In vitro assessment of anti-tumorigenic mechanisms and efficacy of NanoALA, a nanoformulation of aminolevulic acid designed for photodynamic therapy of cancer
Autor: | Antonio Claudio Tedesco, Laise Rodrigues de Andrade, Zulmira G. M. Lacava, Fernando Lucas Primo, Jaqueline Rodrigues da Silva |
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Přispěvatelé: | Center of Nanoscience and Nanobiotechnology, Universidade Estadual Paulista (Unesp), Universidade de São Paulo (USP) |
Rok vydání: | 2017 |
Předmět: |
Programmed cell death
Cell Survival Photodynamic therapy (PDT) medicine.medical_treatment Biophysics Apoptosis Photodynamic therapy 02 engineering and technology Dermatology Pharmacology Nanocapsules Mice 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Polylactic Acid-Polyglycolic Acid Copolymer Cell Line Tumor medicine Animals Pharmacology (medical) Lactic Acid Poly(lactide-co-glycolide) (PLGA) Cytotoxicity Membrane Potential Mitochondrial Photosensitizing Agents Cell Death Aminolevulinic Acid Prodrug Aminolevulic-acid (ALA) 021001 nanoscience & nanotechnology PLGA Photochemotherapy Mammary carcinoma Oncology chemistry 030220 oncology & carcinogenesis Female Nanocarriers Reactive Oxygen Species 0210 nano-technology Polyglycolic Acid |
Zdroj: | Scopus Repositório Institucional da UNESP Universidade Estadual Paulista (UNESP) instacron:UNESP |
ISSN: | 1572-1000 |
DOI: | 10.1016/j.pdpdt.2017.08.011 |
Popis: | Made available in DSpace on 2018-12-11T16:49:15Z (GMT). No. of bitstreams: 0 Previous issue date: 2017-12-01 Instituto Nacional de Ciência e Tecnologia de Doenças Tropicais Background The development of nanocarriers is an important approach to increase the bioavailability of hydrophilic drugs in target cells. In this work, we evaluated the anti-tumorigenic mechanisms and efficacy of NanoALA, a novel nanoformulation of aminolevulic acid (ALA) based on poly(lactide-co-glycolide) (PLGA) nanocapsules designed for anticancer photodynamic therapy (PDT). Methods For this purpose, physicochemical characterization, prodrug incorporation kinetics, biocompatibility and photocytotoxicity tests, analysis of the cell death type and mitochondrial function, measurement of the intracellular reactive oxygen species production and DNA fragmentation were performed in murine mammary carcinoma (4T1) cells. Results NanoALA formulation, stable over a period of 90 days following synthesis, presented hydrodynamic diameter of 220 ± 8.7 nm, zeta potential of −30.6 mV and low value of polydispersity index (0.28). The biological assays indicated that the nanostructured product promotes greater ALA uptake by 4T1 cells and consequently more cytotoxicity in the PDT process. For the first time in the scientific literature, there is a therapeutic efficacy report of approximately 80%, after only 1 h of incubation with 100 μg mL−1 prodrug (0.6 mM ALA equivalent). The mitochondria are probably the initial target of treatment, culminating in energy metabolism disorders and cell death by apoptosis. Conclusions NanoALA emerges as a promising strategy for anticancer PDT. Besides being effective against a highly aggressive tumor cell line, the treatment may be economically advantageous because it allows a reduction in the dose and frequency of application compared to free ALA. University of Brasília Institute of Biological Sciences Center of Nanoscience and Nanobiotechnology São Paulo State University (UNESP) School of Pharmaceutical Sciences Department of Chemistry Center of Nanotechnology and Tissue Engineering – Photobiology and Photomedicine Research Group Faculty of Philosophy Sciences and Letters of Ribeirão Preto University of São Paulo São Paulo State University (UNESP) School of Pharmaceutical Sciences |
Databáze: | OpenAIRE |
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