纳米载体
脂质体
药物输送
药品
靶向给药
药理学
生物利用度
毒品携带者
医学
纳米技术
化学
材料科学
作者
Maria P. Nikolova,Enamala Manoj Kumar,Murthy Chavali
出处
期刊:Pharmaceutics
[MDPI AG]
日期:2022-10-15
卷期号:14 (10): 2195-2195
被引量:21
标识
DOI:10.3390/pharmaceutics14102195
摘要
Liposomes are well-known nanoparticles with a non-toxic nature and the ability to incorporate both hydrophilic and hydrophobic drugs simultaneously. As modern drug delivery formulations are produced by emerging technologies, numerous advantages of liposomal drug delivery systems over conventional liposomes or free drug treatment of cancer have been reported. Recently, liposome nanocarriers have exhibited high drug loading capacity, drug protection, improved bioavailability, enhanced intercellular delivery, and better therapeutic effect because of resounding success in targeting delivery. The site targeting of smart responsive liposomes, achieved through changes in their physicochemical and morphological properties, allows for the controlled release of active compounds under certain endogenous or exogenous stimuli. In that way, the multifunctional and stimuli-responsive nanocarriers for the drug delivery of cancer therapeutics enhance the efficacy of treatment prevention and fighting over metastases, while limiting the systemic side effects on healthy tissues and organs. Since liposomes constitute promising nanocarriers for site-targeted and controlled anticancer drug release, this review focuses on the recent progress of smart liposome achievements for anticancer drug delivery applications.
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