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多西他赛与纳米紫杉醇(一种载有多西他赛的胶束制剂)使用培养细胞和血细胞的比较毒性研究。

Comparative Toxicity Study of Docetaxel and Nanoxel, a Docetaxel-Loaded Micellar Formulation Using Cultured and Blood Cells.

作者信息

Do Van Quan, Park Kwang-Hoon, Park Jung-Min, Lee Moo-Yeol

机构信息

College of Pharmacy, Dongguk University, Goyang, Korea.

出版信息

Toxicol Res. 2019 Apr;35(2):201-207. doi: 10.5487/TR.2019.35.2.201. Epub 2019 Apr 15.

DOI:10.5487/TR.2019.35.2.201
PMID:31015902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6467357/
Abstract

Nanoxel-PM (Nanoxel) is a docetaxel-loaded methoxy-poly(ethylene glycol)--poly(D,L-lactide) (mPEG-PDLLA). This newly developed and marketed nanoformulation exhibits an improved pharmacokinetic profile, efficacy, and safety. Although the safety of Nanoxel to docetaxel as well as its bioequivalence must be clinically confirmed, all biological activities have not been examined in or studies. Here, the toxicity in a cultured cell system and the effects on blood cells were tested with Nanoxel and docetaxel. The cytotoxicity of Nanoxel was found to be comparable to or slightly lower than that of docetaxel depending on the concentrations tested or the cell types. Neither docetaxel nor Nanoxel induced erythrocytes hemolysis and produced reactive oxygen species up to 100 μM. However, Nanoxel was able to enhance the aggregatory response of platelets to collagen, whereas docetaxel attenuated such aggregation in a range of 50-100 μM, while thrombin-induced aggregation was not affected by either of them. Docetaxel or Nanoxel did not alter basal level of Ca and 5-hydroxytryptamine-evoked Ca transient in vascular smooth muscle cells. These results suggest that the mPEG-PDLLA micellar formulation alters the toxicological properties of docetaxel, and that extra cautions are needed when evaluating the safety of nanomedicine.

摘要

纳米紫杉醇-PM(Nanoxel)是一种负载多西他赛的甲氧基聚(乙二醇)-聚(D,L-丙交酯)(mPEG-PDLLA)。这种新开发并上市的纳米制剂具有改善的药代动力学特征、疗效和安全性。尽管Nanoxel对多西他赛的安全性及其生物等效性必须经过临床确认,但尚未在体内或体外研究中考察其所有生物学活性。在此,用Nanoxel和多西他赛测试了其在培养细胞系统中的毒性以及对血细胞的影响。根据测试浓度或细胞类型,发现Nanoxel的细胞毒性与多西他赛相当或略低于多西他赛。多西他赛和Nanoxel在高达100μM时均未诱导红细胞溶血或产生活性氧。然而,Nanoxel能够增强血小板对胶原的聚集反应,而多西他赛在50-100μM范围内减弱这种聚集,而凝血酶诱导的聚集不受它们任何一个的影响。多西他赛或Nanoxel不会改变血管平滑肌细胞中钙的基础水平以及5-羟色胺诱发的钙瞬变。这些结果表明,mPEG-PDLLA胶束制剂改变了多西他赛的毒理学特性,并且在评估纳米药物的安全性时需要格外谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/6467357/d39abf0a8438/tr-35-201f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/6467357/d717b455cf3e/tr-35-201f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/6467357/6d18506ccca7/tr-35-201f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/6467357/ce5c1a12f705/tr-35-201f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/6467357/f7cd44d1b5db/tr-35-201f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/6467357/d39abf0a8438/tr-35-201f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/6467357/d717b455cf3e/tr-35-201f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/6467357/6d18506ccca7/tr-35-201f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/6467357/ce5c1a12f705/tr-35-201f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/6467357/f7cd44d1b5db/tr-35-201f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/6467357/d39abf0a8438/tr-35-201f5.jpg

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