Evaluation of Antitumor Efficacy of Chitosan-Tamarind Gum Polysaccharide Polyelectrolyte Complex Stabilized Nanoparticles of Simvastatin
Authors Malviya R, Raj S, Fuloria S, Subramaniyan V, Sathasivam K, Kumari U, Unnikrishnan Meenakshi D, Porwal O, Hari Kumar D, Singh A, Chakravarthi S, Kumar Fuloria N
Received 8 January 2021
Accepted for publication 15 March 2021
Published 29 March 2021 Volume 2021:16 Pages 2533—2553
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Professor Israel (Rudi) Rubinstein
Rishabha Malviya,1,* Shakshi Raj,1,* Shivkanya Fuloria,2,* Vetriselvan Subramaniyan,3,* Kathiresan Sathasivam,4 Usha Kumari,5 Dhanalekshmi Unnikrishnan Meenakshi,6 Omji Porwal,7 Darnal Hari Kumar,8 Amit Singh,1 Srikumar Chakravarthi,9 Neeraj Kumar Fuloria2,*
1Department of Pharmacy, SMAS, Galgotias University, Greater Noida, U.P., India; 2Department of Pharmaceutical Chemistry, Faculty of Pharmacy, AIMST University, Kedah, 08100, Malaysia; 3Department of Pharmacology, Faculty of Medicine, Bioscience and Nursing, MAHSA University, Kuala Lumpur, 42610, Malaysia; 4Department of Biotechnology, Faculty of Applied Science, AIMST University, Kedah, 08100, Malaysia; 5Department of Physiology, Faculty of Medicine, AIMST University, Kedah, 08100, Malaysia; 6Department of Pharmacology, College of Pharmacy, National University of Science and Technology, Muscat, 130, Oman; 7Department of Pharmacognosy, Faculty of Pharmacy, Tishk International University, Erbil, 44001, KRG, Iraq; 8Department of Pathology, Jeffrey Cheah School of Medicine and Health Sciences, Monash University, Johor Bahru, 80200, Malaysia; 9Department of Pathology, Faculty of Medicine, Bioscience and Nursing, MAHSA University, Kuala Lumpur, 42610, Malaysia
*These authors contributed equally to this work
Correspondence: Neeraj Kumar Fuloria
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, AIMST University, Kedah, 08100, Malaysia
Tel +60 164037685
Email [email protected]
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, AIMST University, Kedah, 08100, Malaysia
Tel +60 143034057
Email [email protected]
Purpose: The present study was intended to fabricate chitosan (Ch)-tamarind gum polysaccharide (TGP) polyelectrolyte complex stabilized cubic nanoparticles of simvastatin and evaluate their potential against human breast cancer cell lines.
Materials and Methods: The antisolvent precipitation method was used for formulation of nanoparticles. Factorial design (32) was utilized as a tool to analyze the effect of Ch and TGP concentration on particle size and entrapment efficiency of nanoparticles.
Results: Formulated nanoparticles showed high entrapment efficiency (67.19± 0.42– 83.36± 0.23%) and small size (53.3– 383.1 nm). The present investigation involved utilization of two biological membranes (egg and tomato) as biological barriers for drug release. The study revealed that drug release from tomato membranes was retarded (as compared to egg membranes) but the release pattern matched that of egg membranes. All formulations followed the Baker–Lansdale model of drug release irrespective of the two different biological barriers. Stability studies were carried out for 45 days and exhibited less variation in particle size as well as a reduction in entrapment efficiency. Simvastatin loaded PEC stabilized nanoparticles exhibited better control on growth of human breast cancer cell lines than simple simvastatin. An unusual anticancer effect of simvastatin nanoparticles is also supported by several other research studies.
Conclusion: The present study involves first-time synthesis of Ch-TGP polyelectrolyte complex stabilized nanoparticles of simvastatin against MCF-7 cells. It recommends that, in future, theoretical modeling and IVIVC should be carried out for perfect designing of delivery systems.
Keywords: polysaccharide, polyelectrolyte, cubic nanoparticles, simvastatin, breast cancer, tamarind
Abnormal growth and uncontrolled division of cells is known as cancer. Studies suggest that breast cancer is the second most common cancer after skin cancer. Breast cancer may spread into other organs of the body and becomes life-threatening.1 Conventional treatment of cancer involves radiotherapy, chemotherapy, and surgery. Several cancer treatment approaches are often ineffective, as attributed to their side-effects. Natural anticancer agents offering minimal side-effects are of great interest to many investigators. Studies suggest the anticancer potential of bio constituents of tamarinds seeds.2,3
Simvastatin is now the second most significant reductase inhibitor in the class of compounds known as hydroxy-methylglutaryl-coenzyme, a reductase inhibitor researched in humans. Simvastatin is now being provided for periods of up to 2 years to over 1,800 patients for the management of hypercholesterolemia.4
In a study examining the effect of simvastatin on hepatocellular carcinoma, it was observed that simvastatin induces G0/G1 arrest by upregulation of p21 and p27 by activation of AMPK and inhibition of the STAT3-Skp2 axis, respectively.5
Simvastatin also triggered caspase-dependent apoptosis in A549 lung cancer cells, where that was associated with decreased expression of phosphorylate Akt and low-regulatory survival of mRNA and protein.6 Another research study on prostate cancer using microarrays demonstrated that simvastatin therapy resulted in an up-regulation of Annex A10 (ANXA10) in PC-3 cells. ANXA10 is assumed to also have anti-tumor effects.6
Tamarind (Tamarindus indica) belongs to the Fabaceae family and is widely distributed in India, especially South India. The tamarind gum polysaccharide (TGP) is extracted from the kernel of tamarind seeds. The TGP is also known as galactoxyloglucan and its molecular weight is around 52,350 D, which constitutes about 60% of the total seed content.7 The TGP exhibits good gelling ability and muco-adhesion properties. The TGP is used as a carrier for oral and parenteral drug delivery systems.8,9 In liquid dosage form, TGP has been used as suspending, emulsifying, and thickening agents. Moreover, TGP is also known for its nontoxic, biodegradability and biocompatibility properties.10 As discussed by authors in previous studies, a major component of tamarind seed pulp is carbohydrate (70.8%), followed by protein (3.1%) and fiber (3.0%). Tamarind seed polysaccharide consists of the -OH group attached with cyclic structure. Galactose, xylose, and glucose are present in a 3:1:2 molar ratio. This ratio predicts that galactose is the major component of tamarind seed polysaccharide followed by glucose and xylose.9,11,12
Chitosan (Ch) is obtained from chitin. Crustacean and insect cuticle exoskeletons are known as rich natural sources of chitin. Chitin a natural biopolymer, is also found in fungal cell walls and mollusk shells.13 Tailoring of Ch by involving amino, acetamide, or hydroxy groups can generate derivatives with improved solubility and remarkable anticancer activity.14,15
Studies have shown that both Ch and its derivatives selectively permeate through cancer cell membranes and exhibit anticancer activity via enzymatic, immunoenhancing, antiangiogenic, antioxidant defense mechanisms, and the apoptotic pathways of cells.15 Wimardhani et al's study revealed that cell cycle arrest and induction of apoptosis is the basic reason behind the anticancer activity of Ch.16
Investigation suggests that nanoparticles are a promising tool for enhancement of cancer treatment because of their bioavailability enhancement property.19 Nanoparticles are reported to enhance the bioavailability of less water-soluble drugs and prevent their degradation from various environmental factors. Nano-encapsulation is a novel approach to improve the solubility of dissolution controlled hydrophobic biologically active compounds.20
Since the last century, polyelectrolyte complex (PEC) based drug delivery systems have attracted researchers on the basis of their pharmaceutical and biomedical applications. One study reported the complex formation of Ch with a natural polymer (alginate) to retard the swelling and erosion of Ch that leads to retardation in drug release.21 The PEC formation is a novel strategy used to elevate the biological and pharmaceutical properties of polymers.22
The PEC formation and nanotechnology approach, combined, have been used by researchers to improve the bioavailability of active pharmaceutical ingredients (APIs).23 Rajabi et al developed Ch-gum Arabic polyelectrolyte based nanocarriers for the delivery of saffron bioactive compounds. Prepared nano capsules were spherical in shape, with a diameter of about 193 nm.24 When oppositely charged macromolecules are allowed to interact with each other, polyelectrolyte or poly salt complexes are formed. Between oppositely charged molecules, like drug-polymer or polymer-polymer or polymer-drug-polymer, a few association complexes are formed, which are called PECs. Between these oppositely charged polyelectrolytes the electrostatic interaction may take place.25 PECs have been used to prepare systems for drug delivery.26
Structurally, these are neutral polymer-polymer complexes consisting of macromolecules with opposite charges causing the electrostatic interactions to bind macromolecules together. In PEC formation, ion dipole interactions, hydrogen bonding and hydrophobic interactions play a major role. This complexity leads to the loss of polymer chain conformation and translational entropy that must be counter-balanced. Electrostatic force is considered a major contributor to the formation of PECs. However, other components of hydrogen bonding in dipole forces and hydrophilic interaction also significantly contribute to their complexation process.27,28 When low molecular weight counter ions are released, there is a gain in entropy. It is the main driving force for complex formation. In recent decades, researchers have tried to develop PEC stabilized nanoparticles for drug delivery. The shape of the nanoparticles is a key factor that affects biodistribution, bio-circulation, cellular penetration, and targeting sites. In most of the cases nanoparticles are spherical in shape, maybe due to less awareness about the effect of shape of formulation on therapeutic effect and simplicity of process. Recently, the focus of biomedical scientists, globally, has shifted towards the shape-specific fabrication of nanoparticles. The shape of nanoparticles also dictates the fate of pharmacokinetics and pharmacodynamics of active pharmaceutical ingredients. In recent decades, the formulation of cubic nanoparticles has attracted much attention. Fabrication of cubic nanoparticles has tuned the association of particles with specific receptors. Research claims that the PRINT method has been used to prepare cube-shaped nanoparticles. Also, the solvent–antisolvent precipitation method assists in the preparation of spherical nanoparticles.29,30
It was observed that none of the researchers used solvent–antisolvent precipitation method for the fabrication of Ch-TGP polyelectrolyte stabilized cubic nanoparticles. Interaction between the amino group of Ch and the hydroxyl group of TGP leads to formation of PECs. As PECs are formed between biocompatible, biodegradable, and nontoxic polymers, they are expected to offer good bio-acceptability. Self-organization, reversible and spontaneous association between oppositely charged molecules without covalent cross-linkers is a distinguished feature of formed PECs. Formed PECs are biodegradable, biocompatible, and non-toxic in nature. The study of Verma et al found that formation of PECs between poly acid and poly base leads to the formation of crystal-like structures.31
Keeping with the idea of Verma et al, it was expected that Ch- and TGP-based PECs will produce crystalline nanoparticles.31 As per our knowledge, it was the first attempt to explore the formulation of Ch-TGP polyelectrolyte stabilized crystalline nanoparticles for therapeutic application. Limited information was found on the effect of shape of polyelectrolyte stabilized nanoparticles on human cancer cells. In the present study, an attempt was made to investigate the effect of cubic nanoparticles and needle-shaped pure drugs in human breast cancer cell lines. The outcomes of the study will surely provide basic guidelines for the design of delivery systems against cancer.
Materials and Methods
The chemicals, reagents and solvents were obtained from Merck Specialties, Sigma Aldrich, S D Fine Chemicals Limited, Fisher Chemicals, and HiMedia. Chitosan (medium molecular weight, 75–85% deacetylated) was procured from Sigma Aldrich, St. Louis, USA).
Extraction of Tamarind Gum Polysaccharide
The testa (seed coat) of the seeds of tamarind was removed by drying them in a hot air oven for 20 min at 40°C. Next, the seed coating was removed by simply crushing the seeds from one side. Obtained white portions of the seeds were then utilized for the isolation of gum. The inner white part of seeds was immersed in a beaker with double-distilled water and heated at 40°C for 2 h. The supernatant fluid was discarded after centrifugation. Further, the remaining portion was concentrated by again heating at a constant temperature of 40°C. The slurry was filtered, and filtrate was precipitated using ethyl alcohol. The precipitated product was spread on the petri dish, dried and the size was reduced till a fine powder was obtained. Size reduction was carried out using a pestle and mortar. The powder was passed through sieve #22 and stored for further use.32
The 32 factorial design was used to prepare nanoparticles. In the present research, TGP and Ch concentrations were selected as independent variables; for dependent variables, particle size and entrapment efficiency were selected. Three levels were selected for every independent variable, as shown in Table 1. The NCSS 12 software (Trial version 15/05/2018) was used for the analysis of dependent variables.33
Table 1 Concentration of TGP (% w/v) and Ch (% w/v) for the Preparation of Nanoparticles
Preparation of PEC Stabilized Nanoparticles
Nanoparticles were formulated using various concentrations of TGP and Ch, as shown in Table 1. Solutions of 20 mL TGP and 20 mL of Ch were prepared separately in distilled water and 5% glacial acetic acid, respectively. TGP solution was further transferred into Ch solution and stirred for 20 min at 40°C and for a further 5 min at 50°C. Simvastatin solution (1 μg/1 mL) was prepared using acetone as solvent. For the preparation of simvastatin solution, 10 mg simvastatin was solubilized into 10 mL of acetone, followed by serial dilution to prepare 1 μg/1 mL solution. The drug solution (5 mL) was further added dropwise into the previously prepared TGP-Ch solution (PEC solution) using a syringe (BD Emerald, 5 mL). Next, the solution was stirred for 45 min at 65°C. Finally, the sample was cooled to 35°C and kept in an airtight container.34 Prepared samples consisting of dispersions of nanoparticles were used for further study and nanoparticles were not separated from the dispersions.
In the present investigation, simvastatin solution (1 μg/1 mL) was prepared using acetone as solvent. For the preparation of simvastatin solution, 10 mg simvastatin was solubilized into 10 mL of acetone, followed by serial dilution to prepare a 1 μg/1 mL solution.
Prepared samples consisting of a dispersion of nanoparticles (nanosuspension) were used for further study and nanoparticles were not separated from the dispersion. As the final formulation was nanosuspension, washing was not performed.
FTIR Spectral Analysis
Spectral analysis of native polymers (Ch and TGP), a drug (simvastatin) and a physical mixture of Ch, TGP and simvastatin was done to identify any interaction between drug and polymer. Analysis of all the compounds was done using OPUS software to record the spectra in the range 4000–400 cm−1.
Based on the following parameters, the PEC-based nanoparticles were characterized.
All the nanoparticles prepared were visually checked for turbidity.35
Particle Size Study
Using Zetasizer (Malvern Instruments, model no. 2000), the particle size of the formulated nanoparticles was determined. Zeta potential was also determined along with particle size. For the analysis, a dilute solution of 1% was used.36 As discussed in various literatures, concentrated solutions may create problems during particle size analysis. In the present investigation, a zeta analyzer was used to determine the particle size of THE formulated nanosuspension. A zeta analyzer is based on the principle of dynamic light scattering (DLS). In the concentrated solution, multiple scattering may take place that further leads to false results. To avoid the chance of false measurement, dilute solutions are generally employed to determine the size of suspended particles.37,38
The SEM is primarily used for the determination of the sample morphology. The morphology of the nanoparticles was analyzed by the Zeiss EVO 18 analyzer. The powder was coated with gold and then placed in a sample holder. Nanosuspensions were kept in a sample holder and dried under vacuum, before analysis to prepare powder. The surface properties of PEC stabilized nanoparticles were determined by a different magnification process.39
Absorption analysis of all formulations was carried out via the drug calibration plot to measure entrapment efficiency (%). In order to calculate entrapment efficiency, equation 1 was used. The freshly prepared 10 mL portion of the cooled nanosuspension was centrifuged in microcentrifuge at 10,000 rpm for 10 min. The supernatant was extracted, and the quantity of un-incorporated drug was calculated based on absorption of supernatant solution at 238 nm recorded using a UV spectrophotometer (UV-1800, Shimadzu, Japan).40,41
Tomato membranes and egg-shell membranes were used to determine the drug release from different formulations prepared from PECs.42
Egg Membrane Preparation
The chicken egg was taken for the preparation of the egg membrane. An orifice was created at one end of the egg and the yolk was completely removed through the opening. The egg shell was kept in a beaker containing a solution of distilled water and 0.1 N HCl (3:1 ratio). The egg shell containing calcium carbonate was released as foam when it came in contact with an acidic solution (equation 2). The temperature of the solution was raised to 50°C, which created bubbles. The bubbles stopped after 45 min and the foam disappeared. At last, only the egg membrane was left in the beaker.33
Preparation of Tomato Membrane
At the top of the tomato fruit a cross was made to release the pulp. The tomato was heated in a water bath at 50°C for 5 min and the membrane was then removed slowly and carefully.43
In vitro Drug Release
Formulation was enclosed in the biological membrane (tomato and egg membranes) and tied properly. To enclose the formulation, a 2 cm x 3 cm membrane was cut and used. Initially, drug release was carried out in 0.1N HCl for 2 h followed by release study in a phosphate buffer pH 7.4 up to 24 h. The temperature of both mediums was maintained at 37±0.5°C during the study, at 25 rpm. A sample (5 mL) was withdrawn at fixed time intervals and the same volume of fresh buffer was added. A UV spectrophotometer (UV-1800, Shimadzu, Japan) at wavelength 238 nm was used for the analysis. Equation 3 was used to determine drug release (%).32,44
Kinetic Studies of Drug Release
It is always necessary to determine the dissolution profile of a formulation. Kinetic models are used to determine the dissolution of a drug from the formulation in which the quantity of a dissolved drug is the function of time.45,46 Release kinetics can be influenced by the particle size of drug, type of drug, and solubility of drug. Kinetic study ensured that dissolution was occurring in the proper manner. To study the kinetics of drug release from the controlled release formulation, statistical methods and model-dependent methods were used. Model-dependent approaches included zero order, first order, Hixson–Crowell, Higuchi, Baker–Lonsdale, and Korsmeyer–Peppas.47,48 To calculate the zero-order and first-order rate constants, equations 4 and 5 were used, respectively.
where K is the first-order rate constant (time-1).
Equation 6 was used to determine the rate constant of the Higuchi model.
where Q is the released amount of the drug in time “t” per unit area A; C is the initial concentration of the drug; Cs is the solubility of the drug in the matrix media; and D is the drug molecule diffusivity.
To determine the kinetics of the Hixson–Crowell model release, equation 7 was used.
where W0 is the initial drug amount in the pharmaceutical dosage form and Wt is the remaining drug amount in the pharmaceutical dosage form at time t.
The release rate constant was determined by equation 8 for the Korsmeyer–Peppas model.
where Mt/M∞ is a drug fraction released at time t; k is the release rate constant; n is the release exponent; and κ (kappa) is a constant incorporating the surface volume relation.
Equation 9 was used to determine the rate constant for the Baker–Lonsdale model.
where the release rate constant, k, corresponds to the slope.
In formulation and dossier preparation, the concept of the similarity factor (f2) has been widely adopted. Two new indices (f1 and f2) were proposed by Moore and Flanner to compare test dissolution profiles and a reference formulation expressed in equation 10.49
where f2 is the similarity factor; n is the observation number; and (Rt–Tt) is the difference between the value of test and reference products.
The growth of the particle size of PEC-based nanoparticles was also measured at 25±2°C by determining the particles' size on the 1st, 7th, 14th and 21st days and the possible growth of crystals.50
At 40±2°C and 75±5% RH for 45 days, stability studies were carried out. In terms of particle size and entrapment efficiency, the stability of formulations was determined.51
An in vitro cytotoxicity analysis of pure drug and optimized formulation T5 was performed against breast cancer cell lines (MCF7) at the anti-cancer drug screening facility (ACDSF) at ACTREC, Tata Memorial Centre, Navi Mumbai. Sulphorhodamine B (SRB) was employed for the activity.
In the present analysis, MCF-7 cells were incubated for 24 h at 37 °C in 96-well microtiter plates. After inoculation of the cell, the microtiter plates were incubated with 5% CO2, 100% relative humidity and 95% air for 24 h at 37°C prior to addition of experimental drugs. Initially, test samples were solubilized in dimethyl sulfoxide at 100 mg/mL and diluted with water to 1 mg/mL and stored frozen prior to usage. A frozen concentrate (1 mg/mL) aliquot was thawed and dilutions of 2, 4, 8 and 10 μg/mL test sample solutions were prepared. The plates were incubated for 48 h after the addition of the sample in the standard condition and, by the addition of cold trichloroacetic acid (TCA), reaction was terminated again. The cells were fixed by the gentle addition of 50 µL of cold 30% (w/v) TCA (final concentration, 10% TCA) and further incubated at 4 °C for 60 min. The supernatant was discarded; the plates were washed with tap water five times and air dried. Sulphorhodamine B (SRB) solution (50 µL) at room temperature was added to each well at 0.4% (w/v) in 1% acetic acid and the plates were incubated for 20 min. Washing was done with 1% acetic acid solution for the removal of unbound dye and the plates were then dried. The bound stains were then eluted with 10 mM Trizma base and the absorbance was read on a plate reader at a wavelength of 540 nm with a reference wavelength of 690 nm. Percentage growth inhibition was calculated as shown in equation 11:
Experimentation work was carried out in triplicate and obtained data was presented as an average of results with standard deviation. Data were subjected to one-way analysis of variance (ANOVA) and t-tests were applied to evaluate equality of means. A p-value of >0.05 was considered statistically insignificant.
Results and Discussion
Inter-chain interaction in the solvent between Ch and TGP leads to the formation of PECs driven by electrostatic interaction. Hydrogen bonding, dipole–dipole interaction and hydrophobic interaction also play an important role in the formation of PECs. Figure 1 shows the PEC formation between chitosan and tamarind gum polysaccharide.
Figure 1 Schematic representation of PEC formation between chitosan and tamarind gum polysaccharide.
The weak electrolyte and PEC formation of the Ch and TGP implies a reduction in the free energy of the system. It further improves the stability of the complex formed. All the PEC stabilized nanoparticles were prepared using TGP and Ch. As discussed in another study, for the complex formation, oppositely charged biopolymers are mixed in solution form. Concentration of polymers should be kept below gelling point. So, in the present study, both Ch and TGP were used in very low concentrations to avoid gel formation.54 In the present research, a very low concentration of the drug was used to investigate its unusual anticancer effect. In other research, investigators also used a very low concentration of the drug to identify its unusual effect.55
Most of the available information on nanoparticles is based on the spherical nature of nanoparticles. The solvent–antisolvent method maintains finer control over particle size distribution and is able to modulate particle geometry. Jindal et al identified that nanoparticles deviate from the spherical shape mainly due to solute–solvent or solute–solute interaction.56
Classically, nanoparticles were prepared by solvent evaporation and the emulsification method; in the present investigation, however, novel antisolvent methods were used for the preparation of PEC stabilized nanoparticles. In this method drug nano-precipitates were formed using the antisolvent system and further stabilized with PECs. IR interpretation of TGP data is shown in Table 2. IR interpretation of simvastatin data is shown in Table 3. IR interpretation of chitosan data is shown in Table 4. IR interpretation of IR spectra of the physical mixture of Ch, TGP and simvastatin is shown in Table 5. Figures 2 and 3 show the IR spectra of TGP and simvastatin. Figure 4 shows the IR spectra of chitosan and Figure 5 shows the IR spectra of the physical mixture of Ch, TGP and simvastatin.
Table 2 IR Interpretation of TGP
Table 3 IR Interpretation of Simvastatin
Table 4 IR Interpretation of Chitosan
Table 5 IR Interpretation of IR Spectra of the Physical Mixture of Ch, TGP and Simvastatin
Figure 2 IR spectra of TGP.
Figure 3 IR spectra of simvastatin.
Figure 4 IR spectra of chitosan.
Figure 5 IR spectra of the physical mixture of Ch, TGP and simvastatin.
The IR spectra of TGP shows that it contains O-H stretch, COOH, C≡C stretch, C=C stretch, C-O, and N-H bend functional groups. Results of the IR spectral study weres also supported by Chawananorasest et al's study showing that the average molecular weight of tamarind seed polysaccharide ranges from 700–880 kDa.9 The IR spectra of simvastatin shows that it contains N-H stretch, C-H stretch, C≡O stretch, C=C stretch, C-H bend, and C-N bend functional groups. The IR spectra of chitosan shows that it contains O-H stretch, COOH, C≡C stretch, C=C stretch, C-O, and N-H bend functional groups. The IR spectra of the physical mixture of Ch, TGP and simvastatin shows that it contains COOH, C-H bend, C=C stretch, N-O stretch, C-O stretch, and C=C bend functional groups. The IR spectra shows that, significantly, no interaction occurs between the functional groups of the physical mixture of Ch, TGP and simvastatin.
In the present research,a 32 factorial design was used to evaluate the effect of independent variables (concentration of TGP and Ch) over particle size and the entrapment efficiency of nanoparticles (dependent variable). A reduced equation for measuring response (particle size and entrapment efficiency) with statistical significance for the 32 factorial design is shown as equation 12.
where Y = response of variables (dependent variables); b0= arithmetic mean response of nine batches; and b1= estimated coefficient of factors X1. The coefficient corresponding liner effect (b1 and b2), interaction (b1) and quadratic effect (b1 and b2) were determined from the results of the experiment; and X1 and X2 are quantity of the polymers.
In the present study, only two levels of each factor were shown in equations because the third level of each factor did not significantly affect the overall outputs of the independent variables. To simplify the equation, only two levels are shown in the text.
Figure 6 Surface plot for effect of independent variables over size of nanoparticles.
Figure 7 Surface plot for effect of independent variables over entrapment efficiency of nanoparticles.
Characterization of PEC Stabilized Nanoparticles of Simvastatin
The formulations of nanoparticles were prepared using PEC, checked visually and found to be clear. The prepared nanosuspensions were found to be transparent without any precipitation (Table 6). The particle size of all formulations was observed to be in the range of 53.3 to 383.1 nm. The smallest particle size was observed in the case of formulation T5 (53.3 nm) as it contains the lowest concentration of TGP and Ch. Formulation T1 shows the largest particle size, 383.1 nm, which may be due to the highest concentration of TGP and Ch. The surface volume ratio of the non-spherical particles (like cubic and rod-shaped) is less than that of the spherical particles. Results obtained in the present study were also supported by Oh et al's study, wherein the particles having a lower aspect ratio show better cytotoxicity.57
Table 6 Characterization Parameters of PEC Stabilized Nanoparticles
Perfect designing of nanoformulations should justify high entrapment efficiency, smaller particle size, no or less drug leaching and improved bioavailability. As discussed by many researchers, nanoparticles with a size range of less than 100 nm are capable of entering and remaining within tumor cells and have better therapeutic potential. Small size nanoparticles are selectively accumulated within the tumor cells when distribution takes place. A study by Jansch et al revealedha that the shape of the nanoparticles does not affect the protein binding of formulations.58 Moore et al found that particle sizes below 100 nm have the ability to drift towards the capillary wall (due to hydrodynamics) and show better cellular accumulation.59 Another study found that cellular internalization of nanorods was not significantly altered by the aspect ratio.60 Circulation of non-spherical nanoparticles in blood is significantly affected by the orientation of particles in vessels. Vacha et al observed that surface adhesion energy is the key determining factor for the endocytosis of nanoparticles.61 The T5 was considered the optimal formulation as it has the lowest particle size (53.3 nm). The T5 was further used for the characterization of the in vitro anticancer effect. The potential difference on the surface of nanoparticles was determined. The zeta potential is the electrical potential at the slipping plane location in the interfacial double layer, which is a relative point in the bulk fluid away from the interface. The potential difference between the dispersion medium and the stationary layer of fluid attached to the dispersed particle is zeta potential. Zeta potential was observed in the range of 32.2 mV to 34.3 mV. Formulation T1 shows the largest particle size but lowest zeta potential, 32.2 mV. It may be due to charge neutralization, as both TGP and Ch contain the highest concentration, so their charge neutralizes and results in the lowest zeta potential. Highest zeta potential was observed in the case of formulation T6. The entrapment efficiency of all formulations was found to be greater than 70% except in batch T1. Formulation T1 shows the highest entrapment efficiency, 83.36%, shown in Table 6. Batch T1 consists of TGP and Ch in the highest concentration (Table 1).
The research study suggests that the dispersed nanosuspensions are generally evaluated for their entrapment efficiency. This is because in dispersed nanosuspensions the nanoparticles are distributed in a solvent system and the drug loading capacity (equation 15) requires total weight of nanoparticles.
Therefore, in this study the formulated nanoparticles were not separated out and were only evaluated for their entrapment efficiency/% loading capacity.
Usually in dispersed nanosuspensions, the nanoparticles are distributed in a solvent system and they are not separated out. This research aspect is also supported by several other researchers.62–64
The SEM image of prepared nanoparticles is shown in Figure 8. The scanning electron microscopy of the nanoparticles reveals their crystal shape. The SEM images showed rough surfaces of Ch (Figure 8A) and TGP (Figure 8B). Particles were also observed in the SEM images of TGP (Figure 8B). Drug precipitates were found to be crystalline deposits (Figure 8C), while nanoformulation (T5) was found to be cubic in shape (Figure 8D). Operational voltage (15kV) was applied for SEM images of TGP (X15,000) and Ch (X15,000) and 30 kV for the SEM images of drug precipitates (X10,000) and nanoparticles (T5) (X27,000).
Figure 8 SEM image of (A) Ch, (B) TGP, (C) drug precipitates and (D) nanoparticles-T5.
Karfa et al made comparisons between spherical-shaped and cube-shaped nanoparticles of Ag/AgCl. In their investigation, it was observed that cube-shaped nanoparticles showed higher adsorption capacity to the receptor as compared to spherical nanoparticles. This ability may occur due to the high surface area of a nanocube in comparison to a spherical nanoparticle.65 According to a study conducted by Zhao et al, cube-shaped nanoparticles are more stable than spherical nanoparticles.66 Another study, by Kolhatkar et al, found that cubic-shaped nanoparticles provide better therapeutic effects on binding that spherical nanoparticles.67 So, in the present investigation, cube-shaped nanoparticles were prepared as the drug delivery carrier.
Figure 9 shows drug release of formulation through the egg membrane while Figure 10 shows drug release of formulation through the tomato membrane. The release study was carried out for 24 h. It was observed that the release study through the egg membrane and the tomato membrane did not significantly alter the pattern of drug release. An initial burst release of the drug was observed at 15 min and 90 min followed by sustained release of the drug for 24 h. The retarded drug release was observed when the tomato membrane was used as a biological membrane in place of the egg membrane. Instead of retarded drug release through the tomato membrane, the basic release pattern remained the same as drug release through the egg membrane. Generally, a dialysis membrane is used as a biological barrier to investigate drug release characteristics. In the present investigation, a preliminary attempt was made to identify an alternative membrane for a drug release study. In future, further research will be needed into pore size, membrane stability, etc., in order to develop a new membrane. A correlation between synthetic and proposed natural membranes will need to be developed. Investigators believe this first-time exploratory study into tomato membranes as a novel and alternative natural biological barrier will inform other drug release studies. In future, this membrane can be a novel biological model that canopen up avenues for further research.
Figure 9 DR (%) of formulations via egg membrane (A) T1, T2, T3; (B) T4, T5, T6; and (C) T7, T8, T9.
Figure 10 DR (%) of formulations via tomato membrane (A) T1, T2, T3; (B) T4, T5, T6; and (C) T7, T8, T9.
Times of 50% drug release (T50%) and 80% drug release (T80%) are tabulated in Table 7.
Table 7 T50% and T80% of Prepared Nanoformulations
From the kinetic study data (Tables 8 and 9), it was observed that the Baker–Lonsdale drug release model was followed by most of the formulations. After this model, the Higuchi model was followed as the obtained r2 value was greater than all other models except the Baker–Lonsdale model. The Baker–Lonsdale model was derived from the Higuchi model. The Higuchi model was also used by other researchers investigatingr nanoparticles.68,69 The Higuchi model is based on three hypotheses.70 First, initial drug concentration in the matrix is much higher than drug solubility. Second, as particles are much smaller than system thickness, the drug particles are encapsulated inside the prepared nanoparticles and no drug is on the surface. Third, drug diffusivity is constant. The release occurs through pores in the matrix. This model follows the porous system, as hydrophilic polymer solubilizes easily and releases through pores.20
Table 8 Drug Release Data of PEC-based Nanoparticles Through Egg Membrane
Table 9 Drug Release Data of PEC Based Nanoparticles Through Tomato Membrane
In the study, TGP was used as the polymer, which is hydrophilic and soluble when it comes in contact with the solvent system. Drug release through pores can be expressed by equation 16.
Data predicts that the Baker–Lonsdale model is followed by all formulations irrespective of the membrane used in the study. The calculated similarity factor was found to be 16.82. This means that the membranes are dissimilar in their drug release as the value observed was less than 50. All formulations of nanoparticles were subjected to size analysis on the 7th, 14th and 21st days. The particle sizes of formulations after the mentioned days did not significantly differ from particle sizes on day 1 (data given in Table 10). No crystal growth was observed as particle size analysis showed a single peak during the analysis.
Table 10 Particle Growth Analysis and Zeta Potential After 7th Day, 14th Day and 21st Day
The particle size of nanoparticles in each formulation was found to be somewhat similar to the size of particles on day 1. This means that crystal growth had not yet started, so there was no increase in particle size. After the 14th and 21st days, the size of particles increases as compared to previous days due to crystal growth and accumulation. Potential differences on the surfaces of nanoparticles of formulations were analyzed on the 7th, 14th and 21st days and no significant deviation from initial readings was observed. After 14 days of study, no significant differences (p ‹0.05) were observed in the particle size and zeta potential of nanoformulations. Entrapment efficiency and particle size data on the initial day and after 45 days are tabulated in Table 11. Data obtained from stability studies showed a slight increase in size (maybe due to crystal growth) and a decrease in entrapment efficiency of nanoparticles (maybe due to leaching) after 45 days.
Table 11 Stability Study Parameters of Nanoformulations
Generally, statins (3-hydroxy-3-methylgutaryl CoA reductase inhibitors) are considered to provide curative effects in the treatment of cardiovascular diseases. Based on some of the preclinical studies, they are gaining interest as anticancer agents too.71 The effects of statins on the growth of breast cancer cells were evaluated. Statins have pleiotropic effects as a result of which they are gaining interest as anticancer agents.72 Investigation of simvastatin was carried out on the propagation of human breast cancer cell line MCF-7. As well as a cholesterol-lowering effect, statins may be important the deterrence of human breast cancer. In MCF-7 cells, activity like caspase-3 and DNA fragmentation is enhanced by simvastatin by which MCF-7 cell propagation is inhibited. For the purpose of cell propagation, formation of mevalonate (cholesterol precursor) is required, catalyzed by HMG-CoA reductase.73 Growth of malignant cells can be damaged or weakened by inhibiting the synthesis of mevalonate. Simvastatin is reported to act as an osteolysis inhibitor in a mouse used as a model for breast cancer. Specifically, statins increase the apoptosis and radiosensitivity in different breast cancer cell lines, prevent proliferation and invasion, and decrease tumors' metastatic dissemination. Clinical findings show that statins minimize the recurrence rates of breast cancer when administered post-diagnostically.74,75 Many in vitro and animal studies indicate that statin drugs inhibit the development of breast cancer. Little evidence in human subjects supports a protective impact of statins on incidence of breast cancer, but consistent evidence supports a protective effect on recurrence of the disease.
As per the data given in Figure 11, T5 exhibits significantly higher death of human breast cancer cells (MCF-7) than pure drug in the in vitro conditions. It may be due to the smaller size of prepared nanoformulations than the particle size of pure drug. Smaller size of nanoformulations leads to better dissolution hence their therapeutic potential. Phagocytes exhibit fewer tendencies for non-spherical nanoparticles as compared to spherical nanoparticles. Attachment of elongated nanoparticles with cells with their axis also reduces the chance of phagocytosis. In their study, Huang et al demonstrated that aspect ratio of nanoparticles has a significant effect on internalization, differentiation, proliferation, adhesion and migration when studied in human melanoma cells A375.76 Godin et al evaluated the effect of spherical and non-spherical nanoparticles in murine model of breast cancer. They predicted that non-spherical particles would exhibit higher concentration than spherical particles within the breast cancer cells.77 Table 12 summarizes the outcomes obtained from the chitosan-based PEC nanoparticles.
Table 12 List of Chitosan-based PEC Nanoparticles and Their Outcomes
Figure 11 Anticancerous activity of nanoparticles (T5) and pure drug precipitates.
Figure 12 shows the bright field image of (a) untreated MCF-7 cells, (b) MCF-7 cells treated with T5, and (c) MCF-7 cells treated with pure simvastatin.
Figure 12 Bright field image of (A) untreated MCF-7 cells, (B) MCF-7 cells treated with nanoparticles (T5) and (C) MCF-7 cells treated with pure simvastatin.
Table 13 describes cell death (%) after the administration of pure drug and nanoparticles at different concentrations.
Table 13 Cell Death (%) After Administration of Pure Drug and Nanoparticles at Different Concentrations
As discussed by Zhao et al, cytotoxicity of nanoparticles depends upon shape of the particles as well as types of cells used in the study.78 Hence, the present study specifically exhibited the results obtained on the human breast cancer cell lines. The opposite result was observed by Li et al, as they concluded that cellular uptake of spherical nanoparticles is higher than cube- and rod-shaped particles due to the ease of the bending capability of the cellular membrane around the nanoparticles.79 The observation of Li et al was also supported by Shimoni et al, as they showed that HeLa cell accumulation towards various nanoparticles depends upon the aspect ratio of particles. HeLa cells preferably accumulate towards the particles having a smaller aspect ratio.80
The present study was based on identification of the need to determine the effect of crystalline drug particles and cubic nanoparticles on human breast cancer cell lines (MCF-7). It can be concluded from the study that the antisolvent precipitation method allows control over the fabrication of cubic nanoparticles. This study also recommends that the present method can be easily adopted to control the shape, edge geometry and aspect ratio of nanoparticles. The study shows that solid cubic nanoparticles can be prepared using the solvent–antisolvent method and by utilizing Ch-TGP as a polyelectrolyte complex forming agent. Fabricated PEC-based nanoparticles exhibit good entrapment efficiency and ability to control drug release up to 24 h. Prepared cubic nanoparticles exhibited better control over the growth of human breast cancer cell lines (MCF-7) than pure drug precipitates in in vitro conditions. Simvastatin is an established hypolipidemic agent. Simvastatin has low aqueous solubility. In the present research, nanoparticles were prepared to increase the solubility of simvastatin. The literature also shows that simvastatin has some anticancer activity with hypolipidemic potential. Therefore, the present research provides an idea that use of simvastatin nanoparticles with an anticancer agent can be used for patients who have cancer and hyperlipidemic conditions. Simvastatin shows both hypolipidemic potential and a synergistic effect with an anticancer agent. The present study establishes that cubic nanoparticles of simvastatin have significantly better control over the growth of MCF-7 cells than pure simvastatin drug. In future, an in vivo animal model study will be required to identify the anticancer effects of the anti-hyperlipidemic agent simvastatin.
We gratefully appreciate the Galgotias University, India; AIMST University, Malaysia; MAHSA University, Malaysia; Tishk International University, Iraq; and the National University of Science and Technology, Sultanate Oman, Muscat, for their support in completing this study.
The authors report no conflicts of interest in this work.
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