Transdermal delivery of antibacterial peptides in the management of methicillin-resistant Staphylococcus aureus

Shivraj Sangappa Shivpuje1, Durgacharan A Bhagwat2, Pankaj Ashok Jadhav3

  • 1School of Pharmacy, SRTM University, Nanded, Maharashtra, 431606, India.

PubMed

Insights

Antimicrobial peptides (AMPs) show promise against methicillin-resistant Staphylococcus aureus (MRSA) infections. Microneedle (MN) delivery systems enhance AMP efficacy and stability, overcoming limitations for treating MRSA skin infections.

Area of Science:

  • Biomedical Engineering
  • Infectious Diseases
  • Drug Delivery Systems

Background:

  • Bacterial antimicrobial resistance (AMR) is a global health crisis, with multidrug-resistant (MDR) bacteria like methicillin-resistant Staphylococcus aureus (MRSA) rendering conventional antibiotics ineffective.
  • Antimicrobial peptides (AMPs) offer a promising alternative due to their broad-spectrum activity and lower resistance development potential, but face challenges like degradation and poor bioavailability.
  • Skin and soft tissue infections (SSTIs) caused by MRSA necessitate novel therapeutic strategies to combat rising antibiotic resistance.

Purpose of the Study:

  • To review microneedle (MN)-assisted delivery systems for antimicrobial peptides (AMPs) in treating MRSA infections.
  • To highlight innovative strategies enhancing AMP stability, bioavailability, and targeted delivery.
  • To discuss the challenges and potential of AMPs delivered via MNs for clinical translation against MRSA.

Main Methods:

  • Review of literature on microneedle (MN) technology and nano-formulations for antimicrobial peptide (AMP) delivery.
  • Analysis of innovative strategies such as Janus-type dressings, bioresponsive MNs, and metal-organic frameworks (MOFs).
  • Evaluation of studies combining AMPs with MNs and nanosystems for enhanced biofilm penetration and therapeutic efficacy against MRSA.

Main Results:

  • Microneedle (MN) platforms coupled with nano-formulations improve AMP stability, bioavailability, and targeted release, mitigating cytotoxicity.
  • Innovative approaches like Janus-type dressings, bioresponsive MNs, and MOF-based nanocarriers demonstrate favorable outcomes against MRSA skin infections.
  • Combinations of AMPs and vancomycin with smart MNs and nanosystems show enhanced biofilm penetration and therapeutic efficacy.

Conclusions:

  • Microneedle (MN)-assisted delivery represents a promising strategy to enhance the clinical utility of antimicrobial peptides (AMPs) against MRSA infections.
  • Despite advancements, challenges in AMP stability, cytotoxicity, and manufacturing costs require further research for successful clinical translation.
  • Further development of MN-based delivery systems is crucial for overcoming limitations and realizing the full therapeutic potential of AMPs in combating MRSA.

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