scholarly journals A SEMIAUTOMATIC INSTRUMENT FOR THE RADIOAUTOGRAPHIC COATING TECHNIQUE

1966 ◽  
Vol 14 (12) ◽  
pp. 923-928 ◽  
Author(s):  
BEATRIX MARKUS KOPRIWA
Keyword(s):  
Silver Bromide ◽  
Electron Microscopic ◽  
Simple Method ◽  
Nuclear Track Emulsion ◽  
Withdrawal Speed ◽  
Emulsion Layer ◽  
Semiautomatic Instrument ◽  
Mechanical Coating ◽  
Electron Microscopic Radioautography ◽  
Selection Of

By means of a mechanical coating instrument a fast, simple method to coat specimens with liquid nuclear track emulsion has been devised for quantitative light and electron microscopic radioautography. In both cases, the section is mounted on a glass slide. After the vertically held slide has been immersed in the melted emulsion, the instrument withdraws it at a slow, constant speed. As a result, the specimen is coated with a thin, uniform emulsion layer composed of homogeneously distributed silver bromide crystals. The thickness of the emulsion coat may be standardized by selection of an optimal combination of emulsion dilution, temperature and withdrawal speed.

scholarly journals THE INFLUENCE OF DEVELOPMENT ON THE NUMBER AND APPEARANCE OF SILVER GRAINS IN ELECTRON MICROSCOPIC RADIOAUTOGRAPHY

1967 ◽  
Vol 15 (9) ◽  
pp. 501-515 ◽  
Author(s):  
BEATRIX MARKUS KOPRIWA
Keyword(s):  
Resolving Power ◽  
Silver Bromide ◽  
Grain Development ◽  
Electron Microscopic ◽  
Duration Of Action ◽  
Small Grains ◽  
Silver Grains ◽  
Electron Microscopic Radioautography ◽  
Selection Of ◽  
Duration Of Development

Under conditions similar to those in electron microscopic radioautography, the development of three different nuclear track emulsions—Ilford L4, Gevaert 307 and Kodak NTE—was investigated by varying the type of developer, duration of action and temperature. These three factors influence: (1) the number of silver grains produced from exposed silver bromide crystals and, therefore, the sensitivity of the emulsion; (2) the production of a few silver grains from silver bromide crystals, unexposed to radiation from the specimen, that is, the background fog; and (3) the size and shape of the developed silver grains, thus influencing the resolving power. The developed silver grains increase in number and in size with increasing duration of development. After complete development in most developers, the silver grains consist of highly convoluted silver filaments and are 2 or 3 times as large as the original silver bromide crystals. However, small grains may be obtained by brief development in Loveland's and p-phenylenediamine developers, in which case only development centers are revealed. Such small grain development improves resolving power, but decreases the number of developed silver grains, thus reducing sensitivity. The most satisfactory emulsion-developer combination under the conditions of the experiment appears to be Gevaert 307 emulsion developed for 2 min in D-19b. Data are also presented to facilitate the selection of the optimal emulsion-developer combination for various experimental situations.

Electron Microscopic Demonstration of Adenovirus in Appendix Vermiformis in a Case of Ileocecal Intussusception

PEDIATRICS ◽  
1973 ◽  
Vol 51 (3) ◽  
pp. 566-570
Author(s):  
Eduardo J. Yunis ◽  
Yoshie Hashida
Keyword(s):  
Electron Microscopy ◽  
Electron Microscopic ◽  
Simple Method ◽  
Appendix Vermiformis ◽  
Viral Particles ◽  
History Of ◽  
Ileocecal Intussusception ◽  
Electron Microscopic Demonstration ◽  
Hematoxylin Eosin ◽  
Selection Of

Viral particles identical to those of adenovirus were demonstrated in the intranuclear inclusion bodies of the epithelial cells of an appendix vermiformis removed from a boy with a recent history of intussusception. Viral particles were demonstrated by electron microscopy following reprocessing of a formaldehyde-fixed, paraffin embedded and hematoxylin-eosin stained section. This simple method permits precise selection of the tissue for electron microscopy and in instances such as this gives sufficient tissue preservation to demonstrate viral particles. Our findings support the idea that some cases of intussusception may be the result of the adenovirus infection.

scholarly journals Block-staining tissues with potassium ferrocyanide-reduced osmium tetroxide and lead aspartate for electron microscopic radioautography.

1984 ◽  
Vol 32 (5) ◽  
pp. 552-554 ◽  
Author(s):  
B M Kopriwa
Keyword(s):  
Room Temperature ◽  
Osmium Tetroxide ◽  
Uranyl Acetate ◽  
Potassium Ferrocyanide ◽  
Electron Microscopic ◽  
En Bloc ◽  
Simple Method ◽  
Electron Microscopic Radioautography

In the hope of devising a method for prestaining tissues en bloc for electron microscopic radioautography, pieces of radioiodine-labeled liver were taken through various combinations of ferrocyanide-reduced osmium tetroxide, lead aspartate, and aqueous uranyl acetate at room temperature or at 60 degrees C. Following the tests, the method adopted for routine use was to block-stain tissues for 2 hr in potassium ferrocyanide-reduced osmium tetroxide at 4 degrees C followed by 1 hr in Walton's lead aspartate at room temperature. This simple method, which requires no manipulation before or after emulsion coating and development of the radioautographs, provides adequate contrast without inducing background fog or artifacts.

A simplified method of emulsion coating and development for quantitative electron microscopic radioautography

1978 ◽  
Vol 36 (2) ◽  
pp. 64-65
Author(s):  
K. Yoshida ◽  
F. Murata ◽  
S. Ohno ◽  
T. Nagata
Keyword(s):  
Mass Production ◽  
Identical Condition ◽  
Microscopic Level ◽  
Electron Microscopic Level ◽  
Electron Microscopic ◽  
Simplified Method ◽  
Complicated Process ◽  
Critical Problems ◽  
Electron Microscopic Radioautography ◽  
Quantitative Radioautography

IntroductionSeveral methods of mounting emulsion for radioautography at the electron microscopic level have been reported. From the viewpoint of quantitative radioautography, however, there are many critical problems in the procedure to produce radioautographs. For example, it is necessary to apply and develop emulsions in several experimental groups under an identical condition. Moreover, it is necessary to treat a lot of grids at the same time in the dark room for statistical analysis. Since the complicated process and technical difficulties in these procedures are inadequate to conduct a quantitative analysis of many radioautographs at once, many factors may bring about unexpected results. In order to improve these complicated procedures, a simplified dropping method for mass production of radioautographs under an identical condition was previously reported. However, this procedure was not completely satisfactory from the viewpoint of emulsion homogeneity. This paper reports another improved procedure employing wire loops.

Platelet Incorporation of Labelled Adenosine and Adenosine Diphosphate

1969 ◽  
Vol 22 (02) ◽  
pp. 304-315 ◽  
Author(s):  
E. W Salzman ◽  
T. P Ashford ◽  
D. A Chambers ◽  
Lena L. Neri
Keyword(s):  
Platelet Rich Plasma ◽  
Adenosine Diphosphate ◽  
Platelet Inhibition ◽  
Electron Microscopic ◽  
Platelet Binding ◽  
Minor Degree ◽  
A Minor ◽  
Plasma Marker ◽  
Electron Microscopic Radioautography ◽  
Simultaneous Assessment

SummaryAfter incubation of platelet-rich plasma with labelled adenosine or ADP, platelet incorporation of radioactivity was assessed. Platelets were rapidly separated for counting by filtration through cellulose acetate Millipore. Inulin-H3 served as a plasma marker, and triple isotope techniques permitted simultaneous assessment of the behavior of the adenine and phosphate moieties of ADP without washing of platelets. In other experiments, electron microscopic radioautography was employed to trace the label after platelet incorporation.The results were consistent with previous reports that ADP is dephosphorylated in plasma and is incorporated by platelets only as a dephosphorylated residue, probably adenosine. The label crossed the platelet membrane and entered the platelet, where it was distributed in platelet granules and the agranular cell sap. Concentration within granules occurred to a minor degree.The results support the hypothesis that platelet aggregation by ADP occurs without a persistent bond of ADP to the platelet. Inhibition of aggregation by adenosine probably depends on a metabolic or transport process rather than on competition between adenosine and ADP for platelet binding sites.

scholarly journals Electron Microscopic Radioautographic Study on Protein Synthesis in Mitochondria of Binucleate Hepatocytes of Aging Mice

2007 ◽  
Vol 7 ◽  
pp. 1008-1023 ◽  
Author(s):  
Tetsuji Nagata
Keyword(s):  
Protein Synthesis ◽  
Labeling Index ◽  
Electron Microscopic ◽  
Protein Precursor ◽  
Binucleate Cells ◽  
Mouse Hepatocytes ◽  
Electron Microscopic Radioautography ◽  
Liver Tissues

In order to study the aging changes of intramitochondrial protein synthesis in mouse hepatocytes, 10 groups of aging mice, each consisting of three individuals, total 30, from fetal day 19 to postnatal year 2, were injected with3H-leucine, a protein precursor, sacrificed 1 h later, and the liver tissues processed for electron microscopic radioautography. On electron microscopic radioautograms obtained from each animal, the numbers of mitochondria, the numbers of labeled mitochondria, and the mitochondrial labeling index labeled with3H-leucine that showed protein synthesis in each hepatocyte, both mononucleate and binucleate cells, were counted and the averages in respective aging groups were compared. From the results, it was demonstrated that the numbers of mitochondria, the numbers of labeled mitochondria, and the labeling indices of intramitochondrial protein syntheses in both mononucleate and binucleate hepatocytes of mice at various ages increased due to development of animals. The numbers of mitochondria, the numbers of labeled mitochondria, and the labeling indices of intramitochondrial protein synthesis in binucleate hepatocytes were more than those of mononucleate hepatocytes at the same aging stages.

scholarly journals Selection of dancer member using simple additive weighting

2018 ◽  
Vol 7 (3) ◽  
pp. 1096 ◽  
Author(s):  
Hana Adela ◽  
Kamarul Azmi Jasmi ◽  
Bushrah Basiron ◽  
Miftachul Huda ◽  
Andino Maseleno
Keyword(s):  
Community Life ◽  
Simple Method ◽  
Unitary State ◽  
Simple Additive Weighting ◽  
Selection Of

Travel and dance form in Indonesia is closely related to the development of community life, both in terms of ethnic structure and within the scope of the unitary state. This study determines the criteria for selecting dancer members and how to apply the qualified Simple method. Based on predetermined criteria is the ability to dance physical flexibility, skilled, nimble, confident, have the ability, fill out the form, and certificate of achievement. From the results obtained values then V1, V2, V3, V4, V5 is a member of a qualified dancer and has a highest value with a score of 100 which was obtained from V2. 

scholarly journals Transoperative refusion: a simple and safe method in emergency surgery

2014 ◽  
Vol 41 (4) ◽  
pp. 292-296
Author(s):  
Luiz Carlos Buarque Gusmão ◽  
Sérgio Henrique Chagas Valoes ◽  
José da Silva Leitão Neto
Keyword(s):  
Cost Benefit ◽  
Blood Transfusions ◽  
Factor V ◽  
West Nile Fever ◽  
Clotting Factors ◽  
Blood Contamination ◽  
Simple Method ◽  
Cost Benefit Ratio ◽  
The Cost ◽  
Selection Of

The objective is to reinforce the importance of blood reinfusion as a cheap, safe and simple method, which can be used in small hospitals, especially those in which there is no blood bank. Moreover, even with the use of devices that perform the collection and filtration of blood, more recent studies show that the cost-benefit ratio is much better when autologous transfusion is compared with blood transfusions, even when there is injury to hollow viscera and blood contamination. It is known that the allogeneic blood transfusion carries a number of risks to patients, among them are the coagulation disorders mediated by excess enzymes in the conserved blood, and deficiency in clotting factors, mainly the Factor V, the proacelerin. Another factor would be the risk of contamination with still unknown pathogens or that are not investigated during screening for selection of donors, such as the West Nile Fever and Creutzfeldt-Jacob, better known as "Mad Cow" disease. Comparing both methods, we conclude that blood autotransfusion has numerous advantages over heterologous transfusion, even in large hospitals. We are not against blood transfusions, just do not agree that the patient's own blood is discarded without making sure there will be enough blood in stock to get him out of the hemorrhagic shock.

scholarly journals A multi-site cutting device implements efficiently the divide-and-conquer strategy in tumor sampling

F1000Research ◽  
2016 ◽  
Vol 5 ◽  
pp. 1587 ◽  
Author(s):  
Jose I. Lopez ◽  
Jesus M. Cortes
Keyword(s):  
Synthetic Data ◽  
Daily Practice ◽  
Divide And Conquer ◽  
Intratumor Heterogeneity ◽  
Pathology Laboratory ◽  
Simple Method ◽  
French Fry ◽  
Histological Processing ◽  
Tumor Sampling ◽  
Selection Of

We recently showed that in order to detect intra-tumor heterogeneity a Divide-and-Conquer (DAC) strategy of tumor sampling outperforms current routine protocols. This paper is a continuation of this work, but here we focus on DAC implementation in the Pathology Laboratory. In particular, we describe a new simple method that makes use of a cutting grid device and is applied to clear cell renal cell carcinomas for DAC implementation. This method assures a thorough sampling of large surgical specimens, facilitates the demonstration of intratumor heterogeneity, and saves time to pathologists in the daily practice. The method involves the following steps: 1. Thin slicing of the tumor (by hand or machine), 2. Application of a cutting grid to the slices (e.g., a French fry cutter), resulting in multiple tissue cubes with fixed position within the slice, 3. Selection of tissue cubes for analysis, and finally, 4. Inclusion of selected cubes into a cassette for histological processing (with about eight tissue fragments within each cassette). Thus, using our approach in a 10 cm in-diameter-tumor we generate 80 tumor tissue fragments placed in 10 cassettes and, notably, in a tenth of time. Eighty samples obtained across all the regions of the tumor will assure a much higher performance in detecting intratumor heterogeneity, as proved recently with synthetic data.

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