Electrokinetic characterization of synthetic protein nanoparticles

• Daniel F. Quevedo,
• Cody J. Lentz,
• Adriana Coll de Peña,
• Yazmin Hernandez,
• Nahal Habibi,
• Rikako Miki,
• Joerg Lahann and
• Blanca H. Lapizco-Encinas

Beilstein J. Nanotechnol. 2020, 11, 1556–1567, doi:10.3762/bjnano.11.138

• ZSP ZEN-5600), using standard settings. The average of at least three measurements was reported. Particle zeta potential was measured on the same instrument using a disposable folded capillary cell (DTS1070, Malvern) and using standard settings. Particle concentration was measured using a Pierce BCA

Wafer-level integration of self-aligned high aspect ratio silicon 3D structures using the MACE method with Au, Pd, Pt, Cu, and Ir

• Mathias Franz,
• Romy Junghans,
• Paul Schmitt,
• Adriana Szeghalmi and
• Stefan E. Schulz

Beilstein J. Nanotechnol. 2020, 11, 1439–1449, doi:10.3762/bjnano.11.128

• main etching mechanism remains the same. However, these structures stick together at the topmost point. The nanostructure bundles form during the drying process. This occurs when the capillary forces during drying are high enough to cluster neighbouring single Si wires, and the adhesion force of the

Analysis of catalyst surface wetting: the early stage of epitaxial germanium nanowire growth

• Owen C. Ernst,
• Felix Lange,
• David Uebel,
• Thomas Teubner and
• Torsten Boeck

Beilstein J. Nanotechnol. 2020, 11, 1371–1380, doi:10.3762/bjnano.11.121

• material layer with the maximum stable thickness (i.e., the wetting layer) may persist between the droplets. However, all the calculations shown here apply only to thickness values below the capillary length (>1 µm) of the fluid, since gravity can be neglected within this range [34]. Table S1 (Supporting

Structure and electrochemical performance of electrospun-ordered porous carbon/graphene composite nanofibers

• Yi Wang,
• Yanhua Song,
• Chengwei Ye and
• Lan Xu

Beilstein J. Nanotechnol. 2020, 11, 1280–1290, doi:10.3762/bjnano.11.112

• of two high-voltage power generators (NTPS-35K, Ntsse Co., Korea), a flow pump (LSP01, Longerpump Co., Ltd., China), a syringe (20 mL) with a capillary tip (diameter = 0.5 mm), a copper ring and a parallel electrode collector. The needle tip and the copper ring were clamped on the anode of the high

• due to capillary condensation in the mesopores, which also indicated a high mesoporous content [40]. At relatively low pressure levels (P/P0 < 0.1), the amount of nitrogen adsorbed on the sample was almost insignificant, which indicated the existence of negligible micropores. Moreover, the increased

Influence of the magnetic nanoparticle coating on the magnetic relaxation time

• Mihaela Osaci and
• Matteo Cacciola

Beilstein J. Nanotechnol. 2020, 11, 1207–1216, doi:10.3762/bjnano.11.105

• performed to reduce the sensitivity of nanoparticles to air, humidity and acidity. In addition, it allows for the functionalization and absorption of proteins and creation of hydrophilic molecules at the surface of the nanoparticles to prevent agglomeration, reducing capillary obstruction risk. Coating can

• other hand, organic coating (particularly polymers) has a number of advantages over inorganic coating, such as better particle dispersion, good colloidal stability, biocompatibility, good nanoparticle circulation in the blood, reduced toxicity and low risk of blood capillary obstruction. In the last

Applications of superparamagnetic iron oxide nanoparticles in drug and therapeutic delivery, and biotechnological advancements

• Maria Suciu,
• Corina M. Ionescu,
• Alexandra Ciorita,
• Septimiu C. Tripon,
• Dragos Nica,
• Hani Al-Salami and
• Lucian Barbu-Tudoran

Beilstein J. Nanotechnol. 2020, 11, 1092–1109, doi:10.3762/bjnano.11.94

• hydrophobic surfaces that induce aggregation and/or the formation of large clusters. When in contact with biological structures, this mechanism provokes capillary clotting and reduces tissue and cellular absorption. To prevent this, nanoparticles are coated with stabilizers, which are added during preparation

• to capillary blockage. Despite these issues, 5 to 15 nm SPIONs are currently approved and used for human medical applications, such as MRI, even with acknowledged side effects [73][74]. These features are very important in in vivo applications because different types of cells internalize

Microwave-induced electric discharges on metal particles for the synthesis of inorganic nanomaterials under solvent-free conditions

• Vijay Tripathi,
• Harit Kumar,
• Anubhav Agarwal and
• Leela S. Panchakarla

Beilstein J. Nanotechnol. 2020, 11, 1019–1025, doi:10.3762/bjnano.11.86

• local temperatures are very high, metal fluorides and sulfides melt and fill the nanotubes via capillary forces. The liquids solidify as one-dimensional nanorods inside the nanotubes. The usage of g-C3N4, instead of graphite, was found to be beneficial, especially for obtaining high yields of nanorods

Atomic layer deposition for efficient oxygen evolution reaction at Pt/Ir catalyst layers

• Stefanie Schlicht,
• Korcan Percin,
• Stefanie Kriescher,
• André Hofer,
• Claudia Weidlich,
• Matthias Wessling and
• Julien Bachmann

Beilstein J. Nanotechnol. 2020, 11, 952–959, doi:10.3762/bjnano.11.79

• Meinsberg) mounted in a Haber–Luggin capillary or a Ag/AgCl reference electrode was used. A platinum (coated titanium mesh) electrode was used as the counter electrode (Magneto Special Anodes B.V., The Netherlands). The working electrodes consist of the prepared catalyst-coated titanium electrodes

Key for crossing the BBB with nanoparticles: the rational design

• Sonia M. Lombardo,
• Marc Schneider,
• Akif E. Türeli and
• Nazende Günday Türeli

Beilstein J. Nanotechnol. 2020, 11, 866–883, doi:10.3762/bjnano.11.72

• conjugated with each ligand and their cellular uptake by brain capillary endothelial cells (BCECs) was tested [153]. It was shown that the cellular uptake of liposomes functionalized with peptide-22 was significantly higher than that of liposomes conjugated with angiopep-2 or T7. A dual-crossing glioma

Integrated photonics multi-waveguide devices for optical trapping and Raman spectroscopy: design, fabrication and performance demonstration

• Gyllion B. Loozen,
• Arnica Karuna,
• Mohammad M. R. Fanood,
• Erik Schreuder and
• Jacob Caro

Beilstein J. Nanotechnol. 2020, 11, 829–842, doi:10.3762/bjnano.11.68

• side channels of the microbath, to exploit capillary forces. The interference of the multiple beams produces an array of hot spots around the bath center, each forming a local trap. This property is clearly confirmed in the experiments and is registered in videos. We demonstrate the performance of a 2

• ). The wide side of the funnel measures 250 μm across, a size that is suitable for the thin needle of a syringe. When a droplet is applied to the funnel, capillary forces induce rapid progress of the fluid/air interface towards the microbath. The pinning of the fluid/air interface at sharp edges [11

• . Microfluidic considerations lead to the design of a microbath with side channels for filling with a sample suspension, a process aided by capillary forces. Experiments with two example devices, with 2 and 16 excitation waveguides, show clear trapping events for polystyrene beads of 1 and 3 μm diameter and

Preparation, characterization and photocatalytic performance of heterostructured CuO–ZnO-loaded composite nanofiber membranes

• Wei Fang,
• Liang Yu and
• Lan Xu

Beilstein J. Nanotechnol. 2020, 11, 631–650, doi:10.3762/bjnano.11.50

• sample regions evaluated with SEM. The pore size distributions of CNFMs were measured using capillary flow porometry (Porometer 3G, Quantachrome Instruments, USA). All samples were circular membranes with a diameter of 25 mm and the thickness of 10 μm. FTIR spectra of CNFMs were obtained using Fourier

• different PVDF/PAN weight ratios determined by capillary flow porometry are illustrated in Figure 3, and the calculated data are given in Table 2. At a weight ratio of 3:7 the pore sizes of the CNFMs were the smallest, and at a weight ratio of 7:3 the pore sizes of the CNFMs were the largest. Taking into

Identification of physicochemical properties that modulate nanoparticle aggregation in blood

• Ludovica Soddu,
• Duong N. Trinh,
• Eimear Dunne,
• Dermot Kenny,
• Giorgia Bernardini,
• Ida Kokalari,
• Arianna Marucco,
• Marco P. Monopoli and
• Ivana Fenoglio

Beilstein J. Nanotechnol. 2020, 11, 550–567, doi:10.3762/bjnano.11.44

• platelet deposition in post-capillary venules in the liver and heart, suggesting the role of this protein in nanoparticle-mediated platelet aggregation [14][15]. Silica nanoparticles (SNPs) of different sizes were found to activate glycoprotein IIb/IIIa and to induce the expression of P-selectin in

• function of the pH in the range from 2–9. The NP suspensions were diluted in ultrapure water at a final concentration of 0.5 mg/mL. The pH of the suspensions was adjusted by adding diluted NaOH or HCl solutions and the samples were introduced into disposable folded capillary cuvettes (Malvern Panalytical

Nanoparticles based on the zwitterionic pillar[5]arene and Ag⁺: synthesis, self-assembly and cytotoxicity in the human lung cancer cell line A549

• Dmitriy N. Shurpik,
• Denis A. Sevastyanov,
• Pavel V. Zelenikhin,
• Pavel L. Padnya,
• Vladimir G. Evtugyn,
• Yuriy N. Osin and
• Ivan I. Stoikov

Beilstein J. Nanotechnol. 2020, 11, 421–431, doi:10.3762/bjnano.11.33

• ) were obtained on an AmazonX mass spectrometer (Bruker Daltonik GmbH, Bremen, Germany). The measurements were carried out in the regime of positive ions in the range of m/z from 100 to 2800. The voltage on the capillary was −4500 V. Nitrogen was used as the gas-drier with a temperature of 300 °C and a

An advanced structural characterization of templated meso-macroporous carbon monoliths by small- and wide-angle scattering techniques

• Felix M. Badaczewski,
• Marc O. Loeh,
• Torben Pfaff,
• Dirk Wallacher,
• Daniel Clemens and
• Bernd M. Smarsly

Beilstein J. Nanotechnol. 2020, 11, 310–322, doi:10.3762/bjnano.11.23

• the macropore space. A 1:1 copy of the pristine SiO2 macropore space is obtained (Figure 1, top). In case of the mesopores the filling is based on a substantial capillary pressure, capturing the nonpolar liquid precursor within the mesopores, which are then replicated. The corresponding SEM images

Influence of the epitaxial composition on N-face GaN KOH etch kinetics determined by ICP-OES

• Markus Tautz,
• Maren T. Kuchenbrod,
• Joachim Hertkorn,
• Robert Weinberger,
• Martin Welzel,
• Arno Pfitzner and
• David Díaz Díaz

Beilstein J. Nanotechnol. 2020, 11, 41–50, doi:10.3762/bjnano.11.4

• centrifuge vials under magnetic stirring. The temperature was precisely maintained with an uncertainty of ±1.5 °C, using an ethylene glycol heating bath and an IR laser thermometer. The credibility of temperature measurement was evaluated by comparison between IR and capillary thermometers. Before immersion

The different ways to chitosan/hyaluronic acid nanoparticles: templated vs direct complexation. Influence of particle preparation on morphology, cell uptake and silencing efficiency

• Arianna Gennari,
• Julio M. Rios de la Rosa,
• Erwin Hohn,
• Maria Pelliccia,
• Enrique Lallana,
• Roberto Donno,
• Annalisa Tirella and
• Nicola Tirelli

Beilstein J. Nanotechnol. 2019, 10, 2594–2608, doi:10.3762/bjnano.10.250

• was converted into ζ-potential values by means of the Smoluchowski equation using Malvern Zetasizer software (v7.11). Capillary electrophoresis. Electrophoresis measurements were performed at 25 °C on a P/ACE MDQ Plus (SCIEX, Warrington, UK) equipped with a 50 cm effective length (70 cm total length

• ) capillary with 75 μm internal diameter (Beckam Coulter, Brea, USA) and a photodiode array detector operating at 214 nm. The capillary was first conditioned by successive rinsing steps (all performed at 20 psi): 5 min with 1 M HCl, 2 min with deionized water, 10 min with 0.1 M NaOH, 2 min with deionized

• the end of each measurement, the capillary was rinsed with water for 1 min at 20 psi. Data acquisition and analysis were performed respectively with software packages 32 Karat (SCIEX) and OriginPro 8.5.1 (OriginLab Corporation, US). A calibration curve was obtained by injecting HA at known

Bombesin receptor-targeted liposomes for enhanced delivery to lung cancer cells

• Mohammad J. Akbar,
• Pâmela C. Lukasewicz Ferreira,
• Melania Giorgetti,
• Leanne Stokes and
• Christopher J. Morris

Beilstein J. Nanotechnol. 2019, 10, 2553–2562, doi:10.3762/bjnano.10.246

• , the liposomal suspension was diluted 1:10 with PBS and transferred to a clean folded capillary cell (Malvern, DTS1070). Liposomal stability in PBS and 10% serum An aliquot of the liposomal suspension was diluted 1:10 with either PBS or 10% FBS in PBS and transferred to individual microcentrifuge tubes

Antimony deposition onto Au(111) and insertion of Mg

• Lingxing Zan,
• Da Xing,
• Abdelaziz Ali Abd-El-Latif and
• Helmut Baltruschat

Beilstein J. Nanotechnol. 2019, 10, 2541–2552, doi:10.3762/bjnano.10.245

• compartment with a Luggin capillary. The counter electrode is placed in the compartment where it can be separated from the central compartment by a glass frit. All electrochemical measurements were carried out using a bi-potentiostat purchased from Pine Instruments, Inc. (model AFBPC1) in combination with

• small compartment filled with the same electrolyte and separated from main compartment by a capillary. Pt/Ir (90:10) STM tips with a diameter of 0.25 cm were prepared by etching in a 2 M KOH/4 M KSCN bath and coated with hot-melt glue containing different types of polymer (provided by Steinel) to

Coating of upconversion nanoparticles with silica nanoshells of 5–250 nm thickness

• Cynthia Kembuan,
• Maysoon Saleh,
• Bastian Rühle,
• Ute Resch-Genger and
• Christina Graf

Beilstein J. Nanotechnol. 2019, 10, 2410–2421, doi:10.3762/bjnano.10.231

• (pore size: 0.2 µm; materials: nylon or polytetrafluoroethylene (PTFE) for particles dispersed in cyclohexane and nylon or regenerated cellulose for particles dispersed in ethanol, Rotilab). Zeta potential measurements of the aqueous dispersions were carried out with a Zetasizer Nano ZS in capillary

Microbubbles decorated with dendronized magnetic nanoparticles for biomedical imaging: effective stabilization via fluorous interactions

• Da Shi,
• Justine Wallyn,
• Dinh-Vu Nguyen,
• Francis Perton,
• Delphine Felder-Flesch,
• Sylvie Bégin-Colin,
• Mounir Maaloum and
• Marie Pierre Krafft

Beilstein J. Nanotechnol. 2019, 10, 2103–2115, doi:10.3762/bjnano.10.205

• IONPs at the gas/liquid interface, the variation of the interfacial tension was acquired using a Tracker® tensiometer (Teclis, Civrieux d’Azergues, France). A 5 µL bubble was formed at the end of a steel capillary that had a tip diameter of 1 mm. The rising bubble was saturated with F-hexane by purging

The importance of design in nanoarchitectonics: multifractality in MACE silicon nanowires

• Stefania Carapezzi and
• Anna Cavallini

Beilstein J. Nanotechnol. 2019, 10, 2094–2102, doi:10.3762/bjnano.10.204

• conditions and the capacity dimension of the nanowires was obtained. Keywords: atomic force microscopy (AFM); capillary force; metal-assisted chemical etching (MACE); multifractal analysis; nanoarchitectonics; nanowires; self-assembly; Introduction In the last years, huge progress was made regarding the

• surface [29][30]. Considering two adjacent NWs, first 1) the capillary force between them should be able to overcome the elastic force moving them back to the original straight position, in order to bring them into contact during the evaporation of the liquid. Then a stable bundle will occur if 2) the

• , such that the other end is deflected by a length w, the magnitude of the elastic force acting on it can be calculated from the Euler–Bernoulli elementary beam theory [32], and it is given by where E is the Young modulus of the pillar and I is its area moment of inertia. The magnitude of the capillary

Ion mobility and material transport on KBr in air as a function of the relative humidity

• Dominik J. Kirpal,
• Korbinian Pürckhauer,
• Alfred J. Weymouth and
• Franz J. Giessibl

Beilstein J. Nanotechnol. 2019, 10, 2084–2093, doi:10.3762/bjnano.10.203

• later) without damaging the tip. Moreover, the hydrophobicity reduces capillary formation at the tip–sample contact area. Capillary condensation causes a locally enhanced presence of condensed water molecules [22], which might correspond to a much higher relative humidity near the apex. Furthermore, the

Synthesis of highly active ETS-10-based titanosilicate for heterogeneously catalyzed transesterification of triglycerides

• Muhammad A. Zaheer,
• David Poppitz,
• Khavar Feyzullayeva,
• Marianne Wenzel,
• Jörg Matysik,
• Radomir Ljupkovic,
• Aleksandra Zarubica,
• Alexander A. Karavaev,
• Andreas Pöppl,
• Roger Gläser and
• Muslim Dvoyashkin

Beilstein J. Nanotechnol. 2019, 10, 2039–2061, doi:10.3762/bjnano.10.200

The influence of porosity on nanoparticle formation in hierarchical aluminophosphates

• Matthew E. Potter,
• Lauren N. Riley,
• Alice E. Oakley,
• Panashe M. Mhembere,
• June Callison and
• Robert Raja

Beilstein J. Nanotechnol. 2019, 10, 1952–1957, doi:10.3762/bjnano.10.191

• used in the IW method increases support–metal interactions leading to more rapid deposition. The minimal amount of solvent will also be readily adsorbed into the internal pores of the material by capillary action, encouraging the metal to deposit on the micropores and mesopores and not just on the

• external surface. In contrast, the excess solvent used in WI will promote deposition primarily on the external surface. AE results in a reasonable deposition efficiency (0.49 wt % Au). Likely the evaporation stage of this process also encourages limited capillary action, similar to IW. Excellent agreement

Toxicity and safety study of silver and gold nanoparticles functionalized with cysteine and glutathione

• Barbara Pem,
• Igor M. Pongrac,
• Lea Ulm,
• Ivan Pavičić,
• Valerije Vrček,
• Darija Domazet Jurašin,
• Marija Ljubojević,
• Adela Krivohlavek and
• Ivana Vinković Vrček

Beilstein J. Nanotechnol. 2019, 10, 1802–1817, doi:10.3762/bjnano.10.175

• and D2O was added (or a D2O-filled capillary was used for a lock signal). Along with the disappearance of the 1H NMR signals of the reactant (CYS), a new set of proton signals of the product emerged (Figure 1). All new signals were shifted downfield by approximately 0.2 ppm. According to detailed 1H

• , respectively. The samples were prepared in UPW with the addition of D2O to a final volume ratio of 10%, or in some cases, a capillary filled with D2O was used as an external lock. 1H NMR spectra were recorded in 10–20 min intervals during the NP synthesis, starting immediately after the mixing of reagents (t0