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Published on: February 6, 2016
Antimicrobial lubricant formulations containing poly(hydroxybenzene)-trimethoprim conjugates synthesized by
Idalina Gonçalves1, Cláudia M Botelho, Ana Teixeira
1CEB - Centre of Biological Engineering, University of Minho, 4710-057, Braga, Portugal.
Abstract:
Poly(hydroxybenzene)-trimethoprim conjugates were prepared using methylparaben as substrate of the oxidative enzyme tyrosinase. MALDI-TOF MS analysis showed that the enzymatic oxidation of methylparaben alone leads to the poly(hydroxybenzene) formation. In the presence of trimethoprim, the methylparaben tyrosinase oxidation leads poly(hydroxybenzene)-trimethoprim conjugates. All of these compounds were incorporated into lubricant hydroxyethyl cellulose/glycerol mixtures. Poly(hydroxybenzene)-trimethoprim conjugates were the most effective phenolic structures against the bacterial growth reducing by 96 and 97% of Escherichia coli and Staphylococcus epidermidis suspensions, respectively (after 24 h). A novel enzymatic strategy to produce antimicrobial poly(hydroxybenzene)-antibiotic conjugates is proposed here for a wide range of applications on the biomedical field.
Insights
Researchers developed novel antimicrobial poly(hydroxybenzene)-trimethoprim conjugates using an enzymatic method. These conjugates effectively inhibited bacterial growth, showing significant reductions in Escherichia coli and Staphylococcus epidermidis.
Area of Science:
- Biomaterials Science
- Enzymatic Synthesis
- Antimicrobial Agents
Background:
- Antimicrobial resistance necessitates novel therapeutic strategies.
- Poly(hydroxybenzene) structures offer potential for functionalization.
- Enzymatic synthesis provides a green chemistry approach for conjugate preparation.
Purpose of the Study:
- To develop poly(hydroxybenzene)-trimethoprim conjugates using tyrosinase.
- To evaluate the antimicrobial efficacy of these conjugates.
- To propose an enzymatic strategy for producing antimicrobial conjugates.
Main Methods:
- Enzymatic oxidation of methylparaben catalyzed by tyrosinase.
- Formation of poly(hydroxybenzene) and poly(hydroxybenzene)-trimethoprim conjugates.
- Incorporation of conjugates into hydroxyethyl cellulose/glycerol mixtures.
- Antimicrobial activity testing against Escherichia coli and Staphylococcus epidermidis.
Main Results:
- Enzymatic oxidation of methylparaben yielded poly(hydroxybenzene).
- Poly(hydroxybenzene)-trimethoprim conjugates were successfully synthesized.
- Conjugates demonstrated high efficacy in reducing bacterial suspensions by 96-97% within 24 hours.
- Incorporation into hydroxyethyl cellulose/glycerol mixtures was achieved.
Conclusions:
- A novel enzymatic strategy for preparing antimicrobial poly(hydroxybenzene)-antibiotic conjugates was established.
- The synthesized conjugates show potent antimicrobial activity.
- This approach holds promise for biomedical applications requiring antimicrobial properties.
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