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 inJournal of biomedical materials research. Part A Vol. 91A; no. 3; pp. 939 - 952
Main Authors Chaouch, W., Dieval, F., Le Nouen, D., Defoin, A., Chakfe, N., Durand, B.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.12.2009
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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
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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Snippet Trichloroacetyl isocyanate reacts rapidly and quantitatively with both acid and hydroxyl chain ends to form derivatives that can be readily determined by...
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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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https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjbm.a.32599
https://www.ncbi.nlm.nih.gov/pubmed/19777570
https://search.proquest.com/docview/1671241176
https://search.proquest.com/docview/734099903
https://search.proquest.com/docview/869583124
https://search.proquest.com/docview/883025759
Volume 91A
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