Formulation development of Silybum marianum seed extracts and silymarin nanoparticles, and evaluation of hepatoprotective effect

被引:16
作者
Macit, Meltem [1 ]
Duman, Gulengul [1 ]
Cumbul, Alev [2 ]
Sumer, Engin [3 ]
Macit, Caglar [4 ]
机构
[1] Yeditepe Univ, Fac Pharm, Dept Pharmaceut Technol, TR-34755 Istanbul, Turkiye
[2] Yeditepe Univ, Fac Med, Dept Basic Med Sci, TR-34755 Istanbul, Turkiye
[3] Yeditepe Univ, Fac Pharm, Dept Pharmaceut Toxicol, TR-34755 Istanbul, Turkiye
[4] Istanbul Medipol Univ, Sch Pharm, Dept Pharmacol, TR-34815 Istanbul, Turkiye
关键词
Silymarin; ALT and AST; Liver; Milk thistle; Extraction; INDUCED LIVER-INJURY; POLYMERIC MICELLES; DRUG; BIOAVAILABILITY; RELEASE; HEPATOTOXICITY; ENHANCEMENT; PERSPECTIVE; ACTIVATION; DELIVERY;
D O I
10.1016/j.jddst.2023.104378
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, we formulated silymarin-nanoparticles and assayed their ability to reduce acetaminophen-induced toxicity in vitro and in vivo. After silymarin molecules were encapsulated the loading efficiency and the physi-cochemical properties of fabricated nanoparticles were investigated by HPLC and DLS analysis. The in vivo hepatoprotective studies were conducted on rats in an optimized setting. The nanoformulation was presented a significant (p <= 0.05) hepatoprotective effect by reducing the serum marker enzymes such as AST, and ALT. The histopathological study further confirmed the hepatoprotective activity of the nanoformulations when compared with the acetaminophen-induced, two different silymarin formulations as treatment group and control group. These results indicate that the nano approaches could be used to improve the therapeutic efficacy of the nano-silymarin. The formulation of silymarin-nanoparticles showed a spherical shape with an average diameter be-tween 138.9 nm and 1155 nm, the zeta potential of - 0.0340 mV. The average loading efficiency was found around 32 +/- 0.5%.
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页数:8
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