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Handbook Of Active Materials For Medical Devices
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Book Synopsis Handbook of Active Materials for Medical Devices by : Andres Diaz Lantada
Download or read book Handbook of Active Materials for Medical Devices written by Andres Diaz Lantada and published by CRC Press. This book was released on 2011-09-28 with total page 551 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book covers biodevices, mainly implantable or quirurgical, for the diagnosis or treatment of different pathologies, which benefit from the use of active materials as sensors or actuators. Such active or "intelligent" materials are capable of responding in a controlled way to different external physical or chemical stimuli by changing some of their properties. These materials can be used to design and develop sensors, actuators, and multifunctional systems with a large number of applications for developing biodevices and medical appliances. Current work on these fields entails problems related to synthesis, characterization, modeling, simulation, processing, and prototyping technologies, as well as device testing and validation, all of which are treated in depth in this book, for the several types of active or intelligent materials covered. The research presented in this book helps further development of medical devices, based on the additional functionalities that the use of active or "intelligent" materials, both as sensors and actuators, supplies. The main results exposed may help with the industrial expansion of this kind of materials as part of more complex systems.
Book Synopsis Handbook of Materials for Medical Devices by : Joseph R. Davis
Download or read book Handbook of Materials for Medical Devices written by Joseph R. Davis and published by ASM International(OH). This book was released on 2003 with total page 360 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Handbook of Materials for Medical Devices provides an in-depth review of the properties, processing, and selection of materials used in the environment of the human body - an environment that is surprisingly hostile and aggressive. Among the application areas described are orthopedics (hips, knees, and spinal and fracture fixation), cardiology (stents, heart valves, pacemakers), surgical instruments, and restorative dentistry. Materials discussed include metals and alloys, ceramics, glasses, and glass-ceramics, polymeric materials, composites, coatings, and adhesives and cements. The book is divided into three major sections. The first section provides an expansive overview of biomaterials and their use in medical devices. Charts and diagrams illustrate/list the many parts of the body that can be replaced by manmade materials. Case histories document some of the more common and successful medical device applications. Biocompatibility and mechanical requirements for implantable devices are also reviewed. The second section of the handbook deals with medical (nondental) applications. Stainless steels, cobalt-chromium alloys, titanium alloys, shape memory alloys, and tantalum are among the metallic materials described. Similar information is provided on nonmetallic materials, including new coatings that offer lubricity, biocompatibility, and antimicrobial action to device surfaces. Other coatings can be used to release drugs or make implanted devices more visible to imaging systems. The final section addresses biomaterials for dental applications. Emphasis is placed on corrosion and tribological behavior and corresponding test procedures to determine corrosion and wear resistance. Contents: Introduction: Overview of Biomaterials and Their use in Medical Devices; Physical and Mechanical Requirements for Medical Device Materials. Medical (Nondental) Applications: Metallic Materials; Corrosion of Metallic Implants and Prosthetic Devices; Failure Analysis of Metallic Orthopedic Implants; Ceramic Materials; Polymeric Materials; Adhesives and Cements; Coatings. Dental Applications: Biomaterials for Dental Applications; Tarnish and Corrosion of Dental Alloys; Friction and Wear of Dental Materials; Index.
Book Synopsis Electrically Active Materials For Medical Devices by : Tofail Syed
Download or read book Electrically Active Materials For Medical Devices written by Tofail Syed and published by World Scientific. This book was released on 2016-08-04 with total page 574 pages. Available in PDF, EPUB and Kindle. Book excerpt: Stress induced electrical charges, action potential and electret behavior of bone, muscles, skin and nerve cells have been known for some time. Electrically Active Materials for Medical Devices builds on this knowledge and encourages readers to understand and exploit electrical activity in biomaterials from native, derived, or completely synthetic origin, or a combination thereof. It presents data and insights from both historic and contemporary research that spans over six decades with a view to generate convergence of interdisciplinary knowledge and skills.Divided into four parts, this book first introduces the reader to a general overview of electrically active materials in biology and biomedical science and describes important concepts and pioneering discoveries. The second part discusses common types of materials that are known to generate electrical activity and lays the foundation for these materials for use in medical devices. The third part gives examples of where electrically active materials have been examined for device application. The final part looks for upcoming and emerging concepts, tools and methodologies that are expected to shape the future profile of this field of converging science.Written by specialists in their respective fields, it has been specifically targeted at a readership of professionals, graduate students and researchers in the fields of biomedical engineering, physics, chemistry biology and clinical medicine.
Book Synopsis Handbook on Advanced Design and Manufacturing Technologies for Biomedical Devices by : Andrés Díaz Lantada
Download or read book Handbook on Advanced Design and Manufacturing Technologies for Biomedical Devices written by Andrés Díaz Lantada and published by Springer Science & Business Media. This book was released on 2014-07-08 with total page 381 pages. Available in PDF, EPUB and Kindle. Book excerpt: The last decades have seen remarkable advances in computer‐aided design, engineering and manufacturing technologies, multi‐variable simulation tools, medical imaging, biomimetic design, rapid prototyping, micro and nanomanufacturing methods and information management resources, all of which provide new horizons for the Biomedical Engineering fields and the Medical Device Industry. Advanced Design and Manufacturing Technologies for Biomedical Devices covers such topics in depth, with an applied perspective and providing several case studies that help to analyze and understand the key factors of the different stages linked to the development of a novel biomedical device, from the conceptual and design steps, to the prototyping and industrialization phases. Main research challenges and future potentials are also discussed, taking into account relevant social demands and a growing market already exceeding billions of dollars. In time, advanced biomedical devices will decisively change methods and results in the medical world, dramatically improving diagnoses and therapies for all kinds of pathologies. But if these biodevices are to fulfill present expectations, today’s engineers need a thorough grounding in related simulation, design and manufacturing technologies, and collaboration between experts of different areas has to be promoted, as is also analyzed within this handbook.
Book Synopsis Handbook of Polymer Applications in Medicine and Medical Devices by : Vinny R. Sastri
Download or read book Handbook of Polymer Applications in Medicine and Medical Devices written by Vinny R. Sastri and published by Elsevier Inc. Chapters. This book was released on 2013-12-05 with total page 27 pages. Available in PDF, EPUB and Kindle. Book excerpt: Over the past 2000 years, many devices have been developed and used in the mitigation and diagnosis of diseases. The materials used in these devices have ranged from stone, wood, metal, ceramics, and most recently plastics. Medical devices have also evolved in sophistication and complexity over time. With the formalization of the scientific method in the seventeenth century such devices became more prevalent [1]. Many medical devices were manufactured by doctors or small companies and sold directly to the public with no government standards or oversight. With the explosion of medical technology in the early twentieth century, several intermediaries had evolved between the medical device industry and the public. In 1879, Dr E.R. Squibb, in an address to the Medical Society of the State of New York, proposed the enactment of a national statute to regulate food and drugs [2]. It was not until 27 years later that the Food and Drug Act of 1906 was introduced into the Congress and signed into law by President Theodore Roosevelt [3]. At that time, devices that were harmful to human safety and health proliferated the market but regulation of medical devices by the Bureau of Chemistry (the precursor to the Food and Drug Administration—FDA) was limited to challenging commercial products only after they had been released into the market. Devices in the marketplace that were defective, adulterated, or misbranded were seized and the device manufacturers were prosecuted in a court of law, but only after the products were sold in the market and caused harm to the end users. Thus, there was a strong need for regulating the devices before they entered the marketplace. An FDA report [4], issued in September 1970, detailed as many as 10,000 injuries and 731 deaths from ineffective medical devices. The report recommended the formation of a regulatory system and body that would enforce the production and sale of safe and effective devices to the public. All medical devices already on the market would be inventoried and classified into a three-tiered system based on their criticality of end use. It also detailed requirements for records and reports, registration and inspection of establishments, and uniform quality assurance programs called good manufacturing practices (GMP). After much lobbying by the FDA, Senate bill SR 510, “The Medical Device Amendments of 1973” was introduced by Senator Edward M. Kennedy and was passed by the Senate in 1975. House bill HR 11124, introduced by Representative Paul Rogers, was passed by the House in 1976. These bills eventually became the Medical Device Amendments of 1976, and were signed into law by President Nixon. The Medical Device Amendments of 1976 became the basis for the medical device regulation in the United States to control and regulate the production of finished devices and thus the device manufacturers themselves.
Book Synopsis Handbook of Polymer Applications in Medicine and Medical Devices by : Len Czuba
Download or read book Handbook of Polymer Applications in Medicine and Medical Devices written by Len Czuba and published by Elsevier Inc. Chapters. This book was released on 2013-12-05 with total page 27 pages. Available in PDF, EPUB and Kindle. Book excerpt: This chapter will present a look at the medical device market with a particular focus on the materials of construction of devices and what we can expect in new products looking ahead. A deeper look at some other trends that have an effect on the direction of the medical device industry will be done. Finally, consideration will be given to a number of global factors that can have dramatic effects on our industry.
Book Synopsis Handbook of Polymer Applications in Medicine and Medical Devices by : Sina Ebnesajjad
Download or read book Handbook of Polymer Applications in Medicine and Medical Devices written by Sina Ebnesajjad and published by Elsevier Inc. Chapters. This book was released on 2013-12-05 with total page 61 pages. Available in PDF, EPUB and Kindle. Book excerpt: This chapter focuses on adhesives used in direct physiological contact in dental and medical procedures. Activity in both areas has been quite extensive outside the United States for decades. In contrast, adhesive use in medical devices, patches, and plasters has been ongoing in the United States for a long time. In the case of medical devices, adhesion is concerned with the joining of materials such as plastics, elastomers, textiles, metals, and ceramics, which are examined in other chapters of the present volume and are covered in various references [1–6], The coverage of this chapter is devoted to applications where to adhesives are in direct contact with tissues and other live organs.
Book Synopsis Metallic Biomaterials Processing and Medical Device Manufacturing by : Cuie Wen
Download or read book Metallic Biomaterials Processing and Medical Device Manufacturing written by Cuie Wen and published by Woodhead Publishing. This book was released on 2020-08-20 with total page 606 pages. Available in PDF, EPUB and Kindle. Book excerpt: Metallic Biomaterials Processing and Medical Device Manufacturing details the principles and practices of the technologies used in biomaterials processing and medical device manufacturing. The book reviews the main categories of metallic biomaterials and the essential considerations in design and manufacturing of medical devices. It bridges the gap between the designing of biomaterials and manufacturing of medical devices including requirements and standards. Main themes of the book include, manufacturing, coatings and surface modifications of medical devices, metallic biomaterials and their mechanical behaviour, degradation, testing and characterization, and quality controls, standards and FDA regulations of medical devices. The leading experts in the filed discuss the requirements, challenges, recent progresses and future research directions in the processing of materials and manufacturing of medical devices. Metallic Biomaterials Processing and Medical Device Manufacturing is ideal for those working in the disciplines of materials science, manufacturing, biomedical engineering, and mechanical engineering. Reviews key topics of biomaterials processing for medical device applications including metallic biomaterials and their mechanical behavior, degradation, testing and characterization Bridges the gap between biomaterials design and medical device manufacturing Discusses the quality controls, standards, and FDA requirements for biomaterials and medical devices
Book Synopsis Medical Devices by : Seeram Ramakrishna
Download or read book Medical Devices written by Seeram Ramakrishna and published by Woodhead Publishing. This book was released on 2015-08-18 with total page 253 pages. Available in PDF, EPUB and Kindle. Book excerpt: Medical Devices and Regulations: Standards and Practices will shed light on the importance of regulations and standards among all stakeholders, bioengineering designers, biomaterial scientists and researchers to enable development of future medical devices. Based on the authors’ practical experience, this book provides a concise, practical guide on key issues and processes in developing new medical devices to meet international regulatory requirements and standards. Provides readers with a global perspective on medical device regulations Concise and comprehensive information on how to design medical devices to ensure they meet regulations and standards Includes a useful case study demonstrating the design and approval process
Book Synopsis Microsystems for Enhanced Control of Cell Behavior by : Andrés Díaz Lantada
Download or read book Microsystems for Enhanced Control of Cell Behavior written by Andrés Díaz Lantada and published by Springer. This book was released on 2016-03-23 with total page 457 pages. Available in PDF, EPUB and Kindle. Book excerpt: This handbook focuses on the entire development process of biomedical microsystems that promote special interactions with cells. Fundamentals of cell biology and mechanobiology are described as necessary preparatory input for design tasks. Advanced design, simulation, and micro/nanomanufacturing resources, whose combined use enables the development of biomedical microsystems capable of interacting at a cellular level, are covered in depth. A detailed series of chapters is then devoted to applications based on microsystems that offer enhanced cellular control, including microfluidic devices for diagnosis and therapy, cell-based sensors and actuators (smart biodevices), microstructured prostheses for improvement of biocompatibility, microstructured and microtextured cell culture matrices for promotion of cell growth and differentiation, electrophoretic microsystems for study of cell mechanics, microstructured and microtextured biodevices for study of cell adhesion and dynamics, and biomimetic microsystems (including organs-on-chips), among others. Challenges relating to the development of reliable in vitro biomimetic microsystems, the design and manufacture of complex geometries, and biofabrication are also discussed.
Book Synopsis Handbook of Biomaterial Properties by : William Murphy
Download or read book Handbook of Biomaterial Properties written by William Murphy and published by Springer. This book was released on 2016-06-11 with total page 676 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book provides tabular and text data relating to normal and diseased tissue materials and materials used in medical devices. Comprehensive and practical for students, researchers, engineers, and practicing physicians who use implants, this book considers the materials aspects of both implantable materials and natural tissues and fluids. Examples of materials and topics covered include titanium, elastomers, degradable biomaterials, composites, scaffold materials for tissue engineering, dental implants, sterilization effects on material properties, metallic alloys, and much more. Each chapter author considers the intrinsic and interactive properties of biomaterials, as well as their appropriate applications and historical contexts. Now in an updated second edition, this book also contains two new chapters on the cornea and on vocal folds, as well as updated insights, data, and citations for several chapters.
Book Synopsis Functional Nanocomposite Hydrogels by : Anuj Kumar
Download or read book Functional Nanocomposite Hydrogels written by Anuj Kumar and published by Elsevier. This book was released on 2023-06-22 with total page 617 pages. Available in PDF, EPUB and Kindle. Book excerpt: Functional Nanocomposite Hydrogels: Synthesis, Characterization, and Biomedical Applications reviews how the unique properties of nanoscale composite materials make them ideal candidates for use in biomedical hydrogels. The book covers a range of key nanocomposite materials for use in biomedical hydrogels, including graphene quantum dot, cellulose and collagen nanocomposites. A wide selection of biomedical applications for functional nanocomposite hydrogels is explored, from drug delivery and cancer therapy, to wound healing and bioimaging. This is a key reference for those working in the fields of biomaterials, nanotechnology, pharmacology, biomedical engineering, and anyone with a particular interest in composites and hydrogels. To improve the properties of conventional hydrogels, nanoparticles or nanostructures are incorporated into the hydrogel networks, forming a composite hydrogel with specialized functional properties which are tailored to a specific biomedical application. Reviews the benefits and challenges of nanocomposites as novel materials in biomedical hydrogels, providing the reader with a wider range of choice and improved options for hydrogel development Describes the synthesis and characterization of nanocomposite hydrogels, offering end-to-end analysis of the process Details the range of applications in biomedicine for nanocomposite hydrogels, including biosensing, antimicrobics and drug delivery
Book Synopsis Handbook of Polymer Applications in Medicine and Medical Devices by : Paul Stoodley
Download or read book Handbook of Polymer Applications in Medicine and Medical Devices written by Paul Stoodley and published by Elsevier Inc. Chapters. This book was released on 2013-12-05 with total page 57 pages. Available in PDF, EPUB and Kindle. Book excerpt: The initial design criteria in the choice of indwelling materials for medical and dental purposes may be pragmatic, and based on the necessary mechanical properties required to fashion a functional device. Orthopedic implants require strong materials for weight-bearing, and articulating surfaces such as joints require durability and resistance to wear. Stents and shunts require flexibility and patency, and sutures require a high tensile strength yet also must be flexible enough for intricate manipulation. As the devices became more sophisticated and developments in materials science provided more options for manufacture, implants are being used more frequently and with longer anticipated lifetimes. Concurrently, the design process increasingly incorporated biocompatibility and comfort into the design criteria. However, with longer lifetimes, the more frequent use of invasive surgical procedures involving indwelling devices and biologically-friendly materials, there has been a rise in the number of incidences of device-related infection. Urinary catheters have been estimated to account for 30% of all nosocomial infections [1]. Between 66 and 88% of these occur after urinary catheterization [2]. It is also reported that almost 100% of catheterized patients develop an infection in an openly draining indwelling catheter which has been in place for four days or more [2]. For some procedures, such as orthopedic joint arthroplasties, the diagnosed surgical site infection rates are relatively low (between 1% and 2%; [3]); however, the increasing number of patients undergoing joint-replacement surgery translates to large numbers of patients afflicted with the consequences of complicating infections per year. Furthermore, infection of artificial joints can be devastating, since oral or IV antibiotic therapy frequently fails to resolve the infection, with the only remaining course of action being surgical debridement or partial or total revision. These two examples, the first with very high numbers of patients but of lesser severity in terms of impact to the individual, and the second, low numbers but severe patient impact, reflect the incentive to pursue a third design criteria—that of infection resistance—into materials and devices [4]. In the following sections we will discuss the role of bacterial biofilms in infection, and the growing literature highlighting biofilms as an important cause of device-related infection.
Book Synopsis Medical Devices - Materials for Human Contact (Design Guide) by : Iom Communications
Download or read book Medical Devices - Materials for Human Contact (Design Guide) written by Iom Communications and published by Routledge. This book was released on 1998 with total page 52 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Plastics in Medical Devices by : Vinny R. Sastri
Download or read book Plastics in Medical Devices written by Vinny R. Sastri and published by Elsevier. This book was released on 2010-03-05 with total page 289 pages. Available in PDF, EPUB and Kindle. Book excerpt: No book has been published that gives a detailed description of all the types of plastic materials used in medical devices, the unique requirements that the materials need to comply with and the ways standard plastics can be modified to meet such needs. This book will start with an introduction to medical devices, their classification and some of the regulations (both US and global) that affect their design, production and sale. A couple of chapters will focus on all the requirements that plastics need to meet for medical device applications. The subsequent chapters describe the various types of plastic materials, their properties profiles, the advantages and disadvantages for medical device applications, the techniques by which their properties can be enhanced, and real-world examples of their use. Comparative tables will allow readers to find the right classes of materials suitable for their applications or new product development needs.
Book Synopsis Medical Regulatory Affairs by : Jack Wong
Download or read book Medical Regulatory Affairs written by Jack Wong and published by CRC Press. This book was released on 2022-01-27 with total page 806 pages. Available in PDF, EPUB and Kindle. Book excerpt: This handbook covers medical device regulatory systems in different countries, ISO standards for medical devices, clinical trial and regulatory requirements, and documentation for application. It is the first to cover the medical device regulatory affairs in Asia. Experts from influential international regulatory bodies, including the US Food and Drug Administration (FDA), UK Medicines and Healthcare Products Regulatory Agency, Japan Pharmaceuticals and Medical Devices Agency, Saudi Food and Drug Authority, Korea Testing Laboratory, Taiwan FDA, World Health Organization, Asian Harmonization Working Party, Regulatory Affairs Professionals Society, and British Standards Institution, have contributed to the book. Government bodies, the medical device industry, academics, students, and general readers will find the book immensely useful for understanding the global regulatory environment and in their research and development projects.
Book Synopsis PEEK Biomaterials Handbook by : Steven M. Kurtz
Download or read book PEEK Biomaterials Handbook written by Steven M. Kurtz and published by William Andrew. This book was released on 2011-11-09 with total page 309 pages. Available in PDF, EPUB and Kindle. Book excerpt: PEEK biomaterials are currently used in thousands of spinal fusion patients around the world every year. Durability, biocompatibility and excellent resistance to aggressive sterilization procedures make PEEK a polymer of choice, replacing metal in orthopedic implants, from spinal implants and hip replacements to finger joints and dental implants. This Handbook brings together experts in many different facets related to PEEK clinical performance as well as in the areas of materials science, tribology, and biology to provide a complete reference for specialists in the field of plastics, biomaterials, medical device design and surgical applications. Steven Kurtz, author of the well respected UHMWPE Biomaterials Handbook and Director of the Implant Research Center at Drexel University, has developed a one-stop reference covering the processing and blending of PEEK, its properties and biotribology, and the expanding range of medical implants using PEEK: spinal implants, hip and knee replacement, etc. Covering materials science, tribology and applications Provides a complete reference for specialists in the field of plastics, biomaterials, biomedical engineering and medical device design and surgical applications
