1. Introduction
In recent years, with the continuous development of the social economy, consumers have an increasing demand for cosmetics with whitening properties [
1]. Nicotinamide is an amide compound of nicotinic acid and is currently used as an active ingredient in whitening and freckle-removing cosmetics [
2]. As one of the B vitamins, its whitening and freckle-removing mechanism is different from other traditional components. Specifically, it can reduce the synthesis of melanin in melanocytes by affecting the transport of substances in melanocytes, thereby effectively inhibiting the transmission of melanin to keratinocytes [
3,
4,
5,
6]. In addition, when melanin reaches the skin surface, nicotinamide can also accelerate the renewal rate of skin cells, thereby promoting the shedding of cells containing melanin and achieving the effect of improving skin quality and whitening skin from inside to outside [
7,
8]. However, regardless of its mechanism of action, the whitening agent must first penetrate the skin to exert its whitening effect. Therefore, it is of great significance to study the transdermal absorption of active whitening components to evaluate their whitening effect.
The transdermal absorption of cosmetics can be divided in two ways: 1. The intercellular pathway: chemical substances bypass keratinocytes and penetrate into the subcutaneous tissue through the continuous distribution of intercellular substances between keratinocytes; 2. the transcellular pathway: chemical substances alternately spread directly through the keratinocytes and intercellular substance in the water phase and lipid phase. The direct penetration of chemicals into the dermis through skin appendages such as hair follicles, sebaceous glands, and sweat duct orifices is also known as the bypass pathway. Macromolecular and ionic substances are difficult to pass through the lipid-rich stratum corneum and may enter the skin through this pathway [
9,
10,
11].
In this paper, the Franz diffusion cell method and high-performance liquid chromatography were used to study the transdermal permeation of nicotinamide in vitro by measuring the cumulative transmittance. The cumulative permeability of transdermal absorption under different influencing factors was studied to provide the basic value of transdermal absorption of water-soluble whitening and freckle-removing agents for cosmetics R & D personnel.
2. Materials and Methods
2.1. Experimental Materials
Nicotinamide, purity ≥ 98% (Baihaobo, Shanghai, China); octanoic acid/capric acid triacylglycerol ester, dioctyl carbonate, coconut glycerides, and polyethylene glycol E 400, all of which were cosmetic grade (BASF, Ludwigshafen, Germany); PBS buffer solution (tablet, pH 7.2~7.4) (Soleibao, Beijing, China); Tween 20, Tween 60, Span 60, Tween 80, and Span 80 (Aladdin, Shanghai, China); polyglycerol-4-laurate (Yingchuang, Shanghai, China); methanol and formic acid, chromatographic grade, and anhydrous ethanol, analytically pure (Sane Chemical Technology, Shanghai, China).
2.2. Experimental Methods
2.2.1. Preparing Solutions
Nicotinamide (NA) was accurately weighed and configured into a solution with a mass concentration of 10 mg/mL. It was diluted into 2, 10, 50, 100, 250, 500, 750, 1000, 1250, and 1500 μg/mL NA series standard solutions. The standard curve of nicotinamide was obtained under 2.2 chromatographic conditions.
Nicotinamide was accurately weighed and aqueous solutions with mass fractions of 2%, 3%, 4%, and 5% were prepared as supply pool samples.
2.2.2. Instrument Box Parameter
The transdermal diffusion device used in this experiment was improved on the basis of the static vertical diffusion tester designed by Franz. The transdermal absorption process of cosmetics was reproduced by slow penetration of the skin model. The device includes a supply cell (diameter of 2 cm) and a receiving cell (volume of 8 mL). The skin model was placed horizontally between the donor media and the acceptor media, and the stratum corneum was oriented towards the supply pool and fixed with a screw clip to empty the bubbles.
We used an Agilent Plus C18 chromatographic column (4.6 mm × 250 mm, 5 μm); the injection volume was 10 μL, column temperature was 30 °C, and detection wavelength was 261 nm. The mobile phase was a mixed solution of V (methanol)/V (0.1% formic acid water) = 35:65.
2.2.3. In Vitro Skin Treatment
In this study, pig ear skin, pig skin, and Strat-MTM membrane were used as skin models [
12]. Pig ears and pig skin (pig back skin) used to make in vitro skin samples for transdermal experiments were purchased from a local market. When making a pig ear skin sample, the pig ear was cleaned with clean water and dried with a soft cloth, and the outer skin of the pig ear was taken off with a scalpel. At the same time, no physical damage and no abnormal skin were selected for the experiment. The skin taken off was full-thickness pig ear skin, including stratum corneum, epidermis, and dermis. The hair was removed with an electric razor to a length of about 3 mm close to human hair. The pig’s outer ear skin and excess fat on the pig’s skin were scraped off with a scraper and cut into a square with a side length of 3 cm with a scalpel. After treatment, it was wrapped in tin foil paper and stored at −20 °C for later use. The storage time did not exceed 30 days. The skin was thawed at room temperature before use.
2.2.4. Transdermal Absorption
In vitro transdermal experiments were carried out according to SCCS (2012), OECD (2004a, b) [
13] guidelines. After the installation of the diffusion tank, the bubbles were discharged and placed in a water bath with magnetic stirring and temperature control. The experiment was carried out at a constant temperature, and the receptor chamber was continuously stirred at a speed of 300 rpm to ensure that the skin surface temperature was (32 ± 1) °C. After coating the sample, 200 μL of the sample was taken from the receiving pool 1, 2, 4, 6, and 8 h after coating, and the same dose of PBS buffer was added to the receiving pool at the same time. The content of nicotinamide was determined by high-performance liquid chromatography (HPLC). The cumulative permeation amount (Q
n, μg) and cumulative permeation rate (A, %) were calculated according to the following formula:
We drew a graph with A to t.
V is the volume of the receiving pool;
Vi is the sampling volume;
Qa is the total mass of nicotinamide.
2.2.5. Selection of Transdermal Conditions
In order to explore the effects of receiving solution type [
13,
14], receiving solution pH [
15,
16], skin type [
17,
18,
19,
20,
21,
22,
23,
24,
25], receiving cell temperature [
26], supply solution concentration, and supply solution application dose [
14,
27] on the transdermal absorption of nicotinamide, each factor was explored. For the effect of the solution in the receiving cell, the main body of the solution in the receiving cell was PBS buffer solution (pH 7.4), and the effects of 20% anhydrous ethanol, 2% PEG400, and 2% Tween 20 on the transdermal absorption results were investigated. For the effect of the pH of the receiving liquid solution, The receiving pool solution was PBS buffer solution, and the effects of pH 7.4 and pH 5.4 of PBS buffer solution on the transdermal absorption results were investigated. For the effect of skin type, pig ear skin, pig skin, and Start-M
TM membrane were used to explore the effect of different skins on transdermal absorption. For the effect of the temperature of the receiving liquid, we kept the room temperature at 25 °C and explored the effect of the water bath temperature of the diffusion liquid at 37 °C, 32 °C, and 25 °C on its transdermal absorption results. For the influence of the concentration of the supply solution, the supply solution was niacinamide aqueous solution, and the influence of concentrations of 2 wt%, 3 wt%, 4 wt%, and 5 wt% on the transdermal absorption results was investigated. For the influence of the dosage, the dosage of the supply solution was applied on the epidermis of the pig ear at a dose of 31.4 mg (limited dose) and 2 g (unlimited dose), respectively, to explore the influence of a limited dose and unlimited dose on the results of transdermal absorption.
2.2.6. Preparation of Nicotinamide Makeup: Water, Gel, and Oil-in-Water Emulsion
To prepare nicotinamide-containing toning lotion, at room temperature, the aqueous phase was accurately weighed: nicotinamide, polyacrylate cross-linked polymer-6, and deionized water were weighed in turn, and three portions were weighed in three beakers. Equal masses of glycerol, 1,3-propanediol, and 1,3-butanediol were added to three beakers, respectively, and stirred until the system was uniform. At the same time, phenoxyethanol was added to the aqueous phase and stirred until the system was uniform, and then the material could be discharged.
Nicotinamide gel was prepared. The water phase was accurately weighed at room temperature. Hansheng gum and polyacrylate cross-linked polymer-6 in the water phase were dispersed in water, fully stirred, and uniformly dispersed. The remaining components of the aqueous phase were added in turn: nicotinamide, glycerol, deionized water. These were stirred and dispersed evenly; then, we added phenoxyethanol to the system, stirred it, and dispersed it until the system was uniform and the material could be discharged.
The nicotinamide oil-in-water emulsion was prepared. At room temperature, the water phase (phase A) was accurately weighed, and nicotinamide, polyacrylate crosslinked polymer-6, deionized water, and glycerol were added in turn. We accurately weighed the oil phase (B phase), added caprylic acid/capric acid triglyceride in three beakers, and added monostearate dehydrated sorbitol ester and polyoxyethylene (20) monostearate dehydrated sorbitol ester, monooleate dehydrated sorbitol ester and polyoxyethylene (20) monooleate dehydrated sorbitol ester, and polyglycerol-4-laurate; the monooleic acid dehydrated sorbitol ester and polyoxyethylene (20) monooleic acid dehydrated sorbitol ester were added to two beakers, and dioctyl carbonate and cocoa butyrate were added, respectively. The A phase and B phase were heated to 80 °C, respectively. The B phase was added to the A phase and stirred at 700 rpm for 5 min. Homogeneous emulsification was performed at 15,000 rpm for 3 min; when the temperature was slowly stirred to 36~38 °C, phenoxyethanol (C phase) was added and stirred until the system was uniform and the material could be discharged.
2.2.7. Data Analysis
Microsoft Excel 2023 (Microsoft) and GraphPad Prism 9.02 (GraphPad) were used to process the data. The experimental data were expressed as mean ± SD (n = 3). One-way analysis of variance (ANOVA) was used to compare the data. p < 0.05 indicated significant differences, and p < 0.01 indicated extremely significant differences. Origin 2018 (Origin) was used to draw the chart.
4. Discussion
According to the national standard GB/T 27818-2011 chemical skin absorption in vitro experimental method, the receiving solution should be preferentially selected as the receiving solution [
28], such as PBS buffer (pH 7.4), but also to meet the requirements of the leak test. Generally, a water-soluble solution is selected for drugs with good water solubility, while organic solvents or surfactants such as ethanol may be considered for drugs with poor water solubility, but it may change skin characteristics or dissolve lipid components, and should be added carefully. Although other solutions can also be used as the receiving solution, it is necessary to provide accurate components of the receiving solution and confirm that the test substance can be fully dissolved in the receiving solution without affecting skin absorption; in addition, the receiving fluid does not affect the integrity of the skin. The composition of the receiving solution has a significant effect on the amount of transdermal absorption [
29]. Liu Yafeng et al. [
14] explored the effect of three different cosolvents on the measurement results in the transdermal absorption of sunscreens by adding 2% Tween 20, 20% ethanol, and 4% PEG to the receiving solution in PBS. These three solvents had little effect on the experimental results. Therefore, the co-solvent with a lower dosage and less effect on the physiological state of the skin was preferred. Therefore, 2% Tween 20 was added to PBS as the receiving solution.
Nowak et al. [
30] found that the permeation amount of nicotinamide through the nicotinamide cellulose acetate membrane (CA membrane) was 883 ± 62 μg when the pH value of the receiving solution was 5.4 and 679 ± 21 μg when the pH value of the receiving solution was 7.4, indicating that it was easier to promote the penetration of nicotinamide under acidic conditions. Zhang Tingting et al. [
16] also pointed out that weak acid is conducive to percutaneous penetration in vitro. The pH value of the human skin surface is 5.4, and the pH value of deeper skin layers is 7.4. Combined with the actual human condition, the PBS buffer solution with a pH of 7.4 was used as the receiving solution in the subsequent experiments.
Huang Xiaoping [
11] found that the permeability of pig ear and pig abdominal skin were similar to that of human thigh skin when comparing the difference of drug permeability between different parts of pig skin and human skin. Zhang et al. [
19] found that the permeability of nicotinamide in pig skin was higher than that in human skin. Pulsoni et al. [
25] evaluated the permeability of caffeine (reference to OECD 428 substance) and LIP1 (lipophilic substance), two molecules with similar molecular weights but different lipophilicity, by using Strat-M
TM membrane and pig ear skin for comparative study. By applying this to the skin under infinite dose conditions, it was found that the Strat-MTM membrane was more permeable than the pig ear skin. According to the results, the pig ear skin will be used as an in vitro penetration skin model.
The passive absorption of chemicals is affected by temperature. Zhang Hongyan et al. [
26] studied the transdermal absorption characteristics of fluorescent whitening agents in facial masks by conducting cosmetic transdermal absorption experiments at a constant temperature (37 °C ± 1 °C). According to the national standard GB/T 27818-2011 chemical skin absorption in vitro experimental method, the supply pool and skin should be kept constantly close to the normal skin temperature (32 °C ± 1 °C). Different diffusion cells require different water baths or heating to a certain temperature to ensure that the skin temperature is at its normal physiological standard.
According to a number of test results, the expert panel of the American Cosmetics Raw Materials Review Committee found that the use of 3% NA in cosmetics had no significant irritation, sensitization, and photosensitivity to the skin. When cosmetics containing nicotinamide are used for a long time, the daily dosage is not more than 3 g. The content of nicotinamide in cosmetics is generally 2–5%. A total of 4% of nicotinamide may cause intolerance in 20% of people. Cosmetics containing 5% nicotinamide can block ultraviolet rays in large quantities and reduce skin immunosuppression by smearing. In this experiment, the effect of 2–5 wt% NA on its permeability was explored, and it was found that the concentration had no effect on the cumulative permeability, but had a significant effect on the cumulative permeability (p < 0.05), and the cumulative permeability increased with the increase in concentration.
The application amount of the formula dose applied to the donor room was divided into limited doses and unlimited doses, limited dose ≤ 10 μL/cm
2 and unlimited dose ≥ 10 μL/cm
2. The finite dose represents a closer application and use condition, while the infinite dose helps us to understand and explain the steady-state permeation and the permeation capacity of a constant high formulation concentration. In the study of the effect of dose on the penetration of nicotinamide, Zhang Y et al. [
27] found that the penetration percentage of nicotinamide in the finite dose study was relatively higher than that in the infinite dose study (
p < 0.05).
The formulation also affects the transdermal absorption of chemicals, and the viscosity of the carrier is one of the factors affecting the diffusion of active ingredients and the release rate of the dosage form. Nabiee et al. [
31] found the inter-group difference in the permeation of vitamin K1 by matrix carriers (O/W ≥ W/O > Aqueous) in exploring the transdermal absorption of vitamin K1. López-Sánchez et al. [
30] explored the effects of aqueous solution, oil-in-water emulsion, and gel on the in vitro transdermal absorption of preservatives. It was found that the absorption of Bronidox and Bronopol depended on the formulation. The O/W emulsion was the system that promoted the least absorption of Bronidox, while the absorption of Bronopol by the gel was lower. The aqueous solution provided the maximum transdermal absorption of the two preservatives.
5. Conclusions
In this study, the effects of different types of receiving solution, pH values of receiving solution, skin, temperature, concentration of supply solution, and application amount of supply solution on the transdermal absorption of nicotinamide were studied. The best detection method for the transdermal absorption of nicotinamide was established. When the receiving solution was PBS solution, the pH was 7.4, the skin was pig ear skin, the temperature was 37 °C, the concentration of nicotinamide was 3%, and the application amount was 2 g, the transdermal absorption performance of nicotinamide was better, the system was more stable, the applicability was stronger, and the repeatability was better.
The effects of different formulations on the transdermal absorption of nicotinamide were investigated by using the established nicotinamide transdermal absorption system. The results showed that in the makeup water, the change in polyols had little effect on the transdermal absorption of NA; in the gel, changing the rheological regulator had a significant effect on the transdermal absorption of NA, that is, cumulative permeability: Hansheng gum > polyacrylate cross-linked polymer-6; and in the oil-in-water emulsion, the change in emulsifier and oil had little effect on the transdermal absorption of NA. Different product formulations of nicotinamide have a significant effect on its permeability. Among them, makeup water is most conducive to the penetration of nicotinamide, followed by emulsion, and finally gel.
The construction of this method makes the detection of nicotinamide transdermal absorption more applicable and accurate, provides the basic value of the transdermal absorption of water-soluble whitening and freckle-removing agents for cosmetics R & D personnel, and also provides reference for the future research and development of whitening and freckle-removing agent formulas.
We encourage researchers to build upon our findings and explore testing a range of nicotinamide concentrations to understand their impact on skin response.