- *Corresponding Author:
- N. V. Shah
Department of Pharmacy, Sumandeep Vidyapeeth, Piparia, Vadodara-391 760, India
E-mail: [email protected]
|Date of Submission||07 May 2018|
|Date of Revision||19 September 2018|
|Date of Acceptance||13 February 2019|
|Indian J Pharm Sci 2019;81(2):309-316|
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The present investigation focussed on the development of a novel strategy to enhance the bioavailability of risedronate sodium, which has poor and erratic absorption. Nanosponges were statistically developed by full 32 factorial design using Design of Experiment software considering concentration of polymer and stabilizer as independent variables and particle size and entrapment efficiency as experimental responses by utilizing the modified quasi-emulsion solvent diffusion technique. Optimized formulation showed 67.27±1.05 % entrapment efficiency, 155.8±2.17 nm particle size and –35.4 mV of zeta potential. The data from in vitro release study showed burst release for initial 2 h followed by slow and sustained release up to 24 h, which followed a diffusion-controlled release mechanism by the Higuchi model. Scanning electron microscopy study showed uniformly discrete spherical particles with porous surface without any agglomeration. Stability study demonstrated no significant changes in particle size, entrapment efficiency and in vitro release, which indicated that the nanosponge formulation was stable. In conclusion, it appeared that the nanosponges were a suitable nanocarrier system that could play a significant role in improving osteoporotic condition.
Risedronate sodium nanosponges, quasi-emulsion solvent diffusion, 32 full factorial design, in vitro buoyancy, in vitro drug release
Osteoporosis, derived from the Greek words osteon (bone) and poros (pore), is a progressive bone disease sometime called as “silent disease” because it leads without any sign until a bone fracture occurs due to decrease in bone mass density, bone micro architecture deteriorates and alteration in varieties of bone proteins. Various treatments are available for the management of osteoporosis such as antiresorptive agents such as bisphosphonates, selective oestrogen receptor modulators, hormone replacement therapy, bone forming agents, vitamin D and analogs [1-7].
Bisphosphonates, characterized under Biopharmaceutics Classification System class III category (freely soluble and poor permeability)  have been used for the treatment of osteoporosis due to powerful binding affinity to bones. Nano scale formulation has significant low particle size that may lead to dramatic changes in the pharmacokinetics of drugs with poor solubility or permeability issues. As a consequence, nano formulation allows more passive diffusion and penetration of drug about 15-250 times greater than that of micro particles through the biological membranes . Clinically, it was reported that primary amino-bisphosphonates have adverse effects such as esophagitis or reflux of partially dissolved formulations. The presence of nitrogen in the pyridinyl ring makes risedronate chemically distinct from other amino-bisphosphonates as it contains the nitrogen in primary amine. Risedronate is rapidly absorbed from upper gastro intestinal tract  with a short biological half-life of 1.5 h. Therefore, floating delivery system has been developed to sustain the release of drug for a longer period of time .
Nanosponges (NSs) are minute particles with a size range of about a virus (100-300 nm), which have cavities that can be filled with a hydrophilic or a lipophilic drug. The sponges behave as a 3D network or scaffold that permits better entrapment of drug. As compared to other nanoparticles, NSs are porous, nontoxic and stable at high temperature up to 300° [12-17]. The aim of the present research work was to develop risedronate sodium (RS)-loaded NSs, using design of the experiment, for the better management of osteoporosis.
Materials and Methods
RS was procured from Manus Aktteva Biopharma LLP, Ahmedabad, India. Eudragit RS 100, Eudragit E 12.5, ethyl cellulose (18-22 cps), potassium hydroxide (KOH), methanol, dichloromethane (DCM), polyvinyl alcohol (PVA) were purchased from Loba Chemie, Mumbai, India. All other chemicals used in research work were of analytical grade.
Selection of solvent:
Solvent was selected based on the maximum solubility of RS. An accurate quantity (5 ml) of different solvents was taken in stoppered vials and excess amount of RS was added in to each solvent followed by vortexing for 10 min. Vials were kept at 25±2° under isothermal orbital shaker (MSW-132, Macro Scientific Work Pvt. Ltd., Delhi, India) for 24 h to attain an equilibrium concentration. The samples were centrifuged at 5000 rpm for 15 min using a cooling centrifuge (C-24 BL, Remi Instrument Pvt Ltd, Mumbai, India). Supernatant was separated, diluted and analysed at 262 nm using UV/Vis spectrophotometer (UV-1800, Shimadzu, Kyoto, Japan).
Formulation of drug-loaded NSs:
NSs of RS were prepared by modified quasi emulsion solvent diffusion method. Accurately weighed quantity (20 mg) of RS was dissolved in methanolic KOH with the aid of sonication using bath sonicator (SW-4, Toshniwal Instruments Pvt., Ltd., Ajmer, India). Ethyl cellulose was dissolved in 10 ml of methanol:DCM (1:1) solvent system. The drug solution was added to the polymer solution under sonication to make an internal organic phase. The organic phase was added to external aqueous phase consisting of known strength of PVA solution with continuous stirring on a mechanical stirrer (RQ-121/D, Remi Instrument Pvt., Ltd., Mumbai, India) at 1600 rpm for 1.5 h. The prepared NS were separated by centrifugation at 14 500 rpm at –10° for 90 min [18,19].
Design of the experiment:
Design Expert® (10.0.0.1) program was used for statistical design of present NS formulation. The statistical software was utilized to acquire information not only about critical values required to achieve the desired response but also to study the possible interactions of the selected independent variables on the dependent variables. A design with 4 centre points and 4 points for lack of fit was used to obtain a robust model. Independent variables such as the amount of ethyl cellulose (X1) and % PVA (X2) were used at low, medium and high levels as shown in Table 1. This design has provided 13 runs to study the effect of independent variables on two dependent variables namely particle size (Y1) and % entrapment efficiency (EE, Y2). The amount of RS, volume of organic phase (10 ml), stirring speed (1600 rpm) and stirring time (90 min) were kept constant throughout the optimization process. For this design, statistical significance was set at 0.05 for the determination of probability values. The interaction between independent and dependent variables were graphically shown in contour plots and 3D surface response plots. The reliability of model was confirmed by check point analysis.
|Independent variables||Variables levels|
|Low (-1)||Medium (0)||High (1)|
X1= amount of ethyl cellulose (mg), X2 = % of PVA
Table 1: Variables and Levels for Statistical Design
The prepared NS dispersion was centrifuged by aforementioned experimental parameters. Supernatant was separated, diluted and analysed spectroscopically at 262 nm to determine drug entrapment. Percent EE of the formulation was calculated as follows : % EE=[RS]total–[RS]supernatant/[RS]total×100, where [RS]total is the amount of total incorporated drug and [RS]supernatant is the amount of free drug in the supernatant layer.
Measurement of particle size:
The particle size of NS formulation was measured on a zeta sizer (Nano ZS, Malvern Instruments, Worcestershire, UK) after suitable dilution with distilled water.
Determination of zeta potential and Fouriertransform infrared (FTIR) spectroscopy:
Zeta potential is studied to characterize the surface charge properties of NS. It was measured on the Zetasizer after suitable dilution with distilled water. FTIR spectra were recorded on a FTIR spectrophotometer (IRAffinity-1, Shimadzu, Japan) to study any interaction between RS and the excipients. Samples were mixed with KBr in a ratio of 1:300 and spectra were recorded in the range of 4000-400 cm-1.
In vitro buoyancy studies:
Accurately weighed amount of NS was placed in 0.1 N hydrochloric acid (HCl). The mixture was stirred at 100 rpm using a magnetic stirrer. At the end of 24 h, the floated and settled NS were recovered and collected by centrifugation. Both the fractions of NS were dried by lyophilization (MSW-137, Macro Scientific Work Pvt Ltd, Delhi, India), weighed and buoyancy was determined as follows, buoyancy (%) = WF/(WF+WS)×100, where WF is the weight of floating NS and WS is the weight of settled NS.
In vitro drug release study:
In vitro release study was carried out using dialysis sac method (HiMedia-Dialysis membrane 135, Mol. cut off 12 000-14 000 Da, Mumbai, India) [20-22]. An accurately weighed amount of NS formulation equivalent to 10 mg of RS was dispersed in 5 ml of 0.1 N HCl and introduced into the dialysis sac. The sac was hung in a glass beaker containing 100 ml of 0.1 N HCl. The receptor compartment was stirred continuously at 37±0.5° on a magnetic stirrer. Aliquots from receptor medium was withdrawn at predefined time intervals up to 24 h and replenishing each time with same volume of buffer. The samples were measured spectroscopically at 262 nm .
Surface morphology study:
The surface morphology and shape of NS formulation were determined on a scanning electron microscope (SEM; Jeol JSM-5610LV, England). Prior to examination, the sample was mounted on to the metal stubs using a double-sided adhesive tape under vacuum. The equipment was operated with an acceleration voltage of 15 kV and working distance of 20 μm. Images of NS were taken at various magnifications .
Differential scanning calorimetry (DSC) analysis:
The thermograms of RS, physical mixture and optimized formulation were recorded on a DSC (TA–60, Shimadzu, Japan). Samples were weighed in an aluminium pan and scanned in the temperature range of 50-300° under dry nitrogen atmosphere at a heating rate of 10°/min. The recorded thermograms were analysed for interaction between drug and excipients [20,24].
A stability study was carried out for the optimized formulation as per International Conference on Harmonisation guidelines. The NS were placed in glass vials and stored at 25±2°/60±5 % RH and 40±2°/75± 5 % RH atmospheric conditions in a stability chamber (Macro Scientific Work Pvt. Ltd., Delhi, India) for a period of 1 mo. Samples were analysed for particle size, % EE and in vitro drug release after the stability period.
Results and Discussion
The solubility of RS was studied in various solvents such as methanol, ethanol and DCM. RS has satisfactory solubility in a single organic solvent. However in the preliminary studies, a problem was encountered after the addition of internal organic phase (a mixture of RS and polymer in a single solvent) into the external aqueous phase. RS was precipitated in the aqueous medium, which resulted in low entrapment of RS in NS. Thereafter, a solvent system such as methanol:DCM (1:1) and KOH in methanol was tried for dissolving the polymer and RS, respectively. The internal organic phase comprising of methanol:DCM and KOH in methanol increased RS stability in the external phase, which improved drug entrapment in formulation. Therefore, this mixture of solvents for internal organic phase was selected for the further optimization of NS.
Drug-loaded NS in different combinations were designed and prepared by modified quasi emulsion solvent diffusion technique. Various preliminary trials were carried out before the implementation of a statistical tool for the development of NS. Screening of stirring speed was performed between the range 1300-1900 rpm. At the minimum speed of 1300 rpm, lump formation of particles was observed. This might be due to insufficient rotation speed at which the NS were unable to get separated out. Ruptured particles with irregular surface morphology were found at high stirring speed of 1900 rpm. NS with discrete spherical particles and even surface were formed at a speed of 1600 rpm. Therefore, this speed was selected for further optimization of NS. Second important parameter studied during the preliminary trials was stirring time. Irregular particle formation was observed due to improper solvent evaporation after 1 h stirring, while particles were ruptured after 2 h of stirring due to increased stress on spongy particles. Uniform spherical particles were obtained after 1.5 h stirring; therefore it was selected for further optimization. Polymers such as Eudragit RS 100, Eudragit E 12.5 and ethyl cellulose were utilised in polymer screening process. Poor drug entrapment and irregular shape particles were observed when NS were prepared with Eudragit RS 100 and Eudragit E 12.5. NS prepared with ethyl cellulose showed uniform and discrete morphology with good drug entrapment, therefore this polymer was selected for further process. Statistical correlation was evaluated among the factors and responses by means of statistical Design Expert® software. The statistical design has suggested 13 runs for optimization of NS formulation and all experiments were performed by considering 2 independent variables with 2 experimental responses as shown in Table 2. The primary stage in data analysis was to fit the investigational data for suitable model. An appropriate model was preferred by the statistical tool on the basis of various statistical parameters. Therefore, various models such as linear, quadratic, 2 FI and cubic were studied for experimental responses using predicted residual sum of square (PRESS) statistic for the identification of appropriateness of model fitting. The quadratic model was selected for both variables as it showed lowest value of PRESS measurement compared to other models. The p value was also found less than 0.05 that showed significance in the model fitting as per the ANOVA analysis. The following polynomial Eqns. were obtained to study the relationship between independent and dependent variables. Y1 = 139.4793+33.7X1-10.43X2+11.77X12+24.77X22– 0.77X1X2; Y2 = 66.00+10.25 X1+0.425 X2–11.89 X12– 9.60 X22–4.35 X1X2.
|Batch code||Variable level||Experimental responses|
Values are expressed as mean±SD, n = 3
Table 2: Factorial Layout and Experimental Responses for Nanosponges
The influence of independent variables on experimental responses is depicted graphically in the contour and 3D surface response plots as shown in figure 1. The plots showed that particles size increases gradually with increase in drug to polymer ratio from 1:3, 1:5 to 1:7. The graph also depicted that, particles size increases with 0.5 % w/v of PVA and decreases with 1 % w/v of PVA. On the other end, it was found that the increment in drug to polymer ratio leads to more % entrapment due to the more exposure of polymer environment to the drug. Overlay plot revealed in figure 2 highlighted the area showing upper and lower limits of responses as a function of formulation components.
To set the objective for the selection of optimized formulation, composition of NS with maximum drug entrapment (%) and minimum particle size (nm) was predicted by the software for check point analysis. The predicted formula with 112.64 mg of ethyl cellulose and 1.13 % w/w surfactant concentration was experimentally prepared in triplicate and studied for experimental responses. The practically obtained % entrapment and particle size were significantly identical with predicted values as shown in Table 3. The NS showed considerably smaller mean particle size with less polydispersity index of <0.20 that represent narrow particles distribution within dispersion. The percent error for both responses was very less. Therefore, from this check point analysis it can be confirmed that applied statistical design is a reliable model for the optimization of drug-loaded NS.
|Independent variables||Experimental variables||Predicted value||Observed value±SD||Residual||% error|
X2 - 1.13 % w/w
Values are expressed as mean±SD, n=3
Table 3: Check Point Analysis for Selected Model
Zeta potential greater than 30 imparted good stability to nanoparticles dispersion. The optimized formulation showed zeta potential value of –35.4 mV. At this high potential, nanoparticles would exhibit a great repulsion with each other, which significantly prevented agglomeration of particles. Drug-polymer compatibility studies were carried out using FTIR spectroscopy to establish any possible interaction of drug with the polymer used in the formulation. Figure 3 showed the presence of characteristic peaks of RS in the formulated NS without any significant change in their position indicating no chemical interaction between RS and the excipients.
The buoyancy study showed that 85.10±0.71 % of NS was remained buoyant after 24 h. This showed good stability of NS in acidic media and provide an environment for the maximum absorption of drug from the acidic medium. Hence, it has been concluded that optimized NS was remained in acidic media for the longer period of time (>24 h) which is essential prerequisite for the absorption of drug from acidic environment for the better therapeutic performance of drug.
In vitro release profile of RS from optimized formulation portrayed in figure 4 showed burst release of RS for initial 2 h followed by slow and sustained release up to 24 h. Initial burst release might be due to the adsorbed RS on the surface, which might get released at a faster rate compared to RS entrapped inside the core of NS. The matrix of NSs held RS and controlled the release over the longer period of time. Different kinetic models were applied to find out the release behaviour of the optimized formulation. The release kinetics of the optimized formulation has high linearity for Higuchi model with regression coefficient (R2) value of 0.939. Thus, from all this discussion it could be concluded that optimized NS formulation followed diffusion-controlled release mechanism as per the Higuchi model.
SEM image of diluted sample of NS in figure 5 showed discrete spherical particles with porous surface. The figure showed that the particles were uniformly distributed without any agglomeration. SEM analysis confirmed the nano scale range of the optimized formulation, which was supported by the data obtained from particle size analysis.
The thermogram in figure 6A of pure RS showed sharp endothermic peak at 263.78° corresponding to its melting point indicating crystalline nature of pure drug. Figure 6B represents thermogram of physical mixture of RS and ethyl cellulose with endothermic peaks at 262.12° and 176.13° showing their melting points, respectively. The thermogram in figure 6C for the optimized formulation depicted peaks of polymer and RS at expected places without any variation. The endothermic peak of RS is considerably broadened indicating a decline in crystallinity of RS in NS formulation.
The stability study of optimized formulation was carried out for the period of 1 mo with the specified storage conditions. The EE (%), particle size and in vitro drug release study were evaluated at the end of study as shown in Table 4. It was found that there were no significant changes in the formulation with respect to performed evaluation parameters and thus, it could be concluded that formulation was stable after 1 mo stability study. The result of optimized formulation found at accelerated conditions (40±2°/75±5 % RH) may produce long term reliability of formulation besides the studied period.
|Parameters||Before stability study||After stability study|
|40±2°/75±5 % RH||25 ± 2°/60±5 %RH|
|Particle size ±SD (nm)||139.5±1.29||137.95±2.10||138.52±2.83|
|Entrapment efficiency ±SD (% )||65.48±3.51||63.96±2.57||64.05±1.95|
|In vitro drug release study ±SD||95.83±5.32||93.96±2.21||94.35±3.07|
Values are expressed as mean±SD, n = 3
Table 4: Stability Study Data of Optimized Formulation
The declarations made in present research work are based on the various in vitro studies of the formulation. The present research work concludes that the permeability and bioavailability of BCS class III drugs may be improved if delivered in the form of NS but this statement can be supported only after performing in vivo study. In this research work, an effort was made to formulate NS using modified quasi-emulsion solvent diffusion technique for the improvement in permeability by the GI retention of drug. The work further concludes that the concentration of polymer ethyl cellulose (100 mg) and stabilizer PVA (1 % w/v) play a key role in the optimization of the formulation. The particle size and % EE of drug were vary with the different concentrations of the polymer and the stabilizing agent. The full 32 factorial design represents that the optimized NS showed 155.8±2.17 nm particle size and 67.27±1.05 % EE with sustained drug release up to 24 h. The formulation was remained buoyant up to 24 h that provides the GI absorption of drug. The stability study also showed satisfactory findings with all evaluated parameters. This work concludes that the NSs of the RS could be an exceptional drug delivery system for better management of osteoporosis.
The authors thank Manus Aktteva Biopharma LLP, Ahmedabad, for providing gift sample of RS for this research work. Authors also wish to thank the Department of Pharmacy, Sumandeep Vidyapeeth, Piparia, Vadodara, for providing required facilities to carry out this research work.
Conflict of interest
The authors declare no conflict of interest.
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