Objectives: This review aims to evaluate the combined efficacy of exosomes and PDRN in treating skin aging induced by oxidative stress. By exploring their mechanisms of action, the review highlights their potential to mitigate reactive oxygen species (ROS)-induced damage, promote collagen production, and enhance skin regeneration.
Introduction: Oxidative stress is a key factor in skin aging, caused by an excess of reactive oxygen species (ROS) that damage cellular structures. This process accelerates collagen degradation, inflammation, and loss of elasticity. Emerging therapies such as exosomes and PDRN offer innovative solutions by combating oxidative damage and promoting tissue regeneration.
Materials / method: Recent literature, including clinical trials and experimental studies, was reviewed to evaluate the efficacy of exosomes and PDRN in skin aging. Key metrics such as collagen synthesis, inflammation reduction, and extracellular matrix regeneration were analyzed. The review also integrates lifestyle factors such as diet, antioxidants, and sun protection.
Results: Exosomes effectively reduce inflammation and stimulate fibroblast activity, while PDRN enhances angiogenesis and extracellular matrix repair. Combined, they deliver superior results in improving skin elasticity, reducing wrinkles, and reversing oxidative damage. Lifestyle interventions further amplify these effects, optimizing therapeutic outcomes.
Conclusion: The integration of exosomes and PDRN into dermatological practice represents a breakthrough in addressing oxidative stress-induced skin aging. Their synergistic effects, combined with healthy lifestyle habits, offer a holistic approach to prevention and treatment, setting a new standard for regenerative therapies.
Disclosures
Did you receive any funding to support your research for this TOPIC?
No
Were you provided with any honoraria, payment or other compensation for your work on this study?
No
Do you have any financial relationship with any entity which may closely compete with the medications, materials or instruments covered by your study?
No
Do you own or have you applied for any patents in conjunction with the instruments, medications or materials discussed in your study?
No
This work was not supported by any direct or non direct funding. It is under the author's own responsability