Incorporation of doxorubicin in different polymer nanoparticles and their anticancer activity

• Sebastian Pieper,
• Hannah Onafuye,
• Dennis Mulac,
• Jindrich Cinatl Jr.,
• Mark N. Wass,
• Martin Michaelis and
• Klaus Langer

Beilstein J. Nanotechnol. 2019, 10, 2062–2072, doi:10.3762/bjnano.10.201

• (vinyl alcohol) (PVA, 30,000–70,000 Da), bovine serum albumin (BSA), HSA, and glutaraldehyde were obtained from Sigma-Aldrich Chemie GmbH (Karlsruhe, Germany). Dulbecco's Phosphate buffered saline (PBS) was purchased from Biochrom GmbH (Berlin, Germany). Doxorubicin was obtained from LGC Standards GmbH

Magnetic properties of biofunctionalized iron oxide nanoparticles as magnetic resonance imaging contrast agents

• Natalia E. Gervits,
• Andrey A. Gippius,
• Alexey V. Tkachev,
• Evgeniy I. Demikhov,
• Sergey S. Starchikov,
• Igor S. Lyubutin,
• Alexander L. Vasiliev,
• Vladimir P. Chekhonin,
• Maxim A. Abakumov,
• Alevtina S. Semkina and
• Alexander G. Mazhuga

Beilstein J. Nanotechnol. 2019, 10, 1964–1972, doi:10.3762/bjnano.10.193

• ) was added to the nanoparticle suspension. Then, 920 μL of glutaraldehyde was added and the mixture was incubated for 15 min with constant stirring. After that, the reaction was stopped by adding a glycine solution in water (3 M, 1 mL, pH 9.2), followed by stirring for 1 h. Finally, a NaBH4 solution in

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

• . Subsequently, the brains of the tumor-bearing mice were separated and the tumor tissue were removed and immersed in 2.5% glutaraldehyde for 2 h at 4 °C, followed by washing with PBS and the remaining steps as previously reported [27]. Primary safety evaluation of PNPs The cytotoxicity of PNPs against U87MG and

Nanoarchitectonics meets cell surface engineering: shape recognition of human cells by halloysite-doped silica cell imprints

• Elvira Rozhina,
• Ilnur Ishmukhametov,
• Svetlana Batasheva,
• Farida Akhatova and
• Rawil Fakhrullin

Beilstein J. Nanotechnol. 2019, 10, 1818–1825, doi:10.3762/bjnano.10.176

• , Bruker, USA) operating in a PeakForce Tapping mode in air. The cells incubated with imprints for 15 minutes were washed with buffer; the precipitate was kept in glutaraldehyde (Sigma) for 1 hour, then washed with buffer and Milli-Q. Standard silicon nitride ScanAsyst-Air probes (Bruker) with resonance

Doxorubicin-loaded human serum albumin nanoparticles overcome transporter-mediated drug resistance in drug-adapted cancer cells

• Hannah Onafuye,
• Sebastian Pieper,
• Dennis Mulac,
• Jindrich Cinatl Jr.,
• Mark N. Wass,
• Klaus Langer and
• Martin Michaelis

Beilstein J. Nanotechnol. 2019, 10, 1707–1715, doi:10.3762/bjnano.10.166

• prepared by desolvation as previously described [13][14][15][16][17]. The nanoparticles were stabilised by the cross-linking of free amino groups present in albumin. Three different nanoparticle preparations were produced using glutaraldehyde at amounts that corresponded to a theoretical cross-linking of

• . HSA (0%) nanoparticles displayed a large particle size of almost 1 µm and a high polydispersity of 0.5, confirming that no stable nanoparticles had formed (Table 1). The three HSA nanoparticle preparations stabilised by the different glutaraldehyde concentrations displayed similar diameters between

• doxorubicin (UKF-NB-3rDOX20) and vincristine (UKF-NB-3rVCR1), which both display ABCB1 activity and resistance to doxorubicin. The HSA nanoparticles were prepared by desolvation and stabilised by glutaraldehyde, which crosslinks amino groups present in albumin molecules [13][14][15][16][17]. Glutaraldehyde

A new bioinspired method for pressure and flow sensing based on the underwater air-retaining surface of the backswimmer Notonecta

• Matthias Mail,
• Adrian Klein,
• Horst Bleckmann,
• Anke Schmitz,
• Torsten Scherer,
• Peter T. Rühr,
• Goran Lovric,
• Robin Fröhlingsdorf,
• Stanislav N. Gorb and
• Wilhelm Barthlott

Beilstein J. Nanotechnol. 2018, 9, 3039–3047, doi:10.3762/bjnano.9.282

• microstructure of the setal bases. The hemelytra were cut into several pieces. The pieces were fixed in 2.5% glutaraldehyde and 1.5% osmium tetroxide in cacodylate buffer (380 mOsmol, pH 7.1). After dehydrating in ethanol, the pieces were embedded in Epon 812 via epoxy propane as an intermedium. The clavus and

Enhanced antineoplastic/therapeutic efficacy using 5-fluorouracil-loaded calcium phosphate nanoparticles

• Shanid Mohiyuddin,
• Saba Naqvi and
• Gopinath Packirisamy

Beilstein J. Nanotechnol. 2018, 9, 2499–2515, doi:10.3762/bjnano.9.233

• followed by incubation at an IC50 concentration of CaP@5-FU NPs for around 24 h. The treated cells were later washed with PBS and processed with glutaraldehyde fixation along with a gradient (30%, 50%, 70%) ethanol fixation. In control cells, CaP@5-FU NPs were not added in order to compare the difference

The structural and chemical basis of temporary adhesion in the sea star Asterina gibbosa

• Birgit Lengerer,
• Marie Bonneel,
• Mathilde Lefevre,
• Elise Hennebert,
• Philippe Leclère,
• Emmanuel Gosselin,
• Peter Ladurner and
• Patrick Flammang

Beilstein J. Nanotechnol. 2018, 9, 2071–2086, doi:10.3762/bjnano.9.196

• voluntary detachment, the footprints were rinsed with MilliQ water to prevent the formation of salt crystals. Some of them were stained with a 0.05% (w/v) crystal violet solution in deionised water. Transmission electron microscopy (TEM) For TEM, whole tube feet were fixed by immersion in 3% glutaraldehyde

Fabrication of photothermally active poly(vinyl alcohol) films with gold nanostars for antibacterial applications

• Mykola Borzenkov,
• Maria Moros,
• Claudia Tortiglione,
• Serena Bertoldi,
• Nicola Contessi,
• Silvia Faré,
• Angelo Taglietti,
• Agnese D’Agostino,
• Piersandro Pallavicini,
• Maddalena Collini and
• Giuseppe Chirico

Beilstein J. Nanotechnol. 2018, 9, 2040–2048, doi:10.3762/bjnano.9.193

• properties of the films [20]. Citric acid was chosen as the crosslinking agent as, in comparison with the widely used method of crosslinking with glutaraldehyde, it is a non-toxic compound approved as a food additive, thus providing a green crosslinking route [20][25]. GNSs were synthesized via a seed-growth

Preparation of micro/nanopatterned gelatins crosslinked with genipin for biocompatible dental implants

• Reika Makita,
• Tsukasa Akasaka,
• Seiichi Tamagawa,
• Yasuhiro Yoshida,
• Saori Miyata,
• Hirofumi Miyaji and
• Tsutomu Sugaya

Beilstein J. Nanotechnol. 2018, 9, 1735–1754, doi:10.3762/bjnano.9.165

• ) [30], coating on patterned substrates [31][32][33], self-assembly of collagen fibers [34], and crosslinking, using glutaraldehyde [35], formaldehyde [36], carbodiimide [37], genipin [38][39], riboflavin [40], transglutaminase [41], silane coupling agents [42], as well as thermal dehydration [43][44

• of biological tissues and for the reinforcement of scaffolds. Genipin has low toxicity, being about 10,000 times less cytotoxic than other crosslinking agents, such as glutaraldehyde [47]. Crosslinking with genipin has been shown to result in an improvement in tensile strength, elastic modulus, and

• in the cell culture medium, gelatin surfaces with grooves (500 nm width and 500 nm height) were immersed in Dulbecco’s modified Eagle’s medium (DMEM) containing 10% fetal bovine serum (FBS). After 1 h, 7 days, or 14 days of incubation, the immersed gelatin grooves were fixed with glutaraldehyde and

Noble metal-modified titania with visible-light activity for the decomposition of microorganisms

• Maya Endo,
• Zhishun Wei,
• Kunlei Wang,
• Baris Karabiyik,
• Kenta Yoshiiri,
• Paulina Rokicka,
• Bunsho Ohtani,
• Agata Markowska-Szczupak and
• Ewa Kowalska

Beilstein J. Nanotechnol. 2018, 9, 829–841, doi:10.3762/bjnano.9.77

• times with sterile Milli-Q water and mounted on a piece of copper tape. The bacterial cells were fixed by 2.0% glutaraldehyde and 2.0% paraformaldehyde in 30 mM HEPES buffer for 1 h. After fixation, cells were washed with 30 mM HEPES buffer for 1 min, dehydrated by a graded series of ethanol (30, 50, 70

Ultralight super-hydrophobic carbon aerogels based on cellulose nanofibers/poly(vinyl alcohol)/graphene oxide (CNFs/PVA/GO) for highly effective oil–water separation

• Zhaoyang Xu,
• Huan Zhou,
• Sicong Tan,
• Xiangdong Jiang,
• Weibing Wu,
• Jiangtao Shi and
• Peng Chen

Beilstein J. Nanotechnol. 2018, 9, 508–519, doi:10.3762/bjnano.9.49

• Zhejiang Lishui, China. Graphite powder (40 μm), used as the source for GO, was obtained from Qingdao Henglide Graphite Co., Ltd. Poly(vinyl alcohol) (PVA, Mw ≈ 95,000 g/mol), glutaraldehyde (GA, crosslinker, 25 wt % in H2O), potassium hydroxide (KOH), Sudan III, acetic acid (CH3COOH), hydrogen peroxide

• ), and GO solution (4.5 g, 3.34 wt %) were mixed together by vigorous stirring for 1 h. Sulfuric acid (0.8 mL, 1.0 vol %) was then added to the CNF/PVA/GO solution with pH of approximately 5. Then, a glutaraldehyde solution (0.8 mL, 25 wt %) was added to the resulting CNF/PVA/GO solution with mechanical

Bombyx mori silk/titania/gold hybrid materials for photocatalytic water splitting: combining renewable raw materials with clean fuels

• Stefanie Krüger,
• Michael Schwarze,
• Otto Baumann,
• Christina Günter,
• Michael Bruns,
• Christian Kübel,
• Dorothée Vinga Szabó,
• Rafael Meinusch,
• Verónica de Zea Bermudez and
• Andreas Taubert

Beilstein J. Nanotechnol. 2018, 9, 187–204, doi:10.3762/bjnano.9.21

• ), calcium chloride dihydrate (CaCl2·2H2O, ≥99%, Carl Roth), ethanol (EtOH; 99%, VWR), ethyl acetoacetate (EtAcAc, 99%, Alfa Aesar), glutaraldehyde solution (GA, 25% in H2O, Sigma-Aldrich), hydrogen tetrachloridoaurate(III) trihydrate (HAuCl4·3H2O, 99.99%, Alfa Aesar), poly(ethylene oxide) (PEO780, nominal

• washed three times with 50 mL of water at room temperature. Characterization Samples for all transmission electron microscopy (TEM) investigations were prepared as follows: small pieces (ca. 2 mm2) of the wet hybrid materials were immersed in a 3% glutaraldehyde solution in 0.1 M phosphate buffer (pH 7

Involvement of two uptake mechanisms of gold and iron oxide nanoparticles in a co-exposure scenario using mouse macrophages

• Dimitri Vanhecke,
• Dagmar A. Kuhn,
• Dorleta Jimenez de Aberasturi,
• Sandor Balog,
• Ana Milosevic,
• Dominic Urban,
• Diana Peckys,
• Niels de Jonge,
• Wolfgang J. Parak,
• Alke Petri-Fink and
• Barbara Rothen-Rutishauser

Beilstein J. Nanotechnol. 2017, 8, 2396–2409, doi:10.3762/bjnano.8.239

• , ethanol, and deionized water, phosphate-buffered saline (PBS) at a 10× solution, electron microscopy grade glutaraldehyde (GA) 25% solution, D-saccharose, glycine, biotin-free and molecular biology grade albumin fraction V (BSA), and sodium cacodylate trihydrate were obtained from Carl Roth GmbH + Co. KG

• pixel-dwell times between 30 and 100 μs were used. The image sizes were 2048 × 1768 or 1024 × 884 pixels. The electron dose for an image ranged between 81 and 376 e−/Å2, and was below the limit of radiation damage [49]. Transmission electron microscopy Fixation was carried out with 2.5% glutaraldehyde

A biofunctionalizable ink platform composed of catechol-modified chitosan and reduced graphene oxide/platinum nanocomposite

• Peter Sobolewski,
• Agata Goszczyńska,
• Małgorzata Aleksandrzak,
• Karolina Urbaś,
• Joanna Derkowska,
• Agnieszka Bartoszewska,
• Jacek Podolski,
• Ewa Mijowska and
• Mirosława El Fray

Beilstein J. Nanotechnol. 2017, 8, 1508–1514, doi:10.3762/bjnano.8.151

• microplotter (Sonoplot GIX Microplotter Desktop). As a proof of concept, printed patterns were biofunctionalized with DNA oligonucleotide probes for Streptococcus agalactiae (Group B streptococcus) using glutaraldehyde as a linker. Confocal microscopy revealed the successful hybridization of complementary

• of concept, we reacted our amine-terminated DNA oligonucleotide probes for Group B streptococcus (GBS) to the printed, annealed nanocomposite ink stripes using glutaraldehyde as a linker [15]. Next, the modified structures were allowed to hybridize with Cy3-fluorescence-labeled, PCR-amplified

• the catechol-modified chitosan matrix (Figure 4B). Chitosan/DNA interactions are largely driven by electrostatic interaction and, as a result, solution pH value, degree of deacetylation and molecular weight all play important roles [18]. Following biofunctionalization via glutaraldehyde linker to the

Low uptake of silica nanoparticles in Caco-2 intestinal epithelial barriers

• Dong Ye,
• Mattia Bramini,
• Delyan R. Hristov,
• Sha Wan,
• Anna Salvati,
• Christoffer Åberg and
• Kenneth A. Dawson

Beilstein J. Nanotechnol. 2017, 8, 1396–1406, doi:10.3762/bjnano.8.141

• and processed using Imaris imaging software (BitPlane, Zurich, Switzerland). Transmission electron microscopy After exposure to the nanoparticles as described above, Caco-2 cell monolayers grown on 3.0 μm PTFE transwell membranes were fixed with glutaraldehyde (2.5%, v/v) at room temperature for 1 h

Characterization of ferrite nanoparticles for preparation of biocomposites

• Urszula Klekotka,
• Magdalena Rogowska,
• Dariusz Satuła and
• Beata Kalska-Szostko

Beilstein J. Nanotechnol. 2017, 8, 1257–1265, doi:10.3762/bjnano.8.127

• nanoparticles was functionalized afterwards with –COOH and –NH2 groups to obtain a bioactive layer. To achieve our goal, two different modification approaches were realized. In the first one, glutaraldehyde was attached to the nanoparticles as a linker. In the second one, direct bonding of such nanoparticles

• dispersive X-ray and Mössbauer spectroscopy. The effect of the obtained biocomposites was monitored by Fourier transform infrared spectroscopy. The obtained results show that in some cases the use of glutaraldehyde was crucial (albumin). Keywords: albumin; EDX; glucose oxidase; IR spectroscopy; lipase

• , we have used nanoparticles with or without attached glutaraldehyde that served as a linker between the nanoparticle and enzymes and gives more space for interaction. The enzymes tested in this paper were: albumin, glucose oxidase, lipase, and trypsin. This study is a continuation of our previous

Silicon microgrooves for contact guidance of human aortic endothelial cells

• Sara Fernández-Castillejo,
• Pilar Formentín,
• Úrsula Catalán,
• Josep Pallarès,
• Lluís F. Marsal and
• Rosa Solà

Beilstein J. Nanotechnol. 2017, 8, 675–681, doi:10.3762/bjnano.8.72

• cell adhesion and surface stability following the 3-amimoptopyl triethoxylane (APTES)–glutaraldehyde (GTA)–collagen sequence as described in Experimental section. Cytotoxicity of silicon substrates Cytotoxicity was assessed by measuring LDH activity 24 h, 2 days, 3 days, 6 days and 7 days (D1–D7) after

A novel electrochemical nanobiosensor for the ultrasensitive and specific detection of femtomolar-level gastric cancer biomarker miRNA-106a

• Maryam Daneshpour,
• Kobra Omidfar and
• Hossein Ghanbarian

Beilstein J. Nanotechnol. 2016, 7, 2023–2036, doi:10.3762/bjnano.7.193

• , respectively). Furthermore, the shifted N–H bond has formed a detectable peak at 1502 cm−1 in the spectrum of TMC@Fe3O4 NPs. This curve contains another notable peak at about 1630 cm−1 which arises from the interaction between the N–H groups of TMC and the CHO group of glutaraldehyde known as “Schiff base

• -ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), N-hydroxysuccinimide (NHS), 11-mercaptoundecanoic acid (MUA), streptavidin, K3Fe(CN)6, and K4Fe(CN)6 were purchased from Sigma Chemical Company (USA). Analytical grade HCl, NaCl, D-glucose, glutaraldehyde, N-methylpyrrolidone (NMP), iodomethane, sodium

• were synthesized using D-glucose as the reducing agent via a typical short procedure at 60 °C [36]. In the following, 200 mg of magnetic NPs was exposed to appropriate amount of previously produced TMC (Fe3O4/TMC molar ratio of 1) in a 20 mL solution containing glutaraldehyde (25%, 2 mL), NaCl (0.5 M

Layered composites of PEDOT/PSS/nanoparticles and PEDOT/PSS/phthalocyanines as electron mediators for sensors and biosensors

• Celia García-Hernández,
• Cristina García-Cabezón,
• Fernando Martín-Pedrosa,
• José Antonio De Saja and
• María Luz Rodríguez-Méndez

Beilstein J. Nanotechnol. 2016, 7, 1948–1959, doi:10.3762/bjnano.7.186

• deposited onto the PEDOT/PSS/EM electrode. After drying at room temperature for approximately 45 min., the biosensors were immersed in glutaraldehyde (2.5% v/v, buffer solution) for 5 min and dried in air for 15 min at room temperature. The biosensors were then rinsed with phosphate buffer to remove any

Facile fabrication of luminescent organic dots by thermolysis of citric acid in urea melt, and their use for cell staining and polyelectrolyte microcapsule labelling

• Nadezhda M. Zholobak,
• Anton L. Popov,
• Alexander B. Shcherbakov,
• Nelly R. Popova,
• Mykhailo M. Guzyk,
• Valeriy P. Antonovich,
• Alla V. Yegorova,
• Yuliya V. Scrypynets,
• Inna I. Leonenko,
• Alexander Ye. Baranchikov and
• Vladimir K. Ivanov

Beilstein J. Nanotechnol. 2016, 7, 1905–1917, doi:10.3762/bjnano.7.182

• was determined, according to the protocol of the manufacturer. Cellular staining We used two methods for visualizing cells by synthesized O-dots: without fixing, and with fixing, using a mixture containing 2.5% glutaraldehyde (Sigma) and 4% paraformaldehyde (Sigma) in phosphate-buffered saline (pH 7.2

Viability and proliferation of endothelial cells upon exposure to GaN nanoparticles

• Tudor Braniste,
• Ion Tiginyanu,
• Tibor Horvath,
• Simion Raevschi,
• Serghei Cebotari,
• Marco Lux,
• Axel Haverich and
• Andres Hilfiker

Beilstein J. Nanotechnol. 2016, 7, 1330–1337, doi:10.3762/bjnano.7.124

• fixed, dehydrated, dried, and a thin metallic layer was sputtered on top of them in order to avoid charging effects during scanning. The fixation process was performed at 4 °C in 2.5% glutaraldehyde for 12 h after the samples were kept in 0.2 M sodium cacodylate buffer for 24 h. The dehydration process

Improved biocompatibility and efficient labeling of neural stem cells with poly(L-lysine)-coated maghemite nanoparticles

• Igor M. Pongrac,
• Marina Dobrivojević,
• Lada Brkić Ahmed,
• Michal Babič,
• Miroslav Šlouf,
• Daniel Horák and
• Srećko Gajović

Beilstein J. Nanotechnol. 2016, 7, 926–936, doi:10.3762/bjnano.7.84

• reagent, washed once with DMEM/F-12 medium, separated by centrifugation and fixed overnight with 2% glutaraldehyde in 0.1 M phosphate buffer, post-fixed in 1% osmium tetroxide, and contrasted in 2% uranyl acetate in water. The samples were dehydrated in acetone and embedded in resin Durcupan (Sigma

Active multi-point microrheology of cytoskeletal networks

• Tobias Paust,
• Tobias Neckernuss,
• Lina Katinka Mertens,
• Ines Martin,
• Michael Beil,
• Paul Walther,
• Thomas Schimmel and
• Othmar Marti

Beilstein J. Nanotechnol. 2016, 7, 484–491, doi:10.3762/bjnano.7.42

• measurement according to [31]. The test of the functionality of the setup was performed in bi-distilled water by observing only the trapped particle. For SEM measurements the networks were fixed with 2.5% glutaraldehyde (in 0.1 M phosphate buffer with 1% saccharose) for 30 min and contrasted with OsO4 (2% in

Time-dependent growth of crystalline Au⁰-nanoparticles in cyanobacteria as self-reproducing bioreactors: 2. Anabaena cylindrica

• Liz M. Rösken,
• Felix Cappel,
• Susanne Körsten,
• Christian B. Fischer,
• Andreas Schönleber,
• Sander van Smaalen,
• Stefan Geimer,
• Christian Beresko,
• Georg Ankerhold and
• Stefan Wehner

Beilstein J. Nanotechnol. 2016, 7, 312–327, doi:10.3762/bjnano.7.30

• samples were chemically fixed using glutaraldehyde and osmium tetroxide, dehydrated and embedded in epoxy resin according to standard procedures, see Supporting Information File 1 for a detailed description of the method. Ultrathin sections (about 60 nm thick) were analyzed in a Zeiss EM 902A transmission

• with an overall concentration of 0.8 mM Au3+, samples were taken after 15 minutes, 9.25 hours and 25.75 hours. These samples were processed for analysis by transmission electron microscopy by separating the supernatant and biomass by centrifugation, washing the biomass and fixing it with glutaraldehyde