The impact of molecular tumor profiling on the design strategies for targeting myeloid leukemia and EGFR/CD44-positive solid tumors

• Nikola Geskovski,
• Nadica Matevska-Geshkovska,
• Simona Dimchevska Sazdovska,
• Marija Glavas Dodov,
• Kristina Mladenovska and
• Katerina Goracinova

Beilstein J. Nanotechnol. 2021, 12, 375–401, doi:10.3762/bjnano.12.31

• synthesis of nucleic acids required for DNA replication, while taxanes and vinca alkaloids interfere with the polymerization/depolymerization of the microtubules thus inhibiting mitosis [8]. However, in addition to cancer cells, all of these drugs also affect the normal/healthy tissues with cells that

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

• initiated by the polymerization of clathrin units resulting in the assembly of a basket-like structure (clathrin-coated pit) with a size of 120–150 nm at the inner layer of the plasma membrane [11]. An alternative endocytosis pathway is caveolin-mediated endocytosis (CavME), the second most important route

• exposure of cells to surface-modified MNPs and Noc affect substantially the cell proliferation and morphology. Noc affects microtubule formation, thus interfering with cytoskeleton structure and mitosis, leading to cell cycle arrest in G2/M [26]. As MNPs interfere with tubulin polymerization as well [27

The nanomorphology of cell surfaces of adhered osteoblasts

• Christian Voelkner,
• Mirco Wendt,
• Regina Lange,
• Max Ulbrich,
• Martina Gruening,
• Susanne Staehlke,
• Barbara Nebe,
• Ingo Barke and
• Sylvia Speller

Beilstein J. Nanotechnol. 2021, 12, 242–256, doi:10.3762/bjnano.12.20

• migration for many mammalian cell types [12][13]. Migrating and spreading cells form flat, actin-supported, organelle-free regions, referred to as lamellipodia, and other features that may expand their attachment area [14]. A physical coupling of adhesion molecules to the actin polymerization machinery has

• (effective treatment time to initiate plasma polymerization of allylamine). For Au coating a sputter coater (Cressington 108 auto/SE, UK) was used. The sputter parameters were Ar pressure: 0.06 mbar, sputter current: 30 mA, time: 60 s, and distance between sample and target: 55 mm. The thickness of the

Unravelling the interfacial interaction in mesoporous SiO₂@nickel phyllosilicate/TiO₂ core–shell nanostructures for photocatalytic activity

• Bridget K. Mutuma,
• Xiluva Mathebula,
• Isaac Nongwe,
• Bonakele P. Mtolo,
• Boitumelo J. Matsoso,
• Rudolph Erasmus,
• Zikhona Tetana and
• Neil J. Coville

Beilstein J. Nanotechnol. 2020, 11, 1834–1846, doi:10.3762/bjnano.11.165

• °C, urea hydrolysis took place reducing the nickel precursor to nickel species, which diffused into the silica layers through the mesoporous shell. The nickel species reacted with the surface hydroxides to give nickel phyllosilicate via a Ni–O–Si polymerization reaction. TiO2 (dTiO2 = 30 ± 9 nm) was

Out-of-plane surface patterning by subsurface processing of polymer substrates with focused ion beams

• Serguei Chiriaev,
• Luciana Tavares,
• Vadzim Adashkevich,
• Arkadiusz J. Goszczak and
• Horst-Günter Rubahn

Beilstein J. Nanotechnol. 2020, 11, 1693–1703, doi:10.3762/bjnano.11.151

• mineral-organic polymer (its structure includes both carbon and silicon atoms). It is an elastomer and its elasticity can be tuned within a very broad range by changing the degree and the type of polymerization and by post-curing treatments [19][20]. The high and easily tunable elasticity, combined with

Adsorption and self-assembly of porphyrins on ultrathin CoO films on Ir(100)

• Feifei Xiang,
• Tobias Schmitt,
• Marco Raschmann and
• M. Alexander Schneider

Beilstein J. Nanotechnol. 2020, 11, 1516–1524, doi:10.3762/bjnano.11.134

• surfaces. It was shown that free-base (2H) or metalated DPP molecules assemble in two-dimensional or linear structures on metal surfaces [22][23] and that on-surface dehydrogenative polymerization reactions may be induced [24]. DPP molecules interact via the phenyl rings and the molecular macrocycle. In

Growth of a self-assembled monolayer decoupled from the substrate: nucleation on-command using buffer layers

• Robby Reynaerts,
• Kunal S. Mali and
• Steven De Feyter

Beilstein J. Nanotechnol. 2020, 11, 1291–1302, doi:10.3762/bjnano.11.113

• controlled electrochemical polymerization of thiophene to produce polythiophene nanowires with tunable lengths [36][37]. In the context of their use for controlling surface architectures, insertion of the buffer layers between the assembling moiety and the solid substrate affects the assembly process via the

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

• -lined autoclave for 24 h at different temperatures from 190 to 220 °C. After cooling down to room temperature, the autoclaves were opened and the black precursors were washed with around 2 L of water and then 1 L of ethanol to remove residuals of the polymerization by vacuum filtration. After drying the

High permittivity, breakdown strength, and energy storage density of polythiophene-encapsulated BaTiO₃ nanoparticles

• Adnanullah Khan,
• Amir Habib and
• Adeel Afzal

Beilstein J. Nanotechnol. 2020, 11, 1190–1197, doi:10.3762/bjnano.11.103

• . This article presents the synthesis of polythiophene-encapsulated BaTiO3 (BTO-PTh) nanoparticles via an in situ Cu(II)-catalyzed chemical oxidative polymerization of thiophene monomer on hydrothermally obtained tetragonal BTO nanocrystals. The formed core–shell-type BTO-PTh nanoparticles exhibit

• )-encapsulated BaTiO3 nanoparticles with a 9:1 mass ratio of BTO/PTh, and a facile method for the synthesis of inverted [11] core–shell-type BTO-PTh nanostructures, which yields a uniform PTh coating on the BTO surface. BTO-PTh nanoparticles are prepared by Cu(II)-catalyzed oxidative polymerization of PTh on the

• to dissolve and remove impurities and is dried in an oven at 120 °C. The obtained dried product is pulverized to get BTO nanoparticles. In the next step, core–shell BTO-PTh nanoparticles are synthesized via in situ chemical oxidative polymerization of thiophene on hydrothermally produced BTO

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

• Abstract Surface functionalization of porous materials allows for the introduction of additional functionality coupled with high mechanical stability of functionalized inner pores. Herein, we investigate the surface-initiated ring-opening polymerization (SI-ROP) of phenylalanine-N-carboxyanhydride (PA-NCA

• ; polyphenylalanine; porous alumina membranes; surface-initiated ring-opening polymerization (SI-ROP); Introduction Porous materials with functional surfaces are a topic of immense interest in science and technology. The high surface area and high mechanical stability of such materials allows for applications in

• applications. The most common route to graft polypeptides on surfaces is the surface-initiated ring-opening polymerization (SI-ROP) of α-aminoacid-N-carboxyanhydrides (NCAs). Dense polypeptide films consisting of poly(γ-benzyl-ʟ-glutamate), polylysine or polyphenylalanine with thickness in the range between

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

• charged sulfonic groups. The gel shell can be utilized for the accumulation of cationic species, e.g., the accumulation of a monomer followed by further polymerization [2][22]. Polystyrene-based gel-shell particles have been also used for the accumulation of silver ions followed by their reduction to

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

• components have been utilized to functionalize capsules in many ways. Hollow capsules of approximately 400 nm in size with negligible toxicity to cells were reported by the oxidative self-polymerization of dopamine solution onto silica particles [114]. The thickness of multilayer films is comparable to the

• LbL multistep technique and can be easily controlled by varying the polymerization time. This single-step technique resulted in a wall thickness similar to the LbL multistep technique and was applicable to other particles of different size and porosity. Because of the broad absorption and interesting

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

• was obtained via the polymerization of a 30% ethanolic solution of 1-vinylimidazole in the presence of 2% (by monomer mass) of 2,2-azobis(isobutyronitrile) in argon atmosphere at 60 °C by Prof. Annenkov’s group and the polymer fraction with a molecular weight of 35,000 Da was used for the study

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

• results. As an example of this, cytochalasin D, an inhibitor of actin polymerization [211], has often been used to test the involvement of macropinocytosis and phagocytosis in the uptake of nanomaterials. However, actin has been shown to be important also for other mechanisms, including clathrin-mediated

Using gold nanoparticles to detect single-nucleotide polymorphisms: toward liquid biopsy

• María Sanromán Iglesias and
• Marek Grzelczak

Beilstein J. Nanotechnol. 2020, 11, 263–284, doi:10.3762/bjnano.11.20

• to a conformational change, and stem separation (step 1), followed by polymerization reaction by the polymerase (step 2), forming biotin- and digoxin-attached duplex DNA (step 3). The process was further amplified through the next cycle (step 4). Overall, by the cyclic process, a large number of

• luminescence was recovered after adding target DNA, causing a conformational transition from hairpin to linear DNA. This opening initiated polymerization of DNA (Figure 11C), which in turn displaced previously hybridized target DNA (Figure 11D). In such a design, one target DNA strand could open many hairpin

• DNA strands, increasing the fluoresce signal. An additional increase of the fluorescence signal was achieved by the action of NEase that nicked an extended double helix strand, allowing for a subsequent polymerization process and displacement of the DNA trigger. The authors estimated that the presence

Rational design of block copolymer self-assemblies in photodynamic therapy

• Maxime Demazeau,
• Laure Gibot,
• Anne-Françoise Mingotaud,
• Patricia Vicendo,
• Clément Roux and
• Barbara Lonetti

Beilstein J. Nanotechnol. 2020, 11, 180–212, doi:10.3762/bjnano.11.15

• parallel to this development of stealth nanocarriers, polymer chemistry had progressed strongly with the emergence of controlled polymerization. After the discovery of so-called living polymerization (polymerization without any transfer nor any termination reaction) in the 1950’s, the development of

• controlled radical polymerization in the 1990’s provided polymer scientists with a range of chemical tools to synthesize polymers and copolymers exhibiting various architectures, from block and gradient to grafted polymers [7]. Designing new nanocarriers exhibiting an external shell based on PEG and a core

Molecular architectonics of DNA for functional nanoarchitectures

• Debasis Ghosh,
• Lakshmi P. Datta and
• Thimmaiah Govindaraju

Beilstein J. Nanotechnol. 2020, 11, 124–140, doi:10.3762/bjnano.11.11

• from DNA block copolymer micelles [100]. The block copolymer micelles were synthesized through ring-opening polymerization, followed by the integration of DNA oligonucleotides in a postpolymerization modification process. The DNA acted as a polar head group, while the whole polymer system acted as a

Internalization mechanisms of cell-penetrating peptides

• Ivana Ruseska and
• Andreas Zimmer

Beilstein J. Nanotechnol. 2020, 11, 101–123, doi:10.3762/bjnano.11.10

• in the initiation of macropinocytosis. After the interaction with extracellular ligands, multimerization of syndecans is thought to occur, which in turn induces actin polymerization. Arginine-rich peptides have shown to have this effect on the cellular signal transduction via syndecan multimerization

• . When it binds to the adaptor protein complex on the plasma membrane, clathrin rapidly assembles into icosahedral cages. It is thought that the polymerization of clathrin could be responsible for the membrane curvature. The actin cytoskeleton also contributes to membrane bending during CME. There is

• evidence that rapid actin polymerization occurs in the region surrounding the coat and the base of the growing membrane invagination. After vesicle scission, actin filaments depolymerize in seconds [79][82]. Vesicle scission is the process where the CCV is separated from the donor membrane. This step is

pH-Controlled fluorescence switching in water-dispersed polymer brushes grafted to modified boron nitride nanotubes for cellular imaging

• Saban Kalay,
• Yurij Stetsyshyn,
• Volodymyr Donchak,
• Khrystyna Harhay,
• Ostap Lishchynskyi,
• Halyna Ohar,
• Yuriy Panchenko,
• Stanislav Voronov and
• Mustafa Çulha

Beilstein J. Nanotechnol. 2019, 10, 2428–2439, doi:10.3762/bjnano.10.233

• polymer brushes via polymerization initiated from their surface [12][28]. In particular, BNNTs were covalently modified with hydrophobic polystyrene or poly(glycidyl methacrylate) polymer brushes [28]. The modified nanotubes demonstrated high dispersibility in a large number of organic solvents. In our

• irradiation [43], by mechanical milling [44] or with the iminoborane treatment [45]. The first step in covalent bonding of oligoperoxide to BNNT surfaces is to bind pyromellitic chloroanhydride moieties through available amino groups. The second step involves the grafting polymerization “from the surface” of

• -functionalized BNNTs were dried and used for grafting polymerization (2). Fabrication of P(AA-co-FA)-grafted brushes BNNTs with grafted oligoperoxide [(2) below in Scheme 1] were placed in a container with 0.1 М of AA and 0.01 M FA aqueous solution and sonicated for 20 min. Then, the mixture was heated under

Atomic force acoustic microscopy reveals the influence of substrate stiffness and topography on cell behavior

• Yan Liu,
• Li Li,
• Xing Chen,
• Ying Wang,
• Meng-Nan Liu,
• Jin Yan,
• Liang Cao,
• Lu Wang and
• Zuo-Bin Wang

Beilstein J. Nanotechnol. 2019, 10, 2329–2337, doi:10.3762/bjnano.10.223

• surfaces. Even at unsuitable exposure doses at 200 and 500 μC·cm−2 which polymerization of the SU-8 resist cannot be completed, the pattern of stiffness is still enhanced. In the next step, after the SU-8 film had developed for 1 min, we chose the optimum exposure dose of 1000 μC∙cm−2 to obtain strip

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

• polymerizations provided high control over molecular weight and functionality. A post-polymerization azide–alkyne cycloaddition allowed for the formation of glycopolymers with different mannose valencies (1, 2, 4, and 8). In aqueous media, these macromolecules formed nanoparticles that were able to bind lectins

• : atom transfer radical polymerization (ATRP); glycopolymer; lectin; poly(ethylene glycol); poly(ε-caprolactone); ring-opening polymerization (ROP); Introduction Carbohydrate–protein interactions are involved in many biological processes, including cell recognition and cell–cell adhesion. These

• functionality can influence the macromolecule bioactivity [8]. Controlled radical polymerization (CRP) techniques, such as atom transfer radical polymerization (ATRP), reversible addition fragmentation chain transfer (RAFT) polymerization, single-electron transfer living radical polymerization (SET-LRP) and

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

• polymerization to obtain –[–Ti–O–Ti–]–, –[–Si–O–Si–]–, and –[–Ti–O–Si–]– containing seeds. After aging, the 90 mL solution was divided into two 45 mL parts, each of which was placed into the 70 mL polytetrafluoroethylene (PTFE) reactor. The reactor was closed with a PTFE cap and inserted into a homemade

Nanostructured and oriented metal–organic framework films enabling extreme surface wetting properties

• Andre Mähringer,
• Julian M. Rotter and
• Dana D. Medina

Beilstein J. Nanotechnol. 2019, 10, 1994–2003, doi:10.3762/bjnano.10.196

• example, sol–gel synthesis, electrochemical deposition, anodization, electrochemical polymerization, electrospinning, plasma treatment, chemical or hydrothermal methods, vapor deposition, layer-by-layer assembly or laser ablation [19][27][28][29][30][31][32][33][34][35][36][37][38][39]. However, the

Porous silver-coated pNIPAM-co-AAc hydrogel nanocapsules

• William W. Bryan,
• Riddhiman Medhi,
• Maria D. Marquez,
• Supparesk Rittikulsittichai,
• Michael Tran and
• T. Randall Lee

Beilstein J. Nanotechnol. 2019, 10, 1973–1982, doi:10.3762/bjnano.10.194

• describes the preparation and characterization of a new type of core–shell nanoparticle in which the structure consists of a hydrogel core encapsulated within a porous silver shell. The thermo-responsive hydrogel cores were prepared by surfactant-free emulsion polymerization of a selected mixture of N

• encapsulation of thermo-responsive pNIPAM-co-AAc hydrogel cores within porous silver nanoshells, and for the purpose of comparison, within a complete nonporous silver nanoshell. We adopt a simple surfactant-free emulsion polymerization (SFEP) technique to grow the initial hydrogel core templates [74][75][76

• -growth method and surfactant-free emulsion polymerization, we demonstrated a reliable synthesis of silver nanocapsules encapsulating thermo-responsive pNIPAM-co-AAc hydrogel cores. The 800 nm silver nanocapsules with a capsule thickness of ≈50 nm were characterized by SEM, TEM, and UV–vis spectroscopy

Processing nanoporous organic polymers in liquid amines

• Jeehye Byun,
• Damien Thirion and
• Cafer T. Yavuz

Beilstein J. Nanotechnol. 2019, 10, 1844–1850, doi:10.3762/bjnano.10.179

• polymerization [14], ionic complexation [15], and electrochemical polymerization [16], which require sophisticated techniques. There are only a few reports that show the processing of nanoporous polymers into the desired morphologies, for instance, the nanoporous polymers were directly processed into