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1.武汉工程大学材料科学与工程学院 武汉 430205
2.生物医用高分子材料教育部重点实验室 武汉大学化学与分子科学学院 武汉 430072
Published:2018-6,
Received:25 December 2017,
Revised:6 February 2018,
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Chang Liu, Yu-xin Chen, Jiang-fan Wang, Xuan Luo, Yu-di Huang, Jin-lei Xu, Guo-ping Yan, Si Chen, Xian-zheng Zhang. A Multi-functional Drug Delivery System Based on Dendritic Peptide for Tumor Nuclear Accurate Targeting Therapy. [J]. Acta Polymerica Sinica 0(6):682-691(2018)
Chang Liu, Yu-xin Chen, Jiang-fan Wang, Xuan Luo, Yu-di Huang, Jin-lei Xu, Guo-ping Yan, Si Chen, Xian-zheng Zhang. A Multi-functional Drug Delivery System Based on Dendritic Peptide for Tumor Nuclear Accurate Targeting Therapy. [J]. Acta Polymerica Sinica 0(6):682-691(2018) DOI: 10.11777/j.issn1000-3304.2017.17335.
为了改善在肿瘤治疗过程中,药物载体靶向性差和药物靶点定位效率低等不足,设计了一种能精准靶向肿瘤细胞核,将药物高效递送至作用靶点的多功能纳米载药体系. 利用具有细胞核定位能力的两亲性枝化多肽包载化疗药物阿霉素(DOX)形成载药纳米胶束DD,并通过静电作用将具有肿瘤靶向功能的透明质酸(HA)包覆在DD表面,得到具有靶向肿瘤细胞核能力的纳米药物HDD. HA的存在赋予了HDD对肿瘤的靶向功能和电荷屏蔽能力,可增加体系的稳定性,延长其血液循环时间,降低正常组织和细胞对HDD的非特异性摄取,实现其在肿瘤部位的特异性富集和肿瘤细胞的高效摄取. 进入肿瘤细胞后,HA层的降解有利于纳米胶束DD在多肽的核定位作用下精准、快速地将DOX递送至细胞核,最终实现高效的肿瘤抑制效果.
Though chemotherapeutics has been one of the most widely used treatments for tumor therapy
it is still heavily limited due to its poor pharmacokinetics
undesirable intracellular uptake and inevitable side effects. In order to overcome these barriers
various functional groups have been introduced in drug delivery system to enhance the therapeutic efficiency of chemotherapy. In this study
a novel drug delivery system for tumor nuclear accurate targeting was designed in order to achieve precise tumor nuclear treatment. The chemotherapeutic drug (doxorubicin
DOX) was encapsulated in amphiphilic dendritic peptide with nuclear localization function to form a regular nanoparticle DD. After that
electronegative hyaluronic acid (HA) with ability of tumor targeting was coated on the surface of nanoparticle DD
via
electrostatic interaction to form tumor nuclear targeting drug delivery system HDD. The presence of HA endowed HDD with the tumor targeting ability and charge shielding effect
which could increase the stability of nanodrug
promote the specific internalization by tumor cells and reduce the non-specific uptake by normal tissue/cells. Furthermore
it was found that the drug delivery system HDD could realize the facile internalization by tumor cells
via
CD44 receptor-mediated recognition. After the degradation of HA shell by hyaluronidase (HAase) in endosome
the nuclear targeted nanodrug DD was exposed
and DOX was carried to the region of nuclear accurately by inheriting the ability from nuclear-targeted peptide. The precise targeting of drug to nuclei could be beneficial to the improvement of drug utilization as well as the suppression of tumor cells. The characteristics of this tumor nuclear accurate targeting drug delivery system
including particle sizes
zeta potential
drug loading capacity
drug release behavior
cellular uptake and antitumor efficacy
were evaluated. All of the studies confirmed that the precise tumor nuclear targeting drug delivery system HDD displayed prominent antitumor efficacy with insignificant adverse effects to normal cells
in vitro
which indicated that the precise tumor nuclear targeting delivery system supplies a useful strategy for tumor therapy.
枝化多肽纳米药物肿瘤靶向核定位精准治疗
Dendritic peptideNanodrugTumor-targetingNuclear localizationPrecise treatment
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