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Query: UMLS:C0432222 (SEM)
 47,337 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

In order to examine semi-thin section for light microscopy with the backscattered electron mode (BE mode), identical sites in tissue sections were comparatively observed with both light microscopy and BE mode. Tissue blocks (ca. 3 X 3 X 1 mm) were fixed in glutaraldehyde or combined formaldehyde-glutaraldehyde solution. After dehydration in alcohol, they were embedded in Kushida's GMA-Quetol 523. 1.0 micron sections on glass slides coated with indium oxide were stained with hematoxylin-eosin or toluidine blue or by the Giemsa method, and then treated with osmium tetroxide vapor or aqueous KMnO4 solution or uranyl acetate-lead citrate solution. The identical places of such sections could be examined with the accelerating potential of 6 kV and the probe current of 8 X 10(-10) A using a JSM-35C SEM with BEIS BE detector. Photographs were taken with the 2500-line resolution cathode ray tube and the time of exposure was 100 sec. The sections were placed at a distance of 5mm from the BE detector. BE images from osmium tetroxide vapor staining showed a distinctly improved contrast especially when the sections were previously stained with hematoxylin and eosin. The cellular structure was clearly demonstrated under the electron microscope in the BE mode. Identical sites in tissue samples could be compared exactly with both light and electron micrographs.
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PMID:Observation on backscattered electron image (BEI) of a scanning electron microscope (SEM) in semi-thin sections prepared for light microscopy. 641 5

A prospective study of 10 patients undergoing hemodialysis showed that less neutropenia and complement activation occurred with dialyzer reuse. Neutrophil counts fell 95% +/- 5% (SEM) with first use and 66% +/- 8% and 48% +/- 10% with second and third uses, respectively (p less than 0.05). The production of complement component C5a-desarg, as measured by the bioassay granulocyte aggregation, was decreased by 96% +/- 1% and 93% +/- 2% with second and third uses, respectively (p less than 0.05). We investigated the role of the dialyzer disinfectant formaldehyde in decreased neutropenia. In vitro, formaldehyde inhibited granulocyte aggregation and chemotaxis and the dialyzer membrane's ability to generate granulocyte aggregating activity; however, this occurred only at concentrations higher than those likely to obtain in patients. The ability of dialysis membranes to generate granulocyte aggregating activity in plasma was decreased 55% +/- 5% by their prior sequential preincubation in plasma and then formalin (p less than 0.05) and extensive rinsing, which is similar to the circumstances obtaining with dialyzer reuse. Preincubation of membranes in plasma or formalin alone resulted in no change in the membrane's ability to generate granulocyte aggregating activity. We conclude that the exposure of membranes to both plasma and formalin during dialysis and storage is responsible for the decreased C5a-desarg production with reuse, probably because plasma proteins are fixed to the membrane in such a way that interrupts free interaction between the membrane and plasma complement components.
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PMID:Effect of dialyzer reuse on complement activation and neutropenia in hemodialysis. 647 May 61

Recent information on hazards as they relate to safety in the SEM laboratory has been compiled. The paper concentrates on recent information on formaldehyde, embeddants, and a reminder of the possible hazards of photographic chemicals. A review of formaldehyde does not substantiate it as a human carcinogen or mutagen. However, the other hazards associated with it suggest that formaldehyde needs to be handled with care. The recent substantiation of epoxy resins as mutagens suggests that all operations involving embeddants should be undertaken in an effective fume hood. Other precautions are also important. The hazards of photographic chemicals need to be reiterated. It should also be pointed out that adequate ventilation of dark rooms would do a lot to reduce this hazard.
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PMID:Safety in the scanning electron microscopy laboratory--1984 update. 652 56

In previous studies concerning the morphogenetic movements in the invaginating lens placode of the chick eye, a discrepancy between the TEM and SEM images was observed. With a fixation procedure giving good results in the TEM, certain changes seemed to have occurred in the SEM specimens (opening of apical cell blebs, bubble-like swelling of microvilli). These changes were suspected of being artefacts arisen during processing. Comparing SEM and TEM images of the invaginating lens placode and the surrounding surface applying two different osmolalities of the glutaraldehyde/formaldehyde fixative vehicle, and comparing SEM as well as TEM images with LM images of living embryos using differential interference contrast, yielded to following information. Recent reports in literature that ideal fixation techniques for SEM, certainly those preserving delicate surface structures as apical blebs and microvilli, can differ from those suitable for TEM, were confirmed. Apparently, the cell blebs which can be demonstrated in vivo to be closed, burst during SEM processing as a consequence of a relative hypo-osmolality of the fixative vehicle (a too low effective osmotic pressure). The TEM images appeared to suffer much less from changes in the osmolality of the fixative vehicle. It is suggested, therefore, that the artefacts are brought about by some step specific to the processing for the SEM (E.g. critical point drying).
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PMID:The effective osmotic pressure of the fixative for transmission and scanning electron microscopy. 677 64

The cause of the reduced wound breaking strength (WBS) in adriamycin-treated animals is unknown. Differential staining of histologic sections, collagen fiber diameter measurements by electron microscopy (EM), induction of maturation, and hydroxyproline content analysis were used to examine this defect. Differential staining and formaldehyde induction of maturation revealed no differences between mature and immature collagen content in scars of adriamycin-treated and control animals. Mean collagen fiber diameters in control rats were 76 +/- 27 nm and, in adriamycin treated rats, 62 +/- 10 nm (mean +/- SD) at 21 days. There was no difference in total hydroxyproline content between ADR and C animals. However, significant differences existed between the specific activity of new or 3H-hydroxyproline (scar collagen) at 14 days (controls, 372 +/- 9 cpm; adriamycin-treated, 129 +/- 5 cpm) and at 21 days (controls, 365 +/- 11 cpm; adriamycin treated, 172 +/- 14 cpm; mean +/- SEM; P less than 0.001). It appears that the defect contributing to reduced WBS in adriamycin treated animals is not due to a collagen maturation defect but rather to a reduction in scar collagen accumulation as measured by new hydroxyproline content and reduced fiber diameter as determined by EM measurements.
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PMID:A study of adriamycin-reduced wound breaking strenght in rats. An evaluation by light and electron microscopy, induction of collagen maturation, and hydroxyproline content. 737 12

We measured dialysate protein losses from polysulphone dialyzers undergoing repetitive processing with bleach and formaldehyde. The entire dialysate was collected during the first, fifth and tenth use of F-80 dialyzers. Dialysate protein concentration was 1.5 +/- 0.4 mg/dl N = 11 +/- SEM) during the first use, 2.1 +/- 0.3 mg/dl during the fifth use and 3.6 +/- 0.5 mg/dl (N = 10) during the tenth use. In a follow-up study, dialyzers were evaluated for up to 25 uses. After 12 to 15 uses dialysate protein was 7.9 +/- 0.8 mg/dl (N = 13), after 16 to 20 uses; 12.0 +/- 1.2 mg/dl (N = 13) and after 23 to 25 uses; 19.9 +/- 2.1 mg/dl (N = 5). Mean dialysate volume was 83.9 +/- 1.1 liters (N = 63) yielding total protein losses of up to 20.7 grams per treatment. Dialysate albumin losses, which were unmeasurable during the first use of the dialyzers, revealed a similar increase with reuse resulting in a mean value of 14.4 +/- 3.2 mg/dl after 23 to 25 reuses (N = 5). Dialysate beta-2 microglobulin (beta 2m) levels were 1.05 +/- 0.13 mg/l for dialyzers bleached < 10 times (N = 32) versus 1.54 +/- 0.15 mg/liter for dialyzers bleached > 10 times (N = 31, P < 0.02 vs. < 10 reuses). A random sampling of dialyzers processed without bleach for 8, 14, 15, 24 and 25 reuses revealed minimal protein losses, ranging from 1.4 to 2.7 mg/dl with no relation to reuse number and no measureable albumin.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Dialysate protein losses with bleach processed polysulphone dialyzers. 772 43

The expression of proliferating cell nuclear antigen (PCNA) was examined in normal human and rat liver fixed in either formaldehyde or methanol, and was compared with the incorporation of bromodeoxyuridine (BrdU) in S-phase cells. Codistribution of PCNA and BrdU was assessed in rat liver by double immunohistochemical staining using PC10 and anti-BrdU monoclonal antibodies to identify labelled nuclei of parenchymal and sinusoidal cells. In formaldehyde-fixed human biopsies (n = 13) PCNA-labelling index (PCNA LI) was 0.43 +/- 0.24% (mean +/- SEM) for hepatocytes and 0.09 +/- 0.03% for sinusoidal cells. A great interspecimen variability was observed and a preferential lobular distribution was not evident. In methanol-fixed human liver (n = 8) the immunostaining was strong. PCNA LI was 0.05 +/- 0.01% for hepatocytes and 0.14 +/- 0.01% for sinusoidal cells. 75% of labelled hepatocytes and 60% of labelled sinusoidal cells were found in acinar zone 1. In formaldehyde-fixed rat liver (n = 10) a weak nuclear staining and a great interspecimen variability were evident. LI was 0.13 +/- 0.07% for hepatocytes and 0.40 +/- 0.21% for sinusoidal cells without preferential acinar distribution. In methanol-fixed rat liver (n = 10), PCNA LI was 0.14 +/- 0.02% for hepatocytes and 0.40 +/- 0.04% for sinusoidal cells. 64% of labelled hepatocytes and 50% of labelled sinusoidal cells were found in zone 1. Only on methanol-fixed material did double immunohistochemistry show an almost complete overlap of BrdU and PCNA labelling. The PCNA LIs and the zonal distribution of labelled nuclei as obtained in methanol-fixed material are in keeping with previous reports using 3H-thymidine (3H-Thy) incorporation, suggesting that PCNA immunostaining represents a valid alternative to 3H-Thy.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Immunohistochemical analysis of S-phase cells in normal human and rat liver by PC10 monoclonal antibody. 791 Sep 34

Increased biocompatibility and lower cost are the two major arguments favoring routine dialyzer reprocessing. The impact of longer-term reprocessing is critical to the practical use of polysulfone membranes (PMs), because of the possibility of decreasing efficiency and performance, especially in the removal of beta 2-microglobulin (beta 2M), a protein that has been implicated in the development of dialysis-associated amyloidosis (DDA). In this study, we examine urea clearance (Kd), urea mass transfer coefficient (h0), ultrafiltration coefficient (K(uf)), and percent removal of beta 2M up to 24 uses. The study involved 11 patients on hemodialysis for 5.27 +/- 4.6 years, with a mean age of 62.5 +/- 9.7 years and average run-time treatment of 2.78 +/- 0.3 hours. PMs were tested after being reprocessed manually using bleach and formaldehyde. The efficacy of the dialyzer was examined on uses 1, 5, 10, 15, 20, and 24, and the percent removal of beta 2M was determined except in the twentieth use and corrected for ultrafiltration. The Kd obtained through 24 uses showed no significant change, although h0 was significantly increased in the fifteenth use, and K(uf) was significantly increased in the 10th and 20th use (P < 0.05). The percent removal of beta 2M increased significantly from 44.1 +/- 2.8 (mean +/- SEM) in the first use to 59.4 +/- 2.19 (P < 0.05) in the 10th use, and 62.1 +/- 4.07 and 63.1 +/- 4.27 in the 15th and 24th uses, respectively (P < 0.001).(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:The effect of dialyzer reprocessing on performance and beta 2-microglobulin removal using polysulfone membranes. 846 21

Reprocessing of dialyzers is often performed with nonsterile solutions possibly contaminated with bacterial-derived cytokine-inducing substances. We investigated the retention of cytokine-inducing substances inside the dialyzer during reprocessing in a closed loop in vitro hemodialysis system using a polyamide high flux membrane. After the first in vitro circulation of human whole blood, rinse of the blood compartment (BC) and reverse ultrafiltration (RUF) was performed with either cytokine-inducing substance-free saline or saline contaminated with filtrates from Pseudomonas cultures (6 ng/ml LAL-reactive material); subsequently, dialyzers were stored in 2% formaldehyde. Dialyzers were rinsed with approximately 15 liters pyrogen-free saline before the second circulation using blood from the same donor; the effluates were free of cytokine-inducing substances and formaldehyde. Before and after the blood circulations, peripheral blood mononuclear cells (PBMC) were separated and total production of IL-1 alpha and IL-1 beta was determined after overnight incubation. In noncirculated PBMC as well as in PBMC separated after whole blood circulation with pyrogen-free processed dialyzers, production of IL-1 beta was not detectable. After contaminated rinse of the BC, production of IL-1 beta could be observed (1,600 +/- 1,100 pg/ml, mean +/- SEM). When pyrogen-free RUF was performed after contaminated BC rinse, IL-1 beta production averaged 163 +/- 92 pg/ml when using reused dialyzers, but 1,820 +/- 880 pg/ml when using new dialyzers. After reuse with pyrogen-free BC-rinse and contaminated RUF no IL-1 beta synthesis was observed; however, when pyrogen-free BC-rinse and contaminated RUF was applied to new dialyzers, IL-1 beta synthesis averaged 1,620 +/- 1,200 pg/ml. We conclude that cytokine-inducing substances are retained inside the dialyzer, probably by adsorption to the membrane as well as to the protein layer covering the membrane and are still biologically active after sterilisation. Cytokine-inducing substances adsorbed to the protein layer can be partially removed by RUF. Finally, the protein layer on the membrane appears to reduce the convective transfer of cytokine-inducing substances from the dialysate into the blood compartment.
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PMID:Retention of cytokine-inducing substances inside high-flux dialyzers. 871 62

This article evaluated possible differences between dentin conditioned in vivo and in vitro with 10 percent maleic acid or with 36 percent phosphoric acid. Semispherical Class V cavities were prepared in vivo and in vitro at the cementum-enamel junction and were divided into four groups. After etching procedures, the in vivo samples were extracted and fixated in 10 percent buffered formaldehyde. Both the in vivo and in vitro samples were then fractured in two parts along their long axis, critical-point dried, and subsequently examined with SEM. Both the acids removed completely the smear layer and demineralized the dentin, leaving a layer of collagenous network. No morphological differences were found between in vivo and in vitro dentin samples.
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PMID:Comparison of in vivo and in vitro demineralized dentin with phosphoric and maleic acid. 909 13


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