
ExternalDocumentID 36604336
10_1080_1061186X_2022_2164007
2164007
Genre Research Article
Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID ---
00X
03L
0R~
29K
36B
4.4
53G
5GY
AAGDL
AALUX
AAMIU
AAPUL
AAQRR
ABBKH
ABDBF
ABEIZ
ABJNI
ABLIJ
ABLKL
ABUPF
ABWVI
ABXYU
ACENM
ACGEJ
ACGFS
ACIEZ
ACUHS
ADCVX
ADRBQ
ADXPE
AECIN
AENEX
AEOZL
AFKVX
AFRVT
AGDLA
AGFJD
AGRBW
AGYJP
AIJEM
AIRBT
AJWEG
AKBVH
ALMA_UNASSIGNED_HOLDINGS
ALQZU
ALYBC
AQTUD
BABNJ
BLEHA
BOHLJ
CCCUG
CS3
D-I
DKSSO
EAP
EBC
EBD
EBS
EMB
EMK
EMOBN
EPL
ESX
F5P
H13
HZ~
KRBQP
KSSTO
KWAYT
KYCEM
LJTGL
M4Z
O9-
RNANH
RVRKI
SV3
TASJS
TBQAZ
TDBHL
TERGH
TFDNU
TFL
TFW
TUROJ
TUS
UHWXJ
V1S
~1N
AAYXX
CITATION
0BK
0VX
5VS
AACCU
AALIY
AAPXX
ABCRQ
ACKYO
ADYSH
AFAUU
AFQCT
AGAFX
AJEBJ
AJXHO
AWYRJ
BVLLS
CAG
CGR
COF
CUY
CVF
DEIEU
DLVIE
DTRLO
DZHFC
ECM
EIF
EJD
JFOCU
M44
NPM
NUSFT
QRXOQ
7X8
ID FETCH-LOGICAL-c413t-d37a6d9c2e9df0080ef40e49197d825d196e7c0c26bb897ae7c6155ef05d598e3
IEDL.DBID TFW
ISICitedReferencesCount 3
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000912744600001&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 1061-186X
1029-2330
IngestDate Tue Aug 05 10:51:00 EDT 2025
Wed Feb 19 02:24:15 EST 2025
Sat Nov 29 04:25:30 EST 2025
Tue Nov 18 22:31:39 EST 2025
Mon Oct 20 23:46:03 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 4
Keywords drug targeting
Sertoli cell
biopanning
testis
phage display
Homing peptides
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c413t-d37a6d9c2e9df0080ef40e49197d825d196e7c0c26bb897ae7c6155ef05d598e3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0001-9718-7358
0000-0002-6196-1687
OpenAccessLink https://figshare.com/articles/journal_contribution/Identification_and_validation_of_Sertoli_cell_homing_peptides_as_molecular_steering_for_testis_targeted_drug_delivery/21825368
PMID 36604336
PQID 2761976235
PQPubID 23479
PageCount 12
ParticipantIDs proquest_miscellaneous_2761976235
pubmed_primary_36604336
informaworld_taylorfrancis_310_1080_1061186X_2022_2164007
crossref_citationtrail_10_1080_1061186X_2022_2164007
crossref_primary_10_1080_1061186X_2022_2164007
PublicationCentury 2000
PublicationDate 2023-04-21
PublicationDateYYYYMMDD 2023-04-21
PublicationDate_xml – month: 04
  year: 2023
  text: 2023-04-21
  day: 21
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
PublicationTitle Journal of drug targeting
PublicationTitleAlternate J Drug Target
PublicationYear 2023
Publisher Taylor & Francis
Publisher_xml – name: Taylor & Francis
References CIT0030
CIT0010
CIT0031
CIT0012
CIT0034
CIT0011
CIT0033
Crosnoe LE (CIT0004) 2013; 2
CIT0014
CIT0036
CIT0013
CIT0035
CIT0016
CIT0038
CIT0015
CIT0037
CIT0018
CIT0017
CIT0039
CIT0019
Work LM (CIT0032) 2005; 108
CIT0041
CIT0040
CIT0021
CIT0043
CIT0020
CIT0042
CIT0001
CIT0023
CIT0022
Ehrlich Y (CIT0008) 2015; 4
CIT0025
CIT0002
CIT0024
CIT0005
CIT0027
Cocuzza M (CIT0003) 2007; 1
CIT0026
CIT0007
CIT0029
Garza AZ (CIT0044) 2022
CIT0006
CIT0028
CIT0009
References_xml – ident: CIT0006
  doi: 10.1016/j.urology.2006.02.045
– ident: CIT0017
  doi: 10.1080/1061186031000086063
– volume: 4
  start-page: 381
  issue: 3
  year: 2015
  ident: CIT0008
  publication-title: Transl Androl Urol
– ident: CIT0014
  doi: 10.1038/380364a0
– ident: CIT0026
  doi: 10.1007/s40005-017-0374-0
– ident: CIT0043
  doi: 10.1016/S0066-4103(08)00201-9
– ident: CIT0031
  doi: 10.1007/978-1-60327-569-9_18
– ident: CIT0016
  doi: 10.1126/science.4001944
– ident: CIT0012
  doi: 10.2174/0929867323666160112122724
– ident: CIT0042
  doi: 10.1039/c0ib00013b
– ident: CIT0041
  doi: 10.1021/acs.chemrev.9b00008
– ident: CIT0024
  doi: 10.1161/CIRCULATIONAHA.104.529537
– ident: CIT0007
  doi: 10.1056/NEJMra1407550
– ident: CIT0036
  doi: 10.1093/nar/gkv1100
– ident: CIT0037
  doi: 10.1016/j.chroma.2019.04.037
– ident: CIT0033
  doi: 10.1016/j.jviromet.2017.11.012
– ident: CIT0020
  doi: 10.1038/nm0202-121
– ident: CIT0038
  doi: 10.7150/ijbs.31957
– ident: CIT0001
  doi: 10.1007/978-1-4939-0659-8_18
– ident: CIT0010
  doi: 10.1016/j.ucl.2013.08.012
– ident: CIT0011
  doi: 10.1055/s-0036-1571435
– ident: CIT0023
  doi: 10.1073/pnas.251687998
– ident: CIT0002
  doi: 10.1055/s-0034-1375184
– ident: CIT0029
  doi: 10.1002/j.1939-4640.2004.tb02780.x
– ident: CIT0030
  doi: 10.1016/j.juro.2015.03.076
– ident: CIT0034
  doi: 10.1101/pdb.prot093419
– ident: CIT0040
  doi: 10.1186/gb-2007-8-2-r24
– ident: CIT0015
  doi: 10.1002/med.20225
– ident: CIT0022
  doi: 10.1074/jbc.274.17.11593
– ident: CIT0013
  doi: 10.2174/1573413052953110
– ident: CIT0018
  doi: 10.3109/1061186X.2011.572974
– ident: CIT0028
  doi: 10.1007/s13346-011-0039-x
– ident: CIT0019
  doi: 10.1080/1061186X.2018.1531419
– volume: 2
  start-page: 106
  issue: 2
  year: 2013
  ident: CIT0004
  publication-title: Transl Androl Urol
– ident: CIT0021
  doi: 10.1038/nm1048
– ident: CIT0009
  doi: 10.1038/nrurol.2011.26
– volume-title: Drug elimination
  year: 2022
  ident: CIT0044
– volume: 1
  start-page: 259
  issue: 3
  year: 2007
  ident: CIT0003
  publication-title: Biol Targets Ther
– ident: CIT0025
  doi: 10.1371/journal.pone.0012252
– volume: 108
  start-page: 395
  year: 2005
  ident: CIT0032
  publication-title: Methods Mol Med
– ident: CIT0027
  doi: 10.1016/j.drudis.2014.10.003
– ident: CIT0005
  doi: 10.1002/ijc.20931
– ident: CIT0039
  doi: 10.1093/bioinformatics/btab203
– ident: CIT0035
  doi: 10.1007/978-1-4939-2020-4_17
SSID ssj0013610
Score 2.375911
Snippet The testicle, an organ privileged with immunity because of Blood-Testis Barrier (BTB), poses a major impediment to developing and delivering drugs to the...
SourceID proquest
pubmed
crossref
informaworld
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 390
SubjectTerms Animals
biopanning
drug targeting
Homing peptides
Humans
Male
Mice
Peptide Library
Peptides - chemistry
phage display
Sertoli cell
Sertoli Cells
Testicular Neoplasms
testis
Title Identification and validation of Sertoli cell homing peptides as molecular steering for testis targeted drug delivery
URI https://www.tandfonline.com/doi/abs/10.1080/1061186X.2022.2164007
https://www.ncbi.nlm.nih.gov/pubmed/36604336
https://www.proquest.com/docview/2761976235
Volume 31
WOSCitedRecordID wos000912744600001&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVAWR
  databaseName: Taylor and Francis Online Journals
  customDbUrl:
  eissn: 1029-2330
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0013610
  issn: 1061-186X
  databaseCode: TFW
  dateStart: 19930101
  isFulltext: true
  titleUrlDefault: https://www.tandfonline.com
  providerName: Taylor & Francis
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9swDBa2Yodd9t6abis4YOip7mzJka3jMCzYYShyyLDcDNmitgJpXMTOgPz7kpbcrIeih-3oA22ZIkVSJD8K8VGirb3RZaKasklybU1ilbWJzBWJs-RM0wCZ_704Py-XSzOP1YRdLKvkGNoHoIjhrGbltnU3VsR94igmK_WSojspzyQ5_KGfnDx7lvHF7Oc-j6AjHoHOEiYZe3juesst63QLu_RuD3SwRLOn_-Efnokn0Q2Fz0FunosHuH4hTuYBx3p3Cot9W1Z3Cicw3yNc716KbWjv9fG-D2gVQBJ7EeYzQeuBjqC-XV0A5wXgd3tJBhKuuIDGYQe2g8txKi-QlA1oiEBMgJ4xPzoI5enowG22v8DhiotHdq_Ej9nXxZdvSZzfkDRkGvvEqcJqZxqJxnl2TdHnKeYmM4WjwNSR8mPRpI3UdV2awtIDZ0nRp1M3NSWq1-Jg3a7xUEBt6dyZlib1GnNfp1ZbiVJ7zJBodToR-bhvVRPBzXnGxqrKIgbqyPCKGV5Fhk_E2Q3ZVUD3uI_A_C0UVT9cq_gwA6VS99B-GCWoIh3mDbBrbLddJfkuiTRDTSfiTRCtm-UorRljTh_9w5ffisf0qDgJJrN34qDfbPG9eNT8oS3dHIuHxbI8HvTmGgRjE78
linkProvider Taylor & Francis
linkToHtml http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELZQQYILb8oChUFCPTUlsRMnPiLUVRHLqodF7M1yYptW2m6qTbbS_vvOxEm3PVQ9wDGKJo_xjGc8j28Y-8KdKb2SRSSqoopSaVRkhDERTwWKM6dMUweZP8mn02I-Vzd7Yaisks7QPgBFdHs1KTcFo4eSuK90jEkKOcfjHeeHHD3-rqH8YYa2lsr6ZuM_20yC7BEJZBIRzdDFc9djbtmnW-ild_ugnS0aP_sff_GcPe09UfgWROcFe-CWL9n-SYCy3hzAbNuZ1RzAPpxsQa43r9g6dPj6PuQH-BmAQnsWRjRB7QF3obZenAGlBuC0PkcbCRdUQ2NdA6aB82EwL6CgdYCIgFyAlmA_GggV6s6CXa3_gnULqh_ZvGa_x0ez78dRP8IhqtA6tpEVuZFWVdwp68k7dT6NXaoSlVs8m1rUf5dXccVlWRYqN3hBiVLn48xmqnDiDdtZ1kv3lkFpcOvJChV76VJfxkYa7rj0LnFIK-MRS4eF01WPb05jNhY66WFQB4ZrYrjuGT5ih9dkFwHg4z4CdVMqdNtFVnwYg6LFPbSfBxHSqMa0AGbp6nWjOYWTUDlENmK7QbauP0dISTBz8t0_vPkTe3w8-zXRkx_Tn-_ZE7wlKCfGkw9sp12t3R57VF3i8q4-dupzBc8rFvg
linkToPdf http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9swDBaGbhh22fuRPTlg6KnubMmRreOwLdiwIsghw3ITZIvaCqRxEDsF8u9LWXKzHooetqNh0A-KFEmR_MjYB46mckqWiajLOsmlUYkRxiQ8FyTO3Geaesj8k2I6LRcLNYvVhG0sq_QxtAtAEf1e7ZV7bd1QEffRRzFZKRcU3XF-zMnh7_vJb_fgWCTS88mvfSJBRkACmSWeZmjiue4xV8zTFfDS613Q3hRNHvyHn3jI7kc_FD4FwXnEbuHqMTucBSDr3RHM931Z7REcwmwPcb17wrahv9fFAz-grwAS2dMwoAkaB7QHdc3yFHxiAP40Z2QhYe0raCy2YFo4G8byAolZD4cIxAToPOhHC6E-HS3YzfY3WFz66pHdU_Zz8nX--VsSBzgkNdnGLrGiMNKqmqOyzvum6PIUc5WpwlJkakn7sajTmsuqKlVh6MKnSdGlYztWJYpn7GDVrPAFg8rQxjMuVeok5q5KjTQcuXSYIdHKdMTyYd10HdHN_ZCNpc4iCOrAcO0ZriPDR-z4kmwd4D1uIlB_C4Xu-nMVF4agaHED7ftBgjQpsV8As8Jm22ruD5NINcR4xJ4H0br8HCGlB5mTL__hze_Y3dmXiT75Pv3xit2jO8InxHj2mh10my2-YXfqc1rdzdteeS4ARHkVnA
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=Identification+and+validation+of+Sertoli+cell+homing+peptides+as+molecular+steering+for+testis+targeted+drug+delivery&rft.jtitle=Journal+of+drug+targeting&rft.au=Jirwankar%2C+Yugandhara&rft.au=Dighe%2C+Vikas&rft.date=2023-04-21&rft.issn=1029-2330&rft.eissn=1029-2330&rft.volume=31&rft.issue=4&rft.spage=390&rft_id=info:doi/10.1080%2F1061186X.2022.2164007&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1061-186X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1061-186X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1061-186X&client=summon