Core Ingredient: Crosslinked Dextran
Specification: 0.5mL, 0.75mL, 1.0mL, 1.25mL, 1.5mL; supplied with 27G needles
Indications: This product is applicable for injection into the middle to deep layers and subcutaneous of the facial dermal tissue to correct moderate to severe wrinkles and restore tissue volume
Injection Layer: Middle to deep layers and subcutaneous of the facial dermal tissue
Efficacy: Instant fill and long-lasting collagen stimulation
Suitable For: People who need long-term improvement of skin contours
Dextran is a polymer of glucose molecules found in various plants and fungi, such as mushrooms, yeast, and algae. lt is a white bead-like microsphere with a porous network structure.
Dextran has excellent biocompatibility and drug-carrying capacity, making it a commonly used filling material. In addition, dextran can promote wound healing and help slow down skin aging.

Dextran can be used as a plasma infusion agent and is a recognized safe substance. As a polysaccharide similar to hyaluronic acid, it has good biocompatibility and hydrophilicity. It is 100% decomposed into H2O and CO2 in the body and disappears. The decomposition time
is about 1-2 years. At the same time, its endotoxin levels are low, indicating its high biosafety.

1. Physical Support
By injecting cross-linked dextran gel into the dermal layer or subcutaneous tissue of the skin,
it achieves immediately visible improvement effects utilizing its physical supporting properties.
The network structure of dextran gel degrades relatively slowly in the body, allowing it to maintain long-term filling effects and improve skin condition.
2. Biostimulation of Collagen Regeneration
Once dextran enters the human body, it stimulates macrophages and fibroblasts, promoting
the generation of new collagen and new blood vessels.
·The dextran is eventually enveloped by collagen, forming collagen capsules.
·The dextran itself will decompose, but the collagen capsules still have a space-filling effect
that can last for more than 3 years.

High Safety
Natural Dextran: Singderm® Volast, a natural polysaccharide, can be completely metabolized by the human body and it can exhibit excellent biocompatibility, minimizing allergic reactions and rejections.
Soft Gel Texture
Compared to other regenerative materials, Singderm® Volast prevents embolism and nodule formation.
Self-Crosslinking Technology
This ensures no residual crosslinking agents in Singderm® Volast, guaranteeing product purity.
Natural Results: Soft texture, providing a natural look and feel after filling.
Superior Support: Singderm® Volast with high elasticity (1000-1200Pa) delivers excellent support,
particularly suitable for deep layer injections and contouring. Meanwhile, it has low extrusion force (5-10N) for precise, painless injections.
Dual-Action Rejuvenation
Stimulates Collagen Regeneration:
Promotes the production of type I and type III collagen, improves skin tightness and smoothness.
In addition, the product has anti-inflammatory effects, reducing inflammation after injection.
Immediate Filling: Due to its viscoelastic properties, a small amount of injectoin can significantly
improve sunken areas of the face, providing an immediate lifting effect.
Long-Term Efficacy
While dextran degrades in 1-2 years, Singderm® Volast can induce collagen capsules sustain effects for over 3 years, ensuring durable results.
Over 3 Years
Cheeks
Nose base
Nasolabial folds
Marionette lines
Chin

1. The person who are allergic to any component of the product are prohibited for using.
2. It is prohibited for using in patients under 18 years.
3. It is prohibited for pregnant or lactating women.
4. It should be used with caution for those with a tendency to keloid formation or a history of hypertrophic scar.
5. Patients with atrophic skin diseases should use this product with caution.
6. Those with capillary dilation should use this product with caution.
7. People who are using anticoagulants such as heparin and aspirin should use this product with caution.
1. Intradermal injection carries a risk of infection, consistent with general precautions for dermal injections. Therefore, local disinfection should be performed before injection, and the injection process should follow the aseptic operation regulations of surgical treatment.
2. For patients taking medications that affect platelet function, injections may cause bruising or bleeding at the injection site.
3. Prevent mixing with any other injectable implant products.
4. The total injection volume of each injection should not exceed 3 mL.
5. The medical effect and retention time are affected by the following factors: the nature of the defect itself, the degree of correction, the depth of implantation, the physicians’ injection technique, and individual physical differences
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