Cosmetic compositions and methods providing enhanced penetration of skin care actives
A technology of cosmetic composition and active substance, which is applied in the direction of cosmetics, cosmetic preparations, dressing preparations, etc., and can solve the problems that the effects are rarely studied or determined
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Embodiment 1
[0115] Example 1 - Nicotinamide / Glycerol Assay
[0116] An in vitro skin penetration study was performed to characterize the effect of glycerol on the in vitro skin penetration of radioisotope-labeled niacinamide in several cosmetic compositions. The kinetics of skin penetration of radiolabeled nicotinamide in vitro was determined at a fixed glycerol concentration, and the effect of glycerol and nicotinamide product concentrations on skin penetration of radiolabeled nicotinamide and glycerol over 6 hours was determined. Table 5 provides a general description of the four types of cosmetic compositions tested.
[0117] Table 4: General description of the substrates used in the in vitro skin penetration assay
[0118]
[0119] Blade-thick cadaver skin was purchased from AlloSource (Englewood, CO). Tritiated water was obtained from PerkinElmer (Boston, MA), while 14 C Nicotinamide was purchased from American Radiochemicals (St. Louis, MO). For all studies, blade-thick h...
Embodiment 2
[0127] Example 2 - Niacinamide / Glycerin / Cetyl Alcohol, Niacinamide / Glycerin / Octyl Salicylate Determination
[0128] Cosmetic compositions shown in Table 5 were prepared.
[0129] table 5
[0130]
[0131] Next, the skin samples (cadaveric or porcine skin) were fixed in a standard Franz-type diffusion cell (0.79 cm 2 surface area). Six replicates were prepared for each composition test group. The receiver compartment was filled with 5 mL of phosphate buffered saline solution (PBS-pH 7.4) containing 1% polysorbate-20 and 0.02% sodium azide, and the skin was allowed to equilibrate for two hours. pool for treatment group randomization based on 3 h 2 O flux was performed (administered 150 μl 3 H2O for five minutes, remove them and collect receiver fluid after 60 minutes). Diffusion cells were randomized by ordering each pool according to water flux and spreading the pools across the treatment groups such that each group included cells spanning the range of observed wa...
Embodiment 3
[0133] Example 3 - Niacinamide / Glycerin / Glyceryl Ether / Ester / Octyl Salicylate Determination
[0134] The cosmetic compositions shown in Table 6 were prepared in the same manner as described in Example 2 above.
[0135] Table 6
[0136]
[0137]
[0138] Generally using the same testing procedure as described in Example 2, the DPMs for the individual compartments of each pool were blank corrected and summed to obtain the total recovered radiolabel value for a given pool. The DPM for each compartment was then normalized to the total recovered radiolabel value to obtain the "percent recovered radiolabel" parameter for each compartment (separate receiver collections, epidermis, dermis, and swabs for mass balance ). The cumulative receiver value for each collection time point is calculated as the sum of the individual collections for that time point, where the total receiver value is calculated as the sum of all the individual collections. The percent total recovery va...
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