Cytotoxicity of Co(III) Complexes of Arginine.

P Genova, T Varadinova, R Alexandrova, S Trifunovic, P Radivojsa
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引用次数: 1

Abstract

The cytotoxicity of four Co(III) complexes of arginine on nontumour MDBK cells and on two cell lines derived from transplantable tumors, LSCC-SF(Mc29) and LSR-SF (SR), was evaluated comparative!y. Based on the cytotoxic concentration required to inhibit cell surveillance by 50% cc(nabla') it was found that: (i) the cytotoxicity of complexes tested increases when the concentration decreased; (ii) the cell surveillance depends on both complex and cell specificities. The complex specificity was illustrated by the order 1 > 4 > 2 >/= 3 . The cell specific response was demonstrated by the fact that LSCC-SG (Mc29) cells were up to 60 times more sensitive to 1 while LSR-SF (SR) cells were up to 1000 times more sensitive to 2 as compared to MDBK cells. Furthermore, with the prolongation of action on nontumour cells the cytotoxicity of 4 decreased up to 300 times while for both tumour cells it was independent on the duration of action.

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精氨酸Co(III)配合物的细胞毒性。
比较评价了精氨酸四种Co(III)复合物对非肿瘤MDBK细胞和来源于可移植肿瘤的两种细胞系LSCC-SF(Mc29)和LSR-SF (SR)的细胞毒性。根据抑制细胞监测所需的细胞毒性浓度为50% cc(nabla'),发现:(i)当浓度降低时,所测试复合物的细胞毒性增加;(ii)细胞监测取决于复杂和细胞特异性。复杂特异性表现为1 > 4 > 2 >/= 3。LSCC-SG (Mc29)细胞对1的敏感性比MDBK细胞高60倍,LSR-SF (SR)细胞对2的敏感性比MDBK细胞高1000倍,证明了细胞特异性反应。此外,随着对非肿瘤细胞作用时间的延长,4的细胞毒性下降高达300倍,而对两种肿瘤细胞的作用与作用时间无关。
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