Dhananjaya K V, Antony A
Microbiology and Cell Biology Laboratory, Indian Institute of Science, Bangalore.
J Virol Methods. 1988 Feb;19(2):131-40. doi: 10.1016/0166-0934(88)90156-5.
Immunoliposomes were prepared using the antibody raised against the avian myeloblastosis virus envelope glycoprotein, gp80. Adriamycin was encapsulated into immunoliposomes. More drug was delivered into target cells when the drug encapsulated in immunoliposomes was incubated with the cells. The drug encapsulated in immunoliposomes was able to inhibit the RNA synthesis twice more than free drug in the virus-transformed myeloblasts. Pre-treatment of cells with ammonium chloride, reversed the effect of drug encapsulated in immunoliposomes. The drugs encapsulated in immunoliposomes had marginal effect on the RNA synthesis of non-target cells, the yolk sac cells. Colony formation by virus-transformed cells and focus formation by virus-infected yolk sac cells was inhibited significantly by the drug encapsulated in immunoliposomes.
使用针对禽成髓细胞瘤病毒包膜糖蛋白gp80产生的抗体制备免疫脂质体。将阿霉素包封到免疫脂质体中。当将包封在免疫脂质体中的药物与细胞一起孵育时,更多的药物被递送至靶细胞。在病毒转化的成髓细胞中,包封在免疫脂质体中的药物抑制RNA合成的能力比游离药物强两倍。用氯化铵对细胞进行预处理可逆转包封在免疫脂质体中的药物的作用。包封在免疫脂质体中的药物对非靶细胞(卵黄囊细胞)的RNA合成影响很小。包封在免疫脂质体中的药物可显著抑制病毒转化细胞的集落形成以及病毒感染的卵黄囊细胞的病灶形成。