A multifunctional basic pH indicator probe for distinguishable detection of Co2+, Cu2+and Zn2+with its utility in mitotracking and monitoring cytoplasmic viscosity in apoptotic cells

化学 滴定法 荧光 水溶液中的金属离子 螯合作用 质子核磁共振 分析化学(期刊) 离子 光化学 赫普斯 金属 无机化学 立体化学 有机化学 生物化学 物理 量子力学
作者
Pranjalee Yadav,Sarita Gond,Anusmita Shekher,Subash C. Gupta,Udai P. Singh,Vinod P. Singh
出处
期刊:Dalton Transactions [Royal Society of Chemistry]
卷期号:51 (17): 6927-6935 被引量:28
标识
DOI:10.1039/d2dt00286h
摘要

Metal ions such as Co2+, Cu2+ and Zn2+ have extensive applications in biological and industrial realms, but the toxicity caused by these ions poses a serious threat to mankind. However, there is no report in the literature on the development of a chemosensor for distinguishable detection of these toxic ions. Addressing this challenge, a multifunctional probe as a basic pH indicator with both colorimetric and fluorescence turn-on responses has been reported. The probe selectively discriminates Co2+, Cu2+ and Zn2+ ions with brown, dark yellow and greenish yellow colors, respectively, in DMF : water (9 : 1 v/v, HEPES 10 mM). Additionally, a fluorescence turn-on response specific to Zn2+ has also been observed. The sensing mechanism has been explored using UV-Vis, fluorescence spectroscopy and 1H NMR titration and confirmed with computational results. The inhibition of CN isomerization and excited state intramolecular proton transfer (ESIPT) along with chelation enhanced fluorescence emission (CHEF) result in fluorescence enhancement with Zn2+. Job's plot and HRMS spectra confirm a 1 : 1 (L : M) stoichiometry between the probe and metal ions. The probe is able to exhibit excellent viscochromism in DMF : glycerol medium. Live cell imaging on SiHa cells has been successfully performed for intra-cellular detection of Zn2+ at basic pH. Furthermore, the probe displays its utility in mitotracking and monitoring cytoplasmic viscosity changes in SiHa cells. It is efficiently used to recognize the apoptosis process by displaying an enhancement in fluorescence intensity from cancerous SiHa cells to apoptotic cells.
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