3D Modelling of Human Joints Using Reverse Engineering for Biomedical Applications

Author(s):  
Deepak Kumar ◽  
Abhishek ◽  
Pradeep Kumar Yadav ◽  
Jitendra Bhaskar
Author(s):  
Jai Menon ◽  
Ranjit Desai ◽  
Jay Buckey

Abstract This paper extends the “cross-sectional” approach for reverse engineering, used abundantly in biomedical applications, to the mechanical domain. We propose a combination of “projective” and cross-sectional algorithms for handling physical artifacts with complex topology and geometry. In addition, the paper introduces the concept of constraint-based reverse engineering, where the constraint parameters could include one or more of the following: time, storage (memory, disk-space), network bandwidth, Quality of Service (output-resolution), and so forth. We describe a specific reverse-engineering application which uses ultrasound (tilt-echo) imaging to reverse engineer spatial enumeration (volume) representations from cross-sectional data. The constraint here is time, and we summarize how our implementation can satisfy real-time reconstruction for distribution of the volume data on the internet. We present results that show volume representations computed from static objects. Since the algorithms are tuned to satisfy time constraints, this method is extendable to reverse engineer temporally-varying (elastic) objects. The current reverse engineering processing time is constrained by the data-acquisition (tilt-echo imaging) process, and the entire reverse engineering pipeline has been optimized to compute incremental volume representations in the order of 3 seconds on a network of four processors.


2020 ◽  
Vol 14 ◽  
pp. 101-108
Author(s):  
Aleksandra Salwierz ◽  
Tomasz Szymczyk

Article shows two modern methods of creating realistic 3D spaces. The comparison includes 3D scanning with FARO Focus 3D X330 and 3D modelling in Blender 2.8. Analysis of methods for creating realistic 3D spaces can be useful in many fields e.g.: architecture, 3D printing, games industry, visualization, criminalistics, reverse engineering or monument documentation. The paper also describes process of generating a chosen space for each method. Each of the two approaches is assessed in terms of the expenses, precision and degree of reflecting reality.. Article includes an analysis of encountered problems and their possible sources. The paper also evaluate usefulness and profitability for each method. A research was carried out and focused on degree of immersion for VR visualizations depending on the used method.


Author(s):  
T. L. Hayes

Biomedical applications of the scanning electron microscope (SEM) have increased in number quite rapidly over the last several years. Studies have been made of cells, whole mount tissue, sectioned tissue, particles, human chromosomes, microorganisms, dental enamel and skeletal material. Many of the advantages of using this instrument for such investigations come from its ability to produce images that are high in information content. Information about the chemical make-up of the specimen, its electrical properties and its three dimensional architecture all may be represented in such images. Since the biological system is distinctive in its chemistry and often spatially scaled to the resolving power of the SEM, these images are particularly useful in biomedical research.In any form of microscopy there are two parameters that together determine the usefulness of the image. One parameter is the size of the volume being studied or resolving power of the instrument and the other is the amount of information about this volume that is displayed in the image. Both parameters are important in describing the performance of a microscope. The light microscope image, for example, is rich in information content (chemical, spatial, living specimen, etc.) but is very limited in resolving power.


Author(s):  
Philippe Fragu

The identification, localization and quantification of intracellular chemical elements is an area of scientific endeavour which has not ceased to develop over the past 30 years. Secondary Ion Mass Spectrometry (SIMS) microscopy is widely used for elemental localization problems in geochemistry, metallurgy and electronics. Although the first commercial instruments were available in 1968, biological applications have been gradual as investigators have systematically examined the potential source of artefacts inherent in the method and sought to develop strategies for the analysis of soft biological material with a lateral resolution equivalent to that of the light microscope. In 1992, the prospects offered by this technique are even more encouraging as prototypes of new ion probes appear capable of achieving the ultimate goal, namely the quantitative analysis of micron and submicron regions. The purpose of this review is to underline the requirements for biomedical applications of SIMS microscopy.Sample preparation methodology should preserve both the structural and the chemical integrity of the tissue.


Author(s):  
J. D. Shelburne ◽  
Peter Ingram ◽  
Victor L. Roggli ◽  
Ann LeFurgey

At present most medical microprobe analysis is conducted on insoluble particulates such as asbestos fibers in lung tissue. Cryotechniques are not necessary for this type of specimen. Insoluble particulates can be processed conventionally. Nevertheless, it is important to emphasize that conventional processing is unacceptable for specimens in which electrolyte distributions in tissues are sought. It is necessary to flash-freeze in order to preserve the integrity of electrolyte distributions at the subcellular and cellular level. Ideally, biopsies should be flash-frozen in the operating room rather than being frozen several minutes later in a histology laboratory. Electrolytes will move during such a long delay. While flammable cryogens such as propane obviously cannot be used in an operating room, liquid nitrogen-cooled slam-freezing devices or guns may be permitted, and are the best way to achieve an artifact-free, accurate tissue sample which truly reflects the in vivo state. Unfortunately, the importance of cryofixation is often not understood. Investigators bring tissue samples fixed in glutaraldehyde to a microprobe laboratory with a request for microprobe analysis for electrolytes.


Author(s):  
Yasushi P. Kato ◽  
Michael G. Dunn ◽  
Frederick H. Silver ◽  
Arthur J. Wasserman

Collagenous biomaterials have been used for growing cells in vitro as well as for augmentation and replacement of hard and soft tissues. The substratum used for culturing cells is implicated in the modulation of phenotypic cellular expression, cellular orientation and adhesion. Collagen may have a strong influence on these cellular parameters when used as a substrate in vitro. Clinically, collagen has many applications to wound healing including, skin and bone substitution, tendon, ligament, and nerve replacement. In this report we demonstrate two uses of collagen. First as a fiber to support fibroblast growth in vitro, and second as a demineralized bone/collagen sponge for radial bone defect repair in vivo.For the in vitro study, collagen fibers were prepared as described previously. Primary rat tendon fibroblasts (1° RTF) were isolated and cultured for 5 days on 1 X 15 mm sterile cover slips. Six to seven collagen fibers, were glued parallel to each other onto a circular cover slip (D=18mm) and the 1 X 15mm cover slip populated with 1° RTF was placed at the center perpendicular to the collagen fibers. Fibroblast migration from the 1 x 15mm cover slip onto and along the collagen fibers was measured daily using a phase contrast microscope (Olympus CK-2) with a calibrated eyepiece. Migratory rates for fibroblasts were determined from 36 fibers over 4 days.


2021 ◽  
Author(s):  
Jintong Liu ◽  
Jing Huang ◽  
Lei Zhang ◽  
Jianping Lei

We review the general principle of the design and functional modulation of nanoscaled MOF heterostructures, and biomedical applications in enhanced therapy.


2008 ◽  
Vol 45 ◽  
pp. 161-176 ◽  
Author(s):  
Eduardo D. Sontag

This paper discusses a theoretical method for the “reverse engineering” of networks based solely on steady-state (and quasi-steady-state) data.


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