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1.
Chinese Journal of Ultrasonography ; (12): 236-241, 2020.
Article in Chinese | WPRIM | ID: wpr-868009

ABSTRACT

Objective:To explore the imaging rate and diagnostic rate of positioning the fetal conus medullaris by three-dimensional ultrasound method to detect atlantoaxial intervertebral space, comparing it with the traditional two-dimensional and three-dimensional ultrasound methods.Methods:Consecutively 318 singleton fetuses received routine ultrasound screening during the second trimester were enrolled from November 2017 to December 2018 in Shenzhen Luohu People′s Hospital and Shenzhen People′s Hospital. These fetuses included 276 normal cases and 42 abnormal cases. The abnormal group contained 11 cases tethered cords fetuses(tethered cords group) and 31 cases non-tethered fetuses(non-tethered group). A new ultrasound method named detecting atlanto-axial intervertebral space with three-dimensional ultrasound and traditional two-dimensional and three-dimensional ultrasound methods were used to acquire and store the images. The positions of the fetal conus medullaris were analyzed blindly and recorded by three experienced physicians using three different methods with off-line software.Results:①The χ 2 test comparing multiple sample rates was used to compare the imaging acquisition success rate of fetal conus medullaris by three ultrasound methods. The test level was adjusted to be α′=0.05/4=0.0125, the results showed that there were no statistically significant differences between the three methods in the normal group (χ 2=7.39, P=0.025) and the abnormal group (χ 2=5.32, P=0.070). ②The χ 2 test comparing multiple sample rates was used to compare the diagnostic accuracy of fetal conus medullaris position in normal group by three methods, it showed there was no significant difference in the correct rate of conus medullaris position in the normal group (χ 2=2.52, P=0.284). ③The χ 2 test comparing multiple sample rates was used to compare the diagnostic accuracy of the fetal conus medullaris in tethered cord group and non-tethered group using 3 methods, the difference was not statistically significant in tethered cord group (χ 2=1.22, P=0.543), while the difference was statistically significant in non-tethered group(χ 2=9.69, P=0.008). Conclusions:The method of detecting atlanto-axial intervertebral space with three-dimensional ultrasound has a high imaging rate and diagnostic accuracy in positioning the fetal conus medullaris. Positioning of fetal conus medullaris by detecting atlanto-axial intervertebral space with three-dimensional ultrasound is better than traditional two-dimensional and three-dimensional ultrasound in the abnormal non-tethered fetuses, which can provide more valuable information for prenatal diagnosis consultation and prenatal and postnatal care.

2.
China Pharmacy ; (12): 2369-2373, 2019.
Article in Chinese | WPRIM | ID: wpr-817142

ABSTRACT

OBJECTIVE: To study the chemical constituents of n-Butanol part from the roots of Camellia oleifera, and to provide reference for elucidating the pharmacodynamic substance basis of it’s anti-tumor effect. METHODS: The ethanol extracts were obtained by using 95% ethanol as extraction solvent to extract the roots of C. oleifera, and the n-Butanol part was obatined after the extracts were extratced with ethyl acetate and water-saturated n-butanol solution in turn. The chemical constituents of n-butanol part were isolated and purified by D101 macroporous resin column, silica gel, atmospheric pressure reversed phase column chromatography, sephadex gel SephadexLH-20 column chromatogram and preparative HPLC. The structure of the compounds was identified by spectroscopic analysis of physicochemical constants, electrospray ionization mass spectrometry, 1H-NMR and 13C-NMR. RESULTS: Eight compounds were isolated from the roots of C. oleifera and elucidated as quercetin 3′ -O-β-D-glucoside (compound 1), apigenin-7-O-β-D-glucoside (compound 2), (+)-lyoniresinol-3α-O-β-D-glucopyranoside (compound 3), rubusoside (compound 4), dulcoside B (compound 5), 4-hydroxy-3-methoxyphenol 1-O-β-D-[6-O-(4-hydroxy-3,5-dimethoxylbenzoate)-glucopyranoside (compound 6), 3,4,5-trimethoxyphenyl-6-O- syringoyl-β-D-glucopyranoside (compound 7), gordonoside P (compound 8).  CONCLUSIONS: Compounds 1-8 were isolated from this plant for the first time. This not only enriches the chemical constituents of this genus, but also provides a reference for elucidating the anti-tumor bioactive substances in this part.

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