Improved biocompatibility and efficient labeling of neural stem cells with poly(L-lysine)-coated maghemite nanoparticles

• Igor M. Pongrac,
• Marina Dobrivojević,
• Lada Brkić Ahmed,
• Michal Babič,
• Miroslav Šlouf,
• Daniel Horák and
• Srećko Gajović

Beilstein J. Nanotechnol. 2016, 7, 926–936, doi:10.3762/bjnano.7.84

• ) cells. Prussian blue staining After labeling, nanoparticles were removed, cells were washed three times with phosphate buffered saline (PBS), fixed with 4% paraformaldehyde (Sigma-Aldrich) for 20 min, and stained with a 1:1 mixture of 10% K4Fe(CN)6 (Sigma-Aldrich) and 20% HCl for 20 min. Cells were

Reconstitution of the membrane protein OmpF into biomimetic block copolymer–phospholipid hybrid membranes

• Matthias Bieligmeyer,
• Franjo Artukovic,
• Stephan Nussberger,
• Thomas Hirth,
• Thomas Schiestel and
• Michaela Müller

Beilstein J. Nanotechnol. 2016, 7, 881–892, doi:10.3762/bjnano.7.80

• to dry to get rid of organic solvent. Then, the chambers on both sides of the aperture were filled with degassed KCl saline (1 M KCl, 20 mM Tris (pH 8)) and 2 µL of PIPEO/DPhPC in chloroform was painted across the aperture with a fine brush. Successful self-assembly of a membrane was monitored by

Investigating organic multilayers by spectroscopic ellipsometry: specific and non-specific interactions of polyhistidine with NTA self-assembled monolayers

• Ilaria Solano,
• Pietro Parisse,
• Ornella Cavalleri,
• Federico Gramazio,
• Loredana Casalis and
• Maurizio Canepa

Beilstein J. Nanotechnol. 2016, 7, 544–553, doi:10.3762/bjnano.7.48

• nanografted areas have been then imaged in soft contact mode in ethanol or in saline buffer (Tris-HCl 20 mM, NaCl 150 mM, pH 7.4) with commercial cantilevers (CSC38 Mikromasch, k = 0.03 N/m) at the minimum force detectable (0.1 nN). Images and data were analyzed with XEI (Park Instruments) and Igor Pro

Efficiency improvement in the cantilever photothermal excitation method using a photothermal conversion layer

• Natsumi Inada,
• Hitoshi Asakawa,
• Taiki Kobayashi and
• Takeshi Fukuma

Beilstein J. Nanotechnol. 2016, 7, 409–417, doi:10.3762/bjnano.7.36

• of AC55 with a spring constant of ≈140 N/m were improved by 6.1 times and 2.5 times, respectively, by coating with a PTC layer. We experimentally demonstrate high stability of the PTC layer in liquid by AFM imaging of a mica surface with atomic resolution in phosphate buffer saline solution for more

• nominal spring constants of 42 and 85 N/m (PPP-NCHAuD and AC55). In addition, we demonstrate high stability of the PTC layer in liquid by long-term FM-AFM imaging of mica with atomic resolution in phosphate buffer saline (PBS) solution. Results and Discussion Preparation of PTC layers Figure 1 shows a

Early breast cancer screening using iron/iron oxide-based nanoplatforms with sub-femtomolar limits of detection

• Dinusha N. Udukala,
• Hongwang Wang,
• Sebastian O. Wendel,
• Aruni P. Malalasekera,
• Thilani N. Samarakoon,
• Asanka S. Yapa,
• Gayani Abayaweera,
• Matthew T. Basel,
• Pamela Maynez,
• Raquel Ortega,
• Yubisela Toledo,
• Leonie Bossmann,
• Colette Robinson,
• Katharine E. Janik,
• Olga B. Koper,
• Ping Li,
• Massoud Motamedi,
• Daniel A. Higgins,
• Gary Gadbury,
• Gaohong Zhu,
• Deryl L. Troyer and
• Stefan H. Bossmann

Beilstein J. Nanotechnol. 2016, 7, 364–373, doi:10.3762/bjnano.7.33

• (phosphate buffered saline, pH 7.4). The average Fe(0) core diameter is 13 ± 0.5 nm, the Fe3O4 shell thickness is 2.0 ± 0.5 nm (Figure 3). Using statistical modeling, the optimal number of TCPP units per nanoparticle was determined to be 35 ± 3, and the number of cyanine 5.5 units to be 50 ± 4 [31]. We have

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

• saline and cell culture media [19][20][21][22][23][24][25][26][30]. The term aggregation indicates strongly bonded or fused particles and agglomeration indicates more weakly bonded particles. All of the obtained results for the agglomeration of differently coated AgNPs and SPIONs in BM are given in Table

Sonochemical co-deposition of antibacterial nanoparticles and dyes on textiles

• Ilana Perelshtein,
• Anat Lipovsky,
• Nina Perkas,
• Tzanko Tzanov and
• Aharon Gedanken

Beilstein J. Nanotechnol. 2016, 7, 1–8, doi:10.3762/bjnano.7.1

• properties and the dye fastness was studied for 72 h in saline solution aiming at medical applications. Keywords: antibacterial nanoparticles; coating stability; dyes; sonochemical coating; Introduction The preferred technique for coating with nanoparticles (NPs) in most scientific and industrial examples

• the dye structure. The crystalline structure of the metal oxides was examined by XRD (Bruker D8). Leaching experiments Possible leaching of the MO and dyes from the coated textile was tested in saline solution (0.9 % NaCl). A piece of fabric (70 mg) was placed in 10 mL saline and kept at 40 °C for 72

• h under agitation at 100 rpm. The leaching solutions were analyzed by ICP-OES for the presence of ions. The release of NPs into the saline was examined by a high-resolution transmission electron microscope (HRTEM), JEOL, operated at 200 kV. The difference in colorization of the textiles before and

Ultrastructural changes in methicillin-resistant Staphylococcus aureus induced by positively charged silver nanoparticles

• Dulce G. Romero-Urbina,
• Humberto H. Lara,
• J. Jesús Velázquez-Salazar,
• M. Josefina Arellano-Jiménez,
• Eduardo Larios,
• Anand Srinivasan,
• Jose L. Lopez-Ribot and
• Miguel José Yacamán

Beilstein J. Nanotechnol. 2015, 6, 2396–2405, doi:10.3762/bjnano.6.246

• as described in [56] and as suggested by the CLSI (2011). In brief, single colonies of a microbiological culture were grown in selective chromogenic medium plates (ChromAgar BD Biosciences). The colonies were diluted in saline solution and adjusted to 1.5 × 108 CFU/mL. The bacterial suspensions were

Fabrication of hybrid graphene oxide/polyelectrolyte capsules by means of layer-by-layer assembly on erythrocyte cell templates

• Joseba Irigoyen,
• Nikolaos Politakos,
• Eleftheria Diamanti,
• Elena Rojas,
• Marco Marradi,
• Raquel Ledezma,
• Layza Arizmendi,
• J. Alberto Rodríguez,
• Ronald F. Ziolo and
• Sergio E. Moya

Beilstein J. Nanotechnol. 2015, 6, 2310–2318, doi:10.3762/bjnano.6.237

• 15 kg/mol), polystyrenesulfonate sodium salt, (PSS, Mw 70 kg/mol), sodium hypochlorite with active chlorine 13%, phosphate buffered saline 10× (PBS), glutaraldehyde solution grade II 25% in water, Hank´s balanced salt solution 10×, sodium chloride and graphite powder (<45 μm, ≥99.99% trace metals

Electroviscous effect on fluid drag in a microchannel with large zeta potential

• Dalei Jing and
• Bharat Bhushan

Beilstein J. Nanotechnol. 2015, 6, 2207–2216, doi:10.3762/bjnano.6.226

• deionized water and saline solutions using the colloidal probe atomic force microscopy technique. They also found that an increasing surface charge density results in a decreasing slip length. Thus, the coupling between the surface charge and slip should be considered when study the combined effect of EDL

Synthesis, characterization and in vitro biocompatibility study of Au/TMC/Fe₃O₄ nanocomposites as a promising, nontoxic system for biomedical applications

• Hanieh Shirazi,
• Maryam Daneshpour,
• Soheila Kashanian and
• Kobra Omidfar

Beilstein J. Nanotechnol. 2015, 6, 1677–1689, doi:10.3762/bjnano.6.170

• sodium azide (0.01%) and phosphate buffered saline (PBS) (pH 7.2, 0.01 M), the product was stored at 4 °C in a dark bottle [38]. UV analysis of Au nanoparticles In this study, two modes of analysis were performed to compare the concentration of the Au nanoparticles and the rate at which they were

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

• as described earlier in literature [64]. In brief, cells were quickly rinsed in warm phosphate buffered saline (PBS; 0.01 M phosphate buffer, 0.15 M NaCl, pH 7.4) and fixed with 4% formaldehyde in PBS for 15 min at room temperature (RT). Next, cells were washed with PBS and permeabilized for 5 min at

Scalable, high performance, enzymatic cathodes based on nanoimprint lithography

• Dmitry Pankratov,
• Richard Sundberg,
• Javier Sotres,
• Dmitry B. Suyatin,
• Ivan Maximov,
• Sergey Shleev and
• Lars Montelius

Beilstein J. Nanotechnol. 2015, 6, 1377–1384, doi:10.3762/bjnano.6.142

• gift from Amano Enzyme, Inc. (Nagoya, Japan). The specific activity of BOx, measured to be 140 U·mg−1, was determined using 5 mM 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) as an electron donor dissolved in phosphate buffered saline (PBS; 50 mM phosphate buffer containing 0.15 M NaCl

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

• (C6) (Mw 350.43), phosphate buffered saline (PBS), acetic acid, sulforhodamine B (SRB), trypan blue, ribonuclease A (RNase) from bovine pancreas (Mw 13,700; solution of 50% glycerol), propidium iodide (Mw 668.39, purity ≥ 94%) and Triton XTM-100 were purchased from Sigma-Aldrich (St. Louis, MO, USA

Probing fibronectin–antibody interactions using AFM force spectroscopy and lateral force microscopy

• Andrzej J. Kulik,
• Małgorzata Lekka,
• Kyumin Lee,
• Grazyna Pyka-Fościak and
• Wieslaw Nowak

Beilstein J. Nanotechnol. 2015, 6, 1164–1175, doi:10.3762/bjnano.6.118

• fibronectin isolated from human plasma. Other reagents Other reagents used in the experiments were: (a) phosphate buffered saline (PBS, ICN Biomedicals, pH 7.4, containing 10 mM of PO42−, 137 mM of NaCl and 27 mM of KCl) was used to prepare all protein solutions; (b) 3-aminopropyltriethoxysilane (APTES, Sigma

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

• the polymer shell), by live HeLa cells in the presence or absence of human transferrin (TF) and human serum albumin (HSA) in phosphate-buffered saline (PBS) medium. They studied the uptake of the NPs by quantitative confocal fluorescence microscopy. For comparison, they also studied the cellular

Novel ZnO:Ag nanocomposites induce significant oxidative stress in human fibroblast malignant melanoma (Ht144) cells

• Syeda Arooj,
• Samina Nazir,
• Akhtar Nadhman,
• Nafees Ahmad,
• Bakhtiar Muhammad,
• Ishaq Ahmad,
• Kehkashan Mazhar and
• Rashda Abbasi

Beilstein J. Nanotechnol. 2015, 6, 570–582, doi:10.3762/bjnano.6.59

• washed and harvested in ice-cold phosphate buffer saline at 4 °C. Cells were then lysed in cell lysis buffer (2.5 M NaCl, 10 mM Trizma-base at pH 10.0, 100 mM Na2EDTA, 1% sodium sarcosinate, 1% Triton X-100, 10% DMSO) and centrifuged at 15000g for 10 min at 4 °C. The supernatant was collected and

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

• surfactant substitution and originated from bovine alveolar lavage. It is composed of surfactant proteins SP-B and SP-C as well as phospholipids. It was suspended in PBS (phosphate-buffered saline) at a concentration of 40 mg/mL. Cell culture: ISO-HAS-1 (human microvascular endothelial cell line, originated

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

• for 24 h and analyzed by flow cytometry. Flow cytometry Particle uptake, cell viability, and CD marker staining were measured with a flow cytometer (FACS Canto II, BD, Heidelberg, Germany). The cells were washed with phosphate buffered saline without calcium (PBS−, Invitrogen) and incubated with 28.6

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

• temperature using two different pH values, namely a pH value of 7.4 and 4.8 in phosphate buffered saline (PBS) solutions, based on a method previously described [34][35]. A pH of 7.4 was chosen to demonstrate the drug release of LD in physiological environment, whereas a pH of 4.8 mimics the acidic conditions

• ) SWCNT–COOH and (B) SWCNT–LD. Release profiles of LD from SWCNT–COOH into phosphate-buffered saline solutions at pH 7.4 and pH 4.8. Fitting data for the release of LD from SWCNT–COOH to the pseudo-first-order, pseudo-second-order and the parabolic equation for pH 7.4 (A–C) and pH 4.8 (D–F). MTT assay of

• of the Raman peaks of SWCNT–COOH and SWCNT–LD nanohybrid. Correlation coefficient, rate constant and half-time obtained by fitting the data of the release of LD from SWCNT–COOH into pH 7.4 and pH 4.8 phosphate-buffered saline solutions at 25 °C. Acknowledgements The authors are grateful 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

• took place against phosphate buffered saline (PBS) and the buffer was changed every 24 h (Figure 6A). Around 30% of the radioactivity was found in the dialysate after 24 h. Only around 4% of the radioactivity was detected in the removed buffer after 48 h. Similar results were obtained for samples taken

The fate of a designed protein corona on nanoparticles in vitro and in vivo

• Denise Bargheer,
• Julius Nielsen,
• Gabriella Gébel,
• Markus Heine,
• Sunhild C. Salmen,
• Roland Stauber,
• Horst Weller,
• Joerg Heeren and
• Peter Nielsen

Beilstein J. Nanotechnol. 2015, 6, 36–46, doi:10.3762/bjnano.6.5

• blood-half-live of 3.6 min (59Fe) and 5 min (125I) for adsorbed and 3.8 min (both labels) for covalently bound transferrin. After 2 h, the mice were sacrificed by blood removal and the organs were perfused with saline and measured for radioactivity (Figure 6B and C). With both preformed protein coronas

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

• incubator with 5% CO2 atmosphere at 37 °C (HERA cell 150, Heraeus). Subculture was performed weekly after cells reached confluence. After the medium was removed, the cell monolayer was washed twice with phosphate-buffered saline (PBS, 4 mL) without magnesium and calcium ions and incubated with the chelating

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

• particle and the membrane. As shown in [33], the interaction between a neutral (i.e., zwitterionic) lipid bilayer and negatively charged silica surface is repulsive in pure water but attractive in phosphate buffered saline. The authors also give a plausible theoretical explanation for this finding by

Proinflammatory and cytotoxic response to nanoparticles in precision-cut lung slices

• Stephanie Hirn,
• Nadine Haberl,
• Kateryna Loza,
• Matthias Epple,
• Wolfgang G. Kreyling,
• Barbara Rothen-Rutishauser,
• Markus Rehberg and
• Fritz Krombach

Beilstein J. Nanotechnol. 2014, 5, 2440–2449, doi:10.3762/bjnano.5.253

• . Immediately after the staining procedure, PCLS were mounted in phosphate buffered saline (PBS) on glass slides and observed by using a Leica SP5 confocal laser-scanning microscope (cLSM, Leica Microsystems, Wetzlar, Germany) with a PlanFluotar objective (Leica; 20×; NA 0.5). The excitation wavelength was 488