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Construction of a Novel Magnetic Targeting Anti-Tumor Drug Delivery System: Cytosine Arabinoside-Loaded Bacterial Magnetosome

机译:新型磁性靶向抗肿瘤药物递送系统的构建:胞嘧啶阿拉伯糖苷加载细菌磁小体

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摘要

To ease the side effects triggered by cytosine arabinoside (Ara-C) for acute leukemia treatment, a novel magnetic targeting anti-tumor drug delivery system was constructed through bacterial magnetosomes (BMs) from Magnetospirillum magneticum AMB-1 combined with Ara-C by crosslinking of genipin (GP). The results showed that Ara-C could be bonded onto the membrane surface of BMs effectively through chemical crosslinking induced by dual hand reagents GP. The average diameters of BMs and Ara-C-coupled BMs (ABMs) were 42.0 ± 8.6 and 72.7 ± 6.0 nm respectively, and the zeta potentials (−38.1 ± 9.1) revealed that these systems were stable, confirming the stability of the system. The optimal encapsulation efficiency and drug loading were 89.05% ± 2.33% and 47.05% ± 0.64% respectively when crosslinking reaction lasted for 72 h. The system also presented long-term stability and release behaviors without initial burst release (Ara-C could be released 80% within three months). Our results indicate that BMs have great potential in biomedical and clinical fields as a novel anti-tumor drug carrier.
机译:为了缓解阿糖胞苷(Ara-C)引发的急性白血病的副作用,通过将Magnetospirillum magneticum AMB-1的细菌磁小体(BMs)与Ara-C结合,通过交联构建了一种新型的磁性靶向抗肿瘤药物递送系统genipin(GP)。结果表明,Ara-C可以通过双手试剂GP诱导的化学交联有效地结合到BMs的膜表面上。 BM和Ara-C耦合BM(ABM)的平均直径分别为42.0±8.6和72.7±6.0 nm,ζ电位(−38.1±9.1)表明这些系统稳定,证实了系统的稳定性。当交联反应持续72 h时,最佳包封率和载药量分别为89.05%±2.33%和47.05%±0.64%。该系统还表现出长期稳定性和释放行为,而没有最初的突发释放(Ara-C可以在三个月内释放80%)。我们的结果表明,BMs作为一种新型的抗肿瘤药物载体在生物医学和临床领域具有巨大的潜力。

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