A Comparative Study of Thai and Australian Crocodile Bone for Use as a Potential Biomaterial

2006 ◽  
Vol 309-311 ◽  
pp. 15-18 ◽  
Author(s):  
Kanthi Lewis ◽  
U. Boonyang ◽  
L. Evans ◽  
S. Siripaisarnpipat ◽  
Besim Ben-Nissan
Keyword(s):  
Crystallite Size ◽  
Cortical Bone ◽  
Biomedical Applications ◽  
Environmental Scanning Electron Microscopy ◽  
Crystallinity Index ◽  
Environmental Scanning ◽  
Carbonated Apatite ◽  
Starting Point ◽  
Crocodylus Porosus ◽  
Promising Source

This study aims to characterize the structure and properties of crocodile bone to assess the potential for use in biomedical applications. Crocodile bone samples obtained from Thailand (Crocodylus siamensis) and Australia (Crocodylus porosus), being the tail and the tibia respectively, were treated to remove organic material and the inner spongy (trabecular) material. The dense cortical bone was used for comparative instrumental analyses. Specific comparisons were made against bovine cortical bone and pure synthetic hydroxyapatite. The material was then analyzed using simultaneous differential thermal analysis/thermogravimetric analysis (DTA/TGA), Fourier- Transform infrared spectroscopy (FTIR), and X-ray diffraction analysis (XRD). Imaging of full bone samples was also conducted using an environmental scanning electron microscopy (ESEM). The SEM provided valuable information through the imaging of samples, showing a markedincrease in bone porosity for crocodile material when compared to bovine samples. The crystallinity and/or crystallite size of carbonated hydroxyapatite has been found to be lower than synthetic apatite, with the tibia being the least crystalline of the bone types studied. The crystallinity index (CI) is used as a measure of crystallite size and internal strain. The strain is affected by substitutions in the structure and these results provide a starting point for comparison of the resulting mechanical properties. There is a need for any biomaterial chosen for bone replacement to allow adequate osteointegration. Thus the study this far shows that crocodile bone is a very promising source of carbonated apatite for biomedical applications.

Environmental scanning electron microscopy of fresh human gallstones reveals new morphologies of precipitated calcium salts

1992 ◽  
Vol 50 (2) ◽  
pp. 1322-1323
Author(s):  
Howard S. Kaufman ◽  
Keith D. Lillemoe ◽  
John T. Mastovich ◽  
Henry A. Pitt
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Environmental Scanning Electron Microscopy ◽  
Environmental Scanning ◽  
X Ray Diffraction ◽  
Calcium Salts ◽  
Cholesterol Gallstones ◽  
X Ray ◽  
Ca Carbonate ◽  
Scanning Electron

Gallstones contain precipitated cholesterol, calcium salts, and proteins. Calcium (Ca) bilirubinate, palmitate, phosphate, and carbonate occurring in gallstones have variable morphologies but characteristic windowless energy dispersive x-ray (EDX) spectra. Previous studies of gallstone microstructure and composition using scanning electron microscopy (SEM) with EDX have been limited to dehydrated samples. In this state, Ca bilirubinates appear as either glassy masses, which predominate in black pigment stones, or as clusters, which are found mostly in cholesterol gallstones. The three polymorphs of Ca carbonate, calcite, vaterite, and aragonite, have been identified in gallstones by x-ray diffraction, however; the morphologies of these crystals vary in the literature. The purpose of this experiment was to study fresh gallstones by environmental SEM (ESEM) to determine if dehydration affects gallstone Ca salt morphology.Gallstones and bile were obtained fresh at cholecystectomy from 6 patients. To prevent dehydration, stones were stored in bile at 37°C. All samples were studied within 4 days of procurement.

Detector strategies for environmental scanning electron microscopy

1992 ◽  
Vol 50 (2) ◽  
pp. 1296-1297
Author(s):  
Klaus-Ruediger Peters
Keyword(s):  
High Vacuum ◽  
Environmental Scanning Electron Microscopy ◽  
Charge Carriers ◽  
Environmental Scanning ◽  
Surface Information ◽  
X Ray ◽  
Detector Electrode ◽  
Electrons And Ions ◽  
Low Energy Electrons ◽  
Environmental Sem

Environmental SEM operate at specimen chamber pressures of ∼20 torr (2.7 kPa) allowing stabilization of liquid water at room temperature, working on rugged insulators, and generation of an environmental secondary electron (ESE) signal. All signals available in conventional high vacuum instruments are also utilized in the environmental SEM, including BSE, SE, absorbed current, CL, and X-ray. In addition, the ESEM allows utilization of the flux of charge carriers as information, providing exciting new signal modes not available to BSE imaging or to conventional high vacuum SEM.In the ESEM, at low vacuum, SE electrons are collected with a “gaseous detector”. This detector collects low energy electrons (and ions) with biased wires or plates similar to those used in early high vacuum SEM for SE detection. The detector electrode can be integrated into the first PLA or positioned at any other place resulting in a versatile system that provides a variety of surface information.

scholarly journals 616 Preventing Biofilms on BACTIGON® Coated Camstent Urinary Catheters in Patients Undergoing Elective Colorectal Surgery: A Single Centre Pilot Study

2021 ◽  
Vol 108 (Supplement_2) ◽  
Author(s):  
C Lewis-Lloyd ◽  
J Dubern ◽  
K Kalenderski ◽  
N Halliday ◽  
M Alexander ◽  
...  
Keyword(s):  
Environmental Scanning Electron Microscopy ◽  
Environmental Scanning ◽  
Bacterial Cells ◽  
Urinary Catheters ◽  
Elective Colorectal Surgery ◽  
Mineral Compositions ◽  
Microscopy Data ◽  
Tract Infections ◽  
Biofilm Development ◽  
Hospital Acquired

Abstract Introduction Catheter associated urinary tract infections account for 40% of hospital acquired infections. They are associated with biofilms consisting of bacterial cells enmeshed in a self-generated extracellular matrix adhering to catheter surfaces. We have developed a novel polymer family that, coated onto urinary catheters, creates a “non-stick” surface preventing biofilm development. Method Prospective cohort of elective colorectal patients recruited pre-operatively, received a standard silicone (SS) or Camstent (BACTIGON®) coated urinary catheter. After removal, catheters were cut longitudinally into 3 segments. Biomass and biomineralisation were analysed using confocal fluorescence microscopy. Data were normalised by square rooting the catheter indwelling duration. Environmental scanning electron microscopy and energy dispersive x-ray spectroscopy was performed. Results Of 40 patients, 20 each received a SS or coated catheter. Between SS and coated catheters, average indwelling duration was similar and biofilm biomass was 32.068µg/cm2 (95%CI ±21.950) vs. 1.948µg/cm2 (95%CI ±2.595) (P = 0.0111). Confocal microscopy suggested a 93.93% reduction in biofilm biomass on coated catheters. Mineral compositions were different with biofilm and struvite/apatite on SS and calcium oxalate, endogenously derived, on coated catheters. Conclusions Inert BACTIGON® coated catheters appear superior at preventing biofilm formation than SS catheters. Clinical trials are needed to determine the clinical and health economic benefit of this intervention.

Characterization of Thin Polymer Blend Films using ESEM – No Charging, No Staining.

2001 ◽  
Vol 707 ◽  
Author(s):  
Ian C. Bache ◽  
Catherine M. Ramsdale ◽  
D. Steve Thomas ◽  
Ana-Claudia Arias ◽  
J. Devin MacKenzie ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Environmental Scanning Electron Microscopy ◽  
Environmental Scanning ◽  
Cross Sectional ◽  
Blend Films ◽  
Thin Polymer ◽  
Device Applications ◽  
Scanning Electron

ABSTRACTCharacterising the morphology of thin films for use in device applications requires the ability to study both the structure within the plane of the film, and also through its thickness. Environmental scanning electron microscopy has proved to be a fruitful technique for the study of such films both because contrast can be seen within the film without the need for staining (as is conventionally done for electron microscopy), and because cross-sectional images can be obtained without charging artefacts. The application of ESEM to a particular blend of relevance to photovoltaics is described.

Acetyl Group Distribution in Acetylated Wood Investigated by Microautoradiography

Holzforschung ◽  
2001 ◽  
Vol 55 (3) ◽  
pp. 270-275 ◽  
Author(s):  
Marie Rosenqvist
Keyword(s):  
Cell Wall ◽  
Weight Gain ◽  
Acetic Anhydride ◽  
Wood Cell Wall ◽  
Environmental Scanning Electron Microscopy ◽  
Environmental Scanning ◽  
Accurate Information ◽  
Concentration Gradients ◽  
Good Opportunity ◽  
Acetyl Group

Summary Sapwood of Scots pine (Pinus silvestris L.) was acetylated with 14C- and 3H-labelled acetic anhydride. The distribution of acetyl groups was investigated with microautoradiography and microautoradiographs were evaluated with ESEM, Environmental Scanning Electron Microscopy. The investigation showed that the impregnation of wood with radioisotope-labelled substances provides a good opportunity to investigate the location of substances covalently bonded to the wood material. Introduced 14C-labelled acetyl groups show an even distribution in the wood cell wall, with no discernible concentration gradients at acetylation levels of about 5, 15 and 20% weight gain. 3H-labelled acetyl groups show an even distribution in the wood cell wall at 15 and 20% weight gain, with no discernible concentration gradients. At the 5% weight gain level, however, an uneven distribution of 3H-labelled acetyl groups over the cell wall is observed. Nevertheless, the unevenness is random and no concentration gradient is discernible at this level. 3H with a relatively high resolution, 0.5–1 μm, compared to 14C with a resolution of 2–5 μm, gives more accurate information about where exactly the acetyl groups are situated in the wood cell wall. Acetic anhydride was evenly distributed when a full impregnation procedure was used. The chemical and physical properties of acetic anhydride allow a uniform penetration into the pine cell wall and a complete acetylation takes place when the specimens are heated.

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