The role of protein content on the steady and oscillatory shear rheology of model synovial fluids

Soft Matter ◽  
2014 ◽  
Vol 10 (32) ◽  
pp. 5965-5973 ◽  
Author(s):  
Z. Zhang ◽  
S. Barman ◽  
G. F. Christopher

Model synovial fluid steady shear viscosity to hyaluronic acid solution are identical when interfacial rheology effects are removed.

2012 ◽  
Vol 534 ◽  
pp. 56-60
Author(s):  
Dong Xu ◽  
Qiu Han ◽  
Hui Fang Chen

Adding a mount of MMWPAN to UHMWPAN/DMSO dilute solution is a good way to increase the total PAN content (including MMWPAN and UHMWPAN) while the UHMWPAN content of the solution is hard to be increased. In this paper, the rheological properties of UHMWPAN/MMWPAN/DMSO solution and the role of UHMWPAN in this solution were studied. The complex viscosity (h*) and the steady shear viscosity (h) both increased as the UHMWPAN content rising.


Cells ◽  
2020 ◽  
Vol 9 (7) ◽  
pp. 1606 ◽  
Author(s):  
Weifeng Lin ◽  
Zhang Liu ◽  
Nir Kampf ◽  
Jacob Klein

Hydration lubrication has emerged as a new paradigm for lubrication in aqueous and biological media, accounting especially for the extremely low friction (friction coefficients down to 0.001) of articular cartilage lubrication in joints. Among the ensemble of molecules acting in the joint, phosphatidylcholine (PC) lipids have been proposed as the key molecules forming, in a complex with other molecules including hyaluronic acid (HA), a robust layer on the outer surface of the cartilage. HA, ubiquitous in synovial joints, is not in itself a good boundary lubricant, but binds the PC lipids at the cartilage surface; these, in turn, massively reduce the friction via hydration lubrication at their exposed, highly hydrated phosphocholine headgroups. An important unresolved issue in this scenario is why the free HA molecules in the synovial fluid do not suppress the lubricity by adsorbing simultaneously to the opposing lipid layers, i.e., forming an adhesive, dissipative bridge between them, as they slide past each other during joint articulation. To address this question, we directly examined the friction between two hydrogenated soy PC (HSPC) lipid layers (in the form of liposomes) immersed in HA solution or two palmitoyl–oleoyl PC (POPC) lipid layers across HA–POPC solution using a surface force balance (SFB). The results show, clearly and surprisingly, that HA addition does not affect the outstanding lubrication provided by the PC lipid layers. A possible mechanism indicated by our data that may account for this is that multiple lipid layers form on each cartilage surface, so that the slip plane may move from the midplane between the opposing surfaces, which is bridged by the HA, to an HA-free interface within a multilayer, where hydration lubrication is freely active. Another possibility suggested by our model experiments is that lipids in synovial fluid may complex with HA, thereby inhibiting the HA molecules from adhering to the lipids on the cartilage surfaces.


2010 ◽  
Vol 152-153 ◽  
pp. 924-930
Author(s):  
Mei Li ◽  
Zhi Qiang Li ◽  
Jun Xu ◽  
Dun Sheng Wei ◽  
Hong Wei Zhu ◽  
...  

Modified Poly(3-hydroxybutyrate-co-4-hydroxybutyrate) [P(3HB-co-4HB)] was prepared by melt reactive blending P(3HB-co-4HB) with chain extenders (ADR-4367). Thermal transitions, spherulitic and freeze-fracture morphology, mechanical and rheological properties of the chain extended bio-materials were investigated. The results show that glass transition temperatures and crystallization temperatures increase, crystallinity and diameters of spherulites decrease, there are amorphous parts dispersed among the crystalline phase, and the bio-materials transfer from brittleness to toughness and ductility. Steady shear viscosity of the modified P(3HB-co-4HB) increases by about one order of magnitude, melts of the modified P(3HB-co-4HB) behave more viscoelasticity by storage modulus and loss modulus correlated with oscillatory shear frequency. Addition of ADR-4367 with contents of 4~6 wt% in the blends is enough to branching and coupling the co-polymer chains and brings remarkable effect on improving mechanical properties, steady shear viscosity and viscoelasticity.


2020 ◽  
Vol 142 (11) ◽  
Author(s):  
Elizabeth Feeney ◽  
Devis Galesso ◽  
Cynthia Secchieri ◽  
Francesca Oliviero ◽  
Roberta Ramonda ◽  
...  

Abstract Inferior synovial lubrication is a hallmark of osteoarthritis (OA), and synovial fluid (SF) lubrication and composition are variable among OA patients. Hyaluronic acid (HA) viscosupplementation is a widely used therapy for improving SF viscoelasticity and lubrication, but it is unclear how the effectiveness of HA viscosupplements varies with arthritic endotype. The objective of this study was to investigate the effects of the HA viscosupplement, Hymovis®, on the lubricating properties of diseased SF from patients with noninflammatory OA and inflammatory arthritis (IA). The composition (cytokine, HA, and lubricin concentrations) of the SF was measured as well as the mechanical properties (rheology, tribology) of the SF alone and in a 1:1 mixture with the HA viscosupplement. Using rotational rheometry, no difference in SF viscosity was detected between disease types, and the addition of HA significantly increased all fluids' viscosities. In noninflammatory OA SF, friction coefficients followed a typical Stribeck pattern, and their magnitude was decreased by the addition of HA. While some of the IA SF also showed typical Stribeck behavior, a subset showed more erratic behavior with highly variable and larger friction coefficients. Interestingly, this aberrant behavior was not eliminated by the addition of HA, and it was associated with low concentrations of lubricin. Aberrant SF exhibited significantly lower effective viscosities compared to noninflammatory OA and IA SF with typical tribological behavior. Collectively, these results suggest that different endotypes of arthritis exist with respect to lubrication, which may impact the effectiveness of HA viscosupplements in reducing friction.


1999 ◽  
Vol 30 (5) ◽  
pp. 549-561
Author(s):  
D. M. MUN ◽  
T.-T. HSIEH ◽  
C. TIU ◽  
B. J. SUTHERLAND

Sign in / Sign up

Export Citation Format

Share Document