Supramolecular hydration structure of graphene-based hydrogels: density functional theory, green chemistry and interface application

• Hon Nhien Le,
• Duy Khanh Nguyen,
• Minh Triet Dang,
• Huyen Trinh Nguyen,
• Thi Bang Tam Dao,
• Trung Do Nguyen,
• Chi Nhan Ha Thuc and
• Van Hieu Le

Beilstein J. Nanotechnol. 2025, 16, 806–822, doi:10.3762/bjnano.16.61

• dispersibility and reduced surface area of graphene-based materials in many applications, such as aqueous dispersions, polymer nanocomposites, and water-based paints. Our previous works demonstrated that in graphene-based hydrogel structures, the intercalation of water molecules between graphene-based sheets

• exhibits the aqueous dispersions derived from the sonication of GO-SG-ZH hydrogel and powder in water (see Supporting Information File 1, Figure S3). Ultrasound waves vibrated water molecules and created cavitation in the hydrogel structure, leading to the exfoliation of graphene-based nanosheets in water

• . It is notable that low concentrations (≤50 ppm) are necessary to obtain homogenous dispersions. The ultrasonic dispersion of GO-SG-ZH hydrogels was faster and clearer due to the high content of water intercalation. The GO-SG-ZH powder contained about 10% of water and approximate 60% of nanosilica and

Efficiency of single-pulse laser fragmentation of organic nutraceutical dispersions in a circular jet flow-through reactor

• Tina Friedenauer,
• Maximilian Spellauge,
• Alexander Sommereyns,
• Verena Labenski,
• Tuba Esatbeyoglu,
• Christoph Rehbock,
• Heinz P. Huber and
• Stephan Barcikowski

Beilstein J. Nanotechnol. 2025, 16, 711–727, doi:10.3762/bjnano.16.55

• ), and laser melting (LML) in liquids are aimed at synthesizing nanoparticles (NPs) from bulk targets (LAL), by downsizing (LFL), or by increasing/reshaping (LML) particle dispersions [1]. On the other hand, pulsed laser defect engineering in liquids (PUDEL) processes involve targeted post-treatment of

• stirrers containing the NP or microparticle (MP) dispersions, which are irradiated with a laser beam. However, as dispersion volumes in batch setups are only partially illuminated and there is constant back-diffusion, no uniform fluence and number of pulses-per-particle can be guaranteed. This prohibits

• enhancement in the colloidally stable supernatants of particle dispersions after sedimentation of the colloidally unstable, unfragmented MP educts, determined by UV–vis extinction spectroscopy, which is proportional to the amount of SMPs and NPs [2][22][49]. This extinction enhancement from the unirradiated

Colloidal few layered graphene–tannic acid preserves the biocompatibility of periodontal ligament cells

• Teissir Ben Ammar,
• Naji Kharouf,
• Dominique Vautier,
• Housseinou Ba,
• Nivedita Sudheer,
• Philippe Lavalle and
• Vincent Ball

Beilstein J. Nanotechnol. 2025, 16, 664–677, doi:10.3762/bjnano.16.51

• reaggregation of exfoliated graphene layers [11]. Various surfactants have been employed. For instance, sodium dodecylbenzene sulfonate and sodium cholate have been reported to be able to produce stable graphene colloidal dispersions [13]. However, these synthetic surfactants often raise concerns about toxicity

Aprepitant-loaded solid lipid nanoparticles: a novel approach to enhance oral bioavailability

• Mazhar Hussain,
• Muhammad Farooq,
• Muhammad Asad Saeed,
• Muhammad Ijaz,
• Sherjeel Adnan,
• Zeeshan Masood,
• Muhammad Waqas,
• Wafa Ishaq and
• Nabeela Ameer

Beilstein J. Nanotechnol. 2025, 16, 652–663, doi:10.3762/bjnano.16.50

• encapsulation efficiency The drug content of SLNs formulations ranged from 16.95% ± 0.76% to 96.75% ± 0.24%; the highest APT content was obtained in APT-CD-NP4. The loss of the drug can be attributed to the lyophilization. However, there was no change in color or aggregation observed. Dispersions of lyophilized

• dispersion. SEM studies Scanning electron micrographs of APT-CD-NP4 and APT-PX-NP8 shown in Figure 3 illustrate that polymeric content was deposited on the SLN surface because of organic solvents. After evaporation of the organic solvent, colloidal particles are closely packed. Dispersions in organic

A formulation containing Cymbopogon flexuosus essential oil: improvement of biochemical parameters and oxidative stress in diabetic rats

• Ailton Santos Sena-Júnior,
• Cleverton Nascimento Santana Andrade,
• Pedro Henrique Macedo Moura,
• Jocsã Hémany Cândido dos Santos,
• Cauãn Torres Trancoso,
• Eloia Emanuelly Dias Silva,
• Deise Maria Rego Rodrigues Silva,
• Ênio Pereira Telles,
• Luiz André Santos Silva,
• Isabella Lima Dantas Teles,
• Sara Fernanda Mota de Almeida,
• Daniel Alves de Souza,
• Jileno Ferreira Santos,
• Felipe José Aidar Martins,
• Ana Mara de Oliveira e Silva,
• Sandra Lauton-Santos,
• Guilherme Rodolfo Souza de Araujo,
• Cristiane Bani Correa,
• Rogéria De Souza Nunes,
• Lysandro Pinto Borges and
• Ana Amélia Moreira Lira

Beilstein J. Nanotechnol. 2025, 16, 617–636, doi:10.3762/bjnano.16.48

• containing 10% EOCF were then prepared individually (Table 1), and the dispersions were evaluated macroscopically and characterized 48 h after they were obtained. Physicochemical characterization of the selected microemulsions The polydispersity index and average hydrodynamic radius of the droplets were

Engineered PEG–PCL nanoparticles enable sensitive and selective detection of sodium dodecyl sulfate: a qualitative and quantitative analysis

• Soni Prajapati and
• Ranjana Singh

Beilstein J. Nanotechnol. 2025, 16, 385–396, doi:10.3762/bjnano.16.29

• negative surface charge. The zeta potential is a critical parameter for evaluating the stability of colloidal dispersions; typically, values greater than ±30 mV are associated with high stability due to strong electrostatic repulsion between particles [31]. Despite the zeta potential being less than ±30 mV

Radiosensitizing properties of dual-functionalized carbon nanostructures loaded with temozolomide

• Radmila Milenkovska,
• Nikola Geskovski,
• Dushko Shalabalija,
• Ljubica Mihailova,
• Petre Makreski,
• Dushko Lukarski,
• Igor Stojkovski,
• Maja Simonoska Crcarevska and
• Kristina Mladenovska

Beilstein J. Nanotechnol. 2025, 16, 229–251, doi:10.3762/bjnano.16.18

Characterization of ZnO nanoparticles synthesized using probiotic Lactiplantibacillus plantarum GP258

• Prashantkumar Siddappa Chakra,
• Aishwarya Banakar,
• Shriram Narayan Puranik,
• Vishwas Kaveeshwar,
• C. R. Ravikumar and
• Devaraja Gayathri

Beilstein J. Nanotechnol. 2025, 16, 78–89, doi:10.3762/bjnano.16.8

• Horiba Scientific instrument from Japan. ZnO NP dispersions were prepared at a concentration of 1 mg/mL in deionized water and analyzed at 25 °C. Each sample was analyzed in triplicate, with the Zeta potential results expressed as the mean ± standard deviation (SD) and the zeta average calculated to

A nanocarrier containing carboxylic and histamine groups with dual action: acetylcholine hydrolysis and antidote atropine delivery

• Elina E. Mansurova,
• Andrey A. Maslennikov,
• Anna P. Lyubina,
• Alexandra D. Voloshina,
• Irek R. Nizameev,
• Marsil K. Kadirov,
• Anzhela A. Mikhailova,
• Polina V. Mikshina,
• Albina Y. Ziganshina and
• Igor S. Antipin

Beilstein J. Nanotechnol. 2025, 16, 11–24, doi:10.3762/bjnano.16.2

• cells were grown in a CO2 incubator at 37 °C after being seeded on a 96-well Eppendorf plate at a concentration of 100,000 cells/mL per well in 150 μL of medium. After 24 h of incubation, 150 μL of the tested dispersions were added to each well. Twofold dilutions of the dispersions were prepared

The round-robin approach applied to nanoinformatics: consensus prediction of nanomaterials zeta potential

• Dimitra-Danai Varsou,
• Arkaprava Banerjee,
• Joyita Roy,
• Kunal Roy,
• Giannis Savvas,
• Haralambos Sarimveis,
• Ewelina Wyrzykowska,
• Mateusz Balicki,
• Tomasz Puzyn,
• Georgia Melagraki,
• Iseult Lynch and
• Antreas Afantitis

Beilstein J. Nanotechnol. 2024, 15, 1536–1553, doi:10.3762/bjnano.15.121

• the ZP values of particles (expressing their electrostatic repulsion) controls the stability of colloidal dispersions according to the Derjaguin–Landau–Verwey–Overbeek (DLVO) theory [39]. For the computational analysis, the TIP3P force field was employed for water, while the DREIDING force field was

Interaction of graphene oxide with tannic acid: computational modeling and toxicity mitigation in C. elegans

• Romana Petry,
• James M. de Almeida,
• Francine Côa,
• Felipe Crasto de Lima,
• Diego Stéfani T. Martinez and
• Adalberto Fazzio

Beilstein J. Nanotechnol. 2024, 15, 1297–1311, doi:10.3762/bjnano.15.105

• assess nanomaterials toxicity is to evaluate their colloidal characteristics. GO stock dispersions (400 mg·L−1) were prepared according to OECD Guideline no. 318 [71]. The GO powder (10 mg) was pre-wetted with 1 mL of ultrapure water and left as a wet-paste for 24 h. Then, ultrapure water (25 mL) was

• medium. Furthermore, negative controls were carried out using ultrapure water as the test substance because the GO stock dispersions were prepared in this medium. The nematodes were exposed for 24 h, and live organisms were counted using a stereomicroscope at the end. To evaluate the effect of tannic

Dual-functionalized architecture enables stable and tumor cell-specific SiO₂NPs in complex biological fluids

• Iris Renata Sousa Ribeiro,
• Raquel Frenedoso da Silva,
• Romênia Ramos Domingues,
• Adriana Franco Paes Leme and
• Mateus Borba Cardoso

Beilstein J. Nanotechnol. 2024, 15, 1238–1252, doi:10.3762/bjnano.15.100

• strategies to produce colloidally stable NP dispersions with retained targeting capacity have been widely investigated [17][18][19][20][21]. While a panel of molecules (e.g., polyethylene glycol, zwitterionics, glycans, aptamers) can improve the stability of NPs in biological media by preventing the

• were made in triplicates at room temperature. The 1H NMR spectra were obtained in Bruker spectrometers operating at frequencies of 500 MHz. The NP dispersions (25 mg) were centrifuged and concentrated to 600 μL of D2O with the standard TMSP. The samples were sonicated before measurements. Chemical

• shifts (δ) were related in part per million (ppm) to the standard TMSP. The signal referring to the solvent used, deuterated water, was omitted from the spectra. The elemental analysis measurements were performed on a CHN 2400 Elementary Analyzer (Perkin-Elmer). The NP dispersions were dried in an oven

Exploring surface charge dynamics: implications for AFM height measurements in 2D materials

• Mario Navarro-Rodriguez,
• Andres M. Somoza and
• Elisa Palacios-Lidon

Beilstein J. Nanotechnol. 2024, 15, 767–780, doi:10.3762/bjnano.15.64

• equations for the system, including the presence of the tip, which we have subsequently particularized for 2D materials on insulating supports. Experimental Co-deposited samples of GO and rGO were prepared following the methodology outlined in [61]. In summary, ultradiluted (4 × 10−4 wt %) dispersions of GO

• and/or rGO in Milli-Q type-I water (MQ water) were utilized. A drop of these dispersions was cast onto highly doped p-type silicon (1–10 Ω·cm, Siltronix) with a 300 nm SiO2 layer thermally grown on top. Before deposition, the substrate underwent a thorough cleaning process, which involved rinsing with

Comparative electron microscopy particle sizing of TiO₂ pigments: sample preparation and measurement

• Ralf Theissmann,
• Christopher Drury,
• Markus Rohe,
• Thomas Koch,
• Jochen Winkler and
• Petr Pikal

Beilstein J. Nanotechnol. 2024, 15, 317–332, doi:10.3762/bjnano.15.29

• . As expected, some agglomerates and aggregates persist even after thorough dispersion. In both distributions in Figure 2, the number of particles above 500 nm is low. This is surprising as large agglomerates above 600 nm are typical for hand-shaken dispersions but are not detected here by spICP-MS

• dispersions in a gravitational field. In all cases, the median ECD calculated from the spICP-MS particle size distributions is larger than the corresponding ECD-related results of the electron microscopy measurements, which are, in turn, larger than the MinFeret-related results of the electron microscopy

Development and characterization of potential larvicidal nanoemulsions against Aedes aegypti

• Jonatas L. Duarte,
• Leonardo Delello Di Filippo,
• Anna Eliza Maciel de Faria Mota Oliveira,
• Rafael Miguel Sábio,
• Gabriel Davi Marena,
• Tais Maria Bauab,
• Cristiane Duque,
• Vincent Corbel and
• Marlus Chorilli

Beilstein J. Nanotechnol. 2024, 15, 104–114, doi:10.3762/bjnano.15.10

• volatility, make their formulation a true challenge. In this regard, nanoemulsions (NEs), which are dispersions of two immiscible liquids with one of them dispersed as small droplets [11][12], stand out as new delivery vehicles for these bioactive compounds. They are especially important to enhance the water

• nanoemulsion comprising 5% p-cymene stabilized with 1% Tween 80, with droplet sizes measuring approximately 150 nm, which maintained its stability for 60 days [31]. The zeta potential is used to predict the stability of dispersions, and its value depends on the physicochemical properties of active ingredients

Carboxylic acids and light interact to affect nanoceria stability and dissolution in acidic aqueous environments

• Matthew L. Hancock,
• Eric A. Grulke and
• Robert A. Yokel

Beilstein J. Nanotechnol. 2023, 14, 762–780, doi:10.3762/bjnano.14.63

• during its synthesis; in fact, a carboxylic acid, namely citric acid, is used in many synthesis protocols. Citric acid adsorbs onto nanoceria surfaces, limiting particle formation and creating stable dispersions with extended shelf life. To better understand factors influencing the fate of nanoceria, its

• absorption edge in the UVA region [43]. Studying the effects of UV irradiation on nanoceria would be informative for environmental applications. In biological systems, colloidal nanoceria dispersions were found to be non-toxic to fibroblasts and were capable of preventing damage from UV irradiation [44

• carboxylic acid dispersions Color change In the presence of light, the majority of the nanoceria dispersions changed color from light yellow to colorless (attributed to Ce4+ reduction to Ce3+) [47]. Nanoceria stored in the dark did not change color and remained light yellow. Dynamic light scattering (DLS

Nanoarchitectonics to entrap living cells in silica-based systems: encapsulations with yolk–shell and sepiolite nanomaterials

• Celia Martín-Morales,
• Jorge Fernández-Méndez,
• Pilar Aranda and
• Eduardo Ruiz-Hitzky

Beilstein J. Nanotechnol. 2023, 14, 522–534, doi:10.3762/bjnano.14.43

• cyanobacteria and yeast cells. On the one hand, sepiolite clay mineral was used for the immobilization of these microorganisms taking into account that this natural microfibrous Mg silicate presents a wide range of porosity, the ability to generate very viscous stable dispersions, and the capability to form

On the use of Raman spectroscopy to characterize mass-produced graphene nanoplatelets

• Keith R. Paton,
• Konstantinos Despotelis,
• Naresh Kumar,
• Piers Turner and
• Andrew J. Pollard

Beilstein J. Nanotechnol. 2023, 14, 509–521, doi:10.3762/bjnano.14.42

• dispersions were then mixed to obtain graphite mass fractions as given in Table 1. To prepare the mixed GNPref/sediment samples, a fresh GNPref sample was prepared by sonication as described above. After the initial centrifugation step at 250g, however, the sediment was retained and redispersed in fresh NMP

Polymer nanoparticles from low-energy nanoemulsions for biomedical applications

• Santiago Grijalvo and
• Carlos Rodriguez-Abreu

Beilstein J. Nanotechnol. 2023, 14, 339–350, doi:10.3762/bjnano.14.29

• encapsulated in PLGA nanoparticles derived from PIC nanoemulsions [63]. These antioxidant-loaded nanoparticles feature hydrodynamic sizes between 71 and 160 nm and encapsulation efficiencies higher than 64%. The colloidal stability of the nanoparticle dispersions was not significantly affected by protein

• . Calderó; R. Montes; M. Llinàs; M. J. García-Celma; M. Porras; C. Solans, “Studies on the formation of polymeric nanoemulsions obtained via low-energy emulsification and their use as templates for drug delivery nanoparticle dispersions”, pages 922-931, Copyright (2016), with permission from Elsevier. This

Solvent-induced assembly of mono- and divalent silica nanoparticles

• Bin Liu,
• Etienne Duguet and
• Serge Ravaine

Beilstein J. Nanotechnol. 2023, 14, 52–60, doi:10.3762/bjnano.14.6

• dispersions was adjusted to 1.08 × 1015 part/L and the solution was stored at 4 °C. Assembly of one-patch silica nanoparticles The incubation of the nanoparticles was carried out in 15 mL tubes under rolling motion at 60 rpm at room temperature. A calculated volume of ethanol, water, or salty water (20 mM of

• open air at room temperature and the grids were placed in a box protected from dust. Statistics from image analysis were performed over at least 300 multipods or 200 chains. The ζ potential value of 1-PSN aqueous dispersions (pH ≈5.7) was measured using the Malvern Zetasizer 3000 HS setup (Malvern

Two-step single-reactor synthesis of oleic acid- or undecylenic acid-stabilized magnetic nanoparticles by thermal decomposition

• Mykhailo Nahorniak,
• Pamela Pasetto,
• Jean-Marc Greneche,
• Volodymyr Samaryk,
• Sandy Auguste,
• Anthony Rousseau,
• Nataliya Nosova and
• Serhii Varvarenko

Beilstein J. Nanotechnol. 2023, 14, 11–22, doi:10.3762/bjnano.14.2

• undecylenic (UA) acids, which are both used as a reagent and as a nanoparticle stabilizer, as well as the influence of their ratio to Fe(III) acetylacetonate on the properties of particles were investigated. Stable dispersions of NPM were obtained in 1-octadecene within the OA or UA ratio from 3.3 mol to 1

• mol of acetylacetonate and up to 5.5 mol/mol. Below the mentioned limit, NPM dispersions were colloidally unstable, and at higher ratios no NPM were formed which could be precipitated by an applied magnetic field. Monodisperse nanoparticles of iron oxides were synthesized with a diameter of 8–13 nm

• followed by their thermolysis in solution. This work aims to develop the synthesis of NPM dispersions by thermolysis of Fe(III) oleate or Fe(III) undecylate in a high-boiling-point solvent. Iron oxide nanoparticle dispersions were obtained via two-stage single-reactor synthesis with Fe(III) acetylacetonate

Single-step extraction of small-diameter single-walled carbon nanotubes in the presence of riboflavin

• Polina M. Kalachikova,
• Anastasia E. Goldt,
• Eldar M. Khabushev,
• Timofei V. Eremin,
• Timofei S. Zatsepin,
• Elena D. Obraztsova,
• Konstantin V. Larionov,
• Liubov Yu. Antipina,
• Pavel B. Sorokin and
• Albert G. Nasibulin

Beilstein J. Nanotechnol. 2022, 13, 1564–1571, doi:10.3762/bjnano.13.130

• facilitate chirality separation. Conventional surfactants such as sodium dodecyl sulfate (SDS) and sodium deoxycholate (DOC), as well as polyethylene glycol-based compositions, are used to obtain high-quality dispersions of individual SWCNTs [3][4][5][10]. Although given surfactants show exemplary

• biocompatibility of nucleic acids can support biomedical applications of such dispersions. Unfortunately, an extensive ultrasonic treatment required to obtain a dispersion of individual nanotubes might destroy fragile nucleic acid molecules so that their applications are somewhat inhibited. Flavin compounds are

• isoalloxazine rings and a sidewall of SWCNTs [17][18]. Flavin derivatives compounds are known to extract specific (n,m) SWCNTs from dispersions in organic solvents [19][20]. Moreover, flavin mononucleotide phosphate could be used as a stabilizer for graphene aqueous dispersions [21]. Although proven to

Orally administered docetaxel-loaded chitosan-decorated cationic PLGA nanoparticles for intestinal tumors: formulation, comprehensive in vitro characterization, and release kinetics

• Sedat Ünal,
• Osman Doğan and
• Yeşim Aktaş

Beilstein J. Nanotechnol. 2022, 13, 1393–1407, doi:10.3762/bjnano.13.115

• nanoparticle aqueous dispersion and the mucin. For this purpose, 40 mg mucin powder was dispersed in 50 mL ultrapure water and stirred for 12 h. Then, by centrifugation at 8000 rpm for 15 min, excess mucin was removed and the mucin solution was obtained. Mucin solution and nanoparticle dispersions were mixed

• at a ratio of 1:4 (mucin solution/nanoparticle dispersion, v/v) and vortexed for 90 s. Mucin–nanoparticle mixtures and aqueous dispersions of nanoparticles were incubated at 37 °C and turbidimetric measurements were conducted at 650 nm at predetermined time points (0, 30, 60, and 120 min

Efficient liquid exfoliation of KP₁₅ nanowires aided by Hansen's empirical theory

• Zhaoxuan Huang,
• Zhikang Jiang,
• Nan Tian,
• Disheng Yao,
• Fei Long,
• Yanhan Yang and
• Danmin Liu

Beilstein J. Nanotechnol. 2022, 13, 788–795, doi:10.3762/bjnano.13.69

• KP15 dispersions. The Lambert–Beer law (Equation 3) was then used to measure the concentration of the KP15 dispersions: where A is the absorbance, K is the absorption coefficient of the material, b is the absorbing layer thickness (which in this work is the width of the cuvette, i.e., 1 cm), and C is

• the concentration of the KP15 dispersions. The absorbance A and the absorption coefficient K are related to the wavelength of the incident light. To determine A and K, it is necessary to choose a specific incident wavelength. The bandgap of bulk KP15 is approx. 1.75 eV [20]. However, according to our

• influence of the surface state, a wavelength (800 nm) which is far away from the bandgap of KP15 bulk and surface state in the KP15 nanowires was chosen. Some dispersions for which we predetermined the concentration were prepared to fit and determine the absorption coefficient K. Solutions of five different

Reliable fabrication of transparent conducting films by cascade centrifugation and Langmuir–Blodgett deposition of electrochemically exfoliated graphene

• Teodora Vićentić,
• Stevan Andrić,
• Vladimir Rajić and
• Marko Spasenović

Beilstein J. Nanotechnol. 2022, 13, 666–674, doi:10.3762/bjnano.13.58

• et al. that controlled centrifugation can be used for the selection of liquid-phase exfoliated graphene dispersions with mean flake sizes in the range from 1 to 3.5 µm [29]. Since centrifugation is a much more facile process than exfoliation, and centrifuges are widely available, post-exfoliation

• electrochemically exfoliated graphene, nor have thin films made from dispersions following size selection through centrifugation been studied for their optoelectronic properties. Here, we present size selection through cascade centrifugation of commercially obtained electrochemically exfoliated graphene. We follow