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.

IF 3.5 3区 医学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pharmaceutical Research Pub Date : 2024-09-01 Epub Date: 2024-08-13 DOI:10.1007/s11095-024-03755-6
Zicong Zheng, Vesna Tumbas Šaponjac, Rashim Singh, Jie Chen, Songpol Srinual, Taijun Yin, Rongjin Sun, Ming Hu
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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.

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采用新颖的荧光光谱法将粪便中的 SN-38 含量作为肠道 SN-38 暴露及相关伊立替康诱发的严重迟发性腹泻的替代预测指标
背景:在临床实践中,伊立替康用药可导致严重的迟发性腹泻(SDOD)。目前,还没有可靠的替代指标来预测肠道暴露于 SN-38 和随后的腹泻发生率:方法:采用新型光谱荧光法研究了 Fisher 344 大鼠粪便中 7-乙基-10-羟基喜树碱(SN-38)含量与 SDOD 之间的关系。此外,还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,从而确定组织和粪便 SN-38 暴露之间的关系:结果:成功地采用了荧光光谱法来测量伊立替康用药后第 3 天到第 6 天的粪便中 SN-38 和 CPT-11 的含量。只有第 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。确定了粪便中 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%。粪便中 SN-38 含量与第 3 天回肠中 SN-38 暴露量之间的正相关性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:粪便中的 SN-38 含量可代表大鼠肠道中 SN-38 的暴露量、肠道损伤的指示性指标以及 SDOD 发生率的预测性指标,而光谱荧光法则展示了其转化潜力。
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来源期刊
Pharmaceutical Research
Pharmaceutical Research 医学-化学综合
CiteScore
6.60
自引率
5.40%
发文量
276
审稿时长
3.4 months
期刊介绍: Pharmaceutical Research, an official journal of the American Association of Pharmaceutical Scientists, is committed to publishing novel research that is mechanism-based, hypothesis-driven and addresses significant issues in drug discovery, development and regulation. Current areas of interest include, but are not limited to: -(pre)formulation engineering and processing- computational biopharmaceutics- drug delivery and targeting- molecular biopharmaceutics and drug disposition (including cellular and molecular pharmacology)- pharmacokinetics, pharmacodynamics and pharmacogenetics. Research may involve nonclinical and clinical studies, and utilize both in vitro and in vivo approaches. Studies on small drug molecules, pharmaceutical solid materials (including biomaterials, polymers and nanoparticles) biotechnology products (including genes, peptides, proteins and vaccines), and genetically engineered cells are welcome.
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