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Clindamycin-Loaded Polyhydroxyalkanoate Nanoparticles for the Treatment of Methicillin-Resistant Staphylococcus
Muneeb Ullah1, Juho Lee1, Nurhasni Hasan2
1College of Pharmacy, Pusan National University, Busandaehak-ro 63 beon-gil 2, Geoumjeong-gu, Busan 46241, Republic of Korea.
Abstract:
Background/Objectives: Owing to the growing resistance of methicillin-resistant Staphylococcus aureus (MRSA) to conventional antibiotics, the development of innovative therapeutic strategies for the treatment of MRSA-infected cutaneous wounds poses a significant challenge. Methods: Here, by using polyhydroxyalkanoates (PHA), emerging biodegradable and biocompatible polymers naturally produced by various microorganisms, we developed clindamycin-loaded PHA nanoparticles (Cly-PHA NPs) as a novel approach for the treatment of MRSA-infected cutaneous wounds. Results: Cly-PHA NPs were characterized in terms of mean particle size (216.2 ± 38.9 nm), polydispersity index (0.093 ± 0.03), zeta potential (11.3 ± 0.5 mV), and drug loading (6.76 ± 0.19%). Owing to the sustained release of clindamycin over 2 days provided by the PHA, Cly-PHA NPs exhibited potent antibacterial effects against MRSA. Furthermore, Cly-PHA NPs significantly facilitated wound healing in a mouse model of MRSA-infected full-thickness wounds by effectively eradicating MRSA from the wound bed. Conclusions: Therefore, our results suggest that Cly-PHA NPs offer a promising approach for combating MRSA infections and accelerating cutaneous wound healing.
Insights
Novel clindamycin-loaded polyhydroxyalkanoate nanoparticles (Cly-PHA NPs) effectively treat methicillin-resistant Staphylococcus aureus (MRSA) wound infections. These nanoparticles accelerate healing by eradicating MRSA and providing sustained drug release.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Infectious Diseases
Background:
- Growing antibiotic resistance in methicillin-resistant Staphylococcus aureus (MRSA) necessitates novel therapeutic strategies.
- Developing effective treatments for MRSA-infected cutaneous wounds remains a significant clinical challenge.
Purpose of the Study:
- To develop and evaluate clindamycin-loaded polyhydroxyalkanoate nanoparticles (Cly-PHA NPs) for treating MRSA-infected cutaneous wounds.
- To assess the physicochemical properties, drug release kinetics, antibacterial efficacy, and wound healing potential of Cly-PHA NPs.
Main Methods:
- Polyhydroxyalkanoates (PHA) were utilized to create clindamycin-loaded nanoparticles (Cly-PHA NPs).
- Nanoparticle characterization included particle size, polydispersity index, zeta potential, and drug loading.
- In vitro antibacterial activity against MRSA and in vivo wound healing efficacy in a mouse model were evaluated.
Main Results:
- Cly-PHA NPs demonstrated a mean particle size of 216.2 ± 38.9 nm and drug loading of 6.76 ± 0.19%.
- Sustained release of clindamycin from PHA over 2 days was observed, leading to potent antibacterial effects against MRSA.
- Cly-PHA NPs significantly accelerated wound healing in a mouse model by eradicating MRSA.
Conclusions:
- Clindamycin-loaded PHA nanoparticles represent a promising therapeutic approach for MRSA infections.
- Cly-PHA NPs effectively combat MRSA and promote accelerated cutaneous wound healing.
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