Microfluidic Production of Lysolipid-Containing Temperature-Sensitive Liposomes

被引:3
作者
Cheung, Calvin C. L. [1 ]
Ma, Guanglong [1 ]
Ruiz, Amalia [1 ]
Al-Jamal, Wafa T. [1 ]
机构
[1] Queens Univ Belfast, Sch Pharm, Belfast, Antrim, North Ireland
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2020年 / 157期
基金
英国工程与自然科学研究理事会;
关键词
Bioengineering; Issue; 157; microfluidics; liposomes; thermosensitive; lysolipid; LTSLs; staggered herringbone micromixer; cholesterol-free; indocyanine green (ICG); doxorubicin loading (DOX); INTERDIGITATED GEL PHASE; ON-A-CHIP; CHOLESTEROL; ETHANOL; PHOSPHATIDYLCHOLINE; NANOPARTICLES; RELEASE;
D O I
10.3791/60907
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The presented protocol enables a high-throughput continuous preparation of low temperature-sensitive liposomes (LTSLs), which are capable of loading chemotherapeutic drugs, such as doxorubicin (DOX). To achieve this, an ethanolic lipid mixture and ammonium sulfate solution are injected into a staggered herringbone micromixer (SHM) microfluidic device. The solutions are rapidly mixed by the SHM, providing a homogeneous solvent environment for liposomes self-assembly. Collected liposomes are first annealed, then dialyzed to remove residual ethanol. An ammonium sulfate pH-gradient is established through buffer exchange of the external solution by using size exclusion chromatography. DOX is then remotely loaded into the liposomes with high encapsulation efficiency (> 80%). The liposomes obtained are homogenous in size with Z-average diameter of 100 nm. They are capable of temperature-triggered burst release of encapsulated DOX in the presence of mild hyperthermia (42 degrees C). Indocyanine green (ICG) can also be co-loaded into the liposomes for near-infrared laser-triggered DOX release. The microfluidic approach ensures high-throughput, reproducible and scalable preparation of LTSLs.
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页数:11
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