Fluorescent bioinspired albumin/polydopamine nanoparticles and their interactions with Escherichia coli cells

• Eloïse Equy,
• Jordana Hirtzel,
• Sophie Hellé,
• Béatrice Heurtault,
• Eric Mathieu,
• Morgane Rabineau,
• Vincent Ball and
• Lydie Ploux

Beilstein J. Nanotechnol. 2023, 14, 1208–1224, doi:10.3762/bjnano.14.100

• FITC. These ratios are much higher than expected if only free dye molecules released from NPs had penetrated the cells (1% as estimated above). Hence, they prove that the fluorescence measured in cells was not emitted by free molecules of dye but by molecules bound to NPs. More specifically, the

Bismuth-based nanostructured photocatalysts for the remediation of antibiotics and organic dyes

• Akeem Adeyemi Oladipo and
• Faisal Suleiman Mustafa

Beilstein J. Nanotechnol. 2023, 14, 291–321, doi:10.3762/bjnano.14.26

• the chemical and biochemical oxygen demand and inhibits photosynthesis. Additionally, the uptake of dye molecules or their by-products in excess may be mutagenic, teratogenic, or carcinogenic [68][69]. Myocardial depression and hypertension are reportedly exacerbated by oral exposure to methylene blue

Green synthesis of zinc oxide nanoparticles toward highly efficient photocatalysis and antibacterial application

• Vo Thi Thu Nhu,
• Nguyen Duy Dat,
• Le-Minh Tam and
• Nguyen Hoang Phuong

Beilstein J. Nanotechnol. 2022, 13, 1108–1119, doi:10.3762/bjnano.13.94

• present in solution which can degraded dyes. These radicals can attract MO and MB molecules, oxidize the dye molecules to degradation products, and finally completely degrade the dyes to CO2 and H2O [35][36]. In addition, when ZnO NPs get in contact with E. coli, reactive oxygen species (ROS), such as •OH

Influence of thickness and morphology of MoS₂ on the performance of counter electrodes in dye-sensitized solar cells

• Lam Thuy Thi Mai,
• Hai Viet Le,
• Ngan Kim Thi Nguyen,
• Van La Tran Pham,
• Thu Anh Thi Nguyen,
• Nguyen Thanh Le Huynh and
• Hoang Thai Nguyen

Beilstein J. Nanotechnol. 2022, 13, 528–537, doi:10.3762/bjnano.13.44

• ) [6][7][8][9]. Since the reduction of I3− to I− on the CE plays a vital role in the regeneration of the oxidized dye molecules on the photoanode of the DSSCs, the electrocatalytic behavior of MoS2 CEs was further evaluated regarding the first redox couple (Ox1/Red1). Various parameters including anode

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

• protect UCNPs surfaces from dissolution. In contrast to a more complex polymeric coating, silica surfaces can be easily functionalized with a wide range of coupling agents and biomolecules, and the interior of the silica shell can be modified by integrating dye molecules, for example. However, amorphous

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

• factor that affects the photocatalytic activity of TiO2, is its adsorption capacity for dye molecules. The adsorption capacity of TiO2 can be readily improved by modifying its surface charge density or by increasing its surface area and pore volume [5][20][21]. Further, SiO2 is a good adsorptive material

• et al. [27] observed an improved photocatalytic degradation of rhodamine blue dye in the presence of rattle-type TiO2@void@SiO2 nanostructures. They attributed the improved photoactivity to the ease of dye molecules to access the TiO2 active sites through the void space between the core and the shell

• support for TiO2 creating a photocatalyst with improved photoactivity due to the presence of more active sites for the adsorption of the MV dye molecules. Additionally, from the diffuse reflectance UV–vis data, an optical bandgap of approximately 2.05 eV was obtained for mSiO2@NiPS while that of mSiO2

Electrokinetic characterization of synthetic protein nanoparticles

• Daniel F. Quevedo,
• Cody J. Lentz,
• Adriana Coll de Peña,
• Yazmin Hernandez,
• Nahal Habibi,
• Rikako Miki,
• Joerg Lahann and
• Blanca H. Lapizco-Encinas

Beilstein J. Nanotechnol. 2020, 11, 1556–1567, doi:10.3762/bjnano.11.138

• been reported in the literature in similar EK microdevices [57]. The absence of a difference in trapping voltage even in the presence of different fluorescent dyes shows that the dye molecules themselves have no evident effect on the EK behavior of the particles. Electrokinetic response of SPNPs

Effect of Ag loading position on the photocatalytic performance of TiO₂ nanocolumn arrays

• Jinghan Xu,
• Yanqi Liu and
• Yan Zhao

Beilstein J. Nanotechnol. 2020, 11, 717–728, doi:10.3762/bjnano.11.59

• the catalyst, so the catalyst needs to have a certain adsorption capacity for dye molecules. Due to the presence of oxygen vacancies, the surface of TiO2 is usually negatively charged and has a good adsorption capacity for cationic dye molecules [36]. Commonly used cationic dyes are rhodamine, methyl

Adsorptive removal of bulky dye molecules from water with mesoporous polyaniline-derived carbon

• Hyung Jun An,
• Jong Min Park,
• Nazmul Abedin Khan and
• Sung Hwa Jhung

Beilstein J. Nanotechnol. 2020, 11, 597–605, doi:10.3762/bjnano.11.47

• under different temperatures and applied for the purification of water contaminated with dye molecules of different sizes and charge by adsorption. With increasing pyrolysis temperature, it was found that the hydrophobicity, pore size and mesopore volume increased. A mesoporous PDC sample obtained via

• pyrolysis at 900 °C showed remarkable performance in the adsorption of dye molecules, irrespective of dye charge, especially in the removal of bulky dye molecules, such as acid red 1 (AR1) and Janus green B (JGB). For example, the most competitive PDC material showed a Q0 value (maximum adsorption capacity

• ) 8.1 times that of commercial, activated carbon for AR1. The remarkable adsorption of AR1 and JGB over KOH-900 could be explained by the combined mechanisms of hydrophobic, π–π, electrostatic and van der Waals interactions. Keywords: acid red 1; adsorption; bulky dye molecules; Janus green B

Synthesis and enhanced photocatalytic performance of 0D/2D CuO/tourmaline composite photocatalysts

• Changqiang Yu,
• Min Wen,
• Zhen Tong,
• Shuhua Li,
• Yanhong Yin,
• Xianbin Liu,
• Yesheng Li,
• Tongxiang Liang,
• Ziping Wu and
• Dionysios D. Dionysiou

Beilstein J. Nanotechnol. 2020, 11, 407–416, doi:10.3762/bjnano.11.31

• 0D/2D CuO structure and interfacial interaction between CuO and tourmaline. The initial solution pH affected the photocatalytic performance mainly via changing the adsorption of dye molecules onto photocatalysts (Figure 7a), as adsorption occurred firstly during the photodegradation reactions [42

Comparing a porphyrin- and a coumarin-based dye adsorbed on NiO(001)

• Sara Freund,
• Antoine Hinaut,
• Nathalie Marinakis,
• Edwin C. Constable,
• Ernst Meyer,
• Catherine E. Housecroft and
• Thilo Glatzel

Beilstein J. Nanotechnol. 2019, 10, 874–881, doi:10.3762/bjnano.10.88

• semiconductor TiO2 has become one of the most extensively studied metal oxides, especially in the context of scanning probe microscopy (SPM) [1]. The working principle of an n-type DSSC, which is shown in Figure 1a, relies on the functionalization of TiO2 surfaces with dye molecules enabling the absorption of

• light in the visible region of the sun spectrum. The photons are absorbed by the dye molecules leading to the excitation of an electron from the highest occupied molecular orbital (HOMO) to the lowest unoccupied molecular orbital (LUMO) of the dye and subsequent injection into the conduction band (CB

• ) of the semiconductor [2]. This charge transfer, which occurs from the dye molecules towards the surface of the semiconductor, offers the possibility of designing specific hybrid devices with photoactive anodes consisting of functionalized TiO2. In contrast to TiO2 [3][4][5][6][7][8][9][10][11], wide

Polydopamine-coated Au nanorods for targeted fluorescent cell imaging and photothermal therapy

• Boris N. Khlebtsov,
• Andrey M. Burov,
• Timofey E. Pylaev and
• Nikolai G. Khlebtsov

Beilstein J. Nanotechnol. 2019, 10, 794–803, doi:10.3762/bjnano.10.79

• loading of rhodamine 123 corresponds to the absorption peak of rhodamine 123 in solution, thus confirming the successful inclusion of dye molecules into the PDA shell via amine groups through a simple one-step procedure. The number of R123 molecules per composite particle can be estimated as follows

• . First, from the differential peak adsorption 0.035 and the calibration curve (Figure S2 in Supporting Information File 1), the molar concentration of bound dye molecules is 1.5 µM. Taking into account the estimated number concentration 1012 mL−1 of AuNRs (Section S1 in Supporting Information File 1), we

• obtain a loading efficiency of 103 R123 molecules per one composite AuNRs-PDA-R123-folate particle. This number is comparable with the typical estimations of the loading capacity for AuNRs coated with a mesoporous silica shell [45] (several thousands of dye molecules per particle). In our case, a smaller

Towards rare-earth-free white light-emitting diode devices based on the combination of dicyanomethylene and pyranine as organic dyes supported on zinc single-layered hydroxide

• Jeff L. Nyalosaso,
• Rachod Boonsin,
• Pierre Vialat,
• Damien Boyer,
• Geneviève Chadeyron,
• Rachid Mahiou and
• Fabrice Leroux

Beilstein J. Nanotechnol. 2019, 10, 760–770, doi:10.3762/bjnano.10.75

• before the measurement. Dye molecules used for the preparation of the organic phosphor film. (a) Normalized emission spectra of blue LED light and selected dyes in ethanol solution: DCM and HPTS and (b) their predicted combined spectrum. (a) SEM image, (b) XRD pattern and (c) TGA/DTA of zinc

Ceria/polymer nanocontainers for high-performance encapsulation of fluorophores

• Kartheek Katta,
• Dmitry Busko,
• Yuri Avlasevich,
• Katharina Landfester,
• Stanislav Baluschev and
• Rafael Muñoz-Espí

Beilstein J. Nanotechnol. 2019, 10, 522–530, doi:10.3762/bjnano.10.53

• ; singlet oxygen; Introduction Hybrid polymeric core–shell nanoparticles with encapsulated fluorescent dye molecules are frequently employed for life-science applications, such as cell labeling and drug delivery [1][2][3][4][5]. In recent years, polymeric hybrid nanoparticles and nanocapsules with tailored

• inorganic components on the surface have attracted great interest because of the possibility to tune size, composition, porosity, stability, surface functionality, and colloidal stability [6][7][8][9][10][11][12]. Generally, fluorescent dye molecules are sensitive to the external environment, which leads to

Low cost tips for tip-enhanced Raman spectroscopy fabricated by two-step electrochemical etching of 125 µm diameter gold wires

• Antonino Foti,
• Francesco Barreca,
• Enza Fazio,
• Cristiano D’Andrea,
• Paolo Matteini,
• Onofrio Maria Maragò and
• Pietro Giuseppe Gucciardi

Beilstein J. Nanotechnol. 2018, 9, 2718–2729, doi:10.3762/bjnano.9.254

• on the shaft (red line). Typical laser powers are 1.0–2.5 mW and integration times are 0.5–1.0 s per pixel. TERS spectra of dyes, pigments and biomolecules The tips have been applied to evaluate the spectra of analyze standard dye molecules such as rhodamine 6G (R6G), crystal violet (CV), methylene

The role of adatoms in chloride-activated colloidal silver nanoparticles for surface-enhanced Raman scattering enhancement

• Nicolae Leopold,
• Andrei Stefancu,
• Krisztian Herman,
• István Sz. Tódor,
• Stefania D. Iancu,
• Vlad Moisoiu and
• Loredana F. Leopold

Beilstein J. Nanotechnol. 2018, 9, 2236–2247, doi:10.3762/bjnano.9.208

• AgNP surface by mediating the chemisorption of Cl− ions. Hence, cationic dye molecules are electronically coupled to the silver surface at these SERS-active sites, leading to high-intensity SERS spectra. The appearance of the SERS effect only after the electronic coupling of the analyte to the Ag

• + cations for the generation of SERS-active sites on the nanoparticle surface [28][29]. When using the cit-AgNPs as a SERS substrate, no SERS spectra of the dye molecules could be obtained since the Lee–Meisel colloid does not contain any chloride ions that could form SERS-active sites. Small amounts of Cl

• +, Mg2+ or Ca2+ promote the chemisorption of Cl− ions, thereby generating SERS-active sites for cationic dye molecules. Thus, instead of adding additional Cl− ions, the SERS intensity of the analyte can be increased by adding cations such as Mg2+ or Ca2+, which promote the chemisorption of more Cl− onto

Dumbbell gold nanoparticle dimer antennas with advanced optical properties

• Janning F. Herrmann and
• Christiane Höppener

Beilstein J. Nanotechnol. 2018, 9, 2188–2197, doi:10.3762/bjnano.9.205

• typical in regard of the obtained signal strength and the noise floor. Clearly, for all measurements individual dye molecules are identified. However, the signal contrast strongly deviates for each measurement. Apparently, the best signal-to-noise level is achieved with the CB[8]-mediated dimer antenna

Closed polymer containers based on phenylboronic esters of resorcinarenes

• Tatiana Yu. Sergeeva,
• Rezeda K. Mukhitova,
• Irek R. Nizameev,
• Marsil K. Kadirov,
• Polina D. Klypina,
• Albina Y. Ziganshina and
• Alexander I. Konovalov

Beilstein J. Nanotechnol. 2018, 9, 1594–1601, doi:10.3762/bjnano.9.151

• , p(SRA-B) is decomposed at pH 3 and 44–47% of the dye molecules are released from the cavity into the solution. The dissociation of the capsule can also occur after the addition influence of glucose. When glucose is added to the aqueous solution of Fl@p(SRA-B), a slight increase in the fluorescence

Cr(VI) remediation from aqueous environment through modified-TiO₂-mediated photocatalytic reduction

• Rashmi Acharya,
• Brundabana Naik and
• Kulamani Parida

Beilstein J. Nanotechnol. 2018, 9, 1448–1470, doi:10.3762/bjnano.9.137

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

• well as FIB-drilled single pores is carried out. Subsequently, molecular filtering as a direct application of our nanoporous membranes is demonstrated: Successful size-selective separation of dye molecules and labeled proteins is observed by real-time fluorescence microscopy. Results and Discussion

Perovskite-structured CaTiO₃ coupled with g-C₃N₄ as a heterojunction photocatalyst for organic pollutant degradation

• Ashish Kumar,
• Christian Schuerings,
• Suneel Kumar,
• Ajay Kumar and
• Venkata Krishnan

Beilstein J. Nanotechnol. 2018, 9, 671–685, doi:10.3762/bjnano.9.62

• corresponding R2 values obtained from both kinetic models, it can be concluded that degradation of RhB follows the modified Freundlich model more appropriately. The removal of RhB from its aqueous solution is controlled by adsorption of the dye molecules on the photocatalyst surface followed by their successive

• degradation of adsorbed molecules (Figure S7, Supporting Information File 1). From Figure S7a, it can be seen that the difference in the absorbance of pure RhB solution and after attaining adsorption–desorption equilibrium is much less, which corresponds to about 6% adsorption of dye molecules on the surface

Anchoring of a dye precursor on NiO(001) studied by non-contact atomic force microscopy

• Sara Freund,
• Antoine Hinaut,
• Nathalie Marinakis,
• Edwin C. Constable,
• Ernst Meyer,
• Catherine E. Housecroft and
• Thilo Glatzel

Beilstein J. Nanotechnol. 2018, 9, 242–249, doi:10.3762/bjnano.9.26

• probe microscopy (SPM) [5]. Through the adsorption of a large variety of dye molecules, the ability of sensitized TiO2 to absorb light can be triggered and tuned. Thus, the possibility of designing photoactive devices with anodes consisting of nanostructured and functionalized TiO2 leads to numerous

• [18], but other promising materials have also been intensively researched [19][20][21]. However, for the application in p-DSSCs, NiO is the most extensively studied material [22][23][24]. A detailed understanding of the adsorption properties of dye molecules on NiO cathodes is therefore of crucial

• importance for the comprehension and design of improved and more efficient devices. NiO single-crystal surfaces functionalized with adsorbed dye molecules are ideal candidates to analyze the fundamental properties of such systems by SPM techniques. Because of the large band gap of NiO, which is reported to

Photobleaching of YOYO-1 in super-resolution single DNA fluorescence imaging

• Joseph R. Pyle and
• Jixin Chen

Beilstein J. Nanotechnol. 2017, 8, 2296–2306, doi:10.3762/bjnano.8.229

• ) has great potential to visualize fine DNA structures with nanometer resolution. In a typical PAINT video acquisition, dye molecules (YOYO-1) in solution sparsely bind to the target surfaces (DNA) whose locations can be mathematically determined by fitting their fluorescent point spread function. Many

• , photoswitching, or a combination thereof [34][37][38]. Dye photobleaching is one of the most utilized methods in PAINT fluorescently turn-off the dye molecules and is commonly used in most all types of fluorescent imaging [17][19][20][39][40]. Thus, carefully tuning the photobleaching rate is an important step

• (Figure 4b). Only well-separated single DNA molecules are chosen for the purpose of easy quantification. The DNA strands are prelabeled with YOYO-1 at a dye–DNA base pair ratio of 1:10. The average dye concentration in each DNA is calculated to be ≈300 dye molecules/μm for a given length of a DNA molecule

Carbon nano-onions as fluorescent on/off modulated nanoprobes for diagnostics

• Stefania Lettieri,
• Marta d’Amora,
• Adalberto Camisasca,
• Alberto Diaspro and
• Silvia Giordani

Beilstein J. Nanotechnol. 2017, 8, 1878–1888, doi:10.3762/bjnano.8.188

• functionalization of the CNOs. The high degree of surface functionalization of the oxi-CNOs and the successful attachment of the dye molecules on the oxi-CNOs was observed by TGA analysis. The TGA spectrum of the oxi-CNOs performed in air (Figure 3, blue) showed a decrease in decomposition temperature from 686 °C

• to 668 °C, with a weight loss of 7.70% compared to the p-CNOs. From the TGA weight loss at 450 °C, a total of 122 carboxylic groups per CNO were estimated. The functionalization of oxi-CNOs with the dye molecules causes a further weight loss of the fluo-CNOs of 3.2% compared to the oxi-CNOs, with a

• decomposition temperature of 639 °C. We estimate that around four dye molecules per CNO were present. A high-resolution TEM image of the p-CNOs is given in Supporting Information File 1, Figure S5. The Raman spectra of p-, oxi- and fluo-CNOs showed the D-band (1320 cm−1) and the G-band (1580 cm−1) typical for

Bright fluorescent silica-nanoparticle probes for high-resolution STED and confocal microscopy

• Isabella Tavernaro,
• Christian Cavelius,
• Henrike Peuschel and
• Annette Kraegeloh

Beilstein J. Nanotechnol. 2017, 8, 1283–1296, doi:10.3762/bjnano.8.130

• silica matrix, which is mostly based on non-polar aromatic or conjugated π-electron systems [33], is not easy to achieve due to the hydrophobic character of the organic dye molecules. Commonly, fluorescent silica nanoparticles are obtained by hydrolysis and condensation of a silica precursor via sol–gel

• significant influence of the dye embedding during the particle synthesis could be observed. Variation of the linker, the dye molecules and the dye concentration To study if either the charge of the used dye or the cysteic acid linker have an influence on the particle synthesis, we chose the neutral dye

• nanoparticles were performed. First of all, we studied the influence of the integration of the dyes into the silica matrix on the absorption and fluorescence signal. Comparison of the UV–vis absorption and fluorescence spectra of dye-doped silica nanoparticles and those of free dye molecules indicated no