Colloidal stability and degradability of silica nanoparticles in biological fluids: a review

Author(s):  
Andressa da Cruz Schneid ◽  
Lindomar Jose Calumby Albuquerque ◽  
Gabriela Borba Mondo ◽  
Marcelo Ceolin ◽  
Agustin Silvio Picco ◽  
...  
2018 ◽  
Vol 25 (35) ◽  
pp. 4553-4586 ◽  
Author(s):  
Jonas Schubert ◽  
Munish Chanana

Within the last two decades, the field of nanomedicine has not developed as successfully as has widely been hoped for. The main reason for this is the immense complexity of the biological systems, including the physico-chemical properties of the biological fluids as well as the biochemistry and the physiology of living systems. The nanoparticles’ physicochemical properties are also highly important. These differ profoundly from those of freshly synthesized particles when applied in biological/living systems as recent research in this field reveals. The physico-chemical properties of nanoparticles are predefined by their structural and functional design (core and coating material) and are highly affected by their interaction with the environment (temperature, pH, salt, proteins, cells). Since the coating material is the first part of the particle to come in contact with the environment, it does not only provide biocompatibility, but also defines the behavior (e.g. colloidal stability) and the fate (degradation, excretion, accumulation) of nanoparticles in the living systems. Hence, the coating matters, particularly for a nanoparticle system for biomedical applications, which has to fulfill its task in the complex environment of biological fluids, cells and organisms. In this review, we evaluate the performance of different coating materials for nanoparticles concerning their ability to provide colloidal stability in biological media and living systems.


Langmuir ◽  
2020 ◽  
Vol 36 (39) ◽  
pp. 11442-11449 ◽  
Author(s):  
Andressa da Cruz Schneid ◽  
Camila Pedroso Silveira ◽  
Flávia Elisa Galdino ◽  
Larissa Fernanda Ferreira ◽  
Karim Bouchmella ◽  
...  

ACS Nano ◽  
2017 ◽  
Vol 12 (1) ◽  
pp. 187-197 ◽  
Author(s):  
Dominic W. Malcolm ◽  
Jomy J. Varghese ◽  
Janet E. Sorrells ◽  
Catherine E. Ovitt ◽  
Danielle S. W. Benoit

Langmuir ◽  
2012 ◽  
Vol 28 (20) ◽  
pp. 7598-7613 ◽  
Author(s):  
Christina Graf ◽  
Qi Gao ◽  
Irene Schütz ◽  
Christelle Njiki Noufele ◽  
Wentao Ruan ◽  
...  

ACS Nano ◽  
2012 ◽  
Vol 6 (8) ◽  
pp. 6829-6842 ◽  
Author(s):  
Fiorenza Rancan ◽  
Qi Gao ◽  
Christina Graf ◽  
Stefan Troppens ◽  
Sabrina Hadam ◽  
...  

2004 ◽  
Vol 37 (17) ◽  
pp. 6376-6384 ◽  
Author(s):  
Abdeslam El Harrak ◽  
Géraldine Carrot ◽  
Julian Oberdisse ◽  
Christophe Eychenne-Baron ◽  
François Boué

2021 ◽  
Author(s):  
◽  
Garima Dobhal

<p>Nano-sized extracellular vesicles, released by most types of cells, contain information about the cell they originate from and have been shown to be involved in a variety of cellular processes. However, their detection and characterisation has been challenging and non-standardised, which makes comparisons across literature very challenging. While exosomes are known to exist in complex biological fluids such as saliva, breast milk, blood, and urine, their separation and identification from these media are time-consuming. Many researchers use techniques such as transmission electron microscopy for physical characterisation and western blot for protein identification, which are often not available in medical settings. Additionally, while these fluids can be easily obtained, acquiring similar samples from lung environments is a highly invasive procedure. While breath is known to transmit droplets from the lungs, the presence of exosomes in these condensates is unknown. In this project, functionalised InP/ZnS quantum dots (QDs) were used to target exosomes from a number of biological sources and provide a gateway to more fully characterise their ensemble properties. The InP/ZnS QDs were synthesised, and their size dependency on the band gap was investigated in accordance with the theoretical effective mass approximation model for quantum dots. The QDs were produced with hydrophobic oleylamine ligands, and therefore had to be ligand exchanged to be used in biological applications. A range of ligand exchange methods was surveyed to probe the best balance between retention of original quantum yields and best colloidal stability in aqueous systems.The QDs were further conjugated to an antibody specific for CD63, the protein found on exosomes. The conjugation was confirmed using dynamic light scattering and surface plasmon resonance. Finally, the binding of the QD-Antibody probe to the exosome was confirmed using surface plasmon resonance and confocal microscopy. Further modifications of the assay system could lead to multiplex-detection of the different proteins on the exosomes, their characterisation, and a method for the rapid detection of diseases.</p>


Nanomedicine ◽  
2021 ◽  
Vol 16 (2) ◽  
pp. 85-96
Author(s):  
Andressa C Schneid ◽  
Iris RS Ribeiro ◽  
Flávia E Galdino ◽  
Jefferson Bettini ◽  
Mateus B Cardoso

Aim: This work is focused on obtaining degradable mesoporous silica nanoparticles (DMSNs) which are able to maintain their colloidal stability in complex biological media. Materials & methods: DMSNs were synthesized using different ratios of disulfide organosilane (degradable structural moiety) and further functionalized with sulfobetaine silane (SBS) to enhance colloidal stability and improve biological compatibility. Results: There was a clear trade-off between nanoparticle degradability and colloidal stability, since full optimization of the degradation process generated unstable particles, while enhancing colloidal stability resulted in poor DMSNs degradation. It was also shown that acidic pH improved particle degradation which is commonly triggered by reduction stimulus. Conclusion: A chemical composition window was found where DMSNs presented satisfactory colloidal stability in biologically relevant medium, meaningful degradation profiles and high biocompatibility.


Biomimetics ◽  
2018 ◽  
Vol 3 (3) ◽  
pp. 22 ◽  
Author(s):  
Estelle Rascol ◽  
Cédric Pisani ◽  
Christophe Dorandeu ◽  
Jeff Nyalosaso ◽  
Clarence Charnay ◽  
...  

Careful analysis of any new nanomedicine device or disposal should be undertaken to comprehensively characterize the new product before application, so that any unintended side effect is minimized. Because of the increasing number of nanotechnology-based drugs, we can anticipate that regulatory authorities might adapt the approval process for nanomedicine products due to safety concerns, e.g., request a more rigorous testing of the potential toxicity of nanoparticles (NPs). Currently, the use of mesoporous silica nanoparticles (MSN) as drug delivery systems is challenged by a lack of data on the toxicological profile of coated or non-coated MSN. In this context, we have carried out an extensive study documenting the influence of different functionalized MSN on the cellular internalization and in vivo behaviour. In this article, a synthesis of these works is reviewed and the perspectives are drawn. The use of magnetic MSN (Fe3O4@MSN) allows an efficient separation of coated NPs from cell cultures with a simple magnet, leading to results regarding corona formation without experimental bias. Our interest is focused on the mechanism of interaction with model membranes, the adsorption of proteins in biological fluids, the quantification of uptake, and the effect of such NPs on the transcriptomic profile of hepatic cells that are known to be readily concerned by NPs’ uptake in vivo, especially in the case of an intravenous injection.


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