脂质体
塑料挤出
材料科学
分散性
药物输送
挤压
生物利用度
粒径
纳米技术
生物医学工程
化学工程
药理学
复合材料
医学
工程类
高分子化学
作者
The Dan Pham,Linh Phuong Nguyen,Quynh Thi Huong Pham,Chi Khanh Pham,Dung Thuy Nguyen Pham,Nguyen Thanh Viet,Hong Van Nguyen,Toan Quoc Tran,Duong Thanh Nguyen
标识
DOI:10.1177/08853282221112491
摘要
Liposomal encapsulation is a drug delivery strategy with many advantages, such as improved bioavailability, ability to carry large drug loads, as well as controllability and specificity towards various targeted diseased tissues. Currently, most preparation techniques require an additional extrusion or filtering step to obtain monodisperse liposomes with the size of less than 100 nm. In this study, a compact liposome extruder was designed at a cost of $4.00 and used to synthesize liposome suspensions with defined particle size and high homogeneity for Murrayafoline A (Mu-A) loading and release. The synthesized MuA-loaded liposomes displayed a biphasic drug release and remained stable under the storage condition of 4°C. They also significantly reduced the viability of HepG2 cells in the cancer spheroids by 25%. The low-cost, flexible liposome extruder would allow the researchers to study liposomes and their applications in a cost-effective manner.
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