What is Rejuran (polydeoxyribonucleotide) skin booster used for?

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Rejuran (Polydeoxyribonucleotide) Skin Booster: Clinical Applications

Rejuran is a polydeoxyribonucleotide (PDRN) skin booster used primarily for skin rejuvenation, wound healing acceleration, wrinkle reduction, and treatment of photoaging-associated hyperpigmentation through intradermal injection. 1, 2, 3

Primary Clinical Indications

Skin Rejuvenation and Anti-Aging

  • PDRN promotes physiological tissue repair by activating adenosine A2A receptors and salvage pathways, leading to increased collagen synthesis, improved skin texture, and reduced wrinkles. 3
  • The mechanism involves stimulation of fibroblast proliferation, enhanced angiogenesis, and extracellular matrix remodeling. 1, 3
  • Clinical studies demonstrate significant improvements in skin smoothness, elasticity, moisture content, and overall facial appearance after 3-4 treatment sessions. 4

Wound Healing Enhancement

  • PDRN accelerates impaired wound healing in conditions such as diabetes, thermal injury, and ischemia by promoting cell migration and growth while reducing inflammation. 3
  • It reduces wound hypoxia, decreases oxygen radical levels, and enhances angiogenesis in compromised tissue. 3

Hyperpigmentation Treatment

  • PDRN exhibits novel anti-melanogenesis properties by decreasing melanin content, tyrosinase activity, and MITF/TRP-1 expression through ERK and AKT signaling pathways. 2
  • Clinical evaluation of six female patients showed more than noticeable improvements in facial hyperpigmentation after three intradermal PDRN injection sessions. 2

Molecular Classification and Product Characteristics

Standardized Nomenclature

  • PDRN refers specifically to DNA polymers with molecular weight <1500 kDa, while polynucleotides (PN) denote polymers ≥1500 kDa. 1
  • Commercial PDRN products (Placentex, Rejuvenex, HiDr) are traditionally extracted from salmon sperm cells (Oncorhynchus mykiss or O. keta). 5
  • The molecular weight range typically spans 50-1500 kDa, though recent formulations may include fragments from 1-10,000 kDa. 1

Available Formulations

  • PDRN is commercially available as injectables, gels, creams, serums, and masks for various aesthetic applications. 1

Optimal Treatment Protocol

Injection Technique

  • Use 30-gauge needles with 4mm length for intradermal delivery at shallow angles with bevel facing upward. 6
  • Each injection must create a visible wheal or papule with blanching to confirm proper intradermal placement and avoid deeper vascular structures. 6
  • Space injections 5mm apart across treatment areas including crow's feet, nasolabial folds, perioral wrinkles, and periorbital regions. 6

Treatment Schedule

  • Administer 3-4 initial treatment sessions spaced one month apart, followed by maintenance treatments every 6-12 months. 6
  • Apply topical anesthesia for at least 30 minutes before the procedure and remove completely before injections. 6

Zone-Specific Modifications

  • For delicate periorbital skin, reduce needle gauge further and limit depth to 0.25mm, or consider using a 22G × 2 inches cannula for enhanced safety. 4, 6
  • Warn patients about potential bruising and swelling in the under-eye area. 4, 6

Combination Therapy Strategies

PDRN with Platelet-Rich Plasma (PRP)

  • Combining PDRN (marketed as "skin booster") with PRP demonstrates superior clinical efficacy compared to either treatment alone, with 88.75% total clinical effectiveness and only 6.25% adverse reaction incidence. 7
  • This combination significantly improves facial skin indicators, quality of life, and patient satisfaction with appearance after one treatment course. 7
  • The synergistic effect delivers multiple growth factors for soft tissue repair combined with PDRN's regenerative and anti-inflammatory properties. 8, 7

PDRN with Microneedling

  • Microneedling combined with PDRN acts synergistically to improve acne scars and overall skin rejuvenation outcomes. 4
  • Inject PDRN into problem areas before microneedling when the product is in its most liquid form. 6

PDRN with Hyaluronic Acid

  • A 50:50 mix of PRP (which can be combined with PDRN) and non-crosslinked HA produces highly significant improvement in overall facial appearance (p<0.0001) with 20%, 24%, and 17% increases in FACE-Q scores at 1,3, and 6 months respectively. 8
  • Mix immediately before injection in a single syringe for optimal results. 8

Safety Profile and Adverse Effects

Documented Safety

  • PDRN demonstrates excellent safety with minimal side effects, promoting healing time and wound regeneration without significant complications. 3
  • No serious adverse events have been reported with PDRN monotherapy or combination treatments. 8, 7
  • The anti-inflammatory properties reduce tissue damage and accelerate recovery. 5, 3

Post-Treatment Care

  • Advise patients to avoid sunlight and heavily scented facial products for 24 hours post-procedure. 6
  • Typical healing time is 24-48 hours with potential for mild bruising or swelling. 6

Critical Clinical Pitfalls to Avoid

Injection Depth Errors

  • Never inject deeper than 2.5mm to maintain intradermal safety and avoid vascular complications. 6
  • Failure to create visible papules indicates incorrect depth placement and risks reduced efficacy by missing target dermal fibroblasts. 6

Product Handling

  • PDRN products must be used according to manufacturer specifications regarding storage and preparation. 1
  • When combining with PRP, use PRF within 20-40 minutes after preparation before it clots in the syringe. 6

Treatment Spacing

  • Inadequate spacing between injection points (less than 5mm) may result in uneven treatment coverage and suboptimal outcomes. 6

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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