scholarly journals Mechanistic understanding of in vivo protein corona formation on polymeric nanoparticles and impact on pharmacokinetics

2017 ◽  
Vol 8 (1) ◽  
Author(s):  
Nicolas Bertrand ◽  
Philippe Grenier ◽  
Morteza Mahmoudi ◽  
Eliana M. Lima ◽  
Eric A. Appel ◽  
...  
2015 ◽  
Vol 6 ◽  
pp. 36-46 ◽  
Author(s):  
Denise Bargheer ◽  
Julius Nielsen ◽  
Gabriella Gébel ◽  
Markus Heine ◽  
Sunhild C Salmen ◽  
...  

A variety of monodisperse superparamagnetic iron oxide particles (SPIOs) was designed in which the surface was modified by PEGylation with mono- or bifunctional poly(ethylene oxide)amines (PEG). Using 125I-labeled test proteins (transferrin, albumin), the binding and exchange of corona proteins was studied first in vitro. Incubation with 125I-transferrin showed that with increasing grade of PEGylation the binding was substantially diminished without a difference between simply adsorbed and covalently bound protein. However, after incubation with excess albumin and subsequently whole plasma, transferrin from the preformed transferrin corona was more and more lost from SPIOs in the case of adsorbed proteins. If non-labeled transferrin was used as preformed corona and excess 125I-labeled albumin was added to the reaction mixtures with different SPIOs, a substantial amount of label was bound to the particles with initially adsorbed transferrin but little or even zero with covalently bound transferrin. These in vitro experiments show a clear difference in the stability of a preformed hard corona with adsorbed or covalently bound protein. This difference seems, however, to be of minor importance in vivo when polymer-coated 59Fe-SPIOs with adsorbed or covalently bound 125I-labeled mouse transferrin were injected intravenously in mice. With both protein coronae the 59Fe/125I-labelled particles were cleared from the blood stream within 30 min and appeared in the liver and spleen to a large extent (>90%). In addition, after 2 h already half of the 125I-labeled transferrin from both nanodevices was recycled back into the plasma and into tissue. This study confirms that adsorbed transferrin from a preformed protein corona is efficiently taken up by cells. It is also highlighted that a radiolabelling technique described in this study may be of value to investigate the role of protein corona formation in vivo for the respective nanoparticle uptake.


Biomaterials ◽  
2021 ◽  
pp. 121021
Author(s):  
Tingbin Zhang ◽  
Galong Li ◽  
Yuqing Miao ◽  
Junjie Lu ◽  
Ningqiang Gong ◽  
...  

Author(s):  
Xue Bai ◽  
Jiali Wang ◽  
Qingxin Mu ◽  
Gaoxing Su

Understanding the basic interactions between engineered nanoparticles (ENPs) and biological systems is essential for evaluating ENPs’ safety and developing better nanomedicine. Profound interactions between ENPs and biomolecules such as proteins are inevitable to occur when ENPs are administered or exposed to biological systems, for example, through intravenous injection, oral, or respiration. As a key component of these interactions, protein corona (PC) is immediately formed surrounding the outlayer of ENPs. PC formation is crucial because it gives ENPs a new biological identity by altering not only the physiochemical properties, but also the biobehaviors of ENPs. In the past two decades, most investigations about PC formation were carried out with in vitro systems which could not represent the true events occurring within in vivo systems. Most recently, studies of in vivo PC formation were reported, and it was found that the protein compositions and structures were very different from those formed in vitro. Herein, we provide an in-time review of the recent investigations of this in vivo PC formation of ENPs. In this review, commonly used characterization methods and compositions of in vivo PC are summarized firstly. Next, we highlight the impacts of the in vivo PC formation on absorption, blood circulation, biodistribution, metabolism, and toxicity of administered ENPs. We also introduce the applications of modulating in vivo PC formation in nanomedicine. We further discuss the challenges and future perspectives.


2017 ◽  
Vol 18 (6) ◽  
pp. 1762-1771 ◽  
Author(s):  
Katja Obst ◽  
Guy Yealland ◽  
Benjamin Balzus ◽  
Enrico Miceli ◽  
Mathias Dimde ◽  
...  

Materials ◽  
2019 ◽  
Vol 12 (14) ◽  
pp. 2218 ◽  
Author(s):  
Amalia Ruiz ◽  
Adán Alpízar ◽  
Lilianne Beola ◽  
Carmen Rubio ◽  
Helena Gavilán ◽  
...  

Superparamagnetic iron oxide nanoparticles are one of the most prominent agents used in theranostic applications, with MRI imaging the main application assessed. The biomolecular interface formed on the surface of a nanoparticle in a biological medium determines its behaviour in vitro and in vivo. In this study, we have compared the formation of the protein corona on highly monodisperse iron oxide nanoparticles with two different coatings, dimercaptosuccinic acid (DMSA), and after conjugation, with a bifunctional polyethylene glycol (PEG)-derived molecule (2000 Da) in the presence of Wistar rat plasma. The protein fingerprints around the nanoparticles were analysed in an extensive proteomic study. The results presented in this work indicate that the composition of the protein corona is very difficult to predict. Proteins from different functional categories—cell components, lipoproteins, complement, coagulation, immunoglobulins, enzymes and transport proteins—were identified in all samples with very small variability. Although both types of nanoparticles have similar amounts of bonded proteins, very slight differences in the composition of the corona might explain the variation observed in the uptake and biotransformation of these nanoparticles in Caco-2 and RAW 264.7 cells. Cytotoxicity was also studied using a standard 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay. Controlling nanoparticles’ reactivity to the biological environment by deciding on its surface functionalization may suggest new routes in the control of the biodistribution, biodegradation and clearance of multifunctional nanomedicines.


Nanoscale ◽  
2018 ◽  
Vol 10 (3) ◽  
pp. 1256-1264 ◽  
Author(s):  
Rafaela García-Álvarez ◽  
Marilena Hadjidemetriou ◽  
Ana Sánchez-Iglesias ◽  
Luis M. Liz-Marzán ◽  
Kostas Kostarelos

A detailed study is presented of in vivo protein corona formation on anisotropic gold nanoparticles, after blood circulation in mice.


RSC Advances ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 2856-2869
Author(s):  
Priya S. R. Naidu ◽  
Eleanor Denham ◽  
Carole A. Bartlett ◽  
Terry McGonigle ◽  
Nicolas L. Taylor ◽  
...  

Transferrin (Tf)-functionalized p(HEMA-ran-GMA) nanoparticles were designed to incorporate and release a water-soluble combination of three ion channel antagonists, identified as a promising therapy for secondary degeneration following neurotrauma.


2021 ◽  
Author(s):  
Christian Isalomboto Nkanga ◽  
Young Hun Chung ◽  
Sourabh Shukla ◽  
Jingcheng Zhou ◽  
Jesse V. Jokerst ◽  
...  

The coating of tobacco mosaic virus (TMV) nanoparticles Gd-Cy5-TMV with polydopamine (PDA) increased protein corona formation and shortened plasma circulation, but minimized recognition by anti-TMV antibodies, and extended organ distribution/clearance.


2015 ◽  
Vol 14 (8) ◽  
pp. 1041-1053 ◽  
Author(s):  
Resham Chhabra ◽  
Barbara Ruozi ◽  
Antonietta Vilella ◽  
Daniela Belletti ◽  
Katharina Mangus ◽  
...  

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