Lycopene (Figure 1) belongs to the class of natural pigments, called carotenoids, with a role in protecting the body from the destructive effects of oxidants. Lycopene neutralizes the negative effects of free radicals. Furthermore, recent studies have shown that lycopene has a significant potential to counter free radicals in comparison with β-Carotene. Validation was confirmed by application of standard techniques lycopene determination. Aqueous extract of propolis has a high concentration of polyphenols and is standardized in polyphenol carboxylic acids (caffeic acid), responsible, among other active substances, for its healing and anti-inflammatory action upon tegument affected by dandruff and seborrheic dermatitis. Thus, the antimicrobial and anti-inflammatory action of lycopene is enhanced and regeneration of skin affected by fungal and/or microbial infections is stimulated. The product formulation also considered physiological aspects of the skin, resulting in a product with low allergenic potential and high degreasing capacity. Because of the nanoemulsion pharmaceutical form, it has several advantages over other topical products with similar action. Thus, in contact with skin it quickly releases active substances due to its good adherence to skin and close contact it has a high therapeutic efficiency, easy administration low allergenic potential, good local tolerance and an increased viscosity, allowing the required concentration in bioactive compounds. Figure 2 clearly shows the absorption spectrum of the extracted lycopene solution. The absorption spectrum very closely coincided with the three peaks characteristic of trans-lycopene (λ = 446, 472, 505 nm). Any analytical method (bio analytical, in particular), in order to be validated, must demonstrate first that it is specified in relation to existing endogenous substances in the biological matrix, to metabolism products and reagents used in the sample preparation. For that, the specificity of this method was verified using six different sources of blank solutions. We aimed to see if there was any endogenous interference at the retention times of the experimental analytes. The linearity of the method was verified by the method of smallest squares, on the 0-3.0 mg/L lycopene domain, using internal standard calibration as calibration model. Lycopene area and standard area ratio were calculated for seven levels of concentration in the selected domain and used for calibration curves. For each calibration point we examined the distribution, the relative percentage deviation of recalculated concentration from calibration curve equation. The calibration model was considered correct if residuals were within boundaries of ± 20% at lower limit and ± 15% at other concentrations and did not have a trend of increase or decrease along with concentration. Correlation was considered linear at a value of the determination coefficient greater than 0.99, as seen in Figure 3. Accuracy, expressed as relative percentage deviation of measured concentration in relation to the a obtained concentration, and precision, expressed as standard relative percentage deviation or coefficient of variation CV%, were determined at three concentration levels. Both, precision and accuracy were determined on the same day, based on five measurements on five different samples at each concentration, and accuracy and precision on different days based on the analysis on different days of five standard samples at each of the three levels of tested concentration. The lowest limit of quantification was considered the lowest concentration on the calibration line with an accuracy and precision within ± 20%. Retrieval was assessed at four concentrations, including the lower limit of quantification, comparing the response obtained after application of UV radiation with that obtained with a standard solution of the same concentration in water and similarly processed as biological samples.

All FTIR analysis is considered technically "non-destructive" therefore further analysis can be performed. Composition analysis by FTIR spectroscopy (Fourier Transform Infrared) allows quantitative estimates and the study of links nature that appear during the nanoemulsions process. Following FTIR spectra analysis, no significant differences were apparent between the products. As shown in Figure 4, differences were found in FTIR spectra in the region 900-500 nm regarding experimental conditions and the resulting products. IR spectra highlight the presence of -CH₂- groups illustrated by the characteristic bands at 1450 cm^-1 and 1460 cm^-1 respectively. The nanoemulsion ester group causes the appearance of characteristic frequency bands at 1700 cm^-1 (-C = O stretching) given by a larger amount of propolis and lycopene. Increase in propolis content (the 30% option) determines the appearance of new frequency bands characteristic of the carbonyl group (1900-1600 cm^-1 -C = O stretching). Growth leads (in propolis) to the disappearance of intense bands at 750-1280 cm^-1, assigned to ring vibrations: 1235-1280 cm^-1, 810-905 cm^-1 and 805-875 cm^-1 and can be attributed to characteristic methyl bands shielding or to the dissolution of certain groups during the process of obtaining the nanoemulsion. In the case of the bands group in the range of 1150-1250 cm^-1, characteristic of ester groups (-C-O stretching), an increase in the intensity of the bands is observed, which is reflected in the decrease of its transmittance from 96% to 56%. This is also explained by the increasing of the quantity of propolis from 27% v/v to 35% v/v in the nanoemulsion. High lycopene content of 35% has the effect of increased intensity of certain bands at 1450 cm^-1 (-CH₃ and CH₂ = strain) reflected in the decrease of the transmittance from 92% to 70.846%. An intensity increase was observed at 1730 cm^-1 (-C = O stretching) a characteristic of unsaturated esters. This growth is highlighted by the decrease of transmittance from 97.95% to 47.126% and is explained by 35% propolis content. The intensity significant increase of nanoemulsion bands characteristic is attributed to the increase of distance interactions between atoms and molecules, through altered angles between the links. In the case of experimental formulated nanoemulsions, for second formulation spectral bands intensity was reduced, which is consistent with the reported kinetic data (Table 1). Table 1 shows correlation coefficients of data regarding the release of formulated nanoemulsions, obtained from the Higuchi model, zero order kinetic and release exponent values (n) obtained from the equation Mt/Mo = ktn regarding the prepared nanoemulsions based on propolis lycopene (n = 3). During these experiments no changes were observed in the organoleptic properties of experimental formulations and pH value of the two nanoemulsions remained within the limits of ± 0.3 pH units. No significant changes were noticed in terms of particle size (p < 0.05).

Micrometric properties of the two experimental formulations are shown in Table 2. This experiment highlighted the improved performances of the se emulsions without side effects and adverse reactions by replacing synthetic chemicals with natural products. It has been documented, that some UV radiation absorbers can be partially degraded therefore causing skin alterations while exposed to UV influencing the effectiveness of sunscreen protection. For information on UV absorbers, the nanoemulsions SPF in vitro parameters were investigated. UVA radiation, the UVA/UVB ratio and in vitro SPF were measured using the Diffey and Robson method. The efficiency of these products is measured by a coefficient, index or protective factor, noted SPF (sun protection factor) or PI (protection index), which is the ratio of the minimum dose of solar radiation that causes lowest skin redness, after and before skin application of these preparations.

This experiment was conducted to determine the photoprotection capacity of natural substances in nanoemulsions. In both nanoemulsions we also introduced a UVR-absorber (Saliform), accepted by European standards, to observe its influence on the analyzed samples. In Table 3 presents the absorbance's of two nanoemulsions measured by UVA, UVA/UVB ratio and SPF. The obtained data show that most absorbance in the UV domain in the relative parameter 5 is present in nanoemulsion 2+ absorber-UVR (Saliform) 1:1 (v/v). Regarding UVA/UVB ratio with the relative parameter 0.82, most absorbance is found in the same nanoemulsion and in the case of SPF with absolute parameter 10.9, in nanoemulsion 2. As shown by these results, highest absorbance parameters may be assigned to nanoemulsion 2. Experimental formulations showed a pseudo-plastic rheology, under the influence of shear stress (Figure 5). The viscosity is directly dependent on the formulations content of propolis. Microscopic observations of the experimental nanoemulsions confirmed formation of spherical particles, as shown in Figure 5. Differences in droplet size of these formulations were not statistically significant (droplet size was found to be 45 μm). Nanoemulsions were kept for three weeks at 4°C in order to provide a stable formulation for local application. Nanoemulsion stability is shown in Figure 6, 7 and 8. This study suggests that the nanoemulsions made of aqueous extract of propolis and lycopene and prepared with active substances may confer better therapeutic effects than conventional formulations, as a result of dose controlled local release longer period of time, which could lead to a greater efficiency and to a greater acceptance by the skin (i.e. better compliance). These results are supported by presented data in Table 4. Collagenase (inactive form of pre-collagenase, activated by trypsin) is an enzyme that cleaves the peptide bonds of fibrillar collagen types I and III. Experimental results showed that both nanoemulsions induced a reduction in collagenase activity. The intensity of anti-inflammatory effect varies with time interval covered by the assessment of therapeutic response according to data in Table 4. The activity of propolis and lycopene nanoemulsions (Table 5) was emphasized by measuring the induced inflammation. Produced inflammation decreased by 75% for nanoemulsion 1 and 100% for nanoemulsion 2. The maximal inflammation reduction effect occurred after 8 hours from the initial application. Preliminary tissue examination showed that these formulations did not produce irritation. Local application of the experimental nanoemulsion (propolis and lycopene) has great potential, both in terms of efficacy (analgesia) and therapeutic safety. Nanoemulsions have proved a better therapeutic efficacy compared to standard suspension, was observed improving monitored parameters for a longer period of time (24 hours). These systems can be seen as a viable alternative to conventional creams, due to their ability to improve residence time and thereby, bioavailability.

Aqueous extract of propolis was obtained by refluxing 100 g of propolis powder and 250 ml of double distilled water. It was concentrated in a water bath then filtered resulting in 1.5 cm³ of extract with 95% of dry substance.

Lycopene was obtained from ripe tomatoes (Lycopersicon esculentum) by solvent extraction. Samples were homogenized in a laboratory homogenizer. 5ml 0.05% BHT in acetone, 5 ml of ethanol and 10 ml of hexane were added to 0.6 g homogenated sample. The supplemented homogenate was kept on ice and stirred with a magnetic stirrer for 15 minutes. Then 3 ml of deionized water were added and samples were mixed for additional 5 minutes. Samples were then left at room temperature for 5 minutes to allow phase separation. The absorption of the hexane layer (upper layer) was measured in a 1cm quartz cuvette at a wavelength of 503 nm, against hexane as blank. Lycopene was measured quantitatively by UV-VIS spectrophotometer T60U, PG Instruments Limited, UV WIN^®version 5.05; detection was performed at 503 nm and calculated using the following formula:

Absorbance at 503 nm (A₅₀₃) =

ε (M^-1·cm^-1)·b(cm)

[Lycopene concentration (M)]

The measuring conditions were: scan speed 90 nm/min and an interval of 1 nm. After extraction, was hexane evaporated to dryness in a vacuum evaporator, under a nitrogen stream 34 . All substances were purchased from Sigma Chemical.

Nanoemulsions were prepared by adding lycopene to aqueous solution of propolis (50 mg propolis in 10 ml D.W.), using a magnetic stirrer at ~ 2000 rpm. The mixture was introduced for in an ultrasonic bath at 20 kHz 20 minutes. The nanoparticles that are formed have a lycopene-propolis loaded shape. After ultrasonic treatment the solution is brought at room temperature (22°C).

The excess organic solvent in excess was evaporated using a rotary evaporator and samples were kept for further analysis by lyophilisation. Independent of preparation temperature, samples were kept at 25°C 35 .

For spectral characterization (FTIR spectrometry), samples were prepared as follows: compounds obtained after heat treatment were mixed at a temperature of 1300°C with potassium bromide powder, previously dried for 24 hours at a temperature of 120°C, at a mass ratio of 0.04:1. After a vigorous mix to obtain uniformisation, pills with a thickness of 0.5-0.75 mm and 13 mm in diameter at a pressure of 0.3 GPa in normal atmosphere were prepared. The pills were analyzed using the JASCO 660 PLUS spectrophotometer, which recorded the IR absorption spectra in the area 4000 cm^-1 100-400 cm^-1. For in vitro characterization of the experimental nanoemulsions, permeability studies and rheological measurements were carried out 36 .

Membrane permeability of the experimental nanoemulsions was investigated by filling the donor compartment of a diffusion cell with a 2 g test mixture. All other experimental conditions identical to those described for permeability studies of solid systems 37 .

Apparent viscosity of the experimental nanoemulsions was determined using a viscometer Brookfield Rheostress DV-III + Rheometer. Measurements were performed 3 times at 25°C using SC4 spindle. To determine the influence of shear stress applied to the microstructure of the prepared nanoemulsions, measurements were made at a rotation speed of 1 and 10 rpm.

Apparent viscosity of the controlled product (2% HPMC dispersion in water), were examined under similar conditions 38 .

Enzyme activity is determined by a continuous spectrophotometric method, using as substrate 2-L-leucylglycyl furanacryloyl-L-prolyl-L-alanine (FALGPA, a specific collagenase substrate), as it is preferentially hydrolyzed much faster than other synthetic substrates.

Measurement of the substrate absorbance decrease was done at 345 nm.

Identification and quantification are done according to the methods described in the European Directorate for the Quality of Medicines 39 .

Preparation: adult, young, healthy animals of the species of guinea pigs, breed albino were used. The animals were acclimatized to laboratory conditions for at least five days before test. Animals were divided randomly into treatment and control groups before test. Their skin was cleaned by clipping, shaving or, if possible, by chemical depilation without excoriation (cleaning method is based on the test method used). Animals have been weighed before and after test.

Determination of SPF (sun protection factor) was performed using a spectrophotometer, equipped with an integrating sphere, with appropriate software and a TRANSPOR 3 TM support, with a composition similar to that of natural skin, on which the amount of 2 mg/cm² of nanoemulsion was applied 40 .

Values were expressed as mean ± S.D. Statistical significance was evaluated by Students-„t‟ test at 5% level of significance (p < 0.05).