Zhang Hui, Gong Wei, Wang Zhi-Yuan, Yuan Shou-Jun, Xie Xiang-Yang, Yang Yan-Fang, Yang Yang, Wang Shan-Shan, Yang De-Xuan, Xuan Zi-Xue, Mei Xing-Guo
Beijing Institute of Pharmacology and Toxicology, Beijing 100850, P.R. China.
Beijing Institute of Radiation Medicine, Beijing 100850 P.R. China.
J Pharm Sci. 2014 Jul;103(7):2177-2183. doi: 10.1002/jps.24019. Epub 2014 May 20.
A novel thermosensitive liposome (TL) containing docetaxel (DTX) was designed to enhance DTX-targeted delivery and antitumor effect. TL loading DTX (DTX-TL) were prepared by thin film hydration. The mean particle size of the liposomes was about 100 nm, and the drug entrapment efficiency was more than 95%. The phase transition temperature of liposomes was about 42 °C. In vitro drug release showed that drug released at 37 °C was obviously less than that at 42 °C. For in vivo experiments, the human breast tumor model was established by subcutaneous xenotransplantation on nude mice; liposomes and injection containing DTX were injected i.v. in nude mice, followed by exposure of the tumors to hyperthermia (HT) for 30 min after administration. The tumor inhibition ratio of DTX-TL group was significantly higher than the normal injection group. Combining TL with HT enhanced the delivery of DTX and thereby its antitumor effects. The liposomes reported in this paper could potentially produce viable clinical strategies for improved targeting and delivery of DTX for the treatment of breast cancer.
设计了一种新型的含多西他赛(DTX)的热敏脂质体(TL),以增强DTX的靶向递送和抗肿瘤效果。通过薄膜水化法制备了负载DTX的TL(DTX-TL)。脂质体的平均粒径约为100nm,药物包封率超过95%。脂质体的相变温度约为42℃。体外药物释放表明,37℃时释放的药物明显少于42℃时。对于体内实验,通过裸鼠皮下异种移植建立人乳腺肿瘤模型;将脂质体和含DTX的注射液静脉注射到裸鼠体内,给药后对肿瘤进行30分钟的热疗(HT)。DTX-TL组的肿瘤抑制率明显高于正常注射组。将TL与HT相结合可增强DTX的递送,从而增强其抗肿瘤效果。本文报道的脂质体可能为改善DTX靶向递送治疗乳腺癌提供可行的临床策略策略。
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