Hepatotoxicity, Acute Toxicity and Salmonella/Microsome Mutagenicity Assay (Ames) of Imatinib Microemulsions

被引:0
|
作者
Baspinar, Yucel [1 ,2 ]
Gundogdu, Evren [3 ]
Koksal, Cinel [2 ,4 ]
Karasulu, Hatice Y. [5 ]
Yavasoglu, Nefise U. Karabay [2 ,4 ]
Karasulu, Ercument [2 ,6 ]
机构
[1] Ege Univ, Fac Pharm, Dept Pharmaceut Biotechnol, TR-35100 Izmir, Turkey
[2] Ege Univ, Ctr Drug Res & Dev & Pharmacokinet Applicat, TR-35100 Izmir, Turkey
[3] Ege Univ, Fac Pharm, Dept Radiopharm, TR-35100 Izmir, Turkey
[4] Ege Univ, Fac Sci, Dept Biol, TR-35100 Izmir, Turkey
[5] Ege Univ, Fac Pharm, Dept Pharmaceut Technol, TR-35100 Izmir, Turkey
[6] Ege Univ, Fac Pharm, Dept Biopharmaceut & Pharmacokinet, TR-35100 Izmir, Turkey
来源
LATIN AMERICAN JOURNAL OF PHARMACY | 2016年 / 35卷 / 01期
关键词
Ames test; cytotoxicity; hepatotoxicity; imatinib; microemulsion; oral toxicity; ORAL ABSORPTION; DELIVERY; PHARMACOKINETICS; INHIBITION; MESYLATE; CANCER;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this study was to investigate cytotoxic activities, acute oral toxicity and gene mutagenicity in form of Salmonella/microsome mutagenicity assay (Ames) of imatinib microemulsion systems (IM MEs). The MEs were prepared by the titration method using pseudo ternary phase diagram. For the cytotoxicity tests, the hepatocellular cell lines Hep 3B (CRL-10741) and Hep G2 (HB-8064) were used. The acute oral toxicity was assessed using the limit test in mice with a dose of 2000 mg/kg body weight. The MEs consisted mainly of Labrasol/Capyrol 90/ Cremophor EL/ Cremophor EL-Span 80/Transcutol /water. In conclusion, no cytotoxic effects, no lethality during the acute oral toxicity test and no mutagenic potential in the TA98 nor in the TA100 strains could be observed on the here investigated cells. According to the obtained results, the developed MEs could be a promising alternative to the available marketed oral drug delivery.
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页码:98 / 104
页数:7
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