Tatsuo Aikawa

Preparation of pH-sensitive Anionic Liposomes Designed for Drug Delivery System (DDS) Application

We prepared pH-sensitive anionic liposomes composed solely of anionic bilayer membrane components that were designed to promote efficient release of entrapped agents in response to acidic pH. The pH-sensitive anionic liposomes showed high dispersion stability at neutral pH, but the fluidity of the bilayer membrane was enhanced in an acidic environment. These liposomes were rather simple and were composed of dimyristoylphosphatidylcholine (DMPC), an anionic bilayer membrane component, and polyoxyethylene sorbitan monostearate (Tween 80). In particular, the present pH-sensitive anionic liposomes showed higher temporal stability than those of conventional DMPC/DPPC liposomes. We found that pHsensitive properties strongly depended on the molecular structure, pKa value, and amount of an incorporated anionic bilayer membrane component, such as sodium oleate (SO), dimyristoylphosphatidylserine (DMPS), or sodium β-sitosterol sulfate (SS). These results provide an opportunity to manipulate liposomal stability in a pH-dependent manner, which could lead to the formulation of a high performance drug delivery system (DDS).

A Reactive Oxygen/Nitrogen Species Sensor Fabricated from an Electrode Modified with a Polymerized Iron Porphyrin and a Polymer Electrolyte Membrane

We have developed an electrochemical reactive oxygen/nitrogen species sensor that can detect superoxide anion radicals (O2-•) and nitric oxide (NO). The reactive oxygen/nitrogen species sensor was fabricated by surface modification of an electrode with polymerized iron tetrakis(3-thienyl)porphyrin (FeT3ThP), and it can detect either O2-• or NO by switching the applied potential. Furthermore, we fabricated a sensor with improved selectivity by coating a Nafion® film onto the poly(FeT3ThP)-modified electrode. An interference current caused by NO2- was seen for the poly(FeT3ThP)-modified electrode, while the interference current was significantly reduced at the Nafion®/poly(FeT3ThP)-modified electrode, leading to improved selectivity for NO detection. The current response at the Nafion®/poly(FeT3ThP)-modified electrode exhibited good linearity in the O2-• and NO concentration ranges 1.3 - 4.1, and 0.5 - 10 μM, respectively. The Nafion®/poly(FeT3ThP)-modified and poly(FeT3ThP)-modified electrodes are highly versatile, because these electrodes can detect either O2-• or NO by switching the applied potential. Since the Nafion®/poly(FeT3ThP)-modified and poly(FeT3ThP)-modified electrodes contain no bio-derived compounds, the reactive oxygen/nitrogen species sensor should be safe even when it is used in vivo.

Platinum Nanoparticle-embedded Porous Diamond Spherical Particles as an Active and Stable Heterogeneous Catalyst

Platinum nanoparticle-embedded porous diamond spherical particles (PtNP@PDSPs), as an active and stable catalyst, were fabricated by spray-drying of an aqueous slurry containing nanodiamond (ND) particles, platinum nanoparticles (PtNP), and polyethylene glycol (PEG) to form ND/PtNP/PEG composite spherical particles, followed by removal of PEG and a short-time diamond growth on the surface. The average diameter of the PtNP@PDSPs can be controlled in the range of 1–5 μm according to the spray-drying conditions. The Brunauer-Emmett-Teller (BET) surface area and average pore diameter of the PtNP@PDSPs were estimated to be ca. 170–300 m2 g−1 and ca. 4–13 nm, respectively. When ND with the size of 20–30 nm was used, the size of PtNP in the PtNP@PDSP was almost unchanged at 5–6 nm even after high temperature processes and reuse test for catalytic reaction, showing stable supporting. The catalytic activity of the PtNP@PDSPs for the dehydrogenation of cyclohexane was higher than that for a Pt/C catalyst, which is attributed to the stable PtNP support by the three-dimensional packing of ND and efficient mass transfer via the interconnected through-hole pores in the PDSPs.

Polystyrene latex particles containing europium complexes prepared by miniemulsion polymerization using bovine serum albumin as a surfactant for biochemical diagnosis

Luminescent particles have been attracting significant attention because they can be used in biochemical applications, such as detecting and imaging biomolecules. In this study, luminescent polystyrene latex particles were prepared through miniemulsion polymerization of styrene with dissolved europium complexes in the presence of bovine serum albumin (BSA) and poly(ethylene glycol) monomethoxy methacrylate as surfactants. The solubility of the europium complex in styrene has a strong effect on the yield of the particle. Europium tris(2-thenoyl trifluoroacetonate) di(tri-n-octyl phosphine oxide), which has a high solubility in styrene, was sufficiently incorporated into the polystyrene particles compared to europium tris(2-thenoyl trifluoroacetonate), which has a low solubility in styrene. The luminescence property of the europium complex could remain intact even after its incorporation through the miniemulsion polymerization. In the aqueous dispersion, the resulting particles could emit strong luminescence, which is a characteristic of the europium complex. The antibody fragments were covalently attached to BSA-covered particles after a reaction with a bifunctional linker, N-(6-maleimidocaproyloxy)succinimide. The time-resolved fluoroimmunoassay technique showed that 3.3pg/mL of human α-fetoproteins (AFP) can be detected by using the resulting luminescent particles. An immunochromatographic assay using the resulting particles was also performed as a convenient method to qualitatively detect biomolecules. The detection limit of AFP measured by the immunochromatographic assay was determined to be 2000pg/mL. These results revealed that the luminescent particles obtained in this study can be utilized for the highly sensitive detection of biomolecules and in vitro biochemical diagnosis.

Real-time monitoring of superoxide anion radical generation in response to wounding: electrochemical study

Background The growth and development of plants is deleteriously affected by various biotic and abiotic stress factors. Wounding in plants is caused by exposure to environmental stress, mechanical stress, and via herbivory. Typically, oxidative burst in response to wounding is associated with the formation of reactive oxygen species, such as the superoxide anion radical (O2•−), hydrogen peroxide (H2O2) and singlet oxygen; however, few experimental studies have provided direct evidence of their detection in plants. Detection of O2•− formation in plant tissues have been performed using various techniques including electron paramagnetic resonance spin-trap spectroscopy, epinephrine-adrenochrome acceptor methods, staining with dyes such as tetrazolium dye and nitro blue tetrazolium (NBT); however, kinetic measurements have not been performed. In the current study, we provide evidence of O2•− generation and its kinetics in the leaves of spinach (Spinacia oleracea) subjected to wounding. Methods Real-time monitoring of O2•− generation was performed using catalytic amperometry. Changes in oxidation current for O2•− was monitored using polymeric iron-porphyrin-based modified carbon electrodes (φ = 1 mm) as working electrode with Ag/AgCl as the reference electrode. Result The results obtained show continuous generation of O2•− for minutes after wounding, followed by a decline. The exogenous addition of superoxide dismutase, which is known to dismutate O2•− to H2O2, significantly suppressed the oxidation current. Conclusion Catalytic amperometric measurements were performed using polymeric iron-porphyrin based modified carbon electrode. We claim it to be a useful tool and a direct method for real-time monitoring and precise detection of O2•− in biological samples, with the potential for wide application in plant research for specific and sensitive detection of O2•−.

Lyoprotective Effect of Alkyl Sulfobetaines for Freeze-drying 1,2-Dipalmitoyl-sn-glycero-3- phosphocholine Liposomes

A liposome is a molecular assembly in the form of a vesicle comprised of a phospholipid bilayer. Liposomes can be used as molecular containers in various fields such as pharmaceutical, cosmetic, and food industries. It is difficult to maintain the original structure of liposomes in an aqueous medium. Phospholipids, which are components of liposomes, are susceptible to hydrolysis, which causes disruption of the liposomal structure and dysfunction of the molecular container. In this context, freeze-drying liposomes is a preferable method to improve the shelf life of liposomes. However, when freeze-drying liposomes, a lyoprotective agent is required to preserve their original structure. In this study, we investigate whether alkyl sulfobetaines (SBn, n: number of carbons in the alkyl chain, n = 1-18) can be used as lyoprotectants for 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) liposomes. The results indicated that the length of the alkyl chain of the SBn was an important factor to prevent liposome disruption during the freeze-drying and subsequent rehydration processes. The use of SBn with an alkyl chain of intermediate length (n = 6-10) could prevent liposome disruption and remarkably reduce the gel-to-liquid crystal phase transition temperature (Tm) of the freeze-dried liposomes. This indicates that these SBn could intercalate in the dried bilayer and reduce intermolecular interaction between DPPC in the bilayer. The Tm reduction of the freeze-dried liposomes should contribute to prevention of the gel-to-liquid phase transition of the liposomes during the rehydration process, which has been known to be a main cause of liposome disruption. We expect that the results from this study will provide an insight into the influence of zwitterionic additives on freeze-dried lipid bilayers and the lyoprotective effect, which should be useful in many biochemical and biomedical fields.

Dispersion of Vesicles Composed of Industrially Produced Alkyl (Oligo) Glucoside Using Diol-Boron Complexation

Alkyl (oligo)glucosides (AOG) are known to be environmentally compatible amphiphiles whose commercial applicability should be broadened. The present paper describes the preparation of molecular assemblies of industrially produced AOG, which is a mixture composed of different length of alkyl chains (C9-C12) with oligoglucoside moiety with a few (1-3) of glucose units. It was also described that regulation of the dispersibility of the molecular assemblies prepared by diol-boron complexation between the sugar moiety on AOG and boric acid in a dispersion medium. The molecular assembly of AOG was successfully formed by mixing AOG and cholesterols (CH). When using a suitable amount of CH (20-40 mol% with respect to AOG), the molecular assembly formed a vesicle structure. The dispersion ability of the resulting vesicle was dependent on both the boric acid concentration and pH of the dispersion medium. The light-scattering and ζ-potential measurements revealed that high concentrations (≥10 mM) of boric acid improved dispersibility the vesicles. In contrast, the vesicle agglomerated at low concentrations of boric acid (1-7.5 mM). In the absence of boric acid in dispersion medium, the vesicles were completely agglomerated. The optimum pH range for vesicle dispersion was found to be from neutral to basic (7.4-10.1). The (11)B NMR study revealed that borate ester formation occurred between boric acid and the diol of the sugar moiety on AOG vesicle. The present data suggest that borate ester formation that occurred on the surface of the vesicle provided negative charge to the vesicles, contributing to their dispersion via repulsive forces.