纳米载体
脂质体
临床试验
医学
药物输送
癌症
癌症治疗
不利影响
药理学
纳米技术
药品
重症监护医学
内科学
材料科学
作者
Satyam Sharma,Moitrai Chakraborty,Dharmendra Yadav,Aniket Dhullap,Raghuraj Singh,Rahul Kumar Verma,Sankha Bhattacharya,Sanjiv Singh
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2024-08-20
卷期号:25 (9): 5650-5669
被引量:7
标识
DOI:10.1021/acs.biomac.4c00847
摘要
Liposomes, made up of phospholipid bilayers, are efficient nanocarriers for drug delivery because they can encapsulate both hydrophilic and lipophilic drugs. Conventional cancer treatments sometimes involve considerable toxicities and adverse drug reactions (ADRs), which limits their clinical value. Despite liposomes' promise in addressing these concerns, clinical trials have revealed significant limitations, including stability, targeted distribution, and scaling challenges. Recent clinical trials have focused on enhancing liposome formulations to increase therapeutic efficacy while minimizing negative effects. Notably, the approval of liposomal medications like Doxil demonstrates their potential in cancer treatment. However, the intricacy of liposome preparation and the requirement for comprehensive regulatory approval remain substantial impediments. Current clinical trial updates show continued efforts to improve liposome stability, targeting mechanisms, and payload capacity in order to address these issues. The future of liposomal drug delivery in cancer therapy depends on addressing these challenges in order to provide patients with more effective and safer treatment alternatives.
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