Development of self nanoemulsifying drug delivery system (SNEDDS) to improve antioxidant activity of single garlic extract (Allium sativum L.)

Single garlic has been known have various benefits because it contains many active compounds. The active compounds in garlic, like antioxidants are quickly degraded in the digestive tract. Various attempts have been made to maintain the antioxidants content in garlic through drug delivery systems. O...

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Main Authors: Sri Rahayu Lestari, Sri Rahayu Lestari, Nenes Prastita, Nenes Prastita, Siti lmroatul Maslikah, Siti lmroatul Maslikah, Sunaryono, Sunaryono, Abdul Gofur, Abdul Gofur, Fauziatul Fajaroh, Fauziatul Fajaroh, Yuslinda Annisa, Yuslinda Annisa, Nik Malek, Nik Ahmad Nizam
Format: Conference or Workshop Item
Published: 2023
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Online Access:http://eprints.utm.my/107909/
http://dx.doi.org/10.1063/5.0111654
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Summary:Single garlic has been known have various benefits because it contains many active compounds. The active compounds in garlic, like antioxidants are quickly degraded in the digestive tract. Various attempts have been made to maintain the antioxidants content in garlic through drug delivery systems. One of the drug delivery systems that can protect antioxidants is the Self Nanoemulsifying Drug Delivery System (SNEDDS). This study aims to characterize and test the antioxidant activity of SNEDDS single garlic extract (SGE). The methods used include single garlic extraction with ethanol solvent, SNEDDS formulation, SNEDDS preparation, SNEDDS response test, and physical tests. Characterization of SNEDDS size and morphology using Particle Size Analyzer (PSA) and Transmission Electron Microscopy (TEM). An antioxidant activity test was carried out using the DPPEI method. The results showed that the mean droplet size of SNEDDS-SGE was 23.10 ± 0.69 nm, the polydispersity index (PDI) was 0,46 ± 0,01 and the Zeta potential was -33.07±0.45 mV. The morphology of SNEDDS is a round droplet. The results of the antioxidant activity test showed that the percentage of antioxidant activity of SNEDDS-SGE was 56.74±1,04 which was higher than the percentage of antioxidant activity of SGE that was not prepared with SNEDDS 17.56 ±0.08.