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基于生物可降解聚合物的纳米诊疗一体化的简易制备:疏水性光敏剂的递药、荧光成像和光动力治疗。

Facile development of biodegradable polymer-based nanotheranostics: Hydrophobic photosensitizers delivery, fluorescence imaging and photodynamic therapy.

机构信息

Department of Pharmaceutical Technology (Biotechnology), National Institute of Pharmaceutical Education and Research (NIPER), Sector-67, S.A.S. Nagar, 160062, Punjab, India.

Centre for Pharmaceutical Nanotechnology, Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research (NIPER), Sector-67, S.A.S. Nagar, 160062, Punjab, India.

出版信息

J Photochem Photobiol B. 2019 Apr;193:39-50. doi: 10.1016/j.jphotobiol.2019.02.007. Epub 2019 Feb 21.

Abstract

Photodynamic therapy (PDT) is reported to be a promising technique to eradicate various cancers. As most of the photosensitizers (PSs) are hydrophobic in nature, thus, the effective delivery of PSs at the targeted site is the main hurdle associated with PDT. Zinc phthalocyanine and Zinc naphthalocyanine are reported as good PSs, however, highly hydrophobic characteristics restrict their use for clinical applications. To circumvent this limitation here we developed the advanced polymer-based nano-delivery system having polyethylene glycol (PEG) coated polymeric core with ~90% PS encapsulation. The PEG coating was responsible for the stabilization of probe in the physiological environment and storage conditions. The developed theranostic probes showed efficient in vitro fluorescence and singlet oxygen quantum yields upon irradiation with 620-750 nm (30 mW/cm) light. The clathrin-mediated endocytosis (CME) based mechanism of cellular internalization was evaluated. The fluorescence of treated MCF-7 cells showed the ability of the probes as imaging agents. Moreover, up to 65% cell inhibition showed their cytotoxic efficiency. Further, comparatively higher tumor-accumulation of PSs without significant hepato/nephro-toxicity shown in vivo experimentation using breast tumor-bearing female Sprague Dawley (SD) rats suggested the featured passive targeting ability of preparations and clinically safe to be used. The study explored the exceptional delivery system for hydrophobic PSs with commendable theranostic applications.

摘要

光动力疗法(PDT)被报道为一种有前途的技术,可以消灭各种癌症。由于大多数光敏剂(PSs)本质上是疏水的,因此,将 PSs 有效递送到靶向部位是与 PDT 相关的主要障碍。锌酞菁和锌萘酞菁被报道为良好的 PSs,然而,其高度疏水的特性限制了它们在临床应用中的使用。为了克服这一限制,我们开发了先进的聚合物基纳米递药系统,该系统具有聚乙二醇(PEG)涂覆的聚合物核,可包裹约 90%的 PS。PEG 涂层负责在生理环境和储存条件下稳定探针。所开发的治疗探针在 620-750nm(30mW/cm)光照射下表现出高效的体外荧光和单线态氧量子产率。评估了基于网格蛋白介导的内吞作用(CME)的细胞内化机制。用处理过的 MCF-7 细胞的荧光显示了探针作为成像剂的能力。此外,高达 65%的细胞抑制表明了它们的细胞毒性效率。进一步,在使用乳腺癌荷瘤雌性 Sprague Dawley(SD)大鼠进行的体内实验中,没有明显的肝/肾毒性,观察到 PSs 的肿瘤积累较高,表明制剂具有独特的被动靶向能力,临床使用安全。该研究探索了用于疏水 PSs 的特殊递药系统,具有值得称赞的治疗应用。

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