首页> 外文期刊>Biochimica et Biophysica Acta. General Subjects >Preparation of long-circulating immunoliposomes containing adriamycin by a novel method to coat immunoliposomes with poly( ethylene glycoi)
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Preparation of long-circulating immunoliposomes containing adriamycin by a novel method to coat immunoliposomes with poly( ethylene glycoi)

机译:一种新方法制备含有阿霉素的长循环免疫脂质体,用一种新的方法涂覆聚乙二醇糖衣的免疫脂质体

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摘要

Modifications of liposomes with poly (ethylene glycoi) (PEG) have been reported to prolong blood circulation time of liposomes. In this report, an adriamycin-encapsulated immunoliposomes were modified with PEG by two different approaches: one is the pre-coating method using lipid derivative of PEG as described by Allen et al. The other is post-coating method which is presented here. The former pre-coating method did not allow coupling of antibody due to the steric hindrance of PEG which had been introduced on liposome surface. On the other hand, in the later post-coating method, PEG-succinylcysteine was synthesized and was successfully conjugated with immunoliposomes via maleimido linker. Resultant PEG-coated immunoliposomes containing adriamycin retained their binding activity and cytotoxicity to target cells, and also showed significantly prolonged blood circulating time as compared with conventional immunoliposomes. This is a novel method to coat immunoliposomes with PEG.
机译:据报道,用聚(乙烯-糖基)(PEG)修饰脂质体可延长脂质体的血液循环时间。在该报告中,通过两种不同的方法用PEG修饰了封装有阿霉素的免疫脂质体:一种是如Allen等人所述使用PEG脂质衍生物的预包被方法。另一种是此处介绍的后涂布方法。由于已经引入脂质体表面的PEG的空间位阻,前一种预包被方法不允许偶联抗体。另一方面,在随后的后涂布方法中,合成了PEG-琥珀酰半胱氨酸,并通过马来酰亚胺基连接体成功地将其与免疫脂质体偶联。与常规免疫脂质体相比,所得包含阿霉素的PEG包被的免疫脂质体保留了它们对靶细胞的结合活性和细胞毒性,并且还显示出血液循环时间显着延长。这是用PEG包被免疫脂质体的新方法。

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