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arXiv · 2104.09126

Mixed-charge pseudo-zwitterionic mesoporous silica nanoparticles with lowfouling and reduced cell uptake properties

Noemi Encinas·Mercedes Angulo·Carlos Astorga·Montserrat Colilla·Isabel Izquierdo-Barba·Maria Vallet-Regi
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Abstract

The design of drug delivery systems needs to consider biocompatibility and host body recognition for an adequate actuation. In this work, mesoporous silica nanoparticles (MSNs) surfaces were successfully modified with two silane molecules to provide mixed-charge brushes (-NH3/-PO3) and well evaluated in terms of surface properties, low-fouling capability and cell uptake in comparison to PEGylated MSNs. The modification process consists in the simultaneous direct-grafting of hydrolysable short chain amino (aminopropyl silanetriol, APST) and phosphonate-based (trihydroxy-silyl-propyl-methyl-phosphonate, THSPMP) silane molecules able to provide a pseudo-zwitterionic nature under physiological pH conditions. Results confirmed that both mixed-charged pseudo-zwitterionic MSNs (ZMSN) and PEG-MSN display a significant reduction of serum protein adhesion and macrophages uptake with respect to pristine MSNs. In the case of ZMSNs, his reduction is up to a 70-90% for protein adsorption and c.a. 60% for cellular uptake. This pseudo-zwitterionic modification has been focused on the aim of local treatment of bacterial infections through the synergistic effect between the capability of the nanocarriers to transport and deliver specific drugs and the electrostatic interactions between the mixed-charge systems and bacteria. These findings open promising future expectations for the effective treatment of bacterial infections through the use mixed-charge pseudo-zwitterionic MSNs furtive to macrophages and with antimicrobial properties.

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Noemi Encinas, Mercedes Angulo, Carlos Astorga, Montserrat Colilla, Isabel Izquierdo-Barba, Maria Vallet-Regi. 2021-04-19. Mixed-charge pseudo-zwitterionic mesoporous silica nanoparticles with lowfouling and reduced cell uptake properties. https://doi.org/10.1016/j.actbio.2018.12.012

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