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  • 1
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract. The release of drugs, entrapped into the poly(allylammonium acrylate) (PAAC) polyelectrolyte complex structure, was tested for vitamin B12 (VitB12) and tetracycline (TCY). The PAAC-drug "composites" were obtained by synthesizing PAAC in the presence of either VitB12 or TCY. Weighed samples of the "composites" were sintered as tablets, which were dipped into Dulbecco's PBS (pH 7.3); the release was followed spectrophotometrically. The tests show very low limiting release values, with different kinetic behaviours for TCY and VitB12. The results are discussed and attributed to strong ionic interactions between the polyelectrolyte complex and the dipolar ions VitB12 and TCY.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-4838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: In this paper we report experimental results from specific biocompatibility tests on two different classes of tri-block poly(ester-ether-ester) copolymers, namely copoly(ε-caprolactone-oxyethylene-ε-caprolactone) and copoly(L-lactide-oxyethylene-L-lactide). In particular, the human umbilical vein endothelial cells (HUVEC) metabolism has been studied in the presence both of the copolymers and of their hydrolytic breakdown products. The release of prostacyclin (PGl2) and angiotensin II (AII) has been measured at different times for copolymers with different composition and hydrophilicity. The results obtained seem to indicate that the block copolymers of both series do not alter the PGI2 and AII release by HUVEC populations in vitro. Similar results are found also after a prolonged contact between the cells and the hydrolytic breakdown products of the copolymers. Furthermore, some of the copolymers studied significantly stimulate the release of either PGI2 or AII. This finding might point towards the use of these copolymers as bioactive materials in the field of cardiovascular devices.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-4838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Poly(ester-ether-ester) block copolymers, belonging to a class of biodegradable materials, were synthesized from poly(ethylene glycol) and ε-caprolactone by a simple ring-opening mechanism, which avoids the use of potentially toxic inorganic or organometallic initiators. The morphological and mechanical properties of such materials were investigated by gelpermeation chromatography, vapour pressure osmometry, proton magnetic resonance, infrared spectroscopy, differential scanning calorimetry, X-ray diffractometry and stress-strain tensile tests. The biocompatibility was investigated by cytotoxicity and hemocompatibility tests; the cytotoxicity was tested by the Neutral Red uptake assay, the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay, the Kenacid Blue R-binding method, and by the cell proliferation test on polymer films; the hemocompatibility was tested by the contact activation both of the coagulation cascade (intrinsic pathway), by the plasma prekallikrein activation test, and of the thrombocytes, by measuring the release of platelet factor 4 and β-thromboglobulin. The experimental results show that such a polymerization process permits high-molecular mass block copolymers with relatively good tensile and mechanical properties to be obtained. Their cyto- and hemo-compatibility makes them suitable for employment as biomaterials.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-4838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Abstract In this paper we report about the biodegradation of tri-block poly (ester-ether-ester) copolymers obtained by reaction of preformed poly (ethylene glycol) (PEG) with two different lactone monomers, i.e. ε-caprolactone (CL) and L-lactide (LA). The two series of copolymers will be indicated as PCL-POE-PCL and PLA-POE-PLA. We identified and measured by HPLC analysis the amount of degradation products of the poly (ester-ether-ester) copolymers; three copolymers were tested for each series during 3–8 week experiments. The experiments were carried out both in the presence and absence of fibroblast cell populations. We evaluated at the same time the decrease of copolymer molecular mass after degradation by means of intrinsic viscosity [η] measurements. From the [η] measurements we can conclude that the higher the hydrophilicity of the material, the faster the rate of decrease of its intrinsic viscosity with time. The HPLC results indicate that the amount of the degradation products, i.e., respectively, the monomers 6-hydroxyhexanoic acid and L-lactic acid, is a function of both hydrophilicity of the molecule and the lateral block length. When the fibroblast cell populations were present in the same wells together with the biodegradable copolymers, signs of cellular metabolism of the degraded monomers were detected.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-4838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Abstract Fibers made by a bioresorbable poly(ε-caprolactone)-block-poly(oxyethylene)-block-poly(ε-caprolactone) copolymer, having a number average molecular mass of about 200 000 Da and an average molar composition of 66% oxycaproyl units and 34% oxyethylene units, were melt-spun, with the aim at using them as suture threads. Their properties were investigated by the stress-strain test and by differential scanning calorimetry (DSC). The results obtained show that the properties of this material depend very strongly on the alignment of its macromolecules. In particular, the only partial alignment, obtainable by a relatively moderate drawing just after the extrusion, leads to values of elongation at break too high for use of the fibers as suture threads. The DSC analysis reveals interesting properties of the material, but also confirms their strong dependence on the extrusion procedure and on the mechanical treatment. In conclusion, the results of this preliminary study show that the spinning technique must be improved, and that further investigations are necessary to ascertain the possibility of using these poly(ester-ether-ester)s for the fabrication of suture threads. © 1999 Kluwer Academic Publishers
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1573-4838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Abstract Biomembranes are frequently proposed as devices for “guided bone regeneration.” Such membranes consist generally of a thin sheet of polymeric material, mostly textured from polymeric yarns or clots, which all have a diffuse very fine winding porosity. The cross-section size of the holes of such porosity is nanometric (diameter 〈 0.1 μm); thus these holes can be indicated as nanoholes. Whatever the method of production, the surface density of nanoholes (number per square centimeter) has to be as high as possible. It is important also that no variation of this density occurs. The fine dimension of these microholes allows the crossing of small molecules (O2, CO2, H2O, sugars, many nutritional organic compounds and even some simple proteins) but not other larger molecules and particulates, including cells of any kind. These biomembranes have, consequently, a semipermeable behavior, providing the functional role which is the interposition of a barrier for the cells, separating the bone from the surrounding soft tissues. The kinetic of proliferation of osteoblasts is lower than that of fibroblasts. Most membranes of this kind are not resorbable. The main problem for the resorbable ones is the speed of size increase of the holes during the time. Their diameter must not exceed a threshold value until the reconstruction of bone is complete, otherwise soft tissue cells will invade the growing bone tissue with formation of undesirable mixed tissue. The present paper deals with a resorbable membrane made with a composite polymer/ceramic. A poly(ɛ-caprolactone)-block-poly(oxyethylene)-block-poly(ɛ-caprolactone) copolymer is the polymeric matrix which contains dispersed ceramic hydroxyapatite microgranules, a stiff filling additive. The main possible use is that of periodontal membranes. The copolymer, obtained by thermal polymerization of ɛ-caprolactone onto poly(ethylene-glycol), presents good biological tolerance, is resorbable under physiological conditions and can promote cell growth. Histological tests, performed 6 months after implantation, showed that the polymeric matrix is almost totally resorbed. New-formed bone colonizes even the innermost parts of the membrane, with bone trabeculae closely surrounding the hydroxyapatite granules. © 1999 Kluwer Academic Publishers
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1573-4838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Abstract Composite materials were prepared by mixing in different proportions of hydroxyapatite (HA) and poly(ε-caprolactone-oxyethylene-ε-caprolactone) block copolymer (PCL-POE-PCL) to produce a new resorbable material for biomedical applications. This material has proved to be very interesting for production of periodontal membranes. Mechanical properties are linearly proportional to the amount of HA introduced. Fourier transform infrared (FTIR) investigations have pointed out that HA is able to influence some close ε-caprolactone molecules to start its homopolymerization giving PCL with an end chain ionic bonding. HA grains are therefore surrounded by a film of PCL which grants close connection of HA grains within copolymeric matrix. This interface bond with PCL is, however, an interesting occurrence for preparations of HA/PCL composites. ©1999 Kluwer Academic Publishers
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1573-4838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Poly (L-lactide)-poly (oxyethylene)-poly (L-lactide) block copolymers obtained in bulk, by a ring opening mechanism, from poly (ethylene glycol)s (PEG)s and L-lactide (LA), at 120–140°C, in the absence of added catalysts are described. By using PEGs with different molecular masses, 3000 and 35000, respectively, and varying the initial molar ratio LA to PEG, two series of copolymers with different molecular masses, relative length of blocks and hydrophilicity were obtained. Physico-chemical characterization of the copolymers had been previously performed. The morphological characteristics of the copolymers were investigated by means of X-ray diffractometry, optical and scanning electron microscopy. The biological properties of the materials were determined by evaluating their cytotoxicity, cytocompatibility, hemocompatibility and degradability using different standard tests. The results obtained indicate that the block copolymers synthesized may be useful for biomedical applications, in particular as resorbable drug vehicles. The materials are brittle and their mechanical properties are not appropriate for implant devices.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Cytotechnology 11 (1993), S. S137 
    ISSN: 1573-0778
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract In vitro cytotoxicity (Neutral Red uptake, Kenacid Blue and MTT) and cytocompatibility (cell adhesion and proliferation) tests were applied to the biocompatibility study of a series of poly(ester-ether-ester) block copolymers of potential interest as biomaterials. Our results indicate that the copolymer extracts after 72 hours incubation with a 3T3 mouse fibroblast cell line do not induce significant toxic effects. Furthermore, human umbilical vein endothelial cells seeded on thin copolymer films show a normal pattern of growth. We conclude that thein vitro tests used are a valid instrument to evaluate the potential toxic action of synthetic materials on different cell compartments and that the tested materials seem to be promising for future applications in the field of biomedical devices.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 9 (1998), S. 73-76 
    ISSN: 1573-4838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Abstract Two chitosan-containing polyelectrolyte complexes, chitosan-poly(acrylic acid) and chitosan-poly(styrenesulphonate), were synthesized by polymerizing acrylic acid and sodium styrenesulphonate in the presence of chitosan and chitosan hydrochloride, respectively. The complexes were studied by optical microscopy and tested for cytotoxicity by the Neutral Red uptake, Kenacid Blue R-Binding and 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazolium bromide assays. The optical microscopy confirmed the differences in crystallinity and structure already found for the two polycomplexes by other characterization techniques. The cytoxicity tests showed different influences on the cell activity by the extracts of the two polyelectrolyte complexes. Such results were discussed and correlated to the different structures of the two materials. © 1998 Chapman & Hall
    Type of Medium: Electronic Resource
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