Soybean-derived blue photoluminescent carbon dots

• Shanshan Wang,
• Wei Sun,
• Dong-sheng Yang and
• Fuqian Yang

Beilstein J. Nanotechnol. 2020, 11, 606–619, doi:10.3762/bjnano.11.48

• wavelength [7], and low cost [8]. CDs have been considered as a group of important nanomaterials with potential applications in nanotechnology [9], electrocatalysis [10], metal-ion detection [2], thermal sensing [11], drug delivery [12], and biosensing and bioimaging [1]. Several methods are available for

Identification of physicochemical properties that modulate nanoparticle aggregation in blood

• Ludovica Soddu,
• Duong N. Trinh,
• Eimear Dunne,
• Dermot Kenny,
• Giorgia Bernardini,
• Ida Kokalari,
• Arianna Marucco,
• Marco P. Monopoli and
• Ivana Fenoglio

Beilstein J. Nanotechnol. 2020, 11, 550–567, doi:10.3762/bjnano.11.44

• targeted drug delivery, active pharmaceutical carriers and medical imaging. However, poor knowledge of the side effects related to their use is an obstacle to clinical translation. For the development of molecular drugs, the concept of safe-by-design has become an efficient pharmaceutical strategy with the

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

• Nanotechnology, SRM Institute of Science and Technology, Kattankulathur, Tamil Nadu 603203, India 10.3762/bjnano.11.41 Abstract Multilayer capsules have been of great interest for scientists and medical communities in multidisciplinary fields of research, such as drug delivery, sensing, biomedicine

• , theranostics and gene therapy. The most essential attributes of a drug delivery system are considered to be multi-functionality and stimuli responsiveness against a range of external and internal stimuli. Apart from the highly explored strong polyelectrolytes, weak polyelectrolytes offer great versatility with

• potential applications. Keywords: drug delivery; functionalization; multilayer capsules; synthesis; weak polyelectrolytes; Review Introduction In the last few decades, micrometer and nanometer-sized capsules made of polyelectrolytes (PEs) have been the subject of intensive research because of their

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

• ], which enables the exchange of citrate ligands with amines. The amine-capped GNPs are stable enough to be used as targeting agents for drug-delivery applications [75], as antigens for the generation of antibodies [77], or as antimicrobial agents [78]. These nanoconjugates are nontoxic, effectively

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

• , handling, and simple structure, plant viruses are attractive for some biomedical applications. Plant bromoviruses, such as the brome mosaic virus (BMV), are viral bionanoparticles that have been proposed as platforms for drug delivery in different therapies, and as diagnostic imaging agents in cancer [18

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

• exploit the cellular machinery to enter cells and be trafficked intracellularly, thus they can be used to overcome some of the cellular barriers to drug delivery. Nano-sized drug carriers of very different properties can be prepared, and their surface can be modified by the addition of targeting moieties

• to recognize specific cells. However, it is still difficult to understand how the material properties affect the subsequent interactions and outcomes at cellular level. As a consequence of this, designing targeted drugs remains a major challenge in drug delivery. Within this context, we discuss the

• crucial challenge for drug delivery and recently the debate on the success of nanomedicine for delivering drugs to their target has been very active [26][27][28]. Indeed, it is difficult to design nanoparticles that achieve specific targeting [7][9][29]. This is not only because a better understanding of

Understanding nanoparticle flow with a new in vitro experimental and computational approach using hydrogel channels

• Armel Boutchuen,
• Dell Zimmerman,
• Abdollah Arabshahi,
• John Melnyczuk and
• Soubantika Palchoudhury

Beilstein J. Nanotechnol. 2020, 11, 296–309, doi:10.3762/bjnano.11.22

• , United States Department of Chemistry, Clark Atlanta University, Georgia 30314, United States 10.3762/bjnano.11.22 Abstract Nanoparticles (NPs) are considered as one of the most promising drug delivery vehicles and a next-generation solution for current medical challenges. In this context, variables

• related to flow of NPs such as the quantity of NPs lost during transport and flow trajectory greatly affect the clinical efficiency of NP drug delivery systems. Currently, there is little knowledge of the physical mechanisms dominating NP flow inside the human body due to the limitations of available

• experimental tools for mimicking complex physiological environments at the preclinical stage. Here, we report a coupled experimental and computational fluid dynamics (CFD)-based novel in vitro approach to predict the flow velocity and binding of NP drug delivery systems during transport through vasculature

Facile biogenic fabrication of hydroxyapatite nanorods using cuttlefish bone and their bactericidal and biocompatibility study

• Satheeshkumar Balu,
• Manisha Vidyavathy Sundaradoss,
• Swetha Andra and
• Jaison Jeevanandam

Beilstein J. Nanotechnol. 2020, 11, 285–295, doi:10.3762/bjnano.11.21

• increasing demand of biomaterials for hard tissue repair [6][7]. It is noteworthy that marine species, including corals, crabs, and fish bones, possess natural calcium phosphate and are currently being extracted and utilized as drug delivery carriers, tissue engineering scaffolds and dental cements in the

• loading capacity and slow drug release in drug delivery systems for progressive advancement in osteoporosis and bone tumor treatments [17]. Various studies have reported the synthesis procedure of Hap nanoparticles from annealed cuttlefish bone using a hydrothermal method, which yields calcium oxide (CaO

Phase inversion-based nanoemulsions of medium chain triglyceride as potential drug delivery system for parenteral applications

• Eike Folker Busmann,
• Dailén García Martínez,
• Henrike Lucas and
• Karsten Mäder

Beilstein J. Nanotechnol. 2020, 11, 213–224, doi:10.3762/bjnano.11.16

• Eike Folker Busmann Dailen Garcia Martinez Henrike Lucas Karsten Mader Institute of Pharmacy, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany 10.3762/bjnano.11.16 Abstract Lipid nanoemulsions are attractive drug delivery systems for lipophilic drugs. To produce nanoemulsions

• drug delivery systems such as solid lipid or polymeric nanoparticles, nanocapsules, liquid nanoemulsions, liposomes and micelles can be used to carry poorly water soluble ingredients of pharmaceuticals for parenteral applications [1][2][3]. Thereby, the physical entrapment of the active ingredients

• water, very high surfactant concentrations could be avoided and the resulting MCT nanoemulsions might be suitable as potential drug delivery systems for intravenous applications. The presented phase inversion-based process offers a suitable alternative to the production of nanoemulsions based on high

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

• use of irradiation to promote drug delivery (photochemical internalization). Block copolymers used for vectorization of photosensitizers Most of the used photosensitizers are highly hydrophobic and have the tendency to aggregate in aqueous environments, which is detrimental for their effectiveness in

• influencing the self-assembly behavior and, consequently, the photosensitizer loading ability. Typical endogenous triggers for pH- and redox-responsive drug delivery are i) acidic tumor tissues (pH 6.0–7.0), endosomes (pH 5.0–6.0) and lysosomes (pH 4.0–5.0) microenvironments, ii) high intracellular

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

• , sensors, molecular or nanoelectronics, diagnostics, drug delivery, and biomedical sciences. The remarkable molecular fidelity and sequence-specific molecular recognition make DNA the ideal candidate in the scheme of molecular architectonics to design and construct functional DNA nanoarchitectures. In this

• delivery and nonimmunogenicity of the nanorobot made it a promising candidate for drug delivery in cancer therapeutics. The group of Krishnan reported the construction of a DNA nanodevice to quantitatively determine the activity and location of chloride ion channels and transport under pH stimuli [57]. In

• assembly systems points at potential drug delivery systems for small molecular and gene-based drugs. Mercury is one of the most toxic heavy metals, with a severe impact on human health already at ultralow concentrations [20][72][73][74]. Selective binding of Hg(II) with thymine is a highly feasible

Internalization mechanisms of cell-penetrating peptides

• Ivana Ruseska and
• Andreas Zimmer

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

• influence the cellular uptake mechanism. Keywords: cell-penetrating peptides; direct translocation; drug delivery; endocytosis; internalization; Introduction The cell membrane is a semipermeable barrier, serving as a protective layer for the cells. It is an essential organelle for cell survival and

• provide enzymatic protection and stability for the drug, an improved distribution and target specificity, as well as a lack of toxicity [3]. Cell-penetrating peptides as drug delivery systems Having in mind the attention they have gained, cell-penetrating peptides (CPPs) have become a current hotspot in

• -1), the epidermal growth factor (EGF) and the platelet-derived growth factor or tumor-promoting factors [63]. However, this mechanism provides an effective path for drug delivery. It has been described as the pathway used to deliver arginine-rich CPPs such as octa-arginine and TAT peptides into

The effect of heat treatment on the morphology and mobility of Au nanoparticles

• Sven Oras,
• Sergei Vlassov,
• Simon Vigonski,
• Boris Polyakov,
• Mikk Antsov,
• Vahur Zadin,
• Rünno Lõhmus and
• Karine Mougin

Beilstein J. Nanotechnol. 2020, 11, 61–67, doi:10.3762/bjnano.11.6

• materials used in studies related to nanostructures. The small size and the enhanced properties of Au nanoparticles (NPs) compared to bulk gold make them important for the development of novel applications, for example, in the field of drug delivery [1], sensor technology [2], printing [3] and catalysis [4

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

• Arianna Gennari Julio M. Rios de la Rosa Erwin Hohn Maria Pelliccia Enrique Lallana Roberto Donno Annalisa Tirella Nicola Tirelli Laboratory of Polymers and Biomaterials, Fondazione Istituto Italiano di Tecnologia, 16163 Genova, Italy NorthWest Centre for Advanced Drug Delivery (NoWCADD), School

• 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

• as the cationic component in polyplexes and other drug delivery vehicles [1][2][3]. In comparison to other polycations, its main advantages are the low toxicity and its biodegradability. Biodegradation can occur both enzymatically and oxidatively [4]. A number of methods can be employed to prepare

Fully amino acid-based hydrogel as potential scaffold for cell culturing and drug delivery

• Dávid Juriga,
• Evelin Sipos,
• Orsolya Hegedűs,
• Gábor Varga,
• Miklós Zrínyi,
• Krisztina S. Nagy and
• Angéla Jedlovszky-Hajdú

Beilstein J. Nanotechnol. 2019, 10, 2579–2593, doi:10.3762/bjnano.10.249

• , Nagyvarad square 4, Budapest, Hungary 10.3762/bjnano.10.249 Abstract Polymer hydrogels are ideal scaffolds for both tissue engineering and drug delivery. A great advantage of poly(amino acid)-based hydrogels is their high similarity to natural proteins. However, their expensive and complicated synthesis

• reductive conditions resulted in an increased drug release due to the cleavage of disulfide bridges in the hydrogels. Consequently, these hydrogels provide new possibilities in the fields of both tissue engineering and controlled drug delivery. Keywords: biocompatibility; cystamine; hydrogel; lysine; poly

• the changing environmental conditions. Therefore, hydrogels can be used as drug delivery systems [4], implants [5][6], coatings [7][8] or scaffolds for tissue engineering [2][3][9][10]. Besides these stimuli-responsive properties, the chemical and physical structure, the mechanical properties [10] as

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

• of physicochemical characteristics and siRNA surface density for a long period. Keywords: colloidal stability; gold nanoparticles; scale-up; siRNA delivery; siRNA duplex stability; therapeutic nucleic acids; Introduction Drug delivery to cells is only one application of nanoparticles in biomedicine

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

• 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

• new therapeutic approaches for targeted drug delivery to SCLC are desperately needed. SCLC belongs to a class known as neuroendocrine tumours in which malignant cells secrete hormones and growth factors – a trait inherited from the neuroendocrine cells of the bronchial epithelium that are transformed

Frontiers in pharmaceutical nanotechnology

• Matthias G. Wacker

Beilstein J. Nanotechnol. 2019, 10, 2538–2540, doi:10.3762/bjnano.10.244

• Matthias G. Wacker National University of Singapore, Faculty of Science, Department of Pharmacy, 6 Science Drive 2, 117546 Singapore 10.3762/bjnano.10.244 Keywords: drug delivery; nanocarriers; nanomedicines; nanotheranostics; pharmaceutical nanotechnology; Today, pharmaceutical nanotechnology

• is a very dynamic and evolving research area that integrates a wide variety of disciplines such as chemical, biological and biomedical science. At the frontier of knowledge, nanoparticles, exosomes and even more advanced drug delivery systems [1] blur the line between drug discovery and formulation

• active transport of nanoparticles into the central nervous system using the low-density lipoprotein receptor family [3][4][5][6], provided an entry route for the cytostatic drug doxorubicin into the brain. The drug delivery system has been tested in a phase II clinical trial and hopefully will make its

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

• fluorescent probes for a number of bio-responsive applications, ranging from drug delivery to genomics [29][30][31]. Similar to other nanotubes, the pristine BNNTs were not fluorescent, and a fluorophore (e.g., organic molecule or quantum dot) is added via surface modification to make them fluorescent [29][30

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

• biocompatibility, improved mechanical characteristics tailored for the specific application, in addition to new release mechanisms and improved permeability [9][12][13][14]. The delivery through the mucosa via buccal administration has shown several advantages as a drug delivery target site. The ease of

• to different types of stimulation, during mastication, speech and swallowing, could hinder the development of drug delivery systems for this route [15][16]. In order to avoid these drawbacks, nanostructured systems with mucoadhesive polymers, such as acrylic-acid derivatives, have been investigated

• with the mechanical and rheological characteristics observed. One of the replicate images is showed in Figure 9B. In vitro drug release profile During the development of drug delivery systems for buccal application, in vitro drug release is highly important and is considered a prerequisite for

Dynamics of superparamagnetic nanoparticles in viscous liquids in rotating magnetic fields

• Nikolai A. Usov,
• Ruslan A. Rytov and
• Vasiliy A. Bautin

Beilstein J. Nanotechnol. 2019, 10, 2294–2303, doi:10.3762/bjnano.10.221

• ; viscous liquid; Introduction Magnetic nanoparticles are promising materials in various areas of biomedicine [1][2][3][4], such as magnetic resonance imaging [5][6][7], targeted drug delivery [8][9][10], and magnetic hyperthermia [11][12][13][14][15][16][17][18][19][20]. Iron oxide nanoparticles are most

Microfluidics as tool to prepare size-tunable PLGA nanoparticles with high curcumin encapsulation for efficient mucus penetration

• Nashrawan Lababidi,
• Valentin Sigal,
• Aljoscha Koenneke,
• Konrad Schwarzkopf,
• Andreas Manz and
• Marc Schneider

Beilstein J. Nanotechnol. 2019, 10, 2280–2293, doi:10.3762/bjnano.10.220

• is more than 50% for Pluronic F68 and Pluronic 10500. A considerable increase in size and size distribution would hamper the ability of the particles to serve as efficient drug delivery systems. Thus, all stabilizers that do not prohibit agglomeration are not suitable for our application. To

• microfluidics in combination with a specific muco-inert surface chemistry led to a promising drug delivery system with enhanced mucus penetration. Moreover, a high absolute curcumin encapsulation efficiency of ≈67.15% was obtained using microfluidics. Furthermore, the encapsulation was clearly improved in

Targeted therapeutic effect against the breast cancer cell line MCF-7 with a CuFe₂O₄/silica/cisplatin nanocomposite formulation

• B. Rabindran Jermy,
• Vijaya Ravinayagam,
• Widyan A. Alamoudi,
• Dana Almohazey,
• Hatim Dafalla,
• Lina Hussain Allehaibi,
• Abdulhadi Baykal,
• Muhammet S. Toprak and
• Thirunavukkarasu Somanathan

Beilstein J. Nanotechnol. 2019, 10, 2217–2228, doi:10.3762/bjnano.10.214

• tumor imaging guide and drug delivery system. Keywords: anticancer; cisplatin; copper ferrite; drug delivery; multifunctional; nanomedicine; nanotherapeutics; spherical silica; tumour therapy; Introduction Due to the continuous advancements in the field of nanotechnology, the therapeutic prospects

• expected health crisis [1]. However, the single modal drug delivery system is hampered by low bioavailability (about 5–10%), burst release, and lower target efficiency. Multifunctional theranostic nanoparticles that can respond to an external magnetic field for drug release and assist in bioimaging

• /HYPS, CuFe2O4/AlMSU-F and CuFe2O4/silicalite nanoformulations. The cellulose membrane dialysis tubing was activated, and drug delivery was performed by immersing the bag containing 30 mg of drug formulations in 50 mL of phosphate buffered saline (PBS) at pH 5.6. The release was performed under constant

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