Surface coating affects behavior of metallic nanoparticles in a biological environment

• Darija Domazet Jurašin,
• Marija Ćurlin,
• Ivona Capjak,
• Tea Crnković,
• Marija Lovrić,
• Michal Babič,
• Daniel Horák,
• Ivana Vinković Vrček and
• Srećko Gajović

Beilstein J. Nanotechnol. 2016, 7, 246–262, doi:10.3762/bjnano.7.23

• media like dissolution, adsorption, binding, and aggregation, all influencing biological impacts by affecting reactive oxygen species generation, cellular uptake and NP biodistribution [15][16][17][18]. Metallic NPs usually aggregate in media with high electrolyte content that correspond to biological

Atomic force microscopy as analytical tool to study physico-mechanical properties of intestinal cells

• Christa Schimpel,
• Oliver Werzer,
• Eleonore Fröhlich,
• Gerd Leitinger,
• Markus Absenger-Novak,
• Birgit Teubl,
• Andreas Zimmer and
• Eva Roblegg

Beilstein J. Nanotechnol. 2015, 6, 1457–1466, doi:10.3762/bjnano.6.151

• , differing in lengths as well as diameters. This suggests that the absence of a well-developed brush border in M cells may facilitate the adherence of antigens on the cell surface and, as a consequence, cellular uptake processes [2]. By contrast, the large surface area of intestinal microvilli is more

• fill remaining data gaps on the effects of these parameters on cell mechanics/kinetics and, as a consequence, on cellular uptake processes (e.g., nanoparticulate systems/antigens). Conclusion The current study shows that cytoskeletal structures and the content of F-actin filaments strongly impact

• properties of cells can be directly linked to cell adhesion, adhesion to the smooth and more elastic surface of M cells is enhanced, thus, facilitating the adherence of antigens and, as a consequence, cellular uptake processes. Experimental Cell cultures Raji B cells were a kind gift from R. Fuchs (Medical

PLGA nanoparticles as a platform for vitamin D-based cancer therapy

• Maria J. Ramalho,
• Joana A. Loureiro,
• Bárbara Gomes,
• Manuela F. Frasco,
• Manuel A. N. Coelho and
• M. Carmo Pereira

Beilstein J. Nanotechnol. 2015, 6, 1306–1318, doi:10.3762/bjnano.6.135

• calcitriol remained stable at release conditions throughout the experiment period. Cellular uptake of PLGA NPs and calcitriol-induced morphological changes The internalization of fluorescent C6–calcitriol–PLGA NPs by S2-013, hTERT-HPNE and A549 cells was evaluated by confocal microscopy. Counterstaining of

Protein corona – from molecular adsorption to physiological complexity

• Lennart Treuel,
• Dominic Docter,
• Michael Maskos and
• Roland H. Stauber

Beilstein J. Nanotechnol. 2015, 6, 857–873, doi:10.3762/bjnano.6.88

• composition and the latest findings that help to shed light on temporal evolution of the full serum corona for the first time. Finally, we discuss the most recent advances regarding the molecular-scale mechanistic role of the protein corona in cellular uptake of NPs. Keywords: agglomeration; corona

• charge [4][9] are critical factors determining the formation and nature of the protein corona. The composition and molecular properties of the protein corona have been shown to be influential factors for the cellular uptake of NPs [7][10][11][12] but direct links between structure and effect remain to be

• biological environment. The formation of the biomolecular corona around the NPs modulated their behavior: cells of the blood system seemed to be protected against NP-induced (patho)biological processes by the presence of the corona and also cellular uptake could be promoted [10]. Effect of the corona

Pulmonary surfactant augments cytotoxicity of silica nanoparticles: Studies on an in vitro air–blood barrier model

• Jennifer Y. Kasper,
• Lisa Feiden,
• Maria I. Hermanns,
• Christoph Bantz,
• Michael Maskos,
• Ronald E. Unger and
• C. James Kirkpatrick

Beilstein J. Nanotechnol. 2015, 6, 517–528, doi:10.3762/bjnano.6.54

• ). All predilutions were applied 1:10 in serum-free medium to the cells (96er well and transwells: 10 µL NP-dispersion + 90 µL serumfree medium and ibidi wells: 30 µL NP-dispersion + 270 µL serum-free medium). Preliminary, cellular uptake of the NPs was examined for the monocultures of A549 on ibidi µ

• –NH2 at a concentration of 50 µg/mL (58 ± 22% and 59 ± 10%) and 100 µg/mL (49 ± 25% and 29 ± 15%). No cell loss was observed after incubation with aSNP–COOH. Figure 2 shows the cellular uptake of aSNPs with different surfaces in A549 (–plain, –NH2, –COOH; 50 µg/mL). The cells clearly internalized all

• three aSNPs after an incubation time of 4 h in serum-free medium. An approximate quantification of cellular uptake via fluorescence intensity measurement of the images could not be conducted due to the variable fluorescence intensity of the aSNP labeling itself. Comparing all three aSNPs using same

A surface acoustic wave-driven micropump for particle uptake investigation under physiological flow conditions in very small volumes

• Florian G. Strobl,
• Dominik Breyer,
• Phillip Link,
• Adriano A. Torrano,
• Christoph Bräuchle,
• Matthias F. Schneider and
• Achim Wixforth

Beilstein J. Nanotechnol. 2015, 6, 414–419, doi:10.3762/bjnano.6.41

• physiological flow conditions the particle uptake rates for this system are significantly lower than at low shear conditions. This underlines the vital importance of the fluidic environment for cellular uptake mechanisms. Keywords: acoustic streaming; cellular uptake; flow; nanoparticles; sedimentation; shear

• of experimental data [1]. Providing that the cellular uptake mechanisms are fast enough, the particle uptake rate at a given particle concentration in the medium, Cm , will be limited by the particle motion and the re-supply in the medium. For small particles, diffusion will dominate the delivery

• surrounding for these cells, which are exposed in vivo to shear rates of up to 3000 s−1 [6]. It was recently shown that the glycocalix of endothelial cells is substantially reorganized under shear [7] and several effects of shear stress on cellular uptake mechanisms have been reported [8][9][10]. One solution

Hematopoietic and mesenchymal stem cells: polymeric nanoparticle uptake and lineage differentiation

• Ivonne Brüstle,
• Thomas Simmet,
• Gerd Ulrich Nienhaus,
• Katharina Landfester and
• Volker Mailänder

Beilstein J. Nanotechnol. 2015, 6, 383–395, doi:10.3762/bjnano.6.38

• into the system, toxicity can occur from the nanoparticles themselves or from the associated components of the nanoparticles that might be released during degradation in vivo. In addition to potentially causing toxicity after cellular uptake, nanoparticles could also alter cellular functions such as

• differentiation studies, cellular uptake and cytotoxicity of the particles were quantitatively determined by flow cytometry. After incubation with 300 µg/mL nanoparticles for 24 h, hMSCs showed a reasonable uptake of polystyrene nanoparticles (PS, Figure 1A). Since here only one population was detected in flow

• hHSCs are able to take up different polymeric particles at a reasonable concentration without showing any signs of toxicity. The surface functionalization of the polystyrene particle with carboxy groups did not improve the cellular uptake for hHSCs, while for hMSCs, this effect was confirmed. The

Overview about the localization of nanoparticles in tissue and cellular context by different imaging techniques

• Anja Ostrowski,
• Daniel Nordmeyer,
• Alexander Boreham,
• Cornelia Holzhausen,
• Lars Mundhenk,
• Christina Graf,
• Martina C. Meinke,
• Annika Vogt,
• Sabrina Hadam,
• Jürgen Lademann,
• Eckart Rühl,
• Ulrike Alexiev and
• Achim D. Gruber

Beilstein J. Nanotechnol. 2015, 6, 263–280, doi:10.3762/bjnano.6.25

• . A single technique is often insufficient to address all questions regarding the distribution of NP within the body, the cellular uptake, and the target cells and organs. But a combination of different detection methods may provide reliable information on the NP biodistribution and associated

Release behaviour and toxicity evaluation of levodopa from carboxylated single-walled carbon nanotubes

• Julia M. Tan,
• Jhi Biau Foo,
• Sharida Fakurazi and
• Mohd Zobir Hussein

Beilstein J. Nanotechnol. 2015, 6, 243–253, doi:10.3762/bjnano.6.23

• cellular uptake experiments are required and are currently under investigation. Conclusion In conclusion, a new, versatile nanohybrid based on a very simple method for the administration of LD has been developed. The findings of this study reveal that the loading capacity of SWCNT–COOH is approximately

Tailoring the ligand shell for the control of cellular uptake and optical properties of nanocrystals

• Johannes Ostermann,
• Christian Schmidtke,
• Christopher Wolter,
• Jan-Philip Merkl,
• Hauke Kloust and
• Horst Weller

Beilstein J. Nanotechnol. 2015, 6, 232–242, doi:10.3762/bjnano.6.22

• and specificity in a broad in vitro test is demonstrated. Keywords: biolable; cellular uptake; fluorescence quenching; poylmeric micelles; quantum dots; Introduction One of the main challenges in using high quality nanoparticles for biological applications is to ensure that the ligand system

• . Since cellular uptake mechanisms except from phagocytosis are known to work best with small structures below 150 nm [22], only spherical micelles fulfilling this requirement will be discussed. To ensure a good compatibility between the hydrophobic particles and the inner core of the final micellar

• to enhance the cellular uptake, due to the attractive interaction with the negatively charged cell membrane [35][36]. Therefore, control over the surface chemistry is crucial to study the nanocontainers behavior in vitro and in vivo. Figure 7 shows possible functionalization of PI-b-PEG prior to the

The distribution and degradation of radiolabeled superparamagnetic iron oxide nanoparticles and quantum dots in mice

• Denise Bargheer,
• Artur Giemsa,
• Barbara Freund,
• Markus Heine,
• Christian Waurisch,
• Gordon M. Stachowski,
• Stephen G. Hickey,
• Alexander Eychmüller,
• Jörg Heeren and
• Peter Nielsen

Beilstein J. Nanotechnol. 2015, 6, 111–123, doi:10.3762/bjnano.6.11

• . In MRI, the correlation of the relaxation times to the local nanoparticle concentrations is difficult due to possible agglomeration, where the increase of hydrodynamic diameters caused by opsonization and the difficulty in the quantification of the degradation and the cellular uptake of particles [22

Synthesis of boron nitride nanotubes and their applications

• Saban Kalay,
• Zehra Yilmaz,
• Ozlem Sen,
• Melis Emanet,
• Emine Kazanc and
• Mustafa Çulha

Beilstein J. Nanotechnol. 2015, 6, 84–102, doi:10.3762/bjnano.6.9

• -employed, aminosilane used in many applications. Ciofani et al. used APTES as an agent for silica coating to functionalize BNNTs [15]. For cellular uptake studies, a fluorescent dye, Oregon Green 488 carboxylic acid, succinimidyl ester was covalently bound to the functionalized BNNTs. The NIH/3T3

• of nanomedicine. The covalent grafting of BNNTs with human transferrin, linked through a carbamide bond, was reported [67]. The transferrin–BNNTs were tested on primary human umbilical vein endothelial cells (HUVECs) to investigate their cellular uptake. It was concluded that the functionalization of

• with GC during a 12 h sonication process. The TEM results indicated that the GC–BNNTs had two different configurations: bamboo-like shaped and noncontinuous walled. HUVECs were treated with the GC–BNNTs and the cellular uptake of the GC–BNNTs was observed. However, the uptake mechanism remains unclear

Mammalian cell growth on gold nanoparticle-decorated substrates is influenced by the nanoparticle coating

• Christina Rosman,
• Sebastien Pierrat,
• Marco Tarantola,
• David Schneider,
• Eva Sunnick,
• Andreas Janshoff and
• Carsten Sönnichsen

Beilstein J. Nanotechnol. 2014, 5, 2479–2488, doi:10.3762/bjnano.5.257

• nanoparticles on substrate require in order to prevent their removal by cells seem to be necessary. In previous studies, the cytotoxic impact of apical exposure of the same functionalized nanoparticles to the same epithelial cell line (MDCK II) was presented [18] and the cellular uptake was quantified [20]. It

Intake of silica nanoparticles by giant lipid vesicles: influence of particle size and thermodynamic membrane state

• Florian G. Strobl,
• Florian Seitz,
• Christoph Westerhausen,
• Armin Reller,
• Adriano A. Torrano,
• Christoph Bräuchle,
• Achim Wixforth and
• Matthias F. Schneider

Beilstein J. Nanotechnol. 2014, 5, 2468–2478, doi:10.3762/bjnano.5.256

• course, in a biological system, active mechanisms play a key role in cellular uptake. But these examples show that the significance of physical interactions might often be underestimated. This is also indicated in several studies, showing striking similarities between the uptake of membrane-active

• can be internalized independent from complex cell machineries and that lipid domains (rafts) play a crucial role in cellular uptake mechanisms [13][32][53]. An understanding of the unspecific physical aspects of membrane–particle interactions is of vital importance for a discussion of these findings

Functionalized polystyrene nanoparticles as a platform for studying bio–nano interactions

• Cornelia Loos,
• Tatiana Syrovets,
• Anna Musyanovych,
• Volker Mailänder,
• Katharina Landfester,
• G. Ulrich Nienhaus and
• Thomas Simmet

Beilstein J. Nanotechnol. 2014, 5, 2403–2412, doi:10.3762/bjnano.5.250

• , positively charged particles were found mostly in leukemia xenografts [43]. With particles left in the cell culture media, the cellular uptake reaches equilibrium within 24 h. When particles were removed from the media, there was virtually an exponential decrease of the amount of particles in proliferating

Nanoparticle interactions with live cells: Quantitative fluorescence microscopy of nanoparticle size effects

• Li Shang,
• Karin Nienhaus,
• Xiue Jiang,
• Linxiao Yang,
• Katharina Landfester,
• Volker Mailänder,
• Thomas Simmet and
• G. Ulrich Nienhaus

Beilstein J. Nanotechnol. 2014, 5, 2388–2397, doi:10.3762/bjnano.5.248

• nanoparticles (NPs) with cells are still not well enough understood. NP size is a key parameter that controls the endocytic mechanism and affects the cellular uptake yield. Therefore, we have systematically analyzed the cellular uptake of fluorescent NPs in the size range of 3.3–100 nm (diameter) by live cells

• as the subcellular distribution upon internalization [21][22][23]. Presently, the effect of NP size on cellular uptake is discussed controversially, which may, at least in part, be associated with the diverse experimental conditions and techniques chosen to monitor NP-cell interactions on cultured

• systematically quantify the uptake kinetics of fluorescent NPs in the size range of 3.3–100 nm (diameter) by live cells. This imaging technique is non-invasive and, because of its high temporal and spatial resolution, well suited to watch NPs invade cells in real time. Here we compare the cellular uptake of NPs

Synthesis of radioactively labelled CdSe/CdS/ZnS quantum dots for in vivo experiments

• Gordon M. Stachowski,
• Christoph Bauer,
• Christian Waurisch,
• Denise Bargheer,
• Peter Nielsen,
• Jörg Heeren,
• Stephen G. Hickey and
• Alexander Eychmüller

Beilstein J. Nanotechnol. 2014, 5, 2383–2387, doi:10.3762/bjnano.5.247

• quantification of the QD concentration during cellular uptake to be calculated. Here, the measured amount of radioactivity can be related to the amount or concentration of the QD ensemble or their metabolites (i.e., ionic species). To avoid any potential chemical inconsistencies we replace the typical precursors

Interaction of dermatologically relevant nanoparticles with skin cells and skin

• Annika Vogt,
• Fiorenza Rancan,
• Sebastian Ahlberg,
• Berouz Nazemi,
• Chun Sik Choe,
• Maxim E. Darvin,
• Sabrina Hadam,
• Ulrike Blume-Peytavi,
• Kateryna Loza,
• Jörg Diendorf,
• Matthias Epple,
• Christina Graf,
• Eckart Rühl,
• Martina C. Meinke and
• Jürgen Lademann

Beilstein J. Nanotechnol. 2014, 5, 2363–2373, doi:10.3762/bjnano.5.245

• cellular uptake, including optical microscopy, electron microscopy, X-ray microscopy on cells and tissue sections, flow cytometry of isolated skin cells as well as Raman microscopy on whole tissue blocks. In order to assess the biological relevance of such findings, cell viability and free radical

• epidermis is of high relevance. As a result of the special architecture of the skin, levels of interactions include the translocation step across the skin barrier, cellular uptake as well as biological effects. In fact, biological responses to nanoparticle exposure may occur on the cellular level, but also

• were able to isolate skin cells which had taken up particles from treated ex vivo human skin (Figure 1d) [3][11]. In accordance with previous studies, the particle size appeared to be a major determinant for cellular uptake. Notably, after ex vivo topical application of silica particles on human skin

Effect of silver nanoparticles on human mesenchymal stem cell differentiation

• Christina Sengstock,
• Jörg Diendorf,
• Matthias Epple,
• Thomas A. Schildhauer and
• Manfred Köller

Beilstein J. Nanotechnol. 2014, 5, 2058–2069, doi:10.3762/bjnano.5.214

• the vast number of toxicological and microbiological studies [7][9][21], only a few studies have investigated whether the differentiation potential of hMSCs was maintained after the uptake of different nanoparticles [31][32][33]. Therefore, the aim of this study was to investigate the cellular uptake

• conclusion, silver nanoparticles with a size of 80 nm (hydrodynamic diameter) were ingested into hMSCs as nanoparticulate material. After cellular uptake, these Ag-NP were mainly associated with the endo-lysosomal cell compartment and occurred as silver agglomerates within these organelles. Exposure of hMSCs

Effects of surface functionalization on the adsorption of human serum albumin onto nanoparticles – a fluorescence correlation spectroscopy study

• Pauline Maffre,
• Stefan Brandholt,
• Karin Nienhaus,
• Li Shang,
• Wolfgang J. Parak and
• G. Ulrich Nienhaus

Beilstein J. Nanotechnol. 2014, 5, 2036–2047, doi:10.3762/bjnano.5.212

• the bare NP surface [2][18][19][20]. To control the biological effects of NPs (e.g., to accomplish targeted delivery to specific cells or tissues or to inhibit cellular uptake), it is extremely important to understand how the properties of the NP surface can control the structure and dynamics of the

Carbon nano-onions (multi-layer fullerenes): chemistry and applications

• Juergen Bartelmess and
• Silvia Giordani

Beilstein J. Nanotechnol. 2014, 5, 1980–1998, doi:10.3762/bjnano.5.207

• (Figure 6). The cytotoxicity and immunomodulatory properties of the synthesized fluorescein-CNO derivative were elucidated and compared with similarly functionalized CNTs. We could show that CNOs exhibit efficient cellular uptake, weak inflammatory potential, and low cytotoxicity and are therefore

• particles have demonstrated high cellular uptake, low cytotoxicity and lower inflammatory potential than CNTs and a very promising future for biomedical applications. HRTEM images of (a) diamond nanoparticles, (b) spherical carbon onions, and (c) polyhedral carbon onions. Diamond nanoparticles are

PVP-coated, negatively charged silver nanoparticles: A multi-center study of their physicochemical characteristics, cell culture and in vivo experiments

• Sebastian Ahlberg,
• Alexandra Antonopulos,
• Jörg Diendorf,
• Ralf Dringen,
• Matthias Epple,
• Rebekka Flöck,
• Wolfgang Goedecke,
• Christina Graf,
• Nadine Haberl,
• Jens Helmlinger,
• Fabian Herzog,
• Frederike Heuer,
• Stephanie Hirn,
• Christian Johannes,
• Stefanie Kittler,
• Manfred Köller,
• Katrin Korn,
• Wolfgang G. Kreyling,
• Fritz Krombach,
• Jürgen Lademann,
• Kateryna Loza,
• Eva M. Luther,
• Marcelina Malissek,
• Martina C. Meinke,
• Daniel Nordmeyer,
• Anne Pailliart,
• Jörg Raabe,
• Fiorenza Rancan,
• Barbara Rothen-Rutishauser,
• Eckart Rühl,
• Carsten Schleh,
• Andreas Seibel,
• Christina Sengstock,
• Lennart Treuel,
• Annika Vogt,
• Katrin Weber and
• Reinhard Zellner

Beilstein J. Nanotechnol. 2014, 5, 1944–1965, doi:10.3762/bjnano.5.205

• biological media (i.e., in the presence of proteins) the surface of silver nanoparticles is rapidly coated by a protein corona that influences their physicochemical and biological properties including cellular uptake. Silver nanoparticles are taken up by cell-type specific endocytosis pathways as

• have investigated whether STXM can be applied to investigate the cellular uptake process of silver nanoparticles in human mesenchymal stem cells (hMSC). For this purpose, hMSC were grown on collagen-coated Si3N4-membranes and incubated for 24 h with O2-free aqueous dispersions of silver particles (c

• without major mechanical stress for a cell is a useful tool to detect internalized metallic nanoparticles within cells [86]. As reported in the literature, the cellular uptake of nanoparticles is a conserved process during which extracellular substances are internalized by enclosing them into vesicles

Carbon-based smart nanomaterials in biomedicine and neuroengineering

• Antonina M. Monaco and
• Michele Giugliano

Beilstein J. Nanotechnol. 2014, 5, 1849–1863, doi:10.3762/bjnano.5.196

• were incubated with oxidised NDs, suggesting it was a specific consequence of the surface chemistry of NDs. Nonetheless, Xing and co-workers noted that NDs and oxidised NDs induce overall less DNA damage than that caused by MWCNTs. The investigation of the cellular uptake mechanisms of NDs is also a

• key aspect for biological applications of NDs. Vaijayanthimala and colleagues [75] reported that cellular uptake was strictly related to the surface functionalisation of NDs and that it took place through clathrin-mediated, energy-dependent, endocytosis processes. Schrand et al. [76] also investigated

Biocompatibility of cerium dioxide and silicon dioxide nanoparticles with endothelial cells

• Claudia Strobel,
• Martin Förster and
• Ingrid Hilger

Beilstein J. Nanotechnol. 2014, 5, 1795–1807, doi:10.3762/bjnano.5.190

• indicated a steric stabilization of nanoparticles due to interaction with proteins. After cellular uptake, the CeO2 nanoparticles were localized around the nucleus in a ring-shaped manner. The nanoparticles revealed concentration and time, but no size-dependent effects on the cellular adenosine triphosphate

• predictions are not possible at present. Nevertheless, the different behavior could explained, at least in parts, by the exposure of different intracellular nanoparticle amounts per cell as a result of cell type specific variations in cellular uptake and exocytosis rates. We also investigated the release of

• fibroblasts (BJ cells, American Type Culture Collection (ATCC), USA) were used as positive cells for CD90 (fibroblast phenotype). 10,000 cells were measured for each sample and analysis was performed using CellQuest ProTM software (Becton Dickinson GmbH, Germany). Cellular uptake and intracellular

Influence of surface-modified maghemite nanoparticles on in vitro survival of human stem cells

• Michal Babič,
• Daniel Horák,
• Lyubov L. Lukash,
• Tetiana A. Ruban,
• Yurii N. Kolomiets,
• Svitlana P. Shpylova and
• Oksana A. Grypych

Beilstein J. Nanotechnol. 2014, 5, 1732–1737, doi:10.3762/bjnano.5.183

• cellular uptake of the magnetic nanoparticles and enhance their specific targeting effect, surface functionalization has to be employed to coat the nanoparticle surface with ligands that could specifically interact with the receptors overexpressed in the cell membrane. While the size of the dry