Nanocarrier systems loaded with IR780, iron oxide nanoparticles and chlorambucil for cancer theragnostics

• Phuong-Thao Dang-Luong,
• Hong-Phuc Nguyen,
• Loc Le-Tuan,
• Xuan-Thang Cao,
• Vy Tran-Anh and
• Hieu Vu Quang

Beilstein J. Nanotechnol. 2024, 15, 180–189, doi:10.3762/bjnano.15.17

• their high potential applications in various fields, including theragnostics. The PLGA SPION nanoparticles were modified to carry siRNA for silencing the inflammatory cytokine Cox-2 in activated macrophages and to serve as a tracer for locating activated macrophages in a mouse model of intra-uterine

The steep road to nonviral nanomedicines: Frequent challenges and culprits in designing nanoparticles for gene therapy

• Yao Yao,
• Yeongun Ko,
• Grant Grasman,
• Jeffery E. Raymond and
• Joerg Lahann

Beilstein J. Nanotechnol. 2023, 14, 351–361, doi:10.3762/bjnano.14.30

• based on specific issues. In addition, we considered only plasmid-based transfection systems during literature search (see details about experimental approach and scope in Supporting Information File 1). But we would expect a similar outcome and trend for the mRNA or siRNA NP delivery literature. The

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

• tumor tissue, such as mRNA, siRNA, miRNA, and sgRNA [113]. This strategy can avoid the impact on normal tissues and shows the advantage of low cytotoxicity. However, RNA is highly unstable and can be easily degraded and eliminated by the kidney [114]. Gene delivery technology based on biomimetic NPs

• shows improved RNA delivery efficiency and overcomes the obstacles of body clearance, insufficient targeting, and low biocompatibility [115]. PLGA NPs loaded with siRNA-E7 and PTX were synthesized for cervical cancer treatment. siRNA-E7 enables the knockdown of E7, which leads to upregulation of the

Nanotechnology – a robust tool for fighting the challenges of drug resistance in non-small cell lung cancer

• Filip Gorachinov,
• Fatima Mraiche,
• Diala Alhaj Moustafa,
• Ola Hishari,
• Yomna Ismail,
• Jensa Joseph,
• Maja Simonoska Crcarevska,
• Marija Glavas Dodov,
• Nikola Geskovski and
• Katerina Goracinova

Beilstein J. Nanotechnol. 2023, 14, 240–261, doi:10.3762/bjnano.14.23

• 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

• the limitations of the conjugates [68][69]. Cytotoxic or molecular targeting agents with siRNA Targeting homologous mRNA sequences in cells and knockdown of receptors involved in cell survival and proliferation using RNA interference downregulates receptor protein expression, inhibits cell growth, and

• induces apoptosis. The effect obtained by siRNA is not influenced by the receptor alteration status and significantly decreases the gene's oncogenic potential. Chen et al. compared the efficacy of TKIs in NSCLC cells harboring different mutations with combined therapy consisting of TKIs (gefitinib

Cyclodextrins as eminent constituents in nanoarchitectonics for drug delivery systems

• Makoto Komiyama

Beilstein J. Nanotechnol. 2023, 14, 218–232, doi:10.3762/bjnano.14.21

• nanoarchitectures are highly promising for future applications in medicine, pharmaceutics, and other relevant fields. Keywords: cyclodextrin; drug delivery system (DDS); nanoarchitecture; phototherapy; siRNA; Review 1 Introduction Recently, drug delivery systems (DDSs) have been attracting much interest [1][2][3

• 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

• resultant well-organized orientation of functional groups in CyD-based nanoarchitectures, should be very appropriate to yield both stable encapsulation of nucleic acid drugs and their prompt release when needed. 3.1 CyD-based nanoarchitectures for delivery of siRNA The therapeutic nucleic acid siRNA is

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

• recently due to a very weak luminescence. Lin et al. synthesized mostly linear PEI and demonstrated a siRNA delivery with this luminescent polymer [27]. Sun et al. utilized the luminescence of branched PEI as the imaging modality in polymeric quantum dots (PDOTs) formed from amphiphilic polyethyleneimine

An overview of microneedle applications, materials, and fabrication methods

• Zahra Faraji Rad,
• Philip D. Prewett and
• Graham J. Davies

Beilstein J. Nanotechnol. 2021, 12, 1034–1046, doi:10.3762/bjnano.12.77

• wafer is anodically bonded to a silicon wafer with predefined cavities (Figure 3) [66]. Deng et al. produced a solid pyramidal silicon microneedle array for in vivo delivery of the cholesterol-modified housekeeping gene siRNA to mice ear skin. The microneedles were 200 μm in height with a tip radius of

Comprehensive review on ultrasound-responsive theranostic nanomaterials: mechanisms, structures and medical applications

• Sepand Tehrani Fateh,
• Lida Moradi,
• Elmira Kohan,
• Michael R. Hamblin and
• Amin Shiralizadeh Dezfuli

Beilstein J. Nanotechnol. 2021, 12, 808–862, doi:10.3762/bjnano.12.64

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

• arrest, demonstrating a sensitiveness of the cells to nilotinib that is attributable to IM. Mendonca and co-workers worked on developing a targeted NDDS for а combination of siRNA and TKI in CML treatment [63]. The authors developed sterically stabilized liposomes decorated with transferrin for co

• -delivery of siRNA and IM for specifically silencing the BCR-ABL oncogene. In this case, IM enables the pre-sensitization of tumor cells, as a prerequisite for effective gene silencing, mediated by the siRNA. The results demonstrate that the siRNA/IM ratio affected the efficacy in BCR-ABL silencing and

• higher levels of transferrin receptor expression and lower BCR-ABL mRNA levels were more sensitive to the prepared liposomal formulation. The importance of co-delivery of both agents was also observed as lower siRNA/imatinib ratios were needed to achieve IC50 values equivalent to those of the experiments

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

• with polyethyleneimine and conjugated with CD44 siRNA can be used as non-viral gene therapy vectors. Polyethylene imine is the material of choice for nucleic acid intracellular delivery, as it gives a positive charge to the nanoparticle surface [41]. Polyvinyl alcohol (PVA)-coated SPIONs were tested as

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

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

• chlorotic mottle virus (CCMV); nanocarriers; plant virus-like particles (VLPs); siRNA delivery; small interfering RNA (siRNA); Introduction Despite many efforts taken, the efficient and specific delivery of therapeutic molecules to tumor cells is still a unsolved challenge. Cancer therapies are often

• the capsid [25][27]. Similarly, VLPs from the closely related cowpea chlorotic mottle virus (CCMV) have been loaded with different cargos, including gold nanoparticles, negatively charged chromophores, and polymers [22]. Small interfering RNA (siRNA) is a promising therapeutic solution to address gene

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

• Russian Academy of Sciences, 3, Ulan-Batorskaya St., P.O. Box 278, Irkutsk, 664033, Russia 10.3762/bjnano.11.26 Abstract The present work explores the ability of poly(1-vinylimidazole) (PVI) to complex small interfering RNA (siRNA) silencing vascular endothelial growth factor (VEGF) and the in vitro

• 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

• the polyplex was found to augment the cytotoxic effects of the chemotherapeutic agent 5-fluorouracil. Microarray analysis of the mRNA isolated from cells treated with free siRNA and the polyplex reveal that the VEGF silencing by the polyplex also altered the expression levels of several other genes

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

• -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

• co-workers showed that self-assembled DNA tetrahedron nanoarchitectures with narrow size distribution could deliver siRNA into tumor cells [71]. The programmable DNA strands were functionalized with tumor-targeting folate ligands. The nanoarchitecture consisted of six DNA strands having a total of

• was exactly complementary to the siRNA sequence, and, typically, six siRNAs could be annealed with the tetrahedron unit. To ascertain the in vivo transfection efficiency of the siRNA-loaded DNA tetrahedron nanoarchitecture, pharmacokinetic profiling and organ biodistribution assays were conducted in

Internalization mechanisms of cell-penetrating peptides

• Ivana Ruseska and
• Andreas Zimmer

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

• peptide nucleic acids (PNAs) and phosphorodiamidate morpholino oligonucleotides (PMOs) [3][12]. Concerning charged molecules such as siRNA or miRNA, the covalent conjugation leads to restricted biological activity, most likely due to the steric hindrance caused by the covalently-linked CPP, which is an

• obstacle for the incorporation of siRNA/miRNA into the RISC complex. Because of this, the siRNA/miRNA molecule cannot be loaded into the complex and manifest its effect [13]. Regarding covalent strategies of cargo-attachment, there is a great promise in biorthogonal chemistry, which allows for the design

• -siRNA/miRNA delivery [17]. It has been reported that CPP-siRNA conjugates have reduced transient and stable expression of reporter transgenes in a number of mammalian cell lines [18]. In this case, thiol-containing siRNAs were synthesized and conjugated to penetratin or transportan by a reducible

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

• at a 1:9 TPP/chitosan weight ratio. In the case of siRNA-loaded nanoparticles, TPP was dissolved in deionized nuclease-free water containing siRNA. The chitosan–TPP nanoparticle (template) dispersion was stirred for 30 min and then mixed with 1 mL of acetate buffer (200 mM, pH 5). After 5 min, 1 mL

• the water every 20 min. B) Direct complexation. 500 µL of a 0.069 wt % chitosan solution prepared as described above was mixed with an equal volume of deionized and nuclease-free water containing siRNA or simply with deionized water for 10 min at 25 °C. The resulting dispersion (with or without siRNA

Long-term stability and scale-up of noncovalently bound gold nanoparticle-siRNA suspensions

• Anna V. Epanchintseva,
• Julia E. Poletaeva,
• Dmitrii V. Pyshnyi,
• Elena I. Ryabchikova and
• Inna A. Pyshnaya

Beilstein J. Nanotechnol. 2019, 10, 2568–2578, doi:10.3762/bjnano.10.248

• nanoparticles (AuNPs) are a platform for the creation of nanoconstructions that can have a variety of functions, including the delivery of therapeutic nucleic acids. We previously designed a AuNP/small interfering RNA (siRNA) nanoconstruction consisting of siRNA noncovalently bound on the AuNP surface and

• showed that this construction, when coated with a lipid shell, was an efficient vehicle for the delivery of siRNA into cells. The goal of the present work was to study the possibility of scaling up the synthesis of AuNP-siRNA and its long-term storage without loss of physicochemical characteristics and

• siRNA duplex integrity as well as siRNA surface density. Dynamic light scattering, transmission electron microscopy, UV–vis spectroscopy, and electrophoresis were used to study the effect of scaling up the AuNP-siRNA synthesis and long term storage of its suspension on physicochemical properties of the

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

• selective delivery to these organelles [49]. The peptide Lys–Asp–Glu–Leu (KDEL) has been anchored on gold nanoparticles loaded with siRNA for the selective delivery of the genetic material into the endoplasmic reticulum [50]. The main mechanism for the internalization of nanoparticles within mammalian cells

• is endocytosis [51]. Usually, the nanocarriers enter into the cells into endosomes, which evolve into lysosomes, which can lead to the degradation of the transported cargo, especially in the case of sensitive agents such as genes or siRNA. Therefore, it is necessary to design mechanisms to induce the

• constitutes a formidable barrier for tissue targeting not only in nanomedicine but also in common drug delivery [63]. In this case, liposomes were modified with Angiopep-2 and tLyP-1 homing and penetrating peptides for the simultaneous delivery of siRNA and (docetaxel) DTX. Angiopep-2 showed affinity to the

Enhanced antineoplastic/therapeutic efficacy using 5-fluorouracil-loaded calcium phosphate nanoparticles

• Shanid Mohiyuddin,
• Saba Naqvi and
• Gopinath Packirisamy

Beilstein J. Nanotechnol. 2018, 9, 2499–2515, doi:10.3762/bjnano.9.233

• nanoparticles in biomedical applications is extended to tissue engineering, gene/siRNA delivery, anticancer drug delivery, protein and antigen delivery, vaccine delivery, insulin as well as imaging probe or contrasting agent delivery for bio-imaging. 5-Fluorouracil (5-FU), a well-known anticancer agent

Cationic PEGylated polycaprolactone nanoparticles carrying post-operation docetaxel for glioma treatment

• Cem Varan and
• Erem Bilensoy

Beilstein J. Nanotechnol. 2017, 8, 1446–1456, doi:10.3762/bjnano.8.144

• increased the particle size and decreased the cellular uptake of nanoparticles [66]. Cationic core–shell nanoparticles are also quite suitable for the delivery of negatively charged gene and drug to tumor tissue. Wei et al. used cationic core–shell nanoparticles for the active targeted delivery of siRNA on

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

• ]. For instance, nucleic acids like DNA [10][11][12][13], siRNA [14][15][16][17] and µRNA [18] have been successfully introduced to perform transfection, gene silencing, prophylactic and therapeutic vaccination [19][20][21]. All kinds of synthetic molecules and biomolecules can be transported across the

High antiviral effect of TiO₂·PL–DNA nanocomposites targeted to conservative regions of (−)RNA and (+)RNA of influenza A virus in cell culture

• Asya S. Levina,
• Marina N. Repkova,
• Elena V. Bessudnova,
• Ekaterina I. Filippova,
• Natalia A. Mazurkova and
• Valentina F. Zarytova

Beilstein J. Nanotechnol. 2016, 7, 1166–1173, doi:10.3762/bjnano.7.108

• ’-terminal region of (−)RNA [10][11] were the most chosen regions of IAV segment 5 to be affected by oligonucleotides and their analogs. The coding region close to the stop codon was often used as the target for the action of siRNA [9][12][15][16]. The other regions of the NP gene were also studied as

Hematopoietic and mesenchymal stem cells: polymeric nanoparticle uptake and lineage differentiation

• Ivonne Brüstle,
• Thomas Simmet,
• Gerd Ulrich Nienhaus,
• Katharina Landfester and
• Volker Mailänder

Beilstein J. Nanotechnol. 2015, 6, 383–395, doi:10.3762/bjnano.6.38

• granulopoetic markers was significantly suppressed. Discussion Although nanoparticles are proposed as useful drug and DNA or siRNA delivery vehicles (which could potentially change the fate of stem cells), they could also influence the cellular fate of stem cells with a potentially devastating effect. While

Comparative evaluation of the impact on endothelial cells induced by different nanoparticle structures and functionalization

• Lisa Landgraf,
• Ines Müller,
• Peter Ernst,
• Miriam Schäfer,
• Christina Rosman,
• Isabel Schick,
• Oskar Köhler,
• Hartmut Oehring,
• Vladimir V. Breus,
• Thomas Basché,
• Carsten Sönnichsen,
• Wolfgang Tremel and
• Ingrid Hilger

Beilstein J. Nanotechnol. 2015, 6, 300–312, doi:10.3762/bjnano.6.28

• ; Introduction To advance the field of nanomedicine, innovative nanoparticle formulations with suitable properties for diagnostic imaging, therapy (e.g., magnetic hyperthermia), delivery of drugs and siRNA have been developed. Apart from their feasibility for the respective application many of these

Caveolin-1 and CDC42 mediated endocytosis of silica-coated iron oxide nanoparticles in HeLa cells

• Nils Bohmer and
• Andreas Jordan

Beilstein J. Nanotechnol. 2015, 6, 167–176, doi:10.3762/bjnano.6.16

• and surface charge, were tested in HeLa cells as a model cell line. To elucidate, which molecular pathways are involved in their endocytosis, well-known endocytotic mechanisms [26][27][28] were inhibited by specific knockdown of key proteins via siRNA (Figure 1). Experimental Superparamagnetic iron

• Technologies. To achieve the optimal transfection efficiency, two transfection rounds on day 1 and 3 after cell plating were performed. In preliminary experiments the knockdown technique was optimized to cause no cell death by applying different ranges of transfection reagent with different amounts of siRNA

• were transfected according to the protocol “Thermo Scientific DharmaFECT Transfection Reagents - siRNA Transfection Protocol“ and DharmaFECT 1 siRNA Transfection Reagent (Thermo Fisher Scientific, Cat. No. T-2001-01) was used. Information about the siRNA-mix (SMARTpool®) used is shown in Table 3