共轭体系
JavaScript
缩放
脂质体
点击化学
乳腺癌
特征(语言学)
材料科学
计算机科学
生物医学工程
白蛋白
纳米技术
癌症
化学
医学
高分子化学
物理
光学
生物化学
程序设计语言
内科学
复合材料
语言学
哲学
镜头(地质)
聚合物
作者
Nahid S. Awad,Vinod Paul,Mohammad H. Al‐Sayah,Ghaleb A. Husseini
标识
DOI:10.1080/21691401.2019.1573175
摘要
Targeted liposomes have high potentials in the specific and effective delivery of their loaded therapeutic agents to the tumour site. Once at the tumour site, it is important that these liposomes are triggered to release their load in a controlled and effective manner. In this study, pegylated (stealth) liposomes conjugated to human serum albumin (HSA) were investigated for the delivery of a model drug (calcein) to breast cancer cells. The fluorescent results showed that calcein uptake by the two breast cancer cell lines (MDA-MB-231 and MCF-7) was significantly higher with the HSA-PEG liposomes compared to the non-targeted control liposomes. Furthermore, the exposure to low-frequency ultrasound (LFUS) resulted in a statistically significant uptake of calcein compared to the uptake without ultrasound. The described drug delivery (DD) system, which involves combining the targeted liposomal formulation with ultrasonic triggering techniques, promises a safe, effective and site-specific breast cancer therapy.
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