Preparation of liposome encapsulating angiotensin-I-converting enzyme inhibitory peptides from sunflower protein hydrolysates
- Authors:
- Published online on: January 24, 2018 https://doi.org/10.3892/mmr.2018.8474
- Pages: 5306-5311
Abstract
Introduction
Synthetic angiotensin-I-converting enzyme (ACE) inhibitory (ACEI) drugs, including captopril, lisinopril, enalapril and ramipril, are effective to treat cardiovascular disease. However, side effects accompany the application of these drugs, including proteinuria, altered sense of taste, allergic skin rashes, cough and drug fever (1). Isolation of effective natural ACEI peptides from diets or crops is an attractive prospect. A series of ACEI peptides derived from food protein sources have been identified, including from fermented milk, cheddar cheeses (2), hen egg white (3), tuna (4), rice (5), soybean (6), peanut meal (7), skate (Okamejei kenojei) skin gelatin (8), flaxseed (9) and pumpkin (10). These ACEI peptides were commonly collected using proteolytic hydrolysis methods or during fermentation processing. Although ACEI peptides from natural food are considered to be safe, they exhibit low efficacy in comparison with synthetic ACEI drugs. Sunflower protein is an important source for ACEI peptides. The procedure for the purification of ACEI peptides derived from sunflower protein, includes the gel filtration chromatography, affinity chromatography and reverse-phase chromatography (11,12). However, it is important to improve the entrapment efficiency and to reduce the release of ACEI peptides.
Liposomes have unique physicochemical properties including the ability to incorporate lipophilic, amphiphilic and/or hydrophilic compounds, and the ability to improve the stability and reduce the toxicity of encapsulated drugs (13,14). Different methodologies are reported to prepare multi-lamellar vesicles, large unilamellar vesicles and small unilamellar vesicles (15). Liposomes formed by thin-film ultrasonic methods have also been widely reported in the literatures (16–19). However, the production of these phospholipids vesicles is poorly reproducible as that ACEI peptides-liposomal experimental set-up is not described in detail.
In this study, it was aimed to optimize the encapsulation conditions for producing liposome ACEI peptides by employing response surface methodology (RSM). In addition, fractional factorial design (FFD) and the central composite design were also used to identify the most important variables for optimizing the encapsulation conditions during the experiments.
Materials and methods
Materials and chemical reagents
Defatted sunflower meal was supplied by China Oil & Foodstuffs Corporation (Shihezi Branch, China). Alcalase (ExPASy entry EC 3.4.21.62, Bacillus licheniformis; 2.4 L), and flavourzyme (ExPASy entry EC 3.4.11.1; 1,000 mg) were purchased from Novozymes (Bagsvard, Denmark). ACE (ExPASy entry EC 3.4.15.1, rabbit lung; 0.25 U/ml) and N-[3-(2-furyl) acryloyl]-L-phenyl-alanylglycylglycine (FAPGG) substrate were purchased from Sigma-Aldrich (Merck KGaA, Darmstadt, Germany). Bicinchoninic acid (BCA) protein kit and bovine serum albumin were purchased from Beijing Kangwei Century Biotechnology Co., Ltd. (Beijing, China). Cholesterol, L-α-dipalmitoyl phosphatidylcholine (DPPC), phosphatidylcholine (PC), soybean phospholipids (SP), sphingomyelin (SM), 1-myristoyl-2-palmitoyl-sn-glycero-3-phosphatidylcholine (MPPC), and polyethylene glycol (PEG; molecular weight, 2,000) were purchased from Rizhao Jia Qing Trading Co., Ltd. (Rizhao, China). All other chemicals and reagents were of analytical grade.
Preparation of sunflower protein isolates
Defatted sunflower meal flour (20 g) was extracted by stirring for 1 h in 200 ml 60% ethanol aqueous solution. Following vacuum filtration, the residue was washed twice with distilled water and extracted by stirring for 1 h in 200 ml NaOH (0.05 M) at room temperature. Following centrifugation at 7,155.2 × g for 20 min, an additional extraction was performed with half the volume of alkaline solution. The pH of the supernatant was adjusted to the isoelectric point (pH 4.3) of sunflower proteins, and the precipitate formed was recovered by a centrifugation as described above, washed with distilled water and freeze-dried until further use.
Sunflower protein-derived ACEI peptides were prepared according to Villanueva et al (20) and Dadzie et al (21) with modifications: Adjusted hydrolysis pH for Alcalase from 8 to 8.5 and for Flavourzyme from 7 to 6.5. In the present study, the fraction of molecular mass <3 kDa was gained by ultrafiltration following hydrolysis and then added to an open column (1.6×100 cm) packed with Sephadex G-25 gel Beijing RuiDa HengHui Science and Technology Development Co., Ltd.,(Beijing, China), that had been pre-equilibrated with distilled water.
The ACEI peptides were eluted by distilled water at the speed of 60 ml/h and the elution peaks were monitored at 220 nm. Those fractions (IC50, 2.63±0.08 µg/ml) were vacuum freeze-dried and stored at −20°C until use (22).
Preparation of liposome containing ACEI peptides
Liposomal ACEI peptides were prepared by thin-film ultrasonic method as described by Ferreira et al (23) and Cortesi et al (24) with certain modifications. The obtained liposome preparation was incubated at room temperature under continuous stirring (180 mot/min) for 16–18 h in order to achieve higher entrapment efficiency (25). The preparation of liposome containing ACEI peptides was confirmed by scanning electron microscope (SEM) (JSM-6490LV; JEOL, Ltd., Tokyo, Japan).
Determination of entrapment efficiency
Entrapment efficiency of liposomal ACEI peptides was determined using Centrifree® (EMD Millipore, Billerica, MA, USA) according to previously reported method (26) with certain modifications: The supernatant was analyzed via a BCA Protein Quantitation kit (aforementioned) at 562 nm to determine the amount of unencapsulated ACEIPs. A standard curve was established with bovine serum albumin.
Liposomal ACEI peptides release assay in vitro
An ACEI peptides release experiment was performed using the dialysis method according to Cortesi et al (24) with slight modification: The adjusted molecular weight of the dialysis tube was reduced from 10,000–12,000 to 8,000–10,000. Analysis of ACEIPs content from by HPLC to BCA Protein Quantitation kit.
FFD
A reduced (26-2) factorial design at two levels with resolution IV was selected. The variables were coded according to the following equation: xi=(Xi-X0)/ΔXi; where xi was the coded value of an independent variable, Xi was the real value of an independent variable, X0 was the real value of an independent variable at the central point, and ΔXi was the step change value.
Central composite design (CCD)
In order to describe the nature of the response surface in the optimum region, a central composite design RSM was performed to examine the effect of the three independent variables X1 (phospholipids to cholesterol ratio), X5 (ultrasound time), and X6 (phospholipids to ACEI peptides ratio) at five levels for each variable on the entrapment efficiency.
Statistical analysis
Design expert 8.0.5 software (Stat-Ease, Inc., Minneapolis, MN, USA) was used for analysis of variance (ANOVA) of the mean responses fitted to a second order polynomial to obtain regression equations. Entrapment efficiencies were compared using one-way ANOVA and Bonferroni multiple comparisons test. P<0.05 was considered to indicate a statistically significant difference. The adequacy of the model to navigate the design space of the responses was determined using the coefficient of determination (R2) and a lack of fit test. Two-dimensional (2D) contour plots and three-dimensional (3D) response surface plots for the responses were generated for two independent variables while fixing the remaining variable at coded 0 levels. The release profile of liposome containing ACEI peptides and the fitted curve for the percentage ACEI peptides released and release time were constructed by Origin 8.0 (OriginLab Corporation, Northampton, MA, USA).
Results and Discussion
Effects of phospholipids on preparation of liposome containing ACEI peptides
In order to identify the most appropriate phospholipids for ACEI peptide entrapment, five phospholipids (SP, PC, DPPC, MPPC and SM) were used to prepare the liposome containing ACEI peptides (Fig. 1). The SP formulation had the highest entrapment efficiency (85.57±5.68%), followed by DPPC formulation (81.24±9.41%) and MPPC (77.31±10.32%), and there was no significant difference among them. By contrast, PC and SM formulation exhibited much lower entrapment efficiency (PC, 45.07±0.78%; SM, 50.03±7.55%), which were significantly lower than those of the SP, MPPC and DPPC formulations. These results were consistent with a previous report, in which there were markedly different interactions among peptides and various types of charged liposome (27). Therefore, the SP formulation was chosen to further optimize the entrapment conditions for producing liposomal ACEI peptides because of its higher efficiency and lower cost. Liposomal ACEI peptides were imaged using SEM (Fig. 2).
Screening of preparation conditions for liposomal ACEI peptides using FFD
A 26-2 FFD was applied to evaluate the impact of six factors. The entrapment efficiency of liposomal ACEI peptides markedly varied in a range from 40.28–90.91%. The factorial analysis of variances indicated that the ratio of phospholipids to cholesterol (X1), ultrasound time (X5) and the ratio of phospholipids to ACEI peptides (X6) were significant factors (P<0.001), which affected entrapment efficiency of liposomal ACEI peptides, while PEG-2000 dosage, NaCl concentration in PBS and hydration temperature were non-significant factors (Table I). In this case, there was significant interaction between X1 and X6, between X1 and X4 (P<0.01). Using multiple regression analysis, the response variables and the test variables were related by the second-order polynomial equation as follows: Y1=76.32–4.56X1-9.84X5+7.71X6+3.27X1X4-2.66X1X5+3.52X1X6. The values of R2 and adjusted R2 were 88.76 and 83.58%, respectively, indicating that the model fitted well with the experimental data. The comparable values revealed that non-significant factors were not included in the model. The P-value of lack-of-fit in ANOVA was insignificant for the model at a confidence level of 95% (P=0.0605), suggesting that the model represented the data satisfactorily.
Table I.Analysis of variances results of fractional factorial designs for entrapment efficiency (Y1) of liposomal angiotensin-I-converting enzyme inhibitory peptides. |
CCD and response surface analysis for liposomal ACEI peptides preparation
RSM is a popular and effective method to solve multivariate problems and optimize several responses in many types of experimentation (28,29). Based on the results of FFD analysis, the factors (X1, X5 and X6) were selected for a further optimization of the entrapment efficiency of liposomal ACEI peptides using a Box-Wilson CCD with six replicates at center point for each factor. PEG-2000 dosage (X2), NaCl concentration in PBS (X3), hydration temperature (X4) were set as 4%, 50 mM/l and 45°C, respectively. The second-order polynomial equation is as follows: Y2=78.34+1.89 X1-7.46 X5-9.89 X6-0.13 X1 X5-2.57 X1 X6+2.79 X5 X6-4.06 X12-13.29X52-0.61 X62; where Y2 is the predicted entrapment efficiency in real value, and X1, X5 and X6 are the coded values of independent variable the ratio of phospholipids to cholesterol, ultrasound time and the ratio of phospholipids to ACEI peptides, respectively.
Table II presents results of the second-order response surface model in the form of ANOVA. The Fisher's F-test with a very low probability value [(Prob>F) <0.0001] indicated the model was highly significant. The model fitted the data with an acceptable determination coefficient (R2=0.9761) and no significant lack-of-fit (P=0.1491), which indicated that the sample variation of 97.61% could be attributed to the independent variables, and the model did not explain only 2.39% of the total variations. The adjusted determination coefficient (R2=0.9546) was also satisfactory to confirm the significance of the model. Meanwhile, the low value of coefficient of variation (CV=5.26%) implicated accuracy and reliability of the experiments.
The regression analysis showed that the ultrasound time (X5) and the ratio of phospholipids to ACEI peptides (X6) had a very significant linear effect on entrapment efficiency. Meanwhile the ultrasound time (X5) and the ratio of cholesterol to phospholipids (X1) exhibited a significant quadratic effect (P<0.01). In addition, an interaction between the ultrasound time and the ratio of phospholipids to ACEI peptides for the entrapment efficiency (P<0.05) was also observed. The linear effects of X1, quadratic effect of X62 and interaction effects of X1X5 and X1X6 were demonstrated to be non-significant on the entrapment efficiency of liposomal ACEI peptides.
To illustrate the interaction of the ratio of phospholipids to cholesterol, ultrasound time and ratio of phospholipids to ACEI peptides and to efficiently optimize the variables, 3D response surface plots and the 2D contour plots were obtained. As shown in Fig. 3, a visual interpretation of the interactions between the two independent variables on the entrapment efficiency was observed, while the third variable was held at zero level. The circular contour plots of response surfaces suggest that the interaction is negligible among the corresponding variables. An elliptical or saddle nature of the contour plots indicates the significance of the interactions between the corresponding variables. In the case of saddle contour plots, the optimum values are obtained at the point of intersection of lines, which are formed by joining the locus (30).
Fig. 3A and B demonstrate that entrapment efficiency of liposomal ACEI peptides was increased with the increase of ultrasound time from 5 to 10 min, while it was decreased when the ultrasound time was >10 min. The result was similar to a previous publication (31). The entrapment efficiency was increased with the ratio of phospholipids to cholesterol until a peak was detected at ~3:1 (w:w). In Fig. 3B, the saddle contour plots demonstrated that interactions between phospholipids to cholesterol ratio and phospholipids to ACEI peptides ratio also reached optimum levels. Fig. 3C shows that the entrapment efficiency of liposomal ACEI peptides increased with the decrease of the ratio of phospholipids to ACEI peptides from 25:1 to 15:1 (w:w) when the ratio of phospholipids to cholesterol was set. There was a saddle in the contour plot (Fig. 3C), indicating the significance of interactions between ultrasound time and the ratio of phospholipids to ACEI peptides.
Validation of the experimental design
The optimum conditions for the entrapment efficiency of liposomal ACEI peptides were calculated based on the data obtained using the ‘response optimizer’ option of Design-Expert software. The optimal values of each variable in coded units were as follows: X1=0.55, X5=−0.39 and X6=−1. Their actual values were 4.1:1 (w:w) of phospholipids to cholesterol ratio (X1), 8.05 min of ultrasound time (X5) and 15:1 (w:w) of phospholipids to ACEI peptides ratio (X6), respectively. The model predicted that the entrapment efficiency of liposomal ACEI peptides could reach 90.86% by using the above optimized condition of the variables. The experiments were repeated three times to validate the suitability of the model equations. The entrapment efficiency (91.25±0.182%, n=3) was obtained from the real experiments, indicating validation of the RSM model.
ACEI peptides release assay
The liposomal ACEI peptides were subjected to release experiments in vitro in order to provide information about the efficiency of release of ACEI peptides from liposome. As reported in Fig. 4, the percentage of ACEI peptides released in phosphate buffer was 95.74% after 12 h, whereas it was 77.83% after 12 h for liposomal ACEI peptides. The release of liposome-entrapped ACEI peptides was significantly delayed compared with ACEI peptides in phosphate buffer. Furthermore, the fitted equation of the percentage of ACEI peptides released vs. release time was calculated based on different release models (zero-order dynamic, one-order dynamic, Korsmeyer-Peppas, Higuchi, logistic) (32,33). The logistic model and one-order dynamic model were well-fitted with the release percentage of ACEI peptides (adjusted R2 of 0.9883 and 0.9841, respectively).
In conclusion, liposomal ACEI peptides derived from sunflower protein hydrolysates were prepared with the aims of improving entrapment efficiency and sustaining release. The ratio of phospholipids to cholesterol, ultrasound time and the ratio of phospholipids to ACEIPs were notable factors affecting entrapment efficiency. Under optimal experimental conditions, the entrapment efficiency of liposomal ACEIPs was 91.25±0.182%. The percentage of released of liposomal ACEIPs was reduced by 17.91% compared with ACEIPs in phosphate buffer after 12 h. However, there are some limitations of the present study. The release of liposome-entrapped ACEIPs in simulated gastric fluid and simulated intestinal fluid was not investigated, and the stability of liposomes was also not analyzed under long durations of preservation; further investigation is required.
Acknowledgements
The present study was partially supported by a grant of College Students' Innovative Training Program of China (grant no. 201410759048).
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