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Types of Step-Growth Polymers: Polyesters01:20

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The introduction of polyesters has brought major development to the textile industry. The wrinkle-free behavior of polyester blends has eliminated the need for starching and ironing clothes.
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the...
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Fabricating Superhydrophobic Polymeric Materials for Biomedical Applications
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Electrospun Polycaprolactone (PCL) Degradation: An In Vitro and In Vivo Study.

Juliana R Dias1, Aureliana Sousa2,3, Ana Augusto4

  • 1Center for Rapid and Sustainable Product Development (CDRsp), Polytechnic Institute of Leiria, 2030-028 Marinha Grande, Portugal.

Polymers
|August 26, 2022
PubMed
Summary

Electrospun polycaprolactone (PCL) meshes show promising degradation rates for wound dressings. In vitro studies with lipase achieved 97% degradation, while in vivo tests showed slower but successful integration.

Keywords:
degradationelectrospinning nanofibersenzymatichydrolyticin vitroin vivopolycaprolactone

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Area of Science:

  • Biomaterials Science
  • Tissue Engineering
  • Regenerative Medicine

Background:

  • Polycaprolactone (PCL) is a biocompatible and FDA-approved polymer favored in tissue engineering.
  • The hydrophobic nature of bulk PCL limits its degradation rate for applications like skin regeneration.
  • Electrospun PCL fiber meshes offer a high surface area, potentially accelerating degradation.

Purpose of the Study:

  • To evaluate the in vitro and in vivo degradation of electrospun PCL meshes over 90 days.
  • To assess the suitability of these PCL meshes as wound dressings.
  • To investigate the influence of enzymatic and hydrolytic conditions on PCL mesh degradation.

Main Methods:

  • In vitro degradation studies using enzymatic (lipase) and hydrolytic conditions in a static medium.
  • In vivo degradation assessment over 90 days in subcutaneous pockets.
  • Evaluation of sample integration and tissue response in vivo.

Main Results:

  • In vitro degradation reached 97% for PCL meshes, significantly influenced by lipase.
  • In vivo degradation was slower compared to in vitro conditions.
  • PCL mesh samples were well-integrated into surrounding tissues without rejection.

Conclusions:

  • Electrospun PCL meshes demonstrate tunable degradation profiles suitable for wound dressing applications.
  • Enzymatic activity, particularly lipase, significantly enhances PCL mesh degradation in vitro.
  • The biocompatibility and integration of PCL meshes in vivo support their potential as advanced wound care materials.