Multi-drug loaded eugenol-based nanoemulsions for enhanced anti-mycobacterial activity

Tuberculosis is one of the oldest bacterial infections known to mankind caused by Mycobacterium tuberculosis . The aim of this research is to optimize and formulate a multi-drug loaded eugenol based nanoemulsion system and to evaluate its ability as an antimycobacterial agent and its potential to be...

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Veröffentlicht in:MedChemComm 2023-03, Vol.14 (3), p.433-443
Hauptverfasser: Menon, Parvathy Mohan, Chandrasekaran, Natarajan, C, George Priya Doss, Shanmugam, Sivakumar
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Sprache:eng
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Zusammenfassung:Tuberculosis is one of the oldest bacterial infections known to mankind caused by Mycobacterium tuberculosis . The aim of this research is to optimize and formulate a multi-drug loaded eugenol based nanoemulsion system and to evaluate its ability as an antimycobacterial agent and its potential to be a low cost and effective drug delivery system. All the three eugenol based drug loaded nano-emulsion systems were optimized using response surface methodology (RSM)-central composite design (CCD) and were found stable at a ratio of 1 : 5 (oil : surfactant) when ultrasonicated for 8 minutes. The minimum inhibitory concentration (MIC) values against strains of Mycobacterium tuberculosis highly proved that these essential oil-based nano-emulsions showed more promising results and an even improved anti-mycobacterium activity on the addition of a combination of drugs. The absorbance of 1st line anti-tubercular drugs from release kinetics studies showed a controlled and sustained release in body fluids. Thus, we can conclude that this is a much more efficient and desirable method in treating infections caused by Mycobacterium tuberculosis and even its MDR/XDR strains. All these nano-emulsion systems were stable for more than 3 months. Reformulation of 1st line anti-TB drugs using a eugenol based nanoemulsion system to enhance its drug potency as an anti-mycobacterium agent and to improve its sustainable release.
ISSN:2632-8682
2040-2503
2632-8682
2040-2511
DOI:10.1039/d2md00320a