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首页> 外文期刊>RSC Advances >Folate chitosan conjugated doxorubicin and pyropheophorbide acid nanoparticles (FCDP-NPs) for enhance photodynamic therapy
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Folate chitosan conjugated doxorubicin and pyropheophorbide acid nanoparticles (FCDP-NPs) for enhance photodynamic therapy

机译:叶酸壳聚糖共轭多柔比星和纤维黄酚酸纳米粒子(FCDP-NPS)增强光动力疗法

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摘要

We prepared new folate chitosan conjugated doxorubicin (DOX) and pyropheophorbide acid (PPa) nanoparticles (FCDP-NPs) using an ionic gelation method with tripolyphosphate (TPP) to enhance photodynamic therapy activity, based on the considerations of the long absorption wavelength (683 nm) of pyropheophorbide acid (PPa) in water and the excellent chemotherapeutic characteristics of doxorubicin (DOX) in cancer therapy. The obtained FCDP-NPs demonstrated a typical spherosome structure, a strong near infrared (NIR) absorption (705 nm) and significantly improved stability and dispersity in PBS (pH = 5, 7, 9); as well as a high singlet oxygen quantum yield (Phi(Delta) = 64%) compared to free PPa (Phi(Delta) = 59.1%). In addition, the in vitro cell experiments suggested that FCDP-NPs could be uptaken by HepG2 cells quickly and were mainly located in the cell nucleus. FCDP-NPs showed improved PDT efficiency over pure PPa and DOX at the same concentration after irradiation. Specifically, FCDP-NPs could lead to a 92% inhibition rate on HepG2 cells at 40 mu g mL(-1) (equal to 6 mu g mL(-1) DOX). However, the pure DOX showed little cytotoxicity at 6 mu g mL(-1), which suggests that a small amount of DOX could effectively enhance the PDT activities of PPa and lead to little "dark" cytotoxicity. Moreover, cell morphological changes after PDT treatment further indicated that FCDP-NPs could induce damage and apoptotic cell death efficiently. Finally, the photochemical mechanism of FCDP-NPs during PDT process was investigated by using specific quenching agents sodium azide (SA, a single oxygen quencher) and D-mannitol (DM, a hydroxyl radicals quencher), respectively. The results suggested that Type I and Type II photodynamic reactions can occur simultaneously, yet Type I reaction (the generation of hydroxyl radicals) might play a more important role. All these studies indicated that the FCDP-NPs could be potential nanoparticles in photodynamic cancer treatment.
机译:使用具有三聚磷酸盐(TPP)的离子凝胶化方法,制备新的叶酸壳聚糖缀合的多柔比星(DOX)和磷酸酰胺(PPA)纳米颗粒(FCDP-NPS),以增强光动力治疗活性,基于长吸收波长的考虑(683nm )在水中的纤维酰胺酸(PPA)和癌症治疗中的多柔比星(DOX)的优异化学治疗特征。所获得的FCDP-NPS证明了典型的球状结构,近红外(NIR)吸收(705nm)强并显着提高PBS的稳定性和分散性(pH = 5,7,9);除了游离PPA(PHI(DELTA)= 59.1%)相比,高分子氧量子产率(PHI(DELTA)= 64%)。此外,体外细胞实验表明,FCDP-NPS可以快速地被HepG2细胞膨胀,主要位于细胞核中。 FCDP-NPS在照射后,在纯PPA和DOX上显示出改善的PDT效率。具体地,FCDP-NPS可以在40μgmm(-1)(等于6μgml(-1)dox)上的Hepg2细胞上的92%抑制率。然而,纯DOX在6μgml(-1)时显示出少的细胞毒性,这表明少量DOX可以有效地增强PPA的PDT活性,并导致小“黑暗”细胞毒性。此外,PDT治疗后的细胞形态变化进一步表明FCDP-NPS可以有效地诱导损伤和凋亡细胞死亡。最后,通过使用特异性猝灭剂叠氮化物(SA,单氧猝灭剂)和D-甘露醇(DM,羟基自由基猝灭剂)来研究PDT过程中FCDP-NPS的光化学机理。结果表明,I型和II型光动力反应可以同时发生,但I型反应(羟基自由基的产生)可能发挥更重要的作用。所有这些研究表明FCDP-NPS可以是光动力癌症治疗中的潜在纳米颗粒。

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  • 来源
    《RSC Advances 》 |2017年第70期| 共12页
  • 作者单位

    Harbin Normal Univ Coll Chem &

    Chem Engn Key Lab Photochem Biomat &

    Energy Storage Mat Hei Harbin 150025 Heilongjiang Peoples R China;

    Key Lab Mol Cytogenet &

    Genet Breeding Heilongjia Harbin 150025 Heilongjiang Peoples R China;

    Harbin Normal Univ Coll Chem &

    Chem Engn Key Lab Photochem Biomat &

    Energy Storage Mat Hei Harbin 150025 Heilongjiang Peoples R China;

    Harbin Normal Univ Coll Chem &

    Chem Engn Key Lab Photochem Biomat &

    Energy Storage Mat Hei Harbin 150025 Heilongjiang Peoples R China;

    Harbin Normal Univ Coll Chem &

    Chem Engn Key Lab Photochem Biomat &

    Energy Storage Mat Hei Harbin 150025 Heilongjiang Peoples R China;

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  • 正文语种 eng
  • 中图分类 化学 ;
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