Synthesis and potent cytotoxic activity of a novel diosgenin derivative and its phytosomes against lung cancer cells

• Liang Xu,
• Dekang Xu,
• Ziying Li,
• Yu Gao and
• Haijun Chen

Beilstein J. Nanotechnol. 2019, 10, 1933–1942, doi:10.3762/bjnano.10.189

• targeted drug delivery to tumors. These nanoparticles can passively accumulate in tumors via enhanced permeability and retention (EPR) effect, thus decreasing the toxicity of nonselective bio-distribution [27]. Considering the advantages of liposomes as a drug delivery system for chemotherapeutic drugs and

• between cells treated with free drugs and their corresponding phytosomes. The results indicated that phytosomes could be an ideal drug delivery system for Di and its derivatives to obtain sustained release without affecting drug activity. In vitro anticancer mechanisms of P2P Cell cycle and cell apoptosis

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

• radical surgery [36]. In addition, Mao and co-workers have reported the multitargeted drug delivery system by a d-peptide ligand (d-AE) based EGFRvIII targeting strategy, which provides a promising path for glioma therapy [37]. Through the conjugation of Cy7.5 to PEPHC1-modified PEGylated SPIONs, a

• -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

Microfluidic manufacturing of different niosomes nanoparticles for curcumin encapsulation: Physical characteristics, encapsulation efficacy, and drug release

• Mohammad A. Obeid,
• Ibrahim Khadra,
• Abdullah Albaloushi,
• Margaret Mullin,
• Hanin Alyamani and
• Valerie A. Ferro

Beilstein J. Nanotechnol. 2019, 10, 1826–1832, doi:10.3762/bjnano.10.177

• capability. These results demonstrate that niosomes prepared by microfluidic mixing to encapsulate curcumin are a promising delivery system to reach target cells. Keywords: curcumin; drug delivery; microfluidic mixing; niosomes nanoparticle; Introduction Curcumin is a natural product that is derived from

• the particle sizes, where smaller particles were obtained at a ratio of 3:1 compared to a ratio of 1:1 for both formulations. These results confirm previously reported results about niosomes prepared by microfluidic mixing [15]. Encapsulation of curcumin The potential of a nanoparticle delivery system

• nanoparticles components to be used as a drug delivery system for curcumin and for other therapeutic agents. TEM images of (A) SP80 niosomes prepared at 1:1 FRR, (B) SP80 niosomes prepared at 3:1 FRR, (C) T85 niosomes prepared at 1:1 FRR, (D) T85 niosomes prepared at 3:1 FRR. Curcumin standard curve measured by

Nanoporous smartPearls for dermal application – Identification of optimal silica types and a scalable production process as prerequisites for marketed products

• David Hespeler,
• Sanaa El Nomeiri,
• Jonas Kaltenbach and
• Rainer H. Müller

Beilstein J. Nanotechnol. 2019, 10, 1666–1678, doi:10.3762/bjnano.10.162

• Berlin, Germany Institute of Functional Interfaces, Karlsruher Institute of Technology, Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen, Germany 10.3762/bjnano.10.162 Abstract smartPearls are a dermal delivery system for poorly soluble active agents, consisting of nanoporous silica

• solvent removal) can be industrially realized in a commercial 50 L rotary evaporator. Keywords: amorphous dispersion; bioavailability enhancement; dermal delivery system; rutin; smartPearls; solubility enhancement; Introduction Many interesting active agents in pharma and cosmetics are poorly soluble

Hydrophilicity and carbon chain length effects on the gas sensing properties of chemoresistive, self-assembled monolayer carbon nanotube sensors

• Juan Casanova-Cháfer,
• Carla Bittencourt and
• Eduard Llobet

Beilstein J. Nanotechnol. 2019, 10, 565–577, doi:10.3762/bjnano.10.58

• printed circuit board (PCB), which was then plugged inside a test chamber (see Supporting Information File 1, Figure S7). Gas sensing measurements A 35 mL airtight test chamber in Teflon was connected to an automated gas mixture delivery system controlled by Bronkhorst mass-flow controllers and calibrated

Cytotoxicity of doxorubicin-conjugated poly[N-(2-hydroxypropyl)methacrylamide]-modified γ-Fe₂O₃ nanoparticles towards human tumor cells

• Zdeněk Plichta,
• Yulia Kozak,
• Rostyslav Panchuk,
• Viktoria Sokolova,
• Matthias Epple,
• Lesya Kobylinska,
• Pavla Jendelová and
• Daniel Horák

Beilstein J. Nanotechnol. 2018, 9, 2533–2545, doi:10.3762/bjnano.9.236

• the novel drug-delivery system, cytomorphological study of chromatin hypercondensation in DAPI-stained murine B16 melanoma cells was performed. Cells were incubated with γ-Fe2O3@PHPMA (Figure 10b,c), free Dox (Figure 10d,e), and γ-Fe2O3@P(HPMA-MMAA)-Dox nanoparticles (Figure 10f,g). Both free Dox and

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

• immediately on improving the efficacy. This need could possibly be met by a nanoscale-carrier-facilitated drug delivery system. This rapidly growing field of research has gained interest all over the world with its effective and targeted drug delivery application [3]. Polymer-based nanoformulations have

• insignificant drug release. On the other hand, with increased acidic conditions, there is an augmented probability of more H+ ions available to counteract the nanoparticle–drug formulation, thereby reducing the interactions [28]. This property of the proposed nanoparticle drug delivery system significantly

Nanoconjugates of a calixresorcinarene derivative with methoxy poly(ethylene glycol) fragments for drug encapsulation

• Alina M. Ermakova,
• Julia E. Morozova,
• Yana V. Shalaeva,
• Victor V. Syakaev,
• Aidar T. Gubaidullin,
• Alexandra D. Voloshina,
• Vladimir V. Zobov,
• Irek R. Nizameev,
• Olga B. Bazanova,
• Igor S. Antipin and
• Alexander I. Konovalov

Beilstein J. Nanotechnol. 2018, 9, 2057–2070, doi:10.3762/bjnano.9.195

• use as a supramolecular drug-delivery system. Keywords: calixresorcinarene; drug encapsulation; hemotoxicity; methoxy poly(ethylene glycol); temperature-controlled release; Introduction One of the acute problems of modern medicinal therapy is the development of novel drug-delivery systems with low

Biomimetic and biodegradable cellulose acetate scaffolds loaded with dexamethasone for bone implants

• Aikaterini-Rafailia Tsiapla,
• Varvara Karagkiozaki,
• Veroniki Bakola,
• Foteini Pappa,
• Panagiota Gkertsiou,
• Eleni Pavlidou and
• Stergios Logothetidis

Beilstein J. Nanotechnol. 2018, 9, 1986–1994, doi:10.3762/bjnano.9.189

• completed after 181 days. The burst release of the drug delivery system was very low (11.6%) and, consequently, this nanoplatform will not release the necessary amount of the drug to merge the immunosuppressive effect over a time scale of 181 days. In the same context, the choice of the CA scaffold, the

A visible-light-controlled platform for prolonged drug release based on Ag-doped TiO₂ nanotubes with a hydrophobic layer

• Caihong Liang,
• Jiang Wen and
• Xiaoming Liao

Beilstein J. Nanotechnol. 2018, 9, 1793–1801, doi:10.3762/bjnano.9.170

• anodizing voltage and time, some distinctive nanotube structures have been obtained, including multilayer [10], bamboo-type [11], branched tubes [12], and double-walled tubes [13]. Multilayered TNTs are known as the most controllable and useful drug delivery system [14]. In a previous work, Shi et al. [15

• . Thus, Zn exhibits significant, promising application in the biomedical field. Hence, Zn was selected as a model drug to be loaded into the TiO2 nanotubes for the drug delivery system in this work. In present work, we provide an approach for a visible-light-controlled drug release platform based on the

Atomic-level characterization and cilostazol affinity of poly(lactic acid) nanoparticles conjugated with differentially charged hydrophilic molecules

• María Francisca Matus,
• Martín Ludueña,
• Cristian Vilos,
• Iván Palomo and
• Marcelo M. Mariscal

Beilstein J. Nanotechnol. 2018, 9, 1328–1338, doi:10.3762/bjnano.9.126

• descriptions using computational methodologies still are not totally addressed. Wang et al. [30] carried out dissipative particle dynamics (DPD) simulations to study the PEG–PLA–PEG/paclitaxel delivery system. The results showed a spherical micelle with the drug inside and polymer chains distributed on the

• determine the spatial distribution of cilostazol in polymeric NPs and to explore its potential use in this kind of drug delivery system. Experimental Characterization of copolymer structures by all-atom molecular dynamics simulations The poly(lactic acid) core PLA polymer chains were built in three

Development of polycationic amphiphilic cyclodextrin nanoparticles for anticancer drug delivery

• Gamze Varan,
• Juan M. Benito,
• Carmen Ortiz Mellet and
• Erem Bilensoy

Beilstein J. Nanotechnol. 2017, 8, 1457–1468, doi:10.3762/bjnano.8.145

• cells. The amphiphilic, cationic PC βCDC6 derivative was used as the anticancer drug carrier delivery system for PCX for the first time in this study. There are various studies in which this derivative is used as a gene transfer delivery system; however, there is only example where this derivative was

• used as a drug delivery system. This was a study regarding the non-polar anxiolytic drug diapezam realized by Mendez-Ardoy et al. [22]. Our goal is to evaluate the potential of the polycationic CD nanoparticles as an anticancer drug delivery system. In fact, these polycationic CDs were evaluated for

• their intrinsic apoptotic effect in our first paper [26] in unloaded blank nanoparticle form. This study focuses on the nanocarrier properties and drug delivery system potential of the polycationic CD nanoparticles for PCX, which is an anticancer drug with several serious bioavaibility and toxicity

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

• than 100 nm and a net positive surface charge to facilitate cellular internalization of drug-loaded nanoparticles. Hydroxypropyl cellulose films were prepared to incorporate these nanoparticle dispersions to complete the implantable drug delivery system. Results: The diameter of core–shell

• nanoparticles and their zeta potential can be varied with chitosan coating. When further loaded into films, these nanoparticles seem to be a potential drug delivery system for docetaxel for glioma treatment and a good candidate for further evaluation in animal studies. This film formulation can be implanted

3D Nanoprinting via laser-assisted electron beam induced deposition: growth kinetics, enhanced purity, and electrical resistivity

• Brett B. Lewis,
• Robert Winkler,
• Xiahan Sang,
• Pushpa R. Pudasaini,
• Michael G. Stanford,
• Harald Plank,
• Raymond R. Unocic,
• Jason D. Fowlkes and
• Philip D. Rack

Beilstein J. Nanotechnol. 2017, 8, 801–812, doi:10.3762/bjnano.8.83

• 1 nm was used while varying dwell times per pixel. A previously developed computer aided design program was used to determine the dwell times per pixel necessary to construct complex shapes. The beam energy and current for all patterns was set at 30 keV and 21 pA, respectively. Laser delivery system

• automated axial translation. An objective lens located at the shaft tip projects the 100 µm diameter laser spot with a Gaussian distribution at the coincidence point between the focused electron beam and the gas injection systems. The laser delivery system is a prototype under development by Waviks, Inc

• of different growth conditions. Schematic illustrating the experimental system which includes a laser delivery system, precursor and co-reactant gas delivery systems, and the electron beam all coincident to the same region. The schematic also illustrates the deposition of the 3D suspended bridge

Chitosan-based nanoparticles for improved anticancer efficacy and bioavailability of mifepristone

• Huijuan Zhang,
• Fuqiang Wu,
• Yazhen Li,
• Xiping Yang,
• Jiamei Huang,
• Tingting Lv,
• Yingying Zhang,
• Jianzhong Chen,
• Haijun Chen,
• Yu Gao,
• Guannan Liu and
• Lee Jia

Beilstein J. Nanotechnol. 2016, 7, 1861–1870, doi:10.3762/bjnano.7.178

• mechanism of action. However, application of MIF is limited by its poor water solubility and low oral bioavailability. In this work, we developed a drug delivery system based on chitosan nanoparticles (CNs) to improve its bioavailability and anticancer activity. The MIF-loaded chitosan nanoparticles (MCNs

• curve from 0 to 24 h compared with free MIF. These results demonstrated that MCNs could be developed as a potential delivery system for MIF to improve its anticancer activity and bioavailability. Keywords: anticancer; chitosan; drug delivery; mifepristone; nanoparticles; pharmacokinetics; sustained

• increased its efficacy by sustained release to reduce drug crystallization [33]. These results suggested that MCNs might be a good drug delivery system for delivery of MIF for cancer therapy. Pharmacokinetic study In our previous study, we found MIF showed distinct pharmacokinetic differences between

Gold nanoparticles covalently assembled onto vesicle structures as possible biosensing platform

• M. Fátima Barroso,
• M. Alejandra Luna,
• Juan S. Flores Tabares,
• Cristina Delerue-Matos,
• N. Mariano Correa,
• Fernando Moyano and
• Patricia G. Molina

Beilstein J. Nanotechnol. 2016, 7, 655–663, doi:10.3762/bjnano.7.58

• methodology. This nanomaterial offers interesting possibilities and future applications such as its use in the design of immunosensors. Moreover, the developed methodology can be a promising candidate for other applications as optical addressable delivery system and affinity columns. Experimental Synthesis of

Comparison of the interactions of daunorubicin in a free form and attached to single-walled carbon nanotubes with model lipid membranes

• Dorota Matyszewska

Beilstein J. Nanotechnol. 2016, 7, 524–532, doi:10.3762/bjnano.7.46

• includes liposomes, which are commercially available daunorubicin formulation (Daunoxome®) used in the treatment of Kaposi’s sarcoma [6]. Despite that, there are still numerous studies on the improvement of this drug delivery system aiming at enhancing drug loading into cells by using specific interactions

• . Moreover, it was shown that the surface concentration of the drug on the electrode surface is similar for both the drug in a free form and the drug–nanocarrier adduct. This observation proves that application of single-walled carbon nanotubes as drug delivery system allows for the transport of the

pH-Triggered release from surface-modified poly(lactic-co-glycolic acid) nanoparticles

• Manuel Häuser,
• Klaus Langer and
• Monika Schönhoff

Beilstein J. Nanotechnol. 2015, 6, 2504–2512, doi:10.3762/bjnano.6.260

• Nanoparticles (NP) of poly(lactic-co-glycolic acid) (PLGA) represent a promising biodegradable drug delivery system. We suggest here a two-step release system of PLGA nanoparticles with a pH-tunable polymeric shell, providing an initial pH-triggered step, releasing a membrane-toxic cationic compound. PLGA

• . We present here the idea of a two-step delivery system consisting of core–shell nanoparticles. The outer shell is susceptible to changes of the pH value, such that the release of a membrane-toxic cationic compound is triggered by a reduced pH value in the endolysosomal compartment of the cells. The

Nanofibers for drug delivery – incorporation and release of model molecules, influence of molecular weight and polymer structure

• Jakub Hrib,
• Jakub Sirc,
• Radka Hobzova,
• Zuzana Hampejsova,
• Zuzana Bosakova,
• Marcela Munzarova and
• Jiri Michalek

Beilstein J. Nanotechnol. 2015, 6, 1939–1945, doi:10.3762/bjnano.6.198

• delivery system with the diffusion rate of the therapeutic agent stable throughout the life. The structure of the nanofibrous drug delivery system plays a key role in the drug release process. The fiber diameter, specific surface area, size and total volume of pores significantly influence the convection

Filling of carbon nanotubes and nanofibres

• Reece D. Gately and
• Marc in het Panhuis

Beilstein J. Nanotechnol. 2015, 6, 508–516, doi:10.3762/bjnano.6.53

• delivery and medical imaging applications of SWCNT and MWCNTs have been identified, this line of research has only very recently emerged [117][118][119]. Further investigations into the selective binding of functional groups and various viruses or tumours could provide for an effective drug delivery system

Release behaviour and toxicity evaluation of levodopa from carboxylated single-walled carbon nanotubes

• Julia M. Tan,
• Jhi Biau Foo,
• Sharida Fakurazi and
• Mohd Zobir Hussein

Beilstein J. Nanotechnol. 2015, 6, 243–253, doi:10.3762/bjnano.6.23

• suggests that the newly synthesized nanohybrid is a promising drug delivery system for the delivery of LD to nervous system. Experimental Materials Short, carboxyl single-walled carbon nanotubes (SWCNT–COOH) produced by chemical vapour deposition with a diameter of 1–2 nm an purity of 90% (w/w %) were

Anticancer efficacy of a supramolecular complex of a 2-diethylaminoethyl–dextran–MMA graft copolymer and paclitaxel used as an artificial enzyme

• Yasuhiko Onishi,
• Yuki Eshita,
• Rui-Cheng Ji,
• Masayasu Onishi,
• Takashi Kobayashi,
• Masaaki Mizuno,
• Jun Yoshida and
• Naoji Kubota

Beilstein J. Nanotechnol. 2014, 5, 2293–2307, doi:10.3762/bjnano.5.238

• complex is considered to be useful as a drug delivery system (DDS) for anticancer compounds since it formed a stable polymeric micelle in water. The resistance of B16F10 melanoma cells to PTX was shown clearly through a maximum survival curve. Conversely, the DDMC/PTX complex showed a superior anticancer

• cancer cells; paclitaxel; supramolecular complex; Review Introduction As a means of delivering a drug to a target effectively, the enhanced permeation and retention (EPR) effect and reticuloendothelial system (RES) were enabled by using a polymer drug delivery system (DDS), and it is thought to

• an anticancer agent can be prevented if the agent promotes positive allosteric modulation according to the enzyme reaction model of a 1:1 ratio of a substrate and enzyme, which is the ratio utilized in vivo. Gene delivery system On the other hand, development of the gene delivery system in field of

Carbon-based smart nanomaterials in biomedicine and neuroengineering

• Antonina M. Monaco and
• Michele Giugliano

Beilstein J. Nanotechnol. 2014, 5, 1849–1863, doi:10.3762/bjnano.5.196

• presence of reactive functional groups and of localised π-electrons, which promote the π–π bond with aromatic compounds, render graphene a suitable candidate as a drug delivery system. Several remarkable studies in this area have been performed, including those involving the functionalisation of GO by PEG

Different endocytotic uptake mechanisms for nanoparticles in epithelial cells and macrophages

• Dagmar A. Kuhn,
• Dimitri Vanhecke,
• Benjamin Michen,
• Fabian Blank,
• Peter Gehr,
• Alke Petri-Fink and
• Barbara Rothen-Rutishauser

Beilstein J. Nanotechnol. 2014, 5, 1625–1636, doi:10.3762/bjnano.5.174

• pathway of a NP will have direct consequences on its intracellular localization; hence, understanding the overall NP distribution in a specific compartment, such as endosomes, lysosomes or others, might provide some interesting suggestions for developing a future drug delivery system. To gain more insight

PEGylated versus non-PEGylated magnetic nanoparticles as camptothecin delivery system

• Paula M. Castillo,
• Mario de la Mata,
• Maria F. Casula,
• José A. Sánchez-Alcázar and
• Ana P. Zaderenko

Beilstein J. Nanotechnol. 2014, 5, 1312–1319, doi:10.3762/bjnano.5.144