摘要
目的以大鼠为动物模型研究了海参皂苷单体EchinosideA(EA)在体内的消化吸收特性。方法Wistar大鼠适应饲养1周后,按体质量分为10组,每组3只。禁食不禁水12h后,给大鼠分别按照30mg/kg·BW灌胃配置好的海参皂苷EA溶液1mL,分别在灌胃后0、0.5、1、2、3、4、7、9、11、24h取血,建立并优化血清中海参皂苷EA的HPLC-MS检测方法,检测不同时间节点大鼠血中EA含量。结果实验结果显示,海参皂苷单体EA液质检测的定量限(LOQ)为2.12ng,在0.3~20,ug/mL的浓度范围内线性良好(R。=0.9946)。海参皂苷EA灌胃后在血中迅速出现,在3h出现最高峰值,浓度达到0.83/μg/mL,之后在7h出现另1个较小峰,9h后恢复至4h水平(约0.24/μg/mL),直至24h。结论本文建立了血清中海参皂苷EA的液相色谱-质谱联用检测方法,发现海参皂苷单体EA可经消化道吸收,该结果为海参皂苷在保健食品及药物中的应用提供了科学依据。
Objective To study the digestion and absorption characteristics of sea cucumber saponins Echi- noside A (EA) in rats. Methods Wistar rats were divided into 10 groups (n=3) according to the body weight. After acclimating for 1 week, the animals were fasted for 12 hours, and oral administration of 1 mL sea cucumber saponins EA solution at the dose of 30 mg/kg BW. The blood was collected in 0, 0. 5, 1, 2, 3, 4, 7, 9, 11, 24 h for the serum determination of EA. The HPLC-MS method of serum EA determination was established and optimized. Results The limit of quantification (LOQ) of EA detected by HPLC-MS was 2. 12 ng, and it showed a good linearity in the concentration range from 0. 3 to 20 μg/mL (R2 =0. 9946). Sea cucumber saponins EA was appeared rapidly after oral administration, the highest peak concentration reached 0. 83 μg/mL at 3 h, and another smaller peak showed at 7 h, then returned to the level of 4 h (about 0.24 μg/mL) at 9 h and stayed the level to 24 h. Conclusion This pa- per established HPLC-MS method of sea cucumber saponins EA in serum, and found that the sea cu- cumber saponins EA could be absorbed by gastrointestinal, the results provided scientific evidence for the application of sea cucumber saponins in marine functional food and drugs.
出处
《中国海洋药物》
CAS
CSCD
2015年第5期41-46,共6页
Chinese Journal of Marine Drugs
基金
国家自然科学基金项目(U1406402)
新世纪优秀人才项目(NCET-13-0534)
"泰山学者"建设工程专项经费资助