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Patil, Shailaja R.,Mote, Umesh S.,Patil, Shivajirao R.,Kolekar, Govind B. Korean Chemical Society 2009 Bulletin of the Korean Chemical Society Vol.30 No.12
A simple, rapid, practical and sensitive spectofluorimetric method was developed for the determination of trace amount of heparin (Hep). Under the Optimum conditions, we studied the interaction between NFLX-Ce$^{3+}$-Hep complex by using absorption and fluorescence spectra. It was observed that Hep remarkably enhance the fluorescence intensity of the NFLX-Ce$^{3+}$ complex at ${\lambda}$= 356 nm in the buffer solution of pH = 7.60 and the enhancement effect is shown to relate with the concentration of Hep. The linear range and detection limit for the determination of Hep was obtained. By the Rosenthal graphic method, the association constant (K) and binding numbers (N) of Hep with probe were investigated. This method is relatively free of interference from coexisting substances and successfully applied for the determination of heparin in heparin sodium injection samples. A suitable mechanism of fluorescence enhancement between NFLX-Ce$^{3+}$ and the NFLX-Ce$^{3+}$-Hep systems were proposed and discussed.
Shailaja R. Patil,Umesh S. Mote,Shivajirao R. Patil,Govind B. Kolekar 대한화학회 2009 Bulletin of the Korean Chemical Society Vol.30 No.12
A simple, rapid, practical and sensitive spectofluorimetric method was developed for the determination of trace amount of heparin (Hep). Under the Optimum conditions, we studied the interaction between NFLX-Ce3+-Hep complex by using absorption and fluorescence spectra. It was observed that Hep remarkably enhance the fluorescence intensity of the NFLX-Ce3+ complex at λ = 356 nm in the buffer solution of pH = 7.60 and the enhancement effect is shown to relate with the concentration of Hep. The linear range and detection limit for the determination of Hep was obtained. By the Rosenthal graphic method, the association constant (K) and binding numbers (N) of Hep with probe were investigated. This method is relatively free of interference from coexisting substances and successfully applied for the determination of heparin in heparin sodium injection samples. A suitable mechanism of fluorescence enhancement between NFLX-Ce3+ and the NFLX-Ce3+-Hep systems were proposed and discussed.
Mahajan, Prasad G.,Dige, Nilam C.,Desai, Netaji K.,Patil, Shivajirao R.,Kondalkar, Vijay V.,Hong, Seong-Karp,Lee, Ki Hwan Elsevier 2018 Spectrochimica acta. Part A, Molecular and biomole Vol.198 No.-
<P><B>Abstract</B></P> <P>Nowadays scientist over the world are engaging to put forth improved methods to detect metal ion in an aqueous medium based on fluorescence studies. A simple, selective and sensitive method was proposed for detection of Co<SUP>2+</SUP> ion using fluorescent organic nanoparticles. We synthesized a fluorescent small molecule viz. 4,4′-{benzene-1,4-diylbis-[(Z)methylylidenenitrilo]}dibenzoic acid (BMBA) to explore its suitability as sensor for Co<SUP>2+</SUP> ion and biocompatibility in form of nanoparticles. Fluorescence nanoparticles (BMBANPs) prepared by simple reprecipitation method. Aggregation induced enhanced emission of BMBANPs exhibits the narrower particle size of 68nm and sphere shape morphology. The selective fluorescence quenching was observed by addition of Co<SUP>2+</SUP> and does not affected by presence of other coexisting ion solutions. The photo-physical properties, viz. UV-absorption, fluorescence emission, and lifetime measurements are in support of ligand-metal interaction followed by static fluorescence quenching phenomenon in emission of BMBANPs. Finally, we develop a simple analytical method for selective and sensitive determination of Co<SUP>2+</SUP> ion in environmental samples. The cell culture <I>E</I>. <I>coli</I>, <I>Bacillus</I> sps., and <I>M</I>. <I>tuberculosis H</I> <SUB> <I>37</I> </SUB> <I>RV</I> strain in the vicinity of BMBANPs indicates virtuous anti-bacterial and anti-tuberculosis activity which is of additional novel application shown by prepared nanoparticles.</P> <P><B>Highlights</B></P> <P> <UL> <LI> New fluorescent Nano probe developed for detection of Co<SUP>2+</SUP> in aqueous medium </LI> <LI> Selective fluorescence quenching induced by Co<SUP>2+</SUP> only </LI> <LI> Quenching mechanism disclose ground state complexation and ligand (COO<SUP>–</SUP>) – metal (Co<SUP>2+</SUP>) interaction </LI> <LI> Lower detection limit for Co<SUP>2+</SUP> = 0.102 µg/mL </LI> <LI> The practical application includes analysis of environmental samples and biological activities </LI> </UL> </P> <P><B>Graphical Abstract</B></P> <P>[DISPLAY OMISSION]</P>
Kondalkar, Vijay V.,Mali, Sawanta S.,Mane, Rahul M.,Dandge, P. B.,Choudhury, Sipra,Hong, Chang K.,Patil, Pramod S.,Patil, Shivajirao R.,Kim, Jin H.,Bhosale, Popatrao N. American Chemical Society 2014 INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH - Vol.53 No.47
<P>Nanostructured TiO<SUB>2</SUB> thin films were fabricated via a facile, economical, and energy-efficient microwave-assisted dip-coating (MWDC) technique. Further, the resulting TiO<SUB>2</SUB> films were characterized by means of X-ray diffraction, high-resolution transmission electron microscopy, selected-area electron diffraction, Fourier transform Raman spectroscopy, X-ray photoelectron spectroscopy, and photoluminescence spectroscopy techniques for their phase structure, morphology, and optical and surface properties. TiO<SUB>2</SUB>-mediated photoelectrocatalytic degradation of the antibiotic cefotaxime (CFX) in an aqueous solution was studied by varying the pH under UV illumination. The degradation intermediates and possible reaction degradation path of CFX were analyzed by electrospray ionization time-of-flight mass spectrometry (MS). The MS spectra revealed that degradation of CFX occurs through β-lactum corresponding to the cleavage of the cephem nucleus. Moreover, the antibacterial activity of CFX prior to and after photoelectrocatalytic degradation was carried out to analyze the toxicity against <I>Staphylococcus aureus</I> and salmonella typhi bacteria. Interestingly, it was observed that the antibiotic activity was drastically inhibited after photoelectrocatalytic degradation of the CFX solution. The photoelectrocatalytic stability of a nanostructured TiO<SUB>2</SUB> electrode was evaluated by recycling the degradation experiments. It was observed that there was no significant decrease in the catalytic activity, indicating potential applications of the TiO<SUB>2</SUB> electrode prepared by the MWDC method.</P><P><B>Graphic Abstract</B> <IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/iecred/2014/iecred.2014.53.issue-47/ie501821a/production/images/medium/ie-2014-01821a_0014.gif'></P><P><A href='http://pubs.acs.org/doi/suppl/10.1021/ie501821a'>ACS Electronic Supporting Info</A></P>