Development of a mucoadhesive drug delivery system and its interaction with gastric cells

• Ahmet Baki Sahin,
• Serdar Karakurt and
• Deniz Sezlev Bilecen

Beilstein J. Nanotechnol. 2025, 16, 371–384, doi:10.3762/bjnano.16.28

• assessed with a similar approach in a newly designed synthetic mucus hydrogel barrier system. The authors used differently sized polystyrene nanoparticles with polyethylene glycol (PEG) modifications. PEGylated nanoparticles exhibited better penetration than non-PEGylated formulations, regardless of the

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

Effect of different silica coatings on the toxicity of upconversion nanoparticles on RAW 264.7 macrophage cells

• Cynthia Kembuan,
• Helena Oliveira and
• Christina Graf

Beilstein J. Nanotechnol. 2021, 12, 35–48, doi:10.3762/bjnano.12.3

• particles [45]. Xia et al. investigated cell type-dependent cytotoxicity in RAW 264.7, epithelial (BEAS-2B), human microvascular endothelial (HMEC), hepatoma (HEPA-1), and pheochromocytoma (PC-12) cells after exposure to amine-functionalized polystyrene nanoparticles (NH2-PS) [64]. They observed that

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

• proteins that can interact with nanoparticles and drastically hinder their diffusion [137]. By densely coating 40 nm and 100 nm fluorescent polystyrene nanoparticles with PEG, the nanoparticles were able to diffuse through the brain ECS of live mice, thanks to PEG limiting the adhesive interactions between

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

• ][126][127]. For example, in one study using HEK293 cells, spherical polystyrene nanoparticles of 100 nm were internalized through actin-dependent but clathrin-independent processes, and vice versa, 200 nm nanoparticles entered by clathrin-mediated endocytosis [127]. Similarly, the uptake of 500 nm

• could be internalized by HeLa cells [125]. Moreover, the effects of nanoparticle size on the mechanism of uptake may be different in different cell types. For example, it has been shown that murine RAW 264.7 macrophages have a higher uptake efficiency for carboxylated polystyrene nanoparticles compared

• to human endothelial HCMEC or epithelial HeLa cells [131]. In another study using carboxylated polystyrene nanoparticles of different sizes in different cell types, actin was required for the internalization of nanoparticles of 200 nm, but not for those of 40 nm in 1321N1 astrocytes. Instead, in lung

Interaction-tailored organization of large-area colloidal assemblies

• Silvia Rizzato,
• Elisabetta Primiceri,
• Anna Grazia Monteduro,
• Adriano Colombelli,
• Angelo Leo,
• Maria Grazia Manera,
• Roberto Rella and
• Giuseppe Maruccio

Beilstein J. Nanotechnol. 2018, 9, 1582–1593, doi:10.3762/bjnano.9.150

• polystyrene nanoparticles) are self-assembled onto a substrate to form a 2D crystal used as a lithographic (positive or negative) mask. The size, shape and interspacing can be controlled on the nanoscale by changing the particle diameter as well as the conditions of film deposition. Indeed, the colloidal

Al₂O₃/TiO₂ inverse opals from electrosprayed self-assembled templates

• Arnau Coll,
• Sandra Bermejo,
• David Hernández and
• Luís Castañer

Beilstein J. Nanotechnol. 2018, 9, 216–223, doi:10.3762/bjnano.9.23

• fabrication process of the Al2O3/TiO2 inverse opals is schematically outlined in Figure 1 where the starting step can be seen in Figure 1a and consists of the electrospray deposition of the template layer of ordered polystyrene nanoparticles. Only a side view of one row of four nanoparticles is shown for

• layers of 360 nm polystyrene nanoparticles can be seen. The layer is almost free of defects besides some missing beads that can be identified in the top surface. A focused ion beam (FIB) drill in two orthogonal vertical planes confirms that the order is fully three-dimensional. The total thickness of the

• easily conformally deposited in thin layers of a few nanometers thick and has the advantage that the deposition temperature is compatible with the maximum temperature that the polystyrene nanoparticles can withstand (<100 °C). The ALD process uses trimethylaluminum (TMA) as the precursor gas. The

Synthesis and characterization of noble metal–titania core–shell nanostructures with tunable shell thickness

• Bartosz Bartosewicz,
• Marta Michalska-Domańska,
• Malwina Liszewska,
• Dariusz Zasada and
• Bartłomiej J. Jankiewicz

Beilstein J. Nanotechnol. 2017, 8, 2083–2093, doi:10.3762/bjnano.8.208

• calibration measurement was carried out after measurement of each sample (with the same conditions) using carboxylated polystyrene nanoparticles (100 nm or 200 nm) supplied by the manufacturer. The statistical data for the particle size distribution, including mean particle diameter, mode particle diameter

Low uptake of silica nanoparticles in Caco-2 intestinal epithelial barriers

• Dong Ye,
• Mattia Bramini,
• Delyan R. Hristov,
• Sha Wan,
• Anna Salvati,
• Christoffer Åberg and
• Kenneth A. Dawson

Beilstein J. Nanotechnol. 2017, 8, 1396–1406, doi:10.3762/bjnano.8.141

• transport across it. The low degree of internalisation is particularly striking in comparison to our previous observations of a substantial uptake of silica nanoparticles into (single) lung cells [37]. Moreover, we have previously found sizable uptake of silica and polystyrene nanoparticles into another

Miniemulsion copolymerization of (meth)acrylates in the presence of functionalized multiwalled carbon nanotubes for reinforced coating applications

• Bertha T. Pérez-Martínez,
• Lorena Farías-Cepeda,
• Víctor M. Ovando-Medina,
• José M. Asua,
• Lucero Rosales-Marines and
• Radmila Tomovska

Beilstein J. Nanotechnol. 2017, 8, 1328–1337, doi:10.3762/bjnano.8.134

• period and does not require massive diffusion of the components of the formulation through the aqueous phase. Ham et al. [32][33] used a so-called miniemulsion process in an attempt to cover SWCNTs with polystyrene nanoparticles, where n-pentanol was used as a hydrophobe to minimize Ostwald ripening

Tight junction between endothelial cells: the interaction between nanoparticles and blood vessels

• Yue Zhang and
• Wan-Xi Yang

Beilstein J. Nanotechnol. 2016, 7, 675–684, doi:10.3762/bjnano.7.60

• exposure to NPs (polystyrene nanoparticles, quantum dots, single-wall carbon nanotubes) results in the disruption of the alveolar epithelial barrier, the extent of which also depends on the composition, shape and surface charge of the NPs [31]. Carbon nanotubes also show their capacity to penetrate the

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

• functionalized polystyrene nanoparticles as described in [18]) or by a combination of miniemulsion and emulsion/solvent evaporation techniques (PLLA nanoparticles without and with magnetite, as described in [19][20]). In all cases, SDS was used as a surfactant for the synthesis or formation of the nanoparticles

• differentiation studies, cellular uptake and cytotoxicity of the particles were quantitatively determined by flow cytometry. After incubation with 300 µg/mL nanoparticles for 24 h, hMSCs showed a reasonable uptake of polystyrene nanoparticles (PS, Figure 1A). Since here only one population was detected in flow

• reasonable uptake of the polystyrene nanoparticles after incubation with 300 µg/mL nanoparticles for 24 h and an even greater uptake for the PLLA particles. All four particles showed a double population in the fluorescence histogram for hHSCs, pointing to the possibility that there are still several subsets

Comparative evaluation of the impact on endothelial cells induced by different nanoparticle structures and functionalization

• Lisa Landgraf,
• Ines Müller,
• Peter Ernst,
• Miriam Schäfer,
• Christina Rosman,
• Isabel Schick,
• Oskar Köhler,
• Hartmut Oehring,
• Vladimir V. Breus,
• Thomas Basché,
• Carsten Sönnichsen,
• Wolfgang Tremel and
• Ingrid Hilger

Beilstein J. Nanotechnol. 2015, 6, 300–312, doi:10.3762/bjnano.6.28

• internalization of Au@Fe3O4, Au@MnO and Fe3O4 particles (Figure 6). Caveolae-mediated uptake was blocked by the use of genistein, which was effectively demonstrated for anionic polystyrene nanoparticles in Hela cells [55]. Contrarily, Fernando et al. observed no changes for the internalization route of polymer

• to be a cell-type-specific process [61][62][63]. In this context, the mouse macrophages cell line J774A.1 used macropinocytosis and clathrin-mediated endocytosis for the uptake of 40 nm sized polystyrene nanoparticles, depending on the lack of caveolin-1 expression in this cell line. In contrast, the

Caveolin-1 and CDC42 mediated endocytosis of silica-coated iron oxide nanoparticles in HeLa cells

• Nils Bohmer and
• Andreas Jordan

Beilstein J. Nanotechnol. 2015, 6, 167–176, doi:10.3762/bjnano.6.16

• human alveolar epithelial cells and polystyrene nanoparticles around 100 nm [38] as well as polymer coated gold nanoparticles with a core size around 13 nm [39]. On the other hand there are studies showing the uptake of different nanoparticles by HeLa cells such as quantum dots [35], PEG-PLA particles

Functionalized polystyrene nanoparticles as a platform for studying bio–nano interactions

• Cornelia Loos,
• Tatiana Syrovets,
• Anna Musyanovych,
• Volker Mailänder,
• Katharina Landfester,
• G. Ulrich Nienhaus and
• Thomas Simmet

Beilstein J. Nanotechnol. 2014, 5, 2403–2412, doi:10.3762/bjnano.5.250

• biodistribution. Polystyrene does not degrade in the cellular environment and exhibits no short-term cytotoxicity. Because polystyrene nanoparticles can be easily synthesized in a wide range of sizes with distinct surface functionalizations, they are perfectly suited as model particles to study the effects of the

• particle surface characteristics on various biological parameters. Therefore, we have exploited polystyrene nanoparticles as a convenient platform to study bio–nano interactions. This review summarizes studies on positively and negatively charged polystyrene nanoparticles and compares them with clinically

• used superparamagnetic iron oxide nanoparticles. Keywords: amino groups; apoptosis; carboxyl groups; cell proliferation; leukemia cell lines; macrophages; mTOR; polystyrene nanoparticles; Review Applications of polystyrene Polystyrene, one of the most extensively used types of plastic [1], is an

Effect of silver nanoparticles on human mesenchymal stem cell differentiation

• Christina Sengstock,
• Jörg Diendorf,
• Matthias Epple,
• Thomas A. Schildhauer and
• Manfred Köller

Beilstein J. Nanotechnol. 2014, 5, 2058–2069, doi:10.3762/bjnano.5.214

• aggrecan release demonstrated no differences compared with cells cultured without silver. Similar results were obtained by Tautzenberger et al., who demonstrated that the chondrogenic differentiation of hMSCs was not influenced in the presence of polystyrene nanoparticles [31]. A major difficulty when

Different endocytotic uptake mechanisms for nanoparticles in epithelial cells and macrophages

• Dagmar A. Kuhn,
• Dimitri Vanhecke,
• Benjamin Michen,
• Fabian Blank,
• Peter Gehr,
• Alke Petri-Fink and
• Barbara Rothen-Rutishauser

Beilstein J. Nanotechnol. 2014, 5, 1625–1636, doi:10.3762/bjnano.5.174

• caveolin-1. A549 cells expressed clathrin heavy chain and caveolin-1, but no flotillin-1 uptake-related proteins. Our data revealed an impeded uptake of 40 nm polystyrene nanoparticles by J774A.1 macrophages when actin polymerization and clathrin-coated pit formation was blocked. From this result, it is

• of clathrin-coated vesicles (preventing clathrin-mediated endocytosis). Our data showed that a combination of several distinguishable endocytotic uptake mechanisms are involved in the uptake of 40 nm polystyrene nanoparticles in both the macrophage and epithelial cell line. Keywords: cell lines

Sub-10 nm colloidal lithography for circuit-integrated spin-photo-electronic devices

• Adrian Iovan,
• Marco Fischer,
• Roberto Lo Conte and
• Vladislav Korenivski

Beilstein J. Nanotechnol. 2012, 3, 884–892, doi:10.3762/bjnano.3.98

• -assembled monolayer of polystyrene nanoparticles, reduced in size by an isotropic etching process [20], which we scale to sub-10 nm feature sizes with large-area coverage in a well-defined hexagonal lattice and full integration for electrical circuit biasing and read out. We demonstrate the fabrication

• technique using spin-torque and spin-flip photoemission material combinations, considered promising for gigahertz oscillators and terahertz lasers. Results and Discussion Self-assembled monolayer of nanoparticles The most widely used colloidal lithography medium is polystyrene nanoparticles in aqueous

• particles. (c) A reinforcing layer of aluminum is deposited to serve as a hard mask. (d) A lift-off of the particles by etching completes the fabrication of the nanomask. Polystyrene nanoparticles monolayer after plasma-ICP etching for (a) 165, (b) 180, and (c) 195 seconds. (d) AFM height profiles of the