阿霉素
肺表面活性物质
心脏毒性
药物输送
胶束
药品
化学
材料科学
色谱法
药理学
纳米技术
水溶液
化疗
毒性
有机化学
医学
生物化学
外科
作者
Juyoung Hwang,Ji Yeong Park,Jio Kang,Nuri Oh,Chen Li,Chung‐Yul Yoo,Wooram Um,Minseok Kwak
标识
DOI:10.1002/marc.202400480
摘要
Abstract In this study, oil‐in‐water nanoemulsions are prepared, an isotropic mixture of oil, surfactant, and cosurfactants. The nanoemulsions exhibit stable structures and are capable of efficiently encapsulating hydrophobic drugs such as doxorubicin (Dox). Compared to polymeric micelles, nanoemulsions demonstrate enhanced stability and loading capacity for Dox. Furthermore, nanoemulsions release Dox steadily over 14 days, with 51.6% released within the initial 24 h and up to 80% over the subsequent period. These properties suggest that nanoemulsions can mitigate the side effects related to the burst release of Dox, thereby improving therapeutic efficacy and safety. Additionally, nanoemulsion‐treated cardiomyocytes show increased viability compared to those treated with free Dox, indicating the potential of nanoemulsions to alleviate Dox‐induced cardiotoxicity. Overall, nanoemulsions hold promise as versatile and efficient drug carriers for improving cancer treatment outcomes.
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