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杂化纳米颗粒作为一种用于癌细胞的高效卟啉递送系统以增强光动力疗法

Hybrid Nanoparticles as an Efficient Porphyrin Delivery System for Cancer Cells to Enhance Photodynamic Therapy.

作者信息

Silva Letícia B, Castro Kelly A D F, Botteon Caroline E A, Oliveira Cristiano L P, da Silva Roberto S, Marcato Priscyla D

机构信息

Department of Pharmaceutical Science, GNanoBio, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.

Department of Biomolecular Sciences, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.

出版信息

Front Bioeng Biotechnol. 2021 Sep 17;9:679128. doi: 10.3389/fbioe.2021.679128. eCollection 2021.

Abstract

Photodynamic therapy (PDT) is a potential non-invasive approach for application in oncological diseases, based on the activation of a photosensitizer (PS) by light at a specific wavelength in the presence of molecular oxygen to produce reactive oxygen species (ROS) that trigger the death tumor cells. In this context, porphyrins are interesting PS because they are robust, have high chemical, photo, thermal, and oxidative stability, and can generate singlet oxygen (O). However, porphyrins exhibit low solubility and a strong tendency to aggregate in a biological environment which limits their clinical application. To overcome these challenges, we developed hybrid nanostructures to immobilize 5,10,15,20-tetrakis[(4-carboxyphenyl) thio-2,3,5,6-tetrafluorophenyl] (), a new third-generation PS. The biological effect of this system was evaluated against bladder cancer (BC) cells with or without light exposition. The nanostructure composed of lipid carriers coated by porphyrin-chitosan (), presented a size of 130 nm and low polydispersity ( 0.25). The presence of the porphyrin-chitosan (-chitosan) on lipid nanoparticle surfaces increased the nanoparticle size, changed the zeta potential to positive, decreased the recrystallization index, and increased the thermal stability of nanoparticles. Furthermore, P-chitosan incorporation on nanoparticles increased the stability and enhanced the self-organization of the system and the formation of spherical structures, as observed by small-angle X-ray scattering (SAXS) analysis. Furthermore, the immobilization process maintained the photoactivity and improved the photophysical properties of PS, minimizing its aggregation in the cell culture medium. In the photoinduction assays, the displayed high phototoxicity with IC 3.2-folds lower than free porphyrin. This higher cytotoxic effect can be correlated to the high cellular uptake of porphyrin immobilized, as observed by confocal images. Moreover, the coated nanoparticles showed mucoadhesive properties interesting to its application . Therefore, the physical and chemical properties of nanoparticles may be relevant to improve the porphyrin photodynamic activity in BC cells.

摘要

光动力疗法(PDT)是一种潜在的非侵入性方法,可应用于肿瘤疾病,其原理是在分子氧存在的情况下,特定波长的光激活光敏剂(PS),产生活性氧(ROS),从而触发肿瘤细胞死亡。在这种情况下,卟啉是有趣的光敏剂,因为它们坚固耐用,具有高化学、光、热和氧化稳定性,并且可以产生单线态氧(O)。然而,卟啉在生物环境中表现出低溶解度和强烈的聚集倾向,这限制了它们的临床应用。为了克服这些挑战,我们开发了混合纳米结构来固定5,10,15,20-四[(4-羧基苯基)硫代-2,3,5,6-四氟苯基](),一种新型第三代光敏剂。在有或没有光照的情况下,评估了该系统对膀胱癌细胞(BC)的生物学效应。由卟啉-壳聚糖()包被的脂质载体组成的纳米结构,尺寸为130nm,多分散性低(0.25)。脂质纳米颗粒表面卟啉-壳聚糖(-壳聚糖)的存在增加了纳米颗粒的尺寸,将zeta电位变为正值,降低了重结晶指数,并提高了纳米颗粒的热稳定性。此外,通过小角X射线散射(SAXS)分析观察到,纳米颗粒上卟啉-壳聚糖的掺入增加了系统的稳定性,增强了系统的自组装以及球形结构的形成。此外,固定过程保持了光敏剂的光活性并改善了其光物理性质,使其在细胞培养基中的聚集最小化。在光诱导试验中,显示出高光毒性,其IC比游离卟啉低3.2倍。如共聚焦图像所示,这种更高的细胞毒性作用可能与固定化卟啉的高细胞摄取有关。此外,包被的纳米颗粒显示出对其应用有趣的粘膜粘附特性。因此,纳米颗粒的物理和化学性质可能与提高卟啉在膀胱癌细胞中的光动力活性有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0128/8484888/05e950d16831/fbioe-09-679128-g001.jpg

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