Apigenin loaded nanoparticle delayed development of hepatocellular carcinoma in rats

被引:83
作者
Bhattacharya, Sanchari [1 ]
Mondal, Laboni [1 ]
Mukherjee, Biswajit [1 ]
Dutta, Lopamudra [1 ]
Ehsan, Iman [1 ]
Debnath, Mita C. [2 ]
Gaonkar, Raghuvir H. [2 ]
Pal, Murari M. [1 ]
Majumdar, Subrata [3 ]
机构
[1] Jadavpur Univ, Dept Pharmaceut Technol, Kolkata 700032, W Bengal, India
[2] Indian Inst Chem Biol, CSIR, Infect Dis & Immunol Div, Kolkata, W Bengal, India
[3] Bose Inst, Div Mol Med, Kolkata, W Bengal, India
关键词
Apigenin nanoparticles; Hepatocellular carcinoma; Pharmacokinetics; Gamma scintigraphy; Histopathology; LC-MS/MS; EXPRESSION; APOPTOSIS; LIVER;
D O I
10.1016/j.nano.2018.05.011
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
Hepatocellular carcinoma (HCC) is one of the major causes of cancer related death globally. Apigenin, a dietary flavonoid, possesses antitumor activity against HCC cells in-vitro. Development, physicochemical characterization of apigenin loaded nanoparticles (ApNp), biodistribution pattern and pharmacokinetic parameters of apigenin upon intravenous administration of ApNp, and effect of ApNp treatment in rats with HCC were investigated. Apigenin loaded nanoparticles had a sustained drug release pattern and successfully reached the hepatic cancer cells in-vitro as well as in liver of carcinogenic animals. ApNp predominantly delayed the progress of !ICC in chemical induced hepatocarcinogenesis in rats. Quantification of apigenin by liquid chromatography-mass spectroscopy (LC-MS/MS) showed that apigenin availability significantly increased in blood and liver upon ApNp treatment. Apigenin loaded nanoparticle delivery substantially controlled the severity of hepatocellular carcinoma and could be a future hope for lingering the survival in hepatic cancer patients. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:1905 / 1917
页数:13
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