2021
DOI: 10.1016/j.ijbiomac.2021.03.088
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Extraction, purification, physicochemical properties and antioxidant activity of a new polysaccharide from Ocimum album L. seed

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Cited by 68 publications
(31 citation statements)
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“…X‐ray diffraction (XRD) and scanning electron microscope (SEM) were used as effective methods to analyse the crystal structures of polymers, and they were widely employed in the structural characterisation of polysaccharides (Arab et al ., 2021; Deore & Mahajan., 2021). Figure S2a showed the XRD patterns of XYCS‐P and XYCS.…”
Section: Resultsmentioning
confidence: 99%
“…X‐ray diffraction (XRD) and scanning electron microscope (SEM) were used as effective methods to analyse the crystal structures of polymers, and they were widely employed in the structural characterisation of polysaccharides (Arab et al ., 2021; Deore & Mahajan., 2021). Figure S2a showed the XRD patterns of XYCS‐P and XYCS.…”
Section: Resultsmentioning
confidence: 99%
“…The anomeric resonances for the anomeric carbons appear at δ 90 to 110 ppm, whereas those for the ring carbons are found between 60 and 85 ppm. Specifically, the chemical shifts between 95 and 101 ppm were due to α-linked residue and the chemical shifts in the region of 101-105 ppm were attributed to the β-linked residue [32]. As shown in Figure 3d, the signals at 97.81 and 104.27 ppm were attributed to the anomeric region of the αand β-configuration, respectively.…”
Section: Nmr Analysismentioning
confidence: 92%
“…Most polysaccharides have an amorphous or semi-crystalline structure. Since intermolecular bonds are weaker in amorphous regions rather than in crystalline regions, the solubility and water uptake are higher in the amorphous polysaccharides [32]. It can be seen from the Figure 3e that there were five diffraction peaks (27.36, 31.58, 45.31, 56.33, 66.17) and the corresponding crystal plane spacings were 3.26, 2.83, 2.00, 1.63, and 1.41 Å.…”
Section: X-ray Diffraction Analysismentioning
confidence: 99%
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“…The FT-IR spectrum of TsLTP (Figure 2A) indicated that the broad and strong band at 3397 cm À 1 represented the OÀ H stretching vibration, [18] while the weak band at 2921 cm À 1 was attributed to CÀ H stretching vibration. The absorption peak at approximately 1638 cm À 1 was due to the bound water, [19][20] while the band at around 1402 cm À 1 was assigned to CÀ H bending vibration. [21] In the range of 1200-1000 cm À 1 , the strong and broad absorption peak at 1064 cm À 1 was ascribed to CÀ O stretching vibrations of the pyranose ring.…”
Section: Ft-ir Spectrum Analysismentioning
confidence: 99%