Recombinant Collagen Peony Anti-wrinkle Mask-1
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Recombinant Collagen Peony Anti-wrinkle Mask_1
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Recombinant Collagen Peony Anti-wrinkle Mask

The core material of Recombinant Human Type lll Collagen could help you rapidly replenish the collagen, make your skin like the baby skin.
Peony flower water is rich in polysaccharides and other nutrients, which can help the skin lock in moisture, keep the skin hydrated, and relieve problems such as dryness and tightness.
  • Intensive fine lines, emergency anti-aging, skin regains elasticity and firmness.
  • Intensive antioxidant brightening, emergency remedy for fatigue and dullness from lack of sleep.
  • Repairs the barrier, soothes sensitivity, enhances anti-aging absorption and effectiveness.
  • Deep hydration, strengthens antioxidants, skin texture is more hydrated and resilient.
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Product Details

Product ID MASK-H-008
Key Benefits Repair + Soothe + Hydrate + Anti-wrinkle + Firming
Target Audience women&men skincare
Package 1 pack*0.88fl.oz./25mL*5pcs
Shelf life 3 years
MOQ 125kg
Delivery Time 40-60 days(Once the design draft is finalized)

 

Key Ingredients

Paeonia Suffruticosa Flower Water, Recombinant Human Type lll Collagen, Ceramide NP, Paeonia Suffruticosa Root Extract, Paeonia Suffruticosa Root Water, Sodium Hyaluronate, Sodium Hyaluronate, Arginine

Suitable for

Staying up late causes skin to sag; Deep anti-wrinkle; Emergency skin rejuvenation; Mature skin repair group

Indications

Dullness and dryness

Fine lines and wrinkle

Uneven skin tone

Effects

Repair and hydrate skin, smooth fine lines; restore it to plump, delicate and radiant skin.

Instructions

Apply it on the face with one piece at one time. After 15-20minutes,remove it.

Product Efficacy Report

  1. Repair

Study Protocol: A total of 30 Asian (Chinese) male and female subjects aged 22–60 were recruited for the test (30 enrolled, 30 completed; completion rate: 100.00%). The repair efficacy of the submitted sample was evaluated by comparing changes in skin Transepidermal Water Loss (TEWL) values—measured via instrumentation—against a blank control at baseline (prior to application) and at 2, 4, and 6 hours after a single application of the test sample.

Comparison of Transepidermal Water Loss (TEWL) Values
2 hours after using the sample In the 30 subjects, the transepidermal water loss (TEWL) value of the skin in the test area decreased by 27.27%, while that in the control area decreased by 23.08%; a significant difference was observed between the two groups.
4 hours after using the sample In the 30 subjects, the transepidermal water loss (TEWL) value decreased by 30.91% in the test area and by 23.72% in the control area; a significant difference was observed between the two groups.
6 hours after using the sample Among the 30 subjects, the transepidermal water loss (TEWL) value in the test skin area decreased by 32.12%, while the TEWL value in the control area decreased by 23.72%; a significant difference was observed between the two groups.
conclusion Test results indicate that, under the experimental conditions, the test sample possesses reparative properties.

Statistical analysis of the data was performed using SPSS 26.0 to evaluate the efficacy of the test parameters. A comparative analysis of the mean values ​​before and after product application was conducted. A paired t-test was used to analyze differences between the two datasets when both followed a normal distribution; a rank-sum test was used when they did not. Statistical significance was defined as P < 0.05 (95% confidence interval).

Regarding the correlation between the test parameters and the efficacy claim, “repair” refers to the ability to help maintain the treated area in a normal state. Transepidermal water loss (TEWL) serves as an indicator of skin barrier function; therefore, the repair efficacy of the sample can be assessed by measuring improvements in the TEWL rate before and after application. A lower measured value indicates reduced transepidermal water loss and superior skin barrier function, thereby demonstrating the sample’s repair efficacy.

  1. Anti-wrinkle, firming, soothing, moisturizing

This test employs a biochemical method—specifically an elastase inhibition assay—to measure the sample’s ability to inhibit enzyme activity, thereby evaluating the anti-wrinkle and firming efficacy of cosmetic raw materials and finished products.

This test evaluates the anti-allergic activity of samples based on their hyaluronidase inhibition rate; a higher inhibition rate indicates stronger anti-allergic activity.

This test evaluates the soothing efficacy of cosmetics and raw materials by measuring the sample’s ability to inhibit hyaluronidase activity.

This test establishes an in vitro protocol to assess water-retention capabilities; by measuring the sample’s water-retention performance in a dry environment, the moisturizing efficacy of cosmetics and raw materials is evaluated.

Test Methods:

① Anti-wrinkle and firming (Elastase inhibition rate): Samples were diluted with TESCA buffer solution according to specified ratios. Components were added as shown in the table below, establishing the following groups: Well 1 (Test Group: sample + reagents), Well 2 (Test Control Blank: sample + buffer/solvent without enzyme), Well 3 (Negative Control: enzyme + substrate), and Well 4 (Negative Control Blank: buffer/solvent without enzyme or substrate). Upon completion of the reaction, the reaction mixtures were transferred to a 96-well plate (with three replicates per group), and absorbance (OD value) was measured at 410 nm using a microplate reader.

② Hyaluronidase inhibition rate: Components were added to the sample group and positive control group, both of which had been diluted with purified water according to specified ratios.

③ In vitro moisturizing efficacy evaluation: Three replicates were set up for each test group. Negative and positive control groups were included alongside the test groups; glycerin was used for the positive control, and purified water for the negative control. The procedure was identical for all groups: A clean, dry, stoppered glass weighing bottle was placed in a desiccator (maintained at 25°C ± 1°C with indicating silica gel desiccant at the bottom) for 24 hours prior to the test, and its weight (m0) was accurately recorded. At room temperature, 1 mL of nutrient agar was pipetted into the weighing bottle; after solidification, 200 μL of the test sample was added, and the total mass (m1) was accurately recorded. The bottle was then placed in the desiccator containing desiccant for a total duration of t = 8 hours. For both the sample and control groups, the weighing bottle was removed from the desiccator at 2, 4, 6, and 8-hour intervals; the lid was secured, and the weight (mt) was accurately recorded.

Test Conclusions:

① Under the conditions of this test, the elastase inhibition rate of the sample (BONNEHEURE Recombinant Collagen & Peony Repair, Anti-Wrinkle & Fine Line-Reducing Mask, 10% concentration) was 65.0% ± 1.6% (P < 0.05, indicating a significant difference). It is concluded that the sample inhibits elastase, demonstrating anti-wrinkle and skin-firming efficacy.

② Under the conditions of this test, the hyaluronidase inhibition rate of the sample (BONNEHEURE Recombinant Collagen & Peony Repair, Anti-Wrinkle & Fine Line-Reducing Mask, 10% concentration) was 62.0% ± 1.6% (P < 0.05, indicating a significant difference). It is concluded that the sample inhibits hyaluronidase, demonstrating soothing efficacy.

③ Under the conditions of this test, the results showed that the percentage of weight loss in the sample group at 2, 4, 6, and 8 hours was lower than that of the negative control group, indicating that the sample (BONNEHEURE Recombinant Collagen & Peony Repair, Anti-Wrinkle & Fine Line-Reducing Mask) possesses moisturizing efficacy.

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