Differences in surface chemistry of iron oxide nanoparticles result in different routes of internalization

• Barbora Svitkova,
• Vlasta Zavisova,
• Veronika Nemethova,
• Martina Koneracka,
• Miroslava Kretova,
• Filip Razga,
• Monika Ursinyova and
• Alena Gabelova

Beilstein J. Nanotechnol. 2021, 12, 270–281, doi:10.3762/bjnano.12.22

• proteins were boiled in Laemmli buffer and separated on a 10% polyacrylamide SDS-PAGE gel. After transfer of proteins onto nitrocellulose membranes the following primary antibodies were used: anti-Clathrin Heavy Chain (P1663) (#2410), anti-Caveolin-1 (#3238), anti-Phospho-Caveolin-1 (Tyr14) (#3251), anti

A review on the green and sustainable synthesis of silver nanoparticles and one-dimensional silver nanostructures

• Sina Kaabipour and
• Shohreh Hemmati

Beilstein J. Nanotechnol. 2021, 12, 102–136, doi:10.3762/bjnano.12.9

• ” synthesis method. These techniques are usually accompanied by the addition of stabilizers to provide stability, prevent aggregation, control morphology, and provide physiologically compatible properties [140][141][142]. Chemical methods were previously used to produce silver nanoparticles including sol–gel

• the presence of a stabilizer such as polyvinylpyrrolidone (PVP) or polyvinylalcohol (PVA). The chemical synthesis of nanoparticles is one of the bottom-up techniques due to the fact that particles are formed from collective atoms in a nucleus rather than from the bulk [104]. 2.2.1 Sol–gel process. The

• sol–gel method is one of the most common techniques to synthesize AgNPs. The sol–gel process is considered to be a multifaceted approach for the synthesis of nanoparticles in various forms – especially complex compounds – such as metal-complex oxides, inorganic nanocomposites, and chalcogenides [144

Bulk chemical composition contrast from attractive forces in AFM force spectroscopy

• Dorothee Silbernagl,
• Media Ghasem Zadeh Khorasani,
• Natalia Cano Murillo,
• Anna Maria Elert and
• Heinz Sturm

Beilstein J. Nanotechnol. 2021, 12, 58–71, doi:10.3762/bjnano.12.5

• accelerator used was 100:90:1 w/w/w, respectively. As an additional organic component, bisphenol A polycarbonate from Makrolon 3108 (Goodfellow, UK) with Mw ≈ 49,550 g/mol and Mn ≈ 21,400, as measured by gel permeation chromatography (GPC), was used. As an inorganic component, boehmite (γ-AlOOH) from two

High-responsivity hybrid α-Ag₂S/Si photodetector prepared by pulsed laser ablation in liquid

• Raid A. Ismail,
• Hanan A. Rawdhan and
• Duha S. Ahmed

Beilstein J. Nanotechnol. 2020, 11, 1596–1607, doi:10.3762/bjnano.11.142

• hydrothermal methods, chemical bath deposition, laser ablation in liquid reverse microemulsion, electrospinning, sol–gel, electrochemical method, template method, sonochemical method, and hydrochemical bath deposition [10][11][12][13]. The size of Ag2S NPs depends on the preparation conditions [14]. Ag2S NPs

Antimicrobial metal-based nanoparticles: a review on their synthesis, types and antimicrobial action

• Matías Guerrero Correa,
• Fernanda B. Martínez,
• Cristian Patiño Vidal,
• Camilo Streitt,
• Juan Escrig and
• Carol Lopez de Dicastillo

Beilstein J. Nanotechnol. 2020, 11, 1450–1469, doi:10.3762/bjnano.11.129

• , chemical vapor deposition, electrochemical anodization method, hydrolysis, hydrothermal method, precipitation–hydrothermal method, reverse micellar route, sol–gel method, solution-based synthesis, solvothermal synthesis, and the sonochemical method. The most relevant ones, along with the typical resulting

• different morphologies and sizes. For example, the technique has been used to obtain ultrafine MgO nanoparticles (8–10 nm) [50], TiO2 nanoparticles (10–20 nm) [51], and even flower-like microstructures (diameter ≈6 µm) and microtubes (diameter ≈1 µm and length ≈4 µm) [52]. The sol–gel technique has been

Role of redox-active axial ligands of metal porphyrins adsorbed at solid–liquid interfaces in a liquid-STM setup

• Thomas Habets,
• Sylvia Speller and
• Johannes A. A. W. Elemans

Beilstein J. Nanotechnol. 2020, 11, 1264–1271, doi:10.3762/bjnano.11.110

• suppliers (ACROS Organics or Sigma-Aldrich), independent whether it was vacuum-distilled prior to use or used as received. For TLC analysis, TLC silicagel 60 F254 (Merck, Burlington, MA, USA) and for column chromatography silica gel 0.035–0.070 mm, (Acros, Branchburg, N.J., USA) was used. MALDI-TOF mass

Magnetic-field-assisted synthesis of anisotropic iron oxide particles: Effect of pH

• Andrey V. Shibaev,
• Petr V. Shvets,
• Darya E. Kessel,
• Roman A. Kamyshinsky,
• Anton S. Orekhov,
• Sergey S. Abramchuk,
• Alexei R. Khokhlov and
• Olga E. Philippova

Beilstein J. Nanotechnol. 2020, 11, 1230–1241, doi:10.3762/bjnano.11.107

• ][30][31][32], solvothermal [33] and hydrothermal [34] reactions, the polyol method [35], dehydration or reduction of precursor rod-like particles [8][11], sonochemical oxidation [36], thermal decomposition [23][26], sol–gel reactions [37], synthesis in worm-like surfactant micellar solutions [38][39

Gas sorption porosimetry for the evaluation of hard carbons as anodes for Li- and Na-ion batteries

• Yuko Matsukawa,
• Fabian Linsenmann,
• Maximilian A. Plass,
• George Hasegawa,
• Katsuro Hayashi and
• Tim-Patrick Fellinger

Beilstein J. Nanotechnol. 2020, 11, 1217–1229, doi:10.3762/bjnano.11.106

• hydrothermal treatment and carbonization time under argon flow) are listed in Table 2. Preparation of carbons from resorcinol-formaldehyde gels Porous carbon monoliths were obtained by carbonization of resorcinol–formaldehyde (RF) gels obtained via a sol–gel process as previously reported [28][29]. In short

• wt % methanol) (Sigma-Aldrich, Germany) was added under vigorous stirring. After mixing for 5 min, the solution was kept at 40 °C for 24 h for gelation and then aged at 80 °C for 24 h. The gel was washed with ethanol at 60 °C for 4 h three times and dried at 60 °C. The dried gel was subsequently

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

• sol–gel process, yielding metal-oxide nanoparticles dispersed in a mesoporous matrix. [5]. Other methods used for synthesising these nanoparticles include modifications of the sol–gel method. These methods involve supercritical conditions, such as ethyl alcohol and alkaline co-precipitation, and an

Photothermally active nanoparticles as a promising tool for eliminating bacteria and biofilms

• Mykola Borzenkov,
• Piersandro Pallavicini,
• Angelo Taglietti,
• Laura D’Alfonso,
• Maddalena Collini and
• Giuseppe Chirico

Beilstein J. Nanotechnol. 2020, 11, 1134–1146, doi:10.3762/bjnano.11.98

• heating of gold nanoparticles embedded in an injectable silk protein hydrogel was one of the first examples that used this approach [65]. The NIR laser irradiation at 528 nm for 15 min (450 mW) elevated the maximum gel temperature to 59 °C. The in vivo studies demonstrated a sufficient bacterial reduction

Plant growth regulation by seed coating with films of alginate and auxin-intercalated layered double hydroxides

• Vander A. de Castro,
• Valber G. O. Duarte,
• Danúbia A. C. Nobre,
• Geraldo H. Silva,
• Vera R. L. Constantino,
• Frederico G. Pinto,
• Willian R. Macedo and
• Jairo Tronto

Beilstein J. Nanotechnol. 2020, 11, 1082–1091, doi:10.3762/bjnano.11.93

• suspension was maintained at pH 9.5 ± 0.5 by the slow addition of a 1.0 mol·L−1 solution of NaOH and the system was kept under constant agitation in a N2 atmosphere. The solid resulting from the synthesis was washed with H2O and dried under reduced pressure in a desiccator containing silica gel. The amount

• . After completion of the synthesis, the whole reaction medium was kept at rest for 12 h. The solid resulting from the synthesis was centrifuged and dried under reduced pressure in a desiccator containing silica gel. Coating of bean seeds with a polymeric film Polymeric gels were prepared by dissolving

• sodium alginate in water for 2 h. The bean seeds were immersed in the gel and subsequently in a 5.0% solution of Ca(NO3)2 for 10 s to initiate the formation of films on the seeds surface. To homogenize the films, before being used in the bioassays, the seeds were dried in a drying oven at 25 °C for 2 h

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

• microscopy; Introduction The synthesis of nanomaterials in short time intervals with fewer chemicals has become increasingly important in materials science. Traditional routes of synthesizing nanomaterials, including sol–gel synthesis, solvothermal synthesis, arc-discharge synthesis, or laser ablation

Wet-spinning of magneto-responsive helical chitosan microfibers

• Dorothea Brüggemann,
• Johanna Michel,
• Naiana Suter,
• Matheus Grande de Aguiar and
• Michael Maas

Beilstein J. Nanotechnol. 2020, 11, 991–999, doi:10.3762/bjnano.11.83

• 4 to 12 MPa were previously obtained for wet-spinning of bare chitosan solutions into ammonia [35]. These results were in good agreement with the Young’s modulus values obtained for our helical chitosan fibers. On the other hand, gel-spinning in combination with a post-drying step led to much higher

A 3D-polyphenylalanine network inside porous alumina: Synthesis and characterization of an inorganic–organic composite membrane

• Jonathan Stott and
• Jörg J. Schneider

Beilstein J. Nanotechnol. 2020, 11, 938–951, doi:10.3762/bjnano.11.78

• well as the mechanisms of gel formation have been studied in detail. Hydrophilic gels with functional side groups enable stimuli-responsive hydrogels with interesting properties with regards to drug release systems. A drawback of these gels is their low mechanical stability, which can however be

• improved by chemical crosslinking of the gel structures [26][27]. A three-dimensional fibrillar network due photo-crosslinking gelation of poly(γ-benzyl-ʟ-glutamate-co-allylglycine) was achieved by Vacogne et al. These authors have demonstrated that the network-like structure remains intact after

• -grafted gel might be interesting in membrane separation technology or supported drug release/adsorption systems. We investigate the ability of polyphenylalanine to form organo-gels in situ within a porous inorganic environment with respect to different volume fractions of DCM in the solvent mixture. We

Band tail state related photoluminescence and photoresponse of ZnMgO solid solution nanostructured films

• Vadim Morari,
• Aida Pantazi,
• Nicolai Curmei,
• Vitalie Postolache,
• Emil V. Rusu,
• Marius Enachescu,
• Ion M. Tiginyanu and
• Veaceslav V. Ursaki

Beilstein J. Nanotechnol. 2020, 11, 899–910, doi:10.3762/bjnano.11.75

• the composition range x = 0.00–0.40 has been prepared by sol–gel spin coating on Si substrates with a post-deposition thermal treatment in the temperature range of 400–650 °C. The morphology of the films was investigated by scanning electron microscopy and atomic force microscopy while their light

• of the alloy composition. Thin films were also prepared by aerosol spray pyrolysis deposition using the same sol–gel precursors for the purpose of comparison. The prepared films were tested for photodetector applications. Keywords: aerosol spray pyrolysis deposition; energy band tails; photodetector

• (MOCVD) [18][19], hydrothermal [4], chemical bath deposition (CBD) [20], sol–gel spin coating [21][22][23][24][25][26][27][28][29], and spray pyrolysis [28][29][30][31][32][33][34]. Among these techniques, the sol–gel spin coating method has the advantage of ensuring easy control and handling of

A novel dry-blending method to reduce the coefficient of thermal expansion of polymer templates for OTFT electrodes

• Xiangdong Ye,
• Bo Tian,
• Yuxuan Guo,
• Fan Fan and
• Anjiang Cai

Beilstein J. Nanotechnol. 2020, 11, 671–677, doi:10.3762/bjnano.11.53

• a sol–gel precursor by adding tetraethyl orthosilicate (TEOS) to polyvinyl pyrrolidone (PVP), and then synthesized a silica/PVP nanofiber composite by electrospinning. The content of silica nanofibers in the composite is 9.1 wt %, and the CTE was decreased by ca. 40%. Jeyranpour et al. [13] studied

• reduce the CTE of the composite. More recently, Wang et al. [16] hydrolyzed various organic compounds to synthesize a solution of APrTEOS-capped poly(amic acid) (EPI) using the sol–gel method, and then added a maximum content of 32.16 wt % tetramethyl orthosilicate (TMOS) and water (as a diluent) into

Silver-decorated gel-shell nanobeads: physicochemical characterization and evaluation of antibacterial properties

• Marta Bartel,
• Katarzyna Markowska,
• Marcin Strawski,
• Krystyna Wolska and
• Maciej Mazur

Beilstein J. Nanotechnol. 2020, 11, 620–630, doi:10.3762/bjnano.11.49

• of composite nanobeads with antibacterial properties. The particles consist of polystyrene cores that are surrounded by sulfonic gel shells with embedded silver nanoparticles. The nanocomposite beads are prepared by sulfonation of polystyrene particles followed by accumulation of silver ions in the

• shell layer and subsequent reduction with sodium borohydride. The resulting material has been characterized by electron microscopy, vibrational and X-ray photoelectron spectroscopy and several other experimental techniques. It was shown that sodium borohydride reduces silver ions embedded in the gel

• layer producing silver nanoparticles but also transforms a fraction of sulfonic groups in the polymer to moieties with sulfur in a lower oxidation state, likely thiols. It is hypothesized that the generated thiol groups are anchoring the nanoparticles in the gel shell of the nanobeads stabilizing the

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

• in an ultrasonic bath and then heated for 5 min at 95 °C to complete the protein denaturation. The protein corona was resolved in a 4% stacking gel / 12% acrylamide and the electrophoretic analysis was conducted at 130 V as previously described [26]. After the electrophoretic separation, the gels

• were stained in Imperial Protein stain (Thermo Scientific) for 1 h and distained overnight (in ultrapure water). The densitometry analysis was performed using the software ImageJ (NIH). Mass spectrometry analysis The samples were run on a sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS

• -PAGE) instrument for 10 min before the protein bands were excised from the gel in order to allow the whole corona proteins to migrate into a single gel band. The proteins in the gel pieces were reduced with dithiothreitol, alkylated with iodoacetamide and digested with trypsin (Promega Corporation

Correction: Photocatalytic antibacterial performance of TiO₂ and Ag-doped TiO₂ against S. aureus. P. aeruginosa and E. coli

• Kiran Gupta,
• R. P. Singh,
• Ashutosh Pandey and
• Anjana Pandey

Beilstein J. Nanotechnol. 2020, 11, 547–549, doi:10.3762/bjnano.11.43

• ., India Department of Biotechnology, Motilal Nehru National Institute of Technology, Allahabad, Prayagraj, 211004, U.P., India 10.3762/bjnano.11.43 Keywords: Ag-doped TiO2; antimicrobial activity; sol–gel; The following is a correction to the section “XRD of TiO2 and Ag-doped TiO2”, which contains a new

Multilayer capsules made of weak polyelectrolytes: a review on the preparation, functionalization and applications in drug delivery

• Varsha Sharma and
• Anandhakumar Sundaramurthy

Beilstein J. Nanotechnol. 2020, 11, 508–532, doi:10.3762/bjnano.11.41

• ]. It was reported that when an 8- or 16-layer capsule core was dissolved at pH 5 and 4.5, respectively, the structure showed high mean heights suggesting trapped silica gel inside the capsules which may be due to an unsuitable pH or thick shells. However, the dissolution of the core containing 8 layers

• were successfully employed for hollow capsule fabrication [31]. Another important feature was that they can be porous or nonporous. During LbL assembly on porous cores, PE complexes were also formed in the interior and its core dissolution gave rise to a gel matrix, which helped in both protecting the

• have been demonstrated with silica or carbonate cores. The crystallization of CaCO3 from supersaturated solutions results in porous gel-like cores which also play an important role for applications in industry and medicine [32]. Such formation depends on the experimental conditions such as pH, salt

Interfacial charge transfer processes in 2D and 3D semiconducting hybrid perovskites: azobenzene as photoswitchable ligand

• Nicole Fillafer,
• Tobias Seewald,
• Lukas Schmidt-Mende and
• Sebastian Polarz

Beilstein J. Nanotechnol. 2020, 11, 466–479, doi:10.3762/bjnano.11.38

• temperature. The solvent was removed, and the residue was dissolved in ethyl acetate (EA) and methanol (MeOH) (5:1) and filtered over silica gel. The solvent was removed and a yellowish powder was obtained [61]. The product was characterized by using 1H NMR spectroscopy. 1H NMR (400 MHz, DMSO-d6) n = 1: δ

Correction: Biocatalytic oligomerization-induced self-assembly of crystalline cellulose oligomers into nanoribbon networks assisted by organic solvents

• Yuuki Hata,
• Yuka Fukaya,
• Toshiki Sawada,
• Masahito Nishiura and
• Takeshi Serizawa

Beilstein J. Nanotechnol. 2020, 11, 370–371, doi:10.3762/bjnano.11.27

• Technology (PRESTO), Japan Science and Technology Agency (JST), 4-1-8 Honcho, Kawaguchi-shi, Saitama 332-0012, Japan DKS Co. Ltd., 5 Ogawaracho, Kisshoin, Minami-ku, Kyoto-shi, Kyoto 601-8391, Japan 10.3762/bjnano.11.27 Keywords: cellulose oligomer; gel; nanoarchitectonics; nanoribbon networks

Poly(1-vinylimidazole) polyplexes as novel therapeutic gene carriers for lung cancer therapy

• Gayathri Kandasamy,
• Elena N. Danilovtseva,
• Vadim V. Annenkov and
• Uma Maheswari Krishnan

Beilstein J. Nanotechnol. 2020, 11, 354–369, doi:10.3762/bjnano.11.26

• efficiency of the formed complexes in A549 lung cancer cells. The polyplex formed was found to exhibit 66% complexation efficiency. The complexation was confirmed by gel retardation assays, FTIR and thermal analysis. The blank PVI polymer was not toxic to cells. The polyplex was found to exhibit excellent

• : The polyplexes with a tracking dye (bromophenol blue, 2 µL), were loaded on a 1% agarose gel. The electrophoresis was carried in Tris/boric acid buffer (TBE) buffer at 80 V for 45 min. The gel was imaged after staining with ethidium bromide in a UV transilluminator using a gel documentation system

• heparin/siRNA (v/v) ratio. The samples were electrophoresed on a 1% agarose gel containing 0.5 μg/mL ethidium bromide at 80 V for 20 min. The bands were imaged using the gel documentation system. In vitro studies Cell viability: The effect of blank polymer and polyplex was determined using MTS (3-(4,5

Interactions at the cell membrane and pathways of internalization of nano-sized materials for nanomedicine

• Valentina Francia,
• Daphne Montizaan and
• Anna Salvati

Beilstein J. Nanotechnol. 2020, 11, 338–353, doi:10.3762/bjnano.11.25

• Section 2.1. Recently, computer simulations and in vitro studies of nanoparticle–membrane interactions have shown that the surface of nanomaterials can in itself induce several changes at the plasma membrane, by determining sol–gel transitions in the lipid bilayer and impairing lipid lateral diffusion

Understanding nanoparticle flow with a new in vitro experimental and computational approach using hydrogel channels

• Armel Boutchuen,
• Dell Zimmerman,
• Abdollah Arabshahi,
• John Melnyczuk and
• Soubantika Palchoudhury

Beilstein J. Nanotechnol. 2020, 11, 296–309, doi:10.3762/bjnano.11.22

• ). The swelling behavior was highly influenced by the pH value of the solution. The selected gel formulation synthesized with 1.3 mL DI water showed an increased mass of 25% at pH 2, 30% at pH 13, and a maximum of 60% at pH 11. Figure 3 shows the scanning electron microscopy (SEM) images of the different

• showed the smoothest surface of all gel formulations. The gels prepared with 1.5 mL DI water showed a distinctly porous surface structure. Therefore, the 1.3 mL DI water hydrogels were most suitable for making flow channels of negligible friction to resemble the vascular microenvironment. The hollow 3D

• hydrogel channels were formed via a facile experimental technique using a newly constructed syringe and plastic tube assembly (Figure 4). The liquid gel was allowed to solidify overnight within the syringe–tube assembly and slowly removed from the assembly after solidification. The resultant final product