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Paper-like electronic displays: large-area rubber-stamped plastic sheets of electronics and microencapsulated electrophoretic inks.

Electronic systems that use rugged lightweight plastics potentially offer attractive characteristics (low-cost processing, mechanical flexibility, large area coverage, etc.) that are not easily achieved with established silicon technologies. This paper summarizes work that demonstrates many of these characteristics in a realistic system: organic active matrix backplane circuits (256 transistors) for large ( approximately 5 x 5-inch) mechanically flexible sheets of electronic paper, an emerging type of display. The success of this effort relies on new or improved processing techniques and materials for plastic electronics, including methods for (i) rubber stamping (microcontact printing) high-resolution ( approximately 1 microm) circuits with low levels of defects and good registration over large areas, (ii) achieving low leakage with thin dielectrics deposited onto surfaces with relief, (iii) constructing high-performance organic transistors with bottom contact geometries, (iv) encapsulating these transistors, (v) depositing, in a repeatable way, organic semiconductors with uniform electrical characteristics over large areas, and (vi) low-temperature ( approximately 100 degrees C) annealing to increase the on/off ratios of the transistors and to improve the uniformity of their characteristics. The sophistication and flexibility of the patterning procedures, high level of integration on plastic substrates, large area coverage, and good performance of the transistors are all important features of this work. We successfully integrate these circuits with microencapsulated electrophoretic "inks" to form sheets of electronic paper.

Journal Article↗

Table detection in online ink notes.

In documents, tables are important structured objects that present statistical and relational information. In this paper, we present a robust system which is capable of detecting tables from free style online ink notes and extracting their structure so that they can be further edited in multiple ways. First, the primative structure of tables, i.e., candidates for ruling lines and table bounding boxes, are detected among drawing strokes. Second, the logical structure of tables is determined by normalizing the table skeletons, identifying the skeleton structure, and extracting the cell contents. The detection process is similar to a decision tree so that invalid candidates can be ruled out quickly. Experimental results suggest that our system is robust and accurate in dealing with tables having complex structure or drawn under complex situations.

Algorithms↗

A comparison of the apical dye penetration patterns shown by methylene blue and india ink in root-filled teeth.

This study compared the linear leakage patterns shown by 5% aqueous solution of methylene blue (MB) and India ink (II). One-hundred and twenty-five roots with single canals from extracted human teeth were used. The canals were cleaned and shaped using the step-back technique under copious irrigation. Three groups were arranged to receive root fillings of gutta-percha and one of three proprietary sealers using standard lateral condensation techniques: Sealapex (40 roots), Tubli-Seal (40 roots) and Ketac-Endo (20 roots). The remaining roots were used as controls: positive with gutta-percha and no sealer and negative with the apices sealed with nail varnish. The roots were randomly selected for 7-day immersion in either MB or II, then sectioned longitudinally; dye penetration was assessed using a Wild Leitz stereomicroscope. In all groups MB showed more penetration than II. The results were statistically significant at the P = 0.01 level, with the exception of the positive control groups. Negative controls showed no penetration. It is concluded that MB, which has a low molecular weight penetrated more deeply along root canal fillings than II, which has a large particle size.

Calcium Hydroxide↗

Multiple ink nanolithography: toward a multiple-Pen nano-plotter

The formation of intricate nanostructures will require the ability to maintain surface registry during several patterning steps. A scanning probe method, dip-pen nanolithography (DPN), can be used to pattern monolayers of different organic molecules down to a 5-nanometer separation. An "overwriting" capability of DPN allows one nanostructure to be generated and the areas surrounding that nanostructure to be filled in with a second type of "ink."

Journal Article↗

Ink and vinegar, a simple staining technique for arbuscular-mycorrhizal fungi

We developed a reliable, inexpensive, and simple method for staining arbuscular-mycorrhizal fungal colonizations in root tissues. Apart from applications in research, this nontoxic, high-quality staining method also could be of great utility in teaching exercises. After adequate clearing with KOH, an ink-vinegar solution successfully stained all fungal structures, rendering them clearly visible.

Journal Article↗

A pseudo-cryptococcal artefact derived from leucocytes in wet India ink mounts of centrifuged cerebrospinal fluid.

Wet India ink mounts of cerebrospinal fluid (CSF) are useful in the laboratory diagnosis of cryptococcal meningitis. Pseudo-cryptococcal artefacts in such mounts have been attributed to leucocytes in CSF but their mode of formation has not been explained. This report describes the reproduction of such an artefact in cryptococcus free CSF-leucocyte mixtures that had been subjected to high speed centrifugation. The viscosity of DNA that could provide a morphological pseudo-capsule, and the yellow-green fluorescence of the pseudo-capsular material on staining with acridine-orange, suggest that lymphocytic nuclear DNA, which possibly leaked out after damage to the lymphocyte membrane by centrifugation, was responsible for this artefact.

Artifacts↗

Analysis of decreased conductance serotonergic response in Aplysia ink motor neurons.

Micropressure ejection of serotonin (5-hydroxytryptamine, 5-HT) produced excitatory responses in the L14 ink motor neurons of Aplysia that depended on the site of application. Ejection of 5-HT onto the cell body produced a slow response that showed variability in voltage sensitivity between preparations. In contrast, ejection of 5-HT onto the neuropil underneath the cell body produced a response whose amplitude was consistently a linear function of the holding potential, reversing near the predicted potassium equilibrium potential. Subsequent analyses focused on this second response. The neuropil response induced by 5-HT had a linear current-voltage relationship (reversing at ca. -80 mV), was associated with a decrease in input conductance, and was sensitive to changes in the concentration of extracellular K+. Serotonin application in artificial seawater (ASW) containing 30 mM K+ produced a response that reversed close to the altered Nernst potential for K+. The 5-HT response did not appear to be due to secondary activation of interneurons or to depend primarily on extracellular Ca2+, since ejection of 5-HT onto cells bathed in ASW containing 30 mM Co2+ produced responses comparable to, although somewhat attenuated from, those observed in ASW. Serotonin responses similar to those produced in ASW were obtained after perfusing the ganglion with ASW containing Co2+, 4-aminopyridine (4-AP), and tetraethylammonium (TEA). This suggests that the 5-HT-sensitive current is separate from the Ca2+-activated, fast, and delayed rectifying K+ currents. The 5-HT response appeared to be mediated by changes in levels of cAMP. Bath application of the phosphodiesterase inhibitors IBMX (3-isobutyl-1-methylxanthine) or Ro 20-1724, or the adenylate cyclase activator forskolin mimicked the 5-HT response by producing a slow inward current associated with a decrease in membrane conductance. Alteration of cellular cAMP metabolism modulated the response to 5-HT. Exposure of the ganglion to low concentrations of either Ro 20-1724 or forskolin potentiated the 5-HT response. Higher concentrations of these agents largely blocked the response to subsequent 5-HT applications. Bath application of the 8-bromo derivative of either cAMP or cGMP produced a slow inward current associated with a decrease in membrane conductance in cells voltage clamped at the resting potential. Responses to 5-HT were blocked, however, after exposure to 8-bromo-cAMP, but not to 8-bromo-cGMP. These results suggest that 5-HT produces a voltage-independent decrease in a steady-state potassium conductance that may be mediated by cAMP.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Cloning, characterization and expression of escapin, a broadly antimicrobial FAD-containing L-amino acid oxidase from ink of the sea hare Aplysia californica.

A 60 kDa monomeric protein isolated from the defensive purple ink secretion of the sea hare Aplysia californica was cloned and sequenced, and is the first sea hare antimicrobial protein to be functionally expressed in E. coli. Sequence analysis suggested that this protein is a flavin-containing l-amino acid oxidase (LAAO), with one predicted potential glycosylation site, although the glycosylation could not be experimentally confirmed. This protein, which we call ;escapin', has high sequence similarity to several other gastropod proteins. Escapin was verified by NMR, mass spectroscopy and HPLC to have FAD as its flavin cofactor. Escapin's antimicrobial effects, bacteriostasis and bactericidal, were determined using a combination of two assays: (1) incubation of bacteria on solid media followed by assessment of inhibition by direct observation of zones of inhibition or by turbidity measurements; and (2) incubation of bacteria in liquid media followed by counting viable colonies after growing on agar plates. Native escapin inhibited the growth of Gram-positive and Gram-negative bacteria, including marine bacteria (Vibrio harveyii and Staphylococcus aureus) and pathogenic bacteria (Staphylococcus aureus, Streptococcus pyogenes and Pseudomonas aeruginosa). Escapin also inhibited the growth of yeast and fungi, with different efficacies. Escapin's antimicrobial activity was concentration dependent and did not decrease when stored for more than 5 months at room temperature. Escapin was bacteriostatic and not bactericidal in minimal media (e.g. salt media) with glucose, yeast extract, and a mixture of 20 amino acids each at 50 micromol l(-1), but was bactericidal in media enriched with Tryptone Peptone. Escapin was also strongly bactericidal in media with l-lysine at concentrations as low as 3 mmol l(-1) and slightly bactericidal in 50 mmol l(-1) l-arginine, but not in most other amino acids even at 50 mmol l(-1). Escapin had high oxidase activity (producing hydrogen peroxide) with either l-arginine or l-lysine as a substrate and little to no oxidase activity with other l-amino acids. Hydrogen peroxide alone (without escapin or amino acids) was strongly bacteriostatic but poorly bactericidal, similar in this respect to l-arginine but different from l-lysine in the presence of escapin. Together these results suggest that there are multiple mechanisms to escapin's antimicrobial effects, with bacteriostasis resulting largely or entirely from the effects of hydrogen peroxide produced by escapin's LAAO activity, but bactericidal effects resulting from lysine-dependent mechanisms not directly involving hydrogen peroxide. Recombinant escapin expressed in bacteria was also active against Gram-positive and Gram-negative bacteria, suggesting that glycosylation is not essential for antimicrobial activity.

Amino Acid Sequence↗

An investigation of the antitumor peptidoglycan fraction from squid ink.

Squid ink, which has little commercial use and is usually discarded, was extracted using a Tris-HCl buffer (pH 6.8). The extract was fractionated using DEAE Sephacel ion-exchange chromatography and Sephacryl S-300 gel filtration to give a peptidoglycan fraction which exhibited strong antitumor activity against Meth-A fibrosarcoma in BALB/c mice following intraperitoneal administration. The fraction was composed of 7.8% peptide, 57% polysaccharide and 30% pigment. The polysaccharide component had a unique structure with equimolar ratios of GlcA, GalNAc and Fuc. Since the fraction has no direct cytotoxic effect on Meth-A cells, inhibition of tumor growth may be due to stimulation of host-mediated responses.

Animals↗

Lymphatic drainage of Listeria monocytogenes and Indian ink inoculated in the peritoneal cavity of the mouse.

The lymphatic drainage of the peritoneal cavity has been investigated by intraperitoneal inoculation of an intracellular bacterium (Listeria monocytogenes) and an inert marker (Indian ink). The results reveal that both agents are transported, either after phagocytosis by intraperitoneal macrophages or in suspension in the lymph, towards the cranial sternal lymph nodes (Lymphonodi sternales craniales) of the ventral thoracic lymphocentrum (Lymphocentrum thoracicum ventrale) and to the lymph nodes of the mediastinal lymphocentrum (Lymphocentrum mediastinale), prior to systemic dissemination. This mechanism of peritoneal lymph drainage has relevance on experimental studies involving the inoculation of pathogens, and on the investigation of metastatic diffusion of neoplasms from the peritoneum.

Animals↗

Morphogenetic studies on the neural crest of hynobius larvae using vital staining and India ink labeling methods.

The neural crest cells of hynobius larvae during the morphogenesis of the neural crest were studied with the following methods: the region of the primordial neural crest was first determined by vital stainings, and then the movement of individual neural crest cells was traced with India ink labeling. The cytoarchitecture and the fine structure of neural crest cells were further observed by light, transmission and scanning electron microscopy. The primordium of the neural crest is located in the area extending from the lateral part of the neural plate to the medial part of the neural fold. RAVEN (1931) suggested that the lateral part of the neural fold was a part of the primordial neural crest. The result of our vital staining shows that it is the primordial epidermal ectoderm. The morphogenesis of the neural crest was found to proceed as follows: at first both neural folds moved to the dorsal mid line of larva, then contacted and fused to each other. The primordial neural crest cells in the neural folds became polygonal, and these cells from both folds mixed and formed a neural crest cell mass. In this process they lost their junctional apparatuses. When larvae developed at the tail bud stage, the cells in the lateral part of the neural crest extended their cytoplasmic processes and began to migrate.

Animals↗

Protein microdeposition using a conventional ink-jet printer.

Many recent bioanalytical systems based on immunologic and hybridization reactions in a mono- or bidimensional microarray format require technology that can produce arrays of spots containing biospecific molecules. Some microarray deposition instruments are commercially available, and other devices have been described in recent papers. We describe a system obtained by adapting a commercial ink-jet printer and used to produce mono- and bidimensional arrays of spots containing horseradish peroxidase on cellulose paper. In a few minutes, it was possible to obtain bidimensional arrays containing several thousands of spots with a diameter as low as 0.2 mm, with each of which requiring only a few nanoliters of the enzyme deposition solution. The quantity of enzyme in each spot was evaluated with a chemiluminescent reaction and a charge-coupled device-based, low-light imaging luminograph. The chemiluminescence measurements revealed that the reproducibility of the enzyme deposition was satisfactory for analytical purposes, with the variation coefficients being lower than 10% in almost all cases.

Horseradish Peroxidase↗

Large format ink-jet poster production: a case report.

To complement the services offered by the Medical Illustration Department of Frenchay Hospital, Bristol, we decided to look at the possibility of producing posters using the ink-jet process. Our designers wanted to use the full scope of their computers and software to expand their design talents. The method of cutting and pasting sheets of paper onto card seemed old fashioned and denied clients the benefit of the exciting techniques that have become available. After seeking sponsorship, a drug company gave 8000 Pounds towards setting up the department's poster printing service. A Kodak DS1000 printer was installed together with Posterjet and Posterworks software and we went into production, servicing not only our hospital but others in the area who gave their support for the service. High quality photographic reproduction was achieved and clients and consultants were very pleased with the results. The designers were happy that their skills were being used and interest in this and other services in the department have increased. The resulting increased income has helped finance other projects. The printer has enabled us also to see output proofs before sending work off to be offset printed--a very useful tool and a cost-saving process.

Image Processing, Computer-Assisted↗

[The influence of anterior and posterior hypothalamic structures on the engulfment and digestion of an antigen by macrophages and on India ink clearance].

Bilateral electrolytic coagulation of the posterior and supraoptic hypothalamic nuclei of rabbits had practically no effect on the engulfment of sheep erythrocytes labeled with radioactive sodium chromate retarding chiefly the rate of the antigen catabolism and promoting its retention in the subcellular fractions of the macrophages function than injury of the anterior one. Coagulation of the supraoptic nucleus accelerated India ink clearance at all the periods of investigation, whereas injury of the posterior hypothalamus failed to influence this process.

Animals↗

[Qualitative and quantitative studies on the corpus geniculatum laterale (Cgl) of the laboratory rat. IV. Qualitative structure analysis of the pars dorsalis an on India-ink-injected Nissl preparation].

1. The histological organization of the rat dorsal lateral geniculate nucleus (Cgld) has been analysed in Nissl-preparations following vessel injection with india ink. 2. The findings have been collected by means of a non-automatically visual scanning method. Every point is defined by 3 coordinates. 3. Different parameters have been collected in every point: the number of the 5 structural elements of the nervous tissue (neurons, fragments of capillaries, nuclei of astrocytes, oligodendrocytes and microglia) and the hit points per structural element. 4. In addition the differentiation of about 15500 neurons in relay neurons and interneurons has been carried out. The ratio of the 2 types of neurons is about 14:1. 5. The collected values have been statistically analysed by correlation, regression and discriminatory analyses. 6. The results relate to the correlation between the structural elements and the rostrocaudal, lateromedial and ventrodorsal directions as well as the structural elements with another. 7. At 5 levels the Cgld has been mapped on the basis of neuron size, neuron density, capillary density, density of the 3 types of glial nuclei and the relative number of hit points per structural element. 8. In the Cgld we distinguish 2 portions regarding the neuron size. The mediocellular portion occupies the lateral, ventral and caudal parts and encloses a magnocellular portion like a coat. 9. The distribution pattern of the interneurons does not correlate with the size of neurons. 10. The capillaries tend to have a greater density in the lateral area of the Cgld. 11. The correlation and regression coefficientes and the distribution pattern of the astrocytes and oligodendrocytes suggest that both glial types show a reciproke ratio in the Cgld. 12. The distribution pattern of the microglia is relatively uniform. 13. Mapping the Cgld we have got a model conception of its structural condition corresponding with the common mammalian scheme. 14. By the discriminatory analysis zones of input and fields of projection have been discriminated. It was possible to discriminate the ipsi- and contralateral input zones, but not the binocular and monocular projection fields. 15. The discriminatory analysis allows to show the collective biological effect of all structural elements in a uniform mathematical value.

Animals↗

Screen-printing ink transfer in a sexual assault case.

Yellow plastic-like particles were discovered on the clothing and body of a sexual assault victim. These particles were later associated to an athletic jersey with flaking yellow screen-printed numbers and letters, worn by the suspect. Depending on its intended substrate, screen-print ink can vary in color and composition. Particles dislodged from screen-printed garments may exhibit fabric impressions. Screen-printed clothing, commonly encountered in forensic casework, should be viewed as a potential source of trace evidence.

Journal Article↗

[Discussion on Tang edition (TE) and notes of the Tang edition (NT) under the "ink cap" in Zheng lei ben cao (Classified materia medica)].

The TE and NT cited under ink cap in Zheng lei ben cao (Classified Materia Medica) cannot be found in the contents and fragmentary volumes of Xin xiu ben cao (Newly Revised Materia Medica), yet can be seen in the "annotations of Shu ben cao (Materia Medica of Sichuan)", cited by Zhang Yuxi. This showed that the TE and NT were, in fact, coming from Shu ben cao, whose old name was Chong guang ying gong ben cao (Augmented Yinggong's Materia Medica). The so - called Yinggong was Li Ji, who compiled Tang ben cao (Materia Medica of the Tang Dynasty) by the imperial order, and gained the title Master Yingguogong, hence the title. Chong guang ying gong ben cao was meant revised Tang ben cao. This was the reason why Tang Shenwei called Shu ben cao as Tang ben cao right away in his Zheng lei ben cao.

China↗