Skip to main content
Log in

The role of crystallinity on differential attachment/proliferation of osteoblasts and fibroblasts on poly (caprolactone-co-glycolide) polymeric surfaces

  • Research Article
  • Published:
Frontiers of Materials Science Aims and scope Submit manuscript

Abstract

The objective of the present study is to systematically evaluate the role of polymer crystallinity on fibroblast and osteoblast adhesion and proliferation using a series of poly(caprolactone-co-glycolide) (PCL/PGA) polymers. PCL/PGA polymers were selected since they reflect both highly crystalline and amorphous materials. PCL/PGA polymeric materials were fabricated by compression molding into thin films. Five compositions, from PCL or PGA to intermediate copolymeric compositions of PCL/PGA in ratios of 25:75, 35:65 and 45:55, were studied. Pure PCL and PGA represented the crystalline materials while the copolymers were amorphous. The polymers/copolymers were characterized using DSC to assess crystallinity, contact angle measurement for hydrophobicity, and AFM for nanotopography. The PCL/PGA films demonstrated similar hydrophobicity and nanotopography whereas they differed significantly in crystallinity. Cell adhesion to and proliferation on PCL/PGA films and proliferation studies were performed using osteoblasts and NIH-3T3 fibroblasts. It was observed that highly crystalline and rigid PCL and PGA surfaces were significantly more efficient in supporting fibroblast growth, whereas amorphous/flexible PCL/PGA 35:65 was significantly more efficient in supporting growth of osteoblasts. This study demonstrated that while chemical composition, hydrophobicity and surface roughness of PCL/PGA polymers were held constant, crystallinity and rigidity of PCL/PGA played major roles in determining cell responses.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Anderson J M, Rodriguez A, Chang D T. Foreign body reaction to biomaterials. Seminars in Immunology, 2008, 20(2): 86–100

    Article  CAS  Google Scholar 

  2. Yang X B, Roach H I, Clarke N M, et al. Human osteoprogenitor growth and differentiation on synthetic biodegradable structures after surface modification. Bone, 2001, 29(6): 523–531

    Article  CAS  Google Scholar 

  3. Harber G M. Cell-material interactions: fundamental design issues for tissue engineering and clinical considerations. In: Guelcher S A, Hollinger J O, eds. An Introduction to Biomaterials. Boca Raton, FL, USA: CRC Press/Taylor & Francis Group, 2006, 189–210

    Google Scholar 

  4. Kalbacova M, Rezek B, Baresova V, et al. Nanoscale topography of nanocrystalline diamonds promotes differentiation of osteoblasts. Acta Biomaterialia, 2009, 5(8): 3076–3085

    Article  CAS  Google Scholar 

  5. Biggs D L, Lengsfeld C S, Hybertson B M, et al. In vitro and in vivo valuation of the effects of PLA microparticle crystallinity on cellular response. Journal of Controlled Release, 2003, 92(1–2): 147–161

    Article  CAS  Google Scholar 

  6. Degirmenbasi N, Ozkan S, Kalyon D M, et al. Surface patterning of poly(L-lactide) upon melt processing: In vitro culturing of fibroblasts and osteoblasts on surfaces ranging from highly crystalline with spherulitic protrusions to amorphous with nanoscale indentations. Journal of Biomedical Materials Research Part A, 2009, 88A(1): 94–104

    Article  CAS  Google Scholar 

  7. Kawamoto N, Mori H, Terano M, et al. Blood compatibility of polypropylene surfaces in relation to the crystalline-amorphous microstructure. Journal of Biomaterials Science, Polymer Edition, 1997, 8(11): 859–877

    Article  CAS  Google Scholar 

  8. Park A, Cima L G. In vitro cell response to differences in poly-Llactide crystallinity. Journal of Biomedical Materials Research, 1996, 31(1): 117–130

    Article  CAS  Google Scholar 

  9. Wang S, Kempen D H, Yaszemski M J, et al. The roles of matrix polymer crystallinity and hydroxyapatite nanoparticles in modulating material properties of photo-crosslinked composites and bone marrow stromal cell responses. Biomaterials, 2009, 30(20): 3359–3370

    Article  CAS  Google Scholar 

  10. Washburn N R, Yamada K M, Simon C G Jr, et al. Highthroughput investigation of osteoblast response to polymer crystallinity: influence of nanometer-scale roughness on proliferation. Biomaterials, 2004, 25(7–8): 1215–1224

    Article  CAS  Google Scholar 

  11. Winet H, Bao J Y. Comparative bone healing near eroding polylactide-polyglycolide implants of differing crystallinity in rabbit tibial bone chambers. Journal of Biomaterials Science, Polymer Edition, 1997, 8(7): 517–532

    Article  CAS  Google Scholar 

  12. Wang D, Christensen K, Chawla K, et al. Isolation and characterization of MC3T3-E1 preosteoblast subclones with distinct in vitro and in vivo differentiation/mineralization potential. Journal of Bone and Mineral Research, 1999, 14(6): 893–903

    Article  CAS  Google Scholar 

  13. Agrawal C M, Ray R B. Biodegradable polymeric scaffolds for musculoskeletal tissue engineering. Journal of Biomedical Materials Research, 2001, 55(2): 141–150

    Article  CAS  Google Scholar 

  14. Tiaw K S, Teoh S H, Chen R, et al. Processing methods of ultrathin poly(ɛ-caprolactone) films for tissue engineering applications. Biomacromolecules, 2007, 8(3): 807–816

    Article  CAS  Google Scholar 

  15. Cheng Z, Teoh S-H. Surface modification of ultra thin poly (ɛ-caprolactone) films using acrylic acid and collagen. Biomaterials, 2004, 25(11): 1991–2001

    Article  CAS  Google Scholar 

  16. Bramfeldt H, Vermette P. Enhanced smooth muscle cell adhesion and proliferation on protein-modified polycaprolactone-based copolymers. Journal of Biomedical Materials Research Part A, 2009, 88A(2): 520–530

    Article  CAS  Google Scholar 

  17. Chung T-W, Wang Y-Z, Huang Y-Y, et al. Poly (ɛ-caprolactone) grafted with nano-structured chitosan enhances growth of human dermal fibroblasts. Artificial Organs, 2006, 30(1): 35–41

    Article  CAS  Google Scholar 

  18. Ishaug-Riley S L, Okun L E, Prado G, et al. Human articular chondrocyte adhesion and proliferation on synthetic biodegradable polymer films. Biomaterials, 1999, 20(23–24): 2245–2256

    Article  CAS  Google Scholar 

  19. Lee S-H, Kim B-S, Kim S H, et al. Elastic biodegradable poly (glycolide-co-caprolactone) scaffold for tissue engineering. Journal of Biomedical Materials Research Part A, 2003, 66A(1): 29–37

    Article  CAS  Google Scholar 

  20. Otten J E, Wiedmann-Al-Ahmad M, Jahnke H, et al. Bacterial colonization on different suture materials — a potential risk for intraoral dentoalveolar surgery. Journal of Biomedical Materials Research Part B, Applied Biomaterials, 2005, 74B(1): 627–635

    Article  CAS  Google Scholar 

  21. Kowalczyńska H M, Kołos R, Nowak-Wyrzykowska M, et al. Atomic force microscopy evidence for conformational changes of fibronectin adsorbed on unmodified and sulfonated polystyrene surfaces. Journal of Biomedical Materials Research Part A, 2009, 91A(4): 1239–1251

    Article  Google Scholar 

  22. Ajami-Henriquez D, Rodríguez M, Sabino M, et al. Evaluation of cell affinity on poly(L-lactide) and poly(ɛ-caprolactone) blends and on PLLA-b-PCL diblock copolymer surfaces. Journal of Biomedical Materials Research Part A, 2008, 87A(2): 405–417

    Article  CAS  Google Scholar 

  23. Pelham R J Jr, Wang Y. Cell locomotion and focal adhesions are regulated by substrate flexibility. Proceedings of the National Academy of Sciences of the United States of America, 1997, 94 (25): 13661–13665

    Article  CAS  Google Scholar 

  24. Tzvetkova-Chevolleau T, Stéphanou A, Fuard D, et al. The motility of normal and cancer cells in response to the combined influence of the substrate rigidity and anisotropic microstructure. Biomaterials, 2008, 29(10): 1541–1551

    Article  CAS  Google Scholar 

  25. Mo X, Weber H-J, Ramakrishna S. PCL-PGLA composite tubular scaffold preparation and biocompatibility investigation. The International Journal of Artificial Organs, 2006, 29(8): 790–799

    CAS  Google Scholar 

  26. Pamula E, Dobrzynski P, Szot B, et al. Cytocompatibility of aliphatic polyesters — In vitro tudy on fibroblasts and macrophages. Journal of Biomedical Materials Research Part A, 2008, 87A(2): 524–535

    Article  CAS  Google Scholar 

  27. Tsai W B, Chen C H, Chen J F, et al. The effects of types of degradable polymers on porcine chondrocyte adhesion, proliferation and gene expression. Journal of Materials Science: Materials in Medicine, 2006, 17(4): 337–343

    Article  CAS  Google Scholar 

  28. Tang Z G, Callaghan J T, Hunt J A. The physical properties and response of osteoblasts to solution cast films of PLGA doped polycaprolactone. Biomaterials, 2005, 26(33): 6618–6624

    Article  CAS  Google Scholar 

  29. Müller A J, Albuerne J, Marquez L, et al. Self-nucleation and crystallization kinetics of double crystalline poly(p-dioxanone)-b-poly(ɛ-caprolactone) diblock copolymers. Faraday Discussions, 2005, 128: 231–252

    Article  Google Scholar 

  30. Hamley I W, Castelletto V, Castillo R V, et al. Crystallization in poly(L-lactide)-b-poly(ɛ-caprolactone) double crystalline diblock copolymers: A study using X-ray scattering, differential scanning calorimetry, and polarized optical microscopy. Macromolecules, 2005, 38(2): 463–472

    Article  CAS  Google Scholar 

  31. Gough J E, Christian P, Scotchford C A, et al. Craniofacial osteoblast responses to polycaprolactone produced using a novel boron polymerisation technique and potassium fluoride posttreatment. Biomaterials, 2003, 24(27): 4905–4912

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Helen Cui.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cui, H., Sinko, P.J. The role of crystallinity on differential attachment/proliferation of osteoblasts and fibroblasts on poly (caprolactone-co-glycolide) polymeric surfaces. Front. Mater. Sci. 6, 47–59 (2012). https://doi.org/10.1007/s11706-012-0154-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11706-012-0154-8

Keywords

Navigation