Classification and application of metal-based nanoantioxidants in medicine and healthcare

• Nguyen Nhat Nam,
• Nguyen Khoi Song Tran,
• Tan Tai Nguyen,
• Nguyen Ngoc Trai,
• Nguyen Phuong Thuy,
• Hoang Dang Khoa Do,
• Nhu Hoa Thi Tran and
• Kieu The Loan Trinh

Beilstein J. Nanotechnol. 2024, 15, 396–415, doi:10.3762/bjnano.15.36

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

• step was added to the preparation procedure. However, it is important to specify that this step is not required and that bacteria stained by the RhBITC- or FITC-BSA/PDA NPs can be observed alive directly after staining. The samples were fixed with paraformaldehyde (PFA): Samples were centrifuged at

Recognition mechanisms of hemoglobin particles by monocytes – CD163 may just be one

• Jonathan-Gabriel Nimz,
• Pichayut Rerkshanandana,
• Chiraphat Kloypan,
• Ulrich Kalus,
• Saranya Chaiwaree,
• Axel Pruß,
• Radostina Georgieva,
• Yu Xiong and
• Hans Bäumler

Beilstein J. Nanotechnol. 2023, 14, 1028–1040, doi:10.3762/bjnano.14.85

• dependence of HbMP uptake on these receptors. Table 2 gives an overview of the samples of indirect phagocytosis test no. 2; the incubation time with HbMPs was 30 min. All samples were analyzed by flow cytometry. Leucocytes were identified by DNA staining with propidium iodide (PI) or diamidinophenylindole

• (DAPI). The closely spaced emission maxima of DAPI and FITC, or PI and APC, necessitated the use of different dyes for DNA staining depending on which signal, FITC or APC, was of interest in each sample. In each run, 2000 monocytes were analyzed. The mean fluorescence intensity (MFI) of the reference

• well. Neither holding a temperature of 37 °C for 120 min (Incub-wb) nor incubation with DAPI or PI (DAPI-/PI-wb) caused a relevant change in this signal. Neither the blood itself nor the HbMPs or the chosen incubation times had an interfering influence on the test. Staining the monocytes with FITC

Green SPIONs as a novel highly selective treatment for leishmaniasis: an in vitro study against Leishmania amazonensis intracellular amastigotes

• Brunno R. F. Verçoza,
• Robson R. Bernardo,
• Luiz Augusto S. de Oliveira and
• Juliany C. F. Rodrigues

Beilstein J. Nanotechnol. 2023, 14, 893–903, doi:10.3762/bjnano.14.73

• standard model for cutaneous leishmaniasis. The parasites were maintained according to previously published protocols [22]. Prussian blue staining For staining with Prussian blue (Sigma-Aldrich, Germany), promastigote and intracellular amastigotes were treated with 100 µg/mL of SPIONs for 24 h. The

• (*). Bright-field optical microscopy of L. amazonensis promastigotes (A, B) and intracellular amastigotes (C, D) treated with 100 µg/mL of SPIONs for 24 h, after staining with Prussian blue (A–D). (A) The arrows indicate the blue stain characteristic for the reaction with ferrous compounds in the promastigote

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

• without staining. Electron microscopy imaging was conducted using a field-emission scanning electron microscope FEI-NOVA NanoSEM 230 equipped with an Apollo XL silicon drift detector from EDAX-Ametek or using a high-resolution JEOL IT500HR/LA microscope equipped with an energy dispersive X-ray

Quercetin- and caffeic acid-functionalized chitosan-capped colloidal silver nanoparticles: one-pot synthesis, characterization, and anticancer and antibacterial activities

• Akif Hakan Kurt,
• Elif Berna Olutas,
• Fatma Avcioglu,
• Hamza Karakuş,
• Mehmet Ali Sungur,
• Cansu Kara Oztabag and
• Muhammet Yıldırım

Beilstein J. Nanotechnol. 2023, 14, 362–376, doi:10.3762/bjnano.14.31

• . Small volumes of Ch/Q- and Ch/CA-Ag NPs were placed on carbon-coated copper grids and allowed to evaporate at room temperature. For negative staining, a drop of freshly prepared 2% uranyl acetate solution was dripped on the copper grid, and excess liquid is removed by a piece of paper after 2 min. Zeta

• TEM due to energetic electron bombardment causing burn, negative staining using uranyl acetate was performed. Figure 4d shows the TEM image of the Ch/Q-Ag NPs exposed by negative staining. It is seen that the chitosan/quercetin shell structure uniformly covers the core Ag NPs (see insets of Figure 4d

• NPs after negative staining were obtained and confirmed that the chitosan/quercetin shell structure covered the core Ag NPs. Moreover, the amount of quercetin and caffeic acid in the samples of Ch/Q- and Ch/CA-Ag NPs determined by colorimetric methods were found to be 31.0 ± 0.8 and 28.8 ± 0.4 μg/mL

Supramolecular assembly of pentamidine and polymeric cyclodextrin bimetallic core–shell nanoarchitectures

• Alexandru-Milentie Hada,
• Nina Burduja,
• Marco Abbate,
• Claudio Stagno,
• Guy Caljon,
• Louis Maes,
• Nicola Micale,
• Massimiliano Cordaro,
• Angela Scala,
• Antonino Mazzaglia and
• Anna Piperno

Beilstein J. Nanotechnol. 2022, 13, 1361–1369, doi:10.3762/bjnano.13.112

• were added three times at room temperature, every hour, to a solution of nanoG (6.75 mL) to obtain nanoGS determined by a light orange staining of the solution. After each addition of silver ions, the mixture was kept under magnetic stirring at room temperature (20–25 °C) for 1 h. The reduction of

Recent advances in green carbon dots (2015–2022): synthesis, metal ion sensing, and biological applications

• Aisha Kanwal,
• Naheed Bibi,
• Sajjad Hyder,
• Arif Muhammad,
• Hao Ren,
• Jiangtao Liu and
• Zhongli Lei

Beilstein J. Nanotechnol. 2022, 13, 1068–1107, doi:10.3762/bjnano.13.93

Biomimetic chitosan with biocomposite nanomaterials for bone tissue repair and regeneration

• Se-Kwon Kim,
• Sesha Subramanian Murugan,
• Pandurang Appana Dalavi,
• Sebanti Gupta,
• Sukumaran Anil,
• Gi Hun Seong and
• Jayachandran Venkatesan

Beilstein J. Nanotechnol. 2022, 13, 1051–1067, doi:10.3762/bjnano.13.92

• weeks. The emergence of new bone in the defective region is confirmed by microscale computational micrographs and staining assay findings [98]. Ning et al. (2019) developed glycyl-ʟ-histidyl-ʟ-lysine-containing copper ions integrated with mesoporous silica nanoparticles (MSN) and chitosan. Further, the

• activity was increased. In addition, Alizarin red S staining tests detected the development of mineralized nodules [81]. On the Ti substrate, TiO2 nanotubes carrying a gentamicin drug mixture were deposited. Furthermore, a combination of alginate and chitosan was utilized to cover the TiO2–gentamicin

• phosphatase staining revealed the differentiation of mesenchymal stem cells to osteoblasts [66]. The addition of polymethylmethacrylate to powder composites of chitosan/graphene oxide increased the compressive strength by 16.2%, compressive modulus by 69.1%, and bending strength by 24%. After four weeks of

Bioselectivity of silk protein-based materials and their bio-inspired applications

• Hendrik Bargel,
• Vanessa T. Trossmann,
• Christoph Sommer and
• Thomas Scheibel

Beilstein J. Nanotechnol. 2022, 13, 902–921, doi:10.3762/bjnano.13.81

Stimuli-responsive polypeptide nanogels for trypsin inhibition

• Petr Šálek,
• Jana Dvořáková,
• Sviatoslav Hladysh,
• Diana Oleshchuk,
• Ewa Pavlova,
• Jan Kučka and
• Vladimír Proks

Beilstein J. Nanotechnol. 2022, 13, 538–548, doi:10.3762/bjnano.13.45

• microscope (TEM; FEI; Brno, Czech Republic) after negative staining of nanogel samples with uranyl acetate. The number-average diameter (Dn), weight-average diameter (Dw), and dispersity (Ð) were calculated using ImageJ software by counting the hydrogel nanoparticles in the TEM images following these

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