紫杉醇
药物输送
细胞毒性
药品
生物利用度
化疗
超声波
乳状液
靶向给药
回声
药理学
生物医学工程
化学
医学
体外
材料科学
纳米技术
外科
放射科
生物化学
作者
Gayoung Kim,Jongho Won,Chul Woo Kim,Jong‐Ryul Park,Donghee Park
出处
期刊:Langmuir
[American Chemical Society]
日期:2023-12-26
卷期号:40 (1): 91-99
被引量:1
标识
DOI:10.1021/acs.langmuir.3c02005
摘要
Chemotherapy is the most widely used cancer treatment, but it has several drawbacks such as adverse side effects and low bioavailability. To address these limitations, various drug delivery systems have been investigated, including liposomes, micelles, and emulsions. These drug delivery technologies have been improving the efficacy and safety of conventional chemotherapy. This study presents an emerging drug delivery technology for targeted chemotherapy using drug-loaded ultrasound-responsive emulsion (URE) as a drug carrier and ultrasound technology for external activation. URE was designed to be responsive to ultrasound energy and fabricated by using an emulsification technique. To investigate this technology, paclitaxel, as a model drug, was used and encapsulated into URE. The size distribution, morphology, and drug release behavior of paclitaxel-loaded URE (PTX-URE) were characterized, and the echogenicity of PTX-URE was assessed by using ultrasound imaging equipment. The cellular uptake and cytotoxicity of PTX-URE with ultrasound were evaluated in breast cancer cells (MDA-MB-231). Our in vitro results indicate that the combination of PTX-URE and ultrasound significantly enhanced cellular uptake by 10.6-fold and improved cytotoxicity by 24.1% compared to PTX alone. These findings suggest that the URE platform combined with ultrasound is a promising technology to improve the drug delivery efficiency for chemotherapy.
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