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The boundary lubrication of chemically grafted and cross-linked hyaluronic acid in phosphate buffered saline and lipid solutions measured by the surface forces apparatus

Yu, Jing, Banquy, Xavier, Greene, George W., Lowrey, Daniel D. and Israelachvili, Jacob N. 2011, The boundary lubrication of chemically grafted and cross-linked hyaluronic acid in phosphate buffered saline and lipid solutions measured by the surface forces apparatus, Langmuir, vol. 28, no. 4, pp. 2244-2250.

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Title The boundary lubrication of chemically grafted and cross-linked hyaluronic acid in phosphate buffered saline and lipid solutions measured by the surface forces apparatus
Author(s) Yu, Jing
Banquy, Xavier
Greene, George W.ORCID iD for Greene, George W. orcid.org/0000-0003-2250-8334
Lowrey, Daniel D.
Israelachvili, Jacob N.
Journal name Langmuir
Volume number 28
Issue number 4
Start page 2244
End page 2250
Total pages 7
Publisher American Chemical Society
Place of publication Washington, D. C.
Publication date 2011-01-31
ISSN 0743-7463
1520-5827
Keyword(s) abrasive friction
articular joints
basic research
bio-lubrication
boundary lubricants
boundary lubrications
cartilage surfaces
friction force
high coefficient-of-friction
high concentration
high molecular weight
higher loads
hyaluronic acids
joint lubrication
lubricin
mica surfaces
phosphate-buffered salines
phosphocholine
physiological condition
physisorbed
self-assembled
surface damages
surface forces apparatus
synovial fluid
wear damage
wear protection
Summary High molecular weight hyaluronic acid (HA) is present in articular joints and synovial fluid at high concentrations; yet despite numerous studies, the role of HA in joint lubrication is still not clear. Free HA in solution does not appear to be a good lubricant, being negatively charged and therefore repelled from most biological, including cartilage, surfaces. Recent enzymatic experiments suggested that mechanically or physically (rather than chemically) trapped HA could function as an “adaptive” or “emergency” boundary lubricant to eliminate wear damage in shearing cartilage surfaces. In this work, HA was chemically grafted to a layer of self-assembled amino-propyl-triethoxy-silane (APTES) on mica and then cross-linked. The boundary lubrication behavior of APTES and of chemically grafted and cross-linked HA in both electrolyte and lipid 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) solutions was tested with a surface forces apparatus (SFA). Despite the high coefficient of friction (COF) of μ ≈ 0.50, the chemically grafted HA gel significantly improved the lubrication behavior of HA, particularly the wear resistance, in comparison to free HA. Adding more DOPC lipid to the solution did not improve the lubrication of the chemically grafted and cross-linked HA layer. Damage of the underlying mica surface became visible at higher loads (pressure >2 MPa) after prolonged sliding times. It has generally been assumed that damage caused by or during sliding, also known as “abrasive friction”, which is the main biomedical/clinical/morphological manifestation of arthritis, is due to a high friction force and, therefore, a large COF, and that to prevent surface damage or wear (abrasion) one should therefore aim to reduce the COF, which has been the traditional focus of basic research in biolubrication, particularly in cartilage and joint lubrication. Here we combine our results with previous ones on grafted and cross-linked HA on lipid bilayers, and lubricin-mediated lubrication, and conclude that for cartilage surfaces, a high COF can be associated with good wear protection, while a low COF can have poor wear resistance. Both of these properties depend on how the lubricating molecules are attached to and organized at the surfaces, as well as the structure and mechanical, viscoelastic, elastic, and physical properties of the surfaces, but the two phenomena are not directly or simply related. We also conclude that to provide both the low COF and good wear protection of joints under physiological conditions, some or all of the four major components of joints—HA, lubricin, lipids, and the cartilage fibrils—must act synergistically in ways (physisorbed, chemisorbed, grafted and/or cross-linked) that are still to be determined.
Language eng
Field of Research 029901 Biological Physics
030603 Colloid and Surface Chemistry
090301 Biomaterials
Socio Economic Objective 920116 Skeletal System and Disorders (incl. Arthritis)
HERDC Research category C1.1 Refereed article in a scholarly journal
Copyright notice ©2011, American Chemical Society
Persistent URL http://hdl.handle.net/10536/DRO/DU:30048049

Document type: Journal Article
Collection: Institute for Frontier Materials
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