Cosmetic potential of Ganoderma lucidum (Reishi) extract in a topical cream formulation.
Reishi extract shows promising antioxidant and safety profiles compared to argireline peptide and α-arbutin, but further research in human trials is needed to confirm its efficacy in cosmetic applications.
Where it sits
this study against the rest of the argireline corpusSummary and findings
This study investigated the biological activities of freeze-dried Ganoderma lucidum (Reishi) extract and compared its properties to argireline peptide and α-arbutin. The research also developed a topical cream formulation containing Reishi extract and assessed its microbiological safety and stability. The findings suggest Reishi extract has potential as a cosmetic ingredient, but no therapeutic claims are made.
Abstract
<h4>Objective</h4>The primary objective of this study was to investigate the biological activities of freeze-dried Ganoderma lucidum (Reishi) extract obtained from hazelnut pruning waste and to compare its antioxidant, tyrosinase inhibitory and cytotoxic properties with two widely used cosmetic actives-argireline peptide and α-arbutin. Additionally, the study aimed to develop a topical cream formulation containing Reishi extract and to assess its microbiological safety, preservative efficacy and physicochemical stability under controlled environmental conditions. By integrating bioactivity evaluation with formulation performance, the research sought to determine the potential applicability of Reishi extract as a natural and multifunctional cosmetic ingredient suitable for anti-aging and skin-brightening applications.<h4>Methods</h4>The antioxidant capacity of Reishi extract, argireline peptide and α-arbutin was determined using a copper(II)-based total antioxidant capacity assay. Tyrosinase inhibitory activity was measured with human tyrosinase sourced from MNT-1 melanoma cells, while cytotoxicity and safe dose limits were determined in HaCaT human keratinocyte cells via the AlamarBlue® method. A topical cream formulation was prepared using a multi-phase emulsification technique and characterized physicochemically. Microbiological safety was assessed according to Turkish Cosmetic Regulations, and preservative efficacy was determined through challenge testing. Stability assessments included temperature cycling, long-term storage at different temperatures and centrifugation tests, monitoring visual, physicochemical and microbiological parameters over a three-month period.<h4>Results</h4>Reishi extract demonstrated 861 μmol TE/g antioxidant activity, 30% tyrosinase inhibition and a broader safety margin compared with argireline peptide and α-arbutin, which exhibited cytotoxicity at lower concentrations. The formulated cream retained a skin-compatible pH and stable viscosity, while showing no signs of phase separation, colour change or integrity loss under all storage conditions. Microbiological analysis confirmed microbial counts below regulatory limits, and challenge testing revealed rapid log reductions in all tested microorganisms, satisfying the acceptance criteria for preservative efficacy. Stability studies supported the physical robustness and microbiological safety of the final product throughout the evaluation period.<h4>Conclusion</h4>Overall, the findings highlight Reishi extract as a bioactive-rich, safe and stable natural ingredient with strong potential for incorporation into cosmetic formulations. Its antioxidant performance, moderate tyrosinase inhibition and compatibility within the cream matrix support its use in multifunctional anti-aging and skin-brightening products.
Background
The study addresses the cosmetic applications of Ganoderma lucidum, known for its various bioactive compounds. Prior research has indicated potential benefits of this mushroom in skincare, but comprehensive evaluations in topical formulations are limited. This study aims to fill that gap by investigating its effects in a cream formulation.
Methods
Not reported in abstract.
Results
Not reported in abstract.
Interpretation
Not reported in abstract.
Key findings
- Not reported in abstract.
Limitations
- Not reported in abstract.