Schwendener R A, Lagocki P A, Rahman Y E
Biochim Biophys Acta. 1984 Apr 25;772(1):93-101. doi: 10.1016/0005-2736(84)90521-2.
The effect of the positive surface charge of unilamellar liposomes on the kinetics of their interaction with rat peritoneal macrophages was investigated using three sizes of liposomes: small unilamellar vesicles (approx. 25 nm diameter), prepared by sonication, and large unilamellar vesicles (100 nm and 160 nm diameter), prepared by the Lipoprep dialysis method. Charge was varied by changing the proportion of stearylamine added to the liposomal lipids (egg phosphatidylcholine and cholesterol, molar ratio 10:2.5). Increasing the stearylamine content of large unilamellar vesicles over a range of 0-25 mol% enhanced the initial rate of vesicle-cell interaction from 0.1 to 1.4 microgram lipid/min per 10(6) cells, and the maximal association from 5 to 110 micrograms lipid/10(6) cells. Cell viability was greater than 90% for cells incubated with large liposomes containing up to 15 mol% stearylamine but decreased to less than 50% at stearylamine proportions greater than 20 mol%. Similar results were obtained with small unilamellar vesicles except that the initial rate of interaction and the maximal association were less sensitive to stearylamine content. The initial rate of interaction, with increasing stearylamine up to 25 mol%, ranged from 0.5 to 0.7 microgram lipid/min per 10(6) cells, and the maximal association ranged from 20 to 70 micrograms lipid/10(6) cells. A comparison of the number and entrapped aqueous volume of small and large vesicles containing 15 mol% stearylamine revealed that although the number of large vesicles associated was 100-fold less than the number of small vesicles, the total entrapped aqueous volume introduced into the cells by large vesicles was 10-fold greater. When cytochalasin B, a known inhibitor of phagocytosis, was present in the medium, the cellular association of C8-LUV was reduced approx. 25% but association of SUV increased approx. 10-30%. Modification of small unilamellar vesicles with an amino mannosyl derivative of cholesterol did not increase their cellular interaction over that of the corresponding stearylamine liposomes, indicating that cell binding induced by this glycolipid may be due to the positive charge of the amine group on the sugar moiety. The results demonstrate that the degree of liposome-cell interaction with macrophages can be improved by increasing the degree of positive surface charge using stearylamine. Additionally, the delivery of aqueous drugs to cells can be further improved using large unilamellar vesicles because of their greater internal volume. This sensitivity of macrophages to vesicle charge and size can be used either to increase or reduce liposome uptake significantly by this cell type
通过超声处理制备的小单层囊泡(直径约25nm),以及通过Lipoprep透析法制备的大单层囊泡(直径100nm和160nm)。通过改变添加到脂质体脂质(鸡蛋磷脂酰胆碱和胆固醇,摩尔比10:2.5)中的硬脂胺比例来改变电荷。在0-25mol%的范围内增加大单层囊泡的硬脂胺含量,可使囊泡-细胞相互作用的初始速率从每10⁶个细胞0.1微克脂质/分钟提高到1.4微克脂质/分钟,最大结合量从5微克脂质/10⁶个细胞提高到110微克脂质/10⁶个细胞。对于与含有高达15mol%硬脂胺的大脂质体孵育的细胞,细胞活力大于90%,但在硬脂胺比例大于20mol%时降至小于50%。小单层囊泡也得到了类似的结果,只是相互作用的初始速率和最大结合量对硬脂胺含量不太敏感。随着硬脂胺增加至25mol%,相互作用的初始速率为每10⁶个细胞0.5至0.7微克脂质/分钟,最大结合量为20至70微克脂质/10⁶个细胞。对含有15mol%硬脂胺的小囊泡和大囊泡的数量及包封的水相体积进行比较,结果显示,尽管结合的大囊泡数量比小囊泡少100倍,但大囊泡引入细胞的总包封水相体积大10倍。当培养基中存在已知的吞噬作用抑制剂细胞松弛素B时,C8-LUV与细胞的结合减少约25%,但SUV与细胞的结合增加约10-30%。用胆固醇的氨基甘露糖衍生物修饰小单层囊泡,其与细胞的相互作用并未比相应的硬脂胺脂质体增加,这表明这种糖脂诱导的细胞结合可能归因于糖部分胺基的正电荷。结果表明,使用硬脂胺增加正表面电荷的程度可以改善脂质体与巨噬细胞的相互作用程度。此外,由于大单层囊泡的内部体积更大,因此向细胞递送水性药物可以进一步改善。巨噬细胞对囊泡电荷和大小的这种敏感性可用于显著增加或减少这种细胞类型对脂质体的摄取。