The Folin-Ciocalteau (F-C) method of assay is the simplest method available for the measurement of phenolic content in products. It is a development of Folin Denis reagent used in the early 19th century for the determination of tyrosine in proteins [1]. F-C reagent can be prepared by dissolving 100 g sodium tungstate (VI) dihydrate and 25 g sodium molybdate (VI) dihydrate with 700 ml distilled water, 100 ml concentrated hydrochloric acid, and 50 ml of 85% phosphoric acid to which is added 150 g of lithium sulphate hydrate. This reagent is very stable if protected from reductants and even when diluted if protected from light. For many years now, the F-C method of assay has been in use as a measure of polyphenol in natural products, and the basic mechanism is an oxidation/ reduction reaction with the phenolic group being oxidized and the metal ion reduced. Chemistry controlling the reaction with Folin-Ciocalteau reagentFolin-Ciocalteau phenol reagent consists of a mixture of the heteropoly acids, phosphomolybdic and phosphotungstic acids in which the molybdenum and the tungsten are in the 6+ oxidation state. On reaction with a reductant, the molybdenum blue and the tungsten blue are formed and the mean oxidation state of the metals is between 5 and 6. Na 2 WO 4 /Na 2 MO 4 yellow⇒ (Phenol-MoW 11 O 40 ) -4 blue Mo +6 (yellow) + e -1 ⇒ Mo +5 (blue) Mo +5 + e -1 ⇒ Mo +4 (blue) ØOH ⇒ ØO • + H +1The above reaction is slow at acidic pH and faster when basic. It is very sensitive, precise but lack specificity. Singleton and Rossi [2] further improved the method with a molybdotungstophosphoric heteropolyanion reagent that reduced polyphenols more specifically with the λ max for the product at 765 nm.To achieve meaningful, reliable and predictable results, some conditions such as proper volume ratio, optimal reaction time, and temperature for colour development, standard optical density, and use of a particular reference-standard polyphenol are required.The improved method F-C reagent can be used by two principal procedures for the measurement of polyphenolic content i.e. as dual reagent [2,3] and as single reagent [4,5].

These findings have implications for improving the structural integrity of the repaired enthesis and potentially reducing the retear rate after rotator cuff repair, which can ultimately lead to improvements in clinical outcomes.

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Templating of cell spreading and proliferation is described that yields confluent layers of cells aligned across an entire two-dimensional surface. The template is a reactive, two-component interface that is synthesized in three steps in nanometer thick, micron-scaled patterns on silicon and on several biomaterial polymers. In this method, a volatile zirconium alkoxide complex is first deposited at reduced pressure onto a surface pattern that is prepared by photolithography; the substrate is then heated to thermolyze the organic ligands to form surface-bound zirconium oxide patterns. The thickness of this oxide layer ranges from 10 to 70 nanometers, which is controlled by alkoxide complex deposition time. The oxide layer is treated with 1,4-butanediphosphonic acid to give a monolayer pattern whose composition and spatial conformity to the photolithographic mask are determined spectroscopically. NIH 3T3 fibroblasts and human bone marrow-derived mesenchymal stem cells attach and spread in alignment with the pattern without constraint by physical means or by arrays of cytophilic and cytophobic molecules. Cell alignment with the pattern is maintained as cells grow to form a confluent monolayer across the entire substrate surface.

Surface damage to articular cartilage is recognized as the initial underlying process causing the loss of mechanical function in early-stage osteoarthritis. In this study, we developed structure-modifying treatments to potentially prevent, stabilize or reverse the loss in mechanical function. Various polymers (chondroitin sulfate, carboxymethylcellulose, sodium hyaluronate) and photoinitiators (riboflavin, irgacure 2959) were applied to the surface of collagenase-degraded cartilage and crosslinked in situ using UV light irradiation. While matrix permeability and deformation significantly increased following collagenase-induced degradation of the superficial zone, resurfacing using tyramine-substituted sodium hyaluronate and riboflavin decreased both values to a level comparable to that of intact cartilage. Repetitive loading of resurfaced cartilage showed minimal variation in the mechanical response over a 7 day period. Cartilage resurfaced using a low concentration of riboflavin had viable cells in all zones while a higher concentration resulted in a thin layer of cell death in the uppermost superficial zone. Our approach to repair surface damage initiates a new therapeutic advance in the treatment of injured articular cartilage with potential benefits that include enhanced mechanical properties, reduced susceptibility to enzymatic degradation and reduced adhesion of macrophages.