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Search for "membrane" in Full Text gives 453 result(s) in Beilstein Journal of Nanotechnology. Showing first 200.
Fabrication of nanocrystal forms of ᴅ-cycloserine and their application for transdermal and enteric drug delivery systems
Beilstein J. Nanotechnol. 2024, 15, 465–474, doi:10.3762/bjnano.15.42
- was slowly added into 20 mL of tert-butanol (Merck-Millipore) and mixed with an ultrasonic cleaner (Creworks Co., Ltd.) at 40 kHz for 1 min. The mixed solution was filtered by suction filtration using a 0.2 μm filter membrane (Merck KGaA). The filtered solution was centrifuged at 10,000 rpm (Kubota Co
- prepared by the same method used in formulation F, except that the DCS nanocrystals were substituted with the commercial DCS powder. In vitro transdermal delivery study A Strat-M membrane (pore size = 450 nm, Merck KGaA) was mounted on a Franz diffusion cell (PermeGear). The receptor compartment contained
- 8 mL of deionized water. Approximately 1–1.35 mL of the transdermal formulations (Formulation tests 1–3 and A–E) were applied to the membrane over an area of 1 cm2 across the donor compartment. The donor cell was exposed to room temperature with 65% humidity and covered with Parafilm to prevent
Heat-induced morphological changes in silver nanowires deposited on a patterned silicon substrate
Beilstein J. Nanotechnol. 2024, 15, 435–446, doi:10.3762/bjnano.15.39
- pentagonal structure is preserved even for small fragments of NWs that were split as a result of heat treatment as shown in Figure 7 (note that the fragments are kept in place due to contact with the thin carbon membrane of the TEM grid). These findings suggests that heat-induced morphological changes in Ag
Classification and application of metal-based nanoantioxidants in medicine and healthcare
Beilstein J. Nanotechnol. 2024, 15, 396–415, doi:10.3762/bjnano.15.36
- intracellular Ca2+ in cells and tissues. One of the most important criteria of anti-inflammatory drugs is the direct delivery to the inflamed tissue [96][97][98]. To increase the targeting ability, anti-inflammatory agents can be wrapped with a cell membrane camouflage technique [99][100][101]. For example, Ma
- et al. constructed carbon dot-SOD nanozymes and CD98 CRISPR/Cas9 plasmids encapsulated in a metal-organic framework (MOF), and then camouflaged it with macrophage membrane [102]. In this system, the macrophage membrane guided the encapsulated nanozymes and CD98 CRISPR/Cas9 plasmids to accumulate at
- pathophysiology of post-ischemic renal failure. Therefore, by coating with a neutrophil membrane, nanoantioxidants can be specifically delivered to kidneys with I/R injury. A majority of reported anti-inflammatory nanomaterials mainly focus on the degradation of ROS. However, nanomaterials possessing the
Nanomedicines against Chagas disease: a critical review
Beilstein J. Nanotechnol. 2024, 15, 333–349, doi:10.3762/bjnano.15.30
- lipophilicity indicator and the most critical parameter predictor of passive membrane permeability (which for BNZ is 0.9; a clogP value below 1.35 is indicative of low permeability) [29][55]. In contrast, others consider BNZ as a class-IV drug, this is, a poorly soluble and poorly permeable molecule [30] with
- implemented in India in the mid-1990s is an excellent example [61][62]. Amphotericin B binds to parasite ergosterol precursors, such as lanosterol, disrupting the parasite membrane. Since protozoan trypanosomatids such as Leishmania and Trypanosoma present ergosterol as a component of their membranes [63
Exploring the relationships between physiochemical properties of nanoparticles and cell damage to combat cancer growth using simple periodic table-based descriptors
Beilstein J. Nanotechnol. 2024, 15, 297–309, doi:10.3762/bjnano.15.27
- well as in biological systems. Since the cell membrane is negatively charged, the interaction between NPs and cell membrane or organelles can be highly influenced by the zeta potential. There is an increased interest in integrating data on metal oxides in the field of nanotoxicology that would be able
- biocompatibility on NP toxicity. These properties of NPs determine their toxicity and interaction with the cell membrane damaging human health and the environment [12]. The toxic effect of NPs can be used as a medical treatment for diseases at the cellular level, that is, targeting and destroying cancerous cells
- NPs and its influence on toxicity. Methods and Materials Dataset The study is based on two datasets, that is, dataset I (zeta potential) and dataset II (cell membrane damage). Dataset I consists of 18 metal oxide nanoparticles (MeOx NPs) with stoichiometries of MO, MO2, MO3, M2O3, and M3O4. This data
Nanocarrier systems loaded with IR780, iron oxide nanoparticles and chlorambucil for cancer theragnostics
Beilstein J. Nanotechnol. 2024, 15, 180–189, doi:10.3762/bjnano.15.17
- and the glomerular basement membrane during glomerular filtration in the kidney [34]. Thus, it may be assumed that the half-life of our NPs in the bloodstream is longer than that of smaller NPs. In addition to the size of nanoparticles, negatively charged NPs are more likely to have an extended half
Ferromagnetic resonance spectra of linear magnetosome chains
Beilstein J. Nanotechnol. 2024, 15, 157–167, doi:10.3762/bjnano.15.15
- thickness of the lipid magnetosome membrane, as well as on the value of the magnetic damping constant. At the same time, they are practically independent of the number Np of particles in the chain under the condition Np ≥ 10. The FMR spectra of non-oriented assemblies of magnetosome chains are compared with
- chains Np = 20, the particle diameter is D = 40 nm, the membrane shell thickness is Ten = 4 nm, and the magnetic damping constant is κ = 0.1. As Figure 2 shows, the greatest difference in the position of the FMR peaks for chains with different types of anisotropy is observed at angles θ ≤ 15°. In
- with E-type anisotropy (black dots) upon averaging partial FMR spectra of oriented assemblies over the angle θ. Partial FMR spectra at certain angles θ are shown in Figure 4a as solid colored curves. The number of particles in chains is Np = 20, the particle diameter is D = 40 nm, the membrane shell
Development and characterization of potential larvicidal nanoemulsions against Aedes aegypti
Beilstein J. Nanotechnol. 2024, 15, 104–114, doi:10.3762/bjnano.15.10
- conditions. Modified Franz cells, equipped with a polyethersulfone membrane (Sigma-Aldrich) and with a diffusion area of 1.77 cm2 were used in the assays. A Microette (Hanson Research, USA) was used. The receptor compartment was filled with 7.0 mL of a receptor solution composed of 0.1 M phosphate buffer and
Berberine-loaded polylactic acid nanofiber scaffold as a drug delivery system: The relationship between chemical characteristics, drug-release behavior, and antibacterial efficiency
Beilstein J. Nanotechnol. 2024, 15, 71–82, doi:10.3762/bjnano.15.7
- study reported that BBR exhibited excellent antibacterial activity against MRSA by damaging the cell wall structure and membrane integrity and further changing the cell morphology in the concentration range of 64–256 mg/L [44]. Recently, Wu et al. [45] proposed a novel orientation on the antibacterial
Curcumin-loaded nanostructured systems for treatment of leishmaniasis: a review
Beilstein J. Nanotechnol. 2024, 15, 37–50, doi:10.3762/bjnano.15.4
- leishmaniasis. Additionally, this molecule produces reactive oxygen species (ROS) and elevates cytosolic calcium. These occur in the exposure of phosphatidylserine to the outer plasma membrane leaflet and DNA fragmentation, causing the death of the leishmaniasis parasite [47][52]. Despite its promising
- these carriers with the macrophage membrane. As a result, the macrophages uptake the drug-loaded nanocarrier by phagocytosis, where they will directly act on the parasites [65][66][67]. Several types of nanosystems have been studied for carrying antileishmanial drugs, such as polymeric nanoparticles
Nanotechnological approaches in the treatment of schistosomiasis: an overview
Beilstein J. Nanotechnol. 2024, 15, 13–25, doi:10.3762/bjnano.15.2
- permeability through the cellular membrane by making a nanoemulsion of Curcuma longa extract (i.e., the curcumin plant source). The nanoemulsion showed an effect against adults of S. mansoni in vitro (especially males). This is an interesting finding because data from the literature reports that females are
- . mansoni in vivo. After that, the same group, in 2015, developed lipid nanocapsules positively charged (cationic) and tested them with and without oleic acid as a membrane permeabilizer in the composition. Both nanoformulations were able to reduce the whole treatment of schistosomiasis in mice to one
- infection [73]. Late in 2020, while cationic lipid nanocapsules were hemolytic [72], the same group tested lipid nanocapsules with oleic acid on the membrane and miltefosine (20 mg/kg) alone or combined with PZQ. They reported that nanosystems containing miltefosine with or without PZQ were potent (when
TEM sample preparation of lithographically patterned permalloy nanostructures on silicon nitride membranes
Beilstein J. Nanotechnol. 2024, 15, 1–12, doi:10.3762/bjnano.15.1
- submicrometer apertures were milled on SiN membranes using a focused ion beam. Furthermore, we have developed a new TEM sample preparation method, where we fabricated Py nanostructures on a bulk substrate with a SiN buffer layer and etched the substrate to create a thin SiN membrane under the Py nanostructure
- structure. The resist was patterned using an electron beam, which offers higher resolution than other sources (e.g., UV light) because of the smaller wavelength of electrons. Since the use of an ultrasonic bath will destroy the free-standing membrane, the undercut must be deliberately made larger to ensure
- information inside the sample. Results and Discussion Fabrication on a commercial SiN membrane Lift-off The lift-off procedure is described in Figure 1. We use PMMA and its copolymer as a positive resist to create a bilayer resist. The copolymer (AR-P 617.08) is a methyl methacrylate and methacrylic acid
Fluorescent bioinspired albumin/polydopamine nanoparticles and their interactions with Escherichia coli cells
Beilstein J. Nanotechnol. 2023, 14, 1208–1224, doi:10.3762/bjnano.14.100
- destabilization of the bacterial cell membrane by interactions with the nanocarriers (thus allowing for the penetration of the drug into the bacteria) is not known (Figure 1e). Yet, the accumulation of ONPs in bacterial cells is crucial if ONPs are to be used for fluorescent labelling of cells. Also, in the case
- been designed to allow for the modification of their fluorescence properties. This also modified the outer surface chemistry; thus, the ability of the NPs to pass through the cell membrane was possibly facilitated. The localization of the fluorescent BSA/PDA NPs related to the cells was investigated by
- ambient temperature, as shown by the good dispersion and the absence of precipitates and deposition on the container wall (Figure 3c). Good stability and dispersion were maintained after dialysis with a 100 kDa cut-off membrane, which allowed for the removal of free BSA molecules. As shown by Chassepot
Elasticity, an often-overseen parameter in the development of nanoscale drug delivery systems
Beilstein J. Nanotechnol. 2023, 14, 1149–1156, doi:10.3762/bjnano.14.95
- comparable size and surface characteristics but variable Young’s moduli ranging from 45 kPa to 19 MPa. In contrast to many other studies, soft nanoliposomes (NLPs) are taken up better by cells than harder particles used in this study. This is explained by the combination of membrane fusion and clathrin
Curcumin-loaded albumin submicron particles with potential as a cancer therapy: an in vitro study
Beilstein J. Nanotechnol. 2023, 14, 1127–1140, doi:10.3762/bjnano.14.93
- cancer cells, likely attributed to particle uptake through endocytosis pathways, including phagocytosis and macropinocytosis [51]. The uptake process depends on cell membrane and particle properties, including size, shape, composition, and surface properties. These factors play a crucial role in particle
Spatial mapping of photovoltage and light-induced displacement of on-chip coupled piezo/photodiodes by Kelvin probe force microscopy under modulated illumination
Beilstein J. Nanotechnol. 2023, 14, 1059–1067, doi:10.3762/bjnano.14.87
- In this work, a silicon photodiode integrated with a piezoelectric membrane is studied by Kelvin probe force microscopy (KPFM) under modulated illumination. Time-dependent KPFM enables simultaneous quantification of the surface photovoltage generated by the photodiode as well as the resulting
- mechanical oscillation of the piezoelectric membrane with vertical atomic resolution in real-time. This technique offers the opportunity to measure concurrently the optoelectronic and mechanical response of the device at the nanoscale. Furthermore, time-dependent atomic force microscopy (AFM) was employed to
- spatially map voltage-induced oscillation of various sizes of piezoelectric membranes without the photodiode to investigate their position- and size-dependent displacement. Keywords: Kelvin probe force microscopy (KPFM); light-driven micro/nano systems; piezoelectric membrane; surface photovoltage (SPV
Recognition mechanisms of hemoglobin particles by monocytes – CD163 may just be one
Beilstein J. Nanotechnol. 2023, 14, 1028–1040, doi:10.3762/bjnano.14.85
- since both proteins are specific for monocytes. CD163 was tested because of its direct affinity to Hb. Also, we tested the effect of blocking CD204 (scavenger receptor A/SR-A). SR-A is a membrane protein occurring in the monocyte/macrophage lineage. Playing an important role in host defense, it exhibits
- block the monocytic membrane protein, as formerly described by Schaer and co-workers [27]. For a reference sample, the phagocytic capacity of monocytes was fully utilized for the uptake of FITC-labeled E. coli lysate over a period of 10 min at 37 °C (commercially available phagocytosis tests use lysate
- allowed to ingest FITC-labeled E. coli lysate, the MFI was reduced to 39.8% ± 19.8% (EC-prefed-120′, Figure 2a). This circumstance indirectly represents phagocytic activity by monocytes: the lower the MFI, the greater the extent of phagocytosis in the “pre-feeding-step”. Covering the monocytes membrane
Nanoarchitectonics of photothermal materials to enhance the sensitivity of lateral flow assays
Beilstein J. Nanotechnol. 2023, 14, 988–1003, doi:10.3762/bjnano.14.82
- different parts, namely sample pad, conjugate pad, nitrocellulose membrane, and adsorbent pad, maintaining a smooth flow of reagents through the LFA membrane. In the presence of a sample, the analyte initially reacts with affinity molecules, commonly antibodies linked with tracers such as gold nanoparticles
- , before being captured by immobilized biomolecules on a test line in the nitrocellulose membrane [6][7]. In conventional LFAs, most commonly gold nanoparticles and coloured cellulose nanobeads have been used as tracer elements because of strong light absorption and surface plasmon resonance, which yield
- nanomaterials; it also influences the capillary movement of nanoparticles inside the nitrocellulose membrane pores. Herein, we discuss the current development of photothermal nanomaterials regarding the application in LFAs. As an introduction, we discuss the classification of different photothermal
Prediction of cytotoxicity of heavy metals adsorbed on nano-TiO2 with periodic table descriptors using machine learning approaches
Beilstein J. Nanotechnol. 2023, 14, 939–950, doi:10.3762/bjnano.14.77
- toxicity through an ionic mechanism followed by the generation of reactive oxygen species (ROS). Another, biomarker for ROS is lipid peroxidation [38] as free radicals cause lipid peroxidation inside the cell membrane. The catalytic properties of the metals are also responsible for an increased toxicity of
Green SPIONs as a novel highly selective treatment for leishmaniasis: an in vitro study against Leishmania amazonensis intracellular amastigotes
Beilstein J. Nanotechnol. 2023, 14, 893–903, doi:10.3762/bjnano.14.73
- effects on cell proliferation, infectivity percentage, and ultrastructure. SPIONs were internalized by both parasite stages, randomly distributed in the cytosol and located mainly in membrane-bound compartments. The selectivity index for intracellular amastigotes was more than 240 times higher compared to
- , scanning electron microscopy and chemical element mapping analysis were carried out to confirm the uptake of the SPIONs by L. amazonensis intracellular amastigotes after removing the plasma membrane to expose the cytoplasmic environment (Figure 2). Secondary electron imaging revealed intracellular
- different sizes. Furthermore, at high magnification, it is possible to observe that the SPIONS are frequently surrounded by membranes (Figure 3B, arrows). In addition, SPIONs were also observed inside the flagellar pocket (Figure 3C, arrowheads) and closely associated with the membrane. The uptake of SPIONs
A wearable nanoscale heart sound sensor based on P(VDF-TrFE)/ZnO/GR and its application in cardiac disease detection
Beilstein J. Nanotechnol. 2023, 14, 819–833, doi:10.3762/bjnano.14.67
- advancement in wearable electronic devices within the healthcare field, leading to several noteworthy breakthroughs. For instance, D. Wan et al. [11] presented a groundbreaking development in the form of a flexible wearable friction patch. This innovative patch consists of a dual-layer PDMS membrane infused
Nanostructured lipid carriers containing benznidazole: physicochemical, biopharmaceutical and cellular in vitro studies
Beilstein J. Nanotechnol. 2023, 14, 804–818, doi:10.3762/bjnano.14.66
- nanoparticles could accumulate in the site of inflammation delivering the drug in the surroundings of their molecular target. In addition, nanocarriers may pass through the cell membrane via endocytosis to avoid BNZ efflux via the P-glycoprotein efflux pump [14][15][16], thus delivering the drug more
- , hemolytic activity could be caused by several reasons, including the ageing of the blood sample after 48 h of incubation with the concomitant release of hemoglobin, but also by the presence of surfactants that could destabilized the erythrocyte membrane [47]. On the other hand, the differences between NLC
- it to the outer leaflet of the lipid bilayer [49]. Trypanosoma brucei predominant membrane protein variant surface glycoprotein (VSG), which is involved in parasite host immune system evasion, is anchored by a GPI that requires myristate for its synthesis. Analogs of myristate have shown toxicity
Silver nanoparticles loaded on lactose/alginate: in situ synthesis, catalytic degradation, and pH-dependent antibacterial activity
Beilstein J. Nanotechnol. 2023, 14, 781–792, doi:10.3762/bjnano.14.64
- the medium. The antibacterial effectiveness of the nanocomposite varied among the bacterial strains and pH values, which may be related to the antibacterial mechanism of AgNPs and the cell wall and membrane structure of each bacterial strain [50]. These findings suggest that the antibacterial activity
Control of morphology and crystallinity of CNTs in flame synthesis with one-dimensional reaction zone
Beilstein J. Nanotechnol. 2023, 14, 741–750, doi:10.3762/bjnano.14.61
- Malaysia, 81310 Johor Bahru, Malaysia Advanced Membrane Technology Research Center, Universiti Teknologi Malaysia, 81310 Johor Bahru, Malaysia National Research and Innovation Agency, Indonesia 10.3762/bjnano.14.61 Abstract The growth of carbon nanotubes (CNTs) in a flame requires conditions that are
On the use of Raman spectroscopy to characterize mass-produced graphene nanoplatelets
Beilstein J. Nanotechnol. 2023, 14, 509–521, doi:10.3762/bjnano.14.42
- was then vacuum-filtered through alumina membranes (20 nm pore size), rinsed with IPA to remove residual NMP, and dried in a vacuum oven at 60 °C overnight. For samples 2 to 7, 3 mL of the dispersion was filtered, while for sample 1, ca. 30 mL was used to ensure adequate coverage of the membrane
- . Raman spectra of the filtered films on the membrane were recorded using a Renishaw Qontor confocal spectrometer (Renishaw plc., UK) using a 532 nm excitation laser and a 2400 L/mm grating. An area of 20 μm × 20 μm of the film was mapped, with 1 μm distance between measurement locations. Spectra were
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