Organic Synthesis Laboratory, Research and Development Institute - IPD, Vale do Paraíba University, Av. Shishima Hifumi 2911, CEP 12244-000, São José dos Campos, Brazil.
Department of Chemistry, Center of Nanotechnology and Tissue Engineering Photobiology and Photomedicine Research Group, Faculty of Philosophy, Sciences and Letters of Ribeirão Preto, Av. dos Bandeirantes 3900, 14040-901, Vila Monte Alegre, University of São Paulo, Brazil.
Photodiagnosis Photodyn Ther. 2018 Jun;22:169-177. doi: 10.1016/j.pdpdt.2018.04.011. Epub 2018 Apr 20.
Microcapsules fabricated using layer-by-layer self-assembly have unique properties, making them attractive for drug delivery applications. The technique has been improved, allowing the deposition of multiple layers of oppositely charged polyelectrolytes on spherical, colloidal templates. These templates can be decomposed by coating multiple layers, resulting in hollow shells. In this paper, we describe a novel drug delivery system for loading photosensitizer drugs into hollow multilayered microcapsules for photoprocess applications.
Manganese carbonate particles were prepared by mixing NHHCO and MnSO and performing consecutive polyelectrolyte adsorption processes onto these templates using poly-(sodium 4-styrene sulfonate) and poly-(allylamine hydrocholoride). A photosensitizer was also incorporated into the layers. Hollow spheres were fabricated by removing the cores in the acidic solution. The hollow, multilayered microcapsules were studied by scanning electron microscopy, steady-state, and time-resolved techniques. Their biological activity was evaluated in vitro with cancer cells using a conventional MTT assay.
The synthesized CaCO microparticles were uniform, non-aggregated, and highly porous spheres. The phthalocyanine derivatives loaded in the microcapsules maintained their photophysical behaviour after encapsulation. The spectroscopic results presented here showed excellent photophysical behaviour of the studied drug. We observed a desirable increase in singlet oxygen production, which is favourable for the PDT protocol. Cell viability after treatment was determined and the proposed microcapsules caused 80% cell death compared to the control.
The results demonstrate that photosensitizer adsorption into the CaCO microparticle voids together with the layer-by-layer assembly of biopolymers provide a method for the fabrication of biocompatible microcapsules for use as biomaterials.
使用层层自组装技术制造的微胶囊具有独特的性质,使其成为药物输送应用的理想选择。该技术得到了改进,允许在球形胶体模板上沉积多层带相反电荷的聚电解质。通过涂层的多层分解这些模板,得到中空壳。在本文中,我们描述了一种新型药物输送系统,用于将光敏剂药物载入中空多层微胶囊中,用于光处理应用。
通过混合 NHHCO 和 MnSO 并使用聚(对苯乙烯磺酸钠)和聚(盐酸烯丙胺)在这些模板上进行连续的聚电解质吸附过程,制备碳酸锰颗粒。也将一种光敏剂掺入层中。通过在酸性溶液中去除核心来制造中空球体。通过扫描电子显微镜、稳态和时间分辨技术研究中空、多层微胶囊。使用传统的 MTT 测定法在体外用癌细胞评估其生物活性。
合成的 CaCO 微球均匀、不聚集、高度多孔。封装后,负载在微胶囊中的酞菁衍生物保持其光物理行为。这里呈现的光谱结果显示了研究药物的出色光物理行为。我们观察到单线态氧产生的理想增加,这有利于 PDT 方案。通过处理后确定细胞活力,与对照相比,所提出的微胶囊导致 80%的细胞死亡。
结果表明,将光敏剂吸附到 CaCO 微球空隙中与生物聚合物的层层组装一起提供了一种制造用于生物材料的生物相容微胶囊的方法。