Pawlak Zenon, Oloyede Adekunle
Queensland University of Technology, School of Engineering Systems, Brisbane, Australia.
Biosystems. 2008 Dec;94(3):193-201. doi: 10.1016/j.biosystems.2008.05.028. Epub 2008 Jul 31.
Phospholipid (PL) molecules form the main structure of the membrane that prevents the direct contact of opposing articular cartilage layers. In this paper we conceptualise articular cartilage as a giant reverse micelle (GRM) in which the highly hydrated three-dimensional network of phospholipids is electrically charged and able to resist compressive forces during joint movement, and hence loading. Using this hypothetical base, we describe a hydrophilic-hydrophilic (HL-HL) biopair model of joint lubrication by contacting cartilages, whose mechanism is reliant on lamellar cushioning. To demonstrate the viability of our concept, the electrokinetic properties of the membranous layer on the articular surface were determined by measuring via microelectrophoresis, the adsorption of ions H, OH, Na and Cl on phospholipid membrane of liposomes, leading to the calculation of the effective surface charge density. The surface charge density was found to be -0.08+/-0.002cm(-2) (mean+/-S.D.) for phospholipid membranes, in 0.155M NaCl solution and physiological pH. This value was approximately five times less than that measured in 0.01M NaCl. The addition of synovial fluid (SF) to the 0.155M NaCl solution reduced the surface charge density by 30% which was attributed to the binding of synovial fluid macromolecules to the phospholipid membrane. Our experiments show that particles charge and interact strongly with the polar core of RM. We demonstrate that particles can have strong electrostatic interactions when ions and macromolecules are solubilized by reverse micelle (RM). Since ions are solubilized by reverse micelle, the surface entropy influences the change in the charge density of the phospholipid membrane on cartilage surfaces. Reverse micelles stabilize ions maintaining equilibrium, their surface charges contribute to the stability of particles, while providing additional screening for electrostatic processes.
磷脂(PL)分子构成了防止相对的关节软骨层直接接触的膜的主要结构。在本文中,我们将关节软骨概念化为一个巨大的反胶束(GRM),其中高度水合的磷脂三维网络带有电荷,并且能够在关节运动以及因此产生的负荷过程中抵抗压缩力。基于这个假设基础,我们描述了一种通过接触软骨进行关节润滑的亲水 - 亲水(HL - HL)生物对模型,其机制依赖于层状缓冲。为了证明我们概念的可行性,通过微电泳测量脂质体磷脂膜上离子H、OH、Na和Cl的吸附,从而计算有效表面电荷密度,以此确定关节表面膜层的电动性质。在0.155M NaCl溶液和生理pH条件下,发现磷脂膜的表面电荷密度为 -0.08±0.002cm⁻²(平均值±标准差)。这个值大约比在0.01M NaCl中测量的值小五倍。向0.155M NaCl溶液中添加滑液(SF)使表面电荷密度降低了30%,这归因于滑液大分子与磷脂膜的结合。我们的实验表明颗粒带电并与反胶束的极性核心强烈相互作用。我们证明当离子和大分子被反胶束(RM)溶解时,颗粒可以有强烈的静电相互作用。由于离子被反胶束溶解,表面熵影响软骨表面磷脂膜电荷密度的变化。反胶束稳定离子以维持平衡,它们的表面电荷有助于颗粒的稳定性,同时为静电过程提供额外的屏蔽。