Use of nanosystems to improve the anticancer effects of curcumin

• Andrea M. Araya-Sibaja,
• Norma J. Salazar-López,
• Krissia Wilhelm Romero,
• José R. Vega-Baudrit,
• J. Abraham Domínguez-Avila,
• Carlos A. Velázquez Contreras,
• Ramón E. Robles-Zepeda,
• Mirtha Navarro-Hoyos and
• Gustavo A. González-Aguilar

Beilstein J. Nanotechnol. 2021, 12, 1047–1062, doi:10.3762/bjnano.12.78

• anticancer photodynamic therapy [140][141], in which this combined approach induces mitochondria-dependent apoptosis (70% of cell viability inhibition) in a human head and neck cancer cell line (AMC-HN3), as compared to individually using F-CUR (10% inhibition) or phototherapy (50% inhibition). The apoptosis

• greater potential to produce ROS [143]. A similar behavior was observed in cervical carcinoma cell lines treated with nanoemulsion-photostimulated CUR, where cell viability was reduced to <5% and an increase in caspase-3 and caspase-7 activity was apparent [144]. Inostroza et al. [112] reported the

The role of deep eutectic solvents and carrageenan in synthesizing biocompatible anisotropic metal nanoparticles

• Nabojit Das,
• Akash Kumar and
• Raja Gopal Rayavarapu

Beilstein J. Nanotechnol. 2021, 12, 924–938, doi:10.3762/bjnano.12.69

• -directing surfactant [60]. They carried out an in vitro cytotoxicity study exposing Hep-G2 and A549 cells to CTAB- and C12EDMAB-capped gold nanorods. The researchers observed a considerable difference in cell viability at the same concentration levels. Much earlier, a chemical method introduced by Chenxu Yu

Comprehensive review on ultrasound-responsive theranostic nanomaterials: mechanisms, structures and medical applications

• Sepand Tehrani Fateh,
• Lida Moradi,
• Elmira Kohan,
• Michael R. Hamblin and
• Amin Shiralizadeh Dezfuli

Beilstein J. Nanotechnol. 2021, 12, 808–862, doi:10.3762/bjnano.12.64

• inertial cavitation, occurring near or within the droplet, cause the dispersed medium to vaporize [135][136]. It has been shown that ADV can decrease cell viability through the disruption of cell membranes [114]. Some researchers have suggested that ADV can cause cell death while increasing the penetration

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

• that Ag-NPs induced mESCs cell cycle arrest at the G1 and S phases through inhibition of the hyperphosphorylation of Retinoblastoma protein [12]. Kalishwaralal et al. reported that Ag-NPs could inhibit cell proliferation, cell viability, and cell migration through activating caspase-3 and suppressing

• ) formation as cardiac and liver markers [31]. In the present study, the in vitro effect of Ag-NPs was investigated on cardiac differentiation potency as well as TL of MSCs. The suitable concentration of Ag-NPs which prolong the cell viability of MSCs was determined by MTT assay as previously examined by

A review on nanostructured silver as a basic ingredient in medicine: physicochemical parameters and characterization

• Gabriel M. Misirli,
• Kishore Sridharan and
• Shirley M. P. Abrantes

Beilstein J. Nanotechnol. 2021, 12, 440–461, doi:10.3762/bjnano.12.36

• concentrations of Ag+ for 24 h indicate that a concentration of 2.5 ppm decreased cell viability by 60% whereas 5.0 ppm decreased cell viability by 100% in comparison to the control case. On the other hand, 30 ppm of AgNPs prepared immediately before the biological tests, in a system without oxygen and with a

• carrier gas to expel all dissolved oxygen (to prevent oxidation and release of silver ions) reported no reduction in cell viability compared to control [127]. Treatment of burns in rats with AgNPs were carried out both in vitro and in vivo. No significant differences in the levels of urea, creatinine, and

Doxorubicin-loaded gold nanorods: a multifunctional chemo-photothermal nanoplatform for cancer management

• Uzma Azeem Awan,
• Abida Raza,
• Shaukat Ali,
• Rida Fatima Saeed and
• Nosheen Akhtar

Beilstein J. Nanotechnol. 2021, 12, 295–303, doi:10.3762/bjnano.12.24

• cytotoxicity against HepG2 (carcinogenic) and 3T3 (non-carcinogenic) cells was evaluated. Cells were treated for 12 h with PSS-GNRs and analyzed using the MTT assay. As shown in Figure 4, cells treated with PSS-GNRs had no significant reduction in cell viability compared to control cells. The viability

• conjugated one. The cytotoxic efficiency of the DOX-loaded PAA-PEG-GNRs was found to be similar to free DOX and improved with an increase in their concentrations [36]. In a previous study, cell viability was significantly decreased down to 57% using GNR-DOX-cRGD, whereas free DOX demonstrated the highest

Characterization, bio-uptake and toxicity of polymer-coated silver nanoparticles and their interaction with human peripheral blood mononuclear cells

• Sahar Pourhoseini,
• Reilly T. Enos,
• Angela E. Murphy,
• Bo Cai and
• Jamie R. Lead

Beilstein J. Nanotechnol. 2021, 12, 282–294, doi:10.3762/bjnano.12.23

• well characterized, including their transformations during exposure. Additionally, we have assessed bio-uptake quantification, using mass spectrometry, and toxicity/cell viability after exposing human PBMCs to AgNPs at clinically relevant concentrations. We also compared the toxicity of AgNPs with

• . However, for the AgNO3 treatment, this ratio increased in a dose-dependent manner (Table 2). Impact of PVP-AgNPs and Ag ions on viability and metabolic activity of PBMCs Cell membrane integrity as a marker for cell viability was measured by LDH release; a greater LDH release is an indication of more

• control group. Results for cell viability and metabolic activity of PBMCs for each person are presented in Supporting Information File 1, Figure S4 and Figure S5, respectively. The Pearson correlation coefficient was calculated to assess the relationship between uptake and cytotoxicity (LDH assay) of PVP

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

• experiments with the positive controls confirmed the ability of endocytic inhibitors to block the specific route of endocytosis. None of the endocytic inhibitors affected cell viability and proliferation activity with the exception of nocodazole (Noc) (Supporting Information File 1, Figure S2). Short-term

• based on the cell viability determined by MTT assay (Supporting Information File 1, Figure S5 and Figure S6). All inhibitors were purchased from Sigma-Aldrich (Slovakia). The cells exposed to culture medium were used as negative control and cells exposed only to MNPs for 1 h were considered as a

The nanomorphology of cell surfaces of adhered osteoblasts

• Christian Voelkner,
• Mirco Wendt,
• Regina Lange,
• Max Ulbrich,
• Martina Gruening,
• Susanne Staehlke,
• Barbara Nebe,
• Ingo Barke and
• Sylvia Speller

Beilstein J. Nanotechnol. 2021, 12, 242–256, doi:10.3762/bjnano.12.20

• coatings of positively charged plasma-polymerized allylamine (PPAAm) or negatively charged Au were used, see below. Viability tests (MTS) were performed on glass, sputter-deposited Au, polydimethylsiloxane (PDMS), and PPAAm coating with native titanium and cell culture plastic as reference. Cell viability

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

• concentration (c = 200 µg/mL), the cell viability after exposure to UC@thin_NH2 was approx. 51 ± 5%, whereas in the UC@thick_NH2 sample, the cell viability was 75 ± 6%. At the lowest concentration (c = 12.5 µg/mL) the cell viability was 110 ± 12% for UC@thin_NH2 and 95 ± 14% for UC@thick_NH2. UC@thin_RBITC_NH2

• highest concentration values (c = 150 and 200 µg/mL) of UC@thick_NH2, no significant difference in the cell viability was observed between the two values. The cytotoxicity of pure silica without a UCNP core (sample SiO2@RBITC_NH2) was also measured. The cell viability at the lowest concentration was 83

• present study. The sample UC@thin_NH2 has a larger hydrodynamic diameter than the sample UC@thick_NH2 in DMEM and the situation is reversed for sample UC@thin_RBITC_NH2 and sample UC@thick_RBITC_NH2. However, in both cases the cell viability increases with shell thickness. Since the light scattering is

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

• , the same volume of fresh PBS was supplied in the release medium. The concentration of released DOX in all samples was determined by measuring the UV absorbance. The cumulative release rate of DOX was calculated and the measurements were repeated for three times, averaging the results. Cell viability

• dissolve the formazan crystals. The absorbance of the final solution was measured at a wavelength of 570 nm using a microplate spectrophotometer (SpectraMax iD5) to calculate the cell viability. Groups without treatment were used as control. Cellular uptake of DOX-loaded nanocarriers The drug delivery in

• tissues. The DOX molecules are retained in the carriers and subsequently rapidly released from nanotubes at the targeted tumor sites with a slightly acidic environment [42]. Cell viability Cytotoxicity assessment results of different blank carriers and DOX-loaded nanocarrier formulations are shown in

Cardiomyocyte uptake mechanism of a hydroxyapatite nanoparticle mediated gene delivery system

• Hiroaki Komuro,
• Masahiro Yamazoe,
• Kosuke Nozaki,
• Akiko Nagai and
• Tetsuo Sasano

Beilstein J. Nanotechnol. 2020, 11, 1685–1692, doi:10.3762/bjnano.11.150

• (PBS) to remove detached dead cells and the formazan crystals were solubilized in DMSO. The absorbance was measured using a microplate reader at 570 nm. The relative cell viability (%) compared to non-treated cells was calculated by [abs] sample/[abs] control × 100. Transfection efficiency assay HL-1

• approximately 1.3 wt % [24]. Cytotoxicity assay Dose-dependent cytotoxicity of HAp/pDNA complexes on HL-1 cells was investigated in the concentration range of 0.1–10 µg/mL. The 3-(4,5-dimethylhiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay was used to assess cytotoxicity. No differences in cell

• viability were observed among the three concentrations of HAp/pDNA complexes used at 24 and 72 h (Figure 2). The results suggested that HAp exhibits little cytotoxicity within the concentration range used in this study. Transfection efficiency To test the gene transfection potential of the HAp nanoparticle

Gram-scale synthesis of splat-shaped Ag–TiO₂ nanocomposites for enhanced antimicrobial properties

• Mohammad Jaber,
• Asim Mushtaq,
• Kebiao Zhang,
• Jindan Wu,
• Dandan Luo,
• Zihan Yi,
• M. Zubair Iqbal and
• Xiangdong Kong

Beilstein J. Nanotechnol. 2020, 11, 1119–1125, doi:10.3762/bjnano.11.96

• antibacterial properties of TiO2 in the presence of silver were examined. The formation of Ag–TiO2 NCs was analyzed through various characterization techniques. The cell viability experimental results demonstrated that the Ag–TiO2 NCs have good biocompatibility. The antibacterial activity of the prepared Ag

• obtain homogeneous Ag–TiO2 nanocomposites with a high yield. The prepared compounds were characterized by XRD, SEM, EDS, FTIR and UV–vis spectrophotometry. The cell viability upon exposure to the splat-shaped Ag–TiO2 nanocomposites was evaluated by using the Cell Counting Kit-8 assay. The antimicrobial

Applications of superparamagnetic iron oxide nanoparticles in drug and therapeutic delivery, and biotechnological advancements

• Maria Suciu,
• Corina M. Ionescu,
• Alexandra Ciorita,
• Septimiu C. Tripon,
• Dragos Nica,
• Hani Al-Salami and
• Lucian Barbu-Tudoran

Beilstein J. Nanotechnol. 2020, 11, 1092–1109, doi:10.3762/bjnano.11.94

• reported no cytotoxicity, when not stimulated, and 15% cell viability in vitro and tumor reduction in vivo when activated by a laser. Horák and collaborators [169] used the toxicity of free Fe ions for antitumor activity. The authors synthesized maghemite nanoparticles covered with poly(N,N

A few-layer graphene/chlorin e6 hybrid nanomaterial and its application in photodynamic therapy against Candida albicans

• Selene Acosta,
• Carlos Moreno-Aguilar,
• Dania Hernández-Sánchez,
• Beatriz Morales-Cruzado,
• Erick Sarmiento-Gomez,
• Carla Bittencourt,
• Luis Octavio Sánchez-Vargas and
• Mildred Quintana

Beilstein J. Nanotechnol. 2020, 11, 1054–1061, doi:10.3762/bjnano.11.90

• 48 h after being treated with PDT using FLG-Ce6 as the photosensitizer is highly reduced, as shown in Figure 4b. The photoactivation of C. albicans without a photosensitizer does not cause any change in the cell viability, nor does the incubation with any of our photosensitizers without light

• singlet oxygen production. The ascending arrows denote the irradiation time (5, 10 and 15 min). c) Details of the LED excitation source. The LED emission spectrum is centered at 632 nm, as shown on the left, and a scheme of the 6 LEDs array is shown on the right. Cell viability assays. a) C. albicans

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

• test their cytotoxicity in vitro [33]. In this work, the CCK-8 assay was performed to measure the viability of L929 cells upon exposure to FGDA nanocubes. Figure 4a indicates that at 12 h after treatment there were no differences in cell viability between the control and groups treated with different

• conclusion, FGDA nanocubes have no negative impact on cell viability or proliferation, which suggests that these nanocubes can be used for in vivo applications. In vivo MRI with FGDA nanocubes as a contrast agent To visualize the contrast and image quality provided by the FGDA nanocubes in vivo, T1-weighted

• panel) and Fe3O4 nanocubes (bottom panel). (d) Transverse relaxation rate, r2, of FGDA nanocubes (black line) and Fe3O4 nanocubes (red line). (a) CCK-8 cell viability test of L929 cells incubated with FGDA at different Fe concentrations for 12, 24, and 48 h. (b) Live–dead staining of control and FGDA

Luminescent gold nanoclusters for bioimaging applications

• Nonappa

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

•  6D–F). Interestingly, the NC frameworks led to a higher cell viability compared to [Au25(SG)18]. This is attributed to the fact that smaller nanoparticles produce reactive oxygen species and possibly aggregate in the cellular medium. The superstructures were also found to show excellent

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

• held at the accelerating voltage of 80 kV in scanning TEM mode using an Oxford Instruments X-Maxn 80T EDS detector. In vitro cell viability The characterization of the A549 cell viability changes under the pillar[5]arenes 3 and 4 action was performed by the MTT assay. A cell suspension of 150 μL/well

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

• viruses were incubated for 24 h with MDA-MB-231 cells, using 2.6 × 107 viruses per cell. A similar concentration has been used in cell viability tests with CCMV [25][39] and glycol chitosan nanoparticles [40]. The flow cytometry results showed around 90% cell survival after treatment with both viruses

• 7,500 events corresponding to single cells were collected and the Attune Cytometric Software (v2.1) was used to analyze results. For the controls, the same amount of free NanoOrange was used as the one used to load viruses. Cell viability assay MDA-MB-231 cells were seeded in 12-well plates, as

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

• carrier. The present work aims to synthesize poly(1-vinylimidazole) for the delivery of anti-VEGF siRNA to lung cancer cells and explore for the first time the effect of VEGF silencing on differential expression of genes and on cell viability, migration and chemosensitization. Experimental Materials PVI

• heparin/siRNA (v/v) ratio. The samples were electrophoresed on a 1% agarose gel containing 0.5 μg/mL ethidium bromide at 80 V for 20 min. The bands were imaged using the gel documentation system. In vitro studies Cell viability: The effect of blank polymer and polyplex was determined using MTS (3-(4,5

• incubated for 48 h. The cell viability was then assessed using the MTS reagent as described above. Internalization studies: Internalization of the polyplex in A549 cells was studied with Cy3 fluorophore-tagged siRNA. A549 cells at a seeding density of 105 cells/well were cultured on a cover slip in a 6-well

Phase inversion-based nanoemulsions of medium chain triglyceride as potential drug delivery system for parenteral applications

• Eike Folker Busmann,
• Dailén García Martínez,
• Henrike Lucas and
• Karsten Mäder

Beilstein J. Nanotechnol. 2020, 11, 213–224, doi:10.3762/bjnano.11.16

• the aqueous Kolliphor HS 15 solution to normal human dermal fibroblasts (NHDF) and mouse embryonic fibroblasts (3T3) was investigated. The impact of the nanoemulsions and the surfactant solution on the cell viability of the two cell lines after 4 and 24 h is illustrated in Figure 7. The viability of

• the cells treated with the different nanoemulsions is depicted as a function of the concentration of the surfactant Kolliphor HS 15. The resulting graphs indicate a similar behavior of all three nanoemulsions and the aqueous Kolliphor HS 15 solution, namely a decrease of the cell viability at a

• slightly lower than the inhibiting Kolliphor HS 15 concentration, an increased cell viability was observed, which might be caused by a stimulated metabolism of the cells. Table 2 lists the mean inhibitory concentration (IC50) of Kolliphor HS 15 in an aqueous solution of Kolliphor HS 15 (second column) and

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

The different ways to chitosan/hyaluronic acid nanoparticles: templated vs direct complexation. Influence of particle preparation on morphology, cell uptake and silencing efficiency

• Arianna Gennari,
• Julio M. Rios de la Rosa,
• Erwin Hohn,
• Maria Pelliccia,
• Enrique Lallana,
• Roberto Donno,
• Annalisa Tirella and
• Nicola Tirelli

Beilstein J. Nanotechnol. 2019, 10, 2594–2608, doi:10.3762/bjnano.10.250

• , cells were washed with PBS and incubated for 1 h at 37 °C in medium containing 5% (v/v) of MTS solution. Cell viability was measured by reading the absorbance values at 490 nm (Synergy2 Biotek plate reader using Gen5 software) and normalized against the total protein content in each well (BCA assay

• assay, a colourimetric method that measures mitochondrial metabolic activity (data normalized against the protein content, assumed roughly proportional to the cell number). Independently of the preparative method and the MW of chitosan, all formulations had a negligible effect on the cell viability up

• ) Relative cell viability of RAW 264.7 (left) and HCT-116 (right) cell lines as a function of nanoparticle concentrations (0.01–0.5 mg/mL, 24 h incubation). Percentages are relative to the normalized mitochondrial activity of untreated cells. The differences between preparative methods are not statistically

Fully amino acid-based hydrogel as potential scaffold for cell culturing and drug delivery

• Dávid Juriga,
• Evelin Sipos,
• Orsolya Hegedűs,
• Gábor Varga,
• Miklós Zrínyi,
• Krisztina S. Nagy and
• Angéla Jedlovszky-Hajdú

Beilstein J. Nanotechnol. 2019, 10, 2579–2593, doi:10.3762/bjnano.10.249

• degradation properties of the gels containing LYS and CYS at different ratios were investigated since these attributes are crucial for biomedical applications. The swelling degree was determined at different pH values and under redox conditions. For biocompatibility studies, cell viability tests were carried

• tissue engineering [49]. Cell viability was assessed using the WST-1 reagent [2-(4-iodophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium] (Roche, Switzerland), while the cell morphology was observed under a two-photon microscope. Moreover, the release kinetics of the model drug metoprolol

• serum (FBS, Gibco, USA), 2 mM ʟ-glutamine (Gibco, USA), 100 units/mL penicillin and 100 mg/mL streptomycin (Gibco, USA). When the cell culture became subconfluent, it was passaged at a ratio of 1:20 using a 0.05% trypsin/EDTA solution. Cell viability assay Before performing the cell viability assay, the

Design of a nanostructured mucoadhesive system containing curcumin for buccal application: from physicochemical to biological aspects

• Sabrina Barbosa de Souza Ferreira,
• Gustavo Braga,
• Évelin Lemos Oliveira,
• Jéssica Bassi da Silva,
• Hélen Cássia Rosseto,
• Lidiane Vizioli de Castro Hoshino,
• Mauro Luciano Baesso,
• Wilker Caetano,
• Craig Murdoch,
• Helen Elizabeth Colley and
• Marcos Luciano Bruschi

Beilstein J. Nanotechnol. 2019, 10, 2304–2328, doi:10.3762/bjnano.10.222

• utilized for the formulations. After this period, cell viability was indirectly determined by MTT metabolic assay (Figure 12). The viability of Cal27 was significantly decreased (p < 0.05) by the presence of the formulations, regardless of the presence of CUR. This cytotoxic effect was not observed in the