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用于检测CPT-11/DSPE-甲氧基聚乙二醇纳米制剂内毒素的鲎试剂检测法和动态比浊法:如果传统方法不适用该怎么办?

LAL test and RPT for endotoxin detection of CPT-11/DSPE-mPEG nanoformulation: What if traditional methods are not applicable?

作者信息

Jin Yanan, Jia Juanjuan, Li Chan, Xue Jianqi, Sun Jiabei, Wang Kaiyuan, Gan Yaling, Xu Jing, Shi Yaqin, Liang Xingjie

机构信息

College of Chemistry & Environmental Science, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of the Ministry of Education, Hebei University, Baoding 071002, China.

National Institutes for Food and Drug Control, No. 5, Huatuo Rd., Daxing District, Beijing 102629, China.

出版信息

Asian J Pharm Sci. 2018 May;13(3):289-296. doi: 10.1016/j.ajps.2017.11.003. Epub 2018 Jan 9.

Abstract

Endotoxin detection is an important step in drug characterization. Herein we found that a chemotherapeutic drug nanoformulation composed of irinotecan hydrochloride (CPT-11) and an amphiphilic molecule DSPE-mPEG can interfere with the limulus amebocyte lysate assay (LAL). Furthermore, the rabbit pyrogen test (RPT) results indicated that at a relatively high dosage, the drug irinotecan hydrochloride can induce a hypothermia effect which may render the RPT results ambiguous in determination of the safety of the drug formulation.Our findings demonstrate limitations of endotoxin detection in micellar drugs, and call for the necessity of developing reliable endotoxin detection methods that can overcome the interference of nanomaterials in order to better ensure the drug safety of patients in future pharmaceutical drug development.

摘要

内毒素检测是药物特性鉴定中的重要一步。在此我们发现,由盐酸伊立替康(CPT - 11)和两亲性分子DSPE - mPEG组成的化疗药物纳米制剂会干扰鲎试剂检测法(LAL)。此外,家兔热原试验(RPT)结果表明,在相对较高剂量下,盐酸伊立替康药物可诱导体温过低效应,这可能使RPT结果在药物制剂安全性测定中变得模糊不清。我们的研究结果证明了胶束药物内毒素检测的局限性,并呼吁开发可靠的内毒素检测方法,以克服纳米材料的干扰,从而在未来药物研发中更好地确保患者的用药安全。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b834/7032139/b53e9662d24e/fx1.jpg

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