核苷与低密度脂蛋白(LDL)的共价偶联产生巨噬细胞特异性(药物)载体。

H von Baeyer, H Neitzel, M Nündel, E Riedel, H K Schultis
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引用次数: 0

摘要

描述了胸苷和叠氮胸苷(ZIDOVUDINE)与LDL-Apo B赖氨酸侧链ε -氨基的共价偶联。细胞培养实验证明,该过程产生的ldl -核苷颗粒仅对巨噬细胞的清道夫受体通路具有亲和力。放射自显影显示3h -胸腺嘧啶作为核苷的代表,被运送到细胞核。因此,胸腺嘧啶的内化、溶酶体裂解和三磷酸化明显发生了。这种新的药物靶向方法的应用是巨噬细胞选择性抑制hiv逆转录酶在艾滋病中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Covalent coupling of nucleosides to low density lipoprotein (LDL) generates macrophage specific (drug)-carriers.

Covalent coupling of thymidine and azidothymidine (ZIDOVUDINE) to epsilon-amino groups of lysine side chains of LDL-Apo B is described. This procedure generates LDL-nucleoside particles that exhibits affinity solely for the scavenger receptor pathway on macrophages which is demonstrated by cell culture experiments. Autoradiography shows that 3H-thymidine, as representative of nucleosides, is delivered to the cell nucleus. Hence internalization, lysosomal cleavage and triphosphorylation of thymidine evidently had occurred. The application of this new method of drug targeting is macrophage selective inhibition of HIV-reverse transcriptase in AIDS.

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