Overview of mechanism and consequences of endothelial leakiness caused by metal and polymeric nanoparticles

• Magdalena Lasak and
• Karol Ciepluch

Beilstein J. Nanotechnol. 2023, 14, 329–338, doi:10.3762/bjnano.14.28

• their various applications. NPs are characterized by a high surface-to-volume ratio, which in turn leads to a large functional surface area. The possibility of combining NPs with various ligands and biologically active molecules, such as nucleic acids, fluorescence dyes, drugs, tumor markers, and

Recent progress in cancer cell membrane-based nanoparticles for biomedical applications

• Qixiong Lin,
• Yueyou Peng,
• Yanyan Wen,
• Xiaoqiong Li,
• Donglian Du,
• Weibin Dai,
• Wei Tian and
• Yanfeng Meng

Beilstein J. Nanotechnol. 2023, 14, 262–279, doi:10.3762/bjnano.14.24

• B16F10 cells, breast cancer 4T1 cells, and African green monkey kidney fibroblast COS-7 cells were used to compare the penetration in brain tissue. The NPs coated with B16F10 and 4T1 cell membranes showed excellent fluorescence aggregation signals 8 h after the nanoformulations were administered

• PBS controls under the same treatment conditions in a mouse HCC model. Through homotypic aggregation and immune evasion, as well as the prevention of premature drug leakage from the biomimetic NPs, the drug was efficiently accumulated at the target site. The fluorescence signal showed a predominant

• entering UM-SCC-7 tumor-bearing mice. (C) Distribution of iron from NPs in UM-SCC-7 tumor-bearing mice. (D) Biomimetic NPs showed high accumulation only in the same tumor tissue in the dual-type tumor model. (E, F) Fluorescence signal distribution of H22 and UM-SCC-7 membrane-encapsulated NPs. Figure 3 was

Structural, optical, and bioimaging characterization of carbon quantum dots solvothermally synthesized from o-phenylenediamine

• Zoran M. Marković,
• Milica D. Budimir,
• Martin Danko,
• Dušan D. Milivojević,
• Pavel Kubat,
• Danica Z. Zmejkoski,
• Vladimir B. Pavlović,
• Marija M. Mojsin,
• Milena J. Stevanović and
• Biljana M. Todorović Marković

Beilstein J. Nanotechnol. 2023, 14, 165–174, doi:10.3762/bjnano.14.17

• test internalization of CQDs, Hela cells were treated for 48 h with a concentration of 200 µg/mL CQDs. As shown in Figure 6b, fluorescence imaging demonstrated that CQDs penetrated Hela cells well (compared to Hela cells treated with vehicle control, shown in Figure 6a) and were mainly in the cytoplasm

• exponential function excluding the initial part influenced by light scattering, fluorescence, and the formation of singlet oxygen from excited states of CQDs. Singlet oxygen generation was investigated by UV–vis probe measurements of solutions of 1,3- diphenylisobenzofuran (DPBF) ethanol (20 µM) as well [52

• /L. Samples were irradiated at 365 and 405 nm with intensities of 6 mW/cm2 and 40 mW/cm2, respectively. The fluorescence of the formed hydroxyterephthalic acid (h-TA) solutions taken after different times of irradiation was measured in 1 × 1 cm2 quartz cuvettes in a right-angle arrangement. The

Antimicrobial and mechanical properties of functionalized textile by nanoarchitectured photoinduced Ag@polymer coating

• Jessica Plé,
• Marine Dabert,
• Helene Lecoq,
• Sophie Hellé,
• Lydie Ploux and
• Lavinia Balan

Beilstein J. Nanotechnol. 2023, 14, 95–109, doi:10.3762/bjnano.14.11

• (chosen for its inertness against microorganism proliferation and for the high image quality it provides with upright fluorescence microscopy). Liquid diffusion assay. The samples were placed in individual, sterile dishes and inoculated with 4 mL of E. coli or C. albicans suspensions of 0.1 OD600. Samples

Gap-directed chemical lift-off lithographic nanoarchitectonics for arbitrary sub-micrometer patterning

• Chang-Ming Wang,
• Hong-Sheng Chan,
• Chia-Li Liao,
• Che-Wei Chang and
• Wei-Ssu Liao

Beilstein J. Nanotechnol. 2023, 14, 34–44, doi:10.3762/bjnano.14.4

• (10 μg/mL in PBS buffer) incubation for 20 min to complete the biorecognition process. Finally, the substrate was gently rinsed by deionized water, immersed in PBS buffer solution, and stored at 4 °C in the dark before further characterization. Fluorescence and bright filed microscopic images were

• captured with an epifluorescence microscope (Axio Imager. M2, Carl Zeiss microscopy, Jena, Germany) equipped with an X-Cite 120 LED (Lumen Dynamics Group, Inc., Mississauga, Canada) lamp. Excitation wavelength was set to 480 nm while emission of 535 nm was collected. Fluorescence images were analyzed with

• moieties are conjugated with streptavidin followed by FITC-labeled anti-streptavidin antibody recognition (Figure 1A). This process results in obvious contrast in fluorescence images, allowing the visualization of biorecognition processes at post lift-off regions. XPS spectroscopy is utilized to monitor

Facile preparation of Au- and BODIPY-grafted lipid nanoparticles for synergized photothermal therapy

• Yuran Wang,
• Xudong Li,
• Haijun Chen and
• Yu Gao

Beilstein J. Nanotechnol. 2022, 13, 1432–1444, doi:10.3762/bjnano.13.118

• 30 μM) at 37 °C for 0.5, 1, 2, 4, 6, and 8 h. Then, the cells were washed, digested, and suspended in 500 μL PBS. The fluorescence was detected by flow cytometry (Becton Dickinson FACSAriaIII cell sorter) in PerCP-Cy5.5 channel to detect the fluorescence of BDP according to our previous report [22

• complex nanoparticles with suitable particle size (73 nm) for in vivo application. Besides, at this molar ratio, BDP could be successfully grafted onto the LNPs. Flow cytometry was employed to study the cellular uptake efficiencies of AB-LNPs and free BDP by detecting the fluorescence of BDP in the PerCP

• -Cy5-5 channel. 4T1 cells treated with AB-LNPs showed an evident increase in mean fluorescence intensity with the extension of the incubation time and reached the peak at 6 h (Figure 4a,b). The uptake amount of AB-LNPs after 6 h incubation time was nine times higher than that of the control, indicating

Studies of probe tip materials by atomic force microscopy: a review

• Ke Xu and
• Yuzhe Liu

Beilstein J. Nanotechnol. 2022, 13, 1256–1267, doi:10.3762/bjnano.13.104

• properties, and thus the fluorescence emission can be tuned by controlling different sizes. Due to their unique electronic, physical, and optical properties, metal nanoclusters have attracted great interest in recent years for electronic devices, catalysis, bioimaging, and chemical sensing [18][19][20][21

• , dimethoate, and phorate were broken. The hydrolysis products contain sulfhydryl groups that bind to the silver atoms on the surface of the silver nanoclusters. The formation of non-fluorescent polymers resulted in a significant quenching of the fluorescence of the silver nanoclusters. Cu2+ effectively

• quenched the fluorescence of DNA-templated silver nanoclusters (DNA-AgNCs), while the strong chelation between glyphosate and Cu2+ restored the fluorescence of the nanoclusters. The method showed good linearity in the concentration range of 1 ng/mL–50 ng/mL, and the detection limit reached 0.2 ng/mL. In

A super-oscillatory step-zoom metalens for visible light

• Yi Zhou,
• Chao Yan,
• Peng Tian,
• Zhu Li,
• Yu He,
• Bin Fan,
• Zhiyong Wang,
• Yao Deng and
• Dongliang Tang

Beilstein J. Nanotechnol. 2022, 13, 1220–1227, doi:10.3762/bjnano.13.101

• emission depletion microscopy (STED) can realize the localization of single fluorescent molecules with 1 nm accuracy [2], albeit with the disadvantages of required fluorescence labeling and slow image reconstruction. Super-resolution microscopy based on structured light illumination (SIM) can realize a

Rapid fabrication of MgO@g-C₃N₄ heterojunctions for photocatalytic nitric oxide removal

• Minh-Thuan Pham,
• Duyen P. H. Tran,
• Xuan-Thanh Bui and
• Sheng-Jie You

Beilstein J. Nanotechnol. 2022, 13, 1141–1154, doi:10.3762/bjnano.13.96

• (HR-XPS). The photoluminescence (PL) spectra of the materials was carried out in the form of fluorescence analysis with an excitation wavelength range of 200–900 nm. Finally, the photocatalytic mechanism was determined by trapping tests and ESR measurements. Photocatalytic performance The

• strongly depends on the optical properties. Photoluminescence Fluorescence spectra of MgO and 3% MgO@g-C3N4 are shown in Figure 10a and Figure 10b, respectively. MgO shows strong fluorescence at 270 nm with an excitation wavelength (270 nm) in the UV range. MgO also shows another emission wavelength at 380

• nm with an excitation wavelength (770 nm) in the visible range, which could be caused by the native structural defects in MgO [18]. 3% MgO@g-C3N4 shows intense fluorescence at 420 nm via excitation at 850 nm, due to the recombination of charge carriers. The photogenerated electrons from the valance

Recent advances in green carbon dots (2015–2022): synthesis, metal ion sensing, and biological applications

• Aisha Kanwal,
• Naheed Bibi,
• Sajjad Hyder,
• Arif Muhammad,
• Hao Ren,
• Jiangtao Liu and
• Zhongli Lei

Beilstein J. Nanotechnol. 2022, 13, 1068–1107, doi:10.3762/bjnano.13.93

• . Surface passivation with different functional groups generates surface defects, which produces fluorescence and also generates new active sites for modification for specific applications. CDs can be chemically modified by many heteroatoms, including N, P, and S, and many other chemicals that increase

• applications [36], tumor marker detection [37], bioanalytical studies [38], biomedical [39][40] and biotechnological applications [3], biosensing and bioimaging [31][32], and fluorescence [41] and photoluminescence processes [42]. Many reviews about CDs obtained from natural resources have been published

• contrast, provides homogenous and effective heating and speed up the reaction to merely a few minutes. Hence, this approach is considered the fastest and simplest amongst the synthesis methodologies and has become widely used. The fluorescence emissions of CDs are usually blue and green (i.e., in the low

Biomimetic chitosan with biocomposite nanomaterials for bone tissue repair and regeneration

• Se-Kwon Kim,
• Sesha Subramanian Murugan,
• Pandurang Appana Dalavi,
• Sebanti Gupta,
• Sukumaran Anil,
• Gi Hun Seong and
• Jayachandran Venkatesan

Beilstein J. Nanotechnol. 2022, 13, 1051–1067, doi:10.3762/bjnano.13.92

• were identified by fluorescence imaging. Cells adhered on nanofibers show a better cell phenotype, and this was corroborated by morphological characterisation via SEM [72] (Figure 6). Misra and colleagues developed chitosan–graphene nanocomposite scaffolds that modify cell–scaffold interactions

Gelatin nanoparticles with tunable mechanical properties: effect of crosslinking time and loading

• Agnes-Valencia Weiss,
• Daniel Schorr,
• Julia K. Metz,
• Metin Yildirim,
• Saeed Ahmad Khan and
• Marc Schneider

Beilstein J. Nanotechnol. 2022, 13, 778–787, doi:10.3762/bjnano.13.68

• primary amine functions, and, therefore, it cannot be crosslinked into the particle matrix by glutaraldehyde. FITC-dextran 70 kDa was loaded into nanoparticles by incorporation during precipitation and subsequent crosslinking of the nanoparticles. The fluorescence intensity was measured after enzymatic

• loading of FITC-dextran was determined by dissolving the gelatin network using enzymatic degradation. The fluorescence intensity of the resulting solution was measured [18]. Therefore, 5 mg of freeze-dried GNPs were dispersed in 5 mL PBS containing 2.5 mg trypsin at room temperature. After 6 h of

• incubation, samples were centrifuged. The fluorescence intensity of supernatants was measured with the spectrofluorometer Duetta™ (Horiba Europe GmbH, Oberursel, Germany) using an excitation wavelength of 493 nm and an emission wavelength of 519 nm. Concentrations were calculated using a calibration row made

Recent advances in nanoarchitectures of monocrystalline coordination polymers through confined assembly

• Lingling Xia,
• Qinyue Wang and
• Ming Hu

Beilstein J. Nanotechnol. 2022, 13, 763–777, doi:10.3762/bjnano.13.67

• realized, showing an anisotropic alignment of fluorescent guest molecules and directional fluorescence [122]. To match with the lattice structure, the grown coordination polymer sometimes may rotate to find the best lattice match with the substrate [123]. In most cases, the lattices of the substrate and

Hierarchical Bi₂WO₆/TiO₂-nanotube composites derived from natural cellulose for visible-light photocatalytic treatment of pollutants

• Zehao Lin,
• Zhan Yang and
• Jianguo Huang

Beilstein J. Nanotechnol. 2022, 13, 745–762, doi:10.3762/bjnano.13.66

• reference standard for solid samples. The photoluminescence (PL) spectra were obtained on a Shimadzu RF-5301PC fluorescence spectrometer under a laser excitation of 360 nm. In order to observe the microstructures of the samples, a small amount of a given sample was dispersed in ethanol to generate a

A nonenzymatic reduced graphene oxide-based nanosensor for parathion

• Sarani Sen,
• Anurag Roy,
• Ambarish Sanyal and
• Parukuttyamma Sujatha Devi

Beilstein J. Nanotechnol. 2022, 13, 730–744, doi:10.3762/bjnano.13.65

• (mass, absorption, fluorescence) techniques are time-consuming, laborious, costy, require specific and sophisticated instruments and trained personnel, and most often are not portable to enable on-site detection [5][6]. Electrochemical nanosensors are one of the preferred methodologies due of their fast

Antibacterial activity of a berberine nanoformulation

• Hue Thi Nguyen,
• Tuyet Nhung Pham,
• Anh-Tuan Le,
• Nguyen Thanh Thuy,
• Tran Quang Huy and
• Thuy Thi Thu Nguyen

Beilstein J. Nanotechnol. 2022, 13, 641–652, doi:10.3762/bjnano.13.56

• . MRSA is a Gram-positive bacterium that has a thick and smooth peptidoglycan layer in the cell wall. Furthermore, the above results also revealed that the antibacterial activity of BBR NPs against MRSA is higher than that against E. coli O157:H7. Figure 7a shows an unclear fluorescence stereomicroscopy

• image of MRSA. The image is unclear because the bacterial cells are not self-fluorescent under excitation. In contrast, after incubation with BBR NPs, the BBR molecules adhered to the bacterial cell walls exhibited fluorescence (Figure 7b) upon UV excitation [44]. In our experiment, the samples used for

• observation under the fluorescence microscope were all centrifuged and washed three times in bi-distilled water. However, due to the limited resolution of the stereomicroscope, the interaction of BBR NPs and bacterial cell walls could not be clearly observed. Therefore, the samples were processed by ultrathin

Effects of substrate stiffness on the viscoelasticity and migration of prostate cancer cells examined by atomic force microscopy

• Xiaoqiong Tang,
• Yan Zhang,
• Jiangbing Mao,
• Yuhua Wang,
• Zhenghong Zhang,
• Zhengchao Wang and
• Hongqin Yang

Beilstein J. Nanotechnol. 2022, 13, 560–569, doi:10.3762/bjnano.13.47

• treatment with 20 µM of blebbistatin for 30 min revealed disorganised microfilament bundles on stiff substrates and weaker fluorescence intensity in PC-3 cells rather than in non-blebbistatin-treated cells (Supporting Information File 1, Figure S4b–d). The Young's modulus of HPV-PZ-7 and PC-3 cells on stiff

• washed with PBS and fluorescence images were obtained using an inverted optical microscope (Leica, Germany) with 488 laser lines. The obtained images were linearly analysed and pseudo-coloured using the ImageJ analysis software. Blebbistatin treatment assay To inhibit myosin II, cells were incubated with

• imaging and cell contour maps. (d) Quantitative statistics of the average surface roughness (Ra). (e) Quantification plot of cell height; “ns” means no difference, ** P < 0.01, *** P < 0.001. Cytoskeletal microfilaments respond to changes in substrate stiffness on prostate cancer cells. (a) Fluorescence

Detection and imaging of Hg(II) in vivo using glutathione-functionalized gold nanoparticles

• Gufeng Li,
• Shaoqing Li,
• Rui Wang,
• Min Yang,
• Lizhu Zhang,
• Yanli Zhang,
• Wenrong Yang and
• Hongbin Wang

Beilstein J. Nanotechnol. 2022, 13, 549–559, doi:10.3762/bjnano.13.46

• hydrolysis of the spirolactam ring of Rh6G2, leading to a significant change in the fluorescence of GNPs-GSH-Rh6G2 from an “OFF” to an “ON” state. This strategy is an effective tool to detect Hg2+ ions. In cytotoxicity experiments, GNPs-GSH-Rh6G2 could penetrate living cells and detect mercury ions through

• the fluorescent “ON” form. Keywords: cell imaging; fluorescence probes; glutathione; gold nanoparticles; mercury ions; rhodamine 6G derivatives; Introduction Metal nanoparticles have been widely used in the development and construction of sensor systems and drug carriers due to their excellent

• molecular release system. After adding Cu(II), we observed a switching of the GNP–ʟ-Cys–Rh6G2 fluorescence from “OFF” to “ON” with high stability. Furthermore, it is worth noting that glutathione (GSH) contains a thiol and an amino group. It can not only conjugate to the nanoparticle surfaces through the

Zinc oxide nanostructures for fluorescence and Raman signal enhancement: a review

• Ioana Marica,
• Fran Nekvapil,
• Maria Ștefan,
• Cosmin Farcău and
• Alexandra Falamaș

Beilstein J. Nanotechnol. 2022, 13, 472–490, doi:10.3762/bjnano.13.40

• fluorescence (SEF), these techniques have shown huge potential for applications in biomedicine, biotechnology, and optical sensors. Both methods rely on the high electromagnetic fields created at locations on the surface of plasmonic metal nanoparticles, depending on the geometry of the nanoparticles, their

• surface features, and the specific location of analyte molecules. Lately, ZnO-based nanostructures have been exploited especially as SERS substrates showing high enhancement factors and increased charge transfer effect. Additionally, applications focused on enhancing the fluorescence of analyte molecules

• as well as on tuning the photoluminescence properties of ZnO nanostructures through combination with metal nanoparticles. This review covers the major recent results of ZnO-based nanostructures used for fluorescence and Raman signal enhancement. The broad range of ZnO and ZnO–metal nanostructures

A non-enzymatic electrochemical hydrogen peroxide sensor based on copper oxide nanostructures

• Irena Mihailova,
• Vjaceslavs Gerbreders,
• Marina Krasovska,
• Eriks Sledevskis,
• Valdis Mizers,
• Andrejs Bulanovs and
• Andrejs Ogurcovs

Beilstein J. Nanotechnol. 2022, 13, 424–436, doi:10.3762/bjnano.13.35

• pharmaceuticals [16][17][18], environmental protection [19], and industrial areas (especially food production) [20][21][22][23][24][25]. Measurement techniques including fluorescence [26][27], luminescence [28], spectrometry [29][30], and electrochemistry [31][32][33] are widely used for H2O2 determination

Micro- and nanotechnology in biomedical engineering for cartilage tissue regeneration in osteoarthritis

• Zahra Nabizadeh,
• Mahmoud Nasrollahzadeh,
• Hamed Daemi,
• Mohamadreza Baghaban Eslaminejad,
• Ali Akbar Shabani,
• Mehdi Dadashpour,
• Majid Mirmohammadkhani and
• Davood Nasrabadi

Beilstein J. Nanotechnol. 2022, 13, 363–389, doi:10.3762/bjnano.13.31

• , osteogenic, and chondrogenic potentials of the hMSCs [124]. However, the migration of SWCNTs through the cell wall to the nucleus was detected using fluorescence-labeled CNTs. In line with these results, the long term exposure of chondrocytes to COOH- and PEG-functionalized SWCNTs in 2D cultures, 3D pellet

Coordination-assembled myricetin nanoarchitectonics for sustainably scavenging free radicals

• Xiaoyan Ma,
• Haoning Gong,
• Kenji Ogino,
• Xuehai Yan and
• Ruirui Xing

Beilstein J. Nanotechnol. 2022, 13, 284–291, doi:10.3762/bjnano.13.23

• was used to incubate these cells for 5 min and the fluorescence intensity of the cells was recorded via confocal laser scanning microscopy. Results and Discussion Synthesis and characterization of MZG We chose Zn2+, a typical essential metal, to effectively bond Myr and GSH via coordination

• to effectively protect cells from damage. DCFH-DA was used to probe ROS in cells, which showed no fluorescence signal without ROS, while it turned to highly fluorescent 2′7′-dichlorofluorescein after interacting with ROS in cells. As shown in the confocal laser scanning microscopy (CLSM) images, the

• fluorescence intensity of cells treated with H2O2 and MZG nanoparticles was weaker than that of cells only treated with H2O2 (Figure 4e). The fluorescence intensity of cells was further measured, indicating that the fluorescence intensity of cells treated with a combination of MZG nanoparticles and H2O2 was

A comprehensive review on electrospun nanohybrid membranes for wastewater treatment

• Senuri Kumarage,
• Imalka Munaweera and
• Nilwala Kottegoda

Beilstein J. Nanotechnol. 2022, 13, 137–159, doi:10.3762/bjnano.13.10

• acid (DTPA)-modified CS membranes electrospun in combination with PEO [60]. The maximum adsorption capacities according to the Langmuir model were found to be 177, 142, and 56 mg/g for Cu2+, Pb2+, and Ni2+, respectively. Li and co-workers reported on an electrospun magnetic fluorescence nanofiber

• reached equilibrium within 100 min. Moreover, the authors developed a simplistic method for real-time and non-invasive tracking of adsorption, based on the linear relationship between adsorption and fluorescence intensity of the membranes. Yari et al. fabricated a novel mesoporous nanohybrid sorbent

Tin dioxide nanomaterial-based photocatalysts for nitrogen oxide oxidation: a review

• Viet Van Pham,
• Hong-Huy Tran,
• Thao Kim Truong and
• Thi Minh Cao

Beilstein J. Nanotechnol. 2022, 13, 96–113, doi:10.3762/bjnano.13.7

• spectroscopy (EIS) data, and the nanosecond-level time-resolved fluorescence decay spectra (Figure 11) demonstrated that the SnO2/NCDs/ZHS nanohybrid achieved low charge carrier recombination, high photoactivity, and excellent photoinduced charge transfer to the surface of the semiconductor. This study enables

• of ZHS, SnO2/ZHS, NCDs/ZHS and SnO2/NCDs/ZHS samples, and (d) PL spectra (inset: transient fluorescence decay spectra). Figure 11 was republished with permission of The Royal Society of Chemistry from [76] (“Constructing Z-scheme SnO2/N-doped carbon quantum dots/ZnSn(OH)6 nanohybrids with high redox

Theranostic potential of self-luminescent branched polyethyleneimine-coated superparamagnetic iron oxide nanoparticles

• Rouhollah Khodadust,
• Ozlem Unal and
• Havva Yagci Acar

Beilstein J. Nanotechnol. 2022, 13, 82–95, doi:10.3762/bjnano.13.6

• exact reason behind this luminescence is not known, but it seems like there is not a single mechanism that explains the intrinsic fluorescence of these “periodically amine” containing species. Different factors including delocalization of nonbonding electrons in highly repeating systems, the rigidity of

• in many in vitro studies including, for example, flow cytometry or fluorescence imaging, since the luminescence of the polymer was not detected [18][33][34]. Unfortunately, the luminescence of the fluorophores (dye or quantum dots) that are active in the visible range is usually significantly reduced

• as well as its targeted delivery to epidermal growth factor receptor (EGFR)-positive cancer cell lines, in vitro. Initially, the dose dependent cytotoxicity of the nanoparticles was determined. Then, using a fluorescence microscope, the ability of these nanoparticles to generate intracellular optical