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SCULPTRA

Price range: EGP12,000.00 through EGP24,000.00

  • الحجم: البوكس [ عدد 2 فيال * 150 مليجرام ]
  • بلد الصنع: [الولايات المتحدة]
  • ضمان التخزين: مخزن تحت رقابة حرارية
SKU: N/A Categories: ,

SCULPTRA® (Box of 2 Vials / 2 x 5 mL) | Galderma

Short Description

The standard clinical multi-vial presentation of the pioneer Poly-L-Lactic Acid (PLLA) collagen biostimulator, containing two sterile vials (300 mg total active PLLA microparticles). Calibrated for bilateral full-face structural restoration, multi-planar vector lifting, or combined face-and-neck biostimulation, the 2-vial kit yields 16 to 18 mL of injectable suspension, providing practitioners with a complete, single-session treatment unit to trigger de novo Type I neocollagenesis lasting 24+ months.

Detailed Description

The SCULPTRA® 2-Vial Presentation (CE-marked European and international standard packaging) represents the primary clinical unit utilized by aesthetic physicians for global facial biorejuvenation. Because structural age-related volume loss and elastosis affect facial anatomy symmetrically across deep fat compartments, temporal hollows, and mandibular vectors, single-vial treatments frequently result in under-correction for mature patients. The 2-vial kit supplies the total bio-active load required to treat both facial halves comprehensively within a single session.

Each box contains two individually sealed, sterile glass vials containing:

  • 150 mg of Poly-L-Lactic Acid (PLLA) microparticles (300 mg total per box)

  • 90 mg of Sodium Carboxymethylcellulose (CMC) carrier (180 mg total per box)

  • 127.5 mg of Non-pyrogenic Mannitol (255 mg total per box)

When reconstituted according to modern immediate-hydration protocols, each vial yields approximately 8.0 to 9.0 mL of homogeneous microparticle suspension (yielding 16.0 to 18.0 mL of total working volume per box). This dual-vial volume allows practitioners to address the entire kinetic facial framework—temples, submalar hollows, pre-auricular zones, and jawline borders—without compromising on product dispersion density or biostimulatory coverage.

Bilateral Facial Dosing & Anatomical Mapping (2-Vial Session)

A standard full-face session utilizing the 2-vial kit allocates 1 vial (8–9 mL) per facial side (Left vs. Right), ensuring balanced bilateral symmetry and homogeneous microparticle distribution:

Anatomical Zone Volume Allocation (Per Side) Delivery Plane & Technique Clinical Endpoint
Temporal Fossa 1.0 – 1.5 mL Supraperiosteal depot (needle on bone) or sub-fascial fan Restores temple concavity and lateral orbital vector support
Zygomatic & Submalar Hollows 2.5 – 3.0 mL Subcutaneous plane; 22G/25G cannula retrograde fanning Lifts midface tissue laxity; softens deep medial cheek hollows
Pre-Auricular & Lateral Cheek 2.0 – 2.5 mL Subcutaneous cross-hatching or retrograde vector threading Redensifies thinning skin envelope; softens accordion smile lines
Mandibular Angle & Pre-Jowl Sulcus 1.5 – 2.0 mL Deep subcutaneous plane anterior and posterior to the jowl Sharpens linear jawline definition; effaces pre-jowl depression
Alternative Protocol: Face + Neck Vial 1: Full Face (bilateral) / Vial 2: Transverse neck rings and platysmal bands (hyperdiluted 1:2) Subdermal retrograde fanning with 25G (70 mm) cannula Rejuvenates severe cervical skin crepeyness simultaneously

Simultaneous Reconstitution Protocol (2-Vial Preparation)

To ensure clinical efficiency and particle homogeneity across both facial sides:

[Vial 1 (150 mg PLLA)] + 5.0 mL SWFI ──┐
                                       ├─► [Vigorous Shake 1 Min] ─► Stand 10 Min ─► + 1-2 mL 2% Lindo per vial
[Vial 2 (150 mg PLLA)] + 5.0 mL SWFI ──┘
  1. Aseptic Access: Remove the flip-off caps from both vials and wipe the stoppers with 70% isopropyl alcohol.

  2. SWFI Introduction: Using an 18G draw-up needle on a 10 mL syringe, introduce 5.0 mL of Sterile Water for Injection (SWFI) down the inner glass wall of each vial.

  3. Agitation: Vigorously shake each vial manually for 60 seconds until the lyophilized cake is fully suspended and no dry powder clings to the base or walls.

  4. Hydration Period: Allow both vials to rest undisturbed for 10 to 15 minutes to ensure complete polymer wetting.

  5. Lidocaine Addition: Immediately prior to clinical injection, add 1.0 to 2.0 mL of 2% Lidocaine HCl (with or without epinephrine) to each vial. Gently swirl to mix.

  6. Syringe Loading: Draw the reconstituted suspension into 1 mL or 3 mL Luer-Lock syringes immediately before injection to prevent particle settling. If particles settle in the syringe, invert or roll between palms before extrusion.

The Clinical “Decade Rule” Treatment Staging

In global aesthetic consensus guidelines, the recommended total number of Sculptra vials across an entire multi-session treatment cycle is estimated using the patient’s age:

$$\text{Total Vials Required for Cycle} \approx \frac{\text{Patient Age}}{10}$$
  • Patient in 40s (4 Vials Total):

    • Session 1: 1 Box (2 Vials) — bilateral full face

    • Session 2 (6 weeks later): 1 Box (2 Vials) — structural touch-up and vector reinforcement

  • Patient in 50s (5 Vials Total):

    • Session 1: 1 Box (2 Vials) — structural foundation

    • Session 2 (6 weeks later): 1 Box (2 Vials) — lateral vector lifting and midface redensification

    • Session 3 (6 weeks later): 1 Single Vial — targeted perimeter refinement

  • Patient in 60s+ (6 Vials Total):

    • Session 1: 1 Box (2 Vials)

    • Session 2 (6 weeks later): 1 Box (2 Vials)

    • Session 3 (6 weeks later): 1 Box (2 Vials)

Technical Specifications

Parameter Specification
Product Kit SCULPTRA® (2-Vial Clinic Pack)
Total Active PLLA Content 300 mg per box (150 mg per vial)
Total Inactive Excipients 180 mg Sodium CMC + 255 mg Non-pyrogenic Mannitol
PLLA Particle Morphology 40 – 63 µm crystalline spheroidal microparticles
Packaging Presentation Box containing 2 x sterile glass vials
Total Reconstituted Volume 16.0 to 18.0 mL per box (8.0–9.0 mL per vial)
Injection Instruments 22G / 25G (50–70 mm) blunt-tip microcannulas or 26G needles
Target Injection Planes Deep subcutaneous layer, immediate subdermal plane, or supraperiosteal bone
Recommended Session Gap 4 to 6 weeks between staged sessions
Expected Clinical Duration 24+ months (native Type I collagen matrix remains stable for up to 3 years)
Manufacturer / Origin Galderma Laboratories (Manufactured in Italy / USA)
Regulatory Category US FDA-Approved (PMA) / CE-marked Class III Medical Device / Rx Only

Post-Procedure Care & Patient Compliance

Because two vials deliver 300 mg of solid microparticles across the face, strict mechanical dispersion is critical to prevent focal microparticle clumping:

  • The 5-5-5 Rule: The patient must vigorously massage all treated facial sectors for 5 minutes, 5 times daily, for 5 consecutive days.

  • Hydration & Sunscreen: Advise the patient to avoid direct UV exposure, tanning beds, and high-heat environments (saunas, steam baths) until all acute swelling and needle erythema subside.

  • Delayed Response Expectation: Manage patient expectations by reinforcing that initial fluid fullness resolves within 48 to 72 hours; genuine structural collagen remodeling begins at week 3 and reaches peak clinical projection between months 3 and 6.

Professional Advisory: SCULPTRA® 2-Vial Kit is a prescription-only medical biostimulant intended strictly for certified dermatologists, plastic surgeons, and credentialed aesthetic physicians. Direct injection into the hyper-mobile vermilion lip body, the tear trough / lower eyelid boundary, or the superficial papillary dermis is strictly contraindicated due to the high risk of visible, fibrotic nodule formation.

الحجم

فيال منفرد, بوكس كامل (عدد 2 فيال )

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