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多糖DPC1经口服和腹腔注射给药后的体内药代动力学研究

In Vivo Pharmacokinetic Study of Polysaccharide DPC1 after Oral and Intraperitoneal Administration.

作者信息

Yong Jin, Zhang Chaozheng, Cao Yuening, Tang Shuang, Long Fei, Cao Zhixing, Lu Jun, Peng Teng

机构信息

College of Pharmacy, Chengdu University of TCM, Chengdu 611137, China.

出版信息

Pharmaceuticals (Basel). 2024 Mar 6;17(3):343. doi: 10.3390/ph17030343.

Abstract

(1) Background: is a medicinal plant, and its polysaccharides are used for immunomodulation and the treatment of hyperglycemia. Investigation of the tissue distribution and pharmacokinetics of polysaccharide can further elucidate its pharmacological mechanisms. (2) Methods: A fluorescence-labeling approach using rhodamine B (RhB) as a fluorescent molecular probe was used for the quantitative assessment of the polysaccharide from dried (DPC1) samples, and the pharmacokinetics and tissue distribution of DPC1 were evaluated in mice after intraperitoneal or oral administration. (3) Results: DPC1 was successfully labeled with RhB, showing degrees of fluorescence labeling at 0.453% and 0.568% as determined by the ultraviolet and enzyme marker methods, respectively. DPC1-RhB was rapidly absorbed into the bloodstream after oral and intraperitoneal administration. Pharmacokinetic characteristics showed that oral administration and intraperitoneal administration were consistent with the features of a two-compartment model. (4) Conclusion: After administration, DPC1-RhB was primarily distributed in the tissues of the heart, spleen, and lung, indicating that the drug has a targeted effect on these tissues. Overall, the findings provide a comprehensive reference for the in vivo distribution of DPC1, together with a foundation for further elucidation of its pharmacological mechanisms and the development and application of DPC1 formulations.

摘要

(1) 背景:[植物名称]是一种药用植物,其多糖用于免疫调节和治疗高血糖。研究[植物名称]多糖的组织分布和药代动力学可以进一步阐明其药理机制。(2) 方法:采用以罗丹明B(RhB)为荧光分子探针的荧光标记方法对干燥的[植物名称]样品中的多糖(DPC1)进行定量评估,并在小鼠腹腔注射或口服给药后评估DPC1的药代动力学和组织分布。(3) 结果:DPC1成功用RhB标记,通过紫外和酶标法测定的荧光标记度分别为0.453%和0.568%。口服和腹腔注射后,DPC1-RhB迅速吸收入血。药代动力学特征表明,口服给药和腹腔注射均符合二室模型特征。(4) 结论:给药后,DPC1-RhB主要分布在心脏、脾脏和肺组织中,表明该药物对这些组织具有靶向作用。总体而言,这些发现为DPC1的体内分布提供了全面参考,同时为进一步阐明其药理机制以及DPC1制剂开发和应用奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd5c/10974776/3ec9856a1c2e/pharmaceuticals-17-00343-g001.jpg

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