1.Simultaneous determination of four diterpene lactones in Lianzhi Xiaoyan capsules by QAMS
BI Fujun ; LU Qiaoyin ; LIN Tong
Drug Standards of China 2024;25(1):048-054
Objective: To set up a multi-components by single maker (QAMS) method for determination of four diterpene lactones in Lianzhi Xiaoyan capsules.
Methods: Shimadzu Shim-pack C18 column(250 mm×4.6 mm,5 μm)was adopted with 35 ℃. Acetonitrile-0.1% phosphoric acid aqueous solution as the mobile phase in gradient mode was used at flow rate of 1.0 mL·min-1. The detection wavelength was set at 203 nm. Andrographolide was used as reference to calculate the relative correction factors of the other three components.
Results: The linear relationships of four components were good (r≥0.999 9) within their ranges, and their average recoveries were 100.0%-102.8% with RSDs 1.1%-2.2%. The results obtained by QAMS were close to those obtained by external standard method.
Conclusion: This rapid, precise and reproducible method can be used for the quality control of Lianzhi Xiaoyan capsules.
2.Meta analysis of adenoid bacterial distribution in children with adenoid hypertrophy
Shujing HAN ; Yamei ZHANG ; Jie LU ; Ping CHU ; Qiaoyin LIU ; Yaqiong JIN ; Yongbo YU ; Yunxiao WU ; Yongli GUO ; Jun TAI ; Xin NI
Chinese Archives of Otolaryngology-Head and Neck Surgery 2016;23(6):313-317
OBJECTIVE To illuminate the adenoid bacteria distribution in children with adenoid hypertrophy. METHODS PubMed, Embash, Medline, CNKI, VIP Information and Wanfang data were searched for studies on the adenoid bacteria distribution and adenoid hypertrophy. Random effects meta-analysis was used to pool data. RESULTS Nine studies were included in this meta analysis. The pooled detection rates of haemophilus influenza, staphylococcus aureus and streptococcus pneumonia were 0.21 (95%CI, 0.09-0.32), 0.14 (95%CI, 0.09-0.20) and 0.15 (95%CI , 0.08-0.22) respectively. CONCLUSION Haemophilus influenzae, staphylococcus aureus, and streptococcus pneumoniae are three main kinds of pathogenic bacteria of adenoid hypertrophy in children.
3.Research progress of aptamer and organic nanomaterials based tumor targeting drug delivery systems
Yimin ZHANG ; Xinmei CAI ; Shan ZHOU ; Junyun CHENG ; Ying WANG ; Lu YANG ; Nanjia SONG ; Mengna WANG ; Yuanyuan LI ; Xuanjun LIU ; Qiaoyin LI ; Zeen SUN ; Zhenbao LIU ; Gang YIN
International Journal of Biomedical Engineering 2018;41(1):78-84,89
Aptamers are DNA or RNA fragments that can specifically bind to target substances.Because of the excellent properties such as strong binding force,high specificity,small physical size,chemical synthesis and modification,good biocompatibility,and low immunogenicity aptamers show wide application propects in biomedical researches.Aptamers can also bind specifically to receptors on the surface of cell membranes,and mediate the endocytosis of nanoparticles into cells,making them ideal drug targeting ligands.Organic nanomaterials have excellent application value in nanodrug delivery system because of their good biocompatibility and degradability.In this paper,the recent research progress of aptamers and organic nanomaterials drug delivery systems was reviewed.
4.Genetic analysis of a child with Complex cortical dysplasia with other brain malformations type 6 due to a p.M73V variant of TUBB gene.
Huiqin XUE ; Qiaoyin TANG ; Rong GUO ; Guizhi CAO ; Yu FENG ; Xiayu SUN ; Hongyong LU
Chinese Journal of Medical Genetics 2023;40(12):1541-1545
OBJECTIVE:
To explore the genetic basis for a child with multiple malformations.
METHODS:
A child who had presented at Shanxi Provincial Children's Hospital in February 2021 was selected as the study subject. Clinical data of the patient was collected, and whole exome sequencing (WES) was carried out to screen pathogenic variants associated with the phenotype. Candidate variant was validated by Sanger sequencing of her family members.
RESULTS:
The child had normal skin, but right ear defect, hemivertebral deformity, ventricular septal defect, arterial duct and patent foramen ovale, and separation of collecting system of the left kidney. Cranial MRI showed irregular enlargement of bilateral ventricles and widening of the distance between the cerebral cortex and temporal meninges. Genetic testing revealed that she has harbored a heterozygous variant of NM_178014.4: c.217A>G (p.Met73Val) in the TUBB gene, which was unreported previously and predicted to be likely pathogenic based on the guidelines from the American College of Medical Genetics and Genomics (ACMG). The child was diagnosed with Complex cortical dysplasia with other brain malformations 6 (CDCBM6).
CONCLUSION
CDCBM is a rare and serious disease with great genetic heterogeneity, and CDCBM6 caused by mutations of the TUBB gene is even rarer. Above finding has enriched the variant and phenotypic spectrum of the TUBB gene, and provided important reference for summarizing the genotype-phenotype correlation of the CDCBM6.
Humans
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Child
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Female
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Abnormalities, Multiple
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Blood Group Antigens
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Family
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Malformations of Cortical Development/genetics*
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Brain
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Mutation