Hybrid Inorganic Complexes as Cancer Therapeutic Agents: In-vitro Validation.

Q1 Pharmacology, Toxicology and Pharmaceutics
Murlidhar A Betallu, Shaileshkumar R Bhalara, Kailash B Sapnar, Vijay B Tadke, Keerti Meena, Ananya Srivastava, Gopal C Kundu, Mahadeo Gorain
{"title":"Hybrid Inorganic Complexes as Cancer Therapeutic Agents: In-vitro Validation.","authors":"Murlidhar A Betallu,&nbsp;Shaileshkumar R Bhalara,&nbsp;Kailash B Sapnar,&nbsp;Vijay B Tadke,&nbsp;Keerti Meena,&nbsp;Ananya Srivastava,&nbsp;Gopal C Kundu,&nbsp;Mahadeo Gorain","doi":"10.7150/ntno.81557","DOIUrl":null,"url":null,"abstract":"<p><p>A series of novel mixed transition metal-Magnesium tartarate complexes of general formulation [MMg(C<sub>4</sub>H<sub>4</sub>O<sub>6</sub>)<sub>2</sub> <sup>.</sup>xH<sub>2</sub>O] (where M = Mn, Fe, Co, Ni, Cu and Zn) is prepared with bidentate tartarate ligand. The synthesized complexes (C1 to C6) are characterized by various analytical techniques such as Elemental analysis, Thermo gravimetric analysis, FT-IR Spectroscopy, X-ray Diffraction, Magnetic susceptibility study etc. All complexes exhibit the composition MMgL<sub>2</sub> where M = Mn(II), Fe(II), Co(II), Ni(II), Cu(II) and Zn(II) and L = bidentate tartarate ligand. Analytical data reveals all complexes possesses 1:1 (metal: ligand) ratio. FT-IR spectral study shows that bidentate tartarate ligand coordinate with metal ion in a bidentate manner through two oxygen atoms. Thermo gravimetric analysis of all complexes shows that degradation curves of complexes agrees with recommended formulae of the complexes. X-ray diffraction technique suggests that all complexes (C1 to C6) are polycrystalline in nature. All newly synthesized metal tartarate complexes and ligand were screened <i>in vitro</i> for their anticancer activity against human breast cancer (MDA-MB-231) cell line. The bioassays of all these complexes showed C3 (Co) and C5 (Cu) Mg-tartarate complexes contains maximum antiproliferative activity at 200 µg/ml concentration on MDA-MB-231 cells as compared to other complexes. MDA-MB-231 cells treated with C3 (Co) and C5 (Cu) Mg-tartarate complexes also showed inhibition in cell migration.</p>","PeriodicalId":36934,"journal":{"name":"Nanotheranostics","volume":"7 3","pages":"270-280"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093419/pdf/","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanotheranostics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7150/ntno.81557","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 2

Abstract

A series of novel mixed transition metal-Magnesium tartarate complexes of general formulation [MMg(C4H4O6)2 .xH2O] (where M = Mn, Fe, Co, Ni, Cu and Zn) is prepared with bidentate tartarate ligand. The synthesized complexes (C1 to C6) are characterized by various analytical techniques such as Elemental analysis, Thermo gravimetric analysis, FT-IR Spectroscopy, X-ray Diffraction, Magnetic susceptibility study etc. All complexes exhibit the composition MMgL2 where M = Mn(II), Fe(II), Co(II), Ni(II), Cu(II) and Zn(II) and L = bidentate tartarate ligand. Analytical data reveals all complexes possesses 1:1 (metal: ligand) ratio. FT-IR spectral study shows that bidentate tartarate ligand coordinate with metal ion in a bidentate manner through two oxygen atoms. Thermo gravimetric analysis of all complexes shows that degradation curves of complexes agrees with recommended formulae of the complexes. X-ray diffraction technique suggests that all complexes (C1 to C6) are polycrystalline in nature. All newly synthesized metal tartarate complexes and ligand were screened in vitro for their anticancer activity against human breast cancer (MDA-MB-231) cell line. The bioassays of all these complexes showed C3 (Co) and C5 (Cu) Mg-tartarate complexes contains maximum antiproliferative activity at 200 µg/ml concentration on MDA-MB-231 cells as compared to other complexes. MDA-MB-231 cells treated with C3 (Co) and C5 (Cu) Mg-tartarate complexes also showed inhibition in cell migration.

Abstract Image

Abstract Image

Abstract Image

杂化无机配合物作为癌症治疗剂:体外验证。
用双齿酒石酸盐配体制备了一系列新型混合过渡金属-酒石酸镁配合物[MMg(C4H4O6)2 . xh2o](其中M = Mn, Fe, Co, Ni, Cu和Zn)。用元素分析、热重分析、红外光谱、x射线衍射、磁化率等分析方法对合成的配合物(C1 ~ C6)进行了表征。所有配合物均为MMgL2,其中M = Mn(II), Fe(II), Co(II), Ni(II), Cu(II)和Zn(II), L =双齿酒石酸盐配体。分析数据表明,所有配合物均具有1:1(金属:配体)的比例。红外光谱研究表明,双齿酒石酸盐配体通过两个氧原子与金属离子以双齿方式配位。所有配合物的热重分析表明,配合物的降解曲线符合推荐的配合物配方。x射线衍射技术表明,所有配合物(C1 ~ C6)本质上都是多晶的。对新合成的金属酒石酸盐配合物和配体进行体外抗人乳腺癌(MDA-MB-231)细胞系抗癌活性筛选。生物实验表明,C3 (Co)和C5 (Cu) mg -酒石酸盐配合物在浓度为200µg/ml时对MDA-MB-231细胞的抗增殖活性最大。C3 (Co)和C5 (Cu) mg -酒石酸盐复合物处理的MDA-MB-231细胞也显示出细胞迁移的抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Nanotheranostics
Nanotheranostics Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
10.40
自引率
0.00%
发文量
37
审稿时长
12 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信