Luminescent gold nanoclusters for bioimaging applications

• Nonappa

Beilstein J. Nanotechnol. 2020, 11, 533–546, doi:10.3762/bjnano.11.42

• allowed for plasmonic and magnetic resonance, and luminescence in a single composite system for plasmonic photothermal therapy (PPTT). The bioimaging capability of the plasmonic magneto-luminescent multifunctional nanocarrier (PML-MF) systems were studied in vitro using three types of cancer cells, namely

• potential for photothermal therapy. While PML-MF alone was not toxic to healthy HEK cell lines, the treatment with DPML-MF showed a similar antiproliferative effect on healthy cell lines as that of cancerous cells. Therefore, the selective killing of cancer cells was not achieved. The superparamagnetic

• therapy [93]. The toxicity studies using human oesophageal squamous cancer cells (EC1) showed that when [Au8(C21H27O2)8] was used at a concentration near its IC10 value, the luminescence of the incubated samples increased from 0 to 8 h. The luminescence, however, disappeared after 24 h indicating

Multilayer capsules made of weak polyelectrolytes: a review on the preparation, functionalization and applications in drug delivery

• Varsha Sharma and
• Anandhakumar Sundaramurthy

Beilstein J. Nanotechnol. 2020, 11, 508–532, doi:10.3762/bjnano.11.41

• intensity of radiation successfully breaks the shell and releases the loaded cargo, high intensity leads to the generation of high heat, which helps in destroying the surrounding cancer cells. Even though the advantages of NP incorporation in capsules have been immense, similar work in weak PE assemblies is

• drug-loaded PVPAlk capsules were even shown to overcome multidrug resistance with Dox and paclitaxel against LIM1899 colorectal cancer cells [98]. A new kind of dual (pH and redox) responsive, charge shifting click capsules based on poly(2-diisopropylaminoethyl methacrylate) (PDPA) were also fabricated

• specific to A33 antigens expressed on colorectal cancer cells were adsorbed on capsules from a buffer at pH 7.4 [102]. Both electrostatic and hydrogen bonding contributed to the binding of antibodies to the capsule external layer and to retaining their immunological activity. As mentioned in the previous

Brome mosaic virus-like particles as siRNA nanocarriers for biomedical purposes

• Alfredo Nuñez-Rivera,
• Pierrick G. J. Fournier,
• Danna L. Arellano,
• Ana G. Rodriguez-Hernandez,
• Rafael Vazquez-Duhalt and
• Ruben D. Cadena-Nava

Beilstein J. Nanotechnol. 2020, 11, 372–382, doi:10.3762/bjnano.11.28

• the breast cancer cells. Representative confocal microscopy images showed NanoOrange fluorescence inside the cells (Figure 1A). It is important to point out that the capsids are able to internalize efficiently into tumor cells without any functionalization. The cell internalization has been quantified

• cancer cells was prepared at a concentration of 2 × 106 cells/mL in PBS. 4T1 cells were then inoculated in the left, upper (or 2nd) mammary fat pad (105 cells in 50 µL) of 8-week old Balb/C female mice. One week after the inoculation, palpable tumors were detected in all the mice that were divided into

Poly(1-vinylimidazole) polyplexes as novel therapeutic gene carriers for lung cancer therapy

• Gayathri Kandasamy,
• Elena N. Danilovtseva,
• Vadim V. Annenkov and
• Uma Maheswari Krishnan

Beilstein J. Nanotechnol. 2020, 11, 354–369, doi:10.3762/bjnano.11.26

• efficiency of the formed complexes in A549 lung cancer cells. The polyplex formed was found to exhibit 66% complexation efficiency. The complexation was confirmed by gel retardation assays, FTIR and thermal analysis. The blank PVI polymer was not toxic to cells. The polyplex was found to exhibit excellent

• internalization and escaped the endosome effectively. The polyplex was more effective than free siRNA in silencing VEGF in lung cancer cells. The silencing of VEGF was quantified using Western blot and was also reflected in the depletion of HIF-1α levels in the cells treated with the polyplex. VEGF silencing by

• that have been connected to the proliferation and invasion of lung cancer cells. These results indicate that the PVI complexes can be an effective agent to counter lung cancer. Keywords: anti-VEGF siRNA; gene silencing; lung cancer; microarray; poly(1-vinylimidazole); small interfering RNA (siRNA

Using gold nanoparticles to detect single-nucleotide polymorphisms: toward liquid biopsy

• María Sanromán Iglesias and
• Marek Grzelczak

Beilstein J. Nanotechnol. 2020, 11, 263–284, doi:10.3762/bjnano.11.20

• necrosis [40][41][42][43][44]. Moreover, in solid malignancies, circulating tumor DNA differs from cell-free DNA by somatic mutations [18][46][47]. In leukemia, for example, the increased amount of cfDNA originates from cancer cells. Nonetheless, four main types of gene alterations occurring in cfDNA are

Rational design of block copolymer self-assemblies in photodynamic therapy

• Maxime Demazeau,
• Laure Gibot,
• Anne-Françoise Mingotaud,
• Patricia Vicendo,
• Clément Roux and
• Barbara Lonetti

Beilstein J. Nanotechnol. 2020, 11, 180–212, doi:10.3762/bjnano.11.15

• proposed to overcome the drug resistance of cancer cells. Indeed, it induced membrane permeability of the endo-lysosome and particle disassembly after white-light irradiation thus triggering the release of doxorubicin in the cytosol [96]. In the study by Zheng et al. [100] the AIE fluorophore is used as

• a hydrophilic shell for micelle stabilization, and the derivatized polylysin (Plys) acts as a hydrophobic core to load the photosensitizer (BODIPY), while PMAGP mainly serves to direct the target delivery to hepatoma cancer cells. Folate (FA) has been extensively studied as a targeting moiety [116

• production efficiency was improved. Polymer self-assemblies containing catalase [68] or MnO2 nanoparticles [65][69] have been developed as they can catalytically decompose endogenous H2O2 present in the tumor environment thus increasing the oxygen level in cancer cells. The electrostatic interactions between

Molecular architectonics of DNA for functional nanoarchitectures

• Debasis Ghosh,
• Lakshmi P. Datta and
• Thimmaiah Govindaraju

Beilstein J. Nanotechnol. 2020, 11, 124–140, doi:10.3762/bjnano.11.11

• construction of a DNA origami-based nanorobot for the cargo delivery of payloads into cancer cells [56]. The autonomous DNA nanorobot was constructed using a nucleolin-binding DNA aptamer and was loaded with thrombin protease. The nucleolin protein was overexpressed in tumor-associated endothelial cells, which

• -functionalized iron oxide nanoparticle system was capable of selectively targeting the cancer cells and, potentially, to act as an MRI contrast agent. The programmability of the DNA tetrahedrons provided an opportunity to conjugate other functional nucleic acid sequences, viz., DNA, siRNA, or DNAzymes, to serve

• the ECL quenching via formation of hydrogen peroxide. Kim and co-workers developed an innovative approach of intercalation of the anticancer drug doxorubicin within the DNA tetrahedron that showed improved therapeutic efficacy in drug-resistant breast cancer cells [70]. The doxorubicin-encapsulated

Advanced hybrid nanomaterials

• Andreas Taubert,
• Fabrice Leroux,
• Pierre Rabu and
• Verónica de Zea Bermudez

Beilstein J. Nanotechnol. 2019, 10, 2563–2567, doi:10.3762/bjnano.10.247

• is simultaneously employed as a contrast agent in magnetic resonance imaging (MRI) and for local heating therapy using magnetic particle hyperthermia [33]. In vitro hyperthermia tests showed efficiency in inoculating mouse breast cancer cells. Another study reports the use of alendronate-coated gold

• nanoparticles [34]. The resulting gold–alendronate nanoplatform combines antitumor activity through drug delivery and photothermal therapy, as illustrated in vitro on the inhibition of prostate cancer cells. In the field of hybrid coordination networks, new lanthanide-based networks synthesized by a solvo

Bombesin receptor-targeted liposomes for enhanced delivery to lung cancer cells

• Mohammad J. Akbar,
• Pâmela C. Lukasewicz Ferreira,
• Melania Giorgetti,
• Leanne Stokes and
• Christopher J. Morris

Beilstein J. Nanotechnol. 2019, 10, 2553–2562, doi:10.3762/bjnano.10.246

• vivo cancer imaging. In this report we decorated pegylated liposomes with a GRPR antagonist peptide and studied its interaction with, and accumulation within, lung cancer cells. Results: An N-terminally cysteine modified GRPR antagonist (termed cystabn) was synthesised and shown to inhibit cell growth

• targeting has potential for enhancing drug accumulation in resistant cancer cells. Keywords: bombesin; GRPR; liposome; lung cancer; targeting; Introduction Small-cell lung cancer (SCLC) accounts for approximately one in five lung cancer diagnoses. In spite of global efforts to reduce tobacco smoking in

• (PSMA)-targeted BIND-014 [16] have reached the clinic but detailed information about the clinical advantage of using targeted platforms is still forthcoming. In this study we explored whether surface engraftment of a GRPR antagonist peptide could be used to target GRPR expressing lung cancer cells for

pH-Controlled fluorescence switching in water-dispersed polymer brushes grafted to modified boron nitride nanotubes for cellular imaging

• Saban Kalay,
• Yurij Stetsyshyn,
• Volodymyr Donchak,
• Khrystyna Harhay,
• Ostap Lishchynskyi,
• Halyna Ohar,
• Yuriy Panchenko,
• Stanislav Voronov and
• Mustafa Çulha

Beilstein J. Nanotechnol. 2019, 10, 2428–2439, doi:10.3762/bjnano.10.233

• uptake of P(AA-co-FA)-functionalized BNNTs into human normal prostate epithelium (PNT1A) and human prostate cancer (DU145) cell lines, we used fluorescence microscopy with excitation at 490 nm and emission at 520 nm (Figure 9). The autofluorescence of healthy cells and cancer cells was strictly avoided

• BNNTs clearly showed fluorescence not only in the nuclei but also in the cytosol. The reason for this is likely due to the more internalized material compared to the healthy cells as a result of higher metabolic activity of cancer cells. This study clearly shows that the cellular uptake of P(AA-co-FA

Design of a nanostructured mucoadhesive system containing curcumin for buccal application: from physicochemical to biological aspects

• Sabrina Barbosa de Souza Ferreira,
• Gustavo Braga,
• Évelin Lemos Oliveira,
• Jéssica Bassi da Silva,
• Hélen Cássia Rosseto,
• Lidiane Vizioli de Castro Hoshino,
• Mauro Luciano Baesso,
• Wilker Caetano,
• Craig Murdoch,
• Helen Elizabeth Colley and
• Marcos Luciano Bruschi

Beilstein J. Nanotechnol. 2019, 10, 2304–2328, doi:10.3762/bjnano.10.222

• 8 h and could permeate through the porcine oral mucosa. Cytotoxicity testing revealed that the formulations were selective to cancer cells over healthy cells. Therefore, these systems could improve the physicochemical characteristics of curcumin by providing improved release and permeation, while

• selectivity targeting cancer cells. Keywords: curcumin; mucoadhesion; oral squamous cell carcinoma; permeation; poloxamer 407; Introduction The development of nanostructured systems containing poloxamer 407 (P407) and Carbopol 974P® (C974P) have previously been shown to have rheological and mechanical

• incorporated into the formulation but decreased cytotoxic effects in healthy cells. Therefore, the nanostructured system demonstrated promising results due to the selectivity towards cancer cells in a monolayer cell culture in addition to exhibiting excellent physicochemical properties. Hence, further activity

Use of data processing for rapid detection of the prostate-specific antigen biomarker using immunomagnetic sandwich-type sensors

• Camila A. Proença,
• Tayane A. Freitas,
• Thaísa A. Baldo,
• Elsa M. Materón,
• Flávio M. Shimizu,
• Gabriella R. Ferreira,
• Frederico L. F. Soares,
• Ronaldo C. Faria and
• Osvaldo N. Oliveira Jr.

Beilstein J. Nanotechnol. 2019, 10, 2171–2181, doi:10.3762/bjnano.10.210

• ) and prostate cancer cells (LNCap). Parallel coordinates plot for PSA concentrations from 12.5 to 1111 fg·mL−1 after the feature-selection procedure. The x-axis represents time values, while the y-axis represents Euclidean distances related to the current. IDMAP plot obtained from the data in Figure 1A

• for buffers containing different PSA concentrations and from Figure 3 for prostate cancer cells. In both cases, feature selection was applied before plotting the data. Schematic illustration of the fabrication of sandwich-type electrochemical immunosensors (INμ-SPCEs). Electrode modification with 10

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

• . The expression of efflux transporters such as the ATP-binding cassette (ABC) transporter ABCB1 is an important resistance mechanism in therapy-refractory cancer cells. Drug encapsulation into nanoparticles has been shown to bypass efflux-mediated drug resistance, but there are also conflicting results

• an important step in the development of improved nanoparticle preparations for anticancer therapy. Further research is required to understand under which circumstances nanoparticles can be used to overcome efflux-mediated resistance in cancer cells. Keywords: cancer; doxorubicin; drug release

• cancer [4][5][6][7][8][9]. Another important aspect of the efficacy of nanoparticles as delivery system for anticancer is their uptake and, in turn, the drug transport into cancer cells. Uptake mechanisms may differ between different types of nanoparticles, which may affect their effectiveness as

Review of advanced sensor devices employing nanoarchitectonics concepts

• Katsuhiko Ariga,
• Tatsuyuki Makita,
• Masato Ito,
• Taizo Mori,
• Shun Watanabe and
• Jun Takeya

Beilstein J. Nanotechnol. 2019, 10, 2014–2030, doi:10.3762/bjnano.10.198

• useful for the rapid screening of diseases as a point-of-care diagnostic tool. Owens and co-workers developed organic field-effect transistor systems with PEDOT/PSS materials for the detection of lactate [111]. Enhanced lactate production was detected for cancer cells because of their promoted activity

Synthesis and potent cytotoxic activity of a novel diosgenin derivative and its phytosomes against lung cancer cells

• Liang Xu,
• Dekang Xu,
• Ziying Li,
• Yu Gao and
• Haijun Chen

Beilstein J. Nanotechnol. 2019, 10, 1933–1942, doi:10.3762/bjnano.10.189

• sterol structure similarly to cholesterol, P2 phytosomes (P2Ps) were prepared to further improve the water solubility of P2. The P2Ps exhibited a particle size of 53.6 ± 0.3 nm with oval shape and a zeta potential of −4.0 ± 0.7 mV. P2Ps could inhibit the proliferation of lung cancer cells more

• anticancer activities, such as restraining the hTERT gene expression in A549 lung cancer cells [3], inhibiting breast cancer stem-like cells via Wnt β-catenin signaling [4], impeding hepatocellular carcinoma cells by increasing DDX3 expression [5], and inducing apoptosis of prostate cancer cells through

• phytosomes were prepared by substituting Di and its derivative for cholesterol. The anticancer effects of free drugs and their phytosomes were investigated in non-small-cell lung cancer cells. Results and Discussion Synthesis and characterization of Di derivatives Late-stage functionalization that uses the C

Microfluidic manufacturing of different niosomes nanoparticles for curcumin encapsulation: Physical characteristics, encapsulation efficacy, and drug release

• Mohammad A. Obeid,
• Ibrahim Khadra,
• Abdullah Albaloushi,
• Margaret Mullin,
• Hanin Alyamani and
• Valerie A. Ferro

Beilstein J. Nanotechnol. 2019, 10, 1826–1832, doi:10.3762/bjnano.10.177

• surfactants prepared by the solvent evaporation method, Xu et al. were able to achieve around 92% loading efficiency of curcumin and measured enhanced cytotoxic activity against ovarian cancer cells compared with freely dispersed curcumin [9]. Microfluidic mixing is a recently developed method for the

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

• conceptually very attractive because it can (in contrast to inhibitors of ABCB1 or other transporters) overcome resistance mediated by multiple transporters and does not result in the systemic inhibition of transporter function at physiological barriers. However, cancer cells may be characterised by multiple

• more sophisticated, personalised therapies will need to be developed. Such therapies will depend on an improved understanding of the resistance status of cancer cells to a certain drug beyond its transporter status. If biomarkers become available that predict cancer cell response to a certain drug more

• reliably, nanoparticles can be used to transport drugs under circumvention of transporter-mediated efflux into cancer cells that are likely to respond to them. In conclusion, doxorubicin-loaded HSA nanoparticles produced by desolvation and cross-linking using glutaraldehyde overcome (in contrast to other

Materials nanoarchitectonics at two-dimensional liquid interfaces

• Katsuhiko Ariga,
• Michio Matsumoto,
• Taizo Mori and
• Lok Kumar Shrestha

Beilstein J. Nanotechnol. 2019, 10, 1559–1587, doi:10.3762/bjnano.10.153

• sophisticated strategy to realize chemotherapy targeting at cancer cells using the controlled assembly and disassembly of layer-by-layer hybrid structures made of two dimensional MoS2 nanosheets with DNA [87]. The preparation of functional low-dimensional materials requires preservation of nanoscale features in

The effect of magneto-crystalline anisotropy on the properties of hard and soft magnetic ferrite nanoparticles

• Hajar Jalili,
• Bagher Aslibeiki,
• Ali Ghotbi Varzaneh and
• Volodymyr A. Chernenko

Beilstein J. Nanotechnol. 2019, 10, 1348–1359, doi:10.3762/bjnano.10.133

• to destroy cancer cells through the elevated temperatures [16][17]. The heating efficiency of the NPs as heat sources under ac magnetic fields is often denominated as specific absorption rate (SAR), which is directly related to the area of the magnetic hysteresis loop of the nanoparticles by the

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

• obtained from Promega Corporation (Madison, USA). Urea was purchased from Acros Organics (New Jersey, USA). Human liver cancer cells (HepG2) were kindly provided by the Institute of Food Chemistry of the University of Muenster, Germany. Phosphate-buffered saline (PBS), Dulbecco’s modified Eagle’s medium

The systemic effect of PEG-nGO-induced oxidative stress in vivo in a rodent model

• Qura Tul Ain,
• Samina Hyder Haq,
• Abeer Alshammari,
• Moudhi Abdullah Al-Mutlaq and
• Muhammad Naeem Anjum

Beilstein J. Nanotechnol. 2019, 10, 901–911, doi:10.3762/bjnano.10.91

• dual-functionalized GO for the photothermal enhancement of gene delivery [23]. Xiong et al. studied the synergistic effects of PEG-functionalized GO for chemo-photothermal therapy [24]. Tian et al. revealed that PEG-GO enhanced the uptake of chlorin e6 by cancer cells [25]. Shen et al. exploited the

Tungsten disulfide-based nanocomposites for photothermal therapy

• Tzuriel Levin,
• Hagit Sade,
• Rina Ben-Shabbat Binyamini,
• Maayan Pour,
• Iftach Nachman and
• Jean-Paul Lellouche

Beilstein J. Nanotechnol. 2019, 10, 811–822, doi:10.3762/bjnano.10.81

• . Functionalization of the nanotubes with CAN-mag nanoparticles resulted in a magnetic nanocomposite. When tested in vitro with two types of cancer cells, the functionalized nanotubes showed a better PTT activity compared to non-functionalized nanotubes, as well as reduced aggregation and the ability to add a second

• human cancer cells – HeLa (cervical cancer) and MCF7 (breast cancer). The cells were cultured on 24-well plates. When the cells reached 80% confluence, freshly prepared aqueous dispersions of WS2-NT or WS2-NT-CM (45 µL, 1 mg/mL) were added to two of the plates, and a third plate, with no additives, was

• small percentages. Yet, the composite maintained the magnetic character of the nanoparticles. Moreover, the functionalized nanotubes proved to have a higher activity as PTT agents compared to bare WS2-NTs in in vitro tests done with HeLa and MCF7 cancer cells. In addition, functionalization with CAN-mag

Polydopamine-coated Au nanorods for targeted fluorescent cell imaging and photothermal therapy

• Boris N. Khlebtsov,
• Andrey M. Burov,
• Timofey E. Pylaev and
• Nikolai G. Khlebtsov

Beilstein J. Nanotechnol. 2019, 10, 794–803, doi:10.3762/bjnano.10.79

• fluorescent imaging and plasmonic phothothermal abilities have not been reported previously. The multifunctional nanoparticles were stable in cell buffer, nontoxic and suitable for targeted fluorescent imaging and photothermal therapy of cancer cells. We demonstrate the enhanced accumulation of folate

• ) loading, resulting in the formation of AuNR-PDA-R123-folate nanocomposites (Scheme 1). This platform demonstrates three distinct features: (1) targeting of nanocomposites with folic acid leads to enhanced cellular uptake by folate-positive cancer cells compared with PEG-coated nanorods; (2) the high

• loading with rhodamine 123 makes the nanoparticles suitable for cell imaging with a simple fluorescent microscope; (3) through using NIR-mediated photothermal therapy the cancer cells can be killed with a high efficiency. Results and Discussion Synthesis and characterization of the AuNRs-PDA-R123-folate

Targeting strategies for improving the efficacy of nanomedicine in oncology

• Gonzalo Villaverde and
• Alejandro Baeza

Beilstein J. Nanotechnol. 2019, 10, 168–181, doi:10.3762/bjnano.10.16

• against specific cell populations. As example, Herceptin is an antibody that recognizes the human epidermal growth factor receptor 2 (HER2) overexpressed in breast cancer cells (HER2+). This antibody has been attached on the surface of poly(D,L-lactic-co-glycolic acid) (PLGA) nanoparticles loaded with the

• specifically to αβ-integrin, which is usually upregulated in many different tumoral cell lines such as breast, lung or fibroblast cancer cells, and also by the epithelial cells of the tumoral blood vessels [32][33]. Ruoshlati et al. have reported that the cyclic version of RGD, CRGDKGPDC (called iRGD), which

• destruction of CD13+ cancer cells as human fibrosarcoma cells (HT-1080) [36]. These liposomes released more than 75% of their payload when the temperature reached 41.3 °C whereas they maintained the Dox within their hydrophilic core at physiological temperature. Other systems widely employed for targeting

Surface plasmon resonance enhancement of photoluminescence intensity and bioimaging application of gold nanorod@CdSe/ZnS quantum dots

• Siyi Hu,
• Yu Ren,
• Yue Wang,
• Jinhua Li,
• Junle Qu,
• Liwei Liu,
• Hanbin Ma and
• Yuguo Tang

Beilstein J. Nanotechnol. 2019, 10, 22–31, doi:10.3762/bjnano.10.3

• as an optical process for MCF-7 breast cancer cells. Keywords: bioimaging; gold nanorods; photoluminescence enhancement; quantum dots; Introduction In the past decades, quantum dots (QDs) have proven to be increasingly useful for their unique features [1][2][3][4][5]. The light emission from QDs

• distance using the combined strong electrostatic adsorption. Secondly, FA was conjugated with this composite nanoparticle for biological applications, where the FA renders the nanoparticle useful for the specific targeting of cancer cells [28][29]. According to current knowledge, when bulk semiconductor

• staining appearing in Figure 8 was due to the accumulation of functionalized nanoparticles in the cells, and there was no sign of any damage to the cell, demonstrating passive uptake in MCF-7 breast cancer cells using CdSe/ZnS@FA and GNR@CdSe/ZnS@FA. However, because the PL intensity and cell morphology of