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Search for "targeting" in Full Text gives 176 result(s) in Beilstein Journal of Nanotechnology.
Recent progress on field-effect transistor-based biosensors: device perspective
Beilstein J. Nanotechnol. 2024, 15, 977–994, doi:10.3762/bjnano.15.80
- coupling [55]. The variation of capacitance depends on the intrinsic charge density and the dielectric constant of the target biomolecule [48]. The cavity specification and thereby the sensor device design is also related to the diameter of targeting species, which varied from micro- to nanoscale (Figure 4
- (≈108) and increased sensing speed through the extended cavity in the oxide–source region of the proposed biosensor structure. Furthermore, the fabrication of a silicon NW TFET-based biosensor has been reported by Gao et al. [84], targeting high sensitivity, versatility, and reliability for point-of
- FET-based biosensors. A Schottky barrier (SE SB) FET-based biosensor, engineered with a charge plasma source, has been proposed and simulated by Hafiz et al. [93], targeting biosensing applications. Figure 10 shows the innovative structure of SE SB FET-based biosensor which utilizes a hafnium material
Therapeutic effect of F127-folate@PLGA/CHL/IR780 nanoparticles on folate receptor-expressing cancer cells
Beilstein J. Nanotechnol. 2024, 15, 954–964, doi:10.3762/bjnano.15.78
- and diagnosis, leveraging the advantages of PLGA, folate targeting, and the integration of therapeutic and imaging agents. Keywords: cancer; chlorambucil; drug carrier; IR780; PLGA nanoparticle; theragnostic; Introduction Poly(ᴅ,ʟ-lactic-co-glycolic acid) (PLGA), a copolymer of poly(lactic acid
- used. Its receptor is significantly overexpressed in several types of cancer cells, while there is an undetectable expression in normal cells [12]. Hence, the incorporation of folic acid into nanoparticles is helpful in actively targeting tumors [12][13]. In our previous study, F127 was conjugated with
- discovered to have exceptional inherent tumor-targeting characteristics without any modification, and it is a fluorophore enabling near-infrared imaging. However, IR780 iodide has low water stability and photostability [23] and shows acute toxicity at high doses [24], which limits its clinical application
Electrospun nanofibers: building blocks for the repair of bone tissue
Beilstein J. Nanotechnol. 2024, 15, 941–953, doi:10.3762/bjnano.15.77
- regeneration [25][29]. Polymeric nanofibrous scaffolds Bone has the ability to heal after fractures and to regenerate continuously. Nevertheless, tumor resections, traumatic bone loss, or large defects caused by infections cannot heal without surgical interventions, and treatments targeting skeletal
Identification of structural features of surface modifiers in engineered nanostructured metal oxides regarding cell uptake through ML-based classification
Beilstein J. Nanotechnol. 2024, 15, 909–924, doi:10.3762/bjnano.15.75
- . Ultimately, this cascade leads to damage to cellular organelles and the demise of the cell [13][14][15]. ENMOs have also been explored for potential diagnostic applications, particularly in targeting cancer cells [16][17]. To create target-specific NPs, researchers synthesized magnetofluorescent NPs with an
- modifiers of nanostructured metal oxides. This may facilitate a higher therapeutic response by surface modifier-mediated site-specific targeting to the cell surface receptors of particular cell types. Further availability of sufficient and reliable uptake data of ENMOs in other cell types is also needed for
Radiofrequency enhances drug release from responsive nanoflowers for hepatocellular carcinoma therapy
Beilstein J. Nanotechnol. 2024, 15, 569–579, doi:10.3762/bjnano.15.49
- still diagnosed at an advanced stage [2][3]. Atezolizumab combined with bevacizumab is the primary recommended systematic treatment for advanced HCC according to mainstream guidelines [4][5]. Even if these drugs exhibit strong targeting and notable therapeutic effects, their efficacy is limited by their
- can alleviate tumor hypoxia and regulate TME to improve antitumor efficiency. In addition, PEG-modified NFs may significantly enhance passive targeting and retention via the EPR effect, thus enhancing their efficacy in cancer treatment [30]. The Fe3O4 NCs, Fe3O4 NCs-CUR layer nanoparticles (CUR-Fe NPs
On the additive artificial intelligence-based discovery of nanoparticle neurodegenerative disease drug delivery systems
Beilstein J. Nanotechnol. 2024, 15, 535–555, doi:10.3762/bjnano.15.47
- , protein targeting, the prediction of coated-NP drug release systems [41][42][43][44][45][46][47][48][49], multitarget networks of neuroprotective compounds for a theoretical study of new asymmetric 1,2-rasagiline carbamates [50], a TOPS-MODE model of multiplexing neuroprotective effects of drugs, an
Cholesterol nanoarchaeosomes for alendronate targeted delivery as an anti-endothelial dysfunction agent
Beilstein J. Nanotechnol. 2024, 15, 517–534, doi:10.3762/bjnano.15.46
- , besides targeting areas of active bone remodeling and resorption [5] and osteoclasts, nitrogenous bisphosphonates have been reported to reduce vascular calcification, through direct or indirect interaction with the endothelium [1][6]. Alendronate sodium (ALN) (CAS 121268-17-5, 4-amino-1-hydroxybutylidine
- variable degrees of increased permeability, offering an anatomic-pathological context that favors extravasation and, therefore, the passive targeting of nanoparticulate material towards cells of the diseased vasculature [20]. Moreover, in recent years, the development of targeted nanomedicines for
- increasingly pursued “quality by design” criteria [24]. The development of structurally simple formulations that facilitate their scaling and further characterization is, therefore, a critical task [25]. Also, targeting nanomedicines to circulating cells and vascular walls is difficult since it should occur
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
- three key components: (1) edaravone and nanoceria were responsible for ROS scavenging; (2) poly(ethylene glycol) increased biocompatibility, monodispersity, and extended the half-life in the bloodstream; and (3) angiopep-2 served as targeting ligand, which specifically binds to the low-density
Nanomedicines against Chagas disease: a critical review
Beilstein J. Nanotechnol. 2024, 15, 333–349, doi:10.3762/bjnano.15.30
- daunorubicin) launched in 2017. These liposomes act mainly by passive targeting mechanisms upon intravenous administration. Parenteral liposomes employing the DepoFoam technology are used in clinical analgesia, that is, DepoDurTM and Expare®, approved in 2004 and 2018, respectively. The above summary shows
- potential tissue irritation [132][133]. Also, if ADRs were associated with an intrinsic susceptibility of patients, reducing BNZ plasma levels would not be helpful. Hence, what type of nanomedicines could solve the problem of BNZ-based medication? Targeting BNZ to diseased tissues while avoiding healthy
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
- 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
Vinorelbine-loaded multifunctional magnetic nanoparticles as anticancer drug delivery systems: synthesis, characterization, and in vitro release study
Beilstein J. Nanotechnol. 2024, 15, 256–269, doi:10.3762/bjnano.15.24
- passive targeting and offer multimodal tumor therapy. In recent years, the use of nanotechnology-based cancer drugs has emerged as a promising alternative treatment approach. Utilizing various nanostructures as specific vehicles for drug delivery enhances efficacy and pharmacokinetic properties of
- laser-driven photothermal agent [25]. However, it is challenging to completely eradicate solid tumors using PTT alone because of light scattering and limited absorption in tumor tissues. For this purpose, various modifications have been employed for passive tumor targeting. PEGylation, which involves
- the use of poly(ethylene glycol) (PEG) polymer, is a widely used modification method to improve passive tumor targeting and retention [26][27][28]. In a study presented in the literature, PEGylation was used to impart passive tumor targeting properties to PDA nanoparticles. In in vivo experiments
Ion beam processing of DNA origami nanostructures
Beilstein J. Nanotechnol. 2024, 15, 207–214, doi:10.3762/bjnano.15.20
- DNA origami nanostructures is rarely explored, yet promising applications are foreseen to require such information. DNA nanostructures have been explored as drug delivery vessels for chemotherapeutics [1][2]. With the constant pursuit of effective targeting strategies [3], they could eventually be
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
- oxide) (PEO). To improve the targeting ability of nanoparticles, ligands are typically designed to be located on the exterior of nanoparticles. Typically, ligands are cell-type-specific monoclonal antibodies, RGD peptides for the overexpression of the asialoglycoprotein receptor on cancer cells [5
- . After 24, 48, and 72 h, the CHL levels in the NPs were significantly lower when incubated in pH 5.4 medium compared to that in pH 7.4 medium. The faster CHL drug release at pH 5.4 was due to a faster degradation of PLGA at pH 5.4 than that at pH 7.4 [30]. Targeting of nanoparticles to the cells The NPs
- show a superior targeting effect to cancer cells, which might be due to the fact that cancer cells were cultured in normal cell culture media. Therefore, the expression of folate receptor was not as high compared to that of cancer cells that grew in folic-acid-free cell culture media. Cytotoxicity of
Curcumin-loaded nanostructured systems for treatment of leishmaniasis: a review
Beilstein J. Nanotechnol. 2024, 15, 37–50, doi:10.3762/bjnano.15.4
- systems [19], nanoparticles [20], nanoliposomes [21], micelles [22], and nanocrystals [23] have been utilized. These systems can promote (i) protection of the drug against degradation in physiological media, (ii) increase in drug solubility, and (iii) modification/targeting of the drug enabling transport
- physicochemical properties of the systems, and by the release and targeting features of the loaded nanosystems, rather than by the drug properties themselves [58][59][60][61][62]. The intracellular amastigote form of Leishmania spp. allocates in macrophage phagolysosomes from infected individuals [63]. However
- antileishmanial drugs to such sites. Overall, drug targeting results in increased treatment efficacy and reduced toxicity, mostly by reducing drug doses and preventing its interaction with unwanted receptors [30][65]. In this scenario, active targeting happens by the functionalization of nanocarriers, making drug
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
- article, we discuss examples highlighting the influence of elasticity in nanoscale biological interactions focusing on mucosal delivery and on tumor targeting. Besides this, we discuss the influence of different measurement settings using atomic force microscopy for the determination of mechanical
- time for passive and active drug targeting before particles are filtered out of the circulation system. Overall, it was shown that softer particles have an enhanced blood circulation time. The effects described were observed for different particle types (made from different materials) and also covered
- overruling material properties. The tissue distribution can be important regarding active and passive targeting of different tissues, such as tumors or inflammation sites. It also gives an idea about possible side effects as high nanoparticle concentration usually correlates with high drug concentration
Exploring internal structures and properties of terpolymer fibers via real-space characterizations
Beilstein J. Nanotechnol. 2023, 14, 1004–1017, doi:10.3762/bjnano.14.83
- . Transverse elastic modulus quantifications We present these last results as relative stiffness variations because multiple AFM tips needed to be used to survey these multiple subdomains. Monitoring tip wear is cumbersome when targeting a broad survey of different regions of multiple fibers, so the results
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
- to functionalize with targeting agents such as antibodies and aptamers for LFAs. Therefore, photothermal LFAs are believed to play a significant role in the development of highly sensitive LFAs and other POCT devices. Schematic representation of photothermal LFA (Figure 1 was reprinted from [27
Antibody-conjugated nanoparticles for target-specific drug delivery of chemotherapeutics
Beilstein J. Nanotechnol. 2023, 14, 912–926, doi:10.3762/bjnano.14.75
- affects the targeting ability of the nanoformulation. In this review, we provide recent findings to highlight several antibody conjugation methods such as adsorption, covalent conjugation, and biotin–avidin interaction. This review also provides an overview of the many effects of the protein corona and
- the theranostic applications of ACNPs for the treatment of cancer. Keywords: active targeting; chemical conjugation; chemotherapeutics; drug delivery; monoclonal antibody; Introduction Off-target side effects, such as myelosuppression, mucositis, alopecia, organ dysfunction, and thrombocytopenia
- circulation time and serum stability. Also, they enable drug release in a sustained and controlled manner [4]. Targeted delivery of drug-loaded NPs can be achieved either through passive targeting, where drugs accumulate in tumor tissues via the enhanced permeability and retention (EPR) effect, or through
Titania nanoparticles for photocatalytic degradation of ethanol under simulated solar light
Beilstein J. Nanotechnol. 2023, 14, 616–630, doi:10.3762/bjnano.14.51
- many studies carried out in gas and liquid phases concerning the photodegradation of ethanol through TiO2-based materials, targeting both hydrogen production [25][26] and the photocatalytic oxidation of ethanol to CO2 [27][28]. Hydrogen production and depollution via ethanol photodegradation are of
Plasmonic nanotechnology for photothermal applications – an evaluation
Beilstein J. Nanotechnol. 2023, 14, 380–419, doi:10.3762/bjnano.14.33
- polarizability (causing interband transitions), and χD is the corresponding susceptibility of the conduction electrons (modelled through the Drude assumption of a free electron “sea”). Hence, PT applications targeting plasmonic materials must account for the contributions to the dielectric function of the terms
Polymer nanoparticles from low-energy nanoemulsions for biomedical applications
Beilstein J. Nanotechnol. 2023, 14, 339–350, doi:10.3762/bjnano.14.29
- , nanocarriers need to be engineered to add functionalities, both in their cores and at their surfaces. This includes therapeutic drugs and genes, targeting moieties, performance enhancers (e.g., for barrier penetration and to avoid opsonization), and imaging agents [2][3]. Core and matrix of the nanoparticles
- targeting Renilla luciferase mRNA. Gene inhibition showed an optimum efficiency (40%) at a given nanoparticle/antisense oligonucleotide ratio, which is promising for in vitro cell transfection. When water was replaced with PBS (0.16 M) for the PIC preparation of nanoemulsions starting from
- and cell viabilities higher than 75% (for concentrations below 100 nM). These nanoparticles displayed high gene silencing efficiencies (up to 90%) targeting Renilla luciferase mRNA, particularly when coated with PEG (Figure 3) and did not show hemolysis after incubation with red blood cells. PLGA
Overview of mechanism and consequences of endothelial leakiness caused by metal and polymeric nanoparticles
Beilstein J. Nanotechnol. 2023, 14, 329–338, doi:10.3762/bjnano.14.28
- aspect is the EPR effect, which is a phenomenon characteristic of mature solid tumors. The vascular permeability factors (e.g., VEGF) produced in higher concentrations by cancer cells stimulate the formation of an abnormal vascular structure, which can be used in the passive targeting of nanodrugs
- achievable utilizing NPs less than 100 nm in diameter. In contrast, active targeting strategies involve functionalizing the NP surface with appropriate ligands specific for receptors overexpressed by the cancer cells (e.g., folic acid and transferrin). The combination of the paracellular gap size resulting
- from the EPR effect and active targeting strategies may increase the efficacy of the therapy. Nevertheless, the accumulation in other, non-targeted organs indicates the existence of a method of NP transport through the endothelium other than EPR [26][28][29][32]. Sindhwani et al. identified an active
Recent progress in cancer cell membrane-based nanoparticles for biomedical applications
Beilstein J. Nanotechnol. 2023, 14, 262–279, doi:10.3762/bjnano.14.24
- of Public Health, Shanxi Medical University, Taiyuan, Shanxi 030001, China Department of General Surgery, Shanxi Cardiovascular Hospital, Taiyuan, Shanxi 030024, China 10.3762/bjnano.14.24 Abstract Immune clearance and insufficient targeting have limited the efficacy of existing therapeutic
- nanoparticles exhibit various effects (e.g., homotypic targeting, prolonging drug circulation, regulating the immune system, and penetrating biological barriers) after encapsulation by cancer cell membranes. The sensitivity and specificity of diagnostic methods will also be improved by utilizing the properties
- intended function of the NPs, resulting in changes of biological behavior and loss of function [6][7]. Moreover, the protein corona can accelerate RES/MPS uptake and interfere with the targeting ability of NPs [8]. The biomimetic technique of cell membrane coating, which employs naturally cell-derived
Nanotechnology – a robust tool for fighting the challenges of drug resistance in non-small cell lung cancer
Beilstein J. Nanotechnol. 2023, 14, 240–261, doi:10.3762/bjnano.14.23
- , and evidence has been derived that no single drug can treat the broad spectrum of molecular alterations in NSCLC. Considering the fact that multiple mechanisms are involved in the reactivation of the EGFR signaling pathway, targeting multiple constituents within the EGFR cascade or targeting parallel
- cancer resistance mechanisms successfully [23][24]. In addition, co-delivery of anticancer therapy using surface-engineered nanoparticles for tumor targeting may alleviate some of the unwanted effects on off-site targets and increase the therapeutic concentration at the site of action as well as efficacy
- synergistic effects, and (iv) cytotoxic or molecular targeting agents with small interfering RNA (siRNA) for silencing the mutating genes at protein and messenger RNA (mRNA) level, have made their way to clinical therapy or are under evaluation for their efficacy and safety in many research studies and
Cyclodextrins as eminent constituents in nanoarchitectonics for drug delivery systems
Beilstein J. Nanotechnol. 2023, 14, 218–232, doi:10.3762/bjnano.14.21
- nucleic acids are RNAs, DNAs, and derivatives thereof that regulate the expression of target genes [57][58][59]. Typical examples are antisense DNA, small interfering RNA (siRNA), aptamers, and ribozymes/DNAzymes. Owing to the accurate targeting at pathogenic genes, they are promising for various
- nanoassemblies (pale green balls in the third row from the top). Due to high biocompatibility and tumor-targeting capacity of HA, these ternary nanoassemblies effectively entered cancer cells. Upon UV irradiation (365 nm), the azobenzene isomerizes from the trans form to the cis form, disassembling the α-CyD
- ′-direction to provide an overhang in both ends. Thus, the siRNA was captured by two kinds of antisense DNAs on the β-CyDs through RNA/DNA hybridization and co-assembled to the nanoparticles. Folic acid (for targeting tumors) and an influenza hemagglutinin peptide HA (for endosomal escape) were conjugated
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