4.7 Article

Development of New Natural Lipid-Based Nanoparticles Loaded with Aluminum-Phthalocyanine for Photodynamic Therapy against Melanoma

Journal

NANOMATERIALS
Volume 12, Issue 20, Pages -

Publisher

MDPI
DOI: 10.3390/nano12203547

Keywords

third-generation photosensitizers; drug delivery systems; cancer; photodynamic therapy; Amazon butters

Funding

  1. National Council for Scientific and Technological Development-CNPq [40356/2021, 401957/2016-0, 302355/2016-2]
  2. Coordination for the Improvement of Higher Level Personnel-CAPES [0001]
  3. Financier of Studies and Projects-FINEP [01.08.0457.00]
  4. Federal District Research Support Foundation-FAPDF [00193.00000920/2020-23, 00193.00001053/2021-24]
  5. Sao Paulo Research Foundation [19/23638-7, 19/10261-2]
  6. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [19/23638-7, 19/10261-2] Funding Source: FAPESP

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Photodynamic therapy using solid lipid nanoparticles loaded with photosensitizers is an effective treatment against skin cancers. A new photosensitizing system, SLN-AlPc, based on Amazon butter, exhibited strong in vitro photodynamic activity on melanoma cells.
Photodynamic therapy (PDT) mediated by photosensitizers loaded in nanostructures as solid lipid nanoparticles has been pinpointed as an effective and safe treatment against different skin cancers. Amazon butters have an interesting lipid composition when it comes to forming solid lipid nanoparticles (SLN). In the present report, a new third-generation photosensitizing system consisting of aluminum-phthalocyanine associated with Amazon butter-based solid lipid nanoparticles (SLN-AlPc) is described. The SLN was developed using murumuru butter, and a monodisperse population of nanodroplets with a hydrodynamic diameter of approximately 40 nm was obtained. The study of the permeation of these AlPc did not permeate the analyzed skin, but when incorporated into the system, SLN-AlPc allowed permeation of almost 100% with 8 h of contact. It must be emphasized that SLN-AlPc was efficient for carrying aluminum-phthalocyanine photosensitizers and exhibited no toxicity in the dark. Photoactivated SLN-AlPc exhibited a 50% cytotoxicity concentration (IC50) of 19.62 nM when applied to B16-F10 monolayers, and the type of death caused by the treatment was apoptosis. The exposed phospholipid phosphatidylserine was identified, and the treatment triggered a high expression of Caspase 3. A stable Amazon butter-based SLN-AlPc formulation was developed, which exhibits strong in vitro photodynamic activity on melanoma cells.

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