Pomegranate extract-loaded solid lipid nanoparticles: design, optimization, and in vitro cytotoxicity study
Received 13 October 2017
Accepted for publication 23 December 2017
Published 6 March 2018 Volume 2018:13 Pages 1313—1326
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 6
Editor who approved publication: Prof. Dr. Thomas J. Webster
Noha M Badawi,1 Mahmoud H Teaima,2 Khalid M El-Say,3 Dalia A Attia,1 Mohamed A El-Nabarawi,2 Mohey M Elmazar4
1Department of Pharmaceutics, Faculty of Pharmacy, The British University in Egypt, Cairo, Egypt; 2Department of Pharmaceutics and Industrial Pharmacy, Cairo University, Cairo, Egypt; 3Department of Pharmaceutics, King Abdulaziz University, Jeddah, Saudi Arabia; 4Department of Pharmacology, Faculty of Pharmacy, The British University in Egypt, Cairo, Egypt
Background: Pomegranate extract (PE) is a natural product with potent antioxidant and anticancer activity because of its polyphenols content. The main purpose of this study was to maximize the PE chemotherapeutic efficacy by loading it in an optimized solid lipid nanoparticles (SLNs) formula.
Materials and methods: The influence of independent variables, which were lipid concentration (X1), surfactant concentration (X2) and cosurfactant concentration (X3), on dependent ones, which were particle size (Y1), polydispersity index (Y2), zeta potential (Y3), entrapment efficiency (Y4) and cumulative % drug release (Y5), were studied and optimized using the Box–Behnken design. Fifteen formulations of PE-SLNs were prepared using hot homogenization followed by ultra-sonication technique. Response surface plots, Pareto charts and mathematical equations were produced to study the impact of independent variables on the dependent quality parameters. The anti-proliferative activity of the optimized formula was then evaluated in three different cancer cell lines, namely, MCF-7, PC-3 and HepG-2, in addition to one normal cell line, HFB-4.
Results: The results demonstrated that the particle sizes ranged from 407.5 to 651.9 nm and the entrapment efficiencies ranged from 56.02 to 65.23%. Interestingly, the 50% inhibitory concentration of the optimized formula had more than a 40-fold improved effect on the cell growth inhibition in comparison with its free counterpart. Furthermore, it was more selective against cancer cells than normal cells particularly in MCF-7 breast cancer cells.
Conclusion: These data proved that nanoencapsulation of PE enhanced its anticancer efficacy. Therefore, our results suggested that a PE-loaded SLNs optimized-formula could be a promising chemotherapeutic agent.
Keywords: pomegranate extract, solid lipid nanoparticles, Box–Behnken design, optimization, cancer cell lines
Cancer is a serious disease where the control of growth in one or more cells is lost, causing either a solid mass of cells recognized as a tumor or a liquid cancer (ie, bone marrow or blood-related cancer). It is one of the largest causes of death worldwide and the major treatments include chemotherapy, surgery, and radiotherapy.1 Chemotherapy comprises of treatment with low-molecular-weight drugs in order to destroy tumor cells selectively or, as a minimum, restrict their proliferation. Gastrointestinal tract lesions, bone marrow suppression, nausea, hair loss, and the development of clinical resistance are the main drawbacks of several cytotoxic agents. These side effects exist because cytotoxic agents act on both cancer and normal cells.2
Since ancient periods, natural products and natural bioactive compounds have been utilized by human beings to treat numerous diseases. Remarkably, natural products have been used in recent times for the treatment and prevention of cancer.3,4
The fruit of the Punica granatum L. tree (pomegranate) has been recognized since prehistoric times for its aids to health.5 Pomegranate extract (PE) and its individual polyphenols reveal in vitro and in vivo anticancer effects.6 PE, containing mainly ellagitannins, shows anti-invasive, antiproliferative, proapoptotic, and anti-inflammatory effects in different cancer cell lines in vitro7 such as breast cancer,8 prostate cancer,9 lung tumors, colon cancer,10 and skin cancer in mice xenograft models and culture plates.11
It was found that various PE formulations decreased the proliferation of both types of breast cancer cells which are estrogen-receptor positive and estrogen-receptor negative,8 in addition to MMTV-Wnt-1 mouse mammary cancer stem cells,12 mammary organ culture,13 and moreover decreased the motility and invasion of SUM 149 and MDA-231 cell lines resulting from aggressive cancers.14 These detected findings were accompanied by inhibition of NF-κB expression14 and also inhibition of aromatase enzyme (17b-hydroxysteroid dehydrogenase), that catalyzes conversion of estrone to estradiol.15 Estradiol was found to increase the risk of breast cancer in postmenopausal women.16 It was also previously demonstrated that PE can induce apoptosis and inhibit cell growth in mice implanted with prostate cancer (PC-3 cell line) by modulating the proteins that regulate apoptosis.17,18 In addition, PE has been found to induce chemoprevention of liver cancer through antiproliferative, antioxidant and proapoptotic mechanisms.19
However, although many natural products have been confirmed to have a strong therapeutic efficacy, their low bioavailability and poor solubility have seriously restricted their usage.11 Nanotechnology is considered as one of the most advanced disciplines that has proved successful yields and mechanisms in defeating cancer;20 its approaches are employed to cancer therapeutic agents in order to reduce toxicity, improve stability and bioavailability and endorse selective tumor uptake.21 Therefore, encapsulation of PE into biodegradable and biocompatible nanoparticles may overcome this problem.
Solid lipid nanoparticles (SLNs) are a good choice for the delivery of both hydrophilic and hydrophobic anticancer drugs. The main reason why SLNs show high drug-loading capacity, improve the blood circulation time, control release kinetics, and increase the overall therapeutic effectiveness of anti-cancer drugs is their lipid core.22,23 In addition, SLNs have been considered as novel nanoparticulate carrier systems due to enhanced delivery and stability of drugs.24
Optimization is a method that uses the available resources to achieve the best probable results so that it is implemented for the design and development of a wide range of controlled-release dosage forms. The optimization technique has now replaced the process of trial-and-error which was widely used and thus it is found in a wide diversity of applications in the chemistry and pharmaceutical industry. Employment of applicable experimental designs, production of polynomial relationships and optimum research techniques via appropriate software are represented by such studies.25
We hypothesized that encapsulation of PE in SLNs would improve their anticancer activity. Therefore, the main objective of this study was to develop, characterize and optimize SLNs loaded with PE. The Box–Behnken design (BBD), using Statgraphics® plus software (Manugistics Inc., Rockville, MD, USA), was applied to detect the critical parameters that influence the characteristics of the prepared PE-SLNs in order to select the optimum formula. Subsequently, the anti-proliferative effect of the optimized formula was evaluated in vitro in MCF-7, PC-3 and HepG-2 cancer cell lines as well as one normal cell line, HFB-4, and then compared to the free PE as well as the void optimized formula.
Materials and methods
PE was purchased from Shaanxi Ciyuan Biotech Co., Ltd (Shaanxi, China). Stearic acid, disodium hydrogen phosphate and potassium dihydrogen phosphate were purchased from El-Nasr Pharmaceutical Chemicals Co. (Cairo, Egypt). Tween 80 and lecithin were generously donated by Egyptian International Pharmaceutical Industries Co. (10th of Ramadan City, Egypt). Dialysis tubing cellulose membrane with molecular weight cutoff 12,000 Dalton was purchased from Sigma-Aldrich Co (St Louis, MO, USA). Dimethyl sulfoxide (DMSO), MTT assay and trypan blue dye were purchased from Sigma-Aldrich Co. Fetal bovine serum, DMEM, RPMI-1640, HEPES buffer solution, L-glutamine, gentamycin and 0.25% Trypsin-EDTA were purchased from Lonza (Bornem, Belgium). All other chemicals were of analytical grade.
Design of experiments
The BBD three-level three-factor (33) was implemented in the present study by the use of statistical package Statgraphics® plus software, version 4. It was applied to optimize the formulation variables statistically in order to prepare PE-SLNs, with the aim of achieving optimum particle size, polydispersity index (PDI), zeta potential, high encapsulation efficiency percent and sustained cumulative drug release. Fifteen runs were designed; 12 of them acted as the mid-point to each edge of the multidimensional cube while the remaining three were the duplicates of the cube’s center point. Three different independent variables were estimated: lipid (stearic acid) concentration (X1), surfactant (tween 80) concentration (X2) and cosurfactant (lecithin) concentration (X3), while the particle size (Y1), PDI (Y2), zeta potential (Y3), entrapment efficiency (EE) (Y4) and cumulative % drug release (Y5) were chosen as dependent variables. The independent and dependent variables are presented in Table 1. The composition of the prepared PE-SLNs according to BBD is shown in Table 2. Desirability was estimated for selection of the optimized formula which was exposed for additional investigations.25
Table 1 Independent and dependent variables and their levels for Box–Behnken design
Table 2 Composition of the 33 Box–Behnken design for formulations of pomegranate extract-loaded solid lipid nanoparticles
Preparation of PE-SLNs
Hot homogenization followed by the ultra-sonication technique was selected for the preparation of PE-SLNs.26 The lipid phase was prepared by melting stearic acid, lecithin as well as PE at 10°C above the lipid melting point. Meanwhile, the dissolving of tween 80 in deionized water and then heating to the same temperature of the lipid phase was carried out for the preparation of the aqueous phase. The hot aqueous phase was then added gradually into the lipid phase with continuous stirring using a magnetic stirrer in a water bath for 30 min. Subsequently, sonication of the coarse oil in water (o/w) emulsion was done using a probe sonicator (Vibra-Cell™ VCX130; Sonics, CT, USA) in an ice bath at 100% amplitude for 10 min. The obtained dispersions were collected in glass containers and stored in the refrigerator for further experiments.
Characterization of the prepared PE-SLNs
The 15 prepared formulae were examined for particle size, PDI, zeta potential, EE% in addition to cumulative % drug release.
Measurements of particle size, PDI and zeta potential
The dynamic light scattering (DLS) technique was chosen for particle size as z-average diameter, PDI, and zeta potential of PE-SLNs evaluation by the using of Zetasizer Nano-Zs90, MPT-Z (Malvern Instruments Ltd, Malvern, UK). Dilution with deionized water was carried out for the prepared PE-SLNs before evaluation to achieve optimal kilo counts per second (kcps) of 50 to 200 for measurements.27
The morphology of the prepared PE-SLNs dispersion was evaluated by using 5 μL of the dispersion which was placed onto the surface of a 300-mesh copper grid coated with carbon and then examined by using transmission electron microscopy (TEM) (JEM-2100, JEOL, Tokyo, Japan), operated at an acceleration voltage of 200 kV. The samples were firstly negatively stained using 2% uranyl acetate (w/v), followed by air drying for 15 min and then the excess was removed by filter paper.28
EE% was examined by measuring the amount of free drug in the aqueous phase after separation of the system using the centrifugation method. PE-SLNs dispersion was centrifuged at 12,000 rpm and 4°C for 1 h using cooling centrifuge (2-16KL, Sigma Laborzentrifugen GmbH, Osterode am Harz, Germany); then the supernatant was collected and diluted with phosphate buffer saline pH 7.4 (PBS 7.4) to measure the free drug concentration.29 The drug concentration was measured at 265 nm using ultraviolet-visible spectrophotometer (V-630, Jasco, Tokyo, Japan).30 The percentage of entrapped drug was calculated according to the following equation:27
where Winitial drug was the amount of drug used for the assay and Wfree drug was the amount of free drug detected in the aqueous phase after centrifugation.
In vitro drug release study
The dialysis bag method was selected for accomplishing the in vitro drug release study by using PBS 7.4 as the dissolution medium27 and dialysis membrane with a molecular weight of 12,000 Da which retains SLNs and permits the diffusion of free drug into the dissolution medium. The bags were initially soaked in PBS 7.4 for 24 h before being used; then 2 mL of PE-SLNs dispersion was transferred into the bag and the two ends tied by string.27 Subsequently, the bags were placed in 100 mL dissolution medium which was maintained at 37°C and shaken at 100 rpm in a thermostatically controlled shaking water bath (WSB-18, Daihan Scientific Co. Ltd, Gangwon-do, Korea). The first eight samples were withdrawn every hour and then one sample was withdrawn after 24 h and the final sample after 48 h. Samples were withdrawn at predetermined time intervals, replenished with fresh buffer to retain the sink condition and analyzed spectrophotometrically at 265 nm.30
Prediction of the optimized formula
The optimized formula was predicted after analysis of data using the Statgraphics® plus software by applying constraints on all independent variables to acquire the optimum particle size, PDI, zeta potential, high EE% and sustained cumulative drug release. In addition, drug-loading capacity was calculated for the optimized formula using the following equation:31
To check the validity of the calculated optimal formulation influences and the expected responses established by the software, the recommended optimized formula was prepared and evaluated.
In vitro cytotoxicity study of the PE-SLNs optimized formula
Cytotoxicity evaluation using viability MTT assay
In this experiment, a cytotoxicity study against three different cancer cell lines as well as a normal cell line was evaluated for the optimized SLNs formula loaded with PE and without PE (void) in addition to the free PE. The concentrations that induced 50% growth inhibition as a result of exposure to the optimized PE-SLNs formula, the void optimized formula and the free PE were obtained and compared.
Cell lines chosen for the study and their propagation
Three different cancer cell lines, namely, human breast carcinoma (MCF-7), human prostate carcinoma (PC-3), and human hepatocellular carcinoma (HepG2) in addition to human normal melanocytes (HFB-4) were bought from the American Type Culture Collection (Rockville, MD, USA). Cells were grown in RPMI-1640 supplemented with 10% inactivated fetal calf serum and 50 μg/mL gentamycin. The cells were kept at 37°C in a humidified, 5% CO2 atmosphere and sub-cultured 2 to 3 times a week.
Antiproliferative activity (MTT assay)
The growing cells from different tumor cell lines were incubated in Corning® 96-well tissue culture plates (5×104 cell/well) for 24 h in order to attach the cells to the wall of the plate. Afterward, samples were added into the well plates to accomplish 10 concentrations (1–500 μg/mL) of each sample and then incubated for 24 h using vehicle (0.5% DMSO) as a control. Concisely, the viability of the treated cells was examined by MTT assay in this way, the media was removed and substituted with 100 μL of fresh culture RPMI-1640 medium then 10 μL of the 12 mM MTT stock solution (5 mg of MTT in 1 mL of PBS). Subsequently, cells were kept at 37°C and 5% CO2 for 4 h and then 85 μL aliquot of the media was discarded from the wells and 50 μL of DMSO was added and mixed carefully. The cells were then incubated at 37°C for 10 min. To determine the number of viable cells, the optical density was measured at 590 nm with the SunRise™ microplate reader (Tecan Inc., NC, USA) and the percentage of viability was calculated. In addition, the relation between surviving cells and drug concentration was plotted to develop the survival curve of each tumor cell line after treatment with the specified compound. The concentration that caused 50% inhibition of cell growth in addition to a 95% CI was obtained using GraphPad Prism 5 software (San Diego, CA, USA).32,33
The mean particle size (Y1) ranged from 407.5 to 651.9 nm depending on the variables level selected during production as displayed in Table 3. PDI (Y2) values ranged from 0.329 to 0.601 where all formulations showed good homogeneity. Furthermore, all formulations exhibited negative zeta potential (Y3) which were in the range of −29.8 to −45.5 mV and the EE% (Y4) was in the range of 56.02% to 65.23% due to the variation in factors combination. Moreover, cumulative % drug release (Y5) after 48 h ranged from 60.36% to 75.53% as shown in Table 3.
Table 3 Observed values of responses for 15 formulations of pomegranate extract solid lipid nanoparticles
Estimation of the quantitative effects of the factors
The analysis of variance for investigating the model according to the data of the responses (Y1 to Y5) is presented in Table 4. The influence of factor is considered significant if the effects differ from zero and the p-value <0.05 as stated by ANOVA. A synergistic effect is identified by a positive sign, while an antagonistic effect of the factor is represented by a negative sign. Results in Table 4 show the estimated effects of the selected factors, and the associated p-values for the five responses resulting from ANOVA.
Based on the obtained results from Table 4, X1 had a significant antagonistic effect on Y2 and Y4 with p-values of 0.0015 and 0.0001, respectively, but it had a significant synergistic effect on Y5 with a p-value of 0.0003. In addition, Y1 was significantly affected by the antagonistic effect of X2 and X3 with p-values of 0.0054 and 0.0018, respectively. X3 had a significant synergistic effect on Y3 with a p-value of 0.0001, but it had a significant antagonistic effect on Y5 with a p-value of 0.0219. Furthermore, Y3 was significantly affected by the synergistic effect of the quadratic term of X32 with a p-value of 0.0029; however, X2 and the interaction effect of X1 and X3 affected Y3 antagonistically with p-values of 0.035 and 0.0408, respectively. On the other hand, Y4 was significantly affected by the synergistic effect of the quadratic term of X12 and X22 with p-values of 0.0030 and 0.0347, respectively, and the antagonistic effect of the quadratic term of X32 with a p-value of 0.0390.
In vitro cytotoxicity study of the optimized formula
Results of the cytotoxicity study showed that PE had a statistically anti-proliferative effect on the MCF-7 breast cancer cell line with a 50% inhibitory concentration (IC50) of 49.2 μg/mL with 95%, CI (29.75 to 78.06) followed by the PC-3 prostate cancer cell line with IC50 of 107 μg/mL with 95%, CI (80.98 to 133.1); the lowest effect was on the HepG-2 liver cell line with IC50 of 219 μg/mL with 95%, CI (186.4 to 310.0), while the cytotoxicity on normal cells (HFB-4) showed higher IC50 of 280 μg/mL with 95%, CI (189.4 to 452.1).
In addition, the optimized formula scored IC50 values of 1.05 μg/mL with 95%, CI (0.6090 to 1.419), 2.63 μg/mL with 95%, CI (1.898 to 6.991), 5.68 μg/mL with 95%, CI (2.932 to 10.97) and 19.34 μg/mL with 95%, CI (16.01 to 23.37) in MCF-7, PC-3 and HepG-2 cancer cell lines as well as the HFB-4 normal cell line, respectively. Furthermore, the void optimized formula recorded IC50 values of 4.516 μg/mL with 95%, CI (3.193 to 6.389), 6.43 μg/mL with 95%, CI (4.472 to 9.245), and 11.5 μg/mL with 95%, CI (8.355 to 15.87) in MCF-7, PC-3 and HepG-2 cancer cell lines, respectively.
Response surface methodology for optimization of PE-SLNs
In this study, BBD was employed to optimize and evaluate the main, interaction and quadratic effects of the independent variables at different levels on the dependent variables. Considerable variations between the responses were obtained based on the different combinations of variables and variable levels.
The results revealed that the size distribution exhibited good unimodal behavior as shown in Figure 1 for batch F1 as a sample. Additionally, Figure 2 shows the TEM images of the PE-SLNs; obtained from batch F5 as an example as all the images obtained were similar, which showed spherical particles with no evident sign of aggregation. In addition, all formulations showed negative zeta potential since lipid nanoparticles have negative charge on their surface due to the presence of terminal carboxylic groups in the lipids.34 Furthermore, Figure 3 displays the in vitro release profiles of PE-SLNs dispersion, which revealed a biphasic release pattern characterized by a rapid initial burst drug release followed by sustained release and this behavior has been stated for SLNs.35,36
Figure 1 Particle size distribution for batch F1.
Figure 2 Transmission electron microscopy image for pomegranate extract solid lipid nanoparticles obtained from batch F5.
Figure 3 In vitro release of stearic acid SLNs-loaded PE through cellulose membrane after 48 h.
To illustrate the influence (in decreasing order of importance) of the independent variables and their interactions on the dependent ones, Pareto charts were constructed (Figure 4). The chart involves a vertical reference line at the critical p-value of 0.05 where the effect that exceeds the vertical line is considered to be statistically significant. In addition, 3D response surfaces (Figure 5) were created according to the model polynomial functions to estimate the change of the response surface.
Figure 5 Estimated three-dimensional response surfaces plot for the effect of the studied variables on (A) particle size, (B) polydispersity index, (C) zeta potential, (D) entrapment efficiency % and (E) cumulative % drug release.
From the obtained results, it is obvious that X1 and Y2 have a direct relationship which could also be attributed to the fact that lipid concentration was increased, viscosity of the dispersed phase was also increased which gave rise to particle aggregation that led to higher particle size and PDI and reduced homogenization efficiency.37 In addition, X1 had the main effect on Y4 where a direct correlation was detected and this could be as a result of the higher amount of lipid which offered extra space to accommodate an excess amount of drug during the preparation of SLNs which led to a reduction in the diffusion rate of the drug into the external phase as viscosity of the lipid phase was higher and thus showed higher EE.37,38 On the other hand, X1 had a negative effect on Y5 which could be explained by increasing the particle size and subsequently decreasing the specific surface area and, therefore, reducing the release rate.39 Furthermore, high lipid concentration leads to high medium viscosity and more rigid solidified nanoparticles which would also slow down the drug diffusion to the dissolution medium.40
It was observed that X2 and X3 had a direct relationship with Y1 that could be explained by the reduction in the interfacial tension between lipid and aqueous phase when increasing the concentration of tween 80 and lecithin which may control the aggregation of lipid particles by facilitating the particle partition thus resulting in lower size.41 Additionally, as stated before, higher surfactant concentration stabilizes the lipid matrix successfully by developing a steric barrier on their surface, thus avoiding aggregation.42
On the other hand, X2 had a negative impact on Y3 which may be due to the surface coverage of the SLNs which reduces the electrophoretic mobility of the particles and thus lowers the zeta potential.43 However, X3 showed a positive effect on Y3 which may be due to the ionic nature of lecithin that broadens the electric double layer surrounding the nanoparticles and increases the zeta potential.44 A negative influence on Y5 was observed due to X3, which could be due to the stabilization role of the cosurfactant, since the higher cosurfactant content stabilizes the SLN, and it also restricts the amount of drug released outside SLN.45
Mathematical modeling and statistical analysis of the experimental data
Analysis of the values for the responses (Y1 to Y5) of the formulations of PE-SLNs was performed using Statgraphics® plus software and Equations 3 to 7 show the mathematical model for each response:
Prediction of the optimized PE-SLNs formulation
Analysis of the experimental factors was performed to assess the examined responses so as to reach factors levels with optimum combination which maximize the desirability function. The optimum formulation of the PE-loaded SLN system was designated based on the criteria of achieving the maximum value of EE, cumulative % drug release, zeta potential and minimizing the particle size, PDI by applying the numerical point prediction optimization method of the Statgraphics® plus software. The responses at optimal combination of independent variables were done to confirm the validity of the calculated optimal factors and the expected responses. The composition of the optimized formula, the observed and predicted responses and the residual values for the responses are illustrated in Table 5. Based on these results, it can be concluded that the optimized combination of the independent variables confirmed the preferred particle size, PDI, zeta potential, EE% and cumulative % drug release. In addition, the drug-loading capacity was found to be 1.86%, indicating high drug-loading capacity and the result obtained is in agreement with that obtained by Tran et al.46
Table 5 Composition of the optimized formula of PE-loaded SLNs with the predicted, observed and residual values of the responses
In vitro cytotoxicity study of the optimized formula
Figure 6 shows the results of the MTT cell proliferation assay which was done to examine the cytotoxicity effect of the optimized PE-SLNs formula on the viability of different cancer cell lines compared to the free PE and the void optimized formula by determination of their IC50 (95%, CI).
The highest effect of PE on the MCF-7 cancer cell line is consistent with the great efficacy of PE against breast cancer cells found earlier,6,7,12,47 while the lower effect of PE was noticed on both PC-3 and HepG-2 cancer cell lines.48–50 On the other hand, it was observed that the IC50 value on the HFB-4 normal cell line was higher by 5.7-fold and 2.6-fold compared to MCF-7 and PC-3 cancer cell lines, respectively, which might indicate the selective toxicity of PE against these cancer cells. However, the effect of PE on HepG-2 was not statistically significant when compared with its effect on HFB-4.
To decide whether nanoencapsulation improved the biological activity of PE or not, we compared the influence of free PE against their nanoprototypes (PE-SLNs optimized formula) on the same cancer cell lines. The effect of the optimized formula on MCF-7 was significant statistically when compared with other cell lines. Accordingly, this data is of the utmost importance since as noticeable, the PE-SLNs-optimized formula was superiorly more cytotoxic and effective, reducing the IC50 values by 47-fold for breast cancer followed by 40-fold for prostate cancer, and 38-fold for liver cancer in comparison to the free PE. This may be due to the fact that PE-SLNs provide a safe delivery system which enhances the efficacy of pomegranate bioactive compounds and thus enhances the bioactivity of the chemopreventive phytochemicals from pomegranates.6 Remarkably, the higher IC50 value of the optimized formula on the HFB-4 normal cell line was observed by 18.4-, 7.4- and 3.4-fold over the MCF-7, PC-3 and HepG-2 cancer cell lines, respectively. This indicates that the optimized formulation has a higher selectivity profile and works preferentially against cancer cells.
Furthermore, the void optimized formula was examined for its cytotoxic effect to determine the influence of the ingredients used on the cancer cells. The only significant finding was the difference in IC50 between the PE-SLNs-optimized formula and the void-optimized formula on the MCF-7 cell line. These results could be attributed to the effect of stearic acid, the main component of our SLNs, which has been previously reported for its anticancer effect by inducing apoptosis on breast cancer,51 prostate cancer particularly on the PC-3 cell line52 and liver cancer.53
Formulations of PE-SLNs were optimized and the optimized formula was developed using BBD which was successfully implemented to statistically optimize the formulation variables. It was found that the lipid concentration had the main effect on the PDI, EE and cumulative drug release. In addition, the surfactant concentration had a significant effect on the particle size and zeta potential. Furthermore, the cosurfactant concentration had the main effect on the particle size, zeta potential and cumulative drug release. The performed cytotoxicity study on different cancer cells that was carried out for optimized PE-SLNs formula, free PE and void optimized formula verified that encapsulation of PE in SLNs enhances their bioefficacy, particularly on MCF-7 breast cancer cells where the IC50 was reduced from 49.2 to 1.05 μg/mL by 47-fold. Moreover, the optimized formula showed a preferential cytotoxicity against cancer cells compared to normal cells. Furthermore, we propose the optimized PE-SLNs formula as the formula of choice for further investigations of PE as a promising anticancer agent, particularly for breast cancer.
MHT, DAA, MAE and MME conceived and designed the study. KME performed the Box–Benhken design and prepared all figures and tables for optimization. NMB performed all laboratory experiments. MHT, DAA, MAE and MME supervised the work. NMB wrote the manuscript and DAA and MME edited the final version. All authors contributed toward data analysis, drafting and critically revising the paper and agree to be accountable for all aspects of the work.
The author reports no conflicts of interest in this work.
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