Development of a quantitative, portable, and automated fluorescent blue-ray device-based malaria diagnostic equipment with an on-disc SiO2 nanofiber filter.

There is an urgent need to develop an automated malaria diagnostic system that can easily and rapidly detect malaria parasites and determine the proportion of malaria-infected erythrocytes in the clinical blood samples. In this study, we developed a quantitative, mobile, and fully automated malaria diagnostic system equipped with an on-disc SiO2 nanofiber filter and blue-ray devices. The filter removes the leukocytes and platelets from the blood samples, which interfere with the accurate detection of malaria by the blue-ray devices. We confirmed that the filter, which can be operated automatically by centrifugal force due to the rotation of the disc, achieved a high removal rate of leukocytes (99.7%) and platelets (90.2%) in just 30 s. The automated system exhibited a higher sensitivity (100%) and specificity (92.8%) for detecting Plasmodium falciparum from the blood of 274 asymptomatic individuals in Kenya when compared to the common rapid diagnosis test (sensitivity = 98.1% and specificity = 54.8%). This indicated that this system can be a potential alternative to conventional methods used at local health facilities, which lack basic infrastructure.

Development of a highly sensitive, quantitative, and rapid detection system for Plasmodium falciparum-infected red blood cells using a fluorescent blue-ray optical system.

A highly sensitive diagnostic system for determining low-density infections that are missed by conventional methods is necessary to detect the carriers of Plasmodium falciparum. A fluorescent blue-ray optical system with a polycarbonate scan disc was developed to detect P. falciparum-infected red blood cells (Pf-iRBCs), and nine samples could be analyzed simultaneously. The cultured P. falciparum strain 3D7 was used to examine the potential of the system for diagnosing malaria. After an RBC suspension had been applied to the disc, the cells were dispersed on the disc by rotation. During the 10 min standing period to allow the RBCs to settle on the disc surface, the cells were simultaneously stained with nuclear fluorescence staining dye Hoechst 34580, which was previously adsorbed on the disc surface. RBCs were arranged on the disc surface as a monolayer by removing excess cells through momentary rotation. Over 1.1 million RBCs remained on the disc for fluorescence analysis. A portable, battery-driven fluorescence image reader was employed to detect fluorescence-positive RBCs for approximately 40 min. A good correlation between examination of Giemsa-stained RBCs by light microscopy and the developed system was demonstrated in the parasitemia range of 0.0001-1.0% by linear regression analysis (R2 = 0.99993). The limit of detection of 0.00020% and good reproducibility for parasitemia determination were observed. The ability of the developed system to detect sub-microscopic low-density Pf-iRBCs and provide accurate quantitative evaluation with easy operation was demonstrated.

Application of a cell microarray chip system for accurate, highly sensitive, and rapid diagnosis for malaria in Uganda.

Accurate, sensitive, rapid, and easy operative diagnosis is necessary to prevent the spread of malaria. A cell microarray chip system including a push column for the recovery of erythrocytes and a fluorescence detector was employed for malaria diagnosis in Uganda. The chip with 20,944 microchambers (105 µm width and 50 µm depth) was made of polystyrene. For the analysis, 6 µl of whole blood was employed, and leukocytes were practically removed by filtration through SiO2-nano-fibers in a column. Regular formation of an erythrocyte monolayer in each microchamber was observed following dispersion of an erythrocyte suspension in a nuclear staining dye, SYTO 21, onto the chip surface and washing. About 500,000 erythrocytes were analyzed in a total of 4675 microchambers, and malaria parasite-infected erythrocytes could be detected in 5 min by using the fluorescence detector. The percentage of infected erythrocytes in each of 41 patients was determined. Accurate and quantitative detection of the parasites could be performed. A good correlation between examinations via optical microscopy and by our chip system was demonstrated over the parasitemia range of 0.0039-2.3438% by linear regression analysis (R(2) = 0.9945). Thus, we showed the potential of this chip system for the diagnosis of malaria.

Elution behavior of lambda-DNA with ternary mixed carrier solvents in an open-tubular capillary under laminar flow conditions.

An open-tubular capillary chromatography was developed based on the tube radial distribution of the ternary mixed carrier solvents that generated the inner and outer phases under laminar flow conditions. This is called "tube radial distribution chromatography" (TRDC). In this report, the elution behavior of lambda-DNA (48502 bp) as a biopolymer was examined by the TRDC system. The ternary mixture of water-acetonitrile-ethyl acetate, 15:3:2 or 3:8:4 volume ratio, as a carrier solution was fed into the capillary tube made of polytetrafluoroethylene (PTFE) or fused-silica. The mixture of hydrophobic 1-naphthol and hydrophilic lambda-DNA was subjected to the TRDC system using the water-rich carrier solution. Lambda-DNA and 1-naphthol were distributed between the inner and outer phases due to their hydrophilic and hydrophobic nature, and then eluted in this order, undergoing chromatographic separation. The mixture of hydrophilic 2,6-naphthalenedisulfonic acid and hydrophobic lambda-DNA that was treated with surfactants was also examined with the organic solvent-rich carrier solution. The modified hydrophobic DNA and 2,6-naphthalenedisulfonic acid were distributed and eluted in this order due to their nature.

Metal ion analysis using microchip CE with chemiluminescence detection based on 1,10-phenanthroline-hydrogen peroxide reaction.

We developed a microchip CE method with chemiluminescence (CL) detection using the reaction of 1,10-phenanthroline and hydrogen peroxide for separation and determination of metal ions, where the metal ions acted as catalysts for the CL reaction. The microchip consisted of two microchannels that crossed at the intersection and four reservoirs that accessed the ends of the channels. The metal ions in the sample solution migrated in the channel along with 1,10-phenanthroline included in a running solution, and then mixed with hydrogen peroxide in one of the reservoirs to emit CL. The light was detected with a photomultiplier tube located just above the reservoir. Two metal ion groups, the platinum metal group (Ru(III), Rh(III), Pd(II), Os(VIII), Ir(III), and Pt(IV)) and the fourth periodic transition metal group (Cu(II), Fe(II), Co(II), and Ni(II)) were examined using the present system. The lowest detection limit was observed for Os(VIII); Os(VIII) responded over the range of 7.5x10(-12)-1.0x10(-8 )M with the detection limit of 7.5x10(-12 )M (about 38 zmol) (S/N = 3). The mixed solution of Ru(III), Rh(III), Pd(II), Os(VIII), Ir(III), and Pt(IV) could be analyzed using this system within about 2.5 min. In addition, the system was applied to the determination of Cu(II) concentration in a city water supply.

Improvement of the light-harvesting efficiency in polymer/fullerene bulk heterojunction solar cells by interfacial dye modification.

Enhancement of the light-harvesting efficiency in poly(3-hexylthiophene)/fullerene derivative (P3HT/PCBM) bulk heterojunction solar cells has been demonstrated by the introduction of near-infrared phthalocyanine molecules as the third component at the P3HT/PCBM interface. The introduction of silicon phthalocyanine derivative (SiPc) increased the short-circuit current density and hence improved the overall power conversion efficiency by 20%, compared to the P3HT/PCBM control device. For P3HT/PCBM/SiPc devices, two distinct external quantum efficiency (EQE) peaks were observed at wavelengths for the absorption bands of SiPc as well as P3HT before and after thermal annealing, suggesting that SiPc molecules are located at the P3HT/PCBM interface because of crystallization of the P3HT and PCBM domains. Furthermore, the EQE for the device increased even at wavelengths for the absorption band of P3HT by the introduction of SiPc molecules. This indicates that P3HT excitons can be dissociated into charge carriers more efficiently in the presence of SiPc molecules at the P3HT/PCBM interface by energy transfer from P3HT to SiPc molecules. These findings suggest that there are two origins for the increase in the photocurrent by the introduction of SiPc; SiPc molecules serve not only as a light-harvesting photosensitizer but also as an energy funnel for P3HT excitons at the P3HT/PCBM interface.