Development of polycationic amphiphilic cyclodextrin nanoparticles for anticancer drug delivery

• Gamze Varan,
• Juan M. Benito,
• Carmen Ortiz Mellet and
• Erem Bilensoy

Beilstein J. Nanotechnol. 2017, 8, 1457–1468, doi:10.3762/bjnano.8.145

• dextrose solution, leading to severe necrosis and pain at injection site as well as reported incompatibility with intravenous (iv) infusion sets [7]. In order to overcome these side effects of PCX in clinical applications, alternative approaches are developed and evaluated to increase safety and efficacy

Carbon nanomaterials sensitize prostate cancer cells to docetaxel and mitomycin C via induction of apoptosis and inhibition of proliferation

• Kati Erdmann,
• Jessica Ringel,
• Silke Hampel,
• Manfred P. Wirth and
• Susanne Fuessel

Beilstein J. Nanotechnol. 2017, 8, 1307–1317, doi:10.3762/bjnano.8.132

• synergistic nature (Table 1). Effect on cell death rate Both chemotherapeutics mediate cell death via the initiation of apoptosis. Consequently, the effect of the single and combinatory treatments on apoptosis- and necrosis-mediated cell death was determined. A treatment with carbon nanomaterials or

• chemotherapeutics alone elevated the cell death rates only marginally to moderately (Figure 3 and Figure 4). Co-exposure of DU-145 cells with CNFs and DTX or MMC led to significantly increased cell death rates by additional 80% and 130%, respectively (Figure 3). Notably, apoptosis and not necrosis mainly

• were performed. For cellular viability, cellular proliferation and cell colony formation the averaged results were expressed as percentage of control ± relative mean deviation; the control values were set 100%. For cell death rate averaged fractions of dead cells (%) due to apoptosis and necrosis

Needs and challenges for assessing the environmental impacts of engineered nanomaterials (ENMs)

• Michelle Romero-Franco,
• Hilary A. Godwin,
• Muhammad Bilal and
• Yoram Cohen

Beilstein J. Nanotechnol. 2017, 8, 989–1014, doi:10.3762/bjnano.8.101

• caused necrosis of liver tissues and severe renal damage) [10]. Given the above concerns, decision-makers and relevant stakeholders are confronted with the need to identify and utilize reliable methods to ascertain environmental impacts related to the production, use and disposal of ENMs. The default

Antitumor magnetic hyperthermia induced by RGD-functionalized Fe₃O₄ nanoparticles, in an experimental model of colorectal liver metastases

• Oihane K. Arriortua,
• Eneko Garaio,
• Borja Herrero de la Parte,
• Maite Insausti,
• Luis Lezama,
• Fernando Plazaola,
• Jose Angel García,
• Jesús M. Aizpurua,
• Maialen Sagartzazu,
• Mireia Irazola,
• Nestor Etxebarria,
• Ignacio García-Alonso,
• Alberto Saiz-López and
• José Javier Echevarria-Uraga

Beilstein J. Nanotechnol. 2016, 7, 1532–1542, doi:10.3762/bjnano.7.147

• have been responsible of the greater thermal increase detected in MNpG animals. In order to know the tumor damage induced by hyperthermia, a skilled pathologist carried out the morphological assessment of the samples, performing a visual qualitative analysis of tissue necrosis. Pathologic studies with

• , tumor necrosis was observed, especially in MNpG rats, in spite of temperature increases being very similar in liver and tumor tissues. SG animals showed a median value of tumor necrosis of 4% (range: 1–13%). These minimal necrosis changes must be considered as natural degeneration phenomena in relation

• with tumor growth. Nevertheless, in MNpG animals, the mean percentage of necrotic tumor measured by pathologic analyses was increased by 5-fold, reaching 20%; however, these rats showed a very wide range of tissue necrosis (3–99%) (Figure 6). The fact that nearly no damage could be observed in normal

On the pathway of cellular uptake: new insight into the interaction between the cell membrane and very small nanoparticles

• Claudia Messerschmidt,
• Daniel Hofmann,
• Anja Kroeger,
• Katharina Landfester,
• Volker Mailänder and
• Ingo Lieberwirth

Beilstein J. Nanotechnol. 2016, 7, 1296–1311, doi:10.3762/bjnano.7.121

• : ATP depletion; calcium crystallization; cytotoxicity; endocytosis; HeLa cells; LDH; mesenchymal stem cells; morphology; necrosis; particle size; silica nanoparticles; TEM; Introduction Silicon dioxide nanoparticles (SiNPs) are used in a wide range of commercially available products to improve product

• . Mostly, it is assumed that the smaller a nanoparticle, the more pronounced its toxic effect [7][16][17][18][19][20][21][22]. Furthermore, the mode of cell death occurring is usually believed to be necrosis, but some groups have found that the apoptotic machinery is activated [23][24][25][26]. In addition

• outer membrane and general signs of necrosis like vacuolization, nuclear membrane disintegration and mitochondria containing agglomerates of dark appearance in TEM brightfield micrographs (Figure 8). From the morphological point of view, the size and frequency of these agglomerates correlates with the

Tight junction between endothelial cells: the interaction between nanoparticles and blood vessels

• Yue Zhang and
• Wan-Xi Yang

Beilstein J. Nanotechnol. 2016, 7, 675–684, doi:10.3762/bjnano.7.60

• 8-oxoguanine (8-oxoG) as marker showed the attenuation of both active forms of ERK and AKT protein expression caused by Ag NPs [77]. Another research evaluating the toxicity of quantum dots, found that the production of tumor necrosis factor (TNF)-α and CXC-chemokine ligand (CXCL) 8 in human primary

Unraveling the neurotoxicity of titanium dioxide nanoparticles: focusing on molecular mechanisms

• Bin Song,
• Yanli Zhang,
• Jia Liu,
• Xiaoli Feng,
• Ting Zhou and
• Longquan Shao

Beilstein J. Nanotechnol. 2016, 7, 645–654, doi:10.3762/bjnano.7.57

• nasal administration for nine months, after which the glial cells showed over-proliferation and tissue necrosis was found in hippocampal area. Meanwhile, the expression of genes associated with neurotrophin signaling pathways, such as nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF

• tumor necrosis factor-α (TNF-α) in the mouse hippocampus was promoted. At the same time, histopathological changes were observed in the hippocampus; over-proliferation of glial cells, impaired nuclei, and cellular degeneration were observed, all of which contributed to neuro-inflammation. In addition

Novel roles for well-known players: from tobacco mosaic virus pests to enzymatically active assemblies

• Claudia Koch,
• Fabian J. Eber,
• Carlos Azucena,
• Alexander Förste,
• Stefan Walheim,
• Thomas Schimmel,
• Alexander M. Bittner,
• Holger Jeske,
• Hartmut Gliemann,
• Sabine Eiben,
• Fania C. Geiger and
• Christina Wege

Beilstein J. Nanotechnol. 2016, 7, 613–629, doi:10.3762/bjnano.7.54

• necrosis aborting viral multiplication, which has been analyzed in detail especially for TMV [47]. Consequently, direct genetic fusion of enzyme sequences to the ends, or into exposed loops, of viral CPs frequently failed, and also short peptide tags enabling bioaffinity linkage were inserted only

Overview about the localization of nanoparticles in tissue and cellular context by different imaging techniques

• Anja Ostrowski,
• Daniel Nordmeyer,
• Alexander Boreham,
• Cornelia Holzhausen,
• Lars Mundhenk,
• Christina Graf,
• Martina C. Meinke,
• Annika Vogt,
• Sabrina Hadam,
• Jürgen Lademann,
• Eckart Rühl,
• Ulrike Alexiev and
• Achim D. Gruber

Beilstein J. Nanotechnol. 2015, 6, 263–280, doi:10.3762/bjnano.6.25

• reactions directly induced by NP have to be monitored, such as degeneration and necrosis of target structures, NP-induced inflammation with influx and activation of immune cells, tissue fibrosis or even the induction of tumor growth [2][10][11]. Moreover, if the NP are destined for diagnostic or therapeutic

• using optimized contrast setting and thus were able to analyze 243,000 μm3 of liver tissue in a single setting [154]. Furthermore, the image interpretation of TEM is more challenging than that of light microscopic techniques [20][152]. Tissue responses to NP, such as inflammation, fibrosis or necrosis

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

• block ATP. They concluded that the PLL–BNNTs accumulation occurred in the cell membrane with energy dependent pathways. At a concentration of up to 10 µg/mL, the PLL–BNNTs exhibited no evidence of apoptosis, necrosis and membrane permeabilization [79]. Danti et al. investigated the cellular uptake of

Proinflammatory and cytotoxic response to nanoparticles in precision-cut lung slices

• Stephanie Hirn,
• Nadine Haberl,
• Kateryna Loza,
• Matthias Epple,
• Wolfgang G. Kreyling,
• Barbara Rothen-Rutishauser,
• Markus Rehberg and
• Fritz Krombach

Beilstein J. Nanotechnol. 2014, 5, 2440–2449, doi:10.3762/bjnano.5.253

• response of PCLS to Ag-NPs through LDH assay, WST-1 assay, and ELISA assay for CXCL-1 and tumour necrosis factor-α (TNF-α) release. ZnO-NPs served as a soluble control and quartz particles as a non-soluble control, since both particle types have induced cytotoxic as well as inflammatory responses in in

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

• . The DDMC/PTX complex reacts better to melanoma cells at the point of metastasis. This seemed to be reflected by the hemorrhagic necrosis of the tumor, which was considered to be caused by the discharge of the tumor necrosis factor alpha (TNF-α) cytokine by M1 macrophages. Later, the increase in TNF-α

• ) groups. (b): Reprinted from [62]. Two mice of both PTX (left) and DDMC/PTX4 (right) groups after 208 hours from I.P. In the mice of DDMC/PTX4 group necrosis was induced by TNF-α. The increase of TNF-α in an individual has been checked by the phoresis results after RT-PCR. Reprinted from [62]. α,β-tubulin

PVP-coated, negatively charged silver nanoparticles: A multi-center study of their physicochemical characteristics, cell culture and in vivo experiments

• Sebastian Ahlberg,
• Alexandra Antonopulos,
• Jörg Diendorf,
• Ralf Dringen,
• Matthias Epple,
• Rebekka Flöck,
• Wolfgang Goedecke,
• Christina Graf,
• Nadine Haberl,
• Jens Helmlinger,
• Fabian Herzog,
• Frederike Heuer,
• Stephanie Hirn,
• Christian Johannes,
• Stefanie Kittler,
• Manfred Köller,
• Katrin Korn,
• Wolfgang G. Kreyling,
• Fritz Krombach,
• Jürgen Lademann,
• Kateryna Loza,
• Eva M. Luther,
• Marcelina Malissek,
• Martina C. Meinke,
• Daniel Nordmeyer,
• Anne Pailliart,
• Jörg Raabe,
• Fiorenza Rancan,
• Barbara Rothen-Rutishauser,
• Eckart Rühl,
• Carsten Schleh,
• Andreas Seibel,
• Christina Sengstock,
• Lennart Treuel,
• Annika Vogt,
• Katrin Weber and
• Reinhard Zellner

Beilstein J. Nanotechnol. 2014, 5, 1944–1965, doi:10.3762/bjnano.5.205

• , 0.3, and 3 µg silver cm−2. A transient increase of mRNA expression encoding tumor-necrosis factor-alpha (TNF-α) could be detected after 4 h only for the highest silver nanoparticle concentration. The protein levels of TNF-α were, however, not increased after 4 and 24 h, and moreover, no other effects

Biocompatibility of cerium dioxide and silicon dioxide nanoparticles with endothelial cells

• Claudia Strobel,
• Martin Förster and
• Ingrid Hilger

Beilstein J. Nanotechnol. 2014, 5, 1795–1807, doi:10.3762/bjnano.5.190

• granulocyte macrophage colony-stimulating factor (GM-CSF), interleukin-1 α (IL-1α), tumor necrosis factor α (TNF-α), interferon gamma-induced protein 10 (IP-10), plasminogen activator inhibitor-1 (PAI-1), platelet-derived growth factor (PDGF-BB), epidermal growth factor (EGF) and vascular endothelial growth

In vitro and in vivo interactions of selected nanoparticles with rodent serum proteins and their consequences in biokinetics

• Wolfgang G. Kreyling,
• Stefanie Fertsch-Gapp,
• Martin Schäffler,
• Blair D. Johnston,
• Nadine Haberl,
• Christian Pfeiffer,
• Jörg Diendorf,
• Carsten Schleh,
• Stephanie Hirn,
• Manuela Semmler-Behnke,
• Matthias Epple and
• Wolfgang J. Parak

Beilstein J. Nanotechnol. 2014, 5, 1699–1711, doi:10.3762/bjnano.5.180

• twenty-four hours the viability of the PCLS was tested by lactate dehydrogenase (LDH) analysis for cell membrane damage and a WST-1 assay for mitochondrial activity in the cell culture supernatant as well as the release of the pro-inflammatory cytokines tumor necrosis factor alpha (TNF-α) and interleukin

The cell-type specific uptake of polymer-coated or micelle-embedded QDs and SPIOs does not provoke an acute pro-inflammatory response in the liver

• Markus Heine,
• Alexander Bartelt,
• Oliver T. Bruns,
• Denise Bargheer,
• Artur Giemsa,
• Barbara Freund,
• Ludger Scheja,
• Christian Waurisch,
• Alexander Eychmüller,
• Rudolph Reimer,
• Horst Weller,
• Peter Nielsen and
• Joerg Heeren

Beilstein J. Nanotechnol. 2014, 5, 1432–1440, doi:10.3762/bjnano.5.155

• process that is dependent on the LDL receptor and apolipoprotein E, by hepatocytes. Gene expression analysis of pro-inflammatory markers such as tumor necrosis factor alpha (TNFα) or chemokine (C-X-C motif) ligand 10 (Cxcl10) indicated that 48 h after injection internalized nanocrystals did not provoke

Mimicking exposures to acute and lifetime concentrations of inhaled silver nanoparticles by two different in vitro approaches

• Fabian Herzog,
• Kateryna Loza,
• Sandor Balog,
• Martin J. D. Clift,
• Matthias Epple,
• Peter Gehr,
• Alke Petri-Fink and
• Barbara Rothen-Rutishauser

Beilstein J. Nanotechnol. 2014, 5, 1357–1370, doi:10.3762/bjnano.5.149

• measured the release of lactate dehydrogenase (LDH) as a marker for the cell integrity to assess the cytotoxic potential of cells exposed to Ag NPs. Also included were cultures incubated with lipopolysaccharide (LPS) as a pro-inflammatory stimulus and tumor necrosis factor alpha (TNF-α) as positive control

• dismutase 1 (SOD1) [GenBank: NM_000454], interleukin-8 (IL8) [GenBank: NM_000584] and tumor necrosis factor alpha (TNFA) [GenBank: NM_000594] were determined. Primer sequences (Microsynth AG, Balgach, Switzerland) were the following: GAPDH: forward 5’- AAC AGC CTC AAG ATC ATC AGC-3’, reverse 5’- GGA TGA TGT

Biocalcite, a multifunctional inorganic polymer: Building block for calcareous sponge spicules and bioseed for the synthesis of calcium phosphate-based bone

• Xiaohong Wang,
• Heinz C. Schröder and
• Werner E. G. Müller

Beilstein J. Nanotechnol. 2014, 5, 610–621, doi:10.3762/bjnano.5.72

• scaffold must possess the inorganic/organic 3D structure of bone and an appropriate porosity [69] that allows the ingrowth of cells and an efficient transport of cytokines, growth factors, and nutrients. To avoid necrosis within larger implants, a suitable scaffold must also allow an efficient

Cytotoxic and proinflammatory effects of PVP-coated silver nanoparticles after intratracheal instillation in rats

• Nadine Haberl,
• Stephanie Hirn,
• Alexander Wenk,
• Jörg Diendorf,
• Matthias Epple,
• Blair D. Johnston,
• Fritz Krombach,
• Wolfgang G. Kreyling and
• Carsten Schleh

Beilstein J. Nanotechnol. 2013, 4, 933–940, doi:10.3762/bjnano.4.105

• -dependent decrease in cell viability. In addition, a proinflammatory response was shown by increased levels of tumor necrosis factor-α (TNF-α), macrophage inflammatory protein-2 (MIP-2), and interleukin-1β (IL-1β) [18]. Furthermore, AgNP caused damage to mitochondria and an increased production of reactive

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 cell proliferation at 160 μg/mL. Our aim is the loading of high payloads onto each delivery cell without causing a high level of necrosis or apoptosis of the delivery cells. Even a loading of 320 μg/mL of nanoparticles in the medium inhibits only 50% of the cell proliferation. We are also