Affiliations 

  • 1 Centre of Innovative Nanostructures and Nanodevices (COINN), Universiti Teknologi PETRONAS, Perak Darul Ridzuan, Malaysia
  • 2 Department of Mechanical Engineering, Universiti Teknologi PETRONAS, Perak Darul Ridzuan, Malaysia
  • 3 School of Engineering and the Built Environment, Birmingham City University, Birmingham, UK
  • 4 School of Chemical Sciences, Universiti Sains Malaysia, Penang, Malaysia
  • 5 Institute of Nano Electronic Engineering, Kangar 01000 & Faculty of Chemical Engineering & Technology, Arau 02600, Universiti Malaysia Perlis, Perlis, Malaysia
  • 6 School of Chemical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 38541, Republic of Korea
Crit Rev Anal Chem, 2022 Oct 26.
PMID: 36288094 DOI: 10.1080/10408347.2022.2135090

Abstract

Biopolymers are an attractive green alternative to conventional polymers, owing to their excellent biocompatibility and biodegradability. However, their amorphous and nonconductive nature limits their potential as active biosensor material/substrate. To enhance their bio-analytical performance, biopolymers are combined with conductive materials to improve their physical and chemical characteristics. We review the main advances in the field of electrochemical biosensors, specifically the structure, approach, and application of biopolymers, as well as their conjugation with conductive nanoparticles, polymers and metal oxides in green-based noninvasive analytical biosensors. In addition, we reviewed signal measurement, substrate bio-functionality, biochemical reaction, sensitivity, and limit of detection (LOD) of different biopolymers on various transducers. To date, pectin biopolymer, when conjugated with either gold nanoparticles, polypyrrole, reduced graphene oxide, or multiwall carbon nanotubes forming nanocomposites on glass carbon electrode transducer, tends to give the best LOD, highest sensitivity and can detect multiple analytes/targets. This review will spur new possibilities for the use of biosensors for medical diagnostic tests.

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