Related Experiment Video
Updated: Apr 18, 2026

Facile Protocol for the Synthesis of Self-assembling Polyamine-based Peptide Amphiphiles PPAs and Related Biomaterials
Published on: June 25, 2018
Tailored synthesis of amine N-halamine copolymerized polystyrene with capability of killing bacteria
Qian Cai1, Sarina Bao1, Yue Zhao1
1College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, People's Republic of China.
Abstract:
Novel amine N-halamine copolymerized polystyrene (ANHCPS) nanostructures were controllably fabricated as potent antibiotics by using the surfactant-free emulsion copolymerization for killing pathogenic bacteria. The morphology and size of the ANHCPS were well tailored by tuning reaction conditions such as monomer molar ratio, temperature, and copolymerization time. Effect of chlorination aging time on the oxidative chlorine content in the ANHCPS was established, and the oxidative chlorine content was determined by the modified iodometric/thiosulfate technique. Antibacterial behavior of the ANHCPS on bacterial strain was evaluated using Staphylococcus aureus and Escherichia coli as model pathogenic bacteria via the plate counting technique, inhibition zone study, and time-kill assay. Antimicrobial results illustrated that the ANHCPS possessed superior antibacterial capability of killing pathogenic bacteria. The destruction induced by the ANHCPS on bacterial surface structure was proven by using SEM technique. The effect of the oxidative chlorine content and morphology/size on the antimicrobial capability was constructed as well. This study provides us a novel approach for controllably synthesizing amine N-halamine polymers, and making them the potent candidates for killing bacteria or even the control of microorganism contamination.
More Related Videos
10:53Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions
Published on: October 10, 2016
12:02An Efficient Method for the Synthesis of Peptoids with Mixed Lysine-type/Arginine-type Monomers and Evaluation of Their Anti-leishmanial Activity
Published on: November 2, 2016
Related Concept Videos
Preparation of 1° Amines: Azide Synthesis
Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...
Anionic Chain-Growth Polymerization: Overview
Preparation of Amines: Alkylation of Ammonia and Amines
Each alkylation step makes the nitrogen center more nucleophilic, which triggers successive alkylations until a quaternary ammonium salt is formed. Considering...
Preparation of 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...