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  • Polymer and Materials Science  (28)
  • Proteoglycans  (5)
  • General Chemistry  (4)
  • 1
    Electronic Resource
    Electronic Resource
    The inhibitory effect of cartilage proteoglycans on hydroxyapatite growth (1984)
    Springer
    Calcified tissue international 36 (1984), S. 285-290 
    Details
    ISSN: 1432-0827
    Keywords: Proteoglycans ; Chondroitin 4-sulfate ; Neutral dextran ; Hydroxyapatite growth
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary The calcification of connective tissues, including cartilage, is under the control of many interacting systems. Proteoglycans are thought to retard the deposition of hydroxyapatite crystals, and modification of the proteoglycans presumably facilitates mineralization in those tissues that are actively calcifying. The mechanism underlying these regulations remains speculative. This study investigates this question by comparing the inhibitory effectiveness of several macromolecules at neutral pH and approximately physiological ionic strengths. Inhibitors tested include bovine nasal proteoglycan monomer A1D1D1 and aggregate-containing A1 fractions, glycosaminoglycan chains (chondroitin 4-sulfate), and neutral dextran (as an uncharged analog). Hydroxyapatite growth was assessed either by measuring the time-dependent decreases in solution calcium and phosphate concentrations, or by determining utilization of hydroxyl ion in a pH-Stat. All species studied inhibit hydroxyapatite growth, and the extent of inhibition for each class is concentration-dependent. The proteoglycan aggregate-containing A1 fraction is more effective than the proteoglycan monomer at the same concentration, and the proteoglycan monomer is more effective than chondroitin 4-sulfate. Neutral dextran inhibits hydroxyapatite growth less effectively than proteoglycans. These results suggest that inhibition of hydroxyapatite growth by proteoglycans critically depends on both status (aggregate, monomer, etc.) and hydrodynamic size of this macromolecule, supporting the hypothesis that modification of proteoglycansin vivo functions to modulate the effectiveness of proteoglycans as a hydroxyapatite growth inhibitor.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02405332
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  • 2
    Electronic Resource
    Electronic Resource
    Effect of proteoglycans on in vitro hydroxyapatite formation (1979)
    Springer
    Calcified tissue international 27 (1979), S. 75-82 
    Details
    ISSN: 1432-0827
    Keywords: Proteoglycans ; Hydroxyapatite ; Amorphous calcium phosphate ; Nucleation ; Calcification
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Well-characterized bovine nasal proteoglycan A1 fraction (aggregate) and proteoglycan D1 fraction (subunit) have been shown to be effective inhibitors of hydroxyapatite (HA) formation in two in vitro test systems: (a) the transformation of amorphous calcium phosphate (ACP) to crystalline HA, and, (b) the direct precipitation of HA from low-concentration calcium phosphate solutions. A1 or D1 in solution slowed the transformation kinetics in system (a) without affecting the time to the onset of conversion. In system (b), A1 or D1 in solution increased the time to the onset of HA formation without affecting the HA formation kinetics. In both test systems A1 was a more effective inhibitor than D1, although the difference was not great. In both systems the inhibitory effect was proportional to the A1 or D1 solution concentration. The action of solutions of low and high molecular weight neutral dextrans on both test systems showed that high molecular weight and/or extended spatial molecular conformation has a much stronger correlation with inhibitory ability than solution viscosity. Proteoglycans have been implicated as playing a role in regulating biological mineralization particularly in the epiphyseal growth plate. Our study suggests that just enzymatic cleavage of aggregate into subunit is not sufficient to allow mineralization to occur, since we find that D1 itself is a potent inhibitor of HA formation. Further degradation and/or removal of D1 appears to be necessary for calcification to take place.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02441164
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  • 3
    Electronic Resource
    Electronic Resource
    Histologic identification of polyethylene wear debris using Oil Red O stain (1993)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Biomaterials 4 (1993), S. 119-125 
    Details
    ISSN: 1045-4861
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Ultra high molecular weight polyethylene (UHMWPE) wear particles are frequently implicated in causing failure of total joint arthroplasties by eliciting a foreign body reaction. The majority of these particles are subcellular and many are submicron in size. Identification of these small particles of UHMWPE by conventional histologic techniques is difficult. We have therefore investigated the utility of Oil Red O (ORO) stain to identify UHMWPE on histologic sections.A wide variety of specimens was studied including an experimental rabbit model with subcutaneous implantation of polyethylene particles as well as specimens from clinical cases with joint arthroplasties. The sensitivity and specificity of ORO stain was compared to conventional polarized light microscopy for the identification of particulate UHMWPE debris. The ORO stain was found to be as sensitive in identifying particulate UHMWPE debris as polarized light microscopy. However, ORO stain was less specific: two specimens that did not contain any UHMWPE also stained with ORO. Careful examination of standard hematoxylin and eosin stained sections with polarized light was therefore more specific for the identification of particulate UHMWPE. As a single test, the ORO stain does not appear to offer any clear advantage specifically for the identification of UHMWPE. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jab.770040202
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  • 4
    Electronic Resource
    Electronic Resource
    Age-Related changes in cartilage proteoglycans: Quantitative electron microscopic studies (1994)
    New York, NY [u.a.] : Wiley-Blackwell
    Microscopy Research and Technique 28 (1994), S. 398-408 
    Details
    ISSN: 1059-910X
    Keywords: Aging ; Proteoglycans ; Electron microscopy ; Intervertebral disc ; Hyaline cartilage ; Nucleus pulposus ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Biochemical and biophysical studies have shown that the composition and sedimentation velocity of cartilage proteoglycans change with age, but these investigations cannot demonstrate the alterations in molecular structure responsible for these changes. Development of quantitative electron microscopic methods has made it possible to define the age-related structural changes in aggregating proteoglycans and to correlate the alterations in their structure with changes in tissue composition and morphology. Electron microscopic measurement of human and animal hyaline cartilage proteoglycans has shown that with increasing age the length of the chondroitin sulfate-rich region of aggregating proteoglycan monomers (aggrecan molecules) decreases, the variability in aggrecan length increases, the density of aggrecan keratan sulfate chains increases, the number of monomers per aggregate decreases, and the proportion of monomers that aggregate declines. Proteoglycans from the nucleus pulposus of the intervertebral disc show similar but more dramatic age-related alterations. At birth, nucleus pulposus aggrecan molecules are smaller and more variable in length than those found in articular cartilage. Within the first year of human life, the populations of aggregates and large aggrecan molecules analogous to those found in articular cartilage decline until few if any of these molecules remain in the central disc tissues of skeletally mature individuals. The mechanisms of the age-related changes in cartilage proteoglycans have not been fully explained, but measurement of proteoglycans synthesized by chondrocytes of different ages suggests that alterations in synthesis produce at least some of the age-related changes in aggrecan molecules. Degradation of aggrecan chondroitin sulfate-rich regions in the matrix probably also contributes to the structural changes seen by electron microscopy. Age-related changes in proteoglycan aggregation may be due to alterations in link protein function or inhibition of aggregation of newly synthesized aggrecan molecules by accumulation of degraded aggrecan molecules. © 1994 Wiley-Liss, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jemt.1070280506
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  • 5
    Electronic Resource
    Electronic Resource
    Errata (1993)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Biomaterials 4 (1993), S. 363-363 
    Details
    ISSN: 1045-4861
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jab.770040412
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  • 6
    Electronic Resource
    Electronic Resource
    Polyethylene wear debris and tissue reactions in knee as compared to hip replacement prostheses (1994)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Biomaterials 5 (1994), S. 185-190 
    Details
    ISSN: 1045-4861
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Differences in bearing surface conformity and wear mechanisms suggest that the polyethylene (PE) wear debris generated by total knee replacement (TKR) prostheses should be different than that in total hip replacement prostheses (THR). To address this issue, PE wear debris and the cellular response in periprosthetic tissues from 19 failed TKRs was compared to that from 24 failed THRs using polarized light microscopy and a semiquantitative grading system. The foreign-body inflammatory reaction in the THR cases was characterized by plump macrophages with a diffuse cytoplasmic birefringence when examined under polarized light, indicating the presence of multiple submicron particles of PE. The majority of the PE particles were 〈1 μm in size and only a small fraction of the total were 〉10 μm. The foreign-body inflammatory reaction in the TKR cases was characterized by giant cells with fewer macrophages. In the TKR specimens, the size range of PE particles was broader than in the hips. PE particles between 2 and 20 μm were frequent in TKR specimens; particles 〈1 μm in length were less common than in the THR specimens. Diffuse cytoplasmic birefringence was not a characteristic of the TKR cases. These histologic differences were so consistently distinct that the source of the specimen (i.e., from a THR or TKR) could be blindly determined by light microscopy. The size distribution of the PE wear particles in these cases indicate that THRs generate a higher number of submicron PE particles and relatively few large particles while TKRs generate a broader range of particles that includes fewer submicron particles. The observed differences in the cellular responses is likely a direct result of the differences in the spectrum of PE wear particles. These differences may in part account for differences in periprosthetic bone resorption and loosening in TKRs as compared to THRs. © 1994 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jab.770050302
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  • 7
    Electronic Resource
    Electronic Resource
    The sol/gel contribution to the behavior of γ-irradiated poly(vinylidene fluoride) (1991)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 535-541 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Poly(vinylidene fluoride) films were γ-irradiated in the dose range of 1-20 Mrad, resulting in up to 74% gel. The irradiated polymer undergoes both crosslinking and chain scission, about 5 : 3 events, respectively. Swelling measurements indicate an increasing crosslink density with the gel content, already at the lower doses. Thermal analysis of the gel fraction and the unextracted irradiated samples shows that although crosslinking affects the crystallization, degree of crystallinity, and the melting characteristics, the behavior of the crosslinked material is predominantly controlled by the extractable sol fraction which consists of the more mobile original chains, branched chains, and degraded ones. The crosslinks, already at low density, retard the development of ordinary crystalline polymer morphology.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1991.070430314
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  • 8
    Electronic Resource
    Electronic Resource
    Low dose γ-irradiation of some fluoropolymers: Effect of polymer chemical structure (1992)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 783-795 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The effect of low dose (1-20 Mrad) γ-irradiation on five fluoropolymers (PVF, PVDF, ETFE, FEP, PFA), differing in fluorine content and chain structure, was studied. The radiation effect, reflected by changes in thermal and mechanical properties, as well as NaOH etched surface morphology, was investigated. The main chain structure was found to predominate the irradiated polymers' behavior. The tensile strength of PVF and its resistance to etching increased with radiation dose, while its degree of crystallinity and melting temperature decreased. These changes were correlated with network formation by irradiation and by the incorporation of crosslinked segments into the crystalline phase during recrystallization. Solvent extraction of PVDF (no solvents were found for the other fluoropolymers) revealed increased gel formation with increasing dose. The degree of crystallinity and the tensile strength dependence on radiation dose for PVDF and ETFE reflected the competition between crosslinking and chain scission events. FEP and PFA undergo predominantly chain scission accompanied by reduction of their mechanical properties. PFA even exhibited an increase in both its melting temperature and degree of crystallinity, stemming from a massive degradation process forming shorter chains. Chemical mechanisms are discussed in an attempt to correlate the irradiation effects with the polymers' chain structure.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1992.070450504
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  • 9
    Electronic Resource
    Electronic Resource
    Characterization of cured polystyrylpyridine by model compoundsPresented at the 1979 Pacific Conference on Chemistry and Spectroscopy in Pasadena, California on 10-12 October 1979. (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 1975-1987 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The crosslinking or curing reaction of polystyrylpyridine (PSP) has been studied by means of thermal reactions of its model compounds. Compounds 2,6-distyrylpyridine, 4-stilbazole (4-styrylpyridine), and deuterated 4-stilbazole were pyrolyzed at 200-325°C both in air and under vacuum in a sealed tube. The major pyrolysis products were diarylethane and stilbene, and were characterized by gas chromatography-mass spectrometry. Major dimeric products were naphthalene or quinoline derivatives. Mechanisms for the pyrolysis are suggested, and a crosslinked structure for cured PSP is proposed based on the thermal reaction products of model compounds.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070260621
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  • 10
    Electronic Resource
    Electronic Resource
    Transmission of water through a biocompatible polyurethane: Application to circulatory assist devices (1985)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 19 (1985), S. 1181-1202 
    Details
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The permeability characteristics of a water-segmented polyurethane (Biomer) system under the conditions encountered in circulatory-assist devices were investigated. A diffusion cell and permeability system providing precise control of membrane boundary conditions and allowing continuous measurement of water vapor transmission was designed. Liquid water at 37°C was used as the donor fluid and the system incorporated a constant-flow nitrogen carrier gas and an optical dew point sensor downstream to determine the water vapor mass flow rate as a function of time. The mass flow rate was then numerically integrated and plotted against time to allow calculation of effective diffusion coefficient (D) by the dynamic time lag method. Steady-state permeabilities were found to be insensitive to donor chamber hydrostatic pressure (50-200 mm Hg) indicating that bulk flow is not a transport mechanism in these membranes. The permeability coefficient (P) was independent of membrane thickness (H) over the four samples tested (0.0102, 0.0148, 0.0269, and 0.0366 cm), with an average value of 3.29 × 10-4cm2/s. Thus, diffusion was Fickian with negligible boundary layers. A plot of lag time versus H2 was linear (R = 0.98) yielding a value for D of 2.18 × 10-7cm2/s. A water-Biomer partition coefficient was determined for each sample with an average value of 1525, indicating a moderately hydrophilic membrane with a water sorption of 6.3% at 37°C. Since water transport is by Fickian diffusion in the absence of bulk flow, liquid water cannot be expected to accumulate in circulatory-assist devices unless a condensing surface is maintained within the system.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jbm.820190924
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