Publication: NLC-Based Rifampicin Delivery System: Development and Characterization for Improved Drug Performance Against Staphylococcus aureus
| dc.contributor.author | Carrasco, Javiera | |
| dc.contributor.author | Sandoval, Felipe | |
| dc.contributor.author | Schuh, Christina | |
| dc.contributor.author | Lagos, Carlos | |
| dc.contributor.author | Morales, Javier | |
| dc.contributor.author | Arriagada, Francisco | |
| dc.contributor.author | Ortiz, Andrea | |
| dc.date.accessioned | 2026-08-20T17:10:25Z | |
| dc.date.available | 2026-08-20T17:10:25Z | |
| dc.date.issued | 2025 | |
| dc.description.abstract | Background/Objectives: Rifampicin is a typical antibiotic used for the treatment of Staphylococcus aureus (S. aureus) infections; however, its clinical utility is limited by poor aqueous solubility, chemical instability, and increasing bacterial resistance. Nanostructured lipid carriers (NLCs) offer a promising strategy to improve drug solubility, stability, and antimicrobial performance. Methods: In this study, rifampicin-loaded NLC (NLC-RIF) was developed using a hot homogenization with a low energy method and characterized in terms of particle size, polydispersity index, zeta potential, encapsulation efficiency, colloidal stability, and drug loading. Results: In vitro release studies under sink conditions demonstrated a biphasic release pattern, best described by the Korsmeyer-Peppas model, suggesting a combination of diffusion and matrix erosion mechanisms. Antimicrobial activity against S. aureus revealed a substantial increase in potency for NLC-RIF, with an IC50 of 0.46 ng/mL, approximately threefold lower than that of free rifampicin. Cytotoxicity assays in HepG2 cells confirmed over 90% cell viability across all tested concentrations. Conclusions: These findings highlight the potential of NLC-RIF as a biocompatible and effective nanocarrier system for enhancing rifampicin delivery and antibacterial activity. | |
| dc.description.version | Versión Publicada | |
| dc.identifier.citation | Carrasco-Rojas J, Sandoval FI, Schuh CMAP, Lagos CF, Morales JO, Arriagada F, Ortiz AC. NLC-Based Rifampicin Delivery System: Development and Characterization for Improved Drug Performance Against Staphylococcus aureus. Pharmaceutics. 2025 Jun 19;17(6):799. doi: 10.3390/pharmaceutics17060799. | |
| dc.identifier.doi | https://doi.org/10.3390/pharmaceutics17060799 | |
| dc.identifier.uri | https://hdl.handle.net/11447/11027 | |
| dc.language.iso | en | |
| dc.subject | HepG2 cell | |
| dc.subject | Staphylococcus aureus | |
| dc.subject | Antibiotic | |
| dc.subject | Drug release | |
| dc.subject | Nanostructured lipid carrier | |
| dc.title | NLC-Based Rifampicin Delivery System: Development and Characterization for Improved Drug Performance Against Staphylococcus aureus | |
| dc.type | Article | |
| dcterms.accessRights | Acceso Abierto | |
| dcterms.source | Pharmaceutics | |
| dspace.entity.type | Publication |
Files
Original bundle
1 - 1 of 1
No Thumbnail Available
- Name:
- NLC-Based Rifampicin Delivery System Development and.pdf
- Size:
- 1.23 MB
- Format:
- Adobe Portable Document Format
- Description:
- Texto Completo
License bundle
1 - 1 of 1
No Thumbnail Available
- Name:
- license.txt
- Size:
- 347 B
- Format:
- Item-specific license agreed upon to submission
- Description: