4.5 Article

Poly(3-hydroxybutyrate-co-3-hydroxyvalerate)-based nanofibrous scaffolds to support functional esophageal epithelial cells towards engineering the esophagus

Journal

JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION
Volume 25, Issue 6, Pages 574-593

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/09205063.2014.884427

Keywords

gelatin; nanofiber; PHBV; esophagus; HEEpiC

Funding

  1. Indian Council of Medical Research, India [35/21/2010-BMS]
  2. Nano Mission [SR/S5/NM-07/2006, SR/NM/PG-16/2007]
  3. Department of Science & Technology, India
  4. FIST, Department of Science & Technology, India [SR/FST/LSI-327/2007]
  5. Drugs & Pharmaceuticals Research Programme, Department of Science & Technology, India
  6. SASTRA University
  7. Council of Scientific and Industrial Research [09/1095/(0003)/2013/EMR-I]

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Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) and PHBV-gelatin were electrospun to obtain defect-free nanofibers by optimizing various process and solution parameters. Tensile strength, Young's modulus, and wettability of PHBV-gelatin nanofibrous scaffold were determined and compared with PHBV nanofibrous scaffold. Our results demonstrate that PHBV-gelatin nanofibers exhibited higher tensile strength and Young's modulus than the PHBV nanofibers. Human esophageal epithelial cells (HEEpiC) were cultured on PHBV and PHBV-gelatin nanofiber showed better cell proliferation in PHBV nanofibrous scaffold than the PHBV-gelatin scaffold after 7 days of culture. HEEpiC cultured on PHBV and PHBV-gelatin nanofibrous scaffold exhibited characteristic epithelial cobblestone morphology after 3 days of culture. Further, the HEEpiC extracellular matrix (ECM) proteins (collagen type IV and laminin) and phenotypic marker proteins (cytokeratin-4 and 14) expressions were significantly higher in PHBV-gelatin nanofibrous scaffold than the PHBV nanofiber scaffold. However, the long-term stability and functional state of the cells on the PHBV scaffold give it an edge over the blend scaffolds. Thus, PHBV-based nanofibrous scaffolds could be explored further as ECM substitutes for the regeneration of esophageal tissue.

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