Division of Drugs, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa, 210-9501, Japan.
Division of Drugs, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa, 210-9501, Japan.
Chem Phys Lipids. 2019 Nov;224:104726. doi: 10.1016/j.chemphyslip.2019.01.004. Epub 2019 Jan 17.
Here we report that the size dependence of cellular internalization of liposomes differs depending on the surface charge. We prepared liposomes of various lipid compositions ranging from 100 to 200 nm size. It was found that cationic liposomes composed of 1,2-Dioleoyl-sn-glycero-3-phosphocholine (DOPC) and 1,2-Dioleoyl-3-trimethylammonium-propane (DOTAP) were most effectively internalized into cells when their mean particle sizes were around 180 nm. When their size was reduced to around 90 nm, the level of internalization reduced six-fold. Conversely, hydrogenated soy phosphatidylcholine (HSPC)/N-(carbonyl-methoxypolyethylene glycol 2000)-1,2-distearoyl-sn-glycero-3-phosphoethanolamine (PEG2000-DSPE)/cholesterol(Chol) liposomes, HSPC/PEG2000-DSPE liposomes, and HSPC/Chol liposomes were most readily internalized when they were around 110 to 130 nm in mean particle size. Unlike DOPC/DOTAP liposomes the difference between the maximum and minimum levels of internalization was less than two-fold. It has been suggested that strong electrostatic interactions between cationic liposomes and the negatively charged plasma membrane affect the size dependence and optimal size range for internalization of liposomes. Size dependence of internalization should be carefully monitored for effective formulation development and quality control of liposome drug products.
在这里,我们报告称,脂质体的细胞内化的大小依赖性取决于表面电荷。我们制备了各种脂质组成的脂质体,粒径范围从 100 到 200nm。结果发现,当平均粒径约为 180nm 时,由 1,2-二油酰基-sn-甘油-3-磷酸胆碱(DOPC)和 1,2-二油酰基-3-三甲基铵丙烷(DOTAP)组成的阳离子脂质体最有效地被细胞内化。当它们的尺寸减小到约 90nm 时,内化水平降低了六倍。相反,氢化大豆卵磷脂(HSPC)/N-(羰基-甲氧基聚乙二醇 2000)-1,2-二硬脂酰基-sn-甘油-3-磷酸乙醇胺(PEG2000-DSPE)/胆固醇(Chol)脂质体、HSPC/PEG2000-DSPE 脂质体和 HSPC/Chol 脂质体在平均粒径约为 110 至 130nm 时最容易被内化。与 DOPC/DOTAP 脂质体不同,内化的最大和最小水平之间的差异小于两倍。有人认为,阳离子脂质体与带负电荷的质膜之间的强静电相互作用影响了脂质体内化的大小依赖性和最佳尺寸范围。在有效开发脂质体药物制剂和进行质量控制时,应仔细监测内化的大小依赖性。