In vitro cytotoxic and genotoxic evaluation of peptides used in nuclear medicine (DOTATATE and Ubiquicidin29-41) in CHO-K1 cells

被引:4
|
作者
Ocampo, Ivette Zegarra [1 ]
Souza Passos, Priscila de Queiroz [2 ]
de Carvalho, Luma Ramirez [1 ]
Lira da Cruz, Camila Ayala [1 ]
Esteves-Pedro, Natalia Mencacci [2 ]
Medeiros da Silva, Fabiana [2 ]
Higa, Olga Zazuco [1 ,2 ]
Pereira Dias, Luiz Alberto [3 ]
Okazaki, Kayo [1 ]
Vieira, Daniel Perez [1 ]
机构
[1] Inst Nucl & Energet Res IPEN CNEN SP, Ctr Biotechnol, Radiobiol Lab, Av LineuPrestes 2242, BR-05508000 Sao Paulo, SP, Brazil
[2] Biosynthesis Lab, Sao Paulo, SP, Brazil
[3] Inst Nucl & Energet Res IPEN CNEN SP, Ctr Radiopharmacy Qual Control Management, Sao Paulo, SP, Brazil
关键词
CHO-K1; cell; Cytotoxicity; Genotoxicity; Modified micronucleus assay; DOTATATE; Ubiquicidin(29-41); MICRONUCLEUS ASSAY; PERIPHERAL-BLOOD; VALIDATION; LYMPHOCYTES; FREQUENCY; EXPOSURE; PET/CT;
D O I
10.1007/s10616-016-0024-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Micronucleus (MN) assay constitutes a valuable surrogate to the chromosome aberration technique for in vitro testing of the genotoxicity of substances. As test substances, two peptidic compounds (DOTATATE and Ubiquicidin(29-41)) used in nuclear medicine, were tested for in vitro cytotoxicity and genotoxicity in CHO-K1 cells. None of the compounds showed detectable cytotoxicity (0.5-7.3 ng/mL for DOTATATE and 0.3-4.5 ng/mL for UBI29-41), genotoxicity (0.72, 7.2 and 72.0 ng/ml for DOTATATE and 0.45, 4.5 and 45.0 ng/mL for UBI29-41) or cell cycle changes as compared to untreated controls at the concentrations tested. Statistical analysis showed good concordance between two independent analysts. The results corroborate the notion of the safety of the compounds and present improvements of the in vitro MN assay when performed in a pre-clinical trial context that increase the throughput of small-to-medium testing facilities as an alternative to high content screening systems.
引用
收藏
页码:2301 / 2310
页数:10
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