2013
DOI: 10.1016/j.carbpol.2012.10.057
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Purification, characterization and anticoagulant activity of the polysaccharides from green tea

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Cited by 124 publications
(65 citation statements)
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“…3). It was observed that all samples exhibited typical major broad stretching peak appeared around 3,600-3,200 cm -1 for the -OH group (Cai et al 2013). The relative stronger absorption peak at 1,650.74 cm -1 for N-H bending vibration might be related to the little content of protein in EPS-1 (Gan et al 2011).…”
Section: Uv and Ft-ir Spectra Of Eps-1 And Eps-2mentioning
confidence: 88%
“…3). It was observed that all samples exhibited typical major broad stretching peak appeared around 3,600-3,200 cm -1 for the -OH group (Cai et al 2013). The relative stronger absorption peak at 1,650.74 cm -1 for N-H bending vibration might be related to the little content of protein in EPS-1 (Gan et al 2011).…”
Section: Uv and Ft-ir Spectra Of Eps-1 And Eps-2mentioning
confidence: 88%
“…The peaks toward 1000-1200 cm −1 on the two spectra suggested the presence of C─O─C and C─O─H link bonds, indicating the presence of pyranose. Finally, the peak that appeared at 874 cm −1 of THWP-1 was attributed to D-Man in pyranose [49]. A characteristic band approximately at 816 cm −1 in purified THWP was due to α-D-Glc [49].…”
Section: Ft-ir Spectra Of Thwp Fractionsmentioning
confidence: 94%
“…The interpretations of the 1 H/ 1 H correlated spectroscopy (COSY), 1 H/ 13 C heteronuclear single-quantum coherence (HSQC), and heteronuclear multiple bond coherence (HMBC) spectra were recorded using a state-time proportion phase incrementation for quadrature detection in the indirect dimension. 13 C spectrum was determined with acetone as the internal standard (methyl C atomic chemical shift of 31.5 ppm), and the 1 H spectrum was done with the HOD peak as calibration standard (δ 4.85 ppm) [27,28].…”
Section: Nuclear Magnetism Spectra Analysismentioning
confidence: 99%
“…H-1-2 was labeled with sodium pertechnetate ( 99m Tc) using a stannous chloride (SnCl 2 ) method [31]. DMSO solution H-1-2 (10 mg/mL pH 6.0) was mixed with 300 mL of NaCl aqueous 99m Tc (20)(21)(22)(23)(24)(25)(26)(27)(28)(29)(30) in the presence of 20 mL of HCl aqueous SnCl 2 (2 mg/mL) reaction, at 50 • C for 60 min. The labeling efficiency of 99 mTc to CS was assessed using thin layer chromatography (TLC), using silica gel coated TLC plates (Ann Arbor, MI, USA).…”
Section: Animal Study-biodistribution Of H-1-2mentioning
confidence: 99%