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Sex-Specific Silica Nanoparticle Protein Corona Compositions Exposed to Male and Female BALB/c Mice Plasmas

[Image: see text] As various nanoparticles (NPs) are increasingly being used in nanomedicine products for more effective and less toxic therapy and diagnosis of diseases, there is a growing need to understand their biological fate in different sexes. Herein, we report a proof-of-concept result of se...

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Autores principales: Ashkarran, Ali Akbar, Gharibi, Hassan, Grunberger, Jason W., Saei, Amir Ata, Khurana, Nitish, Mohammadpour, Raziye, Ghandehari, Hamidreza, Mahmoudi, Morteza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936498/
https://www.ncbi.nlm.nih.gov/pubmed/36820312
http://dx.doi.org/10.1021/acsbiomedchemau.2c00040
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author Ashkarran, Ali Akbar
Gharibi, Hassan
Grunberger, Jason W.
Saei, Amir Ata
Khurana, Nitish
Mohammadpour, Raziye
Ghandehari, Hamidreza
Mahmoudi, Morteza
author_facet Ashkarran, Ali Akbar
Gharibi, Hassan
Grunberger, Jason W.
Saei, Amir Ata
Khurana, Nitish
Mohammadpour, Raziye
Ghandehari, Hamidreza
Mahmoudi, Morteza
author_sort Ashkarran, Ali Akbar
collection PubMed
description [Image: see text] As various nanoparticles (NPs) are increasingly being used in nanomedicine products for more effective and less toxic therapy and diagnosis of diseases, there is a growing need to understand their biological fate in different sexes. Herein, we report a proof-of-concept result of sex-specific protein corona compositions on the surface of silica NPs as a function of their size and porosity upon incubation with plasma proteins of female and male BALB/c mice. Our results demonstrate substantial differences between male and female protein corona profiles on the surface of silica nanoparticles. By comparing protein abundances between male and female protein coronas of mesoporous silica nanoparticles and Stöber silica nanoparticles of ∼100, 50, and 100 nm in diameter, respectively, we detected 17, 4, and 4 distinct proteins, respectively, that were found at significantly different concentrations for these constructs. These initial findings demonstrate that animal sex can influence protein corona formation on silica NPs as a function of the physicochemical properties. A more thorough consideration of the role of plasma sex would enable nanomedicine community to design and develop safer and more efficient diagnostic and therapeutic nanomedicine products for both sexes.
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spelling pubmed-99364982023-02-18 Sex-Specific Silica Nanoparticle Protein Corona Compositions Exposed to Male and Female BALB/c Mice Plasmas Ashkarran, Ali Akbar Gharibi, Hassan Grunberger, Jason W. Saei, Amir Ata Khurana, Nitish Mohammadpour, Raziye Ghandehari, Hamidreza Mahmoudi, Morteza ACS Bio Med Chem Au [Image: see text] As various nanoparticles (NPs) are increasingly being used in nanomedicine products for more effective and less toxic therapy and diagnosis of diseases, there is a growing need to understand their biological fate in different sexes. Herein, we report a proof-of-concept result of sex-specific protein corona compositions on the surface of silica NPs as a function of their size and porosity upon incubation with plasma proteins of female and male BALB/c mice. Our results demonstrate substantial differences between male and female protein corona profiles on the surface of silica nanoparticles. By comparing protein abundances between male and female protein coronas of mesoporous silica nanoparticles and Stöber silica nanoparticles of ∼100, 50, and 100 nm in diameter, respectively, we detected 17, 4, and 4 distinct proteins, respectively, that were found at significantly different concentrations for these constructs. These initial findings demonstrate that animal sex can influence protein corona formation on silica NPs as a function of the physicochemical properties. A more thorough consideration of the role of plasma sex would enable nanomedicine community to design and develop safer and more efficient diagnostic and therapeutic nanomedicine products for both sexes. American Chemical Society 2022-11-07 /pmc/articles/PMC9936498/ /pubmed/36820312 http://dx.doi.org/10.1021/acsbiomedchemau.2c00040 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Ashkarran, Ali Akbar
Gharibi, Hassan
Grunberger, Jason W.
Saei, Amir Ata
Khurana, Nitish
Mohammadpour, Raziye
Ghandehari, Hamidreza
Mahmoudi, Morteza
Sex-Specific Silica Nanoparticle Protein Corona Compositions Exposed to Male and Female BALB/c Mice Plasmas
title Sex-Specific Silica Nanoparticle Protein Corona Compositions Exposed to Male and Female BALB/c Mice Plasmas
title_full Sex-Specific Silica Nanoparticle Protein Corona Compositions Exposed to Male and Female BALB/c Mice Plasmas
title_fullStr Sex-Specific Silica Nanoparticle Protein Corona Compositions Exposed to Male and Female BALB/c Mice Plasmas
title_full_unstemmed Sex-Specific Silica Nanoparticle Protein Corona Compositions Exposed to Male and Female BALB/c Mice Plasmas
title_short Sex-Specific Silica Nanoparticle Protein Corona Compositions Exposed to Male and Female BALB/c Mice Plasmas
title_sort sex-specific silica nanoparticle protein corona compositions exposed to male and female balb/c mice plasmas
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936498/
https://www.ncbi.nlm.nih.gov/pubmed/36820312
http://dx.doi.org/10.1021/acsbiomedchemau.2c00040
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