Investigation of the effects of nanoemulsion formulation containing glycyrrhizin in Streptozotocin-induced diabetic rats

被引:1
|
作者
Duysak, Lale [1 ,4 ]
Kaplan, Afife Busra Ugur [2 ]
Gulaboglu, Mine [1 ]
Cetin, Meltem [2 ]
Kutlu, Zerrin [1 ]
Demirci, Tuba [3 ]
机构
[1] Ataturk Univ, Fac Pharm, Dept Biochem, Erzurum, Turkiye
[2] Ataturk Univ, Fac Pharm, Dept Pharmaceut Technol, Erzurum, Turkiye
[3] Ataturk Univ, Fac Med, Dept Histol & Embryol, Erzurum, Turkiye
[4] Ataturk Univ, Fac Pharm, Dept Biochem, TR-25240 Erzurum, Turkiye
关键词
Antioxidant; Diabetes mellitus; Glycyrrhizin; Nanoemulsion; Streptozotocin; OXIDATIVE STRESS; LIPID-PEROXIDATION; ORAL BIOAVAILABILITY; ACID; MODELS; LIVER;
D O I
10.1016/j.fbio.2023.103210
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
This study aims to prepare and in vitro and in vivo characterize nanoemulsion formulation containing GLY (GLY-NE). Firstly, the NE formulation was prepared and in vitro characterized. Later, the hypoglycemic and antioxidant effects of GLY-NE formulations in STZ-induced diabetic rats were investigated. Also, histopathological evaluation was performed. The droplet sizes of blank NE (B-NE; 110.75 +/- 9.60) and GLY-NE (126.44 +/- 3.86) were in the nano-size range. Furthermore, PDI values of B-NE and GLY-NE formulations were less than 0.3. The zeta potential values of B-NE and GLY-NE were (-)19.02 +/- 1.18 mV and (-) 20.52 +/- 0.83 mV, respectively. At the end of the 21st day, comparing the same dose groups administered GLY or GLY-NE, the blood glucose levels of the diabetic rats administered GLY-NE (D-GLY-NE groups) were lower than the diabetic rats administered GLY (D-GLY groups). Furthermore, the blood glucose level of D-GLY-NE (40 mg/kg) was significantly lower than that of D-GLY (40 mg/kg; p < 0.05). Compared with the diabetic control, the serum ALT and AST levels and liver MDA of the diabetic rats treated with GLY or GLY-NE (for all doses) were significantly decreased, while the liver SOD activity and GSH levels were significantly increased (p < 0.05). The NE formulation may be a potential dosage form for oral delivery of GLY.
引用
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页数:9
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