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Cellular pharmacokinetics study of multi-loaded pegylated irinotecan conjugate based on IS-CID
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Yu-qing ZOU, Ke-xin LIU, Jia-wang ZHAO, Zhuo-fan ZHANG, Shi-wen SONG*
Acta Pharmaceutica Sinica | 2026, 61(2) : 577 - 585
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Acta Pharmaceutica Sinica | 2026, 61(2): 577-585
• Original Articles •
Cellular pharmacokinetics study of multi-loaded pegylated irinotecan conjugate based on IS-CID
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Yu-qing ZOU, Ke-xin LIU, Jia-wang ZHAO, Zhuo-fan ZHANG, Shi-wen SONG*
Affiliations
  • School of Pharmacy, Hainan University, Haikou 570100, China
Published: 2026-02-12 doi: 10.16438/j.0513-4870.2025-1152
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Polymer-drug conjugates have shown great potential in the field of drug delivery, but existing systemic pharmacokinetic data are difficult to clarify their pharmacokinetic behavior at the cellular level. In this study, multi-loaded pegylated irinotecan conjugate (PEG-[irinotecan]3) was used as a model drug to build a research idea based on the interaction of polymorphic components to analyze its cellular pharmacokinetics. An HPLC-MS/MS analysis method based on in-source collision-induced dissociation (IS-CID) technology was established to achieve accurate quantitative analysis of PEG-[irinotecan]3 and its intracellular polymorphic components, and comprehensively clarify its intracellular uptake, efflux and subcellular distribution characteristics. Uptake studies have shown the presence of polymorphic components in cells such as bonded drugs (PEG-[irinotecan]x (x = 3, 2, 1)), release material (PEG20K), free drug (irinotecan) and active metabolite (SN-38). Subcellular distribution studies have shown that bonded drugs and release materials are mainly distributed in the cytoplasm, while irinotecan is mainly distributed in the cytoplasm and nucleus. This study expands the cellular pharmacokinetic research system of polymer-drug conjugates, and the key information obtained is of great value in guiding drug design, clarifying intracellular pharmacokinetic behavior, and promoting clinical transformation.

polymer-drug conjugate  /  cellular pharmacokinetics  /  in-source collision-induced dissociation  /  HPLC-MS/MS  /  polyethylene glycol  /  irinotecan
邹雨晴, 刘可欣, 赵佳旺, 张卓凡, 宋诗文. 基于IS-CID技术的多载药聚乙二醇化伊立替康偶联物的细胞药动学研究. 药学学报, 2026 , 61 (2) : 577 -585 . DOI: 10.16438/j.0513-4870.2025-1152
Yu-qing ZOU, Ke-xin LIU, Jia-wang ZHAO, Zhuo-fan ZHANG, Shi-wen SONG. Cellular pharmacokinetics study of multi-loaded pegylated irinotecan conjugate based on IS-CID[J]. Acta Pharmaceutica Sinica, 2026 , 61 (2) : 577 -585 . DOI: 10.16438/j.0513-4870.2025-1152
Year 2026 volume 61 Issue 2
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doi: 10.16438/j.0513-4870.2025-1152
  • Receive Date:2025-09-26
  • Online Date:2026-09-21
  • Published:2026-02-12
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  • Received:2025-09-26
  • Revised:2025-12-03
Affiliations
    School of Pharmacy, Hainan University, Haikou 570100, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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