Preparation of coffee oil-algae oil-based nanoemulsions and the study of their inhibition effect on UVA-induced skin damage in mice and melanoma cell growth

Int J Nanomedicine. 2017 Sep 5:12:6559-6580. doi: 10.2147/IJN.S144705. eCollection 2017.

Abstract

Coffee grounds, a waste by-product generated after making coffee, contains approximately 15% coffee oil which can be used as a raw material in cosmetics. Algae oil rich in docosahexaenoic acid (DHA) has been demonstrated to possess anticancer and anti-inflammation functions. The objectives of this study were to develop a gas chromatography-mass spectrometry (GC-MS) method for the determination of fatty acids in coffee oil and algae oil and prepare a nanoemulsion for studying its inhibition effect on ultraviolet A-induced skin damage in mice and growth of melanoma cells B16-F10. A total of 8 and 5 fatty acids were separated and quantified in coffee oil and algae oil by GC-MS, respectively, with linoleic acid (39.8%) dominating in the former and DHA (33.9%) in the latter. A nanoemulsion with a particle size of 30 nm, zeta potential -72.72 mV, and DHA encapsulation efficiency 100% was prepared by using coffee oil, algae oil, surfactant (20% Span 80 and 80% Tween 80), and deionized water. Differential scanning calorimetry (DSC) analysis revealed a high stability of nanoemulsion when heated up to 110°C at a pH 6, whereas no significant changes in particle size distribution and pH occurred over a 90-day storage period at 4°C. Animal experiments showed that a dose of 0.1% coffee oil-algae oil nanoemulsion was effective in mitigating trans-epidermal water loss, skin erythema, melanin formation, and subcutaneous blood flow. Cytotoxicity test implied effective inhibition of melanoma cell growth by nanoemulsion with an IC50 value of 26.5 µg/mL and the cell cycle arrested at G2/M phase. A dose-dependent upregulation of p53, p21, cyclin B, and cyclin A expressions and downregulation of CDK1 and CDK2 occurred. Also, both Bax and cytochrome c expressions were upregulated and bcl-2 expression downregulated, accompanied by a rise in caspase-3, caspase-8, and caspase-9 activities for apoptosis execution. Collectively, the apoptosis pathway of melanoma cells B16-F10 may involve both mitochondria and death receptor.

Keywords: DHA; GC-MS; coffee ground; coffee oil-algae oil nanoemulsion; melanoma cell apoptosis; mouse skin protection.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Caspases / metabolism
  • Cell Cycle / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Coffee / chemistry*
  • Docosahexaenoic Acids / pharmacology
  • Emulsions / chemistry*
  • Emulsions / pharmacology
  • Fatty Acids / analysis
  • Gas Chromatography-Mass Spectrometry
  • Humans
  • Melanoma / drug therapy
  • Melanoma / metabolism
  • Mice, Inbred BALB C
  • Mitochondria / metabolism
  • Nanostructures / chemistry*
  • Plant Oils / chemistry
  • Plant Oils / pharmacology*
  • Skin / drug effects*
  • Skin / radiation effects
  • Sunscreening Agents / chemistry
  • Sunscreening Agents / pharmacology
  • Ultraviolet Rays / adverse effects

Substances

  • Coffee
  • Emulsions
  • Fatty Acids
  • Plant Oils
  • Sunscreening Agents
  • Docosahexaenoic Acids
  • Caspases