Exploring the Impact of Nanoparticle Stealth Coatings in Cancer Models: From PEGylation to Cell Membrane-Coating Nanotechnology

Nanotechnological platforms offer advantages over conventional therapeutic and diagnostic modalities. However, the efficient biointerfacing of nanomaterials for biomedical applications remains challenging. In recent years, nanoparticles (NPs) with different coatings have been developed to reduce non...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:ACS applied materials & interfaces Ročník 16; číslo 2; s. 2058
Hlavní autoři: Graván, Pablo, Peña-Martín, Jesús, de Andrés, Julia López, Pedrosa, María, Villegas-Montoya, Martín, Galisteo-González, Francisco, Marchal, Juan A, Sánchez-Moreno, Paola
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States 17.01.2024
Témata:
ISSN:1944-8252, 1944-8252
On-line přístup:Zjistit podrobnosti o přístupu
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Abstract Nanotechnological platforms offer advantages over conventional therapeutic and diagnostic modalities. However, the efficient biointerfacing of nanomaterials for biomedical applications remains challenging. In recent years, nanoparticles (NPs) with different coatings have been developed to reduce nonspecific interactions, prolong circulation time, and improve therapeutic outcomes. This study aims to compare various NP coatings to enhance surface engineering for more effective nanomedicines. We prepared and characterized polystyrene NPs with different coatings of poly(ethylene glycol), bovine serum albumin, chitosan, and cell membranes from a human breast cancer cell line. The coating was found to affect the colloidal stability, adhesion, and elastic modulus of NPs. Protein corona formation and cellular uptake of NPs were also investigated, and a 3D tumor model was employed to provide a more realistic representation of the tumor microenvironment. The prepared NPs were found to reduce protein adsorption, and cell-membrane-coated NPs showed significantly higher cellular uptake. The secretion of proinflammatory cytokines in human monocytes after incubation with the prepared NPs was evaluated. Overall, the study demonstrates the importance of coatings in affecting the behavior and interaction of nanosystems with biological entities. The findings provide insight into bionano interactions and are important for the effective implementation of stealth surface engineering designs.
AbstractList Nanotechnological platforms offer advantages over conventional therapeutic and diagnostic modalities. However, the efficient biointerfacing of nanomaterials for biomedical applications remains challenging. In recent years, nanoparticles (NPs) with different coatings have been developed to reduce nonspecific interactions, prolong circulation time, and improve therapeutic outcomes. This study aims to compare various NP coatings to enhance surface engineering for more effective nanomedicines. We prepared and characterized polystyrene NPs with different coatings of poly(ethylene glycol), bovine serum albumin, chitosan, and cell membranes from a human breast cancer cell line. The coating was found to affect the colloidal stability, adhesion, and elastic modulus of NPs. Protein corona formation and cellular uptake of NPs were also investigated, and a 3D tumor model was employed to provide a more realistic representation of the tumor microenvironment. The prepared NPs were found to reduce protein adsorption, and cell-membrane-coated NPs showed significantly higher cellular uptake. The secretion of proinflammatory cytokines in human monocytes after incubation with the prepared NPs was evaluated. Overall, the study demonstrates the importance of coatings in affecting the behavior and interaction of nanosystems with biological entities. The findings provide insight into bionano interactions and are important for the effective implementation of stealth surface engineering designs.
Nanotechnological platforms offer advantages over conventional therapeutic and diagnostic modalities. However, the efficient biointerfacing of nanomaterials for biomedical applications remains challenging. In recent years, nanoparticles (NPs) with different coatings have been developed to reduce nonspecific interactions, prolong circulation time, and improve therapeutic outcomes. This study aims to compare various NP coatings to enhance surface engineering for more effective nanomedicines. We prepared and characterized polystyrene NPs with different coatings of poly(ethylene glycol), bovine serum albumin, chitosan, and cell membranes from a human breast cancer cell line. The coating was found to affect the colloidal stability, adhesion, and elastic modulus of NPs. Protein corona formation and cellular uptake of NPs were also investigated, and a 3D tumor model was employed to provide a more realistic representation of the tumor microenvironment. The prepared NPs were found to reduce protein adsorption, and cell-membrane-coated NPs showed significantly higher cellular uptake. The secretion of proinflammatory cytokines in human monocytes after incubation with the prepared NPs was evaluated. Overall, the study demonstrates the importance of coatings in affecting the behavior and interaction of nanosystems with biological entities. The findings provide insight into bionano interactions and are important for the effective implementation of stealth surface engineering designs.Nanotechnological platforms offer advantages over conventional therapeutic and diagnostic modalities. However, the efficient biointerfacing of nanomaterials for biomedical applications remains challenging. In recent years, nanoparticles (NPs) with different coatings have been developed to reduce nonspecific interactions, prolong circulation time, and improve therapeutic outcomes. This study aims to compare various NP coatings to enhance surface engineering for more effective nanomedicines. We prepared and characterized polystyrene NPs with different coatings of poly(ethylene glycol), bovine serum albumin, chitosan, and cell membranes from a human breast cancer cell line. The coating was found to affect the colloidal stability, adhesion, and elastic modulus of NPs. Protein corona formation and cellular uptake of NPs were also investigated, and a 3D tumor model was employed to provide a more realistic representation of the tumor microenvironment. The prepared NPs were found to reduce protein adsorption, and cell-membrane-coated NPs showed significantly higher cellular uptake. The secretion of proinflammatory cytokines in human monocytes after incubation with the prepared NPs was evaluated. Overall, the study demonstrates the importance of coatings in affecting the behavior and interaction of nanosystems with biological entities. The findings provide insight into bionano interactions and are important for the effective implementation of stealth surface engineering designs.
Author de Andrés, Julia López
Villegas-Montoya, Martín
Galisteo-González, Francisco
Marchal, Juan A
Pedrosa, María
Sánchez-Moreno, Paola
Graván, Pablo
Peña-Martín, Jesús
Author_xml – sequence: 1
  givenname: Pablo
  surname: Graván
  fullname: Graván, Pablo
  organization: BioFab i3D─Biofabrication and 3D (bio)printing laboratory, University of Granada, 18100 Granada, Spain
– sequence: 2
  givenname: Jesús
  orcidid: 0000-0002-5525-2657
  surname: Peña-Martín
  fullname: Peña-Martín, Jesús
  organization: BioFab i3D─Biofabrication and 3D (bio)printing laboratory, University of Granada, 18100 Granada, Spain
– sequence: 3
  givenname: Julia López
  surname: de Andrés
  fullname: de Andrés, Julia López
  organization: BioFab i3D─Biofabrication and 3D (bio)printing laboratory, University of Granada, 18100 Granada, Spain
– sequence: 4
  givenname: María
  surname: Pedrosa
  fullname: Pedrosa, María
  organization: Excellence Research Unit Modelling Nature (MNat), University of Granada, 18016 Granada, Spain
– sequence: 5
  givenname: Martín
  surname: Villegas-Montoya
  fullname: Villegas-Montoya, Martín
  organization: Faculty of Biology, Calzada de las Américas and University, Ciudad Universitaria, 80040 Culiacán, Sinaloa, Mexico
– sequence: 6
  givenname: Francisco
  orcidid: 0000-0001-8941-5752
  surname: Galisteo-González
  fullname: Galisteo-González, Francisco
  organization: Department of Applied Physics, Faculty of Science, University of Granada, 18071 Granada, Spain
– sequence: 7
  givenname: Juan A
  orcidid: 0000-0002-4996-8261
  surname: Marchal
  fullname: Marchal, Juan A
  organization: BioFab i3D─Biofabrication and 3D (bio)printing laboratory, University of Granada, 18100 Granada, Spain
– sequence: 8
  givenname: Paola
  orcidid: 0000-0002-9560-4629
  surname: Sánchez-Moreno
  fullname: Sánchez-Moreno, Paola
  organization: Excellence Research Unit Modelling Nature (MNat), University of Granada, 18016 Granada, Spain
BackLink https://www.ncbi.nlm.nih.gov/pubmed/38159050$$D View this record in MEDLINE/PubMed
BookMark eNpNkD1PwzAYhC1URD9gZUQeWVJsx3ZiNhS1BakFJGCu3rhOG-TYIXYlOvHXiaBITHfDc6fTjdHAeWcQuqRkSgmjN6ADNPU01TRVPD9BI6o4T3Im2OCfH6JxCO-EyJQRcYaGaU6FIoKM0Nfss7W-q90Wx53BD00LOmJf4UdwvoUu1toa_BIN2LjDhYfYowHXDhfgtOnwym-MDbd43vkGP88WB9sj3uHocWGsxSvTlB04kxyzP8XR6J3z1m8P5-i0AhvMxVEn6G0-ey3uk-XT4qG4WyaQZiQmmvJKUqmELBmlUgrOickUZKzMq4qbtJSSKamkAQklcF0JtYFSCEEJ3-QZm6Dr39628x97E-K6qYPuB_bT_D6smSKK5BnNVI9eHdF92ZjNuu3qBrrD-u809g2g_HFx
CitedBy_id crossref_primary_10_1016_j_ccr_2025_216718
crossref_primary_10_1007_s40820_025_01862_6
crossref_primary_10_1038_s44222_025_00321_6
crossref_primary_10_1002_anbr_202400012
crossref_primary_10_1016_j_jconrel_2025_113824
crossref_primary_10_1016_j_mtbio_2025_101716
crossref_primary_10_1002_adfm_202510739
crossref_primary_10_1016_j_jcis_2025_139020
crossref_primary_10_1016_j_ijpharm_2025_125753
crossref_primary_10_3390_ijms25105171
crossref_primary_10_1021_acsbiomaterials_4c02118
crossref_primary_10_3390_nano15131013
crossref_primary_10_1016_j_ijbiomac_2024_137451
crossref_primary_10_1016_j_jconrel_2025_113782
crossref_primary_10_1021_acsami_5c07306
crossref_primary_10_3390_pharmaceutics16101306
crossref_primary_10_1039_D4NR01853B
crossref_primary_10_3390_molecules30061349
crossref_primary_10_1016_j_jddst_2024_106518
crossref_primary_10_1039_D5NR00984G
ContentType Journal Article
DBID CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1021/acsami.3c13948
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle 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 no_fulltext_linktorsrc
Discipline Engineering
EISSN 1944-8252
ExternalDocumentID 38159050
Genre Journal Article
GroupedDBID ---
.K2
23M
4.4
53G
55A
5GY
5VS
5ZA
6J9
7~N
AABXI
AAHBH
ABBLG
ABJNI
ABLBI
ABMVS
ABQRX
ABUCX
ACGFS
ACS
ADHLV
AEESW
AENEX
AFEFF
AHGAQ
ALMA_UNASSIGNED_HOLDINGS
AQSVZ
BAANH
CGR
CUPRZ
CUY
CVF
EBS
ECM
ED~
EIF
F5P
GGK
GNL
IH9
JG~
NPM
P2P
RNS
ROL
UI2
VF5
VG9
W1F
XKZ
7X8
ID FETCH-LOGICAL-a370t-c14f616956b211665440e79a72b8ff4e3b6629696ea6aba4cf59dab555104d872
IEDL.DBID 7X8
ISICitedReferencesCount 25
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=001144606000001&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 1944-8252
IngestDate Fri Jul 11 10:07:33 EDT 2025
Mon Jul 21 05:18:15 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 2
Keywords cell membranes
3D cell culture
coatings
nanoparticles
biointerfacing
protein corona
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-a370t-c14f616956b211665440e79a72b8ff4e3b6629696ea6aba4cf59dab555104d872
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0002-4996-8261
0000-0002-9560-4629
0000-0001-8941-5752
0000-0002-5525-2657
OpenAccessLink https://doi.org/10.1021/acsami.3c13948
PMID 38159050
PQID 2909087179
PQPubID 23479
ParticipantIDs proquest_miscellaneous_2909087179
pubmed_primary_38159050
PublicationCentury 2000
PublicationDate 2024-01-17
PublicationDateYYYYMMDD 2024-01-17
PublicationDate_xml – month: 01
  year: 2024
  text: 2024-01-17
  day: 17
PublicationDecade 2020
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle ACS applied materials & interfaces
PublicationTitleAlternate ACS Appl Mater Interfaces
PublicationYear 2024
SSID ssj0063205
Score 2.53216
Snippet Nanotechnological platforms offer advantages over conventional therapeutic and diagnostic modalities. However, the efficient biointerfacing of nanomaterials...
SourceID proquest
pubmed
SourceType Aggregation Database
Index Database
StartPage 2058
SubjectTerms Cell Membrane - metabolism
Humans
Nanomedicine
Nanoparticles - metabolism
Neoplasms - metabolism
Polyethylene Glycols - metabolism
Serum Albumin, Bovine - metabolism
Title Exploring the Impact of Nanoparticle Stealth Coatings in Cancer Models: From PEGylation to Cell Membrane-Coating Nanotechnology
URI https://www.ncbi.nlm.nih.gov/pubmed/38159050
https://www.proquest.com/docview/2909087179
Volume 16
WOSCitedRecordID wos001144606000001&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText
inHoldings 1
isFullTextHit
isPrint
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV07T8MwELaAMsDA-1FeMhKr1cRxHmZBKKLA0KoDSN0ix7FFpTQpTUBi4q9zdtLCgoTE4u0iyznffffwfQhd2RnmANSJL2VEWJZyEmmXEXDN0jMPKwMqLdlEOBxG4zEftQm3qm2rXNhEa6izUpoceY9yhzuA7kN-M3slhjXKVFdbCo1V1PEAyhitDsfLKkLgUdvCCHE6IxAJ0cXQRur2hKwMwY4nQYxFv8NL62b62__d4A7aagEmvm00YhetqGIPbf4YO7iPPpeNdxjgH360DyVxqTGYWoihG0lsOn3z-gXHpTCt0RWeFDg2OjLHhkAtr65xf15O8eju_qNpqMN1iWOV53igphCEF4q0svbD9TKJf4Ce-3dP8QNpiRiI8EKnJtJlOnADCKVSiBcNXzFzVMhFSNNIa6a8NAioGbOjRCBSwaT2eSZSH9CYw7IopIdorSgLdYywkFynkUq5Uh5T4BhdV2lYMgHA0dVOF10uTjcBRTfVC9hu-VYl3-fbRUfNL0pmzUSOBGCHzx3fOfmD9CnaoABMTBrFDc9QR8M1V-doXb7Xk2p-YTUI1uFo8AWnwNFt
linkProvider ProQuest
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=Exploring+the+Impact+of+Nanoparticle+Stealth+Coatings+in+Cancer+Models%3A+From+PEGylation+to+Cell+Membrane-Coating+Nanotechnology&rft.jtitle=ACS+applied+materials+%26+interfaces&rft.au=Grav%C3%A1n%2C+Pablo&rft.au=Pe%C3%B1a-Mart%C3%ADn%2C+Jes%C3%BAs&rft.au=de+Andr%C3%A9s%2C+Julia+L%C3%B3pez&rft.au=Pedrosa%2C+Mar%C3%ADa&rft.date=2024-01-17&rft.issn=1944-8252&rft.eissn=1944-8252&rft.volume=16&rft.issue=2&rft.spage=2058&rft_id=info:doi/10.1021%2Facsami.3c13948&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1944-8252&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1944-8252&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1944-8252&client=summon