4.7 Article

Synthesis, surface activity, self-aggregation and cytotoxicity of ruthenium(II) and Oxovanadium(IV) based metallo-surfactants

期刊

JOURNAL OF MOLECULAR LIQUIDS
卷 331, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.molliq.2021.115696

关键词

Metallo-surfactants; Ru(II); Oxovanadium (IV); Self-aggregation; Cytotoxicity; Cancer treatment

资金

  1. UGC Govt. of India [F.17-82/2008(SA-II)]
  2. Department of Science and Technology, Govt. of India, New Delhi, India [SR/S1/PC-11/2009]

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The synthesis, surface activity, self-aggregation, and cytotoxicity of a series of amphiphilic Ruthenium(II) and Oxovanadium (IV) metal complexes were investigated. These metal complexes showed sensitivity to their overall geometry, hydrophobicity, and counter ion polarizability, leading to significant inhibition of human cervix carcinoma cell proliferation. The cytotoxicity of the amphiphilic complexes was notably effective with an IC50 value of 57 uM.
Synthesis, surface activity, self-aggregation and cytotoxicity studies of a series of amphiphilic Ruthenium(II) and Oxovanadium (IV) metal complexes are presented. A series of Ruthenium (II) and Oxovanadium (IV) based metallo-surfactants was synthesized and characterized using UV-Visible, H-1 NMR and infrared spectroscopy. The synthesized metallo-surfactants were analysed for their surface activity and self-aggregation properties through tensiometric and conductometric investigations. The surface activity as well as the self-aggregation tendency of the as synthesized amphiphilic Ru (II) and Oxovanadium (IV) based amphiphilic metal complexes was observed to be very sensitive to their overall geometry, hydrophobicity and counter ion polarizability. The metallo-amphiphiles were tested for their potential role in cell growth inhibition. MTT assay results establish that the amphiphilic Ruthenium and Vanadium complexes significantly inhibit the proliferation of human cervix carcinoma, HeLa cell line. The amphiphilic phendione complexes of both Ruthenium (II) and Oxovanadium (IV) exhibited an excellent cytotoxicity with an IC50 value of 57 mu M. (C) 2021 Elsevier B.V. All rights reserved.

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