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Updated: Sep 10, 2025

A Novel Method to Determine the Longitudinal Antibacterial Activity of Drug-Eluting Materials
Published on: March 3, 2023
Dual antibiotic PLGA microspheres for the treatment of traumatic osteomyelitis
Liangguo Si1, Wenping Zhang2, Haifeng Jiang2
1School of Clinical Medicine, Ningxia Medical University , 750004, Yinchuan, China.
Abstract:
Traumatic osteomyelitis (TO) treatment remains challenging due to biofilm formation and poor antibiotic penetration. We developed poly(lactic-co-glycolic acid) (PLGA) microspheres co-loaded with moxifloxacin/rifampicin (M/R-P) to address these limitations. Key findings: In vitro: The microspheres showed (1) no cytotoxicity (CCK-8 assay; live/dead staining; cytoskeletal staining; SEM visualization), and (2) no inhibition of osteogenic potential (ALP activity).In vivo: M/R-P microspheres significantly reduced MRSA burden ( 8 ± 3 × 10³ CFU/g) compared to debridement-only controls (3143 ± 727 × 10³ CFU/g; p < 0.0001), and near-complete infection resolution (histopathology). Conclusion: These results demonstrate that the M/R-P microspheres possess excellent safety profiles, favorable cytocompatibility, and remarkable antibacterial efficacy. The findings confirm the feasibility of our innovative approach using PLGA as a drug delivery carrier for localized antibiotic therapy in chronic osteomyelitis treatment, achieved through technological optimization for combined antibiotic administration. This provides a novel strategic direction for ultimately overcoming the clinical challenge of traumatic osteomyelitis.
Insights
New poly(lactic-co-glycolic acid) (PLGA) microspheres loaded with moxifloxacin/rifampicin effectively treat traumatic osteomyelitis. These microspheres show excellent safety and antibacterial efficacy, offering a promising localized antibiotic therapy.
Area of Science:
- Biomaterials Science
- Infectious Diseases
- Drug Delivery Systems
Background:
- Traumatic osteomyelitis (TO) presents significant treatment challenges, primarily due to bacterial biofilm formation and inadequate antibiotic penetration to the infection site.
- Current treatment strategies often struggle to achieve effective bacterial eradication, leading to chronic infections and prolonged patient suffering.
Purpose of the Study:
- To develop and evaluate poly(lactic-co-glycolic acid) (PLGA) microspheres co-loaded with moxifloxacin and rifampicin (M/R-P) for the localized treatment of traumatic osteomyelitis.
- To assess the safety, cytocompatibility, and in vivo antibacterial efficacy of the M/R-P microspheres against Staphylococcus aureus (MRSA) in a traumatic osteomyelitis model.
Main Methods:
- PLGA microspheres were formulated to co-load moxifloxacin and rifampicin.
- In vitro assessments included cytotoxicity assays (CCK-8, live/dead staining, SEM) and evaluation of osteogenic potential (ALP activity).
- In vivo efficacy was determined by quantifying bacterial burden (CFU/g) and assessing infection resolution via histopathology in a relevant animal model.
Main Results:
- In vitro studies confirmed that the M/R-P microspheres exhibited no cytotoxicity and did not inhibit osteogenic potential.
- In vivo, M/R-P microspheres significantly reduced MRSA bacterial burden compared to debridement-only controls (8 ± 3 × 10³ CFU/g vs. 3143 ± 727 × 10³ CFU/g; p < 0.0001).
- Histopathological analysis indicated near-complete resolution of infection in the M/R-P microsphere treatment group.
Conclusions:
- The developed M/R-P microspheres demonstrate excellent safety profiles, favorable cytocompatibility, and remarkable antibacterial efficacy for traumatic osteomyelitis.
- PLGA microspheres serve as a feasible and effective drug delivery carrier for localized antibiotic therapy in chronic osteomyelitis.
- This innovative approach offers a novel strategic direction for overcoming the clinical challenges associated with traumatic osteomyelitis treatment.
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