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Recombinant Collagen Peony Revitalizing Spray

Recombinant Human Type lll Collagen itself has good moisturizing properties and can help the skin lock in moisture. And can quickly repair damaged skin.Ingredients such as paeonol contained in peony root can inhibit the activity of tyrosinase, reduce the production of melanin, and make the skin whiter and more translucent. The antioxidant capacity of peony extract can also delay skin aging.
  • Anti-wrinkle repair, enhance firmness and luster, improve loose fine lines.
  • Deep antioxidant, combat dullness, even out skin tone.
  • Hydration and moisture retention, refine pores, skin delicate and radiant.
  • Moisturizing enhancement, strengthen antioxidants, skin texture is hydrated and resilient.
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Product Details

Product ID SPRAY-H-008
Key Benefits Repair + Soothe + Hydrate + Anti-wrinkle + Firming
Target Audience women&men skincare
Package 1 box*1.67 fl.oz. / 50mL
Shelf life 3 years
MOQ 50kg
Delivery Time 40-60 days(Once the design draft is finalized)

 

Key Ingredients

Paeonia Suffruticosa Flower Water, Recombinant Human Type lll Collagen, Paeonia Suffruticosa Root Extract, Paeonia Suffruticosa Root Water, Trehalose, Sodium Hyaluronate, Tocopheryl Acetate

Suitable for

Mature skin; Anti-oxidation and anti-wrinkle; Essence care; Target audience: those seeking delicate and radiant skin

Indications

Dry, sensitive skin

Dull and dry skin condition

Revitalizing

Effects

Hydrate, comfort and tone skin,leave skin healthy and youthful looking.

Instructions

Spray onto the skin in a fine mist. Leave on for 2 to 3 minutes, then gently pat dry. Use as often as necessary.

Product Efficacy Report

  1. Repair

Study Protocol: A total of 30 Asian (Chinese) subjects—men and women aged 22 to 60—were recruited for the test (30 subjects enrolled, 30 completed the study, resulting in a 100.00% completion rate). Instrumental measurements were used to compare changes in skin Transepidermal Water Loss (TEWL) values—assessed against an untreated control site—at baseline (prior to application) and at 2, 4, and 6 hours after a single application of the test product, thereby evaluating the product’s repair efficacy.

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 29.01%, 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 33.95% 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 In the 30 subjects, the transepidermal water loss (TEWL) value of the skin in the test area decreased by 35.19%, while that in the control area decreased by 23.72%; a significant difference was observed between the two groups.
conclusion Under the test conditions, the test sample exhibits reparative efficacy.

Statistical analysis was performed using SPSS 26.0. For the comparison of samples before and after use, a difference analysis was conducted on the mean values: a paired t-test was used when both datasets followed a normal distribution, whereas a rank-sum test was used when they did not.

For the comparison between the sample and the control, a difference analysis was conducted on the calculated differences: a paired t-test was used when both datasets followed a normal distribution, whereas a rank-sum test was used when they did not.

The statistical significance level was set at P < 0.05, indicating statistical significance within a 95% confidence interval.

Regarding the association between the test parameter 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 evaluated by measuring the improvement in the TEWL rate in subjects before and after using the sample.

A lower measured value indicates reduced transepidermal water loss and superior skin barrier function, thereby demonstrating the repair efficacy of the sample.

  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 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 are diluted with TESCA buffer solution according to specific requirements, and components are added as shown in the table below. The setup includes: Well 1 Test Group (sample group and positive control group), Well 2 Test Control Blank Group, Well 3 Negative Control Group, and Well 4 Negative Control Blank Group. Upon completion of the reaction, the reaction mixtures are transferred to corresponding 96-well plates (with three replicates per group), and absorbance (OD value) is measured at 410 nm using a microplate reader.

② Hyaluronidase inhibition rate: Components are added to the sample group and positive control group, which have been diluted with purified water according to specific requirements.

③ In vitro moisturizing efficacy evaluation: Three replicates are set up for each test group. Negative and positive control groups are included simultaneously; glycerol is used for the positive control group, and purified water for the negative control group. The procedure is identical to that of the sample group: Take a dry, stoppered glass weighing bottle and place it in a desiccator maintained at 25°C ± 1°C (with indicating silica gel desiccant at the bottom) one day prior to the test; accurately weigh it (m0). At room temperature, pipette 1 mL of nutrient agar into the weighing bottle; after solidification, add 200 μL of the test sample and accurately weigh the total mass (m1). Place the bottle in the desiccator containing desiccant for a total duration of t = 8 hours. For both the sample and control groups, remove the weighing bottle from the desiccator at 2, 4, 6, and 8 hours, secure the lid, and accurately weigh it (mt).

Moisturizing performance was evaluated based on the percentage of weight loss due to drying. Test conclusions are as follows:

① Under the test conditions, the elastase inhibition rate of the sample (BONNEHEURE Recombinant Collagen & Peony Repairing Anti-Wrinkle Essence, 10% concentration) was 54.8% ± 1.5% (P < 0.05, indicating a significant difference). The sample demonstrated inhibitory activity against elastase, suggesting that it possesses anti-wrinkle and skin-firming properties.

②Under the test conditions, the hyaluronidase inhibition rate of the sample (BONNEHEURE Recombinant Collagen & Peony Repairing Anti-Wrinkle Essence, 10% concentration) was 74.9% ± 1.4% (P < 0.05, indicating a significant difference). The sample demonstrated inhibitory activity against hyaluronidase, suggesting that it possesses soothing properties.

③ Under the test conditions, 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 Repairing Anti-Wrinkle Essence) possesses moisturizing properties.

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