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 the clumping of AuNP-siRNA, we used the known property of albumin to increase the dispersion of AuNP suspensions [29]. We added 3% human serum albumin (HSA) (corresponding to 10% serum commonly used in the cell cultivation) to samples ×1 and ×10 (freshly prepared and stored for one or eight days

• . Experimental Materials and methods We used RNA phosphoramidite synthons, dithiothreitol (DTT), sodium citrate (Na3C6H5O7·2H2O, Sigma-Aldrich, USA); Cy-5.5 phosphoramidite (Primetech, Belarus); aurum hydrochloric acid (HAuCl4·3H2O, Aurat, Russia); human serum albumin (HSA, Reanal, Hungary); sodium chloride

• , storage for one day; 2, storage for eight days. Clusters of AuNP-siRNA in samples ×10 after two (A), three (В), and four (С) weeks. The same samples after the addition of 3% human serum albumin (HSA) in the DMEM medium (D, E, F). D–F – contrasting with uranyl acetate. Scale bars correspond to 100 nm. Data

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

• growth. Secondly, the presence of serum proteases could rapidly reduce the integrity of the peptides, as demonstrated for other bombesin-related peptides that displayed mouse and human serum half-lives measured in the tens of hours [26]. The specificity of Tyr4-Bn and cystabn activity was confirmed in

Magnetic properties of biofunctionalized iron oxide nanoparticles as magnetic resonance imaging contrast agents

• Natalia E. Gervits,
• Andrey A. Gippius,
• Alexey V. Tkachev,
• Evgeniy I. Demikhov,
• Sergey S. Starchikov,
• Igor S. Lyubutin,
• Alexander L. Vasiliev,
• Vladimir P. Chekhonin,
• Maxim A. Abakumov,
• Alevtina S. Semkina and
• Alexander G. Mazhuga

Beilstein J. Nanotechnol. 2019, 10, 1964–1972, doi:10.3762/bjnano.10.193

• and human serum albumin coated iron oxide nanoparticles was observed by Mössbauer spectroscopy. Conclusion: This difference in magnetic behavior is explained by the influence of biofunctionalization on the magnetic and electronic properties of the iron oxide nanoparticles. The ZF-NMR spectra analysis

• functionalization of nanoparticles with bovine serum albumin (BSA) and human serum albumin (HSA) is one potential method to enhance their biocompatibility. There are several directions in the development of coating types: coating of the nanoparticles themselves [10], design of BSA microcapsules with iron oxide

Doxorubicin-loaded human serum albumin nanoparticles overcome transporter-mediated drug resistance in drug-adapted cancer cells

• Hannah Onafuye,
• Sebastian Pieper,
• Dennis Mulac,
• Jindrich Cinatl Jr.,
• Mark N. Wass,
• Klaus Langer and
• Martin Michaelis

Beilstein J. Nanotechnol. 2019, 10, 1707–1715, doi:10.3762/bjnano.10.166

• . Here, we tested doxorubicin-loaded human serum albumin (HSA) nanoparticles in the neuroblastoma cell line UKF-NB-3 and its ABCB1-expressing sublines adapted to vincristine (UKF-NB-3rVCR1) and doxorubicin (UKF-NB-3rDOX20). Doxorubicin-loaded nanoparticles displayed increased anticancer activity in UKF

• body distribution of its many substrates including drugs, xenobiotics, and other molecules. HSA nanoparticles may provide an alternative, more specific way to overcome transporter-mediated resistance. Keywords: ABCB1; cancer; doxorubicin; drug resistance; human serum albumin; nanoparticles

• resistance [6]. This includes various nanoparticle and liposome formulations of the ABCB1 substrate doxorubicin [7][8][9][10][11][12]. Here, we here investigated the effects of doxorubicin-loaded human serum albumin (HSA) nanoparticles in ABCB1-expressing neuroblastoma cells. HSA nanoparticles are easy to

Serum type and concentration both affect the protein-corona composition of PLGA nanoparticles

• Katrin Partikel,
• Robin Korte,
• Dennis Mulac,
• Hans-Ulrich Humpf and
• Klaus Langer

Beilstein J. Nanotechnol. 2019, 10, 1002–1015, doi:10.3762/bjnano.10.101

• around poly(lactide-co-glycolide) (PLGA) NPs at different serum concentrations using two substantially different serum types, namely fetal bovine serum (FBS) and human serum. The corona was characterized by means of sodium dodecylsulfate polyacrylamide gel electrophoresis (SDS-PAGE), Bradford protein

• concentration. On PLGA NPs incubated with either FBS or human serum a clear difference in qualitative corona protein composition was identified by SDS-PAGE and LC–MS/MS in combination with bioinformatic protein classification. In the case of human serum a considerable change in corona composition was observed

• protein corona as a function of increasing serum concentration. Therefore, we produced NPs composed of the biodegradable polymer PLGA stabilized with poly(vinyl alcohol) (PVA) and subsequently incubated them with increasing amounts of either fetal bovine serum (FBS) or human serum to induce the formation

Review on nanoparticles and nanostructured materials: history, sources, toxicity and regulations

• Jaison Jeevanandam,
• Ahmed Barhoum,
• Yen S. Chan,
• Alain Dufresne and
• Michael K. Danquah

Beilstein J. Nanotechnol. 2018, 9, 1050–1074, doi:10.3762/bjnano.9.98

• powered by light on the market, representing the first major commercial use of dye-sensitized solar cells. In 2005, Abraxane™, which is a human serum albumin NP material containing paclitaxel, was manufactured, commercialized and released in the pharmaceutical market [41]. In 2014, there were about 1814

Comparison of four methods for the biofunctionalization of gold nanorods by the introduction of sulfhydryl groups to antibodies

• Xuefeng Wang,
• Zhong Mei,
• Yanyan Wang and
• Liang Tang

Beilstein J. Nanotechnol. 2017, 8, 372–380, doi:10.3762/bjnano.8.39

• modification with Traut’s reagent. These results are consistent with the findings that DTT modification introduces more sulfhydryl groups per mol human serum albumin (HSA) than treatment with Traut’s reagent [28]. The conjugating efficiency of antibody-to-nanosphere by Traut’s thiolation was low relative to

• )trimethoxysilane (MPTMS), ethylenediaminetetraacetic acid (EDTA), poly(ethylene glycol) methyl ether thiol (PEG-SH, Mw ≈ 5000), goat anti-human IgG, dithiotreitol (DTT), thiol-poly(ethylene glycol)amine (SH-PEG-NH2), and human serum IgG were provided by Sigma–Aldrich (St. Louis, MO). Traut’s reagent, ZebaTM spin

A novel electrochemical nanobiosensor for the ultrasensitive and specific detection of femtomolar-level gastric cancer biomarker miRNA-106a

• Maryam Daneshpour,
• Kobra Omidfar and
• Hossein Ghanbarian

Beilstein J. Nanotechnol. 2016, 7, 2023–2036, doi:10.3762/bjnano.7.193

• samples that were performed by the fabricated nanobiosensor with five different known concentrations of the target miR-106a added to human serum. The high recovery and low RSD values prove the obvious potential of this nanobiosensor for detecting miR-106a in serum environment. Furthermore, in order to

• confirm the applicability of our nanobiosensor for analyzing circulating miR-106a in real samples, human serum samples from ten newly diagnosed GC patients and ten healthy volunteers were tested. The recorded electrochemical signals presented in Table 2 demonstrate the upregulation of miR-106a in the

• previously reported miRNA-(nano)biosensors, the presented nanobiosensor provides a simpler more time- and cost-effective methodology with a wide linear range and low limit of detection (Table 3). According to the remarkable performance in real biological environments (human serum sample) and no need for RNA

Early breast cancer screening using iron/iron oxide-based nanoplatforms with sub-femtomolar limits of detection

• Dinusha N. Udukala,
• Hongwang Wang,
• Sebastian O. Wendel,
• Aruni P. Malalasekera,
• Thilani N. Samarakoon,
• Asanka S. Yapa,
• Gayani Abayaweera,
• Matthew T. Basel,
• Pamela Maynez,
• Raquel Ortega,
• Yubisela Toledo,
• Leonie Bossmann,
• Colette Robinson,
• Katharine E. Janik,
• Olga B. Koper,
• Ping Li,
• Massoud Motamedi,
• Daniel A. Higgins,
• Gary Gadbury,
• Gaohong Zhu,
• Deryl L. Troyer and
• Stefan H. Bossmann

Beilstein J. Nanotechnol. 2016, 7, 364–373, doi:10.3762/bjnano.7.33

• designed for detecting MMP 1 and MMP 7 are within the ranges defined by all employed peptide sequences. Pieper et al. have analyzed human serum by fractionating serum proteins, followed by two-dimensional electrophoresis, and sequential anion-exchange and size-exclusion chromatography. They have resolved

Au nanoparticle-based sensor for apomorphine detection in plasma

• Chiara Zanchi,
• Andrea Lucotti,
• Matteo Tommasini,
• Sebastiano Trusso,
• Ugo de Grazia,
• Emilio Ciusani and
• Paolo M. Ossi

Beilstein J. Nanotechnol. 2015, 6, 2224–2232, doi:10.3762/bjnano.6.228

• APO in blood plasma, as shown in Figure 7B. The kinetics of APO adsorption onto the gold nanostructured surface are expected to be strongly affected by matrix effects. In particular, the presence of proteins, such as human serum albumin, an abundant plasma protein that binds a wide range of drugs

Optimized design of a nanostructured SPCE-based multipurpose biosensing platform formed by ferrocene-tethered electrochemically-deposited cauliflower-shaped gold nanoparticles

• Wicem Argoubi,
• Maroua Saadaoui,
• Sami Ben Aoun and
• Noureddine Raouafi

Beilstein J. Nanotechnol. 2015, 6, 1840–1852, doi:10.3762/bjnano.6.187

• pertaining to enzymatic kinetics studies. The levels of hIgG in human serum and H2O2 in honey were successfully determined and served as assessment tools of the applicability of the platforms for real samples analysis. Keywords: cauliflower-shaped gold nanoparticles; enzymatic detection; IgG sensing

• competitive proteins using a panel of electrochemical techniques such as cyclic voltammetry (CV), differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS). Application of the two platforms for the detection of hIgG and H2O2 respectively in human serum and in honey are presented

• analytes in complex matrix formed by human serum and honey. The platform is a prelude to a more specific application in the design of point-of-care and portable devices for use in remote areas and on-field monitoring of several types of analytes such as explosives and other warfare agents. Experimental

Protein corona – from molecular adsorption to physiological complexity

• Lennart Treuel,
• Dominic Docter,
• Michael Maskos and
• Roland H. Stauber

Beilstein J. Nanotechnol. 2015, 6, 857–873, doi:10.3762/bjnano.6.88

• revealed a decrease of the collision efficiency (i.e., the overall number of collisions divided by the number of collisions that form an agglomerate) with an increasing protein (human serum albumin, HSA) concentration (Figure 1a). Intriguingly, they found that their colloid was stable at a point where

• understand the interactions between NPs and biological systems. Briefly, they used their LC-MS based method to measure time-resolved corona compositions on silica and polystyrene NPs in human serum. By using NPs of various sizes (diameters of about 35, 120, 140 nm), and surface functionalities (amine

• the polymer shell), by live HeLa cells in the presence or absence of human transferrin (TF) and human serum albumin (HSA) in phosphate-buffered saline (PBS) medium. They studied the uptake of the NPs by quantitative confocal fluorescence microscopy. For comparison, they also studied the cellular

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

• containing SCIONs. To exclude background fluorescence of extracellular adherent SCIONs, single cells were marked by the help of fluorescently labeled transferrin (Transferrin From Human Serum, Alexa Fluor® 488 Conjugate, Invitrogen, Cat.No. T-13342). After that the mean intensity of the SCION fluorescence

Nanoparticle interactions with live cells: Quantitative fluorescence microscopy of nanoparticle size effects

• Li Shang,
• Karin Nienhaus,
• Xiue Jiang,
• Linxiao Yang,
• Katharina Landfester,
• Volker Mailänder,
• Thomas Simmet and
• G. Ulrich Nienhaus

Beilstein J. Nanotechnol. 2014, 5, 2388–2397, doi:10.3762/bjnano.5.248

• on whether internalization was analyzed with the cells in buffer or in medium containing human serum, so that a protein adsorption layer will form on the NPs. These data emphasize that studies of NP-cell interactions on cell line models may not be straightforwardly transferable to the situation in

Coating with luminal gut-constituents alters adherence of nanoparticles to intestinal epithelial cells

• Heike Sinnecker,
• Katrin Ramaker and
• Andreas Frey

Beilstein J. Nanotechnol. 2014, 5, 2308–2315, doi:10.3762/bjnano.5.239

• ], and possible implications for the particle–cell interactions are considered. For example, it was shown that human serum albumin (HSA), BSA and fetal bovine serum can build a protein corona around NPs whereby the particles are stabilized against agglomeration and the colloid stability of the particle

Nanoencapsulation of ultra-small superparamagnetic particles of iron oxide into human serum albumin nanoparticles

• Matthias G. Wacker,
• Mahmut Altinok,
• Stephan Urfels and
• Johann Bauer

Beilstein J. Nanotechnol. 2014, 5, 2259–2266, doi:10.3762/bjnano.5.235

• Technische Universität Darmstadt, Technical Chemistry, D-64287 Darmstadt, Germany Merck KGaA, D-64287 Darmstadt, Germany 10.3762/bjnano.5.235 Abstract Human serum albumin nanoparticles have been utilized as drug delivery systems for a variety of medical applications. Since ultra-small superparamagnetic

• systemic exposition of patients with the carrier [6]. Human serum albumin (HSA) represents a promising candidate that binds a wide range of compounds with different physicochemical characteristics. In 2007, with Abraxane®, a first polymeric nanoparticle formulation consisting of this material has been

• time range. After freeze drying, only USPIO HSA hybrid particles prepared at an iron concentration of 15 µg/mg demonstrated significant agglomeration. Experimental Reagents and chemicals Human serum albumin (Fraction V) and glutaraldehyde 8% aqueous solution were purchased from Sigma (Steinheim

Effects of surface functionalization on the adsorption of human serum albumin onto nanoparticles – a fluorescence correlation spectroscopy study

• Pauline Maffre,
• Stefan Brandholt,
• Karin Nienhaus,
• Li Shang,
• Wolfgang J. Parak and
• G. Ulrich Nienhaus

Beilstein J. Nanotechnol. 2014, 5, 2036–2047, doi:10.3762/bjnano.5.212

• Marburg, Renthof 7, 35037 Marburg, Germany, Department of Physics, University of Illinois at Urbana-Champaign, 1110 West Green Street, Urbana, IL 61801, USA 10.3762/bjnano.5.212 Abstract By using fluorescence correlation spectroscopy (FCS), we have studied the adsorption of human serum albumin (HSA) onto

• four orders of magnitude. These variations can be understood in terms of specific Coulombic interactions between the proteins and the NP surfaces. Keywords: fluorescence correlation spectroscopy; human serum albumin; nanoparticles; protein corona; quantum dots; Introduction In recent years, both

• reliable in our hands. In our original FCS study [45], we investigated the adsorption of human serum albumin (HSA) onto carboxyl-functionalized, polymer-encased iron platinum nanoparticles (Fe–Pt NPs) with a hydrodynamic radius, RH, of 5–6 nm. We prepared HSA solutions of different concentrations in

In vitro interaction of colloidal nanoparticles with mammalian cells: What have we learned thus far?

• Moritz Nazarenus,
• Qian Zhang,
• Mahmoud G. Soliman,
• Pablo del Pino,
• Beatriz Pelaz,
• Susana Carregal-Romero,
• Joanna Rejman,
• Barbara Rothen-Rutishauser,
• Martin J. D. Clift,
• Reinhard Zellner,
• G. Ulrich Nienhaus,
• James B. Delehanty,
• Igor L. Medintz and
• Wolfgang J. Parak

Beilstein J. Nanotechnol. 2014, 5, 1477–1490, doi:10.3762/bjnano.5.161

• fluorescence correlation spectroscopy (FCS), Röcker et al. investigated the adsorption of human serum albumin onto FePt NPs and found clear evidence that the proteins formed a monolayer on the surface of the NP [136]. Additional FCS studies by using other important serum proteins invariably confirmed the

Characterization of protein adsorption onto FePt nanoparticles using dual-focus fluorescence correlation spectroscopy

• Pauline Maffre,
• Karin Nienhaus,
• Faheem Amin,
• Wolfgang J. Parak and
• G. Ulrich Nienhaus

Beilstein J. Nanotechnol. 2011, 2, 374–383, doi:10.3762/bjnano.2.43

• correlation spectroscopy; human serum albumin; nanoparticle; protein adsorption; Introduction Recent years have seen enormous advances in the field of nanotechnology. A huge variety of nanoparticles (NPs), defined as objects with all three spatial dimensions in the range of 1–100 nm, has been developed, with

• understand the structural and dynamic properties of the protein corona at the molecular level. Recently, we have used quantitative fluorescence microscopy, especially fluorescence correlation spectroscopy (FCS), to study protein adsorption of human serum albumin (HSA) on polymer-coated FePt NPs with an