Classification and application of metal-based nanoantioxidants in medicine and healthcare

• Nguyen Nhat Nam,
• Nguyen Khoi Song Tran,
• Tan Tai Nguyen,
• Nguyen Ngoc Trai,
• Nguyen Phuong Thuy,
• Hoang Dang Khoa Do,
• Nhu Hoa Thi Tran and
• Kieu The Loan Trinh

Beilstein J. Nanotechnol. 2024, 15, 396–415, doi:10.3762/bjnano.15.36

• capability to degrade reactive nitrogen species (RNS) are rare. In response, Miao et al. synthesized polyethylene glycol-coated ultrasmall rhodium nanodots (Rh-PEG NDs) for scavenging both ROS and RNS in order to decrease inflammation [106]. Rh-PEG NDs exhibited O2•–, HO•, NO•, ONOO–, and H2O2 scavenging

• of metal-based nanoantioxidants and the reduction of detrimental effects of these nanomaterials on human health. Surface modification can become an effective method to decrease the toxicity of nanomaterials through coating with biocompatible polymers such as chitosan, polydopamine, and polyethylene

• glycol. From this perspective, bio-inspired nanoantioxidants could be a potential solution for safety issues. Furthermore, metal-based nanoantioxidants are still in the early stage of clinical practice and face the issue of less accurate accumulation at a specific site. In the next stage, a deep and wide

Nanomedicines against Chagas disease: a critical review

• Maria Jose Morilla,
• Kajal Ghosal and
• Eder Lilia Romero

Beilstein J. Nanotechnol. 2024, 15, 333–349, doi:10.3762/bjnano.15.30

• , and resulted in 100% survival of an acute murine model [70]. Either orally or intravenously administered to acute and chronic murine models, poly(ᴅ,ʟ-lactide)-block-polyethylene glycol nanocapsules loaded with lychnopholide (LYC-PLA-PEG NCs), a lipophilic sesquiterpene lactone isolated from

• Loncastuximab tesirine, launched in 2021 to treat B-cell lymphoma [84]. Nearly 10% are polymer–drug/protein conjugates such as polyethylene glycol-ʟ-asparaginase (Calaspargase pegol, Asparlas), launched in 2019 in the USA to treat acute lymphoblastic leukemia [85]. Another 10% are protein-based nanoparticles

• , polyethylene glycol (PEG) lipids, and ionizable synthetic lipids (ALC-0315 from BioNTech-Pfizer and SM-102 from Moderna Therapeutics) for enhanced delivery of messenger RNA (mRNA) encoding the spike protein of the SARS-COV-2 virus to antigen-presenting cells [82]. These vaccines were approved by the FDA

Vinorelbine-loaded multifunctional magnetic nanoparticles as anticancer drug delivery systems: synthesis, characterization, and in vitro release study

• Zeynep Özcan and
• Afife Binnaz Hazar Yoruç

Beilstein J. Nanotechnol. 2024, 15, 256–269, doi:10.3762/bjnano.15.24

• ratios as a result of dopamine polymerisation and covalent bonding of thiol-polyethylene glycol (SH-PEG). The VNB/PDA/Fe3O4 nanoparticles have a saturation magnetisation value of 60.40 emu/g in vibrating sample magnetometry, which proves their magnetisation. Vinorelbine, which is used as an effective

• ), and thiol-polyethylene glycol (SH-PEG, purity: ≥95%), ammonium hydroxide (NH4OH, 28–30%), phosphate-buffered saline (PBS) were purchased from Merck. The chemical vinorelbine tartrate CRS (European Pharmacopoeia (EP) Reference Standard, catalog no: Y0000463) was also acquired from Merck. Synthesis of

• -polyethylene glycol was added to the prepared mixture to homogenize the solution. Subsequently, 0.2 mL of ammonium hydroxide (NH4OH, 28–30%,) was added, and the mixture was stirred at room temperature for 70 min [37]. SH-PEG-modified PDA/Fe3O4 NPs were separated from the solution using a magnet, and unreacted

Sulfur nanocomposites with insecticidal effect for the control of Bactericera cockerelli

• Lany S. Araujo-Yépez,
• Juan O. Tigrero-Salas,
• Vicente A. Delgado-Rodríguez,
• Vladimir A. Aguirre-Yela and
• Josué N. Villota-Méndez

Beilstein J. Nanotechnol. 2023, 14, 1106–1115, doi:10.3762/bjnano.14.91

• ]. Furthermore, different kinds of polysaccharides (e.g., chitosan, alginates, and polyethylene glycol) have been used for the synthesis of nanoinsecticides [15]. While other forms of polymer and non-polymer nanoformulations, such as nanofibers, nanocapsules, nanogels, nanomicelles, and nanospheres, have been

• %, CAS number: 10102-17-7), hydrochloric acid (HCl, ACS reagent, 37%, CAS number: 7647-01-0), triethanolamine ((HOCH2CH2)3N, ACS reagent, ≥99.5%, CAS number: 102-71-6), ethanol (CH3CH2OH, CAS number: 64-17-5), and polyethylene glycol (PEG, H(OCH2CH2)nOH, Wt: 6000, CAS number: 25322-68-3), were acquired

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

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

• siRNA from the endosome. In another example, a supramolecular nanoparticle was prepared from a linear CyD-based polymer, hydrophilic polyethylene glycol bearing an adamantane at the end, and siRNA [64]. By attaching a human transferrin protein, this composite was steered to target cancer cells to

Single-step extraction of small-diameter single-walled carbon nanotubes in the presence of riboflavin

• Polina M. Kalachikova,
• Anastasia E. Goldt,
• Eldar M. Khabushev,
• Timofei V. Eremin,
• Timofei S. Zatsepin,
• Elena D. Obraztsova,
• Konstantin V. Larionov,
• Liubov Yu. Antipina,
• Pavel B. Sorokin and
• Albert G. Nasibulin

Beilstein J. Nanotechnol. 2022, 13, 1564–1571, doi:10.3762/bjnano.13.130

• facilitate chirality separation. Conventional surfactants such as sodium dodecyl sulfate (SDS) and sodium deoxycholate (DOC), as well as polyethylene glycol-based compositions, are used to obtain high-quality dispersions of individual SWCNTs [3][4][5][10]. Although given surfactants show exemplary

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

• , polyhydroxyethylmethacrylate, and polyethylene glycol were used in composite preparation for bone tissue engineering applications [10]. To create a fibrous scaffold for bone tissue regeneration, zein and chitosan were combined with polyurethane and functionalized multiwalled carbon nanotubes. The developed scaffolds have

• polyethylene glycol is extremely stable and might be used in bone tissue engineering applications. The drug distribution ability of the scaffolds was investigated using ciprofloxacin, which is a general antibiotic drug. According to the findings, approx. 98% of the medicines had a sustained released within 90

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

• over conventional TE approaches. For HA, this could be obtained via the conjugation of the HA binding domain to a polyethylene glycol (PEG) hydrogel, which would provide HA affinity for the PEG hydrogel and consequently improve cartilage tissue production [179]. Given the generally conserved nature of

Systematic studies into uniform synthetic protein nanoparticles

• Nahal Habibi,
• Ava Mauser,
• Jeffery E. Raymond and
• Joerg Lahann

Beilstein J. Nanotechnol. 2022, 13, 274–283, doi:10.3762/bjnano.13.22

• )ethyl]polyethylene glycol (NHS-PEG-NHS) with a molecular weight of 2000 Da were purchased from Sigma-Aldrich, USA. O,O′-bis[2-(N-succinimidyl-succinylamino)ethyl]polyethylene glycol (NHS-PEG-NHS) with a molecular weight of 400 Da was purchased from Nanocs Inc., USA. EHD jetting EHD jetting followed the

Engineered titania nanomaterials in advanced clinical applications

• Padmavati Sahare,
• Paulina Govea Alvarez,
• Juan Manual Sanchez Yanez,
• Gabriel Luna-Bárcenas,
• Samik Chakraborty,
• Sujay Paul and
• Miriam Estevez

Beilstein J. Nanotechnol. 2022, 13, 201–218, doi:10.3762/bjnano.13.15

• and a reduced toxicity to normal cells of free drug molecules. Surface modification of the nanomaterials with polyethylene glycol (PEG) is reported to be advantageous for multiple reasons, such as inhibition of recognition by the mononuclear phagocytic system, elimination of in vitro toxicity, and

Sputtering onto liquids: a critical review

• Anastasiya Sergievskaya,
• Adrien Chauvin and
• Stephanos Konstantinidis

Beilstein J. Nanotechnol. 2022, 13, 10–53, doi:10.3762/bjnano.13.2

• where platinum/copper (Pt/Cu) NPs were obtained by using an alloy target for the sputtering onto polyethylene glycol (PEG), it was reported that increasing the current from 10 to 50 mA leads to the formation of bigger NPs, from 1.3 to 4.5 nm, respectively [127

Revealing the formation mechanism and band gap tuning of Sb₂S₃ nanoparticles

• Maximilian Joschko,
• Franck Yvan Fotue Wafo,
• Christina Malsi,
• Danilo Kisić,
• Ivana Validžić and
• Christina Graf

Beilstein J. Nanotechnol. 2021, 12, 1021–1033, doi:10.3762/bjnano.12.76

• with ethylene glycol or polyethylene glycol as solvent [29][30]. The authors reasoned the cleavage at the particle tips by weak van der Waals forces between (Sb4S6)n chains, of which the particles consisted, or by strongly bound ligands interfering with the crystal growth, respectively. However, as

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

• in distant tissues. They suggested that cavitation bubbles induced by US caused the release of the DOX into the tumor tissue [88]. Similar findings were obtained by Chen et al. They synthesized PC-polyethylene glycol (PEG) liposomes loaded with FITC (FITC-PC-PEG-L) with a diameter ranging from 150 to

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

• involved in the internalization of polyethylene glycol-coated MNPs. Our data indicate that surface engineering can contribute to an enhanced delivery efficiency of nanoparticles. Keywords: bovine serum albumin; cellular uptake; magnetic iron oxide nanoparticles; polyethylene glycol; surface coating

• functionalization to increase their accumulation in the tumor mass [3]. Numerous coating moieties have been employed to modify the surface properties of MNPs [16]. Among them, polyethylene glycol (PEG), a non-degradable polyether of the monomer ethylene glycol, and bovine serum albumin (BSA), a versatile protein

• of CME under different physiological conditions is poorly understood and other studies are required to bridge this gap in our knowledge. Conclusion MNPs coated with bovine serum albumin (BSA-SO-MNPs) and polyethylene glycol (PEG-SO-MNPs), were found to enter the cells by different routes of

A review on the green and sustainable synthesis of silver nanoparticles and one-dimensional silver nanostructures

• Sina Kaabipour and
• Shohreh Hemmati

Beilstein J. Nanotechnol. 2021, 12, 102–136, doi:10.3762/bjnano.12.9

• , particle sizes varied from 14 to 34 nm, and were of crystallite shape. In another work, AgNP crystallites were produced with an average size of 10–12 nm using the mechanochemical ball milling process by utilizing polyethylene glycol as the stabilizing agent [107]. The relatively small size of the produced

Photothermally active nanoparticles as a promising tool for eliminating bacteria and biofilms

• Mykola Borzenkov,
• Piersandro Pallavicini,
• Angelo Taglietti,
• Laura D’Alfonso,
• Maddalena Collini and
• Giuseppe Chirico

Beilstein J. Nanotechnol. 2020, 11, 1134–1146, doi:10.3762/bjnano.11.98

• engineered to combat bacterial infections by integrating bacterial conjugation and NIR-triggered photothermal sterilization [97]. In a very recent publication, polyethylene glycol (PEG)-MoS2 nanosheets additionally functionalized with an antibody (anti-protein A lgG) and polydopamine were applied to induce

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

• , dendrimers, albumin, silicones, liposomes, poloxamer, poly-ʟ-lysine, sugars, or polyethylene glycol (PEG) [27][28][29][30][31][32][33]. Hyperthermia treatment for cancer therapy is still under scrutiny. It shows great potential due to the property of SPIONs to produce local heat when placed under an

• graphitic-phase carbon nitride and coated with polyethylene glycol for MRI and fluorescence imaging and for photodynamic therapy. This type of nanoplatform seems to be a good one-for-all solution, as it could be controlled to be non-toxic or highly toxic from the outside. In vitro and in vivo analyses

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

• twofold dilutions (initial concentration, 108 cells·mL−1) were immobilized in the wells through simple adsorption, kept for 30 min on a shaker at room temperature. The samples were replaced with 100 μL of 0.05% polyethylene glycol 20000 (PEG), added to each well to block the free binding sites on

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

• been reported using papaya mosaic virus [45]. Both capsids of CCMV and BMV were covered with polyethylene glycol (PEG) to decrease their surface charge and mask the domains of the capsid proteins that could be recognized by the macrophages (Figure 3C,D). PEG is widely used to reduce the immunogenicity

• using polyethylene glycol functionalized with N-hydroxylsuccinimide (NHS-PEG, Sigma Aldrich). The use of NHS-PEG enabled the selective conjugation of nanoparticles with PEG via amide bonds. A solution of NHS-PEG (9.12 nmol) was mixed with the capsids suspension (1 mg/mL) in PBS and gently shaken for 2 h

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

• to reduce protein adsorption and corona formation. This can be achieved for instance by grafting hydrophilic polymers such as polyethylene glycol (PEG) on the surface of nanomedicines, or by introducing zwitterionic modifications to make nanomaterials almost neutral [42][43][44][45]. These

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

• or the use of antifouling polymers such as polyethylene glycol. Finally, the availability of whole-genome sequencing as offered by recently established private companies (e.g., Veritas Genetics and Novogene) allows for the determination of hundreds of mutations from a single sample at relatively low

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

• in vitro. Cystabn was used to prepare a targeted 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[amino(polyethylene glycol)-2000] (DSPE-PEG2000) lipid conjugate that was formulated into liposomes. The liposomes displayed desirable colloidal properties and good stability under storage conditions

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

• glycopolymers can be potentially utilized as targeted anti-pathogenic nanomaterials and as well as for cell-targeted drug delivery. Experimental General procedures Chemicals were purchased by commercial sources and used without further purification, unless otherwise indicated. Polyethylene glycol methyl ether

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

• easily degraded into their monomers, lactic acid and glycolic acid. Furthermore, a copolymer composed of polyethylene glycol (PEG) and PLGA (PLGA-PEG) was used for nanoparticle preparation. PEGylated (“stealth”) nanoparticles display prolonged systemic circulation time, because they avoid agglomeration

• polyethylene glycol (PEG) and PLGA (PLGA-PEG) and polylactic acid (PLA), respectively, were prepared in the presence of doxorubicin by either emulsion diffusion or solvent displacement technique. The resulting particle diameters are presented in Figure 1. Emulsion diffusion (173.5 ± 5.9 nm) and solvent