Khám Phá Hiệu Suất Sinh Học Của Vật Liệu Trong Y Sinh

Khám phá hiệu suất sinh học của vật liệu trong bài viết 'Biological performance of materials 1', cung cấp thông tin chi tiết và ứng dụng thực tiễn.

Trường đại học

Clemson University

Chuyên ngành

Bioengineering

Tác giả

Jonathan Black

Người đăng

Ẩn danh

Thể loại

sách

2006

520
1
0

Phí lưu trữ

135 Point

Mục lục chi tiết

1. CHƯƠNG 1: Biocompatibility: Definitions and Issues

1.1. Introduction

1.2. The Discipline of Biomaterials

1.3. Afterword: Paradigmatic Shift

2. CHƯƠNG 2: Introduction to the Biological Environment

2.1. Comparison of External and Internal Conditions

2.2. Problems in Definition of the Biological Environment

2.3. Elements of the Biological Environment

2.4. Implant Life History

2.5. Preimplantation Handling Effects

3. CHƯƠNG 3: Swelling and Leaching

3.1. Fick’s Laws of Diffusion

3.2. Examples of Undesirable Absorption

3.3. Example of Planned Leaching: Drug Release

3.4. Effects of Swelling and Leaching

4. CHƯƠNG 4: Corrosion and Dissolution

4.1. Chemistry of Corrosion

4.2. Classification of Reactions

4.3. The Pourbaix Diagram

4.4. The Electrochemical Series

4.5. Potential-Current Relationships in Corrosion

4.6. Forms of Corrosion

4.7. Corrosion in Implant Applications

4.8. Engineering Variables Affecting Corrosion Rates

4.9. Corrosion Factors Peculiar to Biological Environments

5. CHƯƠNG 5: Reactions of Biological Molecules with Biomaterial Surfaces

5.1. Mechanical Aspects of Interfaces

5.2. Results of Interfacial Adhesion of Molecules

5.3. Effects of Charged Interfaces and Ions

6. CHƯƠNG 6: Mechanics of Materials: Deformation and Failure

6.1. Mechanics of Materials

7. CHƯƠNG 7: Friction and Wear

Interpart 1. Implant Materials: Properties

8. CHƯƠNG 8: The Inflammatory Process

8.1. The Inflammatory Response

8.2. Effects of Implant Degradation Products

9. CHƯƠNG 9: Coagulation and Hemolysis

9.1. The Coagulation Cascade

9.2. Approaches to Thromboresistant Materials Development

9.3. Tissue Growth Strategies

9.4. Examples of Adaptation in Implant Applications

9.5. A Final Comment on Adaptation

11. CHƯƠNG 11: In Vitro Tissue Growth and Replantation

11.1. What Is Tissue Engineering?

11.2. The Cell–Receptor Paradigm

11.3. Matrices and Cell Sources

11.4. Thinking Twice about Tissue Engineering

11.5. Some Final Comments

12. CHƯƠNG 12: Allergic Foreign Body Response

12.1. Mechanisms of Immune Response

12.2. Classes of Hypersensitivity Reactions

12.3. Hypersensitivity Reactions Associated with Implants

13. CHƯƠNG 13: Chemical and Foreign-Body Carcinogenesis

13.1. Foreign Body Carcinogenesis

13.2. Evidence for Implant Carcinogenesis in Humans

14. CHƯƠNG 14: Mineral Metabolism

14.1. Human Dietary Metal Intake

15. CHƯƠNG 15: Systemic Distribution and Excretion

15.1. Movement of Solid Bodies

15.2. Transport of Dissolved Species

15.3. Distribution and Excretion of Dissolved Species

16. CHƯƠNG 16: Effects of Degradation Products on Remote Organ Function

16.1. Examples of Systemic Effects

16.2. A Review of Systemic Aspects of Host Response

Interpart 2. Implant Materials: Clinical Performance

Interpart 2.1. An Example: Total Hip Replacement

17. CHƯƠNG 17: In Vitro Test Methods

17.1. In Vitro Test Types

17.2. Tissue Culture Tests

17.3. Blood Contact Tests

18. CHƯƠNG 18: In Vivo Implant Models

19. CHƯƠNG 19: Clinical Testing of Implant Materials

19.1. Goal of Clinical Trials

19.2. Design of Clinical Trials

19.3. Conclusions from Clinical Trials

19.4. Aspects of the Decision for General Clinical Use

20. CHƯƠNG 20: Standardization and Regulation of Implant Materials

20.1. Drug Standardization Activities

20.2. Biomaterials Standardization Activities

20.3. Federal Regulation of Medical Devices and Biomaterials

20.4. Regulation of Materials for Implants

20.5. The Biomaterials Supply “Crisis”

21. CHƯƠNG 21: Design and Selection of Implant Materials

21.1. The Design Process

21.2. The Value of Prospective Design

22. CHƯƠNG 22: Clinical Performance of Biomaterials

22.1. Procedures for Device Retrieval and Analysis

22.2. Common Concerns about Device Retrieval and Analysis

22.3. Proposed National Implant Data Retrieval and Analysis Program (NIDRA)

22.4. Elements of a NIDRA System

22.5. Autopsy Retrieval Studies

Tóm tắt

I. Tổng quan về hiệu suất sinh học của vật liệu trong y sinh

Hiệu suất sinh học của vật liệu trong y sinh là một lĩnh vực nghiên cứu quan trọng, liên quan đến việc đánh giá khả năng tương tác giữa vật liệu và cơ thể sống. Các vật liệu này có thể được sử dụng trong các thiết bị y tế, cấy ghép và nhiều ứng dụng khác. Việc hiểu rõ về hiệu suất sinh học giúp cải thiện thiết kế và ứng dụng của vật liệu trong y học.

1.1. Định nghĩa và tầm quan trọng của hiệu suất sinh học

Hiệu suất sinh học được định nghĩa là khả năng của vật liệu tương tác với các mô sống mà không gây ra phản ứng bất lợi. Điều này rất quan trọng trong việc phát triển các vật liệu y sinh an toàn và hiệu quả.

1.2. Các loại vật liệu y sinh phổ biến

Các loại vật liệu y sinh bao gồm vật liệu polymer, kim loại và gốm. Mỗi loại vật liệu có những đặc tính riêng biệt ảnh hưởng đến hiệu suất sinh học của chúng.

II. Thách thức trong việc đánh giá hiệu suất sinh học của vật liệu

Đánh giá hiệu suất sinh học của vật liệu gặp nhiều thách thức, bao gồm sự phức tạp của các phản ứng sinh học và sự đa dạng của các loại vật liệu. Các yếu tố như độ bền, khả năng tương thích và khả năng phân hủy sinh học đều cần được xem xét.

2.1. Các yếu tố ảnh hưởng đến hiệu suất sinh học

Các yếu tố như cấu trúc hóa học, kích thước và hình dạng của vật liệu có thể ảnh hưởng đến cách mà chúng tương tác với mô sống. Việc hiểu rõ những yếu tố này là rất quan trọng.

2.2. Phản ứng của cơ thể đối với vật liệu

Cơ thể có thể phản ứng khác nhau với các vật liệu khác nhau, từ việc chấp nhận cho đến gây ra viêm nhiễm. Điều này cần được nghiên cứu kỹ lưỡng để đảm bảo an toàn cho người sử dụng.

III. Phương pháp nghiên cứu hiệu suất sinh học của vật liệu

Có nhiều phương pháp để nghiên cứu hiệu suất sinh học của vật liệu, bao gồm thử nghiệm in vitro và in vivo. Mỗi phương pháp có những ưu điểm và nhược điểm riêng, và việc lựa chọn phương pháp phù hợp là rất quan trọng.

3.1. Thử nghiệm in vitro

Thử nghiệm in vitro cho phép đánh giá phản ứng của tế bào với vật liệu trong môi trường kiểm soát. Đây là phương pháp nhanh chóng và tiết kiệm chi phí.

3.2. Thử nghiệm in vivo

Thử nghiệm in vivo cung cấp thông tin thực tế về cách mà vật liệu hoạt động trong cơ thể sống. Tuy nhiên, phương pháp này thường tốn kém và phức tạp hơn.

IV. Ứng dụng thực tiễn của vật liệu sinh học trong y học

Vật liệu sinh học được ứng dụng rộng rãi trong y học, từ cấy ghép mô đến thiết bị y tế. Những ứng dụng này không chỉ cải thiện chất lượng cuộc sống mà còn giúp điều trị hiệu quả hơn.

4.1. Cấy ghép mô và cơ quan

Cấy ghép mô và cơ quan là một trong những ứng dụng quan trọng nhất của vật liệu sinh học. Chúng giúp phục hồi chức năng cho các bộ phận cơ thể bị tổn thương.

4.2. Thiết bị y tế

Vật liệu sinh học được sử dụng trong nhiều thiết bị y tế như stent, van tim và các thiết bị hỗ trợ khác. Chúng cần phải có hiệu suất sinh học cao để đảm bảo an toàn cho bệnh nhân.

V. Kết luận và tương lai của vật liệu sinh học trong y sinh

Tương lai của vật liệu sinh học trong y sinh rất hứa hẹn với nhiều nghiên cứu và phát triển mới. Việc cải thiện hiệu suất sinh học sẽ mở ra nhiều cơ hội mới trong điều trị và chăm sóc sức khỏe.

5.1. Xu hướng nghiên cứu mới

Nghiên cứu hiện tại đang tập trung vào việc phát triển vật liệu mới với tính năng vượt trội, như vật liệu nano và vật liệu thông minh.

5.2. Tác động đến ngành y tế

Sự phát triển của vật liệu sinh học sẽ có tác động lớn đến ngành y tế, giúp cải thiện hiệu quả điều trị và giảm thiểu rủi ro cho bệnh nhân.

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Biological performance of materials 1

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FOURTH EDITION BIOLOGICAL PERFORMANCE of MATERIALS Fundamentals of Biocompatibility FOURTH EDITION BIOLOGICAL PERFORMANCE of MATERIALS Fundamentals of Biocompatibility Jonathan Black Boca Raton London New York A CRC title, part of the Taylor & Francis imprint, a member of the Taylor & Francis Group, the academic division of T&F Informa plc. Copyright Jonathan Black. CRC Press Taylor & Francis Group 6000 Broken Sound Parkway NW, Suite 300 Boca Raton, FL 33487-2742 © 2006 by Taylor & Francis Group, LLC CRC Press is an imprint of Taylor & Francis Group, an Informa business No claim to original U. Government works Version Date: 20131106 International Standard Book Number-13: 978-1-4200-5784-3 (eBook - PDF) This book contains information obtained from authentic and highly regarded sources.

Reasonable efforts have been made to publish reliable data and information, but the author and publisher cannot assume responsibility for the validity of all materials or the consequences of their use. The authors and publishers have attempted to trace the copyright holders of all material reproduced in this publication and apologize to copyright holders if permission to publish in this form has not been obtained. If any copyright material has not been acknowledged please write and let us know so we may rectify in any future reprint. Except as permitted under U.

Copyright Law, no part of this book may be reprinted, reproduced, transmit- ted, or utilized in any form by any electronic, mechanical, or other means, now known or hereafter invented, including photocopying, microfilming, and recording, or in any information storage or retrieval system, without written permission from the publishers. For permission to photocopy or use material electronically from this work, please access www. com (http://www.com/) or contact the Copyright Clearance Center, Inc. (CCC), 222 Rosewood Drive, Danvers, MA 01923, 978-750-8400.

CCC is a not-for-profit organization that provides licenses and registration for a variety of users. For organizations that have been granted a photocopy license by the CCC, a separate system of payment has been arranged. Trademark Notice: Product or corporate names may be trademarks or registered trademarks, and are used only for identification and explanation without intent to infringe. Visit the Taylor & Francis Web site at http://www.com and the CRC Press Web site at http://www.com Preface Biocompatibility of materials increasingly occupies the consciousness of engineers dealing with medical and biological problems.

The engineer has long been accustomed to dealing with materials, limits on design. These limits, such as yield stress, endurance limit, and rupture life, are reflected in design margins tailored to the criticality of the specific application. In situ- ations involving biological interactions as a portion of the design problem, the additional materials limit of biocompatibility must be considered. Failure of compatibility (that is, incompatibility) is proving to be the ulti- mate limit to the engineering solution of many biomedical problems.

As a result, it is necessary to incorporate a thorough grounding in the aspects of biocompatibility — or, as I prefer to term it more generally, biological per- formance of materials — into the training of bioengineers. When this book was first conceived, in the early 1970s, no suitable text- books dealing with broad aspects of biomedical materials or, as the field rapidly came to be called, biomaterials, were available. Today, as this field has matured into biomaterials science and engineering (BSE), many edited collections and topical monographs are available for students and workers at many different levels. However, none seems to suit the neophyte: the former are invariably written by a panel of experts and thus tend to be uneven in attempting to be comprehensive and the latter are the work of a single investigator or research group focusing on relatively narrow and parochial interests.

Both of these types of books have a place and many are extremely valuable to the advanced worker, but they all fail to meet the needs of the student or the professional without a background in the field. Thus, it appears that the current work is still needed; it focuses primarily on principles of biological performance at a relatively fundamental level: interactions between living and nonliving materials whose consideration sets BSE apart as a distinct field of investigation and knowledge. Biological Performance of Materials: Fundamentals of Biocompatibility was orig- inally intended for use as an undergraduate text for a one-term, jun- ior–senior-level bioengineering course on biological performance. I and others have used it in this role.

However, with the assignment of selected articles as reading and study sources, it has also proven useful as the central text in undergraduate survey courses on biomaterials and on artificial organs. With additional reading material from the scientific and clinical literature and from materials science texts, it has also been used as the focus of a first-year graduate course in biomaterials for students with engineering (but not biological or medical) backgrounds and, conversely, as a supple- mentary text for courses on implants for nursing students with little or no engineering training. Finally, engineers working in medical device develop- ment and evaluation in industrial as well as governmental settings have found it a useful reference book. The scarcity of reference to actual materials and specific applications has apparently made this diversity of use possible; this revision attempts to maintain the versatility of the work.

Primary train- ing in materials science and biology is useful, but not totally essential, because this book is intended for use in conjunction with undergraduate texts in materials science and biology, as needed, so as to accommodate variations in individual degrees of preparation. We begin with an examination of the concept of “biocompatibility” and arguments for the broader concept of biological performance. Two major sections are devoted to the effect of biological systems on materials (“bio- degradation” = material response) and of materials on biological systems (“biocompatibility” = host response), respectively. Selected additional read- ings are provided at the end of each chapter.

The reader will note an emphasis on methods for determination of biolog- ical performance, throughout and especially in Chapter 17 and Chapter 18. This reflects the centrality of material and host response in the clinical per- formance of medical devices and surgical implants as well as the continued need to select new and modified materials for specific applications. These questions become even more challenging and complex as increasing num- bers of viable and nonviable untraditional materials come under consider- ation for clinical use. The practicing engineer will find this book a useful source of references, test methods, and approaches to the problem of estab- lishing biological performance of materials.

Generic materials properties are tabulated in Interpart 1; Interpart 2 is an example of diagnostic approaches to detection of clinical issues associated with biomaterials in animal models and in patients. The final four chapters deal with design, qualification, stan- dardization, and regulation of implant materials and will be of special assis- tance to the professional. In response to comments on earlier editions, an extensive glossary is also included. Due to the fundamental nature of this examination, I have elected in this revision to retain many earlier examples and studies, providing updated material and more current references only when needed.

The reader is advised to make use of the online resources of the National Library of Medicine (PubMed*) to provide additional, more recent, and more special- ized information. I wish to thank the many undergraduate and graduate students and col- leagues whose ideas, questions, and discussions have contributed signifi- cantly to the scope and content of this work. Special thanks are due to G. Woodman for their seminal contributions to Chapter 14 and Chapter 15.

An appeal for corrections and suggestions was issued to readers of two listserves (BIOMAT-L and BIOMCH-L) and considerable useful feed- back was received.gov/entrez/query.fcgi?db=PubMed. In the preface to the second edition (1992), I suggested that inappropriate host response to implants and premature device failure secondary to mate- rials degradation continue to impose unwanted limits on engineering solu- tions to biological and medical problems. This is still the case today. It can only be hoped that ideas and information contained in this revised work will contribute to the further improvement of biomaterials in their applica- tion to the alleviation of human disability, disorder, and disease.

Jonathan Black Abstract Biological Performance of Materials: Fundamentals of Biocompatibility presents an organized approach to examining and understanding the interactions between materials used in medical devices and implants and living organ- isms. After an introductory section addressing definitions and aspects of biological environments, the work is divided into three principal sections. These deal with material response to biological systems, host response to biomaterials, and test methods for determining biological response in vitro as well as in animal models and clinical settings. Interparts provide summa- ries of physical properties of commonly used metallic, polymeric, and ceramic biomaterials as well as a guide to understanding clinical perfor- mance of implanted biomaterials.

In addition to numerous references to the literature, each chapter includes an additional bibliography; an extensive glossary completes the work. Now in its fourth edition, this work draws on Black’s more than 35 years experience as a teacher, researcher, and consultant in biomaterials science and engineering. The Author Jonathan Black is professor emeritus of bioengineering at Clemson Univer- sity in Clemson, South Carolina. He holds degrees in physics (Cornell Uni- versity), engineering science (Pennsylvania State University), and metallurgy (biomaterials) (University of Pennsylvania).

Before his appoint- ment as the first occupant of the Hunter Chair of Bioengineering at Clemson in 1988, he was a member of the Department of Orthopaedic Surgery at the University of Pennsylvania for 17 years with a secondary appointment in the Department of Bioengineering. From 1992 to 1995, he was a senior vis- iting fellow in the IRC for biomaterials at Queen Mary and Westfield College (London), with support from an SERC fellowship. Black has been active in research and teaching in several areas of bioma- terials, with special reference to the biological performance of metallic implants and to the needs of orthopaedic clinical practice. He is the author of many articles and several textbooks, including Biological Performance of Materials (1981, 1992, 1999, 2005), Orthopaedic Biomaterials in Research and Practice (1988), and, with G.

Hastings, Handbook of Biomaterial Properties (1998). He has a long-term interest in implant retrieval and analysis and is the author of a major 1992–1993 study of the field for the USFDA. Black has been involved in professional activities in biomaterials for more than 30 years and is a charter fellow of biomaterials science and engineering (FBSE). He is a charter member and past president of the Society for Biom- aterials (U.) and has been a frequent presenter and session chair at the Gordon Research Conferences on Biomaterials and an organizer of the tri- ennial Biointeractions conference series in the United Kingdom.

He has served on a number of advisory and editorial boards and was an assistant editor of the Journal of Biomedical Materials Research from 1978 to 1995. Black is an associate member of the American Academy of Orthopaedic Surgeons and recipient of the presidential gold medal from the British Orthopaedic Association. In 1992, Black established and served as principal of IMN Biomaterials, a professional consultancy in biomaterials and orthopaedic engineering. He concentrated his efforts in this area after retirement from Clemson in 1993 and closed this enterprise at the end of 1998.

He continues to chair the Scientific Advisory Board for Stryker Orthopaedics. Contents Part I General Considerations Chapter 1 Biocompatibility: Definitions and Issues .5 The Discipline of Biomaterials .6 Afterword: Paradigmatic Shift. 15 Chapter 2 Introduction to the Biological Environment .2 Comparison of External and Internal Conditions.3 Problems in Definition of the Biological Environment .4 Elements of the Biological Environment .5 Implant Life History .6 Preimplantation Handling Effects. 30 Part II Material Response: Function and Degradation of Materials In Vivo Chapter 3 Swelling and Leaching .2 Fick’s Laws of Diffusion.4 Examples of Undesirable Absorption .7 Example of Planned Leaching: Drug Release.8 Effects of Swelling and Leaching.

47 Chapter 4 Corrosion and Dissolution .1 Chemistry of Corrosion .2 Classification of Reactions.

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