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Updated: Aug 16, 2025

Antimicrobial Peptides Produced by Selective Pressure Incorporation of Non-canonical Amino Acids
Published on: May 4, 2018
Glycopeptide antibiotic drug stability in aqueous solution
Sardar M Jakaria1,2, David E Budil2, James Murtagh1
1Hikma Pharmaceuticals, Bedford, OH 44146 USA.
Stable liquid formulations of glycopeptide antibiotics are achievable. Strategies to prevent chemical and physical degradation enhance the stability of these crucial antibacterial drugs for improved accessibility.
Area of Science:
- Pharmaceutical Sciences
- Microbiology
- Drug Delivery
Background:
- Glycopeptide antimicrobials are vital for treating Gram-positive bacterial infections.
- Current lyophilized formulations present economic and practical challenges.
- Liquid formulations offer significant advantages for drug accessibility and administration.
Purpose of the Study:
- To review recent advancements in stabilizing glycopeptide antibiotics in aqueous solutions.
- To identify key degradation pathways and strategies for mitigation.
- To assess the market availability and stability of existing glycopeptide drugs.
Main Methods:
- Literature review of published studies and patents on glycopeptide stability.
- Analysis of chemical and physical degradation mechanisms.
- Evaluation of formulation strategies including pH control, excipients, and solvent minimization.
Main Results:
- Chemical degradation is influenced by pH, oxygen, and solvent exposure.
- Physical degradation can be reduced by excipients like sugars, amino acids, polyols, and surfactants.
- Several glycopeptide antibiotics show potential for stable aqueous formulations.
Conclusions:
- Understanding degradation mechanisms is key to developing stable liquid glycopeptide formulations.
- Stable aqueous formulations can improve treatment options for multidrug-resistant pathogens.
- This advancement is critical for regions lacking cold-chain infrastructure.
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