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Volume 3, Issue 4 (Suppl)
Polym Sci
ISSN: 2471-9935 Polym Sci, an open access journal
October 12-13, 2017 Osaka, Japan
Annual Meeting on
Biopolymers and Drug Delivery Systems
Biopolymers Meeting 2017
October 12-13 2017
Page 62
Polym Sci 2017, 3:4
DOI: 10.4172/2471-9935-C1-006
Development and transportation pathway of Alpinia galanga oil loaded Self-Micro Emulsifying Drug
Delivery Systems (SMEDDS) for fish anesthesia
Siriporn Okonogi and Nattakanwadee Khumpirapang
Chiang Mai University, Thailand
A
lpinia galangal
, an important edible plant in family Zingiberaceae is commonly used in Asian folk medicinal remedies. The
essential oil of A.
Galanga
Rhizomes (AGO) has many biological activities e.g., antioxidant, antibacterial, antifungal and anti-
inflammatory actions. However, the poor water miscibility of AGO causes the limitation of its clinical use in both human and animals.
The alcohol used to dissolve AGO for fish anesthesia always causes hyperactivity in fish. The aim of this study was to solve this
problem by developing Self-Micro Emulsifying Drug Delivery Systems (SMEDDS) of AGO. Pseudoternary phase diagrams of AGO
were constructed to identify the best AGO-SMEDDS formulation. It was found that the AGO-SMEDDS composed of 20.0% AGO
and 53.3% tween 80 and 26.7% ethanol had a mean droplet size of 82 nm after dispersing in distilled water. The anesthetic activity of
the developed AGO-SMEDDS in koi (
Cyprinus carpio
) was evaluated in comparison with an AGO ethanol solution on the induction
time required to reach the surgical anesthetic stage in which the fish stop all swimming activity and show loss of equilibrium and
responsiveness. Results showed that the induction times of the fish receiving 200, 300 and 400 mg/L AGO-SMEDDS were 233, 130 and
112 seconds, respectively. Importantly, AGO-SMEDDS showed significantly higher anesthetic activity than the AGO ethanol solution
which showed the induction times of 303, 207 and 167 seconds, with the same dose of AGO, respectively. The transportation pathway
of AGO was investigated using a fluorescence microscope. AGO was labeled with Nile red. The brain, gills and skin of fish showed red
fluorescent spots without auto fluorescence phenomena compared to unlabeled AGO. This result suggests that the AGO entered the
fish via gills and skin and was transported to the brain where the anesthetic effect took place.
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