A review on nanostructured silver as a basic ingredient in medicine: physicochemical parameters and characterization

• Gabriel M. Misirli,
• Kishore Sridharan and
• Shirley M. P. Abrantes

Beilstein J. Nanotechnol. 2021, 12, 440–461, doi:10.3762/bjnano.12.36

• macrophages to produce activated ISGs and pro-inflammatory cytokines, such as interleukins (IL-6, IL-8) [76][115][116][117]. Several studies have shown that AgNPs can act against various types of viruses, viz. human immunodeficiency virus type 1 (HIV-1) [111][118], monkeypox virus (MPV) [112], herpes simplex

• necessary and, in general, it is not a long-lasting protective immunity (immunologic memory). Monocytes and macrophages are the most common phagocytic cells in the body and represent the first innate line of defense, in addition to being responsible for the removal of particles [126]. Carlson et al. and

• Castillo et al. verified the interaction between AgNPs and macrophages and they saw that these NPs remained intact, with no evidence of AgNPs dissolution or cytotoxicity. Once inside the cells, and after 24 h of exposure, the nanoparticles remained at approximately the same size they were before incubation

The impact of molecular tumor profiling on the design strategies for targeting myeloid leukemia and EGFR/CD44-positive solid tumors

• Nikola Geskovski,
• Nadica Matevska-Geshkovska,
• Simona Dimchevska Sazdovska,
• Marija Glavas Dodov,
• Kristina Mladenovska and
• Katerina Goracinova

Beilstein J. Nanotechnol. 2021, 12, 375–401, doi:10.3762/bjnano.12.31

• , hematopoietic, which are responsible for the hematopoiesis, and mesenchymal, which produce the stromal, fat, cartilage, and bone tissue. The BM stroma contains fibroblasts, macrophages, adipocytes, osteoblasts, osteoclasts, and endothelial cells. It provides the appropriate microenvironment for efficient

• adsorbs onto the surface of poloxamer 407-coated colloidal particles, thus exhibiting microdomains that are specific for the sinusoidal BM endothelium. Another mechanism of BM targeting is the phagocytosis-mediated uptake from the perisinusoidal macrophages. It is known that the perisinusoidal BM

• macrophages protrude through the vascular endothelial wall to gain access and monitor blood circulation [24]. Hussain et al demonstrated that perisinusoidal macrophages are responsible for the accumulation of the chylomicrons in the BM and, hence, play a crucial role in the delivery of lipids, as a source of

Differences in surface chemistry of iron oxide nanoparticles result in different routes of internalization

• Barbora Svitkova,
• Vlasta Zavisova,
• Veronika Nemethova,
• Martina Koneracka,
• Miroslava Kretova,
• Filip Razga,
• Monika Ursinyova and
• Alena Gabelova

Beilstein J. Nanotechnol. 2021, 12, 270–281, doi:10.3762/bjnano.12.22

• occurs primarily in specialized cells, such as macrophages or monocytes, other endocytic pathways occur in virtually all cells [8]. Clathrin-mediated endocytosis (CME) is the predominant endocytosis pathway and is involved mainly in nutrient intake and intracellular communication [9][10]. CME is

• involved in PC formation. Hence, coating of MNPs with BSA can be considered as a PC per se. As a dysopsonin protein, albumin promotes a prolonged blood circulation time through blocking the recognition by macrophages [42]. A comprehensive characterization of nanoparticles in biological fluids is, therefore

• inhibition of de novo synthesis [52]. While both F and N blocked the internalization of cholera toxin (ChT) into A549 cells, no effect of MBCD on ChT uptake was observed. Similar results were obtained in J774A.1 macrophages [48]. In contrast, Rothen-Rutishauser et al. [50] did not find any inhibition of ChT

Effect of different silica coatings on the toxicity of upconversion nanoparticles on RAW 264.7 macrophage cells

• Cynthia Kembuan,
• Helena Oliveira and
• Christina Graf

Beilstein J. Nanotechnol. 2021, 12, 35–48, doi:10.3762/bjnano.12.3

• cytometry measurements performed on macrophages (RAW 264.7 cells) indicate that cells treated with amino-functionalized particles with a thicker silica shell have a higher viability than those incubated with UCNPs with a thinner silica shell, even if more particles with a thicker shell are taken up. This

• the macrophage cell line RAW 264.7. RAW 264.7 cells are particularly sensitive to the treatment with nanoparticles [42][43][44]. They are an established model of activated macrophages and they actively take up nanomaterials from biological media. This way, RAW264.7 cells mimic the behavior of

• macrophages and other immune cells, which eliminate foreign substances from the organism. Moreover, they have already been applied in studies involving uncoated NaGdF4 [42] and silica particles [43][44][45][46]. Upconversion cores consisting of NaYF4 doped with 18% Yb and 2% Er were synthesized. Microporous

PEG/PEI-functionalized single-walled carbon nanotubes as delivery carriers for doxorubicin: synthesis, characterization, and in vitro evaluation

• Shuoye Yang,
• Zhenwei Wang,
• Yahong Ping,
• Yuying Miao,
• Yongmei Xiao,
• Lingbo Qu,
• Lu Zhang,
• Yuansen Hu and
• Jinshui Wang

Beilstein J. Nanotechnol. 2020, 11, 1728–1741, doi:10.3762/bjnano.11.155

• ]. However, to the best of our knowledge, studies characterizing CNTs according to the dispersibility produced by different oxidizing acids have been scarcely performed. The macrophages of the reticuloendothelial system (RES) cannot recognize nonopsonized nanoparticles circulating in the blood system

Cardiomyocyte uptake mechanism of a hydroxyapatite nanoparticle mediated gene delivery system

• Hiroaki Komuro,
• Masahiro Yamazoe,
• Kosuke Nozaki,
• Akiko Nagai and
• Tetsuo Sasano

Beilstein J. Nanotechnol. 2020, 11, 1685–1692, doi:10.3762/bjnano.11.150

• the presence than in the absence of HAp (Figure 5). Extracellular calcium ions are proposed to act as a stimulant for triggering macropinocytosis in macrophages and neurons [25][36]. The extracellular calcium-sensing receptor (CaSR) is expressed in cardiomyocytes as well as in various other cells [37

• ]. The results suggested that calcium ions from HAp particles might activate macropinocytosis in HL-1 cells. CaSR has different functions depending on the cell type. In osteoclasts, for example, it directs migration toward bone tissue for bone remodeling, whereas in macrophages it aids in the antigen

Applications of superparamagnetic iron oxide nanoparticles in drug and therapeutic delivery, and biotechnological advancements

• Maria Suciu,
• Corina M. Ionescu,
• Alexandra Ciorita,
• Septimiu C. Tripon,
• Dragos Nica,
• Hani Al-Salami and
• Lucian Barbu-Tudoran

Beilstein J. Nanotechnol. 2020, 11, 1092–1109, doi:10.3762/bjnano.11.94

• at a concentration of 400 µg Fe/mL, in contrast to the PEG-coated SPIONs, which reached 50% toxicity at 100 µg Fe/mL. Dextran was shown to get stripped from the nanoparticles in macrophages that were later apoptotic. The authors concluded that apoptosis was caused first by dextran intoxication and

• PVA or PEG, for drug release studies [33][76] because the hydrophobic polymers are rapidly uptaken by macrophages [85]. SPIONs coated with a mixture of PVA and polyvinyl amine were shown to induce very active mitochondrial and endocytic processes in cells and to be highly toxic to cells due to the

• increase in macrophages. The general consideration is that polymer coating offers colloidal stability, but in fact PVA-coated SPIONs are only stable in water at a certain pH value. In cell culture medium they agglomerate. Studies showed that the components of the medium, and not the calf serum added to the

Preparation and in vivo evaluation of glyco-gold nanoparticles carrying synthetic mycobacterial hexaarabinofuranoside

• Gennady L. Burygin,
• Polina I. Abronina,
• Nikita M. Podvalnyy,
• Sergey A. Staroverov,
• Leonid O. Kononov and
• Lev A. Dykman

Beilstein J. Nanotechnol. 2020, 11, 480–493, doi:10.3762/bjnano.11.39

• subsequent presentation of the epitopes on the surface of macrophages are important events in this positive regulation. According to the literature data, GNPs contribute to the penetration of antigens into phagocytic cells [56]. GNPs, in addition to their adjuvant properties, could lead to a more active

• of macrophages, which is required for the activation of specific B-cells. Clearly, such a substitution is more favored for glyco-GNPs based on amine-terminated glycans than for the more stable glyco-GNPs based on thiol-terminated glycans (for B-cell activation, the latter require the addition of

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

• effects on tumor cells in vitro. However, only BMV did not activate macrophages in vitro. This suggests that BMV is less immunogenic and may be a potential carrier for therapy delivery in tumor cells. Furthermore, BMV virus-like particles (VLPs) were efficiently loaded with small interfering RNA (siRNA

• . Surprisingly, a remarkable difference was found. CCMV showed a high activation of macrophages, while BMV showed almost no immunogenic response (Figure 3C,D). There is 80% homology in the amino acids sequences of CCMV and BMV [21], however, they differ in their surface charge. The zeta potential at pH 7 was

• particles tend to be phagocytosed by macrophages [44]. Accordingly, the virus uptake by the macrophages can activate intracellular receptors, i.e., toll-like receptors (TLR) 7/8, which can recognize the viral ssRNA genome, promoting the activation of the macrophages. This mechanism of TLR 7/8 activation has

Interactions at the cell membrane and pathways of internalization of nano-sized materials for nanomedicine

• Valentina Francia,
• Daphne Montizaan and
• Anna Salvati

Beilstein J. Nanotechnol. 2020, 11, 338–353, doi:10.3762/bjnano.11.25

• could be internalized by HeLa cells [125]. Moreover, the effects of nanoparticle size on the mechanism of uptake may be different in different cell types. For example, it has been shown that murine RAW 264.7 macrophages have a higher uptake efficiency for carboxylated polystyrene nanoparticles compared

Internalization mechanisms of cell-penetrating peptides

• Ivana Ruseska and
• Andreas Zimmer

Beilstein J. Nanotechnol. 2020, 11, 101–123, doi:10.3762/bjnano.11.10

• and is restricted to specialized cells (macrophages, monocytes and neutrophils). Pinocytosis, on the other hand, involves the uptake of fluids and solutes and occurs in all cells. At least four different mechanisms have been described for pinocytosis: macropinocytosis, clathrin-mediated endocytosis

The different ways to chitosan/hyaluronic acid nanoparticles: templated vs direct complexation. Influence of particle preparation on morphology, cell uptake and silencing efficiency

• Arianna Gennari,
• Julio M. Rios de la Rosa,
• Erwin Hohn,
• Maria Pelliccia,
• Enrique Lallana,
• Roberto Donno,
• Annalisa Tirella and
• Nicola Tirelli

Beilstein J. Nanotechnol. 2019, 10, 2594–2608, doi:10.3762/bjnano.10.250

• all a higher aspect ratio (Rg/RH) and a lower fractal dimension. We then compared the kinetics of uptake and the (antiluciferase) siRNA delivery performance in murine RAW 264.7 macrophages and in human HCT-116 colorectal tumor cells. The preparative method (and therefore the internal particle

• performing better in macrophages and those with high-MW chitosan in HCT-116. Keywords: aggregation; chitosan; field flow fractionation; light scattering; targeted drug delivery; Introduction Chitosan is a linear copolymer of β-1,4-ᴅ-glucose-2-amine and N-acetyl-ᴅ-glucose-2-amine, and is commonly employed

• presentation of HA [18], which affected the nanoparticle internalization in both RAW 264.7 macrophages [19][20] and XS106 dendritic cells [21]. In both cases, nanoparticles based on chitosan of low molecular weight appeared to be surrounded by a corona of loosely bound HA, which on one hand lowered the maximum

Small protein sequences can induce cellular uptake of complex nanohybrids

• Jan-Philip Merkl,
• Malak Safi,
• Christian Schmidtke,
• Fadi Aldeek,
• Johannes Ostermann,
• Tatiana Domitrovic,
• Sebastian Gärtner,
• John E. Johnson,
• Horst Weller and
• Hedi Mattoussi

Beilstein J. Nanotechnol. 2019, 10, 2477–2482, doi:10.3762/bjnano.10.238

• macrophages to these hybrid materials combined with an improvement in their in vivo tumour accumulation [6]. Weil and co-workers described the use of multimodal platforms, made of diamond dots combined with gold nanoparticles, as imaging probes of live cell cultures [7]. We have recently characterized a

Mannosylated brush copolymers based on poly(ethylene glycol) and poly(ε-caprolactone) as multivalent lectin-binding nanomaterials

• Stefania Ordanini,
• Wanda Celentano,
• Anna Bernardi and
• Francesco Cellesi

Beilstein J. Nanotechnol. 2019, 10, 2192–2206, doi:10.3762/bjnano.10.212

• polymer that does not promote immune responses. Pegylation reduces the nonspecific binding of nanoparticles to blood proteins and macrophages, making them non-immunogenic and non-antigenic [21]. PEG-PCL copolymers are amphihilic materials that can spontaneously assemble in aqueous media, forming colloidal

Nitrogen-vacancy centers in diamond for nanoscale magnetic resonance imaging applications

• Alberto Boretti,
• Lorenzo Rosa,
• Jonathan Blackledge and
• Stefania Castelletto

Beilstein J. Nanotechnol. 2019, 10, 2128–2151, doi:10.3762/bjnano.10.207

• bulk MRI T2 relaxation time was 23.6 ms with an accuracy of 2.8%. Direct experimental MRI measurements of T2 in macrophages prepared for the NV experiment was also performed to determine the accuracy of the reconstruction from the magnetic field images. The distinction between clustered and diffused

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

• -coated iron oxide nanoparticles to target tumor-associated macrophages [36] and D-AE-peptide-modified micelles as a multitarget drug delivery system [37], the benefits of the nanoprobe in this study are described as follows. First, the nanoprobe has a diameter of around 100 nm and can directly pass

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

• ]. IgG is a major effector molecule of the humoral immune response and takes part in the general process of opsonization for presentation to macrophages [26]. Besides, it activates the classical pathway of the complement system. Immediately after binding of IgG to foreign materials it forms a complex

• cases accompanied by hemoglobin release. Hemoglobin adsorbs to NP surfaces and therefore facilitates phagocytosis by macrophages [36]. The LC–MS/MS results are consistent with the data presented in Figures 2–4, leading us to the assumption that the origin of the protein source plays a crucial role in

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

• receptors expressed in tumoral but also in healthy cells, and the rapid uptake by the reticuloendothelial system, macrophages and supportive cells such as fibroblasts the decrease the nanocarrier concentration in the blood stream. Also, the poor penetration capacity into the tumoral mass due to strong

• would be the first step required for a capture by macrophages. When the system reaches the tumoral tissue, the PEG chain is cleaved leaving exposed the targeting ligand for tumoral cell recognition and internalization. In the recent years, several works reported that the use of PEG could induce

Characterization and influence of hydroxyapatite nanopowders on living cells

• Przemyslaw Oberbek,
• Tomasz Bolek,
• Adrian Chlanda,
• Seishiro Hirano,
• Sylwia Kusnieruk,
• Julia Rogowska-Tylman,
• Ganna Nechyporenko,
• Viktor Zinchenko,
• Wojciech Swieszkowski and
• Tomasz Puzyn

Beilstein J. Nanotechnol. 2018, 9, 3079–3094, doi:10.3762/bjnano.9.286

• belong to the CHO cell line, which can be explained by the nature of the reproductive system in which calcium signalling plays a crucial role. For example, calcium signals control cell division in early embryos and are very important in the development of patterning [78]. Macrophages are cells

• –300 µg/mL. Macrophages are used to absorb foreign substances and because of their nature they have no significant difficulties digesting excess hydroxyapatite. In the case of these cells, a problem might be related to the high pH value connected to solubility of HApSA+Si and its lowest crystallinity

Bioinspired self-healing materials: lessons from nature

• Joseph C. Cremaldi and
• Bharat Bhushan

Beilstein J. Nanotechnol. 2018, 9, 907–935, doi:10.3762/bjnano.9.85

• less drastic response in dealing with the injury. As survival (typically) is not as much in question after a PNS injury, the healing response lends for a more restorative path. Macrophages and monocytes, types of white blood cells from the inflammatory immune response, clear material from the wound

Nanoparticle delivery to metastatic breast cancer cells by nanoengineered mesenchymal stem cells

• Liga Saulite,
• Karlis Pleiko,
• Ineta Popena,
• Dominyka Dapkute,
• Ricardas Rotomskis and
• Una Riekstina

Beilstein J. Nanotechnol. 2018, 9, 321–332, doi:10.3762/bjnano.9.32

• phagocytosed by the macrophages and sequestered in the liver, spleen, and lymph nodes [1][2]. To overcome this hurdle, targeted drug delivery using nanoengineered cells with cancer homing capability has emerged as an alternative approach. Based on the characteristic tumour tropism, integration in tumour stroma

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

• Marburg, Renthof 7, 35037 Marburg, Germany 10.3762/bjnano.8.239 Abstract Little is known about the simultaneous uptake of different engineered nanoparticle types, as it can be expected in our daily life. In order to test such co-exposure effects, murine macrophages (J774A.1 cell line) were incubated with

• % after 1 h and 50% after 24 h. J774A.1 mouse macrophages were exposed either to a single exposure of either particle type, or a co-exposure, and were subsequently studied using ESEM. Interestingly, both NP types were already visible at the macrophage filopodia after this short incubation time (Figure 2

• ± 13 nm between AuNPs could be calculated (Figure S14, Supporting Information File 1). Such organisation was not observed for FeOxNPs, which appeared to be randomly dispersed on the cell surface. Interaction of particles with macrophages First, it was studied if the cells indeed react on NPs in their

Development of an advanced diagnostic concept for intestinal inflammation: molecular visualisation of nitric oxide in macrophages by functional poly(lactic-co-glycolic acid) microspheres

• Kathleen Lange,
• Christian Lautenschläger,
• Maria Wallert,
• Stefan Lorkowski,
• Andreas Stallmach and
• Alexander Schiller

Beilstein J. Nanotechnol. 2017, 8, 1637–1641, doi:10.3762/bjnano.8.163

• Schiller University Jena, Institute for Inorganic and Analytical Chemistry, Humboldtstr. 8, 07743 Jena, Germany 10.3762/bjnano.8.163 Abstract We here describe a new approach to visualise nitric oxide (NO) in living macrophages by fluorescent NO-sensitive microspheres based on poly(lactic-co-glycolic acid

• through UV radiation (254 nm) of 10 mM sodium nitroprusside dehydrate (SNP). After incubation, AZO550 microspheres exhibited an about 8-fold increased emission at 550 nm compared to NO550 particles. For biotic NO release, RAW 264.7 murine macrophages were activated with lipopolysaccharide (LPS) of

• the inflamed mucosa [4]. Previously, we have shown that polymeric particles penetrate and accumulate selectively within the inflamed mucosa proving that a particle-based approach is feasible [5][6]. Now, we introduce a cutting-edge strategy to visualise NO in living macrophages as first step, and to

Bright fluorescent silica-nanoparticle probes for high-resolution STED and confocal microscopy

• Isabella Tavernaro,
• Christian Cavelius,
• Henrike Peuschel and
• Annette Kraegeloh

Beilstein J. Nanotechnol. 2017, 8, 1283–1296, doi:10.3762/bjnano.8.130

• A549 cells, as well as to quantify the number of internalised nanoparticles in these cells [45][46][47]. In another study small silica nanoparticles with diameters of 25 and 40 nm and modified with Atto647N dye were used to investigate the uptake in macrophages [48]. Herein we present the improved

Uptake of the proteins HTRA1 and HTRA2 by cells mediated by calcium phosphate nanoparticles

• Olga Rotan,
• Katharina N. Severin,
• Simon Pöpsel,
• Alexander Peetsch,
• Melisa Merdanovic,
• Michael Ehrmann and
• Matthias Epple

Beilstein J. Nanotechnol. 2017, 8, 381–393, doi:10.3762/bjnano.8.40

• remained. In order to obtain adherent cells, THP-1 cells (a human acute monocytic leukemia cell line) were first seeded in 24-well plates (Sarstedt, USA) at a density of 5·105 cells per well in 0.5 mL of cell medium, then differentiated into macrophages by the addition of 100 nM of PMA (4β-phorbol-12β