首页> 美国卫生研究院文献>Acta Pharmaceutica Sinica. B >Injectable peptide hydrogel as intraperitoneal triptolide depot for the treatment of orthotopic hepatocellular carcinoma
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Injectable peptide hydrogel as intraperitoneal triptolide depot for the treatment of orthotopic hepatocellular carcinoma

机译:注射性肽水凝胶作为腹膜内雷公藤内酯醇治疗原位肝细胞癌

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摘要

Chemotherapy is among the limited choices approved for the treatment of hepatocellular carcinoma (HCC) at intermediate and advanced stages. Preferential and prolonged drug exposure in diseased sites is required to maximize the therapeutic index of the drug. Here, we report an injectable supramolecular peptide hydrogel as an intraperitoneal depot for localized and sustained release of triptolide for the treatment of orthotopic HCC. We chose peptide amphiphile C16-GNNQQNYKD-OH-based nanofibers as gelators and carriers for triptolide. Sustained triptolide release from the hydrogel was achieved over 14 days in vitro, with higher accumulation in and cytotoxicity against human HCC Bel-7402 in comparison with L-02 fetal hepatocytes. After intraperitoneal injection, the hydrogel showed prolonged retention over 13 days and preferential accumulation in the liver, realizing HCC growth inhibition by 99.7 ± 0.1% and animal median survival extension from 19 to 43 days, without causing noticeable pathological changes in the major organs. These results demonstrate that injectable peptide hydrogel can be a potential carrier for localized chemotherapy of HCC.
机译:化学疗法是批准用于中晚期肝细胞癌(HCC)治疗的有限选择之一。为了使药物的治疗指数最大化,需要在患病部位进行优先和长时间的药物暴露。在这里,我们报告注射性超分子肽水凝胶作为腹膜内储库的雷公藤内酯醇的局部和持续释放,用于原位肝癌的治疗。我们选择基于肽两亲性C16-GNNQQNYKD-OH的纳米纤维作为雷公藤甲素的胶凝剂和载体。雷公藤内酯醇从水凝胶中持续释放超过14天,与L-02胎儿肝细胞相比,在人HCC Bel-7402中具有更高的积累和对人HCC Bel-7402的细胞毒性。腹膜内注射后,水凝胶显示了13天以上的保留时间延长并在肝脏中优先积累,实现了HCC生长抑制99.7±0.1%和动物中位生存期从19天延长至43天,而没有引起主要器官的明显病理变化。这些结果表明,可注射的肽水凝胶可能是肝癌局部化疗的潜在载体。

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