<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJO</journal-id><journal-title-group><journal-title>Open Journal of Orthopedics</journal-title></journal-title-group><issn pub-type="epub">2164-3008</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojo.2021.1112037</article-id><article-id pub-id-type="publisher-id">OJO-114275</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  The Impact of pH and Air on the Phospholipid Nanostructure Surface
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>M.</surname><given-names>Sojka</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Z.</surname><given-names>Pawlak</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Tribochemistry Consulting, Salt Lake City, UT 84117, USA</addr-line></aff><aff id="aff1"><addr-line>Mechanical Department, Kujawy University, Grudziadz, Poland</addr-line></aff><pub-date pub-type="epub"><day>06</day><month>12</month><year>2021</year></pub-date><volume>11</volume><issue>12</issue><fpage>392</fpage><lpage>398</lpage><history><date date-type="received"><day>21,</day>	<month>October</month>	<year>2021</year></date><date date-type="rev-recd"><day>27,</day>	<month>December</month>	<year>2021</year>	</date><date date-type="accepted"><day>30,</day>	<month>December</month>	<year>2021</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Phospholipids (PLs) in the form of nanostructures are widely employed as a lubricant and antimicrobial agent. The cartilage (AC) surface was characterized using wettability test fresh and depleted AC samples. Cartilage wet surface exposure to air causes increase 
  in 
  surface wettability from 0 to 104 degrees. Effect is explained by flip-flop of the PLs molecules in membrane. The hydrophilic and hydrophobic character of cartilage was determined. Microscopic image of PLs bilayers adsorbed on the surface of pleural tissues and human stomach will be compared with cartilage tissue.
 
</p></abstract><kwd-group><kwd>PLs Bilayers</kwd><kwd> Wettability</kwd><kwd> PLs Flip-Flop</kwd><kwd> Pleural</kwd><kwd> Cartilage Surface</kwd><kwd> Human Stomach Tissue</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The phospholipids (PLs) in human body [<xref ref-type="bibr" rid="scirp.114275-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.114275-ref2">2</xref>] create bilayers and multilayer structures in many places where friction occurs (see Figs. below). The past two decades Hills introduced pioneer model joint lubrication with phospholipid multi-bilayers as lubricantthe surface amorphous layer (SAL). The amphoteric cartilage surface in aqueous media is hydrophilic with wettability ~0˚ and in dry-air condition is hydrophobic with wettability 104˚ [<xref ref-type="bibr" rid="scirp.114275-ref2">2</xref>]. Hills’ lubrication model was well documented by microscopic image of PLs bilayers adsorbed on the surface of (a) pleural tissues, (b) knee joint, (c) human stomach [<xref ref-type="bibr" rid="scirp.114275-ref3">3</xref>] and by analytical determination PLs bilayer numbers on tissue surfaces.</p><p>Phospholipids as lubricants are spontaneously self-assembled biomolecules in an aqueous environment and their structures (hydrophilic/hydrophobic) allow the formation of liposomes, lamellar phases, and membranes (<xref ref-type="fig" rid="fig1">Figure 1</xref>). The (SAL) with porosity (75% to 80%) covers the cartilage, which ensures excellent moisturizing (hydrating) properties.</p><p>Surface-active phospholipid molecules (SAL) adsorbed on the articular cartilage on the negatively charged proteoglycan layer form a phospholipid multibilayer (membrane). The PL bilayer has a negatively charged surface ( -PO 4 − ) and is hydrophilic at pH ~7.4.</p><p>The Hills’ hydrophobic model has been reviewed as erroneous, which will be based on current research [<xref ref-type="bibr" rid="scirp.114275-ref2">2</xref>]. The hydrophobic AC surface has not gained any support in experimental facts and current literature showing that AC is amphoteric and hydrophilic with a negatively charged surface ( -PO 4 − ) [<xref ref-type="bibr" rid="scirp.114275-ref2">2</xref>].</p><p>The surface energy of the model membrane of spherical lipid bilayer vs. pH defends amphoteric property and has the course of the “bell curve” with maximum IEP at pH ~4.0 and the lowest surface energy in the natural joints for pH 6.5 to 9.0 [<xref ref-type="bibr" rid="scirp.114275-ref2">2</xref>].</p><p>This part of the study aimed to show that the wettability of the amphoteric surface of phospholipid bilayers is changing and is an essential parameter of this tissue. Phospholipid bilayers adsorbed on the surface of articular cartilage reduce friction to surprisingly low values [<xref ref-type="bibr" rid="scirp.114275-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.114275-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.114275-ref4">4</xref>]. The surface in many animal organs is capable of adsorbing the surface-active phospholipids as a barrier against adhesion, corrosion, and microorganisms and in the case of cartilage, the phospholipids are involved in the lubrication. The surface so coated has a different wettability depending on the number of bilayers [<xref ref-type="bibr" rid="scirp.114275-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.114275-ref3">3</xref>].</p><p>In this paper, we examine wettability of bovine cartilage (BC) surface in air- dry condition.</p></sec><sec id="s2"><title>2. Experimental</title><p>The articular cartilage specimens were collected from bovine knees aged ~1.5 years. Osteochondral plugs, of 10 mm in diameter, were harvested from lateral and medial femoral condyles. The cartilage discs were cut into 3-mm plugs with full attachment to the underlying bone. The specimens were stored at 253 K in 0.155M NaCl (pH = 6.9) and fully defrosted prior to testing.</p>Wettability Measurements<p>A KSV CAM100 computerized tensiometer was used to measure the contact angle of cartilage samples. A drop of the 0.155M saline solution was deposited on the air-dry cartilage surface. The tests on the normal, partial and completely depleted cartilage samples were repeated five times. Delipidation operation is the removal of lipids from cartilage surface using (chloroform/methanol (2:1, v/v).</p></sec><sec id="s3"><title>3. Results and Discussion</title><p>After evaporation of water from the cartilage surface, the phosphate groups ( -PO 4 − ) are deactivated as a result of conformational changes on the surface (flip- flop) of phospholipid molecules, <xref ref-type="fig" rid="fig2">Figure 2</xref>(b), <xref ref-type="fig" rid="fig2">Figure 2</xref>(c). Hydrophilic bilayer <xref ref-type="fig" rid="fig2">Figure 2</xref>(b) in wet state and after air-dry time turns into a hydrophobic monolayer. The results obtained for all wettability test are presented in <xref ref-type="fig" rid="fig2">Figure 2</xref>(d): Curve: 1) after 19-minute cartilage delipidation (chloroform/methanol (2:1, v/v),</p><p>contact angle is 40˚; 2) after 9 minutes of delipidation, contact angle 63˚, 3) after 3 minutes of delipidation, contact angle is 73˚, 4) the contact angle of the healthy cartilage surface is 104˚. The degradation of the surface of bovine cartilage from super hydrophilic (contact angle ~0˚) to a hydrophobic monolayer is expressed by an increase in surface energy [<xref ref-type="bibr" rid="scirp.114275-ref2">2</xref>].</p><p>Poor lubrication in animal joints, particularly on the articular surface of cartilage, can be attributed to deterioration of the bilayer surface, where the wettability or contact angle (θ) changes from ~100˚ (healthy) to less than 70˚ (unhealthy).</p><p>The smart-surface of articular cartilage constitution of the superficial phospholipid bilayer in (a) aqueous electrolyte solution and (b) air-dry conditions. A change in surface energy leads to conformational changes in the surface of the bovine patella from bilayer (super hydrophilic ~0˚ contact angle) to monolayer (hydrophobic ~100˚).</p><p><xref ref-type="fig" rid="fig3">Figure 3</xref> shows microscopic images of the stomach, cartilage and pleural surfaces [<xref ref-type="bibr" rid="scirp.114275-ref3">3</xref>]. In the case of the stomach with several bilayers for pH &lt; 1 and strong adsorption of phosphatidylcholine quaternary ammonium ion (Me)<sub>3</sub>N<sup>+</sup>-) (see <xref ref-type="fig" rid="fig2">Figure 2</xref>(a) for general structural formula of phosphatidylcholines), which interacts with the negatively charged surface of the stomach and forms a hydrophobic monolayer on the surface. A consistent phospholipid monolayer with a Ca (II) bond between groups ( -PO 4 − ) is created. Consistency of phospholipids at a very low pH prevailing in the stomach becomes a necessity, <xref ref-type="fig" rid="fig4">Figure 4</xref>(a) [<xref ref-type="bibr" rid="scirp.114275-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.114275-ref6">6</xref>].</p><p>The formation of a hydrophobic monolayer was observed in the presence of</p><p>an air/liquid phase at pH 7.4 for the pleural and for pH &lt; 1 for the stomach (see <xref ref-type="fig" rid="fig4">Figure 4</xref>(c) and <xref ref-type="fig" rid="fig4">Figure 4</xref>(a). The model in <xref ref-type="fig" rid="fig4">Figure 4</xref>(c) shows pleural surfaces with a thin layer of tightly packed hydrocarbon chains comparable to that of a hydrophobic stomach. <xref ref-type="fig" rid="fig4">Figure 4</xref>(b) presents the surface of the cartilage with a hydrophilic bilayer structure.</p><p>The stomach model shown in <xref ref-type="fig" rid="fig4">Figure 4</xref>(c) has the following characteristics:</p><p>- The hydrophobic protective phospholipid monolayer is the physical barrier called by Davenport [<xref ref-type="bibr" rid="scirp.114275-ref8">8</xref>] “gastric mucosal barrier”;</p><p>- PL molecules are directly adsorbed on the surface of the gastric mucosa, originally attached by electrostatic attraction between the of phosphatidylcholine quaternary ammonium ion (Me)<sub>3</sub>N<sup>+</sup>-) and the negatively charged membrane. The mean angle of wettability is 85˚ for the surface of the gastric mucosa [<xref ref-type="bibr" rid="scirp.114275-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.114275-ref9">9</xref>].</p><p>The phospholipid monolayer adsorbed on the surface of the mucous membrane contains a protonated phosphate group (-PO<sub>4</sub>H) that is not ionized in the stomach at pH &lt; 1, but is ionized at physiological pH 7.4 (see equation below) [<xref ref-type="bibr" rid="scirp.114275-ref4">4</xref>].</p><p>( Me 3 N + ) ( CH 2 ) 2 PO 4 H-R 1 R 2 pH   &lt;   1 ⇄ ( Me 3 N + ) ( − OH ) ( CH 2 ) 2 PO 4 − -R 1 R 2 pH7 . 4</p><p>The amine functional group of phosphatidylethanolamine (PE) for pH 7.4 is uncharged by a functional group (-NH<sub>2</sub>): ( -NH 3 + ) + OH<sup>−</sup> → -NH<sub>2</sub> + H<sub>2</sub>O). In the case of phosphatidylcholine, a quaternary ammonium ion for pH 7.4 will form ion pair with hydroxide ion (Me<sub>3</sub>N<sup>+</sup>-OH<sup>−</sup>) and will be adsorbed or electrostatically interact with the hydrophilic surface; the ion pair association constant is: K<sub>ass</sub> ~ 5 &#215; 10<sup>5</sup> [<xref ref-type="bibr" rid="scirp.114275-ref10">10</xref>]. Strong adsorption and cohesion are essential parameters for surface-active phospholipids with a strong adsorption of cationic quaternary ammonium ion (QA) on the hydrophilic surface and the presence of the phosphate-bond cohesive barrier with the Ca (II) cation.</p><p>According to Linn and Sokoloff [<xref ref-type="bibr" rid="scirp.114275-ref11">11</xref>] “the secret of low friction (cartilage/car- tilage) is the fact that the surfaces do not touch” and phospholipids participate in the lamellar lubrication mechanism [<xref ref-type="bibr" rid="scirp.114275-ref12">12</xref>]. Phospholipids are spontaneously self- assembled biomolecules in liposomes and under load (pressure) transformed in lamellar phases bilayers and membrane (see <xref ref-type="fig" rid="fig1">Figure 1</xref>). The phospholipid bilayers on the surface of the cartilage are called the surface amorphous layer (SAL). A negatively charged surface by phospholipid group ( -PO 4 − ) and very high cartilage porosity (75% to 80%) provides excellent hydration properties of the articular cartilage [<xref ref-type="bibr" rid="scirp.114275-ref1">1</xref>]. Hydrophilic cartilage surfaces are negatively charged, they repel electrostatically with the participation of lamellar PLs phases (see <xref ref-type="fig" rid="fig1">Figure 1</xref>), the glycoprotein lubricin, hydrated hyaluronan macromolecules are under almost instant contactless pressure [<xref ref-type="bibr" rid="scirp.114275-ref13">13</xref>].</p></sec><sec id="s4"><title>4. Conclusion</title><p>In this work, we demonstrated that PLs the stomach membrane surfaces at pH &lt; 1 are hydrophobic uncharged, and at pH ~7 cartilage is hydrophilic and negatively charged, and pleural surface is hydrophobic at air condition. The cartilage surface was characterized using wettability test fresh and depleted AC samples.</p></sec><sec id="s5"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s6"><title>Cite this paper</title><p>Sojka, M. and Pawlak, Z. (2021) The Impact of pH and Air on the Phospholipid Nanostructure Surface. Open Journal of Orthopedics, 11, 392-398. https://doi.org/10.4236/ojo.2021.1112037</p></sec></body><back><ref-list><title>References</title><ref id="scirp.114275-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Hills, B.A. (1988) The Biology of Surfactant. Cambridge University Press, London.</mixed-citation></ref><ref id="scirp.114275-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Pawlak, Z. (2018) Articular Cartilage: Lamellar-Repulsive Lubrication of Natural Joints. KDP. Print-Book: https://www.amazon.com/dp/1976760283 e-book: https://www.amazon.com/dp/B07B42P1JY</mixed-citation></ref><ref id="scirp.114275-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Hills, B.A. (2002) Surface-Active Phospholipid: A Pandora’s Box of Clinical Applications, Part II. Barrier and Lubricating Properties. Internal Medicine Journal, 32, 242-251. https://doi.org/10.1046/j.1445-5994.2002.00201.x</mixed-citation></ref><ref id="scirp.114275-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Hills, B.A and Butler, B.D. (1984) Surfactants Identified in Synovial Fluid and Their Ability to Act as Boundary Lubricants. Annals of the Rheumatic Diseases, 43, 641-648. https://doi.org/10.1136/ard.43.4.641</mixed-citation></ref><ref id="scirp.114275-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Mre&amp;lstrok;a, A. and Pawlak, Z. (2019) Articular Cartilage. Strong Adsorption and Cohesion of Phospholipids with the Quaternary Ammonium Cations Providing Satisfactory Lubrication, of Natural Joints. Biosystems, 176, 27-31. https://doi.org/10.1016/j.biosystems.2018.12.005</mixed-citation></ref><ref id="scirp.114275-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Mre&amp;lstrok;a, A. and Pawlak, Z. (2018) Articular Cartilage: Chemical, Physical, and Tribological Properties. Journal of New Developments in Chemistry, 1, 7-11. https://doi.org/10.14302/issn.2377-2549.jndc-18-2159</mixed-citation></ref><ref id="scirp.114275-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Mre&amp;lstrok;a, A. and Pawlak, Z. (2018) Articular Cartilage: Amphoteric Nature and Interfacial Energy. Journal of Clinical and Molecular Medicine, 1, 1-2. https://doi.org/10.15761/JCMM.1000114</mixed-citation></ref><ref id="scirp.114275-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Davenport, H.W. (1965) Is the Apparent Hyposecretion of Acid by Patients with Gastric Ulcer a Consequence of Broken Barrier to Diffusion of Hydrogen Ions into the GASTRIC mucosa? Gut, 6, 513. https://doi.org/10.1136/gut.6.5.513</mixed-citation></ref><ref id="scirp.114275-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Hills, B.A. and Crawford, R.W. (2003) Normal and Prosthetic Synovial Joints Are Lubricated by Surface-Active Phospholipid: A Hypothesis. Journal of Arthroplasty, 18, 499-505. https://doi.org/10.1016/S0883-5403(03)00072-X</mixed-citation></ref><ref id="scirp.114275-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Petelska, A.D. and Figaszewski, Z.A. (2002) Effect of pH on the Interfacial Tension of Bilayer Lipid Membrane Formed from Phosphatidylcholine or Phosphatidylserine. Biochimica et Biophysica Acta (BBA)—Biomembranes, 1561, 135-146. https://doi.org/10.1016/S0005-2736(01)00463-1</mixed-citation></ref><ref id="scirp.114275-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Linn, F.C. and Sokoloff, L. (1965) Movement and Composition of Interstitial Fluid of Cartilage. Arthritis and &amp; Rheumatism, 8, 481-494. https://doi.org/10.1002/art.1780080402</mixed-citation></ref><ref id="scirp.114275-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Mrela, A. and Pawlak, Z. (2018) Hydrophilic and Charged Cartilage Surface for Reducing the Friction Coefficient. Frontiers in Nanoscience and Nanotechnology, 4, 1-3. https://doi.org/10.15761/FNN.1000175</mixed-citation></ref><ref id="scirp.114275-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Israelachvili, J.N. and Wennerstrom, H. (1996) Role of Hydration and Water Structure in Biological and Colloidal Interactions. Nature, 379, 219-225. https://doi.org/10.1038/379219a0</mixed-citation></ref></ref-list></back></article>