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通过将光敏剂和荧光团后加载到聚丙烯酰胺纳米颗粒上来开发用于荧光成像和光动力治疗的多功能纳米平台。

Multifunctional nanoplatforms for fluorescence imaging and photodynamic therapy developed by post-loading photosensitizer and fluorophore to polyacrylamide nanoparticles.

机构信息

PDT Center, Buffalo, New York 14263, USA.

出版信息

Nanomedicine. 2012 Aug;8(6):941-50. doi: 10.1016/j.nano.2011.11.011. Epub 2011 Nov 22.

DOI:10.1016/j.nano.2011.11.011
PMID:22115602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3516373/
Abstract

We report a novel post-loading approach for constructing a multifunctional biodegradable polyacrylamide (PAA) nanoplatform for tumor-imaging (fluorescence) and photodynamic therapy (PDT). This approach provides an opportunity to post-load the imaging and therapeutic agents at desired concentrations. Among the PAA nanoparticles, a formulation containing the photosensitizer, HPPH [3-(1'-hexyloxyethyl)pyropheophorbide-a], and the cyanine dye in a ratio of 2:1 minimized the undesirable quenching of the HPPH electronic excitation energy because of energy migration within the nanoparticles and/or Förster (fluorescence) resonance energy transfer (FRET) between HPPH and cyanine dye. An excellent tumor-imaging (NIR fluorescence) and phototherapeutic efficacy of the nanoconstruct formulation is demonstrated. Under similar treatment parameters the HPPH in 1% Tween 80/5% aqueous dextrose formulation was less effective than the nanoconstruct containing HPPH and cyanine dye in a ratio of 2 to 1. This is the first example showing the use of the post-loading approach in developing a nanoconstructs for tumor-imaging and therapy.

摘要

我们报告了一种构建多功能可生物降解聚丙烯酰胺(PAA)纳米平台的新型后加载方法,用于肿瘤成像(荧光)和光动力治疗(PDT)。这种方法提供了在所需浓度下后加载成像和治疗剂的机会。在 PAA 纳米颗粒中,含有光敏剂 HPPH [3-(1'-己氧基乙基)焦脱镁叶绿酸-a]和花菁染料的配方以 2:1 的比例最小化了 HPPH 电子激发能的不利猝灭,因为能量在纳米颗粒内迁移和/或 HPPH 和花菁染料之间的Förster(荧光)共振能量转移(FRET)。证明了纳米结构制剂具有优异的肿瘤成像(近红外荧光)和光疗功效。在相似的治疗参数下,1%吐温 80/5%水性葡萄糖配方中的 HPPH 不如含有 HPPH 和花菁染料比例为 2:1 的纳米结构制剂有效。这是第一个证明后加载方法在开发用于肿瘤成像和治疗的纳米结构中的应用的例子。

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