Essential oils have been widely used for their antimicrobial and antifungal properties, but their instability to light and high volatility limit their clinical use. Useful strategies to improve their biopharmaceutical properties are vesicular drug delivery systems, particularly liposomes. The aim of the present study was to extract, characterize, and formulate the essential oil of Artemisia annua L. in liposomes. The optimized vesicles were evaluated for their performance against different drug-resistant Candida strains. Main constituents of AEO were camphor (22.6%), artemisia ketone (17.3%) and 1,8-cineole (15.8%). Optimized nanoliposomes were loaded with 10 mg/ml of AEO. Size was 250 nm, ?-potential was -10mV, and polydispersity index was 0.21. Encapsulation efficiency was about 75%, recovery % was more than 90%. The drug release study showed that after 14 h almost 100% of AEO was released from the vesicles. Minimum fungicidal concentration (MFC) values ranged from 10 to 42 mg/ml for pure AEO. MFC of AEO-loaded in nanoliposomes ranged from 5 to 10 mg/ml. The most susceptible species to AEO loaded in nanoliposome was C. norvegensis (5.00 mg/ml), followed by C. krusei. These findings suggest that AEO could be an interesting by-product of A. annua, and the proper entrapment of AEO into nanoliposomes could optimize the biological properties and defeat fungal infections.
Artemisia annua essential oil extraction, characterization, and incorporation in nanoliposomes, smart drug delivery systems against Candida species
Salvatici MC;
2020
Abstract
Essential oils have been widely used for their antimicrobial and antifungal properties, but their instability to light and high volatility limit their clinical use. Useful strategies to improve their biopharmaceutical properties are vesicular drug delivery systems, particularly liposomes. The aim of the present study was to extract, characterize, and formulate the essential oil of Artemisia annua L. in liposomes. The optimized vesicles were evaluated for their performance against different drug-resistant Candida strains. Main constituents of AEO were camphor (22.6%), artemisia ketone (17.3%) and 1,8-cineole (15.8%). Optimized nanoliposomes were loaded with 10 mg/ml of AEO. Size was 250 nm, ?-potential was -10mV, and polydispersity index was 0.21. Encapsulation efficiency was about 75%, recovery % was more than 90%. The drug release study showed that after 14 h almost 100% of AEO was released from the vesicles. Minimum fungicidal concentration (MFC) values ranged from 10 to 42 mg/ml for pure AEO. MFC of AEO-loaded in nanoliposomes ranged from 5 to 10 mg/ml. The most susceptible species to AEO loaded in nanoliposome was C. norvegensis (5.00 mg/ml), followed by C. krusei. These findings suggest that AEO could be an interesting by-product of A. annua, and the proper entrapment of AEO into nanoliposomes could optimize the biological properties and defeat fungal infections.File | Dimensione | Formato | |
---|---|---|---|
Journal of Drug Delivery Science and Technology 59 (2020) 101849.pdf
solo utenti autorizzati
Tipologia:
Versione Editoriale (PDF)
Licenza:
NON PUBBLICO - Accesso privato/ristretto
Dimensione
1.68 MB
Formato
Adobe PDF
|
1.68 MB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.