Skip to main content
Log in

Cellulose-based polymeric liquid crystals as a biomimetic modifier for suppressing protein adsorption

  • Biomaterials
  • Published:
Journal of Wuhan University of Technology-Mater. Sci. Ed. Aims and scope Submit manuscript

Abstract

A novel biomimetic protein-resistant modifier based on cellulose-based polymeric liquid crystals was described (PLCs). Two types of PLCs of propyl hydroxypropyl cellulose ester (PPC) and octyl hydroxypropyl cellulose ester (OPC) were prepared by esterification from hydroxypropyl cellulose, and then were mixed with polyvinyl chloride and polyurethane to obtain composite films by solution casting, respectively. The surface morphology of PLCs and their composite films were characterized by polarized optical microscopy (POM) and scanning electron microscopy (SEM), suggesting the existence of microdomain separation with fingerprint texture in PLC composite films. Water contact angle measurement results indicated that hydrophilicity of PLC/polymer composite films was dependent on the type and content of PLC as well as the type of matrix due to their interaction. Using bovine serum albumin (BSA) as a model protein, protein adsorption results revealed that PLCs with protein-resistant property can obviously suppress protein adsorption on their composite films, probably due to their flexible LC state. Moreover, all PLCs and their composites exhibited non-toxicity by MTT assay, suggesting their safety for biomedical applications.

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. Ratner BD. The Catastrophe Revisited: Blood Compatibility in the 21st Century[J]. Biomaterials, 2007(28): 5 144–5 147

    Google Scholar 

  2. Chen H, Yuan L, Song W, et al. Biocompatible Polymer Materials: Role of Protein-surface Interactions[J]. Progress in Polymer Science, 2008(33): 1 059–1 087

    Google Scholar 

  3. Jin Z, Feng W, Zhu S, et al. Protein-resistant Polyurethane Via Surface-Initiated Atom Transfer Radical Polymerization of Oligo(Ethylene Glycol) Methacrylate[J]. J. Biomed. Mater. Res., 91A, 2009:1 189–1 201

    Article  Google Scholar 

  4. Suriyanarayanan S, Lee H, Liedberg B, et al. Protein-resistant Hyperbranched Polyethyleneimine Brush Surfaces[J]. Journal of Colloid and Interface Science, 2013, 396: 307–315

    Article  Google Scholar 

  5. Mao C, Qiu Y, Sang H, et al. Various Approaches to Modify Biomaterial Surfaces for Improving Hemocompatibility [J]. Adv. Colloid. Interfac., 2004, 110: 5–17

    Article  Google Scholar 

  6. Zhang W, Fujiwara T, Taskent H, et al. A Polyurethane Surface Modifier: Contrasting Amphiphilic and Contraphilic Surfaces Driven by Block and Random Soft Blocks Having Trifluoroethoxymethyl and PEG Side Chains[J]. Macromol. Chem. Phys., 2012, 213: 1 415–1 434

    Article  Google Scholar 

  7. Chen L, Han D, Jiang L. On improving Blood Compatibility: From Bioinspired to Synthetic Design and Fabrication of Biointerfacial Topography at Micro/Nano Scales[J]. Colloids and Surfaces B: Biointerfaces, 2011, 85: 2–7

    Article  Google Scholar 

  8. Zhang Z, Zhang M, Chen S, et al. Blood Compatibility of Surfaces with Superlow Protein Adsorption[J]. Biomaterials, 2008, 29:4285–4291

    Article  Google Scholar 

  9. Ma H, Li D, Sheng X, et al. Protein-resistant Polymer Coatings on Silicon Oxide by Surface-initiated Atom Transfer Radical Polymerization[J]. Langmuir, 2006, 22:3751–37566

    Article  Google Scholar 

  10. Chen H, Hu X, Zhang Y, et al. Effect of Chain Density and Conformation on Protein Adsorption at PEG-grafted Polyurethane Surfaces[J]. Colloid. Surface B, 2008, 61: 237–243

    Article  Google Scholar 

  11. Jin Z, Feng W, Zhu S, et al. Protein-resistant Polyurethane by Sequential Grafting of poly(2-hydroxyethyl methacrylate) and poly(Oligo(ethylene glycol) Methacrylate) via Surface-initiated ATRP[J]. J. Biomed. Mater. Res. Part A, 2010: 1 223–1 232

    Google Scholar 

  12. Korematsu A, Takemoto Y, Nakaya T, et al. Synthesis, Characterization and Platelet Adhesion of Segmented Polyurethanes Grafted Phospholipid Analogous Vinyl Monomer on Surface[J]. Biomaterials, 2002(23): 263–271

    Google Scholar 

  13. Chen S, Zheng J, Li L, et al. Strong Resistance of Phosphorylcholine Self Assembled Monolayers to Protein Adsorption: Insights into Nonfouling Properties of Zwitterionic Materials[J]. J. Am. Chem. Soc., 2005, 127: 14 473–14 478

    Article  Google Scholar 

  14. Lu C, Zhou N, Xu D, et al. Surface-initiated Reverse Atom Transfer Radical polymerization (SI-RATRP) for Blood-compatible Polyurethane Substrates[J]. Applied Surface Science, 2011, 258: 618–626

    Article  Google Scholar 

  15. Yuan J, Lin S, Shen J. Enhanced Blood Compatibility of Polyurethane Functionalized with Sulfobetaine[J]. Colloid. Surf. B, 2008, 66:90–95

    Article  Google Scholar 

  16. Huang J, Xu W. Zwitterionic Monomer Graft Copolymerization onto Polyurethane Surface Through a PEG Spacer[J]. Applied Surface Science, 2010, 256: 3 921–3 927

    Article  Google Scholar 

  17. Zhang Z, Chen S, Jiang S. Dual-functional Biomimetic Materials: Nonfouling poly(carboxybetaine) with Active Functional Groups for Protein Immobilization[J]. Biomacromolecules, 2006(7): 3 311–3 315

    Google Scholar 

  18. Chen S, Yu F, Yu Q, et al. Strong Resistance of a Thin Crystalline Layer of Balanced Charged Groups to Protein Adsorption[J]. Langmuir, 2006, 22: 8 186–8 191

    Article  Google Scholar 

  19. Langer R, Tirrell DA. Designing Materials for Biology and Medicine [J]. Nature, 2004, 428: 487–492

    Article  Google Scholar 

  20. Hilt J Z. Nanotechnology and Biomimetic Methods in Therapeutics: Molecular Scale Control with Some Help from Nature[J]. Adv. Drug Deliv. Rev., 2004, 56: 1 533–1 536

    Article  Google Scholar 

  21. Shin H, Jo S, Mikos A G. Biomimetic Materials for Tissue Engineering [J]. Biomaterials, 2003(24): 4 353–4 364

    Google Scholar 

  22. Woltman SJ, Jay GD, Crawford G. Liquid-crystal Materials Find a New Order in Biomedical Applications[J]. Nature Materials, 2007(6): 929–938

    Google Scholar 

  23. Hwang JJ, Iyer SN, Li LS, et al. Self-assembling Biomaterials: Liquid Crystal Phases of Cholesteryl Oligo(L-lactic acid) and Their Interactions with Cells[J]. Proceedings of the National Academy of Sciences of the United States of America, 2002, 99(15): 9 662–9 667

    Article  Google Scholar 

  24. Cheng L, Luk Y, Murphy CJ, et al. Compatibility of Lyotropic Liquid Crystals with Viruses and Mammalian Cells That Support the Replication of Viruses[J]. Biomaterials, 2005(26): 7 173–7 182

    Google Scholar 

  25. Lockwood NA, Mohr J, Ji L, et al. Thermotropic Liquid Crystals as Substrates for Imaging the Reorganization of Matrigel by Human Embryonic Stem Cells[J]. Adv. Funct. Mater., 2006, 16(5): 618–624

    Article  Google Scholar 

  26. Fong WK, Hanley T, Boyd B J. Stimuli Responsive Liquid Crystals Provide’ on-demand’ Drug Delivery in vitro and in vivo[J]. Journal of Controlled Release, 2009(135): 218–226

    Google Scholar 

  27. Li LH, Tu M, Mou SS, et al. Preparation and Blood Compatibility of Polysiloxane/Liquid-crystal Composite Membranes[J]. Biomaterials, 2001(22): 2 595–2 599

    Google Scholar 

  28. Tu M, Han W, Zeng R, et al. A Study of Surface Morphology and Phase Separation of Polymer/Cellulose Liquid Crystal Composite Membranes[J]. Colloids and Surfaces A: Physicochem. Eng. Aspects, 2012, 407:126–132

    Article  Google Scholar 

  29. Han W, Tu M, Zeng R, et al. Preparation, Characterization and Cytocompatibility of Polyurethane/Cellulose Based Liquid Crystal Composite Membranes[J]. Carbohydrate Polymers, 2012, 90: 1 353–1 361

    Article  Google Scholar 

  30. L CH, J, WC Y YH, et al. Hemocompatibility and Cytocompatibility of Styrenesulfonate-grafted PDMS-polyurethane-HEMA hydrogel [J]. Colloid. Surf. B, 2009, 70: 132–141

    Article  Google Scholar 

  31. Lin KH, Huang. Texture Evolution of Cholesteric Liquid Crystal Driven by a Thermal Process[J]. Applied Surface Science, 2011, 257: 9 858–9 862

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Mei Tu  (屠美).

Additional information

Funded by the National Natural Science Foundation of China (Nos. 31170911 and 31040027), the Research Development and Innovation Fund of Jinan University (No. 21611410), the Open Fund of the First Affiliated Hospital, Jinan University, Guangzhou(No. 511005024) and the Macao Science and Technology Development Fund(No. 064/2013/A2)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Situ, F., Tan, R., Gong, L. et al. Cellulose-based polymeric liquid crystals as a biomimetic modifier for suppressing protein adsorption. J. Wuhan Univ. Technol.-Mat. Sci. Edit. 30, 416–422 (2015). https://doi.org/10.1007/s11595-015-1163-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11595-015-1163-0

Key words

Navigation