Advanced hybrid nanomaterials

• Andreas Taubert,
• Fabrice Leroux,
• Pierre Rabu and
• Verónica de Zea Bermudez

Beilstein J. Nanotechnol. 2019, 10, 2563–2567, doi:10.3762/bjnano.10.247

• synthesize clusters, so-called colloidal molecules [21]. Nanospherical satellites were covalently bonded via amide groups within the dimples of valence-endowed patchy nanoparticles, allowing the tuning of their topology and self-assembling ability. Polyion complex micelles formed by complexation between poly

• (ethylene oxide)-b-poly(acrylic acid) (PEO-b-PAA) and an oligo-chitosan-type polyamine was used as a structure-directing agent to prepare ordered mesoporous silica materials in the work “pH-mediated control over the mesostructure of ordered mesoporous materials templated by polyion complex micelles” [22

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

• remain constant. Hence, the number of micelles stays constant, and their size is increased to accommodate the growing core–shell particles. Consequently, the formation of core-free silica particles is suppressed. When the negative zeta potential of the particles, which continuously decreased during the

• , the size and the number of the aqueous domains, i.e., the water pools inside the micelles, are determined by the ratio of ammonia water to Igepal CO-520, often denoted as the R-value [30][36][51][52]. Several authors suggested that for an optimal growth process where particles with multiple cores as

• well as coreless particles are absent, the number of micelles has to ideally match the number of particles [36][47]. If in the course of this process the silica shell becomes thicker, ammonia water and surfactant must be added accordingly in order to balance the particle growth, while suppressing the

Design of a nanostructured mucoadhesive system containing curcumin for buccal application: from physicochemical to biological aspects

• Sabrina Barbosa de Souza Ferreira,
• Gustavo Braga,
• Évelin Lemos Oliveira,
• Jéssica Bassi da Silva,
• Hélen Cássia Rosseto,
• Lidiane Vizioli de Castro Hoshino,
• Mauro Luciano Baesso,
• Wilker Caetano,
• Craig Murdoch,
• Helen Elizabeth Colley and
• Marcos Luciano Bruschi

Beilstein J. Nanotechnol. 2019, 10, 2304–2328, doi:10.3762/bjnano.10.222

• elucidated by incorporation kinetics and location studies. They revealed that the drug was quickly incorporated and located in the hydrophobic portion of nanometer-sized polymeric micelles. Moreover, the systems displayed plastic behavior with rheopexy characteristics at 37 °C, viscoelastic properties and a

• characteristics beneficial for pharmaceutical and biomedical use [1]. P407 is a non-ionic block copolymer with polypropylene oxide (PPO) and polyethylene oxide (PEO) segments, which can display thermoresponsive properties forming nanometer-sized micelles, hydrogels and lyotropic liquid crystals [2][3]. The

• increase of temperature can promote the self-assembly from unimers to micelles, with large endothermic heat. In this sense, PPO-groups dehydrate in a hydrophobic core with a surrounding hydrated shell. Higher concentrations of P407 are used (15% to 20%, w/w) as colloidal gelling systems in a cubic

Mannosylated brush copolymers based on poly(ethylene glycol) and poly(ε-caprolactone) as multivalent lectin-binding nanomaterials

• Stefania Ordanini,
• Wanda Celentano,
• Anna Bernardi and
• Francesco Cellesi

Beilstein J. Nanotechnol. 2019, 10, 2192–2206, doi:10.3762/bjnano.10.212

• aggregates (e.g., micelles and vesicles) above their critical aggregation concentration (CAC). The resulting self-assembled nanoparticles can act as drug carriers and delivery systems, being able to accommodate a hydrophobic drug within their hydrophobic core [22], or chemically bind bioactive agents [23][24

Incorporation of doxorubicin in different polymer nanoparticles and their anticancer activity

• Sebastian Pieper,
• Hannah Onafuye,
• Dennis Mulac,
• Jindrich Cinatl Jr.,
• Mark N. Wass,
• Martin Michaelis and
• Klaus Langer

Beilstein J. Nanotechnol. 2019, 10, 2062–2072, doi:10.3762/bjnano.10.201

• 33.9 ± 0.5%, respectively). These loading efficiencies are in the range of those described for similar preparations, although higher drug loads have been described when using alternative PLGA-based formulations such as nanoparticles or micelles with doxorubicin covalently bound to the polymer

• , nanoparticles produced by nanoprecipitation, micelles based on multi-arm star-shaped PLGA–PEG block copolymers, or nanopolymersomes [14][15][16][17][18]. In addition, PLGA nanoparticles prepared at pH 7 displayed a more controlled and sustained doxorubicin release than PLGA nanoparticles prepared without pH

• such as nanoparticles or micelles with doxorubicin covalently bound to the polymer, nanoparticles produced by nanoprecipitation, micelles based on multi-arm star-shaped PLGA–PEG block copolymers, or nanopolymersomes [14][15][16][17][18]. Nanoparticle efficacy in cell culture Finally, the effects of

Review of advanced sensor devices employing nanoarchitectonics concepts

• Katsuhiko Ariga,
• Tatsuyuki Makita,
• Masato Ito,
• Taizo Mori,
• Shun Watanabe and
• Jun Takeya

Beilstein J. Nanotechnol. 2019, 10, 2014–2030, doi:10.3762/bjnano.10.198

• disadvantageous in the formation of host–guest complexes. However, the incorporation of guanidinium functionality into molecular assemblies such as aqueous micelles and lipid bilayers to place recognition sites at a mesoscopic interface increased the binding constants between guanidinium and phosphate to 102–104

Gold-coated plant virus as computed tomography imaging contrast agent

• Alaa A. A. Aljabali,
• Mazhar S. Al Zoubi,
• Khalid M. Al-Batanyeh,
• Ali Al-Radaideh,
• Mohammad A. Obeid,
• Abeer Al Sharabi,
• Walhan Alshaer,
• Bayan AbuFares,
• Tasnim Al-Zanati,
• Murtaza M. Tambuwala,
• Naveed Akbar and
• David J. Evans

Beilstein J. Nanotechnol. 2019, 10, 1983–1993, doi:10.3762/bjnano.10.195

• contrast agents including gold nanoparticles (AuNPs) [13], bromine [14], platinum [15], ytterbium [16], gadolinium [4], and tungsten [15]. Many of the systems are made up of a core that is coated with a polymeric material such as liposomes [17], micelles [13], lipoproteins or polymeric nanoparticles [18

• ]. One of the first examples of such NP-based systems was reported by Caride et al. using brominated phospholipids packaged into liposomes and administered to dogs. Contrast enhancement signals of 40 HU were observed in the liver of imaged animals [14]. Two hours after injection, micelles loaded with

Engineered superparamagnetic iron oxide nanoparticles (SPIONs) for dual-modality imaging of intracranial glioblastoma via EGFRvIII targeting

• Xianping Liu,
• Chengjuan Du,
• Haichun Li,
• Ting Jiang,
• Zimiao Luo,
• Zhiqing Pang,
• Daoying Geng and
• Jun Zhang

Beilstein J. Nanotechnol. 2019, 10, 1860–1872, doi:10.3762/bjnano.10.181

• -coated iron oxide nanoparticles to target tumor-associated macrophages [36] and D-AE-peptide-modified micelles as a multitarget drug delivery system [37], the benefits of the nanoprobe in this study are described as follows. First, the nanoprobe has a diameter of around 100 nm and can directly pass

Microfluidic manufacturing of different niosomes nanoparticles for curcumin encapsulation: Physical characteristics, encapsulation efficacy, and drug release

• Mohammad A. Obeid,
• Ibrahim Khadra,
• Abdullah Albaloushi,
• Margaret Mullin,
• Hanin Alyamani and
• Valerie A. Ferro

Beilstein J. Nanotechnol. 2019, 10, 1826–1832, doi:10.3762/bjnano.10.177

• unwanted side effects [8][9]. Liposomes, solid lipid nanoparticles, dendrimers, micelles, polymeric nanoparticles, gold nanoparticles, and carbon nanotubes are among the most common types of nanoparticle delivery systems [10]. These efforts have been reported in several studies. For example, Guo et al

Materials nanoarchitectonics at two-dimensional liquid interfaces

• Katsuhiko Ariga,
• Michio Matsumoto,
• Taizo Mori and
• Lok Kumar Shrestha

Beilstein J. Nanotechnol. 2019, 10, 1559–1587, doi:10.3762/bjnano.10.153

• guanidinium-functionalized aqueous micelles and lipid bilayers reaches values of 102 to 104 M−1. Surprisingly, the binding constant of the same recognition pair further increases to 106 to 107 M−1 when a macroscopic less dynamic interface, the air–water interface, is used as the recognition medium [157][158

Tailoring the stability/aggregation of one-dimensional TiO₂(B)/titanate nanowires using surfactants

• Atiđa Selmani,
• Johannes Lützenkirchen,
• Kristina Kučanda,
• Dario Dabić,
• Engelbert Redel,
• Ida Delač Marion,
• Damir Kralj,
• Darija Domazet Jurašin and
• Maja Dutour Sikirić

Beilstein J. Nanotechnol. 2019, 10, 1024–1037, doi:10.3762/bjnano.10.103

• in aqueous solutions. In order to fill this void, in this study, the effect of monomers and micelles of (a) monomeric dodecyltrimethylammonium bromide (DTAB), and (b) its corresponding gemini, bis(N,N-dimethyl-N-dodecyl)ethylene-1,2-diammonium dibromide (12-2-12) quaternary ammonium surfactant

• micelles) on the stability of TNWs was assessed in two media, water and aqueous electrolyte solution of sodium bromide, thus increasing the complexity of the investigated systems. The observed effects were quantified by surface complexation modeling (SCM) in order to describe the TNW behavior when

• tension with increase of surfactant concentration up to almost constant σ values, indicating the formation of micelles. As expected, 12-2-12 exhibited considerably lower σ values as well as a lower critical micelle concentration (cmc) than DTAB (Table S1 in Supporting Information) indicating its greater

Self-assembly and wetting properties of gold nanorod–CTAB molecules on HOPG

• Imtiaz Ahmad,
• Floor Derkink,
• Tim Boulogne,
• Pantelis Bampoulis,
• Harold J. W. Zandvliet,
• Hidayat Ullah Khan,
• Rahim Jan and
• E. Stefan Kooij

Beilstein J. Nanotechnol. 2019, 10, 696–705, doi:10.3762/bjnano.10.69

• surface. The self-assembled layers of CTAB molecules on the HOPG terraces prior to nanorod deposition were shown to change the wettability of the surface, and as a result, gold nanorod deposition takes place on nonwetting HOPG terraces. Keywords: CTAB; gold nanorods; micelles; self-assembly; wettability

• ; Introduction In the last few decades there have been many studies that focused on hard colloidal particles and micelles, covering a length scale ranging from nanometers to micrometers. The focus of nanoscience and nanotechnology is increasingly shifting from synthesis to assembly into larger superstructures

• that CTAB surfactant molecules can self-assemble on a highly ordered pyrolytic graphite (HOPG) surface in the form of hemi-cylindrical micelles [43][44][45]. The surface of HOPG is hydrophobic [46][47], while the CTAB molecules have a hydrophilic end group and a hydrophobic tail [48]. Therefore, to

pH-mediated control over the mesostructure of ordered mesoporous materials templated by polyion complex micelles

• Emilie Molina,
• Mélody Mathonnat,
• Jason Richard,
• Patrick Lacroix-Desmazes,
• Martin In,
• Philippe Dieudonné,
• Thomas Cacciaguerra,
• Corine Gérardin and
• Nathalie Marcotte

Beilstein J. Nanotechnol. 2019, 10, 144–156, doi:10.3762/bjnano.10.14

• Coulomb, UMR 5221 CNRS – Université de Montpellier, 34095 Montpellier, France 10.3762/bjnano.10.14 Abstract Ordered mesoporous silica materials were prepared under different pH conditions by using a silicon alkoxide as a silica source and polyion complex (PIC) micelles as the structure-directing agents

• . PIC micelles were formed by complexation between a weak polyacid-containing double-hydrophilic block copolymer, poly(ethylene oxide)-b-poly(acrylic acid) (PEO-b-PAA), and a weak polybase, oligochitosan-type polyamine. As both the micellization process and the rate of silica condensation are highly

• ; hybrid organic–inorganic interface; mesoporous materials; nanostructured materials; polyion complex micelles; polyion electrostatic complexation; Introduction Due to their unique physicochemical properties originating from their uniform pore size and periodically arranged network at the mesoscale

Enhanced antineoplastic/therapeutic efficacy using 5-fluorouracil-loaded calcium phosphate nanoparticles

• Shanid Mohiyuddin,
• Saba Naqvi and
• Gopinath Packirisamy

Beilstein J. Nanotechnol. 2018, 9, 2499–2515, doi:10.3762/bjnano.9.233

• –surfactant molar ratio (MW). By restricting the water–surfactant molar ratio up to 10 (i.e., MW < 10) the reverse micelles can be readily formed with narrow size distribution in a synthetic reaction system [23]. The water molecules restricted inside hydrophilic core resulted in swollen micelles that were

High-throughput micro-nanostructuring by microdroplet inkjet printing

• Hendrikje R. Neumann and
• Christine Selhuber-Unkel

Beilstein J. Nanotechnol. 2018, 9, 2372–2380, doi:10.3762/bjnano.9.222

• densities is highly important in many fields, ranging from nano-optics to biosensor technologies and biomaterials. A well-established method to fabricate quasi-hexagonal patterns of metal nanoparticles is block copolymer micelle nanolithography, which relies on the self-assembly of metal-loaded micelles on

• surfaces by a dip-coating or spin-coating process. Using this method, the spacing of the nanoparticles is controlled by the size of the micelles and by the coating conditions. Whereas block copolymer micelle nanolithography is a high-throughput method for generating well-ordered nanoparticle patterns at

• spacing between a few tens to several hundreds of nanometers is block copolymer micelle nanolithography (BCML) [8]. This technique is based on the self-assembly of metal-containing micelles on surfaces during dip-coating or spin-coating. BCML is very efficient in coating large areas with nanoparticles in

Block copolymers for designing nanostructured porous coatings

• Roberto Nisticò

Beilstein J. Nanotechnol. 2018, 9, 2332–2344, doi:10.3762/bjnano.9.218

• micelles, reverse micelles as well as worm-like structures, lamellar sheets, and vesicles (Figure 5). As mentioned previously, the thermodynamic incompatibility between the blocks forming the polymer chains is the driving force behind the formation of such nanostructures [4][35]. In this context, this

Nanoconjugates of a calixresorcinarene derivative with methoxy poly(ethylene glycol) fragments for drug encapsulation

• Alina M. Ermakova,
• Julia E. Morozova,
• Yana V. Shalaeva,
• Victor V. Syakaev,
• Aidar T. Gubaidullin,
• Alexandra D. Voloshina,
• Vladimir V. Zobov,
• Irek R. Nizameev,
• Olga B. Bazanova,
• Igor S. Antipin and
• Alexander I. Konovalov

Beilstein J. Nanotechnol. 2018, 9, 2057–2070, doi:10.3762/bjnano.9.195

• nanoassociates that are able to encapsulate organic substrates of different hydrophobicity, including drugs (doxorubicin, naproxen, ibuprofen, quercetin). The micelles of the macrocycle slowed down the release of the hydrophilic substrates in vitro. In physiological sodium chloride solution and phosphate

• -buffered saline, the micelles of the macrocycle acquire thermoresponsive properties and exhibit a temperature-controlled release of doxorubicin in vitro. The combination of the low toxicity and the encapsulation properties of the obtained calixresorcinarene–mPEG conjugate shows promising potential for the

• various therapeutics and nanomaterials due to a number of benefits among which its low toxicity the most important [23][24]. PEG has good solubility in water and organic solvents. When being a component of polymeric micelles, it forms the outer hydrophilic shell of the micelle, contributes the colloidal

Self-assembled quasi-hexagonal arrays of gold nanoparticles with small gaps for surface-enhanced Raman spectroscopy

• Emre Gürdal,
• Simon Dickreuter,
• Fatima Noureddine,
• Pascal Bieschke,
• Dieter P. Kern and
• Monika Fleischer

Beilstein J. Nanotechnol. 2018, 9, 1977–1985, doi:10.3762/bjnano.9.188

• /mL and stirred for 2 days. The micelles were loaded with chlorauric acid (HAuCl4, loading parameter (L = 0.5), Sigma-Aldrich) and stirred again for 2 days. Spin-coating was applied to cover the substrate with a monolayer of the gold-loaded micelles (30 s at 2000 rpm). Electroless deposition A quartz

• block [23]. The hydrophobic PS forms the shell, and the hydrophilic P2VP the core of the spherically shaped micelles [24]. Within their core gold salt can be assembled, which is bonded by protonization or complexation [25]. The loaded spherical micelles form a hexagonal array when being deposited on a

• substrate. Exposing them to an aqueous environment promotes a morphological change of the spherical micelles [18]. In the next step, the micelles are treated with UV irradiation, which causes the gold salt particles in the center to grow bigger by photochemical growth [18]. To enlarge the metal precursor

Nanoporous silicon nitride-based membranes of controlled pore size, shape and areal density: Fabrication as well as electrophoretic and molecular filtering characterization

• Axel Seidenstücker,
• Stefan Beirle,
• Fabian Enderle,
• Paul Ziemann,
• Othmar Marti and
• Alfred Plettl

Beilstein J. Nanotechnol. 2018, 9, 1390–1398, doi:10.3762/bjnano.9.131

• . 12 nm) are deposited on the silicon oxide layer with a quasi-hexagonal order by self-organization. This is realized by dip-coating from a solution of Au salt-loaded PS–P2VP diblock copolymer micelles directly on the upper membrane face (coating is done without preceding deposition of appropriate

• self-organization of Au-loaded diblock copolymer micelles followed by plasma treatments. (b) Applying a photochemical growth process the Au NP size can be enlarged in a controlled way. (c) The resulting NP mask is exploited to etch nanopillars by RIE, (d) a Cr layer (black) is evaporated, (e) and the

A simple extension of the commonly used fitting equation for oscillatory structural forces in case of silica nanoparticle suspensions

• Sebastian Schön and
• Regine von Klitzing

Beilstein J. Nanotechnol. 2018, 9, 1095–1107, doi:10.3762/bjnano.9.101

• , aggregates or micelles tend to form a well-ordered layer in close proximity to a confining surface (henceforth called wall) with a density that is higher than that of the bulk. Since the molecules cannot penetrate each other, this layer of increased density is bordering on a region of lower density of

Review on nanoparticles and nanostructured materials: history, sources, toxicity and regulations

• Jaison Jeevanandam,
• Ahmed Barhoum,
• Yen S. Chan,
• Alain Dufresne and
• Michael K. Danquah

Beilstein J. Nanotechnol. 2018, 9, 1050–1074, doi:10.3762/bjnano.9.98

• structures such as dendrimers, micelles, liposomes and polymer NPs. (iv) Composite-based nanomaterials: Composite NMs are multiphase NPs and NSMs with one phase on the nanoscale dimension that can either combine NPs with other NPs or NPs combined with larger or with bulk-type materials (e.g., hybrid

Optical orientation of nematic liquid crystal droplets via photoisomerization of an azodendrimer dopant

• Sergey A. Shvetsov,
• Alexander V. Emelyanenko,
• Natalia I. Boiko,
• Alexander S. Zolot'ko,
• Yan-Song Zhang,
• Jui-Hsiang Liu and
• Alexei R. Khokhlov

Beilstein J. Nanotechnol. 2018, 9, 870–879, doi:10.3762/bjnano.9.81

• different kinds of soft matter, such as light-driven polymers [5][6], elastomers [7][8][9] microgel particles [10][11], micelles [12][13], nematic liquid crystals (NLCs) [7][14], liquid-crystalline (LC) polymers [15][16][17][18] and Langmuir–Blodgett films [19][20] with light-controllable supramolecular

The role of ligands in coinage-metal nanoparticles for electronics

• Ioannis Kanelidis and
• Tobias Kraus

Beilstein J. Nanotechnol. 2017, 8, 2625–2639, doi:10.3762/bjnano.8.263

• particular facets [2]. Their structure-directing action is due to a combination of thermodynamic driving forces (energy differences in facets) and transport modulation, where ligand coverage adjusts diffusion of monomers to the facets [2]. Some ligands also form micelles that can act as templates during the

Fabrication of carbon nanospheres by the pyrolysis of polyacrylonitrile–poly(methyl methacrylate) core–shell composite nanoparticles

• Dafu Wei,
• Youwei Zhang and
• Jinping Fu

Beilstein J. Nanotechnol. 2017, 8, 1897–1908, doi:10.3762/bjnano.8.190

• nanospheres were first fabricated by Kowaleski et al. [31] via successive shell crosslinking, oxidization and carbonization of the micelles resulting from the self-assembly of PAN-b-poly(acrylic acid) (PAA) block copolymer in water. The crosslinked shell can retain the micelle structure during the heat

• treatments, and thus is very crucial to obtain discrete carbon nanospheres after pyrolysis. Jérom et al. [32] obtained discrete carbon nanocapules after pyrolysis of stable PAN-b-PAA micelles with Au-nanoparticle-crosslinked cores. However, the difficulty in synthesis of the block copolymers and the low

• observed in the cavitation of non-covalently-connected micelles composed of carboxyl-ended polybutadiene cores and crosslinked poly(vinyl alcohol) shells in THF/water (9/1, v/v) mixture [44]. It was very possible that the size of PAN chains was too large to diffuse out of the PMMA shell, thus, the

Self-assembly of chiral fluorescent nanoparticles based on water-soluble L-tryptophan derivatives of p-tert-butylthiacalix[4]arene

• Pavel L. Padnya,
• Irina A. Khripunova,
• Olga A. Mostovaya,
• Timur A. Mukhametzyanov,
• Vladimir G. Evtugyn,
• Vyacheslav V. Vorobev,
• Yuri N. Osin and
• Ivan I. Stoikov

Beilstein J. Nanotechnol. 2017, 8, 1825–1835, doi:10.3762/bjnano.8.184

• agreement was observed between the DLS data and the microscopy measurements in the case of the compounds 8 and 10 in cone conformation. This is due to the structure of the macrocycles, which formed spherical charged particles (micelles) with inwardly directed hydrophobic parts (thiacalixarene) and outwardly

• oriented hydrophilic positively charged fragments in the solution (Figure 1). The charge on the micelles prevents them from aggregating when we concentrate the solutions for preparation of the SEM experiment. This leads to the preservation of individual particles of similar size to those that exist in