Osteogenic Surface Modification Based on Functionalized Poly-P-Xylylene Coating

PLoS One. 2015 Sep 17;10(9):e0137017. doi: 10.1371/journal.pone.0137017. eCollection 2015.

Abstract

The biotechnology to immobilize biomolecules on material surfaces has been developed vigorously due to its high potentials in medical applications. In this study, a simple and effective method was designed to immobilize biomolecules via amine-N-hydroxysuccinimide (NHS) ester conjugation reaction using functionalized poly-p-xylylene coating on material surfaces. The NHS ester functionalized coating is synthesized via chemical vapor deposition, a facile and solvent-less method, creating a surface which is ready to perform a one-step conjugation reaction. Bone morphogenetic protein 2 (BMP-2) is immobilized onto material surfaces by this coating method, forming an osteogenic environment. The immobilization process is controlled at a low temperature which does not damage proteins. This modified surface induces differentiation of preosteoblast into osteoblast, manifested by alkaline phosphatase (ALP) activity assay, Alizarin Red S (ARS) staining and the expression of osteogenic gene markers, Alpl and Bglap3. With this coating technology, immobilization of growth factors onto material surface can be achieved more simply and more effectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Alkaline Phosphatase / biosynthesis
  • Alkaline Phosphatase / metabolism
  • Animals
  • Anthraquinones / metabolism
  • Bone Morphogenetic Protein 2 / chemistry*
  • Cell Adhesion / drug effects*
  • Cell Differentiation / drug effects
  • Cell Line
  • Mice
  • Osteoblasts / cytology*
  • Osteoblasts / metabolism
  • Osteogenesis / drug effects*
  • Osteogenesis / physiology
  • Polymers / chemistry
  • Succinimides / chemistry
  • Surface Properties / drug effects*

Substances

  • Anthraquinones
  • Bmp2 protein, mouse
  • Bone Morphogenetic Protein 2
  • Polymers
  • Succinimides
  • Alizarin Red S
  • ALPL protein, mouse
  • Alkaline Phosphatase
  • N-hydroxysuccinimide

Grants and funding

CHC gratefully acknowledges support from the Ministry of Science and Technology of Taiwan (MOST 103-2633-B-002-014; NSC 102-2320-B-002-002-MY2) and National Taiwan University Hospital-Taipei Veterans General Hospital Joint Research Program (NTUH-TVGH VN103-10). This work is further supported by the Ministry of Science and Technology of Taiwan (NSC 101-2628-E-002-034-MY3; NSC-DAAD 102-2911-I-002-507), and National Taiwan University (102R7745; 103R7745) for HYC. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.