Synthesis and Application of Aurophilic Poly(Cysteine) and Poly(Cysteine)-Containing Copolymers

The redox capacity, as well as the aurophilicity of the terminal thiol side groups, in poly(Cysteine) lend a unique characteristic to this poly(amino acid) or polypeptide. There are two major application fields for this polymer: (i) biomedical applications in drug delivery and surface modification o...

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Main Authors: David Ulkoski, Carmen Scholz
Format: Article
Language:English
Published: MDPI AG 2017-10-01
Series:Polymers
Subjects:
Online Access:https://www.mdpi.com/2073-4360/9/10/500
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spelling doaj-2a7f22e0854240c8a8357c6b8cc981902020-11-25T00:38:56ZengMDPI AGPolymers2073-43602017-10-0191050010.3390/polym9100500polym9100500Synthesis and Application of Aurophilic Poly(Cysteine) and Poly(Cysteine)-Containing CopolymersDavid Ulkoski0Carmen Scholz1Department of Chemistry, University of Alabama, 301 Sparkman Dr., Huntsville, AL 35899, USADepartment of Chemistry, University of Alabama, 301 Sparkman Dr., Huntsville, AL 35899, USAThe redox capacity, as well as the aurophilicity of the terminal thiol side groups, in poly(Cysteine) lend a unique characteristic to this poly(amino acid) or polypeptide. There are two major application fields for this polymer: (i) biomedical applications in drug delivery and surface modification of biomedical devices and (ii) as coating for electrodes to enhance their electrochemical sensitivity. The intended application determines the synthetic route for p(Cysteine). Polymers to be used in biomedical applications are typically polymerized from the cysteine N-carboxyanhydride by a ring-opening polymerization, where the thiol group needs to be protected during the polymerization. Advances in this methodology have led to conditions under which the polymerization progresses as living polymerization, which allows for a strict control of the molecular architecture, molecular weight and polydispersity and the formation of block copolymers, which eventually could display polyphilic properties. Poly(Cysteine) used as electrode coating is typically polymerized onto the electrode by cyclic voltammetry, which actually produces a continuous, pinhole-free film on the electrode via the formation of covalent bonds between the amino group of Cysteine and the carbon of the electrode. This resulting coating is chemically very different from the well-defined poly(Cysteine) obtained by ring-opening polymerizations. Based on the structure of cysteine a significant degree of cross-linking within the coating deposited by cyclic voltammetry can be assumed. This manuscript provides a detailed discussion of the ring-opening polymerization of cysteine, a brief consideration of the role of glutathione, a key cysteine-containing tripeptide, and examples for the utilization of poly(Cysteine) and poly(Cysteine)-containing copolymers, in both, the biomedical as well as electrochemical realm.https://www.mdpi.com/2073-4360/9/10/500aurophilicpoly(amino acid)spoly(">l-cysteine)drug deliverysurface modificationelectrochemical based detection
collection DOAJ
language English
format Article
sources DOAJ
author David Ulkoski
Carmen Scholz
spellingShingle David Ulkoski
Carmen Scholz
Synthesis and Application of Aurophilic Poly(Cysteine) and Poly(Cysteine)-Containing Copolymers
Polymers
aurophilic
poly(amino acid)s
poly(
">l-cysteine)
drug delivery
surface modification
electrochemical based detection
author_facet David Ulkoski
Carmen Scholz
author_sort David Ulkoski
title Synthesis and Application of Aurophilic Poly(Cysteine) and Poly(Cysteine)-Containing Copolymers
title_short Synthesis and Application of Aurophilic Poly(Cysteine) and Poly(Cysteine)-Containing Copolymers
title_full Synthesis and Application of Aurophilic Poly(Cysteine) and Poly(Cysteine)-Containing Copolymers
title_fullStr Synthesis and Application of Aurophilic Poly(Cysteine) and Poly(Cysteine)-Containing Copolymers
title_full_unstemmed Synthesis and Application of Aurophilic Poly(Cysteine) and Poly(Cysteine)-Containing Copolymers
title_sort synthesis and application of aurophilic poly(cysteine) and poly(cysteine)-containing copolymers
publisher MDPI AG
series Polymers
issn 2073-4360
publishDate 2017-10-01
description The redox capacity, as well as the aurophilicity of the terminal thiol side groups, in poly(Cysteine) lend a unique characteristic to this poly(amino acid) or polypeptide. There are two major application fields for this polymer: (i) biomedical applications in drug delivery and surface modification of biomedical devices and (ii) as coating for electrodes to enhance their electrochemical sensitivity. The intended application determines the synthetic route for p(Cysteine). Polymers to be used in biomedical applications are typically polymerized from the cysteine N-carboxyanhydride by a ring-opening polymerization, where the thiol group needs to be protected during the polymerization. Advances in this methodology have led to conditions under which the polymerization progresses as living polymerization, which allows for a strict control of the molecular architecture, molecular weight and polydispersity and the formation of block copolymers, which eventually could display polyphilic properties. Poly(Cysteine) used as electrode coating is typically polymerized onto the electrode by cyclic voltammetry, which actually produces a continuous, pinhole-free film on the electrode via the formation of covalent bonds between the amino group of Cysteine and the carbon of the electrode. This resulting coating is chemically very different from the well-defined poly(Cysteine) obtained by ring-opening polymerizations. Based on the structure of cysteine a significant degree of cross-linking within the coating deposited by cyclic voltammetry can be assumed. This manuscript provides a detailed discussion of the ring-opening polymerization of cysteine, a brief consideration of the role of glutathione, a key cysteine-containing tripeptide, and examples for the utilization of poly(Cysteine) and poly(Cysteine)-containing copolymers, in both, the biomedical as well as electrochemical realm.
topic aurophilic
poly(amino acid)s
poly(
">l-cysteine)
drug delivery
surface modification
electrochemical based detection
url https://www.mdpi.com/2073-4360/9/10/500
work_keys_str_mv AT davidulkoski synthesisandapplicationofaurophilicpolycysteineandpolycysteinecontainingcopolymers
AT carmenscholz synthesisandapplicationofaurophilicpolycysteineandpolycysteinecontainingcopolymers
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