| Product ID | MASK-L-010 |
|---|---|
| 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 | 50kg |
| Delivery Time | 40-60 days(Once the design draft is finalized) |
Collagen, Aqua, 1,3-Butylene Glycol, 1,2-Pentylene Glycol, Hydroxyacetophenone, 1,2-Hexanediol, Sodium Hyaluronate, Trehalose, Arginine, Carbomer, Allantoin
Multi-issue skin; Sensitive skin anti-aging; Groups in urgent need of barrier repair
Accelerates skin renewal after laser treatment.
Soothes skin after sun exposure or physical skin damage.
Provides care for sensitive, dull, and irritated skin.
Supports vulnerable skin.
Improves skin condition for post-operative therapy
Lowers the risks after a laser procedure
Fast recovery the skin after laser procedures
Keeps skin moist and prevents it from drying out
Delaying aging, smoothing the skin
Cleanse and dry face thoroughly. Remove mask from packaging and apply to fit the contours of your face.
Leave on for 20-30 minutes and then remove gently. Massage the remaining essence into face and neck.
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 the rate of hyaluronidase inhibition; 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 performance; by measuring the sample’s ability to retain moisture 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 specified ratios. Components are then added as shown in the table below, dividing the setup into: 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 the 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 specified ratios.
③ In vitro moisturizing efficacy evaluation: Three replicates are set up for each test group. Negative control groups (using purified water) and positive control groups (using glycerin) are included, with procedures identical to those for the sample group: Take a dry, stoppered glass weighing bottle and place it in a suitable desiccator maintained at 25°C ± 1°C (with indicating silica gel desiccant at the bottom) the day before 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 mass (m1). Place the bottle in the desiccator containing desiccant for a total duration of t = 8 hours. For both 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).
④ In vitro moisturizing efficacy evaluation: Three replicates are set up for each test group. Negative control groups (using purified water) and positive control groups (using glycerin) are included, with procedures identical to those for the sample group: Take a dry, stoppered glass weighing bottle and place it in a suitable desiccator maintained at 25°C ± 1°C (with indicating silica gel desiccant at the bottom) the day before the test; accurately weigh it (m0). At room temperature, pipette 1 mL of nutrient agar into a weighing bottle; once solidified, add 200 μL of the test sample and accurately weigh the assembly (m1). Place the bottle in a desiccator containing a 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 the bottle (mt).
Test Conclusions:
① Under the conditions of this test, the elastase inhibition rate of the sample “BONNEHEURE Recombinant Collagen Multi-Effect Repair Mask” (10% concentration) was 73.7% ± 0.8% (P < 0.05, indicating a significant difference). It is concluded that the sample inhibits elastase, demonstrating anti-wrinkle and firming properties.
② Under the conditions of this test, the hyaluronidase inhibition rate of the sample “BONNEHEURE Recombinant Collagen Multi-Effect Repair Mask” (10% concentration) was 57.0% ± 0.8% (P < 0.05, indicating a significant difference). It is concluded that the sample inhibits hyaluronidase, demonstrating soothing properties.
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 Essence” possesses moisturizing properties.
The study recruited a total of 33 healthy Asian (Chinese) male and female subjects; data from all 33 subjects were valid, resulting in a validity rate of 100.00%. Instrumental measurements were used to compare changes in skin parameters before and after the use of the test sample, thereby evaluating the repair efficacy of the submitted product.
| Skin transepidermal water loss (TEWL) value | |
| 2 hours after using the sample | In the 33 subjects, the transepidermal water loss (TEWL) value of the skin in the test area decreased by 37.79%, while that in the control area decreased by 27.39%; a significant difference was observed between the two groups. |
|---|---|
| 4 hours after using the sample | In the 33 subjects, the transepidermal water loss (TEWL) value of the skin in the test area decreased by 40.12%, while that in the control area decreased by 28.03%; a significant difference was observed between the two groups. |
| 6 hours after using the sample | In the test areas of the 33 subjects, the transepidermal water loss (TEWL) value decreased by 46.51%, whereas in the control areas, it decreased by 33.76%; a significant difference was observed between the two groups. |
| conclusion | The results indicate that the test samples exhibit reparative effects after 2, 4, and 6 hours of use. |
| Moisture content of the skin’s stratum corneum | |
| 2 hours after using the sample | In the 33 subjects, the stratum corneum moisture content increased by 65.11% in the test areas and by 20.83% in the control areas; a significant difference was observed between the two groups. |
| 4 hours after using the sample | In the 33 subjects, the stratum corneum moisture content in the test areas increased by 41.03%, while that in the control areas increased by 17.19%; a significant difference was observed between the two groups. |
| 6 hours after using the sample | In the 33 subjects, the moisture content of the stratum corneum in the test areas increased by 38.57%, while that in the control areas increased by 20.83%; a significant difference was observed between the two groups. |
| Skin Hemoglobin EI Value | |
| 2 hours after using the sample | In the 33 subjects, the skin hemoglobin EI value in the test area decreased by 18.90%, while that in the control area decreased by 10.94%; a significant difference was observed between the two groups. |
| 4 hours after using the sample | In the 33 subjects, the skin hemoglobin EI value decreased by 24.02% in the test area and by 11.70% in the control area; a significant difference was observed between the two groups. |
| 6 hours after using the sample | In the 33 subjects, the skin hemoglobin EI value in the test area decreased by 24.80%, while that in the control area decreased by 13.21%; a significant difference was observed between the two groups. |
| conclusion | The results indicate that the test samples exhibit reparative effects after 2, 4, and 6 hours of use. |
Statistical analysis was performed using SPSS 26.0. The test data were first assessed for normal distribution; a t-test was employed for normally distributed data, while a rank-sum test was used for non-normally distributed data. A significance level of P<0.05 was adopted, indicating statistical significance within a 95% confidence interval.
Regarding the relationship 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 a sample can be evaluated by measuring changes in the subject’s TEWL rate, hemoglobin (EI) value, and stratum corneum moisture content before and after application. Lower measured values indicate reduced transepidermal water loss and superior skin barrier function, thereby demonstrating the sample’s repair efficacy.
Molecular
HIGH-PERFORMANCE SKINCARE SOLUTIONS
Powered by recombinant human Type III collagen, we provide professional skincare solutions for skin repair, barrier care, anti-aging and customized OEM/ODM development.
News