Scanning and transmission electron microscopy of biodegradable microspheres (DSM) in blood vessels

1989 ◽  
Vol 13 (5) ◽  
pp. 427-436 ◽  
Author(s):  
MAKITA ◽  
ICHIMAL ◽  
KAGABU ◽  
MANBA ◽  
NAITO ◽  
...  
2001 ◽  
Vol 95 (3) ◽  
pp. 489-494 ◽  
Author(s):  
Joëlle Veziers ◽  
Maurice Lesourd ◽  
Christophe Jollivet ◽  
Claudia Montero-Menei ◽  
Jean-Pierre Benoit ◽  
...  

Object. Stereotactically guided implantation of biodegradable microspheres is a promising strategy for delivery of neurotrophic factors in a precise and spatially defined brain area. The goal in this study was to show the biocompatibility of poly(D,L,lactide-co-glycolide) microspheres with brain tissue at the ultrastructural level and to analyze the three-dimensional (3D) ultrastructure after intrastriatal implantation of these microparticles. Methods. Scanning and transmission electron microscopy were used to study the microspheres and their environment after implantation in an inert material (gelatin) and in the rat striatum. Observations were made at different time periods, ranging from 24 hours to 2 months postimplantation. Conclusions. The progressive degradation of the microspheres, with vacuolization, deformation, and shrinkage, was well visualized. This degradation was identical in microspheres implanted in the inert material and in the rat brain tissue, independent of the presence of macrophages. The studies preformed in the striatum permitted the authors to demonstrate the structural integrity of axons in contact with microspheres, confirming the biocompatibility of the polymer. Furthermore, scanning electron microscopy showed the preservation of the 3D ultrastructure of the striatum around the microparticles. These microparticles, which can be stereotactically implanted in functional areas of the brain and can release neurotrophic factors, could represent, for some indications, an alternative to gene therapy.


2020 ◽  
Author(s):  
Christian Meyer ◽  
Thomas André ◽  
Günter Purschke

Abstract Background: The sedentary polychaete Sabellaria alveolata, the sandcastle or honeycomb worm, possesses four different kinds of appendages besides the parapodia: opercular papillae, tentacular filaments, palps, and branchiae. It exhibits a highly specialized anterior end, the operculum, formed by the prostomium, peristomium, and two anterior segments. Besides the median organ, the operculum comprises opercular papillae, tentacular filaments, and palps. Paired branchiae are present from the second thoracic chaetiger onwards on the posteriorly following segments except for the last ones. Only the palps have been studied thus far by transmission electron microscopy in late larvae of a different species. In order to bridge the data gap, we investigated the appendages of S. alveolata by applying light microscopy, confocal laser scanning microscopy, scanning, and transmission electron microscopy. Results: In S. alveolata the entire body is covered by a thin cuticle characterized by the absence of layers of parallel collagen fibers with no differentiation between the various body regions including the branchiae. The opercular papillae bear numerous tufts of receptor cells and lack motile cilia. The tentacular filaments show a distinctive ciliation pattern; their most conspicuous morphological feature is their cell-free cartilaginous endoskeletal structure enclosed by ECM. Besides musculature the filaments include a single coelomic cavity but blood vessels are absent. The palps are ciliated with two coelomic cavities and a single blind-ending blood vessel. Besides external ciliation and receptor cells, the coelomate branchiae are highly vascularized and equipped with numerous blood spaces extending deep into the basal regions of the epidermal cells (diffusion distances: 150–400nm). Conclusions: All appendages, including the branchiae, bear receptor cells and, as such, are sensory. The opercular papillae resemble typical parapodial cirri. In contrast, the tentacular filaments have a double function: sensing, collecting and transporting particles. A similarity to branchiae can be excluded. The palps are typical grooved palps similar to another sabellariid studied. A revised classification of polychaete branchiae is suggested; thereby, the branchiae of S. alveolata belong to the most common type comprising coelom, musculature, and blood vessels. The results indicate that diffusion distances between blood and environment have been underestimated in many cases.


Author(s):  
Shirley Siew ◽  
Mehboob Fatteh

Renal oncocytoma is a comparatively rare tumor, having an incidence 1/20th that of renal cell carcinoma, from which it has to be differentiated. We report a case of a 61 year old man who was found to have albuminuria 100 mg/dL on a routine physical examination. A retrograde pyelogram showed splaying of the right upper pole infundibula. Two right renal tumors were shown on renal CT scan and there were multiple hypervascular masses on angiography. A right radical nephrectomy was performed. The kidney weighed 176 grains and measured 11 × 7.5 × 5 cm. There were several dark brown nodules in the upper pole, lower pole and midportion of the kidney. Some of the nodules protruded onto the cortical surface, stretching the overlying capsule, but, there was no evidence of capsular nor renal vein invasion. The largest nodule measured 4.5 × 4 × 4 cm. Histologic examination showed a distinct line of demarcation between the tumors and the normal kidney. Occasional thickened vessels were noted at the border. For the greater part, the tumor showed a tubular or acinar architecture, although the lumina of some of the tubules were narrow. The tubules were lined by large, polygonal eosinophilic cells with a granular cytoplasm. There was no evidence of nuclear atypicality nor mitotic activity. Thin walled blood vessels were present between the tubules. Transmission electron microscopy showed the presence of irregular tubules, surrounded by a well formed basement membrane. The tubules were separated by thin walled blood vessels (Fig. 1). The luminal surface of the cells lacked microvilli – Nuclei were comparatively small and irregular in shape. Lysosomes were concentrated towards the luminal surface. There were occasional lipid vacuoles. The cytoplasm contained large numbers of mitochondria with membranous cristae (Fig. 2) . These ultrastructural characteristics are in keeping with those of a renal oncocytoma. Comment: The term oncocyte1 is applied, at the light microscopic level, to large epithelial cells, which have a markedly eosinophilic and granular cytoplasm. Transmission electron microscopy shows the presence of an abundance of mitochondria filling the cytoplasm. Oncocytomas are tumors composed of a uniform population of such cells. Renal oncocytoma is considered to be a benign cortical adenoma. It has been postulated that it arises from proximal tubular epithelium. Features that distinguish renal oncocytoma from other adenomas are that they may reach a large size (7cm) and that they maybe multicentric in the same kidney (reported in 5% of cases). The dark brown bulging nodules present in our case are typical of the gross appearance of renal oncocytoma. Various theories have been proposed to account for the marked increase of mitochondria, including that it is due to a neoplastic proliferation of them, at the expense of other subcellular organelles. The diagnosis of oncocytoma is established by the ultrastructural demonstration of the abnormal abundance of mitochondria.


Author(s):  
G. G. Shaw

The morphology and composition of the fiber-matrix interface can best be studied by transmission electron microscopy and electron diffraction. For some composites satisfactory samples can be prepared by electropolishing. For others such as aluminum alloy-boron composites ion erosion is necessary.When one wishes to examine a specimen with the electron beam perpendicular to the fiber, preparation is as follows: A 1/8 in. disk is cut from the sample with a cylindrical tool by spark machining. Thin slices, 5 mils thick, containing one row of fibers, are then, spark-machined from the disk. After spark machining, the slice is carefully polished with diamond paste until the row of fibers is exposed on each side, as shown in Figure 1.In the case where examination is desired with the electron beam parallel to the fiber, preparation is as follows: Experimental composites are usually 50 mils or less in thickness so an auxiliary holder is necessary during ion milling and for easy transfer to the electron microscope. This holder is pure aluminum sheet, 3 mils thick.


Author(s):  
R. W. Anderson ◽  
D. L. Senecal

A problem was presented to observe the packing densities of deposits of sub-micron corrosion product particles. The deposits were 5-100 mils thick and had formed on the inside surfaces of 3/8 inch diameter Zircaloy-2 heat exchanger tubes. The particles were iron oxides deposited from flowing water and consequently were only weakly bonded. Particular care was required during handling to preserve the original formations of the deposits. The specimen preparation method described below allowed direct observation of cross sections of the deposit layers by transmission electron microscopy.The specimens were short sections of the tubes (about 3 inches long) that were carefully cut from the systems. The insides of the tube sections were first coated with a thin layer of a fluid epoxy resin by dipping. This coating served to impregnate the deposit layer as well as to protect the layer if subsequent handling were required.


Author(s):  
S. Fujishiro

The mechanical properties of three titanium alloys (Ti-7Mo-3Al, Ti-7Mo- 3Cu and Ti-7Mo-3Ta) were evaluated as function of: 1) Solutionizing in the beta field and aging, 2) Thermal Mechanical Processing in the beta field and aging, 3) Solutionizing in the alpha + beta field and aging. The samples were isothermally aged in the temperature range 300° to 700*C for 4 to 24 hours, followed by a water quench. Transmission electron microscopy and X-ray method were used to identify the phase formed. All three alloys solutionized at 1050°C (beta field) transformed to martensitic alpha (alpha prime) upon being water quenched. Despite this heavily strained alpha prime, which is characterized by microtwins the tensile strength of the as-quenched alloys is relatively low and the elongation is as high as 30%.


Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi

It is very useful if we can observe the identical cell elements within the same sections by light microscopy (LM), transmission electron microscopy (TEM) and/or scanning electron microscopy (SEM) sequentially, because, the cell fine structure can not be indicated by LM, while the color is; on the other hand, the cell fine structure can be very easily observed by EM, although its color properties may not. However, there is one problem in that LM requires thick sections of over 1 μm, while EM needs very thin sections of under 100 nm. Recently, we have developed a new method to observe the same cell elements within the same plastic sections using both light and transmission (conventional or high-voltage) electron microscopes.In this paper, we have developed two new observation methods for the identical cell elements within the same sections, both plastic-embedded and paraffin-embedded, using light microscopy, transmission electron microscopy and/or scanning electron microscopy (Fig. 1).


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