This product is a bio-material for tissue restoration. A syringe is filled with 0.3% lidocaine hydrochloride with a derivative of cross-linked sodium hyaluronate originated from bacterial fermentation gel.
It is intended to be used for facial tissue augmentation for mid-to-deep dermal implantation for the correction of moderate to severe facial wrinkles and nasolabial folds. The addition of lidocaine provides a pain-relieving eff ect during treatment.
Luxfill Plus is safe by integrating chemical and physical crosslinking and has high viscoelasticity and cohesion. Cross-linking, referring to the binding hyaluronic acid, is done by using BDDE, the most commonly employed crosslinking agent.
Luxfi ll Plus can be used safely by minimizing the amount of BDDE input (about 60% of BDDE used for popular fillers), and minimizing impurities such as BDDE residues that are not completely crosslinked through a strict purifi cation process.
It also uses ingredients listed in the European Directorate for the Quality of Medicines & Healthcare (EDQM) including hyaluronic acid, lidocaine, and BDDE to ensure safety.
In addition, it applies physical crosslinking performed by the High-Density Tapping Process(h-DTP) , a manufacturing system unique to the company, for which a patent has been applied. The h-DTP maintains the high viscoelasticity of the HA filler despite the use of a small amount of crosslinking agent, helping to extend the duration after the procedure.
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