1H-NMR spectroscopic study of the effect of aging vascular prostheses made of poly(ethylene terephthalate) on the macromolecular weight
Trichloroacetyl isocyanate reacts rapidly and quantitatively with both acid and hydroxyl chain ends to form derivatives that can be readily determined by 1H‐NMR spectroscopy. This method provides a convenient mean for characterization of polyethylene terephthalate (PET) end‐groups. The 1H‐NMR spectr...
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Published in | Journal of biomedical materials research. Part A Vol. 91A; no. 3; pp. 939 - 952 |
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Abstract | Trichloroacetyl isocyanate reacts rapidly and quantitatively with both acid and hydroxyl chain ends to form derivatives that can be readily determined by 1H‐NMR spectroscopy. This method provides a convenient mean for characterization of polyethylene terephthalate (PET) end‐groups. The 1H‐NMR spectroscopy has been applied to describe the chemical aging of the PET vascular prostheses by determination of the hydroxyl and carboxyl end‐group concentrations and therefore the macromolecular weight. To validate 1H‐NMR results, we used chemical titration of the end‐groups and classical viscosimetric method as complementary techniques. The analyses made on the explants of different lifetime demonstrated a significant deterioration compared with the virgin prostheses. A high degradation of macromolecular weight is observed. This phenomenon is explained by a random scission of the ester linkages. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2009 |
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AbstractList | Trichloroacetyl isocyanate reacts rapidly and quantitatively with both acid and hydroxyl chain ends to form derivatives that can be readily determined by (1)H-NMR spectroscopy. This method provides a convenient mean for characterization of polyethylene terephthalate (PET) end-groups. The (1)H-NMR spectroscopy has been applied to describe the chemical aging of the PET vascular prostheses by determination of the hydroxyl and carboxyl end-group concentrations and therefore the macromolecular weight. To validate (1)H-NMR results, we used chemical titration of the end-groups and classical viscosimetric method as complementary techniques. The analyses made on the explants of different lifetime demonstrated a significant deterioration compared with the virgin prostheses. A high degradation of macromolecular weight is observed. This phenomenon is explained by a random scission of the ester linkages. Trichloroacetyl isocyanate reacts rapidly and quantitatively with both acid and hydroxyl chain ends to form derivatives that can be readily determined by 1H-NMR spectroscopy. This method provides a convenient mean for characterization of polyethylene terephthalate (PET) end-groups. The 1H-NMR spectroscopy has been applied to describe the chemical aging of the PET vascular prostheses by determination of the hydroxyl and carboxyl end-group concentrations and therefore the macromolecular weight. To validate 1H-NMR results, we used chemical titration of the end-groups and classical viscosimetric method as complementary techniques. The analyses made on the explants of different lifetime demonstrated a significant deterioration compared with the virgin prostheses. A high degradation of macromolecular weight is observed. This phenomenon is explained by a random scission of the ester linkages. [copy 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2009 Trichloroacetyl isocyanate reacts rapidly and quantitatively with both acid and hydroxyl chain ends to form derivatives that can be readily determined by super(1)H-NMR spectroscopy. This method provides a convenient mean for characterization of polyethylene terephthalate (PET) end-groups. The super(1)H-NMR spectroscopy has been applied to describe the chemical aging of the PET vascular prostheses by determination of the hydroxyl and carboxyl end-group concentrations and therefore the macromolecular weight. To validate super(1)H-NMR results, we used chemical titration of the end-groups and classical viscosimetric method as complementary techniques. The analyses made on the explants of different lifetime demonstrated a significant deterioration compared with the virgin prostheses. A high degradation of macromolecular weight is observed. This phenomenon is explained by a random scission of the ester linkages. Trichloroacetyl isocyanate reacts rapidly and quantitatively with both acid and hydroxyl chain ends to form derivatives that can be readily determined by 1H‐NMR spectroscopy. This method provides a convenient mean for characterization of polyethylene terephthalate (PET) end‐groups. The 1H‐NMR spectroscopy has been applied to describe the chemical aging of the PET vascular prostheses by determination of the hydroxyl and carboxyl end‐group concentrations and therefore the macromolecular weight. To validate 1H‐NMR results, we used chemical titration of the end‐groups and classical viscosimetric method as complementary techniques. The analyses made on the explants of different lifetime demonstrated a significant deterioration compared with the virgin prostheses. A high degradation of macromolecular weight is observed. This phenomenon is explained by a random scission of the ester linkages. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2009 |
Author | Chaouch, W. Le Nouen, D. Durand, B. Dieval, F. Defoin, A. Chakfe, N. |
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References | Jun SC,Ji HY,Won HJ,Suk WK,Wan SH,Dong IY. Cyclization routes for formation of cyclic oligomers in poly(ethylene terephthalate). Macromol. Chem Phys 2001; 202: 998-1003. Kurata M,Tsunashima Y,Iwana M,Kamada K. In: Bandrup J,Immergut EH, editors. Polymer Handbook,2nd ed, New York: Wiley; 1975, p 35. Zhang H,Ward IM. Kinetics of hydrolytic degradation of poly (ethylene naphthalene-2,6-dicarboxylate). Macromolecules 1995; 28: 7622-7629. Dannoux M,Cassagnau Ph,Michel A. Synthesis of oligoester a, w-diols by alcoholysis of PET through the reactive extrusion process. The Can J Chem Eng 2002; 80: 1075-1082. Goodlett VW. Use of in situ reactions for characterization of alcohols and glycols by nuclear magnetic resonance. Anal Chem 1965; 37: 431-432. Chakfe N,Dieval F,Riepe G,Mathieu D,Zbali I,Thaveau F,Heintz C,Kretz JG,Durand B. Influence of the textile structure on the degradation of explanted aortic endoprostheses. Eur J Vasc Endovasc Surg 2004; 27: 33-41. Chakfe N,Dieval F,Thaveau F,Taghavi I,Lemagnen JF,Laroche G,Hassani O,Riepe G,Durand B,Kretz JG. Aneurysm of an expanded polytetrafluoroethylene vascular graft: An ultrastructural evaluation. Eur Vasc Endovasc Surg 2003; 25: 360-366. Ma Y,Agarwal US. Solvent assisted post-polymerization of PET. Polymer 2005; 46: 5447-5455. Jordens K,Wilkes GL,Janzen J,Rohlfing DC,Welch MB. The influence of molecular weight and thermal history on the thermal, rheological, and mechanical properties of metallocene-catalyzed linear polyethylenes. Polymer 2000; 41: 7175-7192. Tang W,Murthy NS,Mares F,Mcdonnell ME,Curran SA. Poly(ethylene terephthalate)-poly(caprolactone) block copolymer. I. synthesis, reactive extrusion, and fiber morphology. JAppl Polym Sci 1999; 74: 1858-1867. Grosvenor MP,Staniforth JN. The effect of molecular weight on the rheological and tensile properties of poly-(ϵ-caprolactone). Int J Pharm 1995; 135: 103-109. Pohl A. Determination of carboxyl end-groups in a polyester, polyethylene terephthalate. Anal Chem 1954; 26: 1614-1616. Rwei S-P,Ni S-K. Formation, characterization, and prevention of dust generated during fiber or fabric processing of pet materials. Text Res J 2004; 74: 581-586. Richard DA,Moad G. A novel method for determination of polyester end-groups by MNR spectroscopy. Polymer 2005; 46: 5005-5011. Sammon C,Yarwood J,Everall N. An FT- IR study of the effect of hydrolytic degradation on the structure of thin PET films. Polym Degrad Stab 2000; 67: 149-158. Patrick C,Isabelle E. Physique des polymères, Tome I. Structure, Fabrication, Emploi. Paris: Hermann Editeurs des Sciences et des Arts; 2005, p 42. Chakfe N,Riepe G,Dieval F,Lemagnen JF,Wang L,Urban E,Beaufigeau M,Durand B,Imig H,Kretz JG. Longitudinal ruptures of polyester knitted vascular prostheses. J Vasc Surg 2001; 33: 1015-1021. Susumu T,Haruhiko N. Thermal degradation and melt viscosity of ultra-high-molecular-weight poly(ethylene terephthalate). Polymer 1996; 37: 1583-1587. Postma A,Davis Thomas P,Donovan A,Richard Li G,Moad G,Mulder R,O'shea Michael S. A simple method for determining protic end-groups of synthetic polymers by 1H-NMR spectroscopy. Polymer 2006; 47: 1899-1911. Kenwright AM,Peace SK,Richards RW,Bunn A,Macdonald WA. End-group modification in poly(ethylene terephthalate). Polymer 1999; 40: 2035-2040. Al-Abdulrazzak S,Lofgren EA,Jabrin SA. End-group determination in poly(ethylene terephthalate) by infrared spectroscopy. Polym Int 2002; 51: 174-182. Maarek JM,Guidoin R,Aubin M,Prud'homme RE. Molecular weight characterization of virgin and explanted polyester arterial prostheses. J Biomed Mater Res 1984; 18: 881-894. Ma Y,Agarwal US,Vekemans JM,Sikkema DJ. NMR based determination of minute acid functionality: End-groups in PET. Polymer 2003; 44: 4429-4434. Spyros A. Quantitative determination of the distribution of free hydroxylic and carboxylic groups in unsaturated polyester and alkyd resins by 31P-NMR spectroscopy. J Appl Polym Sci 2002; 83: 1635-1642. Zhang H,Rankin A,Ward IM. Determination of the end-group concentration and molecular weight of poly(etylene naphthalene-2,6-dicarboxylate) using infrared spectroscopy. Polymer 1996; 37: 1079-1085. Ma Y,Agarwal US,Sikkema DJ,Lemstra PJ. Solid-state polymerization of pet: Influence of nitrogen sweep and high vacuum. Polymer 2003; 44: 4085-4096. Conix A. On the molecular weight determination of poly-(ethylene terephthalate). Makromol Chem 1958; 26: 226-235. Maurice MJ,Huizinga F. The determination of carboxyl groups in polyethylene terephthalate. Anal Chim Acta 1960; 22: 363-368. Kern Von W,Munk R,Schmidt KH. Lineare polyester mit carboxylendruppen und derenbestimmung. Makromol Chem 1956; 17: 219-230. Jabarin SA,Lofgren EA. Solid state polymerisation of poly- (ethylene terephthalate): Kinetic and property parameters. J Appl Polym Sci 1986; 32: 5315-5335. Lee KH,Won CY,Chu CC,Gitsov I. Hydrolysis of biodegradable polymers by superoxide ions. J Polym Sci Part A: Polym Chem 1999; 37: 3558-3567. 2004; 27 1986; 32 2000; 67 2002; 51 2000; 41 1975 2005 1995; 135 1954; 26 1956; 17 1999; 40 2002; 80 1965; 37 1996; 37 2001; 202 2005; 46 2004; 74 1960; 22 1995; 28 2002; 83 1958; 26 2006; 47 1999; 37 2003; 25 1984; 18 1999; 74 2001; 33 2003; 44 |
References_xml | – volume: 135 start-page: 103 year: 1995 end-page: 109 article-title: The effect of molecular weight on the rheological and tensile properties of poly‐(ϵ‐caprolactone) publication-title: Int J Pharm – volume: 83 start-page: 1635 year: 2002 end-page: 1642 article-title: Quantitative determination of the distribution of free hydroxylic and carboxylic groups in unsaturated polyester and alkyd resins by P‐NMR spectroscopy publication-title: J Appl Polym Sci – start-page: 35 year: 1975 – volume: 80 start-page: 1075 year: 2002 end-page: 1082 article-title: Synthesis of oligoester a, w‐diols by alcoholysis of PET through the reactive extrusion process publication-title: The Can J Chem Eng – volume: 17 start-page: 219 year: 1956 end-page: 230 article-title: Lineare polyester mit carboxylendruppen und derenbestimmung publication-title: Makromol Chem – start-page: 42 year: 2005 – volume: 37 start-page: 3558 year: 1999 end-page: 3567 article-title: Hydrolysis of biodegradable polymers by superoxide ions publication-title: J Polym Sci Part A: Polym Chem – volume: 37 start-page: 1079 year: 1996 end-page: 1085 article-title: Determination of the end‐group concentration and molecular weight of poly(etylene naphthalene‐2,6‐dicarboxylate) using infrared spectroscopy publication-title: Polymer – volume: 32 start-page: 5315 year: 1986 end-page: 5335 article-title: Solid state polymerisation of poly‐ (ethylene terephthalate): Kinetic and property parameters publication-title: J Appl Polym Sci – volume: 41 start-page: 7175 year: 2000 end-page: 7192 article-title: The influence of molecular weight and thermal history on the thermal, rheological, and mechanical properties of metallocene‐catalyzed linear polyethylenes publication-title: Polymer – volume: 27 start-page: 33 year: 2004 end-page: 41 article-title: Influence of the textile structure on the degradation of explanted aortic endoprostheses publication-title: Eur J Vasc Endovasc Surg – volume: 44 start-page: 4085 year: 2003 end-page: 4096 article-title: Solid‐state polymerization of pet: Influence of nitrogen sweep and high vacuum publication-title: Polymer – volume: 74 start-page: 581 year: 2004 end-page: 586 article-title: Formation, characterization, and prevention of dust generated during fiber or fabric processing of pet materials publication-title: Text Res J – volume: 47 start-page: 1899 year: 2006 end-page: 1911 article-title: A simple method for determining protic end‐groups of synthetic polymers by H‐NMR spectroscopy publication-title: Polymer – volume: 26 start-page: 1614 year: 1954 end-page: 1616 article-title: Determination of carboxyl end‐groups in a polyester, polyethylene terephthalate publication-title: Anal Chem – volume: 18 start-page: 881 year: 1984 end-page: 894 article-title: Molecular weight characterization of virgin and explanted polyester arterial prostheses publication-title: J Biomed Mater Res – volume: 74 start-page: 1858 year: 1999 end-page: 1867 article-title: Poly(ethylene terephthalate)–poly(caprolactone) block copolymer. I. synthesis, reactive extrusion, and fiber morphology publication-title: JAppl Polym Sci – volume: 28 start-page: 7622 year: 1995 end-page: 7629 article-title: Kinetics of hydrolytic degradation of poly (ethylene naphthalene‐2,6‐dicarboxylate) publication-title: Macromolecules – volume: 33 start-page: 1015 year: 2001 end-page: 1021 article-title: Longitudinal ruptures of polyester knitted vascular prostheses publication-title: J Vasc Surg – volume: 51 start-page: 174 year: 2002 end-page: 182 article-title: End‐group determination in poly(ethylene terephthalate) by infrared spectroscopy publication-title: Polym Int – volume: 46 start-page: 5447 year: 2005 end-page: 5455 article-title: Solvent assisted post‐polymerization of PET publication-title: Polymer – volume: 202 start-page: 998 year: 2001 end-page: 1003 article-title: Cyclization routes for formation of cyclic oligomers in poly(ethylene terephthalate). Macromol publication-title: Chem Phys – volume: 40 start-page: 2035 year: 1999 end-page: 2040 article-title: End‐group modification in poly(ethylene terephthalate) publication-title: Polymer – volume: 37 start-page: 431 year: 1965 end-page: 432 article-title: Use of in situ reactions for characterization of alcohols and glycols by nuclear magnetic resonance publication-title: Anal Chem – volume: 37 start-page: 1583 year: 1996 end-page: 1587 article-title: Thermal degradation and melt viscosity of ultra‐high‐molecular‐weight poly(ethylene terephthalate) publication-title: Polymer – volume: 44 start-page: 4429 year: 2003 end-page: 4434 article-title: NMR based determination of minute acid functionality: End‐groups in PET publication-title: Polymer – volume: 25 start-page: 360 year: 2003 end-page: 366 article-title: Aneurysm of an expanded polytetrafluoroethylene vascular graft: An ultrastructural evaluation publication-title: Eur Vasc Endovasc Surg – volume: 67 start-page: 149 year: 2000 end-page: 158 article-title: An FT‐ IR study of the effect of hydrolytic degradation on the structure of thin PET films publication-title: Polym Degrad Stab – volume: 46 start-page: 5005 year: 2005 end-page: 5011 article-title: A novel method for determination of polyester end‐groups by MNR spectroscopy publication-title: Polymer – volume: 26 start-page: 226 year: 1958 end-page: 235 article-title: On the molecular weight determination of poly‐(ethylene terephthalate) publication-title: Makromol Chem – volume: 22 start-page: 363 year: 1960 end-page: 368 article-title: The determination of carboxyl groups in polyethylene terephthalate publication-title: Anal Chim Acta |
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SubjectTerms | 1H-NMR spectroscopy Blood Vessel Prosthesis chemical aging Derivatives Humans Hydrolysis Macromolecular Substances macromolecular weight Magnetic Resonance Spectroscopy - methods Materials Testing Models, Chemical Molecular Weight polyethylene terephthalate Polyethylene terephthalates Polyethylene Terephthalates - chemistry Prostheses Prosthesis Failure Prosthetics Reproduction Scission Spectroscopy Surgical implants Time Factors vascular prosthesis Viscosity |
Title | 1H-NMR spectroscopic study of the effect of aging vascular prostheses made of poly(ethylene terephthalate) on the macromolecular weight |
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