The cleaner, the greener? Product sustainability assessment of the biomimetic façade paint Lotusan^® in comparison to the conventional façade paint Jumbosil^®

• Florian Antony,
• Rainer Grießhammer,
• Thomas Speck and
• Olga Speck

Beilstein J. Nanotechnol. 2016, 7, 2100–2115, doi:10.3762/bjnano.7.200

• , dispersion-based façade paint. In accordance with the reporting guideline [31], Jumbosil® consists of polymer dispersion, titanium dioxide, calcium carbonate, silicate fillers, talcum, water, glycol ether, aliphatic compounds, additives and preserving agents [33]. Jumbosil® is characterized by a density of

From iron coordination compounds to metal oxide nanoparticles

• Mihail Iacob,
• Carmen Racles,
• Codrin Tugui,
• George Stiubianu,
• Adrian Bele,
• Liviu Sacarescu,
• Daniel Timpu and
• Maria Cazacu

Beilstein J. Nanotechnol. 2016, 7, 2074–2087, doi:10.3762/bjnano.7.198

• ] using FeCl3∙6H2O and FeCl2·4H2O at a molar ratio of 1:2, calcium acetate ((CH3COO)2Ca) and glacial acetic acid. The identity of the compound obtained was confirmed by FTIR (KBr) ν: 3421 (s), 1586 (vs), 1420 (vs), 1349 (m), 1050 (w), 1033 (w), 715 (m), 663 (s), 618 (m), 468 (w), 561 (w); Anal. calcd for

“Sticky invasion” – the physical properties of Plantago lanceolata L. seed mucilage

• Agnieszka Kreitschitz,
• Alexander Kovalev and
• Stanislav N. Gorb

Beilstein J. Nanotechnol. 2016, 7, 1918–1927, doi:10.3762/bjnano.7.183

• acetylation [38][39]. The presence of calcium ions slows down water transfer to cellulose and pectins and thus increases the cell-wall stiffness [19][40][41]. Also the presence of boron in the pectic network causes the reduction of the amount of water and contributes the cell-wall strength [19][40]. We can

Facile fabrication of luminescent organic dots by thermolysis of citric acid in urea melt, and their use for cell staining and polyelectrolyte microcapsule labelling

• Nadezhda M. Zholobak,
• Anton L. Popov,
• Alexander B. Shcherbakov,
• Nelly R. Popova,
• Mykhailo M. Guzyk,
• Valeriy P. Antonovich,
• Alla V. Yegorova,
• Yuliya V. Scrypynets,
• Inna I. Leonenko,
• Alexander Ye. Baranchikov and
• Vladimir K. Ivanov

Beilstein J. Nanotechnol. 2016, 7, 1905–1917, doi:10.3762/bjnano.7.182

• [56][57], with some modifications: instead of one polyanionic layer on the surface of microcapsules, a layer of negatively charged O-dots was used (Figure 8). Calcium carbonate microparticles were used as the template for fabrication of the nanocomposite shells. The first polyelectrolyte layer was

• the following layers: PAH/PSS/PAH/O-dots/PAH/PSS (Figure 8). The core–polyelectrolyte particles were washed three times with deionized water after each adsorption step. Finally, the calcium carbonate cores were dissolved in ethylenediaminetetraacetic acid (EDTA) for 30 min. The microcapsules were

3D printing of mineral–polymer bone substitutes based on sodium alginate and calcium phosphate

• Aleksey A. Egorov,
• Alexander Yu. Fedotov,
• Anton V. Mironov,
• Vladimir S. Komlev,
• Vladimir K. Popov and
• Yury V. Zobkov

Beilstein J. Nanotechnol. 2016, 7, 1794–1799, doi:10.3762/bjnano.7.172

• calcium phosphate (CP) for bone tissue engineering. The fabrication of 3D composite structures was performed through the synthesis of inorganic particles within a biopolymer macromolecular network during 3D printing process. The formation of a new CP phase was studied through X-ray diffraction, Fourier

• diameter ≈800 μm) and were found to possess compressive strengths from 0.45 to 1.0 MPa. This new approach can be effectively applied for fabrication of biocompatible scaffolds for bone tissue engineering constructions. Keywords: 3D printing; bone graft; calcium phosphate; composite materials; sodium

• number of biocompatible materials, such as polymers of different nature (both natural and synthetic), as well as a variety of calcium phosphates (CPs) are used for this purpose [2]. In this respect, the alginate-based materials are of particular interest. Alginate (extracellular polysaccharide) is a

Influence of hydrothermal synthesis parameters on the properties of hydroxyapatite nanoparticles

• Sylwia Kuśnieruk,
• Jacek Wojnarowicz,
• Agnieszka Chodara,
• Tadeusz Chudoba,
• Stanislaw Gierlotka and
• Witold Lojkowski

Beilstein J. Nanotechnol. 2016, 7, 1586–1601, doi:10.3762/bjnano.7.153

• ; Introduction Hydroxyapatite (HAp) is a naturally occurring mineral (a form of calcium apatite), which is also an inorganic component of bones, with approximately 8 wt % water, 22 wt % protein and 70 wt % mineral. HAp is a form of calcium phosphate with the chemical formula Ca10(PO4)6(OH)2 and a hexagonal

• biological apatite, the main substituent is carbonate, which normally occurs at 5 to 8 wt % in bone mineral. Moreover, calcium deficiency is always observed in biological apatites along with a relatively low degree of crystallinity – with diameter on the order of 0.2 µm and smaller [16][17][18]. In the

• hydroxyapatite structure, PO43− anions can be substituted to a certain extent by carbonate groups, whereas calcium ions can be substituted by magnesium (≈0.7 wt %), sodium (≈0.9 wt %), potassium (0.03 wt %) chlorine (0.13 wt %), fluorine (0.03 wt %) and a few trace elements: Sr, Pb, Zn, Cu, and Fe. The

Photothermal effect of gold nanostar patterns inkjet-printed on coated paper substrates with different permeability

• Mykola Borzenkov,
• Anni Määttänen,
• Petri Ihalainen,
• Maddalena Collini,
• Elisa Cabrini,
• Giacomo Dacarro,
• Piersandro Pallavicini and
• Giuseppe Chirico

Beilstein J. Nanotechnol. 2016, 7, 1480–1485, doi:10.3762/bjnano.7.140

• porosity and permeability as measured in Gurley seconds: substrate 1 (>40000 Gurley seconds, semi-permeable, two coating layers ), substrate 2 (7360 Gurley seconds, permeable, calcium carbonate (major component) and kaolin coating) and substrate 3 (non-permeable, latex coating). The PEG-decorated GNS were

On the pathway of cellular uptake: new insight into the interaction between the cell membrane and very small nanoparticles

• Claudia Messerschmidt,
• Daniel Hofmann,
• Anja Kroeger,
• Katharina Landfester,
• Volker Mailänder and
• Ingo Lieberwirth

Beilstein J. Nanotechnol. 2016, 7, 1296–1311, doi:10.3762/bjnano.7.121

• : ATP depletion; calcium crystallization; cytotoxicity; endocytosis; HeLa cells; LDH; mesenchymal stem cells; morphology; necrosis; particle size; silica nanoparticles; TEM; Introduction Silicon dioxide nanoparticles (SiNPs) are used in a wide range of commercially available products to improve product

• overall appearance of the cell – the more advanced the necrotic cellular breakdown the more distinct the dark material inside the mitochondria. These agglomerates might be due to deposition of Ca2+ salts within the mitochondria. EELS and EDX measurements revealed a significantly raised content of calcium

• increasing the permeability of the plasma membrane. The accumulation of calcium taking the form of insoluble hydroxyapatite (Ca phosphate) inside mitochondria during a necrotic process is a well-known and documented phenomenon during this process [37][38]. A lot of data concerning cytotoxicity of

Preparation of alginate–chitosan–cyclodextrin micro- and nanoparticles loaded with anti-tuberculosis compounds

• Albert Ivancic,
• Fliur Macaev,
• Fatma Aksakal,
• Veaceslav Boldescu,
• Serghei Pogrebnoi and
• Gheorghe Duca

Beilstein J. Nanotechnol. 2016, 7, 1208–1218, doi:10.3762/bjnano.7.112

• -mannuronate and α-L-guluronate units [29]. Sodium alginate forms gels in the presence of certain bivalent cations, particularly calcium ions, and entrap other materials in the formed gel structures [30]. Chitosan is a naturally occurring aminopolysaccharide [31] consisting of randomly distributed of β-1,4

• , probably due to the excess of β-cyclodextrin that adhered to the surface of alginate–chitosan matrix. The particles of systems 2, 3 and 5, compared to systems 1 and 4, are almost spherical. System 4 contains filamentous formations, characteristic for calcium alginate. Particles with sizes below 100 nm

• stretching band of the COO− group from 1595 cm−1 to 1604 cm−1. This leads to the conclusion that alginate ions interacted with calcium ions. Also we observe a shift of the band characteristic for OH groups: 3265 cm−1 for system 2, compared to 3279 cm−1 for β-CD, 3226 cm−1 for sodium alginate and 3289 cm−1

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

• ]. Solvent and monomers were purified prior to use. Toluene was stirred over Na–K alloy and benzophenone. Isoprene and ethylene oxide were purified in a two-step procedure: First, the monomers were stirred over calcium hydride for 1 h at −70 °C (dry ice–ethanol mixture), then transferred to a second flask

Influence of calcium on ceramide-1-phosphate monolayers

• Joana S. L. Oliveira,
• Gerald Brezesinski,
• Alexandra Hill and
• Arne Gericke

Beilstein J. Nanotechnol. 2016, 7, 236–245, doi:10.3762/bjnano.7.22

• interaction of C1P with the C2 domain of cPLA2α, an effector protein that needs the presence of submicromolar concentrations of calcium ions. The aim of this study was to determine the phase behaviour and structural properties of C1P in the presence and absence of millimolar quantities of calcium in a well

• -defined pH environment. For that purpose, we used monomolecular films of C1P at the soft air/liquid interface with calcium ions in the subphase. The pH was varied to change the protonation degree of the C1P head group. We used surface pressure versus molecular area isotherms coupled with other monolayer

• techniques as Brewster angle microscopy (BAM), infrared reflection–absorption spectroscopy (IRRAS) and grazing incidence X-ray diffraction (GIXD). The isotherms indicate that C1P monolayers are in a condensed state in the presence of calcium ions, regardless of the pH. At higher pH without calcium ions, the

Fabrication and characterization of novel multilayered structures by stereocomplexion of poly(D-lactic acid)/poly(L-lactic acid) and self-assembly of polyelectrolytes

• Elena Dellacasa,
• Li Zhao,
• Gesheng Yang,
• Laura Pastorino and
• Gleb B. Sukhorukov

Beilstein J. Nanotechnol. 2016, 7, 81–90, doi:10.3762/bjnano.7.10

• ) (PLLA) were alternately adsorbed directly on calcium carbonate (CaCO3) templates and on poly(styrene sulfonate) (PSS) and poly(allylamine hydrochloride) (PAH) multilayer precursors in order to fabricate a novel layer-by-layer (LBL) assembly. A single layer of poly(L-lysine) (PLL) was used as a linker

• deposition. The multilayer structure (PSS/PAH)4/PSS/PLL(PDLA/PLLA)3/PSS was built on calcium carbonate cores, and then moved from acetonitrile to water. A drop of the aqueous dispersion was let to evaporate at room temperature. In this sample, the structure of the calcium carbonate core is visible in some

• points where no shell is present. The different morphologies between the bare calcium carbonate core and the coated surface can be clearly noticed, confirming the successful assembly of the capsule shell. Since particles coated with (PSS/PAH)4/PSS/PLL(PDLA/PLLA)3 and (PSS/PAH)4/PSS/PLL(PDLA/PLLA)3/PSS

Green and energy-efficient methods for the production of metallic nanoparticles

• Mitra Naghdi,
• Mehrdad Taheran,
• Satinder K. Brar,
• M. Verma,
• R. Y. Surampalli and
• J. R. Valero

Beilstein J. Nanotechnol. 2015, 6, 2354–2376, doi:10.3762/bjnano.6.243

• reduced to spherical NPs and their sizes range from 18 to 40 nm depending on pH, temperature, and the Au3+/dextran ratio. However, in acidic conditions, the reduction is very slow and large Au NPs with different shapes are formed [35]. Saha et al. utilized calcium alginate gel beads as a template for Ag

• showed that the more Au atoms than Ag atoms are loaded on calcium alginate [98]. Venkatpurwar and Pokharkar mentioned a single step method for synthesis of Ag NPs by using sulfated polysaccharide extracted from marine red algae (Porphyra vietnamensis) in a 15 min reaction at 70 °C. The produced NPs

Self-organization of gold nanoparticles on silanated surfaces

• Htet H. Kyaw,
• Salim H. Al-Harthi,
• Azzouz Sellai and
• Joydeep Dutta

Beilstein J. Nanotechnol. 2015, 6, 2345–2353, doi:10.3762/bjnano.6.242

• and after functionalization of glass substrates for 24 h with 1% APTES are shown in Figure 1. The survey spectra (Figure 1a) show oxygen, carbon, silicon, tin, potassium, calcium and sodium KLL peaks of non-functionalized glass substrates as well as APTES-modified glass substrates (The core peak of Na

Electrochemical coating of dental implants with anodic porous titania for enhanced osteointegration

• Amirreza Shayganpour,
• Alberto Rebaudi,
• Pierpaolo Cortella,
• Alberto Diaspro and
• Marco Salerno

Beilstein J. Nanotechnol. 2015, 6, 2183–2192, doi:10.3762/bjnano.6.224

• affinity to tri-calcium phosphates or hydroxylapatite. Both the Stark and S&M implants were made using grade 4 Ti. Actually, grade 5 Ti is commonly used only for abutments and other parts, since it presents higher mechanical performance (e.g., yield stress of 860 MPa vs 550 MPa) but is less biocompatible

Nanotechnology in the real world: Redeveloping the nanomaterial consumer products inventory

• Marina E. Vance,
• Todd Kuiken,
• Eric P. Vejerano,
• Sean P. McGinnis,
• Michael F. Hochella Jr.,
• David Rejeski and
• Matthew S. Hull

Beilstein J. Nanotechnol. 2015, 6, 1769–1780, doi:10.3762/bjnano.6.181

• oxide [17]. Calcium and magnesium were listed together in dietary supplements. Nano-ceramics and silver are used in combination in water filtration products, cosmetics, and a humidifier. These results demonstrate the use of nanohybrids [23] in consumer products and indicate that the use of

• variety of nanomaterial compositions (silver, nano-organics, calcium, gold, silicon dioxide, magnesium, ceramics, etc.) were also advertised to be used for health applications, such as dietary supplements (11%). Potential exposure pathways Since critical information such as nanomaterial size and

Towards multifunctional inorganic materials: biopolymeric templates

• Claudia Steinem and
• Joachim Bill

Beilstein J. Nanotechnol. 2015, 6, 1698–1699, doi:10.3762/bjnano.6.172

• structure formation of inorganic components in an aqueous environment. Accordingly, composites made of inorganic solids (i.e., calcium phosphate or carbonate) and biopolymers are formed. Furthermore, the resulting combination of inorganic and bioorganic components yields biominerals with unique

Thermal energy storage – overview and specific insight into nitrate salts for sensible and latent heat storage

• Nicole Pfleger,
• Thomas Bauer,
• Claudia Martin,
• Markus Eck and
• Antje Wörner

Beilstein J. Nanotechnol. 2015, 6, 1487–1497, doi:10.3762/bjnano.6.154

• temperature range between 285 to 450 °C were performed. The heat transfer medium Hitec XL® was used. The material tests of the quartzite rocks as well as sand were successful, apart from the observed calcium carbonate crust formation in the high temperature tests. Implementations in commercial-scale solar

• power plants do not exist so far because of concerns due to the calcium carbonate crust formation and its treatment in a large scale thermal storage unit. The stability of the filler material is influenced by the molten salt (Solar Salt, HITEC XL®, etc.) and by the maximum operation temperature. In the

• ®. Cofalit® is manufactured by the INERTAM Company in France and is produced by high-temperature plasma treatment (1500 °C) of asbestos-containing waste called ACW. Cofalit® is a calcium magnesium iron alumina-silicate [26]. The thermophysical properties meet the required criteria of potential filler

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

• targeting gene expression via both genomic and nongenomic pathways [1]. Although known as an important regulator of calcium homeostasis and bone mineralization [3], several studies support that vitamin D also plays a major role in tumor pathogenesis, progression and therapy [2]. Calcitriol is also regarded

Self-assembled anchor layers/polysaccharide coatings on titanium surfaces: a study of functionalization and stability

• Ognen Pop-Georgievski,
• Dana Kubies,
• Josef Zemek,
• Neda Neykova,
• Roman Demianchuk,
• Eliška Mázl Chánová,
• Miroslav Šlouf,
• Milan Houska and
• František Rypáček

Beilstein J. Nanotechnol. 2015, 6, 617–631, doi:10.3762/bjnano.6.63

• a long-term immersion. Based on the stability observations, the alginate monolayers bound to the neridronate or PDA anchor layers can be potentially used for the immobilization of a thin alginate hydrogel carrier of bioactive compounds (such as calcium phosphates or other biologically active

In situ scanning tunneling microscopy study of Ca-modified rutile TiO₂(110) in bulk water

• Giulia Serrano,
• Beatrice Bonanni,
• Tomasz Kosmala,
• Marco Di Giovannantonio,
• Ulrike Diebold,
• Klaus Wandelt and
• Claudio Goletti

Beilstein J. Nanotechnol. 2015, 6, 438–443, doi:10.3762/bjnano.6.44

• Abstract Despite the rising technological interest in the use of calcium-modified TiO2 surfaces in biomedical implants, the Ca/TiO2 interface has not been studied in an aqueous environment. This investigation is the first report on the use of in situ scanning tunneling microscopy (STM) to study calcium

• -modified rutile TiO2(110) surfaces immersed in high purity water. The TiO2 surface was prepared under ultrahigh vacuum (UHV) with repeated sputtering/annealing cycles. Low energy electron diffraction (LEED) analysis shows a pattern typical for the surface segregation of calcium, which is present as an

• impurity on the TiO2 bulk. In situ STM images of the surface in bulk water exhibit one-dimensional rows of segregated calcium regularly aligned with the [001] crystal direction. The in situ-characterized morphology and structure of this Ca-modified TiO2 surface are discussed and compared with UHV-STM

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

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

• fluorochrome can be monitored independently of the fluorochrome concentration [102]. FLIM gains its information from the fluorescence decay curves and applications of this technique include environmental sensing of, amongst others, polarity, local pH, and calcium concentrations, as well as the study of protein

• muscle cells and characterized the local calcium distribution by using spectromicroscopy at the calcium L3,2 edges [150]. Despite the advantages of soft X-ray microscopy compared with fluorescence or electron microscopy techniques, it has only been applied for few biomedical samples so far due to the

• ) allows for 2D-mapping of tissues or cells. As a result, the distribution of specific elements such as phosphorus, calcium and iron can be identified [173] and conclusions about toxic effects induced by NP may be drawn. In summary, TEM is thus regarded as a useful addition to a series of microscopic tools

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

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

• functionalization of silica particles with amino groups in order to turn the surface potential of the particles from initially negative to highly positive did not significantly affect cellular uptake rates in whole-tissue experiments. However, immortalized human keratinocytes (HaCaT, Human Adult Low Calcium High