COMPOSITION FOR COSMETIC TATTOO LIGHTENING AND METHOD OF USING SAME
20220354763 · 2022-11-10
Inventors
Cpc classification
International classification
Abstract
An enhanced alkaline pigment lightening suspension formulation for fading of unwanted cosmetic tattoos is proposed. The improved formulation of the claimed chemical tattoo lightening suspension is additionally complemented with a suggested neutralizing technique. The proposed innovative method includes the application of alkaline solution followed by an acid solution to reduce side effects. Additionally, a unique method of administration of the post-removal skin rehabilitation is proposed. The treatment is proven effective in scar reduction and consists of the administration of percutaneous collagen induction treatments following the aforementioned tattoo lightening treatments.
Claims
1. A composition for fading of cosmetic tattoo, comprising: isopropanol, triethanolamine, Calcium oxide, Zinc oxide, Magnesium Oxide, propylene glycol, silicon dioxide, ethyl cellulose and deionized water.
2. The composition of claim 1, wherein the composition consists of (by weight): 27.15% of deionized water, 56.6% isopropanol, 3% of triethanolamine, 7% of Calcium oxide, 1% of Zinc oxide, 0.5% of Magnesium Oxide, 4% of propylene glycol, 0.5% silicon dioxide, 0.25% ethyl cellulose.
3. A method of neutralization of fading suspension, systematic lightening of cosmetic tattoo and rehabilitation of skin scarring due to cosmetic tattoo application or/and removal attempts by using a composition comprising: isopropanol, triethanolamine, Calcium oxide, Zinc oxide, Magnesium Oxide, propylene glycol, silicon dioxide, ethyl cellulose and deionized water.
4. The method of claim 3, wherein the composition consists of (by weight): 27.15% of deionized water, 56.6% isopropanol, 3% of triethanolamine, 7% of Calcium oxide, 1% of Zinc oxide, 0.5% of Magnesium Oxide, 4% of propylene glycol, 0.5% silicon dioxide, 0.25% ethyl cellulose.
Description
BRIEF DESCRIPTION OF THE DRAWINGS:
[0024]
[0025]
[0026]
[0027]
[0028]
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
Ingredients Included in the Proposed Composition
[0029]
TABLE-US-00001 CAS Mass IUPAC of Registry (g) per the ingredient number EC code Molecular formula Percentage 1 L Deionized Water 7732-18-5 231-79-2 H2O 27.15 271.5 Isopropanol 67-63-0 200-661-7 C3H8O 56.6 566 Triethanolamine 102-71-6 203-049-8 (HOCH2CH2)3N 3 30 Calcium Oxide 1305-78-8 215-138-9 CaO 7 70 Zinc Oxide 1314-13-2 215-222-5 ZnO 1 10 Magnesium Oxide 1309-48-4 215-171-9 MgO 0.5 5 Propylene Glycol 57-55-6 200-338-0 C3H8O2 4 40 Silicon Dioxide 7631-86-9 231-545-4 SiO2 0.5 5 Ethyl Cellulose 9004-57-3 618-384-9 C6H7O2(OR1)(OR2) 0.25 2.5 *where R1 and R2 may be any of the following: —H or —CH2CH3
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
Advantages of the Invented Composition and Method
[0030] The Composition Performance Improvement:
[0031] A small amount of propylene glycol has been added to keep the products from melting in high heat or from freezing during the avia shipment. Propylene glycol also helps active ingredients of the composition penetrate the epidermis.
[0032] Aerosil, or amorphous anhydrous colloidal silicon dioxide (used in pharmaceutical products), was added as a viscosity increasing agent to thicken and thixotropize the suspension and as well as an anti-setting, anti-sagging agent.
[0033] Ethyl cellulose (widely used in pharmaceutical compositions) was added as a binding and thickening agent. Its coating properties allow it to serve as a disperser for the mineral compounds used in the composition.
[0034] As a result of the abovementioned implemented changes, the suspension obtained has a smooth, creamy texture (suitable for the precise local applications) and is stable in time and impervious to temperature fluctuations during shipments.
[0035] The Innovative Method of the Application:
[0036] The well-balanced new composition softens collagen fiber and does not require any mechanical application. Topical application for 5-10 minutes (depending on the client's skin texture and thickness) allows softening of the epidermal layers. Wiping the treated area with a water-soaked cotton pad is the second step in the described method.
[0037] Clinical studies show that topical treatment of alkaline burns with a weak acid results in more rapid tissue neutralization, reduction of injury, and improved epithelial regeneration. Based on this evidence, the proposed new tattoo-lightening method relies on immediate topical introduction of a mild solution of tricarboxylic acid on the area where the alkaline suspension was previously applied. It is recommended to then keep the treated area moist with the acid solution applied for one minute before wiping dry with a clean cotton pad. This step will assure the neutralization of any residual substance in the treated area and minimize the possibility of side effects.
[0038] After the neutralization phase has been completed, treatment with derma pen, using the nano module, is indicated, to peel off the keratinocytes disassembled by the fading composition application.
[0039] Dexapanthenol-containing creams are highly effective for skin barrier repair after alkali-induced irritation. An aftercare instruction manual with a list of dexapanthenol-containing pharmaceutical creams is developed and will be suggested to the treated customers.
[0040] A clinical study has found a notable increase of collagen and elastin following percutaneous collagen induction therapy. Compared with collagen in the scar tissues, the collagen in the treated area was cross-linked, the stratum corneum was structured normally, and a thickening of the epidermis of about 40% was observed. The method being suggested includes a sequence of follow-up treatments of percutaneous collagen induction therapy to the area previously treated with the tattoo fading suspension to enhance the skin texture.
[0041] Through the gathering of clinical data and practical experience, the afore-described method was developed and named “REVITAL”. REVITAL is potentially an effective approach in fading unwanted cosmetic tattoo and reviving the skin to regain normal texture and function.
EXAMPLES OF USE OF THE INVENTED METHOD AND COMPOSITION
[0042] Volunteers seeking tattoo-fading treatment were enrolled in a study that resulted in outcomes described hereafter. The suggested composition and method for fading unwanted cosmetic tattoo is effective for the following needs:
[0043] Lightening of fresh (one month since application) cosmetic tattoo and correcting mistakes made by the tattoo artist see in
[0044] Lightening of old cosmetic tattoo; 2-6 years after application. See in
[0045] Extraction of pigment substance from the excess of collagen formed above its surface due to unsuccessful laser tattoo removal, and reducing scarring formed as a result of aggressive application of cosmetic tattoo, see
[0046] Moreover, the words “example” or “exemplary” are used herein to mean serving as an example, instance, or illustration. Any aspect or design described herein as “exemplary” is not necessarily to be construed as preferred or advantageous over other aspects or designs. Rather, use of the words “example” or “exemplary” is intended to present concepts in a concrete fashion. As used in this application, the term “or” is intended to mean an inclusive “or” rather than an exclusive “or”. That is, unless specified otherwise, or clear from context, “X employs A or B” is intended to mean any of the natural inclusive permutations. That is, if X employs A; X employs B; or X employs both A and B, then “X employs A or B” is satisfied under any of the foregoing instances. In addition, the articles “a” and “an” as used in this application and the appended claims should generally be construed to mean “one or more” unless specified otherwise or clear from context to be directed to a singular form.