AI Article Synopsis

  • A new cost-effective photo probe using Tb-simvastatin was developed for spectrofluorometric detection of four important biological compounds across various environments.
  • The complex displays strong luminescence at 545 nm, which decreases when folic acid, progesterone, testosterone, and vitamin D are present, with optimal testing conditions determined at different pH levels.
  • The method was validated and found to be accurate and specific, making it suitable for routine analysis and early detection of chronic diseases linked to these compounds.

Article Abstract

An innovative, simple and cost effective Tb-simvastatin photo probe was designed and used as a core for a spectrofluorometric approach to sensitively determine four vital biological compounds in different matrices. A Tb-simvastatin complex displays a characteristic electrical band with at 545 nm with significant luminescence intensity, which is quenched in the presence of folic acid, progesterone, testosterone and vitamin D at four variant sets of pH: 5.0, 6.2, 7.5 and 9.0, respectively. The conditions were optimized and the best solvent for operation was found to be acetonitrile at at 340 nm. Folic acid was successfully estimated in tablet dosage form, urine and serum in the concentration range of 2.49 × 10 to 1.28 × 10 mol L. Progesterone, testosterone and vitamin D were also assessed in serum samples using the same optimal conditions within concentration ranges of 5 × 10 to 1.9 × 10, 5 × 10 to 2.8 × 10 and 5 × 10 to 4.2 × 10 mol L, respectively. The proposed luminescence method was validated in accordance with ICH guidelines and found to be accurate, precise, and specific and free from any interference at the working pH for each analyte. The cost effectiveness and applicability of the method make it a good choice for routine analysis of the four compounds and early diagnosis of chronic diseases associated with abnormalities in their physiological levels.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042109PMC
http://dx.doi.org/10.1039/d1ra05368jDOI Listing

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