首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >IL-6 Antibody and RGD Peptide Conjugated Poly(amidoamine) Dendrimer for Targeted Drug Delivery of HeLa Cells
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IL-6 Antibody and RGD Peptide Conjugated Poly(amidoamine) Dendrimer for Targeted Drug Delivery of HeLa Cells

机译:IL-6抗体和RGD肽缀合的聚(酰胺基胺)树状大分子用于HeLa细胞的靶向药物递送

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摘要

In this study, PAMAM dendrimer (G4.5) was conjugated with two targeting moieties, IL-6 antibody and RGD peptide (G4.5-IL6 and G4.5-RGD conjugates). Doxorubicin anticancer drug was physically loaded onto G4.5-IL6 and G4.5-RGD with the encapsulation efficiency of 51.3 and 30.1% respectively. The cellular internalization and uptake efficiency of G4.5-IL6/DOX and G4.5-RGD/DOX complexes was observed and compared by confocal microscopy and flow cytometry using HeLa cells, respectively. The lower IC50 value of G4.5-IL6/DOX in comparison to G4.5-RGD/DOX is indication that higher drug loading and faster drug release rate corresponded with greater cytotoxicity. The cytotoxic effect was further verified by increment in late apoptoticecrotic cells due to delivery of drug through receptor-mediated endocytosis. On the basis of these results, G4.5-IL6 is a better suited carrier for targeted drug delivery of DOX to cervical cancer cells.
机译:在这项研究中,PAMAM树状聚合物(G4.5)与两个靶向部分IL-6抗体和RGD肽(G4.5-IL6和G4.5-RGD缀合物)缀合。将阿霉素抗癌药物物理加载到G4.5-IL6和G4.5-RGD上,其包封效率分别为51.3%和30.1%。分别通过共聚焦显微镜和流式细胞术使用HeLa细胞观察并比较了G4.5-IL6 / DOX和G4.5-RGD / DOX复合物的细胞内在化和摄取效率。与G4.5-RGD / DOX相比,G4.5-IL6 / DOX的IC50值较低,表明较高的载药量和较快的药物释放速率与较大的细胞毒性相对应。通过由于受体介导的内吞作用递送药物而导致的晚期凋亡/坏死细胞增加,进一步证实了细胞毒性作用。基于这些结果,G4.5-IL6是更适合将DOX靶向药物递送至宫颈癌细胞的载体。

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