Novel ZnO:Ag nanocomposites induce significant oxidative stress in human fibroblast malignant melanoma (Ht144) cells

• Syeda Arooj,
• Samina Nazir,
• Akhtar Nadhman,
• Nafees Ahmad,
• Bakhtiar Muhammad,
• Ishaq Ahmad,
• Kehkashan Mazhar and
• Rashda Abbasi

Beilstein J. Nanotechnol. 2015, 6, 570–582, doi:10.3762/bjnano.6.59

• (565)NP control and Abs(565)blank represent the background optical density and was measured in NPs only and media only samples. HCEC cells were included as a normal control cell line. Mitochondrial function: cell survival and proliferation assay MTT assay was used to investigate mitochondrial function

• measured relative to the NTC by using MTT assay. Statistical analysis The results are presented as mean ± SD. ANOVA and two tailed t-test were used to investigate the differences between NTC, nanoparticles treated and solvent exposed samples. The photo-oxidative effect of the NPs was measured by comparing

• scavengers mannitol, NaN3 and DMSO on the photo-oxidative activity of ZnO and ZnO:Ag nanocomposites as measured by MTT assay in HT144 (skin cancer) cells. Viability (mean ± SD) was calculated relative to the NTC samples. (a) ZnO, (b) ZnO:Ag (10%), (c) ZnO:Ag (20%), and (d) ZnO:Ag (30%). *p < 0.01, **p

Oxygen-plasma-modified biomimetic nanofibrous scaffolds for enhanced compatibility of cardiovascular implants

• Anna Maria Pappa,
• Varvara Karagkiozaki,
• Silke Krol,
• Spyros Kassavetis,
• Dimitris Konstantinou,
• Charalampos Pitsalidis,
• Lazaros Tzounis,
• Nikos Pliatsikas and
• Stergios Logothetidis

Beilstein J. Nanotechnol. 2015, 6, 254–262, doi:10.3762/bjnano.6.24

• may lead to improved surface properties without affecting the morphology or the mechanical behaviour of the system. In depth nanoindentation measurements were conducted for the scaffolds under optimal conditions to assess the mechanical performance. MTT assay along with imaging techniques were used to

• locations of the samples to 300 nm maximum penetration depth. The nanoindentation load–displacement curves were analyzed by using the Oliver–Pharr model to calculate the elastic modulus of the samples versus the indenter penetration (contact) depth [31]. Cell studies MTT assay: MTT assay (Sigma-Aldrich

• the O2-plasma modified ones, with P = 20 W and P = 40 W. The elastic modulus values of the untreated PCL electrospun scaffolds and the plasma-modified ones (20 W) versus the contact depth. Every curve comes from a nanoindentation measurement to a different surface location of the samples. (a,b) MTT

Release behaviour and toxicity evaluation of levodopa from carboxylated single-walled carbon nanotubes

• Julia M. Tan,
• Jhi Biau Foo,
• Sharida Fakurazi and
• Mohd Zobir Hussein

Beilstein J. Nanotechnol. 2015, 6, 243–253, doi:10.3762/bjnano.6.23

• well-described by a pseudo-second-order kinetic model. A cytotoxicity assay of the synthesized nanohybrid was also carried out in PC12 cell lines (a widely used, in vitro Parkinson’s model for neurotoxicity studies) using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay in order

• carbon nanotubes; levodopa; MTT assay; nanomedicine; Parkinson’s disease; PC12 cells; sustained release; Introduction Over the past few years, the revolutionary development of nanomedicine has emerged as one of the most prominent research areas in biomedical science. This interdisciplinary technology is

• neurons more susceptible to LD. In another related work, conducted by Kura et al. [31], viability of PC12 cells was found to decrease with increasing concentration of LD after 72 h, as determined by MTT assay. In contrast, SWCNT–COOH and SWCNT–LD did not compromise the cell viability of PC12 cells and the

Synthesis of boron nitride nanotubes and their applications

• Saban Kalay,
• Zehra Yilmaz,
• Ozlem Sen,
• Melis Emanet,
• Emine Kazanc and
• Mustafa Çulha

Beilstein J. Nanotechnol. 2015, 6, 84–102, doi:10.3762/bjnano.6.9

• normal MRC-5 fibroblast lung cells were investigated [76]. The hemolytic activity of the pure BNNTs was investigated by UV–vis spectroscopy and the results showed no significant hemolysis of cells that were exposed to the BNNTs. The metabolic activity of the BNNT-exposed cells using an MTT assay was

Anticancer efficacy of a supramolecular complex of a 2-diethylaminoethyl–dextran–MMA graft copolymer and paclitaxel used as an artificial enzyme

• Yasuhiko Onishi,
• Yuki Eshita,
• Rui-Cheng Ji,
• Masayasu Onishi,
• Takashi Kobayashi,
• Masaaki Mizuno,
• Jun Yoshida and
• Naoji Kubota

Beilstein J. Nanotechnol. 2014, 5, 2293–2307, doi:10.3762/bjnano.5.238

• elasticity [32], such as a self-structural change, so that it may become advantageous functionally according to the structural change of a substrate and an intermediary body. MTT assay (WST8) The WST-8 (2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium) method is superior to

• the traditional MTT assay with regard to sensitivity and cell cytotoxicity. The results of survival analysis in vitro by a direct MTT assay (WST8) are shown for PTX-resistant melanoma B16F10 cells (Figure 5a). The resistance of this melanoma cell line to PTX changed clearly, as can be seen from the

Influence of surface-modified maghemite nanoparticles on in vitro survival of human stem cells

• Michal Babič,
• Daniel Horák,
• Lyubov L. Lukash,
• Tetiana A. Ruban,
• Yurii N. Kolomiets,
• Svitlana P. Shpylova and
• Oksana A. Grypych

Beilstein J. Nanotechnol. 2014, 5, 1732–1737, doi:10.3762/bjnano.5.183

• the modified particles were characterized by transmission electron microscopy and dynamic light scattering with regard to morphology, particle size and polydispersity. In vitro survival of human stem cells was then investigated by using the methyl thiazolyl tetrazolium (MTT) assay, which showed that D

• -mannose- and poly(N,N-dimethylacrylamide)-coated γ-Fe2O3 particles exhibit much lower level of cytotoxicity than the non-coated γ-Fe2O3. Keywords: maghemite; magnetic; MTT assay; nanoparticles; stem cells; Introduction One of the most important applications of nanoparticles in biomedicine is the direct

• zero remanent magnetization of the particles, the risk of formation of aggregates in physiological liquids is reduced. MTT assay In order to achieve an efficient cell labeling, the response of intracellular γ-Fe2O3 content on the metabolism of the cells should be taken into account because the

Protein-coated pH-responsive gold nanoparticles: Microwave-assisted synthesis and surface charge-dependent anticancer activity

• Dickson Joseph,
• Nisha Tyagi,
• Christian Geckeler and
• Kurt E.Geckeler

Beilstein J. Nanotechnol. 2014, 5, 1452–1462, doi:10.3762/bjnano.5.158

• OVA > BGG > LYS > BSA > BHG > HIS, OVA > BGG > LYS > BHG > BSA > HIS and OVA > BGG > BSA > BHG > LYS > HIS for the HCT116, HeLa and SCC-7 cell lines, respectively (Table S3, Supporting Information File 1). The MTT assay on the blank proteins showed cell viabilities greater than 80% (Figure S7

• cytotoxicity studies. The reactions were also carried out in the absence of AgNO3, keeping all of the other conditions the same as above. Cell culture and cell viability test (MTT assay) In a similar manner to the methods described in [61], Mouse embryonic fibroblasts (NIH-3T3), human colorectal cancer cells

• and (F) BGG. Scale bar: 20 nm. Variation in the zeta potential of AuNPs prepared by using different proteins as a function of the pH in aqueous medium. Cell viability studies by using MTT assay on (A) NIH-3T3, (B) HCT116, (C) HeLa and (D) SCC-7 cells treated with AuNPs prepared by using different

The protein corona protects against size- and dose-dependent toxicity of amorphous silica nanoparticles

• Dominic Docter,
• Christoph Bantz,
• Dana Westmeier,
• Hajo J. Galla,
• Qiangbin Wang,
• James C. Kirkpatrick,
• Peter Nielsen,
• Michael Maskos and
• Roland H. Stauber

Beilstein J. Nanotechnol. 2014, 5, 1380–1392, doi:10.3762/bjnano.5.151

• MTT assay (Figure 6). Similar to the lung surfactant [32], also epithelial cell of the GI tract are covered by an additional biobarrier, i.e., by mucous matrices [33]. To investigate the impact of mucus associated to GI tract cells on the observed effects, we included the mucus-secreting colorectal

• 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay as described in [54]. Briefly, following NP exposure, cells were incubated with MTT (400 μg/mL; 965 μM; Life Technologies, Carlsbad, USA) for 4 h. The MTT was removed, the cells were washed with PBS and solubilized in dimethyl

• by using the MTT assay. Data are depicted as percentage compared to untreated control cells, which was set to 100% vitality. Results are shown as means ± SD (n = 3). *P < 0.05, **P < 0.01 and ***P < 0.001. Automated microscopy to analyze the impact of exposure to ASP30 on the cell viability. Caco-2

Magnetic-Fe/Fe₃O₄-nanoparticle-bound SN38 as carboxylesterase-cleavable prodrug for the delivery to tumors within monocytes/macrophages

• Hongwang Wang,
• Tej B. Shrestha,
• Matthew T. Basel,
• Raj K. Dani,
• Gwi-Moon Seo,
• Sivasai Balivada,
• Marla M. Pyle,
• Heidy Prock,
• Olga B. Koper,
• Prem S. Thapa,
• David Moore,
• Ping Li,
• Viktor Chikan,
• Deryl L. Troyer and
• Stefan H. Bossmann

Beilstein J. Nanotechnol. 2012, 3, 444–455, doi:10.3762/bjnano.3.51

• of the nanoparticles in the cells and compared to the side scatter of control cells. 10,000 cells were counted and analyzed. This procedure was repeated three times. Data were analyzed by using Cytosoft software (Guava Easycyte Plus System, Millipore Corporation, MA). MTT Assay The MTT assay [46] was

• . Different concentrations of nanoparticles were taken up by double-stable Mo/Ma cells over 24 h; the nanoparticle-concentration ranged from 0 to 320 μg/mL MNP-SN38 in fresh medium. After 24 h, the inhibition of cell proliferation was measured by using the MTT assay (Figure 4). We found only 20% of inhibition

• of nanoparticles contained 0.427 mg of iron, indicating that this amount of iron would be high enough for alternating magnetic field hyperthermia in combination with chemotherapy [54]. The MTT assay indicated that 8 pg of iron can be easily loaded in each cell (20% inhibition of cell proliferation