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

• preparation by solvent displacement led to the smallest nanoparticles. In PLGA nanoparticles, the drug load could be optimised using solvent displacement at pH 7 reaching 53 µg doxorubicin/mg nanoparticle. These PLGA nanoparticles displayed sustained doxorubicin release kinetics compared to the more burst

• -like kinetics of the other preparations. In neuroblastoma cells, doxorubicin-loaded PLGA-PEG nanoparticles (presumably due to their small size) and PLGA nanoparticles prepared by solvent displacement at pH 7 (presumably due to their high drug load and superior drug release kinetics) exerted the

• [50]. To optimise the loading efficiency and drug release kinetics of PLGA nanoparticles the pH value of the stabiliser solution used during nanoparticle preparation was increased to 7. At this pH value, doxorubicin exists in the more lipophilic deprotonated form [51]. The use of PVA solution at pH 7

Pulsed laser synthesis of highly active Ag–Rh and Ag–Pt antenna–reactor-type plasmonic catalysts

• Kenneth A. Kane and
• Massimo F. Bertino

Beilstein J. Nanotechnol. 2019, 10, 1958–1963, doi:10.3762/bjnano.10.192

• . Afterwards, 0.015 mL of fresh aqueous 10−1 M NaBH4 was spiked into the mixture, as reducing agent, and the time-dependent absorption spectrum was recorded. As NaBH4 was used in excess, the reaction kinetics are assumed to follow a first-order rate law. The absorption peak at 400 nm (Abs400nm) forms

• to be stable, and the activity was measured for a variety of Ag–Rh/Pt loading ratios, demonstrating that the enhancement persisted at low loading ratios. Further and future inquiry will include: (1) studying the reaction kinetics in the absence of visible light to confirm plasmonic enhancement; (2

Biocatalytic oligomerization-induced self-assembly of crystalline cellulose oligomers into nanoribbon networks assisted by organic solvents

• Yuuki Hata,
• Yuka Fukaya,
• Toshiki Sawada,
• Masahito Nishiura and
• Takeshi Serizawa

Beilstein J. Nanotechnol. 2019, 10, 1778–1788, doi:10.3762/bjnano.10.173

• ], distorted nanosheets with a bilayer structure [35], helical nanorods with a bilayer structure [35], and network structures composed of nanoribbon-shaped lamellar crystals [33][42][43][44][45][46] have been successfully constructed by changing the enzymatic reactions, tuning the self-assembly kinetics

Growth dynamics and light scattering of gold nanoparticles in situ synthesized at high concentration in thin polymer films

• Corentin Guyot,
• Philippe Vandestrick,
• Ingrid Marenne,
• Olivier Deparis and
• Michel Voué

Beilstein J. Nanotechnol. 2019, 10, 1768–1777, doi:10.3762/bjnano.10.172

• mass ratio increases, the absorbance reaches an increasing plateau value. Moreover, increasing the annealing temperature increases the reduction kinetics. The plateau value is reached within shorter times. Besides playing a role in the growth kinetics of the nanoparticles by promoting the reduction of

TiO₂/GO-coated functional separator to suppress polysulfide migration in lithium–sulfur batteries

• Ning Liu,
• Lu Wang,
• Taizhe Tan,
• Yan Zhao and
• Yongguang Zhang

Beilstein J. Nanotechnol. 2019, 10, 1726–1736, doi:10.3762/bjnano.10.168

• electrochemical impedance spectroscopy (EIS) analysis to analyze the charge transfer kinetics in Li/S batteries with pristine and TiO2/GO-coated separators. Figure 8 presents the Nyquist plots of Li/S batteries with pristine and TiO2/GO-coated separators before and after cycling. As shown in Figure 8a, the charge

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

• paclitaxel with albumin may differ from that of doxorubicin. Hence, variations in drug binding and drug release kinetics may be responsible for this difference. Despite the prominent role of ABCB1 as a drug resistance mechanism, attempts to exploit it as drug target have failed so far, despite the

Tuning the performance of vanadium redox flow batteries by modifying the structural defects of the carbon felt electrode

• Ditty Dixon,
• Deepu Joseph Babu,
• Aiswarya Bhaskar,
• Hans-Michael Bruns,
• Joerg J. Schneider,
• Frieder Scheiba and
• Helmut Ehrenberg

Beilstein J. Nanotechnol. 2019, 10, 1698–1706, doi:10.3762/bjnano.10.165

• configuration, showed poor electrochemical performance for the positive (V5+/V4+) redox reaction. Taking into account that the negative redox reaction is the limiting reaction in VRFB, the overall enhancement in the full cell performance was purely attributed to enhancement in the V3+/V2+ redox kinetics due to

Layered double hydroxide/sepiolite hybrid nanoarchitectures for the controlled release of herbicides

• Ediana Paula Rebitski,
• Margarita Darder and
• Pilar Aranda

Beilstein J. Nanotechnol. 2019, 10, 1679–1690, doi:10.3762/bjnano.10.163

• that they remain attached to the silicate fibers (Figure 6F). In vitro release of MCPA in water The release of MCPA from the hybrid nanoarchitectures was evaluated in in vitro tests in deionized water (pH approx. 5.5), simulating the conditions of rain. The kinetics of the release depends on the

• nanoarchitecture composition (Figure 7), but in all cases an initial fast release is observed, followed by another zone showing slower kinetics. These two regimes could be due to the initial release of more accessible MCPA, most likely related to interparticle diffusion, while the second zone could be due to

• hydration or the presence of OH− species in the systems consolidated at lower temperature, which determines a different mechanism of attack of H+ to produce the degradation of the LDH and the subsequent release of entrapped MCPA. The fastest kinetics is observed with the lowest LDH content (Figure 7 and

Nanoporous smartPearls for dermal application – Identification of optimal silica types and a scalable production process as prerequisites for marketed products

• David Hespeler,
• Sanaa El Nomeiri,
• Jonas Kaltenbach and
• Rainer H. Müller

Beilstein J. Nanotechnol. 2019, 10, 1666–1678, doi:10.3762/bjnano.10.162

• the skin. The dissolution kinetics of rutin from the smartPearls is much faster than from the raw rutin powder. With smartPearls, the solubility saturation is reached after almost 1 min, for the raw rutin powder, it takes 5–10 min. For the dermal formulation the kinetics is not relevant, only the

Stationary beam full-field transmission helium ion microscopy using sub-50 keV He⁺: Projected images and intensity patterns

• Michael Mousley,
• Santhana Eswara,
• Olivier De Castro,
• Olivier Bouton,
• Nico Klingner,
• Christoph T. Koch,
• Gregor Hlawacek and
• Tom Wirtz

Beilstein J. Nanotechnol. 2019, 10, 1648–1657, doi:10.3762/bjnano.10.160

• kinetics related to charge build-up and charge dissipation processes. To explore the possible correlation between the local surface morphology and the observed intensity patterns, the same BN sample was also imaged in the prototype THIM, where Figure 4C shows the THIM intensity pattern. Through a

Synthesis of P- and N-doped carbon catalysts for the oxygen reduction reaction via controlled phosphoric acid treatment of folic acid

• Rieko Kobayashi,
• Takafumi Ishii,
• Yasuo Imashiro and
• Jun-ichi Ozaki

Beilstein J. Nanotechnol. 2019, 10, 1497–1510, doi:10.3762/bjnano.10.148

• applied to all types of N-containing compounds, e.g., naturally occurring ones. However, fundamental studies on the kinetics and mechanisms of ORR activity enhancement induced by PN-doping are required to clarify the remaining questions and will be conducted in due course. Experimental CPAT N- and P

Hierarchically structured 3D carbon nanotube electrodes for electrocatalytic applications

• Pei Wang,
• Katarzyna Kulp and
• Michael Bron

Beilstein J. Nanotechnol. 2019, 10, 1475–1487, doi:10.3762/bjnano.10.146

• energy conversion and storage, since they, in addition to their nonpolluting nature and low operating temperature, run on an easily handled and cheap liquid fuel. However, the slow kinetics of methanol oxidation at the anode and the methanol crossover through the electrolyte membrane from anode to

• cathode are still major obstacles that hinder the broad market implementation of DMFCs. The slow kinetics are mainly caused by incomplete methanol oxidation accompanied by the formation of adsorbed carbonaceous reaction intermediates, which poison the Pt surface [14][15][16][17][18][19]. Most strategies

Selective gas detection using Mn₃O₄/WO₃ composites as a sensing layer

• Yongjiao Sun,
• Zhichao Yu,
• Wenda Wang,
• Pengwei Li,
• Gang Li,
• Wendong Zhang,
• Lin Chen,
• Serge Zhuivkov and
• Jie Hu

Beilstein J. Nanotechnol. 2019, 10, 1423–1433, doi:10.3762/bjnano.10.140

• significantly impact its response. The gas adsorption and desorption kinetics and the chemical activation of WO3 are closely related to the working temperature [6]. The optimal working temperature for various gases is different due to the redox reaction energy required. This therefore provides the possibility

• temperature further increases. For the detection of H2S, NH3 and CO for all four sensors, the maximum response values were achieved at 90 °C, 150 °C and 210 °C, respectively. The thermodynamics and kinetics of the gas adsorption and desorption on the surface of WO3 could be responsible for this “increased

BiOCl/TiO₂/diatomite composites with enhanced visible-light photocatalytic activity for the degradation of rhodamine B

• Minlin Ao,
• Kun Liu,
• Xuekun Tang,
• Zishun Li,
• Qian Peng and
• Jing Huang

Beilstein J. Nanotechnol. 2019, 10, 1412–1422, doi:10.3762/bjnano.10.139

• -order kinetics model [38]: ln C/C0 = kt, where the apparent reaction rate constant and degradation time are expressed by k and t, and the initial concentration of RhB and the concentration at transit time t are represented by C0 and C, respectively. Supporting Information File 1, Figure S2a shows the UV

Highly ordered mesoporous silica film nanocomposites containing gold nanoparticles for the catalytic reduction of 4-nitrophenol

• Mohamad Azani Jalani,
• Leny Yuliati,
• Siew Ling Lee and
• Hendrik O. Lintang

Beilstein J. Nanotechnol. 2019, 10, 1368–1379, doi:10.3762/bjnano.10.135

• exceeded that of 4-NP (and remains constant throughout the experiment), both films were found to follow pseudo-first order kinetics [41]. This reduction followed the Langmuir–Hinshelwood model, where both reactants (4-NP and BH4−) were adsorbed on the AuNP surface at a fast rate. In the next step, electron

Construction of a 0D/1D composite based on Au nanoparticles/CuBi₂O₄ microrods for efficient visible-light-driven photocatalytic activity

• Weilong Shi,
• Mingyang Li,
• Hongji Ren,
• Feng Guo,
• Xiliu Huang,
• Yu Shi and
• Yubin Tang

Beilstein J. Nanotechnol. 2019, 10, 1360–1367, doi:10.3762/bjnano.10.134

• constants of all as-prepared materials with good linearity following first-order kinetics. The kinetic constant with added 2.5 wt % Au/CBO is 4.76 times higher than that with bare CBO. Recycling experiments were performed to test the stability of Au/CBO (Figure 6d). There was a slight decrease of

• using 2.5 wt % Au/CBO as a photocatalyst. (c) First-order kinetics of the TC degradation curves using different photocatalysts. (d) Three consecutive runs of TC degradation over 2.5 wt % Au/CBO photocatalyst. (a) Photocurrent response and (b) EIS spectra of bare CBO and 2.5 wt % Au/CBO composite under

Alloyed Pt₃M (M = Co, Ni) nanoparticles supported on S- and N-doped carbon nanotubes for the oxygen reduction reaction

• Stéphane Louisia,
• Yohann R. J. Thomas,
• Pierre Lecante,
• Marie Heitzmann,
• M. Rosa Axet,
• Pierre-André Jacques and
• Philippe Serp

Beilstein J. Nanotechnol. 2019, 10, 1251–1269, doi:10.3762/bjnano.10.125

• promising technologies in the field of renewable energy (and especially for transport applications), but the cost and lifetime are factors still to be improved in order to achieve widespread dissemination of this technology [1][2]. Due to the sluggish reaction kinetics for the ORR, the cathode active layer

Molecular attachment to a microscope tip: inelastic tunneling, Kondo screening, and thermopower

• Rouzhaji Tuerhong,
• Mauro Boero and
• Jean-Pierre Bucher

Beilstein J. Nanotechnol. 2019, 10, 1243–1250, doi:10.3762/bjnano.10.124

• tunneling through excitation of molecular vibration modes. Parameter-dependent transport in a molecular junction In order to gain additional information about the kinetics of carriers not contained in the current–voltage characteristics we want to evaluate the impact of the zero-bias peak on the thermopower

Porous N- and S-doped carbon–carbon composite electrodes by soft-templating for redox flow batteries

• Maike Schnucklake,
• László Eifert,
• Jonathan Schneider,
• Roswitha Zeis and
• Christina Roth

Beilstein J. Nanotechnol. 2019, 10, 1131–1139, doi:10.3762/bjnano.10.113

• in higher currents compared to the only carbonized samples. The obtained data suggest that the kinetics regarding the VO2+/VO2+ redox couple follow the order of carbonized < composite (N-doped) < composite (co-doped with N and S). This means that the redox reaction of the vanadium ions proceeds more

Glucose-derived carbon materials with tailored properties as electrocatalysts for the oxygen reduction reaction

• Rafael Gomes Morais,
• Natalia Rey-Raap,
• José Luís Figueiredo and
• Manuel Fernando Ribeiro Pereira

Beilstein J. Nanotechnol. 2019, 10, 1089–1102, doi:10.3762/bjnano.10.109

• electrocatalyst used for the reaction. The most commonly used electrocatalyst to supply faster kinetics and a four-electron pathway are platinum-based materials [3][4], which are costly and may assume up to 50% of the total cost of a fuel cell [5]. Transition metals [6][7], metal oxides [8][9] and carbon

• frequencies, indicating a lower charge transfer resistance, which allows the kinetics of the ORR to increase, and consequently, a higher onset potential is observed for sample AG6h (the values of the onset potential are shown in Supporting Information File 1, Table S4). In addition, these results also suggest

• that a more developed microporous structure favors the electrolyte diffusion to the most electrochemically active pores, which also contributed to the ORR kinetics. Moreover, clear differences regarding ionic transportation are also observed at medium frequencies. Sample AG1h shows a more defined

Serum type and concentration both affect the protein-corona composition of PLGA nanoparticles

• Katrin Partikel,
• Robin Korte,
• Dennis Mulac,
• Hans-Ulrich Humpf and
• Klaus Langer

Beilstein J. Nanotechnol. 2019, 10, 1002–1015, doi:10.3762/bjnano.10.101

• surface and are immediately replaced by high-affinity proteins with lower abundance and slower kinetics, such as apolipoproteins and immunoglobulins [4][24]. According to the predominant protein band at MW = 66 kDa, we suggest an enrichment of HSA in the corona of the PLGA NPs following incubation with 1

In situ AFM visualization of Li–O₂ battery discharge products during redox cycling in an atmospherically controlled sample cell

• Kumar Virwani,
• Younes Ansari,
• Khanh Nguyen,
• Francisco José Alía Moreno-Ortiz,
• Jangwoo Kim,
• Maxwell J. Giammona,
• Ho-Cheol Kim and
• Young-Hye La

Beilstein J. Nanotechnol. 2019, 10, 930–940, doi:10.3762/bjnano.10.94

• to the kinetics of the reaction taking place at the cathode [37]. The constant phase element CPEdl represents the capacitance of the double layer formed at the cathode. The diffusion of oxygen and lithium ions in the electrolye results in a low-frequency linear Warburg component, Ws. The slope of the

• charge transfer resistance, improves the kinetics of the reaction. Topographical observations using AFM AFM was used to monitor morphological changes on the glassy carbon cathode surface. The topography images in Figure 3 and Figure 4 each show one of the nine scanned regions at two different water

Fabrication of silver nanoisland films by pulsed laser deposition for surface-enhanced Raman spectroscopy

• Bogusław Budner,
• Mariusz Kuźma,
• Barbara Nasiłowska,
• Bartosz Bartosewicz,
• Malwina Liszewska and
• Bartłomiej J. Jankiewicz

Beilstein J. Nanotechnol. 2019, 10, 882–893, doi:10.3762/bjnano.10.89

• deposition changes the kinetics of Ag nanoisland growth, which gives a higher average EF value while maintaining the relative intensity deviation at 17%. In contrast, an increase in the temperature of the furnace to the 340 ± 3 °C (samples H and I) leads to a reduction of EF to less than half the value of

An efficient electrode material for high performance solid-state hybrid supercapacitors based on a Cu/CuO/porous carbon nanofiber/TiO₂ hybrid composite

• Mamta Sham Lal,
• Thirugnanam Lavanya and
• Sundara Ramaprabhu

Beilstein J. Nanotechnol. 2019, 10, 781–793, doi:10.3762/bjnano.10.78

• , more reliable, low cost, highly efficient and environmentally benign energy storage devices must be explored. Among many energy storage devices, supercapacitors are an ideal option for fast energy storage due to their high specific power (>10 kW kg−1), fast charge–discharge kinetics (in units of

• amount of charge than double layer supercapacitors and exhibits superior energy density [6]. Pseudo-supercapacitors have limited electrical conductivity and slow charge–discharge kinetics, resulting in a significant decrease in power density. Supercapacitors have been explored by realizing both faradaic

Ultrasonication-assisted synthesis of CsPbBr₃ and Cs₄PbBr₆ perovskite nanocrystals and their reversible transformation

• Longshi Rao,
• Xinrui Ding,
• Xuewei Du,
• Guanwei Liang,
• Yong Tang,
• Kairui Tang and
• Jin Z. Zhang

Beilstein J. Nanotechnol. 2019, 10, 666–676, doi:10.3762/bjnano.10.66

• water. The mechanism of this transformation between the CsPbBr3 PNCs and Cs4PbBr6 PNCs and their morphology change are studied, involving ions equilibrium, anisotropic growth kinetics, and CsBr-stripping process. Keywords: CsPbBr3 PNCs; Cs4PbBr6 PNCs; polar-solvent-free; reversible transformation

• between 0.5 and 1.5 mL, the morphology of PNCs gradually becomes irregular and some hexagonal shapes emerge (Figure 5c–e). As the amount of OAm increase to 3.0 mL, Cs4PbBr6 PNCs with homogeneous hexagonal shape can be achieved (Figure 5h). These results suggest that the growth kinetics of this process can

• images (Figure 4c–h) clearly confirm that the morphology of these PNCs can be tuned easily by changing the amount of OAm in the precursor solution, while keeping the amount of OA unchanged. We attribute this morphology change to the crystal anisotropy induced by the growth kinetics. The capping ligands