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粪便中SN-38含量作为肠道SN-38暴露的替代预测指标以及通过荧光分光光度法的新应用预测伊立替康诱导的严重迟发性腹泻

Fecal SN-38 Content as a Surrogate Predictor of Intestinal SN-38 Exposure and Associated Irinotecan-induced Severe Delayed-Onset Diarrhea by a Novel Use of the Spectrofluorimetric Method.

作者信息

Zheng Zicong, Šaponjac Vesna Tumbas, Singh Rashim, Chen Jie, Srinual Songpol, Yin Taijun, Sun Rongjin, Hu Ming

机构信息

Department of Pharmacological and Pharmaceutical Sciences, College of Pharmacy, University of Houston, 4349 Martin Luther King Blvd, Houston, TX, 77204, USA.

Sanarentero LLC, 514 N. Elder Grove Dr., Pearland, TX, 77584, USA.

出版信息

Pharm Res. 2024 Sep;41(9):1855-1867. doi: 10.1007/s11095-024-03755-6. Epub 2024 Aug 13.

DOI:10.1007/s11095-024-03755-6
PMID:39138788
Abstract

BACKGROUND

Irinotecan administration can lead to severe delayed-onset diarrhea (SDOD) in clinical practice. Currently, there is no reliable surrogate predictor of intestinal exposure to SN-38 and subsequent diarrhea incidence.

METHODS

The relationship between fecal 7-ethyl-10-hydroxycamptothecin (SN-38) content and SDOD was investigated in Fisher 344 rats using a novel spectrofluorimetric method. Additionally, a pharmacokinetic study of irinotecan was performed to evaluate the biodistribution of SN-38 to establish the relationship between tissue and fecal SN-38 exposure.

RESULTS

The spectrofluorimetric method was successfully employed to measure fecal SN-38 and CPT-11 content from Day 3 to Day 6 post-irinotecan administration. Only fecal SN-38 content on Day 3 exhibited a significantly positive correlation with SDOD incidence on Days 4 and 5. A cutoff value of SN-38 ≥ 0.066 mg/g in feces was identified, predicting severe diarrhea incidence with 81% accuracy and 80% specificity. The positive correlation between fecal SN-38 content and SN-38 exposure in the ileum on Day 3 was also reflected in the changes of indicators during intestinal injury, such as prostaglandin E2 level and antioxidant activity.

CONCLUSION

Fecal SN-38 content proves to be representative of intestinal exposure to SN-38, indicative of intestinal injury, and predictive of SDOD incidence in rats, while the spectrofluorimetric method demonstrates the translational potential.

摘要

背景

在临床实践中,使用伊立替康可导致严重的迟发性腹泻(SDOD)。目前,尚无可靠的替代指标来预测肠道对SN-38的暴露及随后的腹泻发生率。

方法

采用一种新型荧光分光光度法,在Fisher 344大鼠中研究粪便中7-乙基-10-羟基喜树碱(SN-38)含量与SDOD之间的关系。此外,进行了伊立替康的药代动力学研究,以评估SN-38的生物分布,从而建立组织与粪便中SN-38暴露之间的关系。

结果

荧光分光光度法成功用于测量伊立替康给药后第3天至第6天的粪便SN-38和CPT-11含量。仅第3天的粪便SN-38含量与第4天和第5天的SDOD发生率呈显著正相关。确定粪便中SN-38≥0.066 mg/g的临界值,预测严重腹泻发生率的准确率为81%,特异性为80%。第3天粪便SN-38含量与回肠中SN-38暴露之间的正相关也反映在肠道损伤期间的指标变化中,如前列腺素E2水平和抗氧化活性。

结论

粪便SN-38含量被证明可代表肠道对SN-38的暴露,指示肠道损伤,并可预测大鼠SDOD的发生率,而荧光分光光度法显示出转化潜力。

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1
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2
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Acta Pharm Sin B. 2023 Aug;13(8):3444-3453. doi: 10.1016/j.apsb.2023.01.011. Epub 2023 Jan 10.
3
Targeting oxidative stress in disease: promise and limitations of antioxidant therapy.
针对疾病中的氧化应激:抗氧化治疗的前景和局限性。
Nat Rev Drug Discov. 2021 Sep;20(9):689-709. doi: 10.1038/s41573-021-00233-1. Epub 2021 Jun 30.
4
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Drug Metab Dispos. 2021 Aug;49(8):683-693. doi: 10.1124/dmd.121.000476. Epub 2021 Jun 1.
5
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6
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7
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Int J Oncol. 2019 Apr;54(4):1376-1386. doi: 10.3892/ijo.2019.4714. Epub 2019 Feb 11.
8
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Chem Commun (Camb). 2018 Feb 6;54(12):1485-1488. doi: 10.1039/c7cc07668a.
9
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NPJ Biofilms Microbiomes. 2017 Nov 1;3:27. doi: 10.1038/s41522-017-0034-1. eCollection 2017.
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