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Theranostic Properties of Crystalline Aluminum Phthalocyanine Nanoparticles as a Photosensitizer.
Makarov, Vladimir I; Pominova, Daria V; Ryabova, Anastasiya V; Romanishkin, Igor D; Voitova, Arina V; Steiner, Rudolf W; Loschenov, Victor B.
Afiliação
  • Makarov VI; Prokhorov General Physics Institute, Russian Academy of Sciences, Moscow 119991, Russia.
  • Pominova DV; Department of Laser Micro-, Nano- and Biotechnologies, National Research Nuclear University MEPhI, Moscow 115409, Russia.
  • Ryabova AV; Prokhorov General Physics Institute, Russian Academy of Sciences, Moscow 119991, Russia.
  • Romanishkin ID; Department of Laser Micro-, Nano- and Biotechnologies, National Research Nuclear University MEPhI, Moscow 115409, Russia.
  • Voitova AV; Prokhorov General Physics Institute, Russian Academy of Sciences, Moscow 119991, Russia.
  • Steiner RW; Department of Laser Micro-, Nano- and Biotechnologies, National Research Nuclear University MEPhI, Moscow 115409, Russia.
  • Loschenov VB; Prokhorov General Physics Institute, Russian Academy of Sciences, Moscow 119991, Russia.
Pharmaceutics ; 14(10)2022 Oct 06.
Article em En | MEDLINE | ID: mdl-36297557
ABSTRACT
The study of phthalocyanines, known photosensitizers, for biomedical applications has been of high research interest for several decades. Of specific interest, nanophotosensitizers are crystalline aluminum phthalocyanine nanoparticles (AlPc NPs). In crystalline form, they are water-insoluble and atoxic, but upon contact with tumors, immune cells, or pathogenic microflora, they change their spectroscopic properties (acquire the ability to fluoresce and become phototoxic), which makes them upcoming agents for selective phototheranostics. Aqueous colloids of crystalline AlPc NPs with a hydrodynamic size of 104 ± 54 nm were obtained using ultrasonic dispersal and centrifugation. Intracellular accumulation and localization of AlPc were studied on HeLa and THP-1 cell cultures and macrophages (M0, M1, M2) by fluorescence microscopy. Crystallinity was assessed by XRD spectroscopy. Time-resolved spectroscopy was used to obtain characteristic fluorescence kinetics of AlPc NPs upon interaction with cell cultures. The photodynamic efficiency and fluorescence quantum yield of AlPc NPs in HeLa and THP-1 cells were evaluated. After entering the cells, AlPc NPs localized in lysosomes and fluorescence corresponding to individual AlPc molecules were observed, as well as destruction of lysosomes and a rapid decrease in fluorescence intensity during photodynamic action. The photodynamic efficiency of AlPc NPs in THP-1 cells was almost 1.8-fold that of the molecular form of AlPc (Photosens). A new mechanism for the occurrence of fluorescence and phototoxicity of AlPc NPs in interaction with cells is proposed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article