Photothermal ablation of murine melanomas by Fe₃O₄ nanoparticle clusters

• Xue Wang,
• Lili Xuan and
• Ying Pan

Beilstein J. Nanotechnol. 2022, 13, 255–264, doi:10.3762/bjnano.13.20

• irradiation for 10 min or left intact. After 24 h, cells were washed with PBS, pelleted by centrifugation and underwent Annexin V and propidium iodide staining as per manufacturer’s instructions (ThermoFisher Scientific, Waltham, USA). Samples were analyzed in the FACS Calibur flow cytometry (BD Biosciences

• by NIR irradiation. Immunohistochemical staining of harvested tumors revealed HSP70 to be elevated (brown signals) by PTT. Schematic representation of Fe3O4 NPC-mediated photothermal therapy in melanoma. Supporting Information Supporting Information File 46: Additional figures. Funding This study

Alteration of nanomechanical properties of pancreatic cancer cells through anticancer drug treatment revealed by atomic force microscopy

• Xiaoteng Liang,
• Shuai Liu,
• Xiuchao Wang,
• Dan Xia and
• Qiang Li

Beilstein J. Nanotechnol. 2021, 12, 1372–1379, doi:10.3762/bjnano.12.101

• under (almost) physiological conditions in situ. It offers nanoscale force sensitivity, the ability to work in liquid phases, and requires no staining [12][13][14]. With the development of AFM, researchers have been able to conduct extensive research on biological issues through imaging the

Biocompatibility and cytotoxicity in vitro of surface-functionalized drug-loaded spinel ferrite nanoparticles

• Sadaf Mushtaq,
• Khuram Shahzad,
• Tariq Saeed,
• Anwar Ul-Hamid,
• Bilal Haider Abbasi,
• Nafees Ahmad,
• Waqas Khalid,
• Muhammad Atif,
• Zulqurnain Ali and
• Rashda Abbasi

Beilstein J. Nanotechnol. 2021, 12, 1339–1364, doi:10.3762/bjnano.12.99

• HT144) were quantitatively determined by fluorescence microscopy using acridine orange and propidium iodide (AOPI) staining. Cells were treated with drug-loaded NPs for 3 h at concentration values of 5 and 10 μg/mL. NTC, NPs-PMA (10 μg/mL) and free drugs (DOX and MTX, 5 μM each) were included as

• controls. After treatment and staining with AOPI, cells were observed under a fluorescence microscope where viable cells appeared green, apoptotic cells appeared orange/yellow, and necrotic cells appeared red in color (Figure 5a). Percentage fractions of live, necrotic, and apoptotic cells were calculated

An overview of microneedle applications, materials, and fabrication methods

• Zahra Faraji Rad,
• Philip D. Prewett and
• Graham J. Davies

Beilstein J. Nanotechnol. 2021, 12, 1034–1046, doi:10.3762/bjnano.12.77

• cross-section of brain displaying cells (Hoechst staining), astrocytes (GFAP staining), and neurons (cresyl violet staining) at the insertion location of the microneedle [66]. Figure 3a–h were reprinted from [66], Sensors and Actuators B, Chemical, vol. 209, by Lee, H. J.; Son, Y.; Kim, D.; Kim, Y. K

Silver nanoparticles induce the cardiomyogenic differentiation of bone marrow derived mesenchymal stem cells via telomere length extension

• Khosro Adibkia,
• Ali Ehsani,
• Asma Jodaei,
• Ezzatollah Fathi,
• Raheleh Farahzadi and
• Mohammad Barzegar-Jalali

Beilstein J. Nanotechnol. 2021, 12, 786–797, doi:10.3762/bjnano.12.62

• differentiation of BM-MSCs via TL extension as an effective factor in reducing cell senescence of BM-MSCs. Results Multilineage differentiation of BM-MSCs The BM-MSCs appeared as spindle-shaped cells (Figure 1A,B). The adipogenic and osteogenic differentiation was specified by Oil red O and Alizarin red staining

• , respectively. After staining, the presence of oil vacuoles confirmed the adipogenic differentiation (Figure 1C). Also, the redness of the nodules indicated the presence of mineralized compartments as a result of the osteogenic confirmation (Figure 1D). Phenotypical characterization of BM-MSCs Flow cytometry

• -well plates were cultured in the cardiomyogenic differentiation medium for 14 days. The medium was refreshed twice weekly. Cardiomyogenic differentiation was confirmed by ICC. Immunofluorescence staining BM-MSCs were seeded in 8-well slide containing cardiomyogenic differentiation medium for 14 days

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

• ). Single-cell clones were selected and amplified by dilution cloning in 6-well plates. Immunofluorescence staining Cells were grown on glass coverslips in 48-well plates overnight before incubation with Alexa Fluor 594–Transferrin conjugate (25 µg/mL) or cholera Toxin B subunit–FITC conjugate (5 mg/mL) at

• . For F-actin staining, the coverslips were incubated with Alexa Fluor 488 Phalloidin or Alexa Fluor 546 Phalloidin (Life Technologies, Thermo Fisher Scientific) (dilution 1:500) at 37 °C for 1 h. After washing with PBS, 4,6-diamide-2-phenylindole (DAPI) (dilution 1: 500) was added for nuclear staining

Bio-imaging with the helium-ion microscope: A review

• Matthias Schmidt,
• James M. Byrne and
• Ilari J. Maasilta

Beilstein J. Nanotechnol. 2021, 12, 1–23, doi:10.3762/bjnano.12.1

• range of applications to thin sections, similar to the transmission option in SEMs. In combination with the well-established heavy-metal staining techniques used in transmission electron microscopy (TEM), this would allow for ultrastructural research comparable to standard TEM. SRIM [57] simulations

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

• loading buffer and transferred into a 15 mL tube. Following staining with 5 µL of Annexin V-FITC and PI, the cells were incubated for 15 min at 4 °C. The cell suspensions were then immediately analyzed by FCM, with 488 nm excitation wavelength and 575 nm emission wavelength. Groups without staining with

Uniform Fe₃O₄/Gd₂O₃-DHCA nanocubes for dual-mode magnetic resonance imaging

• Miao Qin,
• Yueyou Peng,
• Mengjie Xu,
• Hui Yan,
• Yizhu Cheng,
• Xiumei Zhang,
• Di Huang,
• Weiyi Chen and
• Yanfeng Meng

Beilstein J. Nanotechnol. 2020, 11, 1000–1009, doi:10.3762/bjnano.11.84

• slightly higher than that measured for the control groups (P < 0.01). In order to further test the cytotoxicity of FGDA nanocubes, live–dead staining was performed. The results showed that there was no difference in cellular morphology or viability between the control and treated groups (Figure 4b,c). In

• maintained an oversaturated state and kept generating the T2 signals since its concentration was higher than Gd2O3 in the nanocubes. Prussian blue staining further confirmed the presence of iron in lumbar muscles, indicating that the T1 and T2 signal changes were indeed induced by the FGDA nanocubes (Figure

• processed for hematoxylin and eosin (H&E) staining for a qualitative evaluation of the in vivo toxicity. Figure 5e demonstrated that the FGDA nanocubes did not cause significant side effects in major organs when compared with the control group. This result reinforces that FGDA nanocubes are safe to be used

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

• nanobeads, which likely stabilizes these structures. The hybrid particles reveal considerable antibacterial properties. This has been evaluated based on the determination of MIC and MBIC values and an estimation of bacterial viability through fluorescence staining. Experimental Chemicals All chemicals were

• staining [53], was taken as the MBIC. Each determination was performed in triplicate. Confocal laser scanning microscopy was used to assess the bacterial viability in biofilms using the LIVE/DEAD BacLight bacterial viability kit. Overnight cultures of P. aeruginosa and S. aureus were 100-fold diluted in MH

Examination of the relationship between viscoelastic properties and the invasion of ovarian cancer cells by atomic force microscopy

• Mengdan Chen,
• Jinshu Zeng,
• Weiwei Ruan,
• Zhenghong Zhang,
• Yuhua Wang,
• Shusen Xie,
• Zhengchao Wang and
• Hongqin Yang

Beilstein J. Nanotechnol. 2020, 11, 568–582, doi:10.3762/bjnano.11.45

• . Confocal imaging of the microfilament skeleton The cytoskeletal organization in ovarian cancer cells was investigated by confocal imaging. The cells were seeded into 35 mm cover glass bottom culture dishes (Nest) at a density of 5 × 104 mL−1 and cultured in the 37 °C incubator for 2 days prior to staining

Nanoparticles based on the zwitterionic pillar[5]arene and Ag⁺: synthesis, self-assembly and cytotoxicity in the human lung cancer cell line A549

• Dmitriy N. Shurpik,
• Denis A. Sevastyanov,
• Pavel V. Zelenikhin,
• Pavel L. Padnya,
• Vladimir G. Evtugyn,
• Yuriy N. Osin and
• Ivan I. Stoikov

Beilstein J. Nanotechnol. 2020, 11, 421–431, doi:10.3762/bjnano.11.33

• [2][3][4]. Silver is well known for its antimicrobial activity, and Ag+ ion is usually considered a biologically active substance [5][6][7][8]. However, it is known that the effect of Ag+ on the human body is toxic and can cause diseases such as argyria (irreversible staining of the skin in gray

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

• , or FITC were added to the culture (1.3 × 106 virions per cell) and incubated for 4 h. The amount of virus used is consistent with previous studies with plant viruses [32][35][36][37][41]. Virus internalization was monitored on live cells or cells fixed with paraformaldehyde, after staining 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

• : The polyplexes with a tracking dye (bromophenol blue, 2 µL), were loaded on a 1% agarose gel. The electrophoresis was carried in Tris/boric acid buffer (TBE) buffer at 80 V for 45 min. The gel was imaged after staining with ethidium bromide in a UV transilluminator using a gel documentation system

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

• subcellular localization was monitored. An organelle-staining study indicated the localization of the tetrahedrons within the cytoplasm and demonstrated efficient cellular uptake of DNA tetrahedrons without the need for any transfection agents or procedures. One of the advantages of DNA tetrahedrons is that

Internalization mechanisms of cell-penetrating peptides

• Ivana Ruseska and
• Andreas Zimmer

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

• -dependent process is the major route for the internalization of CPPs. Nonetheless, novel studies on living cells show that the uptake of arginine-rich peptides could be a combination of both direct translocation and endocytosis. What supports this hypothesis is the mixture of punctate and diffuse staining

• 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

Bombesin receptor-targeted liposomes for enhanced delivery to lung cancer cells

• Mohammad J. Akbar,
• Pâmela C. Lukasewicz Ferreira,
• Melania Giorgetti,
• Leanne Stokes and
• Christopher J. Morris

Beilstein J. Nanotechnol. 2019, 10, 2553–2562, doi:10.3762/bjnano.10.246

• -Target-lipo group. Cells exposed to FL-Control-lipo displayed a diffuse cell membrane-like staining with few green fluorescent puncta. Whereas, the target-lipo exposed cells displayed many more fluorescent puncta as well as a widespread increase in cellular fluorescence. Our observations here indicate

Evaluation of click chemistry microarrays for immunosensing of alpha-fetoprotein (AFP)

• Seyed Mohammad Mahdi Dadfar,
• Sylwia Sekula-Neuner,
• Vanessa Trouillet,
• Hui-Yu Liu,
• Ravi Kumar,
• Annie K. Powell and
• Michael Hirtz

Beilstein J. Nanotechnol. 2019, 10, 2505–2515, doi:10.3762/bjnano.10.241

• immobilized on the surface. This enables the identification of the sites were unlabeled AFP bound by subsequent staining with fluorescently labeled streptavidin (Figure S3). After incubation a fluorescent microarray pattern becomes visible again (Figure S4). Conclusion In this study, we present the

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

• for the staining of cell membranes [4]. In two separate studies, Chan and co-workers described two interesting hybrid systems. In the first, a charge driven self-assembly of AuNPs and different-colour QDs into multicolour, non-blinking nanohybrids was introduced. These nanohybrids were then coupled to

• observed, as indicated by the significant fluorescence staining of the cells (see Figure 1D). Additional confocal images collected from two sets of cultures, one incubated with nanohybrids prepared with His6-MBP-γ and the other with His6-MBP (gamma-free MBP), and serving as control. Only the culture

• incubated with nanohybrids prepared with His6-MBP-γ yielded pronounced intracellular staining; the control cultures did not show any cellular uptake (see Figure 1D and Figures S3 and S4 in Supporting Information File 1). In addition, the distribution of the QD staining (shown in Figure 1E, top panels) is

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

• fixed in 4% paraformaldehyde/PBS (pH 7.0) for 15 min at ambient temperature (25 °C). Cells were rinsed three times for 5 min with PBS (10 mL) and incubated in 0.2% Triton X-100 for further 10 min. After three five-minute rinses with PBS and preincubation with 2% BSA to block nonspecific staining, cells

Synthesis and potent cytotoxic activity of a novel diosgenin derivative and its phytosomes against lung cancer cells

• Liang Xu,
• Dekang Xu,
• Ziying Li,
• Yu Gao and
• Haijun Chen

Beilstein J. Nanotechnol. 2019, 10, 1933–1942, doi:10.3762/bjnano.10.189

• late apoptosis in human cervical HeLa cancer cells [26]. In order to explore the death mechanism of P2, A549 and PC9 cells were treated with P2 and Di for 48 h and the proportion of cells undergone apoptosis was counted through Annexin V-FITC/PI staining and followed by flow cytometry analysis. As

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

• ), followed by negative staining with 2% phosphotungstic acid. The mean hydrodynamic diameter and zeta potential of the nanoprobes were measured with a Malvern Zetasizer Nano ZS (Malvern, UK) instrument. The quantitative measurement of the Fe content in PNPs was conducted by inductively coupled plasma

• sections. After staining with DAPI, fluorescence images of the brain slices were obtained with a laser confocal microscope (ZEISS, 710, LSM, Germany). For electron microscopy samples, the tumor-bearing mice were sacrificed by heart perfusion with saline and 4% paraformaldehyde 24 hours after injection

• at 48 h after PNP injection at a Fe concentration of 20 mg/kg every 2 days for 4 weeks and subjected to H&E staining and microscopic examination (Leica, Germany). Statistical analysis Differences in the assessment between experimental groups was evaluated using an unpaired student’s t-test. A value

Toxicity and safety study of silver and gold nanoparticles functionalized with cysteine and glutathione

• Barbara Pem,
• Igor M. Pongrac,
• Lea Ulm,
• Ivan Pavičić,
• Valerije Vrček,
• Darija Domazet Jurašin,
• Marija Ljubojević,
• Adela Krivohlavek and
• Ivana Vinković Vrček

Beilstein J. Nanotechnol. 2019, 10, 1802–1817, doi:10.3762/bjnano.10.175

• apoptotic/dead cells were determined by flow cytometry analysis after staining with CAM and EthD dyes. The doses that caused low or no significant reduction in cell viability (Figure 4a) showed apoptotic processes in a dose-response manner for all tested species (Figure 4b). In accordance with the MTT data

• -aminoactinomycin D (7-AAD) staining. Annexin V binds phosphatidylserine, which can only be found on the outer leaflet of cell membranes during apoptosis, while 7-AAD is a DNA-binding agent that cannot penetrate the membrane of living cells and can only stain dead or late apoptotic ones. The treatment involved 24 h

• joined, centrifuged at 800g for 5 min and washed with PBS containing 2% bovine serum albumin (1 mL per sample). The cells were then stained using Muse® Annexin V and a dead cell assay kit (Merck KGaA, Darmstadt, Germany) according to the manufacturer’s instructions. After staining, the cells were washed

Scavenging of reactive oxygen species by phenolic compound-modified maghemite nanoparticles

• Małgorzata Świętek,
• Yi-Chin Lu,
• Rafał Konefał,
• Liliana P. Ferreira,
• M. Margarida Cruz,
• Yunn-Hwa Ma and
• Daniel Horák

Beilstein J. Nanotechnol. 2019, 10, 1073–1088, doi:10.3762/bjnano.10.108

• phenolic compound-modified nanoparticles (100 μg/mL), they were incubated with L-929 and LN-229 cells for 3 h, and 2 mM H2O2 was added for 30 min, followed by staining with CM-H2DCFDA for 1 h. Figure 6 shows the representative flow cytometry results of nanoparticle internalization and the intracellular ROS

Enhanced inhibition of influenza virus infection by peptide–noble-metal nanoparticle conjugates

• Zaid K. Alghrair,
• David G. Fernig and
• Bahram Ebrahimi

Beilstein J. Nanotechnol. 2019, 10, 1038–1047, doi:10.3762/bjnano.10.104

• that does not stain with toluidine blue. In control (no virus) and vehicle (DMSO)-treated cells, the cell monolayer in the well was evenly stained (Supporting Information File 1, Figure S3). In the presence of virus, there were substantial areas where cells had lysed (plaques) and there was no staining