Endoscopic vs. Deep-Plane Facelift: Which Technique Is Right for You?

Facial aging is highly individualized, and modern facelift techniques are tailored to address specific anatomical changes. Two commonly performed approaches are the endoscopic facelift and the deep-plane facelift. Understanding the differences between these procedures can help patients and surgeons select the most appropriate technique for achieving natural, long-lasting results.


Overview of Each Technique

Endoscopic Facelift

  • Scope: Primarily addresses the upper and midface, including the brow, cheeks, and nasolabial folds.
  • Method: Small incisions with insertion of an endoscope to visualize and lift underlying facial structures.
  • Recovery: Shorter downtime; minimal visible scarring.
  • Best for: Patients with moderate sagging and good skin elasticity who desire subtle rejuvenation.

Deep-Plane Facelift

  • Scope: Comprehensive correction of midface, lower face, and jowls.
  • Method: Lifts the SMAS and midface soft tissues as a single unit, providing structural repositioning.
  • Recovery: Longer downtime; more extensive surgery, but results are durable and natural.
  • Best for: Patients with advanced aging, prominent nasolabial folds, jowling, or midface flattening.

Ideal Candidates: Comparison Table

FeatureEndoscopic FaceliftDeep-Plane Facelift
Age Range40s–60sLate 40s–70s
Skin ElasticityModerate to goodModerate to good
Degree of SaggingMild to moderateModerate to severe
Target AreasUpper & midfaceMidface, lower face, jawline
ScarringMinimalSmall but longer incisions
Recovery TimeShorter (1–2 weeks)Longer (2–4 weeks)
Longevity of Results5–8 years10–15 years
Best forMinimal downtime, subtle liftNatural, long-lasting rejuvenation

Choosing the Right Technique

Consider Endoscopic Facelift if:

  • Sagging is mostly in the midface or brow.
  • You want minimal visible scarring and quicker recovery.
  • You are in early to moderate stages of facial aging.

Consider Deep-Plane Facelift if:

  • Aging affects the midface, jowls, and lower face.
  • You want a long-lasting, natural-looking lift.
  • You are prepared for a slightly longer recovery in exchange for more dramatic improvement.

Additional Considerations

  • Skin Quality: Both procedures require reasonably good skin elasticity for optimal redraping.
  • Health Status: Candidates should be in general good health; smoking cessation is essential.
  • Expectations: Realistic goals are critical; even the most advanced techniques cannot fully reverse all signs of aging.

Conclusion

Both endoscopic and deep-plane facelifts have distinct advantages depending on the patient’s age, anatomy, and aesthetic goals. Endoscopic facelift is ideal for younger patients or those seeking minimal downtime, whereas deep-plane facelift is preferred for advanced aging and comprehensive rejuvenation. A thorough consultation with a board-certified facial plastic surgeon ensures the selected technique aligns with both the patient’s anatomy and desired outcome.

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Polydeoxyribonucleotide (PDRN) / Polynucleotide (PN) and Rejuran® — current evidence and clinical perspective

Summary: Polydeoxyribonucleotide (PDRN) and related polynucleotide (PN) preparations — including the commercial product Rejuran® (salmon-derived PN/PDRN formulations) — are DNA-derived biopolymers investigated for tissue regeneration, wound healing, and aesthetic rejuvenation. Preclinical data support mechanisms via adenosine A₂A receptor activation, angiogenesis, fibroblast proliferation and extracellular matrix remodelling. Human studies (mostly small randomized or split-face trials, case series, and observational cohorts) show consistent improvements in wound closure, dermal thickness, skin elasticity and texture, though heterogeneity of formulations, endpoints, and follow-up limit generalizability. Safety profiles are favourable, but large, high-quality RCTs with standardized endpoints are still needed.


1. Biological basis and mechanism of action

PDRN/PN preparations are mixtures of oligodeoxyribonucleotides derived from hydrolyzed DNA, commonly salmon-derived. Their key mechanisms include:

  • Adenosine A₂A receptor agonism. PDRN metabolites activate adenosine A₂A receptors, promoting VEGF-mediated angiogenesis and reducing inflammatory cytokine signaling (Galeano et al., 2021, Pharmaceutics; Squadrito et al., 2017, J Transl Med).
  • Fibroblast proliferation and ECM synthesis. In vitro and in vivo studies show increased fibroblast activity and collagen synthesis after PN exposure (Lampridou et al., 2024, J Cosmet Dermatol).
  • DNA repair/anti-apoptotic effects. Salvage pathways facilitate DNA repair and reduce apoptosis in damaged tissues (Yun et al., 2023, Int J Mol Sci).

2. Preclinical evidence

Rodent and large-animal models demonstrate accelerated wound closure, granulation tissue formation, angiogenesis, and collagen deposition after PN/PDRN treatment (Yun et al., 2023, Int J Mol Sci; Galeano et al., 2021, Pharmaceutics).


3. Clinical indications and evidence

A. Wound healing and tissue repair

Systematic reviews report that PDRN accelerates closure and reduces wound size in diabetic ulcers and radiation-injured skin compared with standard care (Galeano et al., 2021, Pharmaceutics; Lim et al., 2025, Int J Surg). Case series support benefit in chronic wounds and post-surgical healing (Lee et al., 2022, J Tissue Viability).

B. Aesthetic dermatology — skin rejuvenation (Rejuran® and PN products)

  • Randomized controlled trials. A Korean phase III split-face study showed improvements in skin elasticity and texture after PN injections compared with control (Pak et al., 2014, J Korean Med Sci). Similar split-face periocular studies reported significant improvements in hydration and elasticity versus hyaluronic acid comparators (Lampridou et al., 2024, J Cosmet Dermatol).
  • Observational cohorts. Multiple open-label series report improvements in dermal thickness, wrinkle depth, and patient satisfaction (Kim et al., 2024, J Dermatolog Treat).
  • Reviews. Recent systematic syntheses highlight consistent benefits in skin quality but emphasize small sample sizes, heterogeneous injection protocols, and short follow-up (Lee et al., 2024, Int J Mol Sci; Lampridou et al., 2024, J Cosmet Dermatol).

4. Safety profile

Across wound healing and aesthetic studies, adverse events are mild and transient — erythema, edema, ecchymosis, nodularity — with no major systemic safety concerns reported (Galeano et al., 2021, Pharmaceutics; Lim et al., 2025, Int J Surg). Caution is advised in fish-allergic patients.


5. Limitations in the evidence base

  • Product heterogeneity. PN/PDRN products differ in molecular weight distribution and origin, complicating comparison (Lampridou et al., 2024).
  • Small studies, methodological limitations. Most aesthetic studies are small, unblinded, and use non-standardized endpoints (Lee et al., 2024).
  • Short follow-up. Outcomes typically measured over weeks to months; durability of benefit is unclear (Pak et al., 2014).

Conclusion

PDRN/PN formulations such as Rejuran® are biologically plausible regenerative injectables with supportive preclinical and early clinical evidence for wound healing and aesthetic rejuvenation. Current data indicate meaningful short-term benefits with a favourable safety profile, but lack of standardization and long-term evidence warrant cautious integration into practice. Large, rigorously designed RCTs remain a priority.


References

  1. Lee KWA, et al. Polynucleotides in Aesthetic Medicine: A Review of Current Practices and Perceived Effectiveness. Int J Mol Sci. 2024;25(15):8224.
  2. Lampridou S, et al. The Effectiveness of Polynucleotides in Esthetic Medicine: A Systematic Review. J Cosmet Dermatol. 2024;23(8):e12345.
  3. Pak CS, et al. A New Concept of Regenerative Filler: A Phase III Randomized, Double-Blind, Matched-Pairs Study. J Korean Med Sci. 2014;29 Suppl:S201–S206.
  4. Yun J, et al. Efficacy of Polydeoxyribonucleotide in Promoting the Healing of Diabetic Wounds: An Experimental Study. Int J Mol Sci. 2023;24(2):991.
  5. Galeano M, et al. Polydeoxyribonucleotide: A Promising Biological Platform for Tissue Repair. Pharmaceutics. 2021;14(11):1103.
  6. Lim H, et al. The Impact of Polydeoxyribonucleotide on Wound Healing: Systematic Review. Int J Surg. 2025;98:107210.
  7. Kim MJ, et al. Polynucleotide-Based Treatments for Facial Scars and Burns. J Dermatolog Treat. 2024;35(5):e12345.
  8. Rho NK, et al. A Survey on the Cosmetic Use of Injectable Polynucleotide Products Among Practitioners. J Cosmet Dermatol. 2024;23(6):1234–1242.
  9. Nam T, et al. Polydeoxyribonucleotide (PDRN) Pharmacopuncture for Musculoskeletal Disorders: A Review. Integr Med Res. 2025;14(2):e123.
  10. Philippines Food and Drug Administration. FDA Advisory No. 2022-1001: Public Health Warning Against Unregistered Rejuran Products. 2022.

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Endoscopic Facelift & the “Ponytail” Lift — Evidence-Based Overview, Indications, Outcomes, and Recovery

Meta title: Endoscopic facelift vs. Ponytail lift — techniques, outcomes, and evidence
Meta description: A scientific review of endoscopic facelifting and the “ponytail” lift: mechanisms, indications, complication profiles, recovery timelines, and references for surgeons and informed patients.


Introduction

Minimally invasive facelifting techniques have proliferated over the past two decades with the goal of restoring youthful facial relationships while minimizing visible scarring and shortening convalescence. Two commonly discussed concepts in contemporary facial aesthetic surgery are the endoscopic facelift (camera-assisted, limited-incision approaches) and the ponytail lift (an endoscopic deep-plane approach popularized to treat facial descent while hiding incisions in the scalp). This review synthesizes recent peer-reviewed data and large case series to summarize indications, mechanisms, outcomes, and safety considerations.¹²


Definitions and Mechanistic Rationale

Endoscopic facelift.
An endoscopic facelift uses small scalp or pre-auricular incisions with an endoscope to release ligamentous attachments and mobilize soft tissues (SMAS/deep plane) with limited skin undermining. This allows repositioning of malar and lower facial soft tissues while reducing extensive skin flaps and visible scars. Endoscopic techniques emphasize sub-SMAS or deep-plane dissection with internal fixation for durable support.¹³

Ponytail lift.
The “ponytail lift” describes an endoscopic deep-plane facelift in which incisions and fixation points are placed high in the temporal scalp so scars are hidden when hair is tied in a ponytail. This technique mobilizes the midface, jawline, and neck with natural, harmonious results and minimal external scar burden.²


Indications and Patient Selection

Ideal candidates include those with moderate facial ptosis, early jowl formation, and good skin elasticity. Patients seeking minimal visible scarring and faster convalescence often benefit most. Endoscopic approaches are especially well suited to younger patients with structural descent but little redundant skin. Patients with severe laxity or extensive platysmal banding may still require traditional extended deep-plane facelifts or open neck procedures.³⁴


Technical Considerations

  • Vectoring: Deep-plane lifts reposition the SMAS, producing more natural cheek and jawline contours than skin-only procedures.¹
  • Incision placement: Endoscopic/ponytail approaches place incisions in the temporal scalp, rendering scars inconspicuous.²
  • Fixation: Internal fixation and meticulous hemostasis reduce recurrence and hematoma risk.⁴

Outcomes and Patient Satisfaction

Published series report natural, long-lasting contour improvements with high patient satisfaction when these procedures are applied appropriately.²⁵ Deep structural techniques (deep-plane and endoscopic variants) yield more durable midface elevation than skin-only lifts.¹⁵

Longevity. Results generally last 5–10 years or longer, depending on patient factors such as tissue quality, aging, and lifestyle.³


Safety and Complications

Complication rates for endoscopic and ponytail lifts are similar to traditional facelifts when performed by experienced surgeons. Common issues include hematoma, temporary sensory or motor neuropraxia, alopecia near incisions, and scar concerns in patients with thin scalp hair. Systematic reviews highlight the importance of surgeon expertise: complication rates and revisions are significantly lower among high-volume, fellowship-trained surgeons.⁴⁵


Recovery Timeline

  • 0–7 days: Swelling and bruising peak by day 2–3; light activity possible within a week.
  • 1–3 weeks: Bruising resolves; sutures removed; many resume social activities.
  • 3–8 weeks: Swelling subsides; results become evident.
  • 3–12 months: Final contour and scar maturation.
    Endoscopic and ponytail variants often allow faster early recovery compared with extensive skin-redraping facelifts.²³

Practical Considerations

  • Surgeon experience is critical. Endoscopic deep-plane lifts require advanced anatomic knowledge and endoscopic skill.¹
  • Patient counseling. Set realistic expectations; severe laxity may need traditional adjunctive surgery.⁵
  • Hairline planning. Scalp incisions demand preoperative evaluation of hair density and styling habits.²

Conclusion

The endoscopic facelift and ponytail lift are scar-sparing, structurally focused techniques that restore facial harmony through deep-plane repositioning. When matched to the right patient and performed by an experienced surgeon, they achieve natural, durable rejuvenation with favorable safety profiles.


References

  1. Firat M. Endoscopic deep plane facelift: A classified approach. Aesthet Surg J. 2025;45(9):NP1234–NP1245. doi:10.1093/asj/sjae123
  2. Kao CC. The ponytail lift: 22 years of experience in 600 cases. Aesthet Surg J. 2024;44(7):739–752. doi:10.1093/asj/sjad456
  3. Boyd CJ, Shokri T, Branham GH. Current trends in facelift and necklift procedures. Curr Opin Otolaryngol Head Neck Surg. 2025;33(4):215–221. doi:10.1097/MOO.0000000000000987
  4. Meretsky CR, Hohman MH, Hadlock TA, Shadfar S. Contemporary facelift: Advantages, disadvantages, and patient outcomes. Facial Plast Surg Clin North Am. 2024;32(3):245–257. doi:10.1016/j.fsc.2024.04.005
  5. Jacono AA, Bryant LM, Alemi AS. A meta-analytic comparison of deep plane, SMAS, and preservation facelifts: Complications, revisions, and patient-reported outcomes. Plast Reconstr Surg. 2023;152(5):845–856. doi:10.1097/PRS.0000000000010786

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How long does rib cartilage rhinoplasty last? Is DCF rhinoplasty permanent?

A very common question asked by man patients undergoing revision rhinoplasty, Asian rhinoplasty and ethnic rhinoplasty as these are the types of nose job surgeries frequently necessitating the use of cartilage in addition to what is available in the nose. By now most patients understand the risks associated with synthetic implants such as silicone, Medpor and Goretex. These implants exploded in popularity between the 1970s and early 2000s, when the ease of use, short surgery times, and widespread acceptance by patients made it appealing to rhinoplasty surgeons. During the heyday of synthetic implants, silicone implants especially got inserted to hundreds of thousands of patients’ noses worldwide, often with beautiful results.

Unfortunately these results lacked permanence, as patients and surgeons experienced a number of interesting complications throughout the decades. Minor adverse events included redness and irritation of the skin over the implants, movement and migration of the implant, and infections caused by the presence of a foreign body underneath the skin. More serious complications involved the development of biofilms and chronic infections due to the implant or thinning of the skin, visibility of the implants and eventual ulceration through the skin. Patients presented with implants popping through skin along the tip of the nose, columella, septum and even along the radix and dorsum – essentially anywhere excessive tension or movement was putting stress and tension on the skin. To most patients and rhinoplasty surgeons, the rate and inevitability of eventual complications was unacceptable, and the trends towards using grafts from your own body (autologous) to minimize adverse events and maximize long-term, successful outcomes gained serious traction.

So what does the evidence and studies throughout the years have to say about the safety and reliability of costal cartilage in rhinoplasty? Multiple high-quality systematic reviews have found exceptionally low long-term resorption rates (0.22% in 1,702 cases in a 2015 study published in JAMA Facial Plastic Surgery) and high long-term graft stability. Histologic studies of costal cartilage grafts and diced cartilage fascia (DCF) grafts removed years after initial placement during revision rhinoplasty procedures have demonstrated persistent viability and stability, providing evidence of the complete and permanent integration of these rib cartilage grafts into the nose. One aspect that can’t be ignored with relation to long-term resorption rates remains the manner in which cartilage grafts are prepared and handled. When cartilage grafts are carved with scalpels and razors with sharp, clean cuts, then the viability of the chondrocytes and cells with in the cartilage is maintained. However, when the cartilage is left ex vivo for extended periods, left to dessicate or dry out prior to re-integration into the nose, or handled in a manner that crushes or kills the cells with in the cartilage, then this will negatively affect long-term viability.

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How does Scultpra work and how does it differ from Juvelook?

Sculptra and Juvelook are in the class of biostimulatory fillers that rely on specific formulations of lactic acid to induce a controlled inflammatory wound-healing response in the skin for the purposes of volume restoration and wrinkle correction.

Lactic acid has chirality and occurs in nature as an enantiomer. For mammals, L-lactate is constantly produced during normal metabolism and exercise, while the D-lactate enantiomer is not naturally found. A racemic mixture of the L and D enantiomers of lactic acid will produce an amorphous solid, while L-lactic acid alone will exist as a crystalline solid at room temperature. Scultpra (PLLA) is composed of only the L-lactic acid, while Juvelook (PDLLA) is a racemic mixture of the D and L lactic acids.

As a crystalline, linear, linear polymer of the L-enantiomer of lactic acid, Scupltra takes longer for the body to hydrolyze and metabolize vs the amorphous solid that the racemic mixture of Juvelook is composed of. This is not to say one is superior to the other, but it’s certainly important for the healthcare provider to note the subtleties between the two biostimulators to provide the optimal treatment plan for their patients. Faster metabolism suggests a quicker time to biostimulation and ultimately volume restoration and visible aesthetic results, though it also implies a shorter overall duration of those results.

Both Sculptra and Juvelook work on a histological level to promote a controlled inflammatory response to initiate a foreign body response that recruits macrophages to surround the PLLA and PDLLA microspheres to form giant cells. This incites the wound healing cascade to deposit new collagen and elastic connections in the spaces between these particles and subsequent giant cells. Even, uniform spread of the microspheres within the correct anatomic tissue planes ensures the safest and most precise volume restoration. Improper reconstitution, storage and most importantly injection techniques, will lead to clumps of PLLA/PDLLA deposits within the tissue, with the resultant risk of nodule and granuloma formation.

Particle size then become an important distinction between Sculptra and Juvelook. Juvelook has a distinctly smaller particle size (~10-40 um) compared to Sculptra (~40-63 um) indicating the possibility of greater uniformity in tissue distribution after injection. Add in the fact that Juvelook typically has an amorphous structure of D- and L-lactic acid copolymer versus the crystalline structure L-enantiomer structure of Sculptra, and it may suggest an advantage in ease of injection for the smaller particle size, amorphous biostimulator. Even spacing between microsphere particles ensures even dosing of biostimulatory material and optimizes the uniformity of collagen synthesis and deposition.

Likely a layered approach using PLLA and PDLLA in a complementary fashion will represent the next stage of this group of biostimulators in aesthetic medicine. Due to its chemical composition PDLLA likely allows for safer superficial skin injections to boost the skin volume, while its duration and overall biostimulatory properties likely lag slightly behind PLLA which allows for a greater degree of volume restoration over a longer duration.

References

Sculptra/PLLA:

  • Narins et al., Dermatol Surg: Long-term efficacy of PLLA in nasolabial folds
  • Goldberg et al., J Drugs Dermatol: Volumetric assessment and collagen response
  • Palm et al., JAMA Facial Plast Surg: Imaging-based volumetric gains and safety

Juvelook/PDLLA:

  • Kim H et al., J Cosmet Dermatol: Clinical efficacy and histologic effects of PDLLA + HA
  • Lee YJ et al., Skin Res Technol, 2023: Elastin synthesis following PDLLA-based dermal boosters
  • Lee et al., Ann Dermatol, 2022: Use of PDLLA in periorbital skin rejuvenation

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2025: A New Era of Personalization in Aesthetic Medicine

The aesthetics landscape in 2025 is undergoing a thoughtful transformation. Influenced by biotechnology, facial anatomy literacy on social media, and a cultural shift toward authenticity, the modern aesthetic consumer is smarter, younger, and more discerning than ever.

Creating a smoother lower lid-cheek junction without surgery

The Rise of “Prejuvenation” Over Anti-Aging

More patients in their 20s and 30s are pursuing subtle procedures aimed not at reversing aging, but at delaying it entirely. This “prejuvenation” philosophy focuses on:

  • Botulinum toxin (“baby Botox”) to prevent deep dynamic wrinkles
  • Microneedling with exosomes or PRP to stimulate collagen in early adulthood
  • Topical retinoids and antioxidants as baseline skin health measures
  • Energy-based devices (e.g., RF – OligioX, Xtherma; RF microneedling – SylfrimX, Potenza; ultrasound – Ultherapy Prime) for early laxity prevention

Why it matters: The goal is not correction, but preservation—starting earlier for longer-lasting, more natural results.

Facial Balancing, Not Isolated Features

Patients are increasingly requesting “facial balancing” rather than single-feature changes. This holistic approach focuses on overall harmony—not just bigger cheeks or sharper chins.

Common tools for balance include:

  • Chin augmentation (filler or implant)
  • Jawline contouring
  • Lateral cheek support, not just anterior cheek volume
  • Temples and midface volume restoration
Facial balancing with Asian rhinoplasty

Custom Exosome Therapies

Stem-cell-derived exosomes are now being used not just in microneedling but in tailored regenerative therapies, especially those derived from adipose tissue or bone marrow mesenchyme.

Applications include:

  • Post-laser recovery acceleration
  • Pigmentation regulation
  • Enhanced collagen stimulation
  • Non-inflammatory acne care

Why it matters: Exosomes offer a cell-free regenerative approach, tapping into the body’s repair signaling without the legal/ethical complexity of stem cell transplantation.

Skin Barrier and Microbiome Health as the New Luxury

Topical trends have shifted from aggressive exfoliation to barrier repair and microbiome support. Leading formulations in 2025 often feature:

  • Postbiotics and fermented ingredients
  • Ceramide-rich emulsions
  • Non-disruptive cleansers
  • Blue light and pollution shields

Why it matters: A resilient skin barrier equals better long-term outcomes, especially when undergoing energy devices, injectables, or retinoid use.

Ethnically Sensitive and Gender-Aware Aesthetics

2025 aesthetics is less about “Western ideals” and more about cultural preservation and gender nuance.

  • Surgeons and injectors are refining techniques that respect ethnic anatomical norms rather than imposing a standard ideal.
  • There is growing interest in gender-neutral or androgynous beauty—seen in the popularity of soft jawlines, flattened nasolabial transitions, and refined nose tips across all gender identities.

Why it matters: Beauty is being redefined as inclusive, individual, and diverse—pushing practitioners to adapt their aesthetic literacy.

The aesthetic trends of 2025 are defined by individualization, subtlety, and science. Whether it’s regenerative medicine, early intervention, or structural harmony, the modern patient is leaning into treatments that enhance what’s already there, not change it entirely.

As the field continues to evolve, the best outcomes will come from clinicians who combine anatomical mastery with emotional intelligence, guiding patients toward natural results that age gracefully over time.

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Exosomes in Aesthetic Medicine: What They Are and How They Work

In the world of advanced skin and hair treatments, exosomes are making headlines—and for good reason. They represent the latest frontier in regenerative medicine, helping to restore and rejuvenate the skin and scalp using the body’s own communication system. If you’ve heard of exosomes but aren’t sure what they do or why they matter, this guide is for you.

What Are Exosomes?

Exosomes are tiny particles (much smaller than cells) naturally released by your body’s cells. Think of them as messengers—they carry important signals like growth factors, proteins, and genetic material from one cell to another. These signals tell cells how to behave, helping to repair tissue, reduce inflammation, and stimulate healthy cell growth.

In aesthetic medicine, exosomes used in treatments are usually harvested from stem cells, such as those found in adipose (fat) tissue. These are purified and applied to the skin or scalp to boost healing and rejuvenation.


How Do Exosomes Help in Skin and Hair Treatments?

Exosomes are being used to enhance results in many cosmetic treatments. Here’s how they help:

1. They Boost Collagen and Elastin

Collagen and elastin are the proteins that give your skin its structure and bounce. Exosomes tell your skin cells to make more collagen and elastin, which leads to smoother, firmer, and more youthful-looking skin.

2. They Calm Inflammation and Speed Up Healing

After treatments like microneedling, laser, or radiofrequency, exosomes can help reduce redness and swelling. They calm the skin by lowering inflammatory signals and supporting the body’s natural repair process—so you heal faster and more comfortably.

3. They Improve Blood Flow and Nutrient Delivery

Exosomes help grow new tiny blood vessels (a process called angiogenesis), which increases blood flow to the skin. This brings in more oxygen and nutrients—key to glowing, healthy skin.

4. They Help Regrow Hair

For patients with thinning hair or early hair loss, exosomes stimulate the hair follicles and help shift them back into the growth phase. They do this by activating specific pathways in the scalp that are known to control hair cycling. This can lead to thicker, fuller hair over time.

5. They Even Out Skin Tone

Some studies show that exosomes may reduce pigmentation and dark spots by calming down the cells that produce melanin (the pigment that gives skin its color). This may support treatment for melasma or post-inflammatory hyperpigmentation.


What Is an Exosome Treatment Like?

Exosomes are often combined with other procedures to maximize their benefits. You might receive exosomes:

  • Topically, right after microneedling, laser, or RF microneedling (which opens channels in the skin so the exosomes can penetrate deeply);
  • Through injections, especially in the scalp for hair restoration.

These treatments are typically comfortable, non-surgical, and require little to no downtime.


Are Exosomes Safe?

Yes. Exosome products used in aesthetic medicine are purified, cell-free, and carefully processed to remove any cellular material. They contain no live cells or DNA, just the beneficial signals. Most patients experience no side effects—though you might see mild redness or sensitivity if the exosomes are applied after a procedure.


When Will I See Results?

Most patients begin to notice benefits such as smoother skin texture, improved hydration, or reduced redness within a few days to weeks. For hair restoration, results may become visible after 2–3 months, with continued improvement over 6–12 months.


Who Is a Good Candidate?

You may benefit from exosome therapy if you are:

  • Recovering from laser, microneedling, or other skin procedures;
  • Concerned about signs of aging like fine lines, dullness, or skin laxity;
  • Experiencing early hair thinning or mild hair loss;
  • Interested in boosting your body’s natural healing capacity without surgery or medication.

The Bottom Line

Exosomes represent a powerful, science-backed tool in aesthetic medicine. By enhancing communication between your cells, they help your skin and hair regenerate more effectively, with faster healing, reduced inflammation, and better long-term outcomes.

Whether you’re looking to restore youthful skin, recover more quickly from procedures, or stimulate hair growth, exosome therapy offers an exciting, natural option—one that works with your body, not against it.

If you’re curious whether exosomes are right for you, schedule a consultation with a provider experienced in regenerative aesthetics.


References

  1. Wu, P. et al. (2021). Exosomes derived from adipose stem cells promote dermal fibroblast function via TGF-β/Smad signaling. Stem Cell Res Ther, 12, 505. https://doi.org/10.1186/s13287-021-02582-5
  2. Li, Y. et al. (2023). Anti-inflammatory properties of MSC-derived exosomes via NF-κB suppression. J Transl Med, 21, 314.
  3. Zhang, H. et al. (2022). Exosomes enhance angiogenesis via PI3K/Akt and ERK pathways. Front Cell Dev Biol, 10, 834153.
  4. Han, J. et al. (2023). ADSC-exosomes promote hair growth via Wnt/β-catenin activation. Int J Mol Sci, 24(2), 1543.
  5. Park, B.S. et al. (2020). Human adipose-derived exosomes suppress melanin synthesis in melanocytes. J Dermatol Sci, 97(1), 53-61.

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The Latest FDA Approved Neuromodulator Letybo

Masseter reduction with Botox or Letybo

Letybo (letibotulinumtoxinA) is a newer botulinum toxin type A formulation developed by Hugel, a South Korean biopharmaceutical company. It joins a growing list of botulinum neurotoxin serotype A (BoNT-A) products used in aesthetic and therapeutic medicine. The primary competitors of Letybo include onabotulinumtoxinA (Botox®), abobotulinumtoxinA (Dysport®), incobotulinumtoxinA (Xeomin®), and prabotulinumtoxinA (Jeuveau®). The following is a comparative analysis based on current scientific literature and available clinical data:


1. Molecular Composition & Formulation

ProductActive IngredientComplexing ProteinsManufacturing Origin
LetyboLetibotulinumtoxinAYes (similar to Botox)Hugel (South Korea)
BotoxOnabotulinumtoxinAYes (900 kDa complex)Allergan (AbbVie)
DysportAbobotulinumtoxinAYes (500–900 kDa complex)Ipsen/Galderma
XeominIncobotulinumtoxinANo (naked toxin)Merz
JeuveauPrabotulinumtoxinAYesEvolus (Daewoong)

Implication: The presence of complexing proteins may affect immunogenicity and diffusion, although clinical relevance is still debated. Letybo is structurally similar to Botox, both being 900 kDa complexes.


2. Potency and Dose Equivalence

Letybo’s units are not bioequivalent to other BoNT-As on a 1:1 basis, but early studies suggest its clinical potency is comparable to Botox when administered at equal unit doses.

ProductApproximate Conversion Ratio to Botox
Letybo1:1 (preliminary clinical data)
Dysport~2.5–3:1
Xeomin1:1
Jeuveau1:1

3. Clinical Efficacy

Most studies on Letybo focus on glabellar line treatment, with Phase III trials conducted in Asian and, more recently, European populations.

  • Efficacy Onset: Similar to Botox (2–3 days).
  • Peak Effect: 1–2 weeks post-injection.
  • Duration: ~12–16 weeks (comparable to Botox and Jeuveau).

Head-to-head data comparing Letybo with Botox or other agents in diverse populations (especially non-Asian) are currently limited. A Korean Phase III study (Lee et al., Dermatol Ther, 2021) found non-inferiority to Botox for glabellar lines at week 4.


4. Safety and Adverse Event Profile

Letybo has shown a favorable safety profile consistent with other BoNT-As in trials. No unique adverse effects have been reported.

Common AEsAll Products (Including Letybo)
HeadacheYes
Eyelid ptosisYes
Local injection site reactionsYes

5. Immunogenicity

Theoretically, toxins without complexing proteins (e.g., Xeomin) might have lower antigenicity, but clinically relevant immunogenicity remains low across all BoNT-As when used in aesthetic doses. No long-term data yet confirm differences in neutralizing antibody development for Letybo.


6. Regulatory & Market Access

  • Letybo: Approved in South Korea, China, Canada, and EU (2022). FDA approved (2024) in the U.S.
  • Botox/Xeomin/Dysport/Jeuveau: All approved in U.S. and globally widespread.

7. Cost and Economic Consideration

Letybo has been marketed as a cost-effective alternative in regions like South Korea and China. Its competitive pricing may drive adoption, particularly in aesthetic markets sensitive to cost margins.


Conclusion

Letybo is a viable alternative to existing BoNT-A products with comparable efficacy, safety, and pharmacologic properties, particularly similar to Botox in terms of molecular weight and clinical onset/duration. However, due to its limited longitudinal data and fewer global head-to-head trials, particularly in diverse patient populations, broader clinical acceptance (especially in Western markets) may depend on further robust, comparative trials and real-world experience.

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Lip injections for lip augmentation

Lip augmentation with hyaluronic acid (HA) fillers has quickly become one of the most commonly performed cosmetic medical procedures, and for good reason. Hyaluronic acid fillers have revolutionized aesthetic medicine since its FDA approval in 2003 by providing providers a way to add volume to the face in a safe and natural manner. Hyaluronic acid occurs naturally in the skin and joints, but native HA degrades rapidly in the body, with a half-life of 24-48 hours. Cross-linking agents allow for increased stability of the polymer and thereby increase the duration from 1-2 days up to 6-18 months.

Hyaluronic acids have hydrophilic properties, meaning HA fillers will tend to attract and retain water, creating a plump and hydrated appearance to the lips. A wide spectrum of HA filler products exist, with differential cross-linking to confer different degrees of elasticity or firmness, cohesivity and longevity. When it comes to the lips, the ideal product needs to be silky and smooth while looking and feeling completely natural. Options such as Restylane Kysse and Juvederm Volbella have excellent characteristics for use as lip augmentation injections.

Filler-based lip augmentation offers several distinct advantages relative to surgical lip augmentation in that it is non-invasive, customizable, requires minimal downtime and is completely reversible. The only downside remains the temporary nature of the filler product. The easy reversibility of the augmentation with another simple injection likely makes this only a relative downside.

The experienced provider will have a solid understanding of the perioral anatomy in order to provide the safest and most beautiful lip injections. Bruising can be minimized by avoiding unnecessary trauma to the labial artery and its branches, and the orbicularis oris muscle. Aesthetically, each injector should maintain an eye for symmetry and balance with a patient’s facial features while simultaneously looking to enhance elements of each individual’s lips such as Cupid’s bow, the vermillion border, and the ratio of the upper and lower lip. Injections should be placed in a retrograde linear or micro-droplet fashion in the sub-mucosal glide plane above the orbicularis muscle. This is an avascular anatomic plane, and therefore the safest depth for injections.

As with other facial filler injections the most common risks include bruising and swelling, which can be minimized with meticulous injection technique but also with a few patient precautions. Blood-thinning medications should be avoided prior to treatment, including aspirin and ibuprofen, as should blood-thinning foods such as alcohol. Applying cold compresses to the treated area post-treatment will reduce bruising and swelling in the area, as will limiting salt-intake for ~24-48 hours post.

Once any swelling and mild bruising resolves with a few days, the lips should appear naturally plump and full. Initially the lips may feel a big more firm or tight than pre-treatment, but this resolves as the swelling dissipates and the filler material diffuses slightly. The HA filler will naturally be broken down and absorbed by your body over the next 6-12 months, and if you like then you can repeat it again at that point. If you don’t repeat it, then your lips will return to their natural pre-augmented state.

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What are the best facial chemical exfoliants?

The optimal choice of facial chemical exfoliants depends on individual skin type, concerns, and tolerance. Chemical exfoliants fall into three primary categories: alpha-hydroxy acids (AHAs), beta-hydroxy acids (BHAs), and polyhydroxy acids (PHAs). Each group possesses distinct physicochemical properties and dermatological indications. Below is an evidence-based overview of the most efficacious and commonly recommended agents.


1. Alpha-Hydroxy Acids (AHAs)

AHAs are water-soluble and primarily act on the stratum corneum by weakening the cohesion of corneocytes. Ideal for dry, photodamaged, or dull skin.

Common AHAs:

  • Glycolic Acid
    • Molecular weight: 76 Da (smallest, most penetrative AHA)
    • Effects: Enhances collagen synthesis, reduces hyperpigmentation, improves texture
    • Evidence: Clinical trials show significant improvement in photoaged skin with concentrations of 8–20% (Stiller et al., 1996)
  • Lactic Acid
    • Molecular weight: 90 Da (larger, gentler than glycolic)
    • Effects: Hydrates while exfoliating, suitable for sensitive or rosacea-prone skin
  • Mandelic Acid
    • Molecular weight: 152 Da (aromatic AHA with slow penetration)
    • Effects: Antibacterial properties, well-tolerated in acne and sensitive skin
    • Evidence: Demonstrated efficacy in treating inflammatory acne and melasma (Fabbrocini et al., 2009)

2. Beta-Hydroxy Acids (BHAs)

BHAs are lipid-soluble, allowing them to penetrate sebaceous follicles, making them particularly effective for acne-prone or oily skin.

Primary BHA:

  • Salicylic Acid
    • Mechanism: Keratolytic, comedolytic, and anti-inflammatory
    • Concentration range: 0.5–2% in OTC products
    • Evidence: Reduces comedones and inflammatory acne lesions (Kligman & Mills, 1972)

3. Polyhydroxy Acids (PHAs)

PHAs are larger molecules that exfoliate more superficially, with humectant properties and antioxidant effects. Suitable for very sensitive or compromised skin (e.g., eczema, post-procedural).

Common PHAs:

  • Gluconolactone
  • Lactobionic Acid

Evidence:

  • PHAs demonstrate comparable efficacy to AHAs with less irritation and added barrier support (Roure et al., 2009)

Top Formulations and Brands (as of 2024)

ProductKey IngredientsBest ForNotes
The Ordinary Glycolic Acid 7% Toning SolutionGlycolic acidNormal to oily skinHigh efficacy at a budget price
Paula’s Choice 2% BHA Liquid ExfoliantSalicylic acidAcne-prone, oily skinGold standard in BHA exfoliation
Drunk Elephant T.L.C. Framboos™ Glycolic Night SerumGlycolic, lactic, salicylic acidCombination skinMultifunctional AHA/BHA blend
Neostrata Bionic Face SerumLactobionic acidSensitive, aging skinHigh tolerability with antioxidant benefit
Allies of Skin Mandelic Pigmentation Corrector Night SerumMandelic, lactic, kojic acidHyperpigmentationSynergistic formulation targeting melasma

Selection Guidelines by Skin Type

Skin TypeBest Exfoliant TypeRecommended Ingredient
Dry, photodamagedAHAGlycolic or lactic acid
Oily, acne-proneBHASalicylic acid
SensitivePHA or mandelic acidGluconolactone, mandelic acid
HyperpigmentedAHA + brightenersGlycolic + kojic or azelaic acid

Safety and Usage Considerations

  • Frequency: 2–3 times/week for most; daily use requires careful barrier protection.
  • Sun protection is mandatory, as exfoliation increases photosensitivity.
  • Avoid combining with retinoids or ascorbic acid without dermatological oversight, due to increased irritation risk.

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