Polyglycolide

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Polyglycolide
IUPAC name 1,4-Dioxane-2,5-dione
Identifiers
3D model (JSmol)
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Properties
(C2H2O2)n
Molar mass N/A
Density 1.530 g/cm³ at 25 °C
Melting point
Boiling point
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox disclaimer and references

Polyglycolide or Polyglycolic acid (PGA) is a biodegradable, thermoplastic polymer and the simplest linear, aliphatic polyester. It can be prepepared starting from glycolic acid by means of polycondensation or ring-opening polymerization. PGA has been known since 1954 as a tough fiber-forming polymer. Owing to its hydrolytic instability, however, its use has initially been limited.[1] Currently polyglycolide and its copolymers (poly(lactic-co-glycolic acid) with lactic acid, poly(glycolide-co-caprolactone) with ε-caprolactone, and poly (glycolide-co-trimethylene carbonate) with trimethylene carbonate) are widely used as a material for the synthesis of absorbable sutures and are being evaluated in the biomedical field.[2]

Physical properties

Polyglycolide has a glass transition temperature between 35-40 °C and its melting point is reported to be in the range of 225-230 °C. PGA also exhibits an elevated degree of crystallinity, around 45-55%, thus resulting insoluble in water.[2] The solubility of this polyester is somewhat unique, in that its high molecular weight form is insoluble in almost all common organic solvents (acetone, dichloromethane, chloroform, ethyl acetate, tetrahydrofuran), while low molecular weight oligomers sufficiently differ in their physical properties to be more soluble. However polyglycolide is soluble in highly fluorinated solvents like hexafluoroisopropanol (HFIP) and hexafluoroacetone sesquihydrate, that can be used to prepare solutions of the high MW polymer for melt spinning and film preparation.[3] Fibers of PGA exhibit high strength and modulus (7 GPa) and are particularly stiff.[2]

Synthesis

Polyglycolide can be obtained through several different processes starting with different materials:

  1. polycondensation of glycolic acid;
  2. ring-opening polymerization of glycolide;
  3. solid-state polycondensation of halogenoacetates;
  4. acid catalyzed reaction of carbon monoxide and formaldehyde

Polycondensation of glycolic acid is the simplest process available to prepare PGA, but it is not the most efficient because it yields a low molecular weight product. Briefly, the procedure is as follows: glycolic acid is heated at atmospheric pressure and a temperature of about 175-185°C is maintained until water ceases to distill. Subsequently, pressure is reduced to 150 mm Hg, still keeping the temperature unaltered for about two hours and the low MW polyglycolide is obtained.[4]

The most common synthesis used to produce a high molecular weight form of the polymer is ring-opening polymerization of "glycolide", the cyclic diester of glycolic acid. Glycolide can be prepared by heating under reduced pressure low MW PGA, collecting the diester by means of distillation. Ring-opening polymerization of glycolide can be catalyzed using different catalysts, including antimony compounds, such as antimony trioxide or antimony trihalides, zinc compounds (zinc lactate) and tin compunds like, stannous octoate (tin(II) 2-ethylhexanoate) or tin alkoxides. Stannous octoate is the most common used initiator, since it is approved by the FDA as a food stabilizer. Usage of other catalysts has been undisclosed as well, among these are aluminum isopropoxide, calcium acetylacetonate, and several lanthanide alkoxides (e.g. yttrium isopropoxide).[4][5][6]The procedure followed for ring-opening polymerization is briefly outlined: a catalytic amount of initiator is added to glycolide under a nitrogen atmosphere at a temperature of 195°C. The reaction is allowed to proceed for about two hours, then temperature is raised to 230°C for about half an hour. After solidification the resulting high MW polymer is collected.[4]

File:Pga synthesis.png
Ring-opening polymerization of glycolide to polyglycolide

Another procedure consists in the thermally induced solid-state polycondensation of halogenoacetates with general formula X-—CH2COO-M+ (where M is a monovalent metal like sodium and X is a halogen like chlorine), resulting in the production of polyglycolide and small crystals of a salt. Polycondensation is carried out by heating an halogenoacetate, like sodium chloroacetate, at a temperature between 160-180°C, continuously passing nitrogen through the reaction vessel. During the reaction polyglycolide is formed along with sodium chloride which precipitates within the polymeric matrix; the salt can be conveniently removed by washing the product of the reaction with water.[7]

PGA can also be obtained by reacting carbon monoxide, formaldehyde or one of its related compunds like paraformaldehyde or trioxane, in presence of an acidic catalyst. In a carbon monoxide atmosphere an autoclave is loaded with the catalyst (chlorosulfonic acid), dichloromethane and trioxane, then it is charged with carbon monoxide until aspecific pressure is reached; the reaction is stirred and allowed to proceed at a temperature of about 180°C for two hours. Upon completion the unreacted carbon monoxide is discharged and a mixture of low and high MW polyglycolide is collected.[8]

Degradation

Polyglycolide is characterized by hydrolytic instability owing to the presence of the ester linkage in its backbone. The degradation process is erosive and appears to take place in two steps during which the polymer is converted back to its monomer glycolic acid: first water diffuses into the amorphous (non-crystalline) regions of the polymer matrix, cleaving the ester bonds; the second step starts after the amorphous regions have been eroded, leaving the crystalline portion of the polymer susceptible to hydrolytic attack. Upon collapse of the crystalline regions the polymer chain dissolves.

When exposed to physiological conditions, polyglycolide is degraded by random hydrolysis and apparently it is also broken down by certain enzymes, especially those with esterase activity. The degradation product, glycolic acid, is non toxic and it can enter the tricarboxylic acid cycle after which it is excreted as water and carbon dioxide. A part of the glycolic acid is also excreted by urine.[9]

Studies undergone using polyglycolide-made sutures have shown that the material loses half of its strength after two weeks and 100% after four weeks. The polymer is completely resorbed by the organism in a time frame of four to six months.[2]

Uses

While known since 1954, PGA had found little use because of its ease of degradation when compared to other synthetic polymers. However in 1962 this polymer was used to develop the first synthetic absorbable suture which was marketed under the tradename of Dexon[1] by the Davis & Geck subsidiary of the American Cyanamid Corporation. Because polyglycolide give strongs fibers and degrades into water soluble monomers, sutures made with this polymer have found use in certain surgical applications, since there is no need for further medical attention to remove them. Implantable medical devices have been produced with PGA as well, including anastomosis rings, pins, rods, plates and screws.[2]

The traditional role of PGA as a biodegradable suture material has led to its evaluation in other biomedical fields, such as tissue engineering or controlled drug delivery. Tissue engineering scaffolds made with polyglycolide have been produced following different approaches, but generally most of these are obtained through textile technologies in the form of non-woven meshes.

References

  1. 1.0 1.1 Gilding, D. K. (December 1979). "Biodegradable polymers for use in surgery - polyglycolic/poly (lactic acid) homo- and copolymers: 1". Polymer. 20: 1459–1464. doi:doi:10.1016/0032-3861(79)90009-0 Check |doi= value (help). Unknown parameter |coauthors= ignored (help)
  2. 2.0 2.1 2.2 2.3 2.4 Middleton, J. (March 1998). "Synthetic biodegradable polymers as medical devices" (HTML). Medical Plastics and Biomaterials Magazine. Retrieved 2006-07-04. Unknown parameter |coauthors= ignored (help)
  3. Schmitt, E.: "Polyglycolic acid in solutions", U.S. Pat 3 737 440, 1973
  4. 4.0 4.1 4.2 Lowe, C. E.: "Preparation of high molecular weight polyhydroxyacetic ester", U.S. Pat 2 668 162, 1954
  5. Bero, Maciej (18 June 1999). "Application of Calcium Acetylacetonate to the Polymerization of Glycolide and Copolymerization of Glycolide with ε-Caprolactone and L-Lactide". Macromolecules. ACS. 32 (14): 4735–4737. doi:doi:10.1021/ma981969z Check |doi= value (help). Unknown parameter |coauthors= ignored (help); line feed character in |title= at position 42 (help)
  6. Stridsberg, Kajsa M. (2002). "Controlled Ring-Opening Polymerization: Polymers with designed Macromolecular Architecture". Advances in Polymer Science. Springer. 157: 41–65. ISSN 0065-3195. Unknown parameter |coauthors= ignored (help)
  7. Epple, Matthias (1999). "A detailed characterization of polyglycolide prepared by solid-state polycondensation reaction". Macromolecular Chemistry and Physics. Wiley. 200 (10): 2221–2229.
  8. Masuda et al.: "Biodegradable plastic composition", U.S. Pat 5 227 415, 1993
  9. Gunatillake, Pathiraja A. (2003). "Biodegradable Synthetic Polymers for tissue engineering" (PDF). European Cells and Materials. 5: 1–16. ISSN 1473-2262. Retrieved 2006-07-04. Unknown parameter |coauthors= ignored (help)

eo:Poliglikolido it:Acido poliglicolico


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