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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5361_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •Aim and Scope
- •Preface
- •Acknowledgments
- •Contents
- •Contributors
- •About the Editors
- •1.1 Introduction
- •1.2.1 Friction
- •1.2.1.3 Friction Under Lubricated Conditions
- •1.7.1 Joint Tribology
- •1.7.2 Skin Tribology
- •1.7.3 Oral Tribology
- •1.8 Summary
- •References
- •2.1 Introduction
- •2.3.1 Fluid Pressurization/Fluid-Film Lubrication
- •2.3.2 Boundary Lubrication
- •2.3.3 Hydrodynamic Lubrication
- •2.3.4 Squeeze-Film Lubrication
- •2.3.5 Synovial Fluid
- •2.3.6 Hydration Lubrication
- •2.5.2 Scaffolds
- •2.5.3 Synthetic Polymer
- •2.5.4 Polyacrylamide
- •2.5.5 PEG Hydrogel
- •2.5.6 PVA Hydrogel
- •2.5.7 Double Network Hydrogel
- •2.5.8 Triple Network Hydrogel
- •2.6.1 Polyacrylamide
- •2.6.2 PEG Hydrogel
- •2.6.3 PVA Hydrogel
- •2.6.4 Double Network Hydrogel
- •2.6.5 Triple Network Hydrogel
- •2.7.1 Mechanical Properties
- •2.7.2 Structural Properties
- •2.8 Conclusion
- •References
- •3.1 Introduction
- •3.3.1 Label-Based Biosensors
- •3.3.2 Label-Free Biosensors
- •3.4 Different Nanobiosensing Techniques
- •3.4.1 Optical Sensing
- •3.4.2 Electrochemical/Electrical Sensing
- •3.4.3 Magnetic Sensing
- •3.4.4 Mass-Based Sensing
- •3.6.2 Neurodegenerative Diseases
- •3.6.3 Infectious Diseases
- •3.6.4 Metabolic Diseases
- •References
- •4.1 Introduction
- •4.2.1 Surface Functionalization
- •4.2.2 Bioconjugation
- •4.3 Synthesis Approach
- •4.3.1 Hydrothermal Method
- •4.3.2 Chemical Vapor Deposition (CVD)
- •4.3.3 Wet Chemical Method
- •4.4 Plasmonic Black Bodies (PBBs)
- •4.4.1 Gold NP (AuNPs)-Based PBB
- •4.4.2 Silver NPs (Ag NPs)-Based PBB
- •4.4.3 Platinum NPs (Pt NPs)-Based PBB
- •4.5 Biomimetic NP
- •4.6 Upconverting NP (UCNP)
- •4.6.1 Synthesis
- •4.7 Inorganic NP
- •4.7.1 Synthesis
- •4.8 Photothermal Therapy (PTT)
- •4.9 Conclusion
- •References
- •5.1 Introduction
- •5.2 Human Skin
- •5.10 Future Scope
- •5.11 Conclusion
- •References
- •6.1 Introduction
- •6.1.1 Class 1
- •6.1.2 Class 2
- •6.1.3 Class 3
- •6.4.1.1 Surface Patterning
- •6.4.1.2 Direct-Write Patterning
- •6.4.1.5 Dip-Pen Nanotechnology
- •6.4.1.7 Composing Using Beams
- •6.4.1.8 Direct Write Photolithography (DWP)
- •6.4.1.9 Light-Beam Lithography Electron
- •6.4.1.10 Focused Ion Beam Lithography
- •6.4.2 Fabrication Techniques
- •6.4.2.4 Non-invasive Glucose Monitoring Devices Technique
- •6.4.2.6 Cost-Effective Electrochemical Voltametric Sensors Techniques
- •6.4.2.7 Three-Dimensional (3D) Printing Techniques
- •6.4.2.8 UV-LED Stereolithography Printer Technique
- •6.4.2.9 4D Printing Techniques
- •6.4.2.10 Advanced Biomedical Techniques Involving Biorobots
- •References
- •7.1 Introduction
- •7.6 Mechanical Biocompatibility Challenges
- •7.7 Poor Bio-Printing Resolution
- •7.9 Limited Biomaterial Selection
- •7.11 Conclusion
- •8.2 Animal Tribology
- •8.2.1 Joint
- •8.2.3 Integumentary Change
- •References
- •8.1 Introduction
- •8.3.1 Nanotribology
- •8.4 Green Tribology
- •8.5 Conclusion
- •References
- •9.1 Introduction
- •9.2 Bio-Tribological Issues
- •9.3.2 Bone Fracture Fixation
- •9.3.4 Cardiovascular Devices
- •9.3.5 Minimal Invasive Surgical Devices
- •References
- •10.1 Introduction
- •10.2.2.1 Structural Integrity
- •10.2.2.2 Controlled Release Properties
- •10.2.2.3 Enhanced Drug Loading Capacity
- •10.2.2.4 Tailored Material Properties
- •10.2.3.1 Biocompatibility
- •10.2.3.3 Mechanical Properties
- •10.2.3.4 Drug Compatibility
- •10.2.3.5 Fabrication Compatibility
- •10.3.1 Matrix Material Properties
- •10.3.4 Biocompatibility Assessment
- •10.3.4.1 In Vitro Cell Culture Studies
- •10.3.4.2 Hemocompatibility Studies
- •10.3.4.3 In Vivo Animal Studies
- •10.3.4.4 Histological Analysis
- •10.3.4.5 Immune Response Evaluation
- •10.3.4.6 Biodegradation Assessment
- •10.4 Surface Engineering Considerations
- •10.4.2.1 Surface Coatings
- •10.4.2.2 Plasma Treatment
- •10.4.2.3 Surface Grafting
- •10.4.2.4 Dip Coating
- •10.4.2.5 Spray Coating System
- •10.4.2.6 Electrotreated Coating
- •10.4.2.9 Microfabrication Techniques
- •10.4.2.10 Surface Roughness Control
- •10.5.1.2 Mechanical Properties
- •10.5.1.3 Surface Characteristics
- •10.5.1.4 Release Kinetics Analysis
- •10.5.1.5 Biological Compatibility
- •10.5.1.7 Other Analyses
- •10.6 Advanced Fabrication Techniques
- •10.8 Conclusion
- •References
- •11.1 Introduction
- •11.2 Shape Memory Alloys (SMA)
- •11.3 Shape Memory Polymers
- •11.3.1 Heat
- •11.3.2 Light
- •11.3.3 Magnetic Field
- •11.4 Shape-Changing Hydrogels
- •11.5 Biomedical Applications
- •11.6 Conclusion
- •References
- •12.1 Introduction
- •12.3 Bioresorbable Orthopedic Implants
- •12.4.1 Polylactides
- •12.4.2 Poly (Ortho Esters)
- •12.4.3 Polyphosphoesters
- •12.4.4 Polyphosphazenes
- •12.4.5 Polycaprolactone
- •12.4.6 Polyurethanes
- •12.4.7 Polycarbonates
- •12.5.1 Compression Molding
- •12.5.2 Transfer Molding
- •12.5.3 Injection Molding
- •12.5.4 Extrusion
- •12.5.5 Blow Molding
- •12.5.6 Calendering Process
- •12.5.7 Fiber Spinning
- •12.5.8 Thermoforming
- •12.5.9 Polymer Foaming
- •12.7 Challenges
- •12.8 Conclusion
- •References
- •13.1 Introduction
- •13.3.1.1 Total Hip Replacement (THR)
- •13.3.2 Resurfacing Hip Replacement (RHR)
- •13.5.1 Adhesive Wear
- •13.5.2 Abrasive Wear
- •13.5.3 Fatigue Wear
- •13.5.4 Corrosion/Oxidative Wear
- •13.5.5 Surface Cracking
- •13.6.1 Metallic Implants
- •13.6.1.1 Stainless Steel
- •13.6.1.2 Co-Cr Alloys
- •13.6.1.3 Ti-Alloy
- •13.6.2 Ceramic Implants
- •13.6.3 Polymer Implants
- •13.6.4 Composite Implants
- •13.6.5.2 Surface Coatings
- •13.7.2.1 Hydrodynamic Lubrication
- •13.7.2.2 Boundary Lubrication
- •13.7.2.3 Elastohydrodynamic Lubrication
- •13.7.3 Biomimetic Lubrication Approaches
- •13.7.3.1 Replicating Natural Lubrication Mechanisms
- •13.7.4.1 Implant Wear
- •13.7.4.3 Synovial Fluid Degradation
- •13.8.1 Hydroxyapatite Coatings
- •13.8.1.1 Bone Integration
- •13.8.1.2 Implant Stability
- •13.8.1.4 Biocompatibility
- •13.8.2 Diamond-Like Carbon Coatings
- •13.8.3 Metal Nitride Coatings
- •13.8.4 Polymeric Coatings
- •13.8.5 Nanocomposite Coatings
- •13.9.1 Pin-on-Disk Testing
- •13.9.2 Hip Joint Simulators
- •13.9.3 Knee Joint Simulators
- •13.9.4 Tribo-Corrosion Testing
- •13.9.5 Wear Debris Analysis Techniques
- •13.9.5.1 Scanning Electron Microscopy (SEM)
- •13.9.5.2 Energy-Dispersive X-Ray Spectroscopy (EDS)
- •13.10.1.1 Tailored Geometries
- •13.10.1.2 Improved Wear Characteristics
- •13.10.1.3 Accelerated Innovation
- •13.10.2.1 Real-Time Wear Monitoring
- •13.10.2.2 Functionality Assessment
- •13.10.2.3 Implant Status Monitoring
- •13.10.2.4 Patient-Centric Healthcare
- •13.10.3.1 Advanced Biomaterials
- •13.10.3.4 Multidisciplinary Approaches
- •13.10.4.1 Wear Data Analysis
- •13.10.4.2 Predictive Wear Patterns
- •13.10.4.3 Early Intervention Strategies
- •13.10.4.4 Personalized Treatment Plans
- •13.11 Conclusion
- •References
- •14.1 Introduction
- •14.2.1 Powder Bed Fusion (PBF)
- •14.2.2 Directed Energy Deposition
- •14.3.1 Extrusion-Based AM
- •14.5 Biomanufacturing
- •14.5.1 Tissue Engineering
- •14.5.2 Organ-on-a-Chip Models
- •14.6 Conclusion
- •References
- •Index

22
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and Zr Addition in Thermal Stabilization of Nano-Crystalline Cu Synthesized by Ball Milling.
Materials Letters 2020, 271, 127780. https://doi.org/10.1016/j.matlet.2020.127780.
81. Soumya Mandal, Ashish Kumar Gupta, Elena Echeverria, David N. McIlroy, Jonathan
D.Poplawsky, R.Sachan. Laser-Assisted Nanofabrication of Multielement Complex Oxide.
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82. Gupta, A.K.; Gupta, S.; Mandal, S.; Sachan, R.Laser Irradiation-Induced Nanoscale Surface
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84. Kumar A, Shrama AK, Gupta TVK, Katiyar JK (2022) Inuence of hexagonal boron nitride
additive nanocutting uid on the machining of AA6061-T6 alloy using minimum quality lubrication. Proc Inst Mech Eng Part E J Process Mech Eng 09544089221110980.
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Polym Compos 10–11.
86. Parihar A, Kumar A, Panda U, Khan R, Parihar DS, Khan R (2023) Cryopreservation: A
Comprehensive Overview, Challenges, and Future Perspectives. Adv Biol 2200285.
87. Parihar A, Pandita V, Kumar A, Parihar DS, Puranik N, Bajpai T, Khan R (2021) 3D Printing:
Advancement in Biogenerative Engineering to Combat Shortage of Organs and Bioapplicable
Materials. Regen Eng Transl Med 1–27.
88. Parmar V, Kumar A, Mani Sankar M, Datta S, Vijaya Prakash G, Mohanty S, Kalyanasundaram
D (2018) Oxidation facilitated antimicrobial ability of laser micro-textured titanium alloy
against gram-positive Staphylococcus aureus for biomedical applications. J Laser Appl 30.
25

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89. Parmar V, Kumar A, Prakash GV, Datta S, Kalyanasundaram D (2019) Investigation, modelling and validation of material separation mechanism during ber laser machining of medical
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90. Singh M, Kumar A, Khan AR (2020) Capillary as a liquid diode. Phys Rev Fluids 5:102101.
91. Singh RK, Kumar A, Kant R, Gupta A, Suresh E, Bhattacharya S (2014) Design and fabrication of 3-dimensional helical structures in polydimethylsiloxane for ow control applications.
Microsyst Technol 20:101–111.
92. Subramanian Y, Gajendiran J, Veena R, Azad AK, Sabarish VCB, Muhammed Ali SA, Kumar
A, Gubendiran RK (2023) Structural, Photoabsorption and Photocatalytic Characteristics
of BiFeO3-WO3 Nanocomposites: An Attempt to Validate the Experimental Data Through
SVM-Based Articial Intelligence (AI). J Electron Mater 1–11.
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Technologies for Sustainable Manufacturing. CRC Press, pp67–83.
94. Gupta, A., Choudhari, A., Kadaka, T., Rayar, P. (2019). Design and Analysis of Vertical Vacuum
Fryer. In: Vasudevan, H., Kottur, V., Raina, A. (eds) Proceedings of International Conference
on Intelligent Manufacturing and Automation. Lecture Notes in Mechanical Engineering.
Springer, Singapore. https://doi.org/10.1007/978- 981- 13- 2490- 1_13.
95. Choudhari, A., Rayar, P., Shimpi, S., Pawar, N., Ambetkar, S. (2023). Design and Development
of Vacuum Frying Machine for the Production of High-Quality Fried Products. In: Vasudevan,
H., Kottur, V.K.N., Raina, A.A. (eds) Proceedings of International Conference on Intelligent
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Singapore. https://doi.org/10.1007/978- 981- 19- 7971- 2_50.
96. Talkar, S., Choudhari, A., Rayar, P. (2020). Building Envelope Optimization and CostEffective Approach in HVAC to Support Smart Manufacturing. In: Vasudevan, H., Kottur,
V., Raina, A. (eds) Proceedings of International Conference on Intelligent Manufacturing
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Conservation and Effective Utilization of Waste Heat from Air Conditioner’, IOP Conference
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A. Kumar et al.

Chapter 2
Characterization ofHydrogel Properties
intheAdvancement ofBio-Tribology
NusratChowdhury , SakibFaisal , AbhishekKumar ,
AmitChoudhari , AshishKumarGupta , AvinashKumar ,
andAshwaniKumar
Abstract Nature-driven artifacts have the most precise form of tribological proper-
ties. Because of hydration lubrication, biological tissues like articular cartilage have
the lowest friction and wear. However, these natural tissues are hard to repair in case
of injury, accident, or fracture. Recent advances in bio-tribology include replacement material development like hydrogel through surface property analysis and
using hydrogel as an ECM microenvironment for cell proliferation. Hydrogels are
used as potential biological tissue development because of the biphasic low friction
nature of the material as it contains almost 90% water content like biological tissue.
Hydration lubrication enables improved surface characterization and improves tribological properties. The chapter will primarily concentrate on characterizing the
surface and structure of hydrogels and exploring the potential they offer as substitutes for biological tissue.
Keywords Articular cartilage · Cell proliferation (maybe) · Hydrogel types ·
Elastic modulus · Structural · Mechanical characteristics · Tribological properties ·
Bio-tribology · Structural properties · Tissue engineering
N. Chowdhury (*)
University of Illinois Urbana-Champaign, Urbana, IL, USA
e-mail: nusratc2@illinois.edu
S. Faisal
South Dakota State University, Brookings, SD, USA
A. Kumar
J.Mike Walker ’66 Department of Mechanical Engineering, Texas A&M University,
College Station, TX, USA
Department of Mechanical Engineering, University of California, Merced, CA, USA
e-mail: akumar71@tamu.edu
A. Choudhari
Mechanical Engineering Department, Cleveland State University, Cleveland, OH, USA
e-mail: a.choudhari@vikes.csuohio.edu
A. Kumar etal. (eds.), Applications of Biotribology in Biomedical Systems,
https://doi.org/10.1007/978-3-031-58327-8_2
27© The Author(s), under exclusive license to Springer Nature Switzerland AG 2024

28
N. Chowdhury etal.
2.1 Introduction
Tribological properties, encompassing the science of friction, wear, and lubrication,
play a pivotal role in the efcient functioning of various materials and systems.
Nature’s ingenious designs have provided remarkable examples of precise tribological properties, as evidenced by biological tissues like articular cartilage, which
exhibit minimal friction and wear due to the phenomenon of hydration lubrication.
However, the innate limitations of these natural tissues, such as the challenge of
repair after injury or damage, have driven the exploration of innovative solutions in
the realm of bio-tribology [1]. Recent advancements in bio-tribology have spurred
the development of potential replacement materials, particularly hydrogels, by
leveraging in-depth surface property analysis. Hydrogels, characterized by their
biphasic nature and high water content akin to biological tissues, have emerged as
promising candidates for mimicking natural tissue behavior. Their unique properties, including low friction characteristics and potential for creating a favorable
extracellular matrix (ECM) microenvironment, have sparked interest in their application for biological tissue regeneration [2].
This chapter aims to delve into the intricacies of tribological properties exhibited
by articular cartilage, the specialized tissue found in synovial joints responsible for
smooth and resilient joint motion. We will explore the development of hydrogels as
potential substitutes for biological tissues, focusing on their mechanical and structural attributes. By examining the interplay between tribological properties,
mechanical characteristics, and structural features, we seek to unravel the relationship underpinning these materials’ functionality. In the subsequent sections, we will
embark on a journey through the fundamentals of articular cartilage‘s tribological
prowess, the evolution of hydrogels as replacement materials, and the mechanical
and structural attributes that dene their behavior. By investigating how tribological
properties are intricately linked to these material characteristics, we aim to shed
light on the promising role of hydrogels as substitutes for biological tissues, opening new avenues in tissue engineering and regenerative medicine.
A. K. Gupta
School of Mechanical and Aerospace Engineering, Oklahoma State University,
Stillwater, OK, USA
e-mail: ashish.gupta10@okstate.edu
A. Kumar
Department of Mechanical Engineering, Indian Institute of Information Technology Design &
Manufacturing (IIITDM), Kancheepuram, Chennai, Tamil Nadu, India
Department of Mechanical Engineering, Stanford University, Stanford, CA, USA
e-mail: avikr@iiitdm.ac.in
A. Kumar
Department of Mechanical Engineering, Technical Education Department Uttar Pradesh
(under Government of Uttar Pradesh), Kanpur, Uttar Pradesh, India

2 Characterization ofHydrogel Properties intheAdvancement ofBio-Tribology
29
2.2 Tribological Properties ofArticular Cartilage
Articular cartilage, located in synovial joints, is a durable tissue that serves as a
protective layer. The thickness of articular cartilage in humans typically ranges
from 1 to 5mm. It covers the surface where bones articulate, providing resilience
and smooth movement during joint motion. The extracellular matrix (ECM) of
articular cartilage contains dispersed chondrocytes, forming a connective tissue that
offers various functions like structural support, resilience, and lubrication. ECM
mainly consists of collagen (15–22%), water (60–85%), and proteoglycans (protein
chains glycosaminoglycan (GAG)) (4–7%). Figure2.1 shows the layers and crosssectional view of various zones in cartilage. The articular cartilage has four clearly
dened zones: the deep zone, calcied zone, middle zone, and supercial zone [1].
The supercial zone accounts for 10–20% of the total thickness, of articular
cartilage, is in direct contact with the joint space, and contains collagen bers and
high cell density oriented parallelly to the articular surface, enabling it to withstand
shear forces effectively and promote smooth sliding without friction [1–3]. The ori-
entation of collagen bers in the middle/transitional zone of articular cartilage is
distinct from that in the supercial zone, which is in the oblique or perpendicular to
the articular surface, attened and elongated shape chondrocytes [4]. The deep cartilage zone contains almost 30% of the cartilage, collagen ber, and chondrocytes
arranged in vertical columns or clusters aligned perpendicularly to the articular surface. Additionally, within the calcied zone of articular cartilage, chondrocytes and
a calcied matrix are present, serving as an anchor between the cartilage and the
subchondral bone and aiding in the transmission of mechanical loads during joint
movement [5–10].
The organization of bers and chondrocytes is the determination of the mechanical and structural properties of the tissue. However, the load-carrying ability and
frictional characteristics of articular cartilage depend on its surface structure and
supercial layer properties. An acellular non-brous, highly viscous synovial uid,
Fig. 2.1 A depiction of the different zones in articular cartilage in a cross-sectional view [170]

30
Fig. 2.2 Two types of
defects in articular
cartilage. (a) Chondral
defect, (b) Osteochondral
defect [14]
N. Chowdhury etal.
acceptable granular electron-dense material zone exists atop the transitional zone
[11, 12]. The surface layer’s regenerative mechanism is dened by the mechanical
characteristics and movement of liquid-like synovial uid, GAGS, and lipid
throughout the cartilage surface and solid matrix structure when deformed [13].
Articular cartilage does not have progenitor cells, adequate nutrients, or perichondrium, as proteoglycan is the water-attracting component in articular cartilage. It
limits the healing capability of this cartilage and is known as cartilage damage or
osteoarthritis. Two primary kinds of imperfections may occur osteochondral defects
(C), which extend into the subchondral bone, and chondral defects (B), affecting
only the cartilage. Figure2.2a,b shows the cartilage defect and osteochondral defect
caused by age, bone defect, and accident [2, 14, 15].
In articular cartilage tissue engineering shown in Fig.2.3, the traditional approach
involves using primary chondrocytes or stem cells, scaffolds, growth factors, and
biomechanical methods to create potential cartilage replacements. The development
of biomimetic articial cartilage relies on improving engineered cartilage’s frictional properties. Tribological properties like friction, wear, and lubrication are very
important because of maintain healthy and functional articular cartilage joints.
These tribological properties contribute to a crucial part in the degeneration of
joints, cartilage, and OA [16].

2 Characterization ofHydrogel Properties intheAdvancement ofBio-Tribology
Fig. 2.3 In tissue engineering of articular cartilage, the conventional method involves using primary chondrocytes or stem cells, scaffolding materials, growth factors, and morphogens, to
develop constructs for potential cartilage replacement. Experimental biomechanical methods are
presently utilized in current functional approaches techniques. Achieving biomimetic articial cartilage will depend on advancements in the frictional properties of engineered cartilage [171]
31
2.3 Lubrication Mechanism ofArticular Cartilage
2.3.1 Fluid Pressurization/Fluid-Film Lubrication
Research ndings have provided insights into how lubrication occurs in the articular
cartilage. In the early understanding of diarthrodial joints, it was hypothesized that
articular cartilage relied on the lubrication mechanism of a uid lm, aided by the
viscous synovial uid. This uid full-lm lubrication prevented direct contact
between the cartilage surfaces. However, subsequent studies revealed that synovial
uid is rapidly depleted within a short time as it lters through the porous layers of
cartilage [17].
According to the biphasic theory, when articular cartilage experiences compression, the uid and solid components of the tissue, which are nearly incompressible,
provide the initial support for the applied stress during conned compression, where
rigid walls surround the specimen, the tissue cannot undergo an isochoric (volumeconserving) deformation. Therefore, the interstitial uid builds pressure to counteract the applied load. The extruded water forms a pressurized uid layer on the
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