Determination of 13 Heparan Sulfate Disaccharides in PANC-1 and CFPAC-1 Cells Tumor Bearing Mice with Pancreatic Cancer by Precolumn Derivatization/High Performance Liquid Chromatography and Fluorescence Detection
Scientific Papers|更新时间:2025-05-09
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Determination of 13 Heparan Sulfate Disaccharides in PANC-1 and CFPAC-1 Cells Tumor Bearing Mice with Pancreatic Cancer by Precolumn Derivatization/High Performance Liquid Chromatography and Fluorescence Detection
Journal of Instrumental AnalysisVol. 44, Issue 5, Pages: 811-821(2025)
ZHANG Lei,WANG Si-ya,ZHANG Yun-tao,REN Qiang.Determination of 13 Heparan Sulfate Disaccharides in PANC-1 and CFPAC-1 Cells Tumor Bearing Mice with Pancreatic Cancer by Precolumn Derivatization/High Performance Liquid Chromatography and Fluorescence Detection[J].Journal of Instrumental Analysis,2025,44(05):811-821.
ZHANG Lei,WANG Si-ya,ZHANG Yun-tao,REN Qiang.Determination of 13 Heparan Sulfate Disaccharides in PANC-1 and CFPAC-1 Cells Tumor Bearing Mice with Pancreatic Cancer by Precolumn Derivatization/High Performance Liquid Chromatography and Fluorescence Detection[J].Journal of Instrumental Analysis,2025,44(05):811-821. DOI: 10.12452/j.fxcsxb.240913396.
Determination of 13 Heparan Sulfate Disaccharides in PANC-1 and CFPAC-1 Cells Tumor Bearing Mice with Pancreatic Cancer by Precolumn Derivatization/High Performance Liquid Chromatography and Fluorescence Detection
A precolumn derivatization/high performance liquid chromatography-fluorescence detection(HPLC-FLD) method for the determination of 13 heparan sulfate(HS) disaccharides in PANC-1 and CFPAC-1 cells tumor bearing mice with pancreatic cancer was established. HS disaccharides were obtained from pancreatic cancer samples by defatting and protease enzymatic hydrolysis,and then reacted with 2-aminoacridone(AMAC) derived reagents. The separation was performed by Thermo Scien
tific HYRERSIL ODS-2 C
18
column,and the mobile phase gradient elution was performed with methanol-60 mmol/L ammonium acetate(pH 5.6) at excitation wavelength of 425 nm and emission wavelength of 520 nm. The results showed that the 13 HS disaccharides had a good linear relationship within the corresponding mass concentration ranges(
r
2
≥0.999 0),with detection limits(LODs) of 0.012-0.313 µg/mL and the quantitation limits(LOQs) of 0.117-1.250 µg/mL. The relative standard deviations(RSDs) of precision ranged from 0.040% to 0.63%,the RSD of intra-day stability ranged from 0.34% to 3.6%,the RSD of inter-day stability ranged from 1.8% to 6.4%. The recoveries ranged from 80.7%-109%,and RSD was 0.50%-17%. 9 HS disaccharides were detected in the tumor tissue of the two types of pancreatic cancer cells,among which ΔUA-GlcN(ⅣH) accounted for the highest proportion,with concentrations of 28 627.558 nmol/g and 66 938.786 nmol/g,respectively. ΔUA-GlcNAc(ⅣA) and ΔUA-GlcN,6S(ⅡH) took the second place,and the results of molecular docking showed that ⅣH had the strongest binding force with heparin-binding epidermal growth factor(HB-EGF) and ⅡH had the strongest binding force with fibroblast growth factor-2(FGF-2). The characteristics of HS sulfated sequence and its interaction with HB-EGF and FGF-2 regulate the occurrence and development of pancreatic cancer. The findings of this study may provide valuable insights for the early treatment and diagnosis of pancreatic cancer.
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