Skip to main content

Cosmetic Research Analysis

5 papers

August’s cosmetic-focused research coalesced around noninvasive dermatologic oncology, injectable aesthetics, and perioperative biomaterials. A phase III randomized trial established red-light ALA-PDT as an effective, cosmetically favorable treatment for superficial basal cell carcinoma, while a network meta-analysis clarified trade-offs in Bowen’s disease between long-term clearance and scar quality. Translational biomaterials advanced with an injectable zwitterionic hydrogel that eliminated po

Summary

August’s cosmetic-focused research coalesced around noninvasive dermatologic oncology, injectable aesthetics, and perioperative biomaterials. A phase III randomized trial established red-light ALA-PDT as an effective, cosmetically favorable treatment for superficial basal cell carcinoma, while a network meta-analysis clarified trade-offs in Bowen’s disease between long-term clearance and scar quality. Translational biomaterials advanced with an injectable zwitterionic hydrogel that eliminated postoperative adhesions in animals, signaling potential reductions in surgical morbidity. Non-surgical lower-face contouring gained randomized support for onabotulinumtoxinA, and preclinical work identified eucalyptol as a direct β2 integrin antagonist to curb neutrophil-driven inflammation. Across the month, AI-enabled objective grading and modern in vitro models continued to elevate evidence standards for cosmetic outcomes.

Selected Articles

1. Red light photodynamic therapy with 10% aminolevulinic acid gel showed efficacy for treatment of superficial basal cell carcinoma in a randomized, vehicle controlled, double-blind, multicenter phase III study.

81Journal of the American Academy of Dermatology · 2025PMID: 40846240

A pivotal multicenter double-blind phase III RCT (n=187) showed 10% ALA gel plus red-light PDT achieved 75.9% histologic and 83.4% clinical clearance for superficial BCC versus 19.0% and 21.4% with vehicle; safety was acceptable and 88.1% of patients rated cosmetic results as good/very good.

Impact: Establishes a noninvasive, cosmetically superior therapy for sBCC with level I evidence, expanding options in cosmetically sensitive areas and potentially reducing surgical morbidity.

Clinical Implications: Consider 10% ALA–PDT as a first-line or alternative for superficial BCC when cosmesis is prioritized or surgery is contraindicated; discuss retreatment potential and pending long-term durability.

Key Findings

  • Histologic clearance of 75.9% vs 19.0% with vehicle (P < .0001).
  • Clinical clearance of 83.4% vs 21.4% with vehicle (P < .0001).
  • 88.1% of patients rated esthetic outcome as good/very good with acceptable safety.

2. Interventions for Bowen's disease: A systematic review and network meta-analysis of randomized controlled trials.

78.5Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG · 2025PMID: 40827908

A PROSPERO-registered network meta-analysis of nine RCTs (672 patients, 844 lesions) ranked treatments for Bowen’s disease: LA-PDT led initial clearance, surgery led long-term clearance, and PDT/LA-PDT/5-FU had the best cosmetic outcomes while surgery performed worst cosmetically.

Impact: Simultaneously ranks efficacy and cosmetic outcomes to support shared decision-making where recurrence risk and cosmesis must be balanced.

Clinical Implications: Use rankings to tailor care: prioritize LA-PDT/PDT for better cosmesis, or surgery for durability; explicitly communicate lower clearance with cryotherapy/imiquimod.

Key Findings

  • LA-PDT ranked first for initial lesion clearance.
  • Surgery ranked first for long-term clearance.
  • PDT/LA-PDT/5-FU had the most favorable cosmetic outcomes; surgery worst.

3. Chimonanthus salicifolius essential oil protects against endotoxin-induced acute lung injury via suppression of β2 integrin-mediated neutrophil adhesion and chemotaxis.

81Journal of Ethnopharmacology · 2025PMID: 40816582

Preclinical studies identified eucalyptol as a direct β2 integrin antagonist that reduces neutrophil adhesion/chemotaxis and mitigates LPS-induced lung injury, with multi-assay confirmation of target engagement and in vivo efficacy.

Impact: Opens a druggable pathway to modulate neutrophil trafficking with potential relevance to inflammatory complications after cosmetic or surgical procedures.

Clinical Implications: If human PK/PD and safety translate, eucalyptol-derived agents could limit neutrophil-driven tissue damage in ALI/ARDS or post-procedural inflammation; requires dosing, off-target, and formulation studies.

Key Findings

  • Eucalyptol directly bound β2 integrin (MST Kd ~19.5 μM) and disrupted β2 integrin/ICAM-1 interaction.
  • In vitro, neutrophil adhesion and chemotaxis were inhibited; in vivo, neutrophil recruitment and ALI severity were reduced.
  • CSEO and eucalyptol attenuated inflammatory signaling (e.g., NF-κB, MPO/NE, ROS).

4. An Injectable Zwitterionic Hydrogels with Multiple Intermolecular Interactions for Effective Prevention of Abdominal Adhesions.

77.5Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025PMID: 40827578

A multifunctional injectable zwitterionic hydrogel (PSA-ZnO) completely prevented postoperative peritoneal adhesions in rat models and outperformed commercial hyaluronic acid gel, combining antifouling, antibacterial, rapid hemostatic, and anti-fibrin properties.

Impact: Targets a long-standing unmet need—adhesion prevention—potentially reducing reoperation and morbidity in aesthetic and general surgery.

Clinical Implications: Pending large-animal and human data, such hydrogels could be integrated into abdominopelvic and aesthetic procedures to prevent adhesions and improve recovery.

Key Findings

  • Completely prevented or markedly reduced peritoneal adhesions at 7–14 days in rats.
  • Outperformed commercial hyaluronic acid gel and achieved >95% antibacterial clearance.
  • Enabled rapid hemostasis and favorable cytokine modulation while inhibiting pathological fibrin organization.

5. Improvement of Lower Facial Shape After Treatment With OnabotulinumtoxinA: Secondary Results From a Phase 2 Dose Escalation Study.

78Plastic and Reconstructive Surgery · 2025PMID: 40801407

In a randomized, placebo-controlled phase 2 trial (n=187), intramuscular onabotulinumtoxinA to the masseters significantly reduced lower facial width and mandibular angle at 90 days, with effects persisting to 180 days and improved patient-reported outcomes.

Impact: Delivers randomized evidence with objective morphometrics supporting a durable, non-surgical option for lower-face contouring.

Clinical Implications: Supports use of onabotulinumtoxinA for masseter prominence with expected durability up to six months; integrate morphometrics and PROs into counseling and dose selection.

Key Findings

  • All doses (24–96 U) reduced facial width and mandibular angle vs placebo at day 90; effects persisted to day 180.
  • Improved Masseter Muscle Prominence Scale grades and patient satisfaction.
  • Randomized, placebo-controlled, dose-ranging design with objective endpoints.