Cargando…

Microfluidic-Assisted Fabrication of Dual-Coated pH-Sensitive Mesoporous Silica Nanoparticles for Protein Delivery

Microfluidics has become a popular method for constructing nanosystems in recent years, but it can also be used to coat other materials with polymeric layers. The polymeric coating may serve as a diffusion barrier against hydrophilic compounds, a responsive layer for controlled release, or a functio...

Descripción completa

Detalles Bibliográficos
Autores principales: Küçüktürkmen, Berrin, Inam, Wali, Howaili, Fadak, Gouda, Mariam, Prabhakar, Neeraj, Zhang, Hongbo, Rosenholm, Jessica M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8946851/
https://www.ncbi.nlm.nih.gov/pubmed/35323451
http://dx.doi.org/10.3390/bios12030181
_version_ 1784674290043453440
author Küçüktürkmen, Berrin
Inam, Wali
Howaili, Fadak
Gouda, Mariam
Prabhakar, Neeraj
Zhang, Hongbo
Rosenholm, Jessica M.
author_facet Küçüktürkmen, Berrin
Inam, Wali
Howaili, Fadak
Gouda, Mariam
Prabhakar, Neeraj
Zhang, Hongbo
Rosenholm, Jessica M.
author_sort Küçüktürkmen, Berrin
collection PubMed
description Microfluidics has become a popular method for constructing nanosystems in recent years, but it can also be used to coat other materials with polymeric layers. The polymeric coating may serve as a diffusion barrier against hydrophilic compounds, a responsive layer for controlled release, or a functional layer introduced to a nanocomposite for achieving the desired surface chemistry. In this study, mesoporous silica nanoparticles (MSNs) with enlarged pores were synthesized to achieve high protein loading combined with high protein retention within the MSN system with the aid of a microfluidic coating. Thus, MSNs were first coated with a cationic polyelectrolyte, poly (diallyldimethylammonium chloride) (PDDMA), and to potentially further control the protein release, a second coating of a pH-sensitive polymer (spermine-modified acetylated dextran, SpAcDEX) was deposited by a designed microfluidic device. The protective PDDMA layer was first formed under aqueous conditions, whereby the bioactivity of the protein could be maintained. The second coating polymer, SpAcDEX, was preferred to provide pH-sensitive protein release in the intracellular environment. The optimized formulation was effectively taken up by the cells along with the loaded protein cargo. This proof-of-concept study thus demonstrated that the use of microfluidic technologies for the design of protein delivery systems has great potential in terms of creating multicomponent systems and preserving protein stability.
format Online
Article
Text
id pubmed-8946851
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-89468512022-03-25 Microfluidic-Assisted Fabrication of Dual-Coated pH-Sensitive Mesoporous Silica Nanoparticles for Protein Delivery Küçüktürkmen, Berrin Inam, Wali Howaili, Fadak Gouda, Mariam Prabhakar, Neeraj Zhang, Hongbo Rosenholm, Jessica M. Biosensors (Basel) Article Microfluidics has become a popular method for constructing nanosystems in recent years, but it can also be used to coat other materials with polymeric layers. The polymeric coating may serve as a diffusion barrier against hydrophilic compounds, a responsive layer for controlled release, or a functional layer introduced to a nanocomposite for achieving the desired surface chemistry. In this study, mesoporous silica nanoparticles (MSNs) with enlarged pores were synthesized to achieve high protein loading combined with high protein retention within the MSN system with the aid of a microfluidic coating. Thus, MSNs were first coated with a cationic polyelectrolyte, poly (diallyldimethylammonium chloride) (PDDMA), and to potentially further control the protein release, a second coating of a pH-sensitive polymer (spermine-modified acetylated dextran, SpAcDEX) was deposited by a designed microfluidic device. The protective PDDMA layer was first formed under aqueous conditions, whereby the bioactivity of the protein could be maintained. The second coating polymer, SpAcDEX, was preferred to provide pH-sensitive protein release in the intracellular environment. The optimized formulation was effectively taken up by the cells along with the loaded protein cargo. This proof-of-concept study thus demonstrated that the use of microfluidic technologies for the design of protein delivery systems has great potential in terms of creating multicomponent systems and preserving protein stability. MDPI 2022-03-18 /pmc/articles/PMC8946851/ /pubmed/35323451 http://dx.doi.org/10.3390/bios12030181 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Küçüktürkmen, Berrin
Inam, Wali
Howaili, Fadak
Gouda, Mariam
Prabhakar, Neeraj
Zhang, Hongbo
Rosenholm, Jessica M.
Microfluidic-Assisted Fabrication of Dual-Coated pH-Sensitive Mesoporous Silica Nanoparticles for Protein Delivery
title Microfluidic-Assisted Fabrication of Dual-Coated pH-Sensitive Mesoporous Silica Nanoparticles for Protein Delivery
title_full Microfluidic-Assisted Fabrication of Dual-Coated pH-Sensitive Mesoporous Silica Nanoparticles for Protein Delivery
title_fullStr Microfluidic-Assisted Fabrication of Dual-Coated pH-Sensitive Mesoporous Silica Nanoparticles for Protein Delivery
title_full_unstemmed Microfluidic-Assisted Fabrication of Dual-Coated pH-Sensitive Mesoporous Silica Nanoparticles for Protein Delivery
title_short Microfluidic-Assisted Fabrication of Dual-Coated pH-Sensitive Mesoporous Silica Nanoparticles for Protein Delivery
title_sort microfluidic-assisted fabrication of dual-coated ph-sensitive mesoporous silica nanoparticles for protein delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8946851/
https://www.ncbi.nlm.nih.gov/pubmed/35323451
http://dx.doi.org/10.3390/bios12030181
work_keys_str_mv AT kucukturkmenberrin microfluidicassistedfabricationofdualcoatedphsensitivemesoporoussilicananoparticlesforproteindelivery
AT inamwali microfluidicassistedfabricationofdualcoatedphsensitivemesoporoussilicananoparticlesforproteindelivery
AT howailifadak microfluidicassistedfabricationofdualcoatedphsensitivemesoporoussilicananoparticlesforproteindelivery
AT goudamariam microfluidicassistedfabricationofdualcoatedphsensitivemesoporoussilicananoparticlesforproteindelivery
AT prabhakarneeraj microfluidicassistedfabricationofdualcoatedphsensitivemesoporoussilicananoparticlesforproteindelivery
AT zhanghongbo microfluidicassistedfabricationofdualcoatedphsensitivemesoporoussilicananoparticlesforproteindelivery
AT rosenholmjessicam microfluidicassistedfabricationofdualcoatedphsensitivemesoporoussilicananoparticlesforproteindelivery