Lanlan Xiang, Hao Wang, Jiajie Liu, Yuchen Shen, Yanfen Hu, Wenchen Che, Ran Li, Sisi Yang, Xin Teng
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引用次数: 0
摘要
背景/目的:多西他赛是一种有效的抗癌药物,能够治疗多种类型的癌症。然而,当与标准增溶剂Tween-80一起使用时,通常会引起一系列不良反应,因此需要在给药前用地塞米松预防过敏。为了减轻过敏反应的风险,纳米胶束由于其增强的溶解度和热力学稳定性而引起了人们的极大兴趣。方法:设计m = 45, n = 10的mPEG-PLA-Lys(Fmoc)胶束载体包封多西紫杉醇,并研究其胶束自组装。此外,还对动物进行了过敏反应研究。结果:研究结果表明,该制剂不会引起兔溶血、血管或肌肉刺激,也不会引起豚鼠过敏反应。结论:纳米微球包封多西紫杉醇可减轻注射多西紫杉醇引起的过敏反应,为提高多西紫杉醇的治疗价值提供了新的途径。
Docetaxel Micelles: A New Formulation to Diminish Hypersensitivity Reactions.
Background/Objectives: Docetaxel is a potent anti-cancer agent capable of treating various types of cancer. However, it often induces a range of adverse reactions when used with its standard solubilizer, Tween-80, necessitating allergy prophylaxis with dexamethasone prior to administration. To mitigate the risk of allergic reactions, with nanomicelles garnering significant interest due to their enhanced solubility and thermodynamic stability. Methods: In this research, a mPEG-PLA-Lys(Fmoc) micellar carrier with m = 45 and n = 10 was engineered to encapsulate docetaxel, and its self-assembly into micelles was investigated. Additionally, allergic reaction studies were conducted on animals. Results: The findings indicated that the formulation did not cause hemolysis, vascular, or muscle irritation in rabbits, nor did it elicit an allergic response in guinea pigs. Conclusions: These results suggest that nanomicelle-encapsulated docetaxel can diminish the allergic reactions associated with docetaxel injections, offering a novel approach to enhance the therapeutic utility of this outstanding anti-cancer drug.
PharmaceuticsPharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍:
Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications, and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.