Affiliations 

  • 1 School of Computer Science and Engineering, Faculty of Innovation and Technology, Taylor's University Lakeside Campus, No. 1, Jalan Taylor's, Subang Jaya 47500, Selangor, Malaysia
  • 2 Center of Nanotechnology and Advanced Materials, Faculty of Science and Engineering, University of Nottingham Malaysia Campus, Jalan Broga, Semenyih 43500, Selangor, Malaysia
  • 3 Department of Mechanical, Materials & Manufacturing Engineering, University of Nottingham, University Park, Nottingham NG7 2RD, UK
  • 4 Department of Chemical and Environmental Engineering, University of Nottingham China, 199 Taikang East Road, Ningbo 315100, China
Polymers (Basel), 2021 Aug 07;13(16).
PMID: 34451170 DOI: 10.3390/polym13162629

Abstract

Poly(N-isopropylacrylamide) (polyNIPAm) microspheres were synthesized via the suspension polymerization technique. Thermal and redox initiators were compared for the polymerization, in order to study the effect of initiator type on the surface charge and particle size of polyNIPAm microspheres. The successful polymerization of NIPAm was confirmed by FTIR analysis. Microspheres of diameter >50 µm were synthesized when a pair of ammonium persulfate (APS) and N,N,N',N'-tetramethylene-diamine (TEMED) redox initiators was used, whilst relatively small microspheres of ~1 µm diameter were produced using an Azobis-isobutyronitrile (AIBN) thermal initiator. Hence, suspension polymerization using a redox initiator pair was found to be more appropriate for the synthesis of polyNIPAm microspheres of a size suitable for human embryonic kidney (HEK) cell culturing. However, the zeta potential of polyNIPAm microspheres prepared using an APS/TEMED redox initiator was significantly more negative than AIBN thermal initiator prepared microspheres and acted to inhibit cell attachment. Conversely, strong cell attachment was observed in the case of polyNIPAm microspheres of diameter ~90 µm, prepared using an APS/TEMED redox initiator in the presence of a cetyl trimethyl ammonium bromide (CTAB) cationic surfactant; demonstrating that surface charge modified polyNIPAm microspheres have great potential for use in cell culturing.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.