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基于纳米技术的 siRNA 递药策略治疗转移性结直肠癌。

Nanotechnology-based siRNA delivery strategies for metastatic colorectal cancer therapy.

机构信息

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen, 208, 4200-135 Porto, Portugal; INEB - Instituto de Engenharia Biomédica, Universidade do Porto, Rua Alfredo Allen, 208, 4200-135 Porto, Portugal; IPO Porto - Instituto Português de Oncologia do Porto, Rua Dr António Bernardino de Almeida, 4200-072 Porto, Portugal; ICBAS - Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, Rua Jorge de Viterbo Ferreira, 228, 4050-313 Porto, Portugal.

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen, 208, 4200-135 Porto, Portugal; INEB - Instituto de Engenharia Biomédica, Universidade do Porto, Rua Alfredo Allen, 208, 4200-135 Porto, Portugal.

出版信息

Int J Pharm. 2019 Sep 10;568:118530. doi: 10.1016/j.ijpharm.2019.118530. Epub 2019 Jul 16.

Abstract

Colorectal cancer (CRC) is the second most common cause of cancer-related death in the world, mainly due to distant metastases events. The metastatic CRC (mCRC) stages are resistant to the therapeutic recommended. Therefore, it urges the development of more efficient strategies to impair the disease. Small interfering RNA (siRNA) is a well-known silencing tool with impact on targeted cancer therapy, even though in vivo challenges difficult its clinical application. Here, multiple solutions to overcome the extracellular and intracellular barriers encountered by intravenous delivery of siRNA are discussed. Moreover, it is emphasized the association of siRNA with nanoparticles to enable the long-term release and to counteract the toxicity issues of siRNA. Particular attention is paid on the potential of poly(lactic-co-glycolic acid) (PLGA) nanoparticles for systemic siRNA delivery in mCRC. Despite of being less used so far due to technological difficulties, multiple strategies to successfully encapsulate siRNA into PLGA nanocarriers are summarized.

摘要

结直肠癌(CRC)是世界上第二大常见的癌症相关死亡原因,主要是由于远处转移事件。转移性结直肠癌(mCRC)对推荐的治疗方法具有耐药性。因此,迫切需要开发更有效的策略来损害这种疾病。小干扰 RNA(siRNA)是一种众所周知的沉默工具,对靶向癌症治疗具有影响,尽管其在体内的应用具有挑战性,这使其难以应用于临床。在这里,讨论了多种克服 siRNA 静脉内给药时遇到的细胞外和细胞内障碍的解决方案。此外,还强调了将 siRNA 与纳米粒子结合以实现长期释放并对抗 siRNA 的毒性问题的重要性。特别关注聚(乳酸-共-乙醇酸)(PLGA)纳米粒子在 mCRC 系统中 siRNA 传递的潜力。尽管由于技术困难,到目前为止使用较少,但总结了将 siRNA 成功包封到 PLGA 纳米载体中的多种策略。

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