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基于阿仑膦酸钠聚乙二醇偶联壳聚糖的靶向纳米粒用于递送 siRNA 和姜黄素治疗骨转移乳腺癌的应用。

Targeted Nanoparticles Based on Alendronate Polyethylene Glycol Conjugated Chitosan for the Delivery of siRNA and Curcumin for Bone Metastasized Breast Cancer Applications.

机构信息

School of Chemistry and Molecular Biosciences, The University of Queensland, Cooper Road, Brisbane, Queensland, 4072, Australia.

Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Corner of College and Cooper Road, Brisbane, Queensland, 4072, Australia.

出版信息

Macromol Biosci. 2024 Feb;24(2):e2300268. doi: 10.1002/mabi.202300268. Epub 2023 Oct 15.

Abstract

Bone metastasized breast cancer reduces the quality of life and median survival. Targeted delivery of small interfering RNA (siRNA) and chemotherapeutic drugs using nanoparticles (NPs) is a promising strategy to overcome current limitations in treating these metastatic breast cancers. This research develops alendronate conjugated polyethylene glycol functionalized chitosan (ALD-PEG-CHI) NP for the delivery of cell death siRNA (CD-siRNA) and curcumin (CUR) and explores its targeting ability and in vitro cell cytotoxicity. Polyethylene glycol functionalized CHI (mPEG-CHI) NPs serve as control. The size of CD-siRNA loaded NPs is below 100 nm while CUR loaded NPs is below 200 nm, with near neutral zeta potential for all NPs. The CUR encapsulation efficiency (EE) is 70% and 88% for targeted and control NPs, respectively, while complete encapsulation of CD-siRNA is achieved in both NP systems. The bone targeting ability of CY5-dsDNA loaded ALD-PEG-CHI NPs using hydroxyapatite discs is fivefold compared to control indicating ALD presentation at the targeting NP surface. Delivery of CD-siRNA loaded NPs and CUR loaded NPs show synergistic and additive growth inhibition effects against MCF-7 cells by mPEG-CHI and ALD-PEG-CHI NPs, respectively. Overall, these in vitro results illustrate the potential of the targeted NPs as an effective therapeutic system toward bone metastasized breast cancer.

摘要

骨转移乳腺癌降低了生活质量和中位生存期。使用纳米粒子(NPs)靶向递送小干扰 RNA(siRNA)和化疗药物是克服治疗这些转移性乳腺癌当前局限性的一种很有前途的策略。本研究开发了阿仑膦酸钠偶联聚乙二醇功能化壳聚糖(ALD-PEG-CHI)NP,用于递送电死亡 siRNA(CD-siRNA)和姜黄素(CUR),并探讨了其靶向能力和体外细胞细胞毒性。聚乙二醇功能化 CHI(mPEG-CHI)NP 用作对照。载有 CD-siRNA 的 NP 的粒径小于 100nm,而载有 CUR 的 NP 的粒径小于 200nm,所有 NP 的 Zeta 电位均接近中性。靶向和对照 NP 中 CUR 的包封效率(EE)分别为 70%和 88%,而在两种 NP 系统中均实现了 CD-siRNA 的完全包封。使用羟磷灰石盘的 CY5-dsDNA 负载的 ALD-PEG-CHI NP 的骨靶向能力比对照 NP 高五倍,表明在靶向 NP 表面呈现 ALD。载有 CD-siRNA 的 NP 和载有 CUR 的 NP 的递送均显示出针对 MCF-7 细胞的协同和相加生长抑制作用,分别通过 mPEG-CHI 和 ALD-PEG-CHI NP。总的来说,这些体外结果表明,靶向 NP 作为针对骨转移乳腺癌的有效治疗系统具有潜力。

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