Amantino Camila F, de Baptista-Neto Álvaro, Badino Alberto C, Siqueira-Moura Marigilson P, Tedesco Antonio C, Primo Fernando L
Department of Engineering of Bioprocess and Biotechnology, School of Pharmaceutical Sciences, São Paulo State University - UNESP, Araraquara, 14800-903, São Paulo, Brazil.
Graduate Program of Chemical Engineering, Federal University of São Carlos, São Carlos, 13565-905, São Paulo, Brazil.
Photodiagnosis Photodyn Ther. 2020 Sep;31:101815. doi: 10.1016/j.pdpdt.2020.101815. Epub 2020 May 12.
Photodynamic therapy has been applied for the treatment of many diseases, especially skin diseases. However, poor aqueous solubility and toxicity of some photosensitizer drugs are the main disadvantages for their direct clinical applications. Thus, biotechnology and nanotechnology are important tools in the development of new ways of obtaining photoactive compounds that are biocompatible. We investigated the potential of a new nanostructured photosensitizer, an anthraquinone derivative produced by biotechnological process; then we associated nanotechnology to obtain a nanostructured anthraquinone active molecule. For this, it was prepared a classical nanocapsule formulations containing poly(lactide-co-glycolide) (PLGA) coating for encapsulation of anthraquinone derivative. These formulations were characterized by their physicochemical, morphological, photophysical properties, and stability. We performed in vitro biocompatibility and photodynamic activity assays of free and nanostructured anthraquinone. Nanocapsule formulations containing anthraquinone derivative showed a nanometric profile with particle size around 250 nm, negative zeta potential around -30 mV, and partially monodisperse. Besides that, characteristic spherical morphology of nanocapsules and homogeneous particle surface were observed by AFM analyses. The in vitro biocompatibility assay showed absence of cytotoxicity for all tested RD/NC concentrations and also for unloaded/NC in NIH3T3 cells. In vitro photoactivation assay using NIH3T3 cells showed that nanocapsules promoted greater drug uptake by NIH3T3 cells, around of 87%, of cell death compared to free drug showed around 48% of cell death. The anthraquinone derivative showed potential for use in PDT. Besides the association with nanocapsules improved cell uptake of photosensitizer resulting in increased cell death compared to free anthraquinone.
光动力疗法已被应用于多种疾病的治疗,尤其是皮肤病。然而,一些光敏剂药物的水溶性差和毒性是其直接临床应用的主要缺点。因此,生物技术和纳米技术是开发具有生物相容性的光活性化合物新方法的重要工具。我们研究了一种新型纳米结构光敏剂的潜力,该光敏剂是一种通过生物技术过程生产的蒽醌衍生物;然后我们结合纳米技术获得了一种纳米结构的蒽醌活性分子。为此,制备了含有聚(丙交酯-乙交酯)(PLGA)涂层的经典纳米胶囊制剂,用于包裹蒽醌衍生物。这些制剂通过其物理化学、形态、光物理性质和稳定性进行了表征。我们对游离和纳米结构的蒽醌进行了体外生物相容性和光动力活性测定。含有蒽醌衍生物的纳米胶囊制剂呈现纳米级特征,粒径约为250 nm,zeta电位约为-30 mV,且部分呈单分散性。除此之外,通过原子力显微镜分析观察到纳米胶囊具有特征性的球形形态和均匀的颗粒表面。体外生物相容性测定表明,所有测试的RD/NC浓度以及NIH3T3细胞中未负载的/NC均无细胞毒性。使用NIH3T3细胞进行的体外光活化测定表明,与游离药物相比,纳米胶囊促进NIH3T3细胞摄取更多药物,细胞死亡率约为87%,而游离药物的细胞死亡率约为48%。蒽醌衍生物显示出用于光动力疗法的潜力。此外,与纳米胶囊结合可提高光敏剂的细胞摄取,与游离蒽醌相比,导致细胞死亡增加。