4.7 Article

Hydrolytic degradation of porous poly(hydroxybutyrate-co-hydroxyvalerate) scaffolds manufactured using selective laser sintering

期刊

POLYMER DEGRADATION AND STABILITY
卷 187, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.polymdegradstab.2021.109545

关键词

biopolymer; bone scaffold; hydrolytic degradation; PHBV

资金

  1. Medical Engineering @ The University of Queensland (UQ) SEED grant
  2. UQ NSRSU [NS-1803]
  3. Australian Research Council (ARC) through its DECRA Fellowship program [DE190101152]
  4. UQ PhD Scholarship by the University of Queensland (UQ)
  5. Australian Research Council [DE190101152] Funding Source: Australian Research Council

向作者/读者索取更多资源

The long-term hydrolytic degradation of SLS PHBV bone scaffolds was explored by incubating them in PBS solution for 20 weeks. The degradation occurred predominantly by bulk degradation, leading to reduction in molecular weight and compressive stiffness while increasing crystallinity. The weight loss was minimal in the first 8 weeks, with gradual increase thereafter, and the concentration of COOH groups on the scaffold surface initially increased before declining due to surface erosion from hydrolysis.
The long-term hydrolytic degradation of porous poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV) bone scaffolds manufactured using Selective Laser Sintering (SLS) process have yet to be explored. In this study, SLS PHBV scaffolds were incubated in phosphate-buffered saline (PBS) solution for up to 20 weeks. The result showed that degradation of the PHBV scaffolds occurred predominantly by bulk degradation. With increasing incubation time, the molecular weight and compressive stiffness of the scaffolds reduced while their crystallinity increased. In the first 8 weeks, the weight loss of the scaffolds was insignificant, indicating very limited amount of soluble product was produced by the hydrolysis process. Weight loss started to occur from Week 8; the average weight loss per fortnight was minimal and in the range of 0.33-0.51 %. The pristine PHBV scaffolds had a highly crystalline surface layer with low concentration of the hydrophilic carboxylic acid (COOH) end-groups. The concentration of COOH groups on the scaffold surface increased initially upon immersion in PBS due to the preferential chain rearrangement to expose hydrophilic segments. During immersion surface hydrolysis proceeded and the quantity of COOH groups declined from Week 2 to 6 due to erosion of the surface layer. (C) 2021 Elsevier Ltd. All rights reserved.

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