Triclosan antimicrobial polymers

Richard C. Petersen; Richard C. Petersen

doi:10.3934/molsci.2016.1.88

AIMS Molecular Science

2016, Volume 3, Issue 1: 88-103. doi: 10.3934/molsci.2016.1.88

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Review

Triclosan antimicrobial polymers

Richard C. Petersen ^,

Department of Biomaterials and Restorative Sciences, University of Alabama at Birmingham, Birmingham, AL, USA

Received: 30 December 2015 Accepted: 22 March 2016 Published: 29 March 2016

Triclosan antimicrobial molecular fluctuating energies of nonbonding electron pairs for the oxygen atom by ether bond rotations are reviewed with conformational computational chemistry analyses. Subsequent understanding of triclosan alternating ether bond rotations is able to help explain several material properties in Polymer Science. Unique bond rotation entanglements between triclosan and the polymer chains increase both the mechanical properties of polymer toughness and strength that are enhanced even better through secondary bonding relationships. Further, polymer blend compatibilization is considered due to similar molecular relationships and polarities. With compatibilization of triclosan in polymers a more uniform stability for nonpolar triclosan in the polymer solid state is retained by the antimicrobial for extremely low release with minimum solubility into aqueous solution. As a result, triclosan is projected for long extended lifetimes as an antimicrobial polymer additive. Further, triclosan rapid alternating ether bond rotations disrupt secondary bonding between chain monomers in the resin state to reduce viscosity and enhance polymer blending. Thus, triclosan is considered for a polymer additive with multiple properties to be an antimicrobial with additional benefits as a nonpolar toughening agent and a hydrophobic wetting agent. The triclosan material relationships with alternating ether bond rotations are described through a complete different form of medium by comparisons with known antimicrobial properties that upset bacterial cell membranes through rapid fluctuating mechanomolecular energies. Also, triclosan bond entanglements with secondary bonding can produce structural defects in weak bacterial lipid membranes requiring pliability that can then interfere with cell division. Regarding applications with polymers, triclosan can be incorporated by mixing into a resin system before cure, melt mixed with thermoplastic polymers that set on cooling into a solid or alternatively applied as a coating through several different methods with dissolving into an organic solvent and dried on by evaporation as a common means.

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Citation: Richard C. Petersen. Triclosan antimicrobial polymers[J]. AIMS Molecular Science, 2016, 3(1): 88-103. doi: 10.3934/molsci.2016.1.88

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Abstract

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