食品科学 ›› 2026, Vol. 47 ›› Issue (11): 131-139.doi: 10.7506/spkx1002-6630-20251210-089

• 营养卫生 • 上一篇    

荧光标记枸杞多糖在小鼠体内的药代动力学研究

向小青,任婧楠,李阳,范刚,马利奋,张智锋,武康宁   

  1. (1.华中农业大学食品科学技术学院,环境食品学教育部重点实验室,果蔬加工与品质调控湖北省重点实验室,湖北 武汉 430070;2.武汉市蔡甸区公共检验检测中心,湖北 武汉 430100;3.宁夏枸杞产业发展中心,宁夏 银川 750011;4.宁夏华信达健康科技有限公司,宁夏 灵武 751400)
  • 发布日期:2026-07-02
  • 基金资助:
    “十四五”国家重点研发计划重点专项(2024YFF1106605);银川市科技计划项目(2024NYHZC006)

Pharmacokinetics of Fluorescently Labeled Lycium barbarum Polysaccharides in Mice

XIANG Xiaoqing, REN Jingnan, LI Yang, FAN Gang, MA Lifen, ZHANG Zhifeng, WU Kangning   

  1. (1. Key Laboratory of Environment Correlative Dietology, Ministry of Education, Hubei Key Laboratory of Fruit & Vegetable Processing & Quality Control, College of Food Science and Technology, Huazhong Agricultural University, Wuhan 430070, China; 2. Wuhan Caidian District Public Inspection and Testing Center, Wuhan 430100, China; 3. Ningxia Goji Berry Industry Development Center, Yinchuan 750011, China; 4. Ningxia Huaxinda Health Technology Co. Ltd., Lingwu 751400, China)
  • Published:2026-07-02

摘要: 以纯化枸杞多糖(Lycium barbarum polysaccharides,LBP)为研究对象,用荧光标记法研究LBP经口服后在小鼠体内的血清吸收、组织分布和排泄特性。结果表明:LBP能够被异硫氰酸荧光素(fluorescein isothiocyanate,FITC)和菁染料(sulfo-cyanine 7,Cy7)成功标记。活体成像结果表明小鼠口服LBP-Cy7后,在小肠和肝脏部位有较强荧光强度,小肠在1 h时有最大荧光强度,肝脏部位在6 h时有最大荧光强度,多糖经小肠吸收后主要在肝脏蓄积。经过验证,LBP-FITC测量方法在血清、组织、粪便和尿液中具有良好的精密度(日内和日间相对标准偏差(relative standard deviation,RSD)<15%)、稳定性(RSD<15%)和回收率(97.2%~100.8%)。小鼠单次灌胃50 mg/mL LBP-FITC后在血清中2 h时检测到最大吸收浓度,在血清中消除半衰期t1/2为(8.67±1.23)h,消除缓慢;组织分布结果表明,灌胃后LBP-FITC主要分布在胃、小肠、大肠和肝脏中,组织分布排序为小肠>胃>大肠>肝>肾>肺>心>脾,并在肝脏中6 h达到最大蓄积量;灌胃后,在48 h以内有87% LBP-FITC通过尿液和粪便排泄,并且大部分通过粪便排泄。本研究为枸杞多糖的体内检测技术及吸收分布规律研究提供了技术与理论支撑。

关键词: 枸杞多糖;荧光标记;药代动力学

Abstract: This study investigated serum absorption, tissue distribution, and excretion characteristics of purified Lycium barbarum polysaccharides (LBP) in mice following oral administration using a fluorescent labeling method. The results showed that LBP were successfully labeled with fluorescein isothiocyanate (FITC) and sulfo-cyanine 7 (Cy7). In vivo imaging revealed strong fluorescence intensity in the small intestine and liver after oral administration of LBP-Cy7. The small intestine exhibited peak fluorescence intensity at 1 h, while the liver showed peak intensity at 6 h, indicating that polysaccharides absorbed in the small intestine primarily accumulate in the liver. The LBP-FITC assay was validated for its excellent precision (intra-day and inter-day relative standard deviation (RSD) < 15%), stability RSD < 15%, and recovery rates (97.2%–100.8%) in serum, tissues, feces, and urine. Following a single oral gavage of 50 mg/mL LBP-FITC in mice, its peak serum concentrations were detected at 2 h, with a long elimination half-life (t1/2) of (8.67 ± 1.23) h. Tissue distribution analysis indicated that LBP-FITC primarily distributed in the stomach, small intestine, large intestine, and liver after oral administration. The decreasing order of tissue distribution was small intestine > stomach > large intestine > liver > kidney > lung > heart > spleen, with maximum accumulation in the liver occurring at 6 h. Within 48 h post-gavage, 87% of LBP-FITC was excreted via urine and feces, with the majority excreted through feces. This study provides technical and theoretical support for the in vivo detection of LBP and to further explore their absorption and distribution patterns.

Key words: Lycium barbarum polysaccharides; fluorescent labeling; pharmacokinetics

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