PEG/PEI-functionalized single-walled carbon nanotubes as delivery carriers for doxorubicin: synthesis, characterization, and in vitro evaluation

• Shuoye Yang,
• Zhenwei Wang,
• Yahong Ping,
• Yuying Miao,
• Yongmei Xiao,
• Lingbo Qu,
• Lu Zhang,
• Yuansen Hu and
• Jinshui Wang

Beilstein J. Nanotechnol. 2020, 11, 1728–1741, doi:10.3762/bjnano.11.155

• ) and different DOX-loaded nanocarrier formulations for 12 h. (B) Fluorescence intensity of free DOX and different DOX-loaded nanocarrier formulations (n = 3). Student t-test was used for statistical analysis. (A) Confocal microscopy images of MCF-7 cells after treatment with free DOX (control) and

Hexagonal boron nitride: a review of the emerging material platform for single-photon sources and the spin–photon interface

• Stefania Castelletto,
• Faraz A. Inam,
• Shin-ichiro Sato and
• Alberto Boretti

Beilstein J. Nanotechnol. 2020, 11, 740–769, doi:10.3762/bjnano.11.61

• ]. This has prompted the investigation of SP confocal microscopy to observe SPEs from various h-BN types of materials from bulk to monolayers, however with similar unclear attributions. Despite the PL variability in h-BN, very recently, deep-level, atom-like luminescent defects in h-BN have been

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

• circles), PSSAg (blue squares) and silver nanoparticles (red squares) as a function of the pH value. TGA thermograms of sulfonated PSS (dashed line) and PSSAg nanobeads (solid line). Confocal microscopy images of P. aeruginosa cells in biofilms (A) without PSSAg nanobeads and (B) incubated with 0.5 µg/mL

• PSSAg. Green cells are viable, red cells are dead. Confocal microscopy images of S. aureus cells in biofilms incubated (A) without nanocomposite, (B) with 0.5 µg/mL PSSAg. Green cells are viable, red cells are dead. MIC and MBIC values of PSSAg were obtained at least three times independently; no

Luminescent gold nanoclusters for bioimaging applications

• Nonappa

Beilstein J. Nanotechnol. 2020, 11, 533–546, doi:10.3762/bjnano.11.42

• (d, e) electron tomography of the AuNCF superstructure. D) Photographs under ambient light (top) and UV light (bottom) with varying concentrations of SnCl2 added to Au-GSH NCs. E) Confocal microscopy images of NIH3T3 cell lines incubated with AuNCFs for 1 day (a) bright-field image, (b) confocal

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

• PE capsules by changing the open and closed state of the capsules. PAH/PMA microcapsules were successfully loaded with fluorescein isothiocyanate-bovine serum albumin (FITC-BSA) at pH < 4 [70]. Confocal microscopy was used to visualize the open and closed state of the capsules at pH 3 and 7

Brome mosaic virus-like particles as siRNA nanocarriers for biomedical purposes

• Alfredo Nuñez-Rivera,
• Pierrick G. J. Fournier,
• Danna L. Arellano,
• Ana G. Rodriguez-Hernandez,
• Rafael Vazquez-Duhalt and
• Ruben D. Cadena-Nava

Beilstein J. Nanotechnol. 2020, 11, 372–382, doi:10.3762/bjnano.11.28

• the breast cancer cells. Representative confocal microscopy images showed NanoOrange fluorescence inside the cells (Figure 1A). It is important to point out that the capsids are able to internalize efficiently into tumor cells without any functionalization. The cell internalization has been quantified

• possible detachment of NanoOrange from the capsids, FITC fluorophore was covalently conjugated to the capsid surface and analyzed by confocal microscopy (Figure 2 and Figure S1, Supporting Information File 1). The confocal images showed FITC fluorescence inside the cells without colocalization of the

• cytometry analysis showed a 70% virus internalization in the cells treated with both CCMV and BMV capsids (Figure 1B,C). In addition, confocal microscopy images showed that almost all the cells contained plant viruses with loaded NanoOrange or with covalently conjugated FITC (Figure 1A and Figure 2). The

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

• cells were stained with Hoechst 33258 and imaged with laser scanning confocal microscopy (Olympus FV1000, Tokyo, Japan). Gene expression analysis: VEGF gene silencing was determined using reverse transcriptase-polymerase chain reaction (RT-PCR, AG22331, Eppendorf, Germany). About 3 × 105 A549 cells were

• absence of free siRNA in the polyplex lanes treated with heparin shows the stability of the complex formed. (A) Intracellular uptake of the polyplex monitored by using laser scanning confocal microscopy after 4 h of treatment with Cy3-labeled anti-VEGF siRNA (emission wavelength = 568 nm) at a final siRNA

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

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

• data (Figure 8c) showed the movement of ions through the lipid–nanopore interface via the formation of a toroidal pore. The binding of porphyrin-tethered nanopores with giant unilamellar vesicles was analyzed by confocal microscopy (Figure 8d). The inherent fluorescent signal of porphyrin showed their

Internalization mechanisms of cell-penetrating peptides

• Ivana Ruseska and
• Andreas Zimmer

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

• observed using confocal microscopy [39][40]. It is assumed that the punctate staining indicates endocytic uptake, while the diffuse staining is correlated with direct translocation. The switch between different uptake mechanisms might be concentration-dependent. It has been shown that at low concentration

Small protein sequences can induce cellular uptake of complex nanohybrids

• Jan-Philip Merkl,
• Malak Safi,
• Christian Schmidtke,
• Fadi Aldeek,
• Johannes Ostermann,
• Tatiana Domitrovic,
• Sebastian Gärtner,
• John E. Johnson,
• Horst Weller and
• Hedi Mattoussi

Beilstein J. Nanotechnol. 2019, 10, 2477–2482, doi:10.3762/bjnano.10.238

• -γ loading of per nano-assembly, using confocal microscopy (Figure 1E). A close examination of the images allows us to distinguish three different colour distributions: the cell nuclei shown in blue (stained with DAPI), the endosomal compartments counterstained in red (labelled with Cy5-transferin

• cellular fate of these structures rather than appearance in solution. The confocal microscopy data were further exploited to generate a z-stack, to visualize the fluorescence distribution of the nanocomposites side-by-side with that of the Cy5 dye and cell nuclei. The 3D-stack, shown in Figure 2A, confirms

• and 14 His6-MBP-γ equiv/AuNP, scale bar = 50 µm. (E) Confocal microscopy images of HeLa cells incubated with nanohybrids for 1 h; c(QD) = 50 nM and 7 His6-MBP-γ equiv/AuNP. 60× magnification was used. Scale bar = 20 µm. (Top panels) data correspond to nanohybrids containing His6-MBP (no γ-peptide

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

• thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), dynamic light scattering (DLS), ultraviolet–visible spectrophotometry (UV–vis), laser scanning confocal microscopy (LSCM) and scanning electron microscopy (SEM). The DLS results demonstrated that P(AA-co-FA)-functionalized BNNTs

• mixed with KBr to form a pellet. The spectra in the range of 7800–350 cm−1 with a 5 cm−1 step were collected in reflection or in transmission mode. Laser scanning confocal microscopy (LSCM) P(AA-co-FA)-functionalized BNNTs were imaged with a Zeiss Axio Imager M2 laser scanning confocal microscope (Carl

• are revealed by the stretching vibrations at 1120 and 1050 cm−1. All of this spectral information confirms the successful fabrication of grafted P(AA-co-FA) brushes on oligoperoxide-functionalized BNNTs. The optical properties of P(AA-co-FA)-functionalized BNNTs were studied by absorption and confocal

Deterministic placement of ultra-bright near-infrared color centers in arrays of silicon carbide micropillars

• Stefania Castelletto,
• Abdul Salam Al Atem,
• Faraz Ahmed Inam,
• Hans Jürgen von Bardeleben,
• Sophie Hameau,
• Ahmed Fahad Almutairi,
• Gérard Guillot,
• Shin-ichiro Sato,
• Alberto Boretti and
• Jean Marie Bluet

Beilstein J. Nanotechnol. 2019, 10, 2383–2395, doi:10.3762/bjnano.10.229

• emission of at least a factor of 6 using micro-photoluminescence systems. Using custom confocal microscopy setups, we characterized the emission of VSi measuring an enhancement by up to a factor of 20, and of NCVSi with an enhancement up to a factor of 7. The experimental results are supported by finite

• the VSiVC and NCVSi. A detailed confocal microscopy study of NCVSi in the pillars is given in the next section. A summary of the PL-measured color centers in each sample is reported in Table 1. Confocal microscopy Confocal fluorescence scanning microscopy was performed using two custom-built systems

• , and dead time set at 2 μs) to measure the NCVSi emission (Figure 4). In the first confocal microscopy setup a variable wavelength super continuum NKT Photonics, Fianium WhiteLase pulsed laser was used for sample illumination at 730 nm. The laser has a pulse width of 30 ps and a repetition rate

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

• ], confocal microscopy, scanning electron microscopy (SEM) [12] and atomic force microscopy (AFM) [16][17] have been employed to investigate cell–substrate interactions. Fluorescence and confocal microscopy are traditional techniques to investigate the intra- and intercellular processes in biological studies

Nitrogen-vacancy centers in diamond for nanoscale magnetic resonance imaging applications

• Alberto Boretti,
• Lorenzo Rosa,
• Jonathan Blackledge and
• Stefania Castelletto

Beilstein J. Nanotechnol. 2019, 10, 2128–2151, doi:10.3762/bjnano.10.207

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

• . Fluorescence microscopy confirmed that the VCAM1-PEG5000Au-CPMV can selectively bind to their target, whereas, the IgG-PEG5000Au-CPMV control did not show any fluorescence signal, which is indicative that no binding to the surface of the cells occurred (Figure 4A). The merged confocal microscopy image in

• of growth surface and were used between passages 2 and 3. Subculture occurred after 60–70% confluence after trypsinization (0.025% trypsin, 0.5 mM EDTA, 10 mM HEPES buffer pH 6.5). RAW264.7 cell labeling and confocal microscopy: Cells of a murine endothelial line (100 μL of 1 × 106 cells/mL, RAW264.7

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

• confocal microscopy (Figure 3a). Subsequently, the targeting capability of the PEPHC1 peptide to U87MG-EGFRvIII cells was identified. After incubation with the peptide PEPHC1, U87MG-EGFRvIII cells demonstrated significantly higher fluorescence intensity than U87MG (Figure 3c). A further FACS assay revealed

• that the binding of PEPHC1 peptide with U87MG-EGFRvIII cells was 6.5-fold that of U87MG (Figure 3d), which agreed well with the results observed by confocal microscopy (Figure 3c). These results indicated that U87MG-EGFRvIII cells overexpressed EGFRvIII and PEPHC1 peptide had special targeting to U87MG

Nanoarchitectonics meets cell surface engineering: shape recognition of human cells by halloysite-doped silica cell imprints

• Elvira Rozhina,
• Ilnur Ishmukhametov,
• Svetlana Batasheva,
• Farida Akhatova and
• Rawil Fakhrullin

Beilstein J. Nanotechnol. 2019, 10, 1818–1825, doi:10.3762/bjnano.10.176

• Milli-Q, and studied with AFM and SEM. Cells recognition by imprints The recognition of HeLa cells with imprints was visualised using bright-field optical microscopy (Axio Imager Z2, Carl Zeiss), and laser confocal microscopy (LSM 780: 405 nm and 633 nm lasers). For fluorescence microscopy imaging

• /halloysite imprints templated on HeLa cells; (D) EDX spectrum taken from the sample shown in (C), demonstrating the typical silica and halloysite elemental distribution; (E) optical and (F) confocal microscopy images demonstrating the recognition of HeLa cells with cell-templated imprints (cell nuclei

The nanoscaled metal-organic framework ICR-2 as a carrier of porphyrins for photodynamic therapy

• Jan Hynek,
• Sebastian Jurík,
• Martina Koncošová,
• Jaroslav Zelenka,
• Ivana Křížová,
• Tomáš Ruml,
• Kaplan Kirakci,
• Ivo Jakubec,
• František Kovanda,
• Kamil Lang and
• Jan Demel

Beilstein J. Nanotechnol. 2018, 9, 2960–2967, doi:10.3762/bjnano.9.275

• using confocal microscopy. Figure 7 clearly shows that the nanoparticles accumulate in intracellular vesicles, which strongly co-localize with the fluorescent marker of lysosomes. This is similar to the results of a previous study performed with PCN-222 nanoparticles [22]. Toxicity and phototoxicity

• resazurin assay (Sigma-Aldrich). Dark toxicity experiments were performed in the same way in the dark. Confocal microscopy: HeLa cells were seeded onto dishes with a glass bottom (MatTek) in full culture medium. After 24 h, the cells received fresh medium without serum and phenol red, and were mixed with

• were 405 nm and 488 nm, respectively. During the confocal microscopy, the cells were maintained at 37 °C and 5% CO2 atmosphere. Flow cytometry: The cells were plated onto 6-well plates in full culture medium. The next day, they were treated with indicated amount of nanoparticles for the indicated

Fabrication of photothermally active poly(vinyl alcohol) films with gold nanostars for antibacterial applications

• Mykola Borzenkov,
• Maria Moros,
• Claudia Tortiglione,
• Serena Bertoldi,
• Nicola Contessi,
• Silvia Faré,
• Angelo Taglietti,
• Agnese D’Agostino,
• Piersandro Pallavicini,
• Maddalena Collini and
• Giuseppe Chirico

Beilstein J. Nanotechnol. 2018, 9, 2040–2048, doi:10.3762/bjnano.9.193

• (Figure S2). We studied the distribution of the GNSs within the PVA films by means of reflection confocal microscopy (Figure 2). By acquiring z-stacks (20 planes, 1 μm spacing) on a 25.8 μm field of view, it was possible to estimate the density of particles in the film with 20% accuracy (see Experimental

Photoluminescence of CdSe/ZnS quantum dots in nematic liquid crystals in electric fields

• Margarita A. Kurochkina,
• Elena A. Konshina and
• Daria Khmelevskaia

Beilstein J. Nanotechnol. 2018, 9, 1544–1549, doi:10.3762/bjnano.9.145

• . Figure 3 shows confocal microscopy images of QDs and their aggregates in the active (a, b, c) and the passive (d, e) LC matrix. We have obtained the images in Figure 3a,d after filling the LC cells without the application of an electric field. The images in Figure 3b,e correspond to the maximal PL of QDs

Optical near-field mapping of plasmonic nanostructures prepared by nanosphere lithography

• Gitanjali Kolhatkar,
• Alexandre Merlen,
• Jiawei Zhang,
• Chahinez Dab,
• Gregory Q. Wallace,
• François Lagugné-Labarthet and
• Andreas Ruediger

Beilstein J. Nanotechnol. 2018, 9, 1536–1543, doi:10.3762/bjnano.9.144

• spots due to higher and localized enhancement. Nevertheless, this technique is diffraction limited to a few hundred of nanometers as it is based on confocal microscopy measurements. Galarreta et al. [26] coated such triangular structures with an azopolymer thin film sensitive to laser irradiation and

Room-temperature single-photon emitters in titanium dioxide optical defects

• Kelvin Chung,
• Yu H. Leung,
• Chap H. To,
• Aleksandra B. Djurišić and
• Snjezana Tomljenovic-Hanic

Beilstein J. Nanotechnol. 2018, 9, 1085–1094, doi:10.3762/bjnano.9.100

• section “Results and Discussion”, it is preferable to obtain a clear indication of deposited nanopowder on the substrate. Confocal microscopy Figure 1 is a schematic of the scanning confocal microscope used to investigate the TiO2 defects. The samples were illuminated by a frequency-doubled Nd:YAG laser

• Confocal microscopy of various TiO2 morphologies The various TiO2 samples were investigated at room temperature using scanning confocal microscopy. This form of microscopy allows for high-resolution images that resolve fluorescence signals from individual defects. The motivation in exploring different TiO2

• signals in the emission peaks by suppressing the contributions due to phonon sidebands. Conclusion This study investigated thin films, single crystals and nanopowders of TiO2 via confocal microscopy. For the first time, it has been observed that TiO2 defects exhibit antibunching behaviour within thin

Green synthesis of fluorescent carbon dots from spices for in vitro imaging and tumour cell growth inhibition

• Nagamalai Vasimalai,
• Vânia Vilas-Boas,
• Juan Gallo,
• María de Fátima Cerqueira,
• Mario Menéndez-Miranda,
• José Manuel Costa-Fernández,
• Lorena Diéguez,
• Begoña Espiña and
• María Teresa Fernández-Argüelles

Beilstein J. Nanotechnol. 2018, 9, 530–544, doi:10.3762/bjnano.9.51

• unequivocally affirm that the C-dots synthesized here have a strong potential for bioanalytical and clinical applications. First, results obtained from fluorescence confocal microscopy studies have demonstrated that the C-dots from spices can be easily tracked when incorporated into cells, because their self

Temperature-tunable lasing from dye-doped chiral microdroplets encapsulated in a thin polymeric film

• Gia Petriashvili,
• Mauro Daniel Luigi Bruno,
• Maria Penelope De Santo and
• Riccardo Barberi

Beilstein J. Nanotechnol. 2018, 9, 379–383, doi:10.3762/bjnano.9.37

• water evaporation, the formed thin film can be easily detached from the glass (Figure 4). In Figure 5, a picture of the microdroplets obtained through confocal microscopy (Leica,DM6000 TCS SP8) is shown, which confirms the stabilization through PVA by preventing the coalescence of droplets during the