Co-Encapsulation of Violacein and Iron Oxide in Poly(lactic acid) Nanoparticles for Simultaneous Antibacterial and Anticancer Applications
Journal of biomedical nanotechnology, ISSN: 1550-7033, Vol: 18, Issue: 3, Page: 729-739
2022
- 5Citations
- 9Captures
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Metrics Details
- Citations5
- Citation Indexes5
- Captures9
- Readers9
Article Description
To date, the possibility of drug-resistant bacterial infections in hospitals and intensive care units comprises a significant concern especially for immunocompromised cancer patients. In the current study, violacein and superparamagnetic iron oxide nanoparticles were co-encapsulated in polylactic acid nanoparticles (vio-Fe₃O₄-PLA) and tested for their antimicrobial and anticancer activity. The loaded nanoparticles presented efficient saturation magnetization that rendered this nanosystem a promising candidate for magnetic targeting. Moreover, violacein released from the nanoparticles at 500 μg/mL successfully inhibited the growth of the "superbug" methicillin-resistant Staphylococcus aureus (MRSA) with an IC50 value of 595.8 μg/mL, while it did not prove effective against multi-drug-resistant Escherichia coli at concentrations of 10-1000 μg/mL. Finally, a concentration of 500 μg/mL of drug loaded magnetic nanoparticles induced an over 80% growth inhibition of glioblastoma and melanoma cancer cell lines with IC50 values of 221.30 and 201.60 μg/mL, respectively. Since bacterial infections are a key clinical problem for cancer patients due to their compromised immune systems, the presented results suggest that our system should be further studied for its simultaneous anti-bacterial and anti-cancer properties, as it comprises a promising strategy for combating bacterial infections and providing anticancer activity through magnetic-targeted delivery.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85132454172&origin=inward; http://dx.doi.org/10.1166/jbn.2022.3305; http://www.ncbi.nlm.nih.gov/pubmed/35715912; https://www.ingentaconnect.com/content/10.1166/jbn.2022.3305; https://dx.doi.org/10.1166/jbn.2022.3305; https://www.ingentaconnect.com/content/asp/jbn/2022/00000018/00000003/art00008
American Scientific Publishers
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