2009
DOI: 10.1016/j.aca.2009.06.041
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Exploitation of phosphorescent labelling reagent of fullerol-fluorescein isothiocyanate and new method for the determination of trace alkaline phosphatase as well as forecast of human diseases

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Cited by 10 publications
(4 citation statements)
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“…Fluorescein (1) has been derivatized and/or functionalized particularly on the top ring with an isothiocyanate (−NC S) group named fluorescein isothiocyanate (FITC, Figure 2). FITC has been widely utilized as diverse forms to understand various physicochemical, photophysical, and biological implications; FITC-labeled PEO−PCL−PEO triblock copolymer, 12 FITC−deacetylated chitin conjugates, 13 FITC-labeled human plasma, 14 FITC-labeled collagen, 15 FITC−PEO conjugate, 16 FITC−cyclodextrin conjugates, 17 FITC−fullerol conjugates, 18 insulin−fluorescein conjugates, 19 bifunctional polyacrylamides containing vancomycin and fluorescein, 20 a fluorescein− ruthenium−octa-arginine conjugate, 21 lithocholyl−lysyl−fluorescein conjugates, 22 dimethylamionapthamide−fluorescein conjugates, 23 FITC-labeled lectin, 24 FITC labeling at the 5′end of DNA with intercalating compound conjugates, 25 and FITC−dextran conjugates. 26 Fluorescein also functionalized on the top ring with a carboxylic acid group fluorescein carboxylic acid (FCA), which has been used as precursor for the synthesis of oligonucleotides (e.g., fluorescein phosphoramidites, FAM), 27 fluorescein-tagged peptoid conjugates, 28,29 characterizing RecA−DNA interaction, 30 fluorescein-C-and O-glycosides, 31 fluorescein labeled 7methylguanosinemonophosphate, 32 and ifenprodil conjugates.…”
Section: ■ Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Fluorescein (1) has been derivatized and/or functionalized particularly on the top ring with an isothiocyanate (−NC S) group named fluorescein isothiocyanate (FITC, Figure 2). FITC has been widely utilized as diverse forms to understand various physicochemical, photophysical, and biological implications; FITC-labeled PEO−PCL−PEO triblock copolymer, 12 FITC−deacetylated chitin conjugates, 13 FITC-labeled human plasma, 14 FITC-labeled collagen, 15 FITC−PEO conjugate, 16 FITC−cyclodextrin conjugates, 17 FITC−fullerol conjugates, 18 insulin−fluorescein conjugates, 19 bifunctional polyacrylamides containing vancomycin and fluorescein, 20 a fluorescein− ruthenium−octa-arginine conjugate, 21 lithocholyl−lysyl−fluorescein conjugates, 22 dimethylamionapthamide−fluorescein conjugates, 23 FITC-labeled lectin, 24 FITC labeling at the 5′end of DNA with intercalating compound conjugates, 25 and FITC−dextran conjugates. 26 Fluorescein also functionalized on the top ring with a carboxylic acid group fluorescein carboxylic acid (FCA), which has been used as precursor for the synthesis of oligonucleotides (e.g., fluorescein phosphoramidites, FAM), 27 fluorescein-tagged peptoid conjugates, 28,29 characterizing RecA−DNA interaction, 30 fluorescein-C-and O-glycosides, 31 fluorescein labeled 7methylguanosinemonophosphate, 32 and ifenprodil conjugates.…”
Section: ■ Introductionmentioning
confidence: 99%
“…Fluorescein ( 1 ) has been derivatized and/or functionalized particularly on the top ring with an isothiocyanate (−NCS) group named fluorescein isothiocyanate (FITC, Figure ). FITC has been widely utilized as diverse forms to understand various physicochemical, photophysical, and biological implications; FITC-labeled PEO–PCL–PEO triblock copolymer, FITC–deacetylated chitin conjugates, FITC-labeled human plasma, FITC-labeled collagen, FITC–PEO conjugate, FITC–cyclodextrin conjugates, FITC–fullerol conjugates, insulin–fluorescein conjugates, bifunctional polyacrylamides containing vancomycin and fluorescein, a fluorescein–ruthenium–octa-arginine conjugate, lithocholyl–lysyl–fluorescein conjugates, dimethylamionapthamide–fluorescein conjugates, FITC-labeled lectin, FITC labeling at the 5′-end of DNA with intercalating compound conjugates, and FITC–dextran conjugates …”
Section: Introductionmentioning
confidence: 99%
“…As a result, F-ol could emit strong and steady RTP. Then the reaction was carried out between HOOC-in Cyt C molecule and -OH in F-ol molecule [18], then a nonphosphorescence compound F-olCyt C formed (Scheme 3) causing the RTP of F-ol quenching sharply (Figure 1, curve 5.5 � ).…”
Section: Mechanism Of Reactionmentioning
confidence: 99%
“…Therefore, searching for a high sensitive and accurate method for the determination of Cyt C in biological samples and discussing the relativity between the content of Cyt C and cell apoptosis have become research focus with high academic value and great significance. There have been many reports on the synthesis of multihydroxyl C 60 derivatives, F-ol derivatives, aminophenol derivatives, dendritic fullerene derivatives [13][14][15], the fluorescent property of water-soluble F-ol [16], and the determination of alkaline phosphatase [17,18], glucose [19], As (V) [20], and Mn 2+ [21] based on phosphorescent property of F-ol, showing broad prospects of F-ol in analytical application.…”
Section: Introductionmentioning
confidence: 99%