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Journal of Pharmaceutics
Volume 2013 (2013), Article ID 151035, 11 pages
Plantago ovata F. Mucilage-Alginate Mucoadhesive Beads for Controlled Release of Glibenclamide: Development, Optimization, and In Vitro-In Vivo Evaluation
1Department of Pharmaceutics, Seemanta Institute of Pharmaceutical Sciences, Jharpokharia, Mayurbhanj, Odisha 757086, India
2Department of Pharmaceutical Sciences, Guru Ghasidas Vishwavidyalaya (A Central University), Koni, Bilashpur, Chhattisgarh 495 009, India
Received 20 December 2012; Revised 25 February 2013; Accepted 26 February 2013
Academic Editor: Nayanabhirama Udupa
Copyright © 2013 Amit Kumar Nayak et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The current study deals with the development and optimization of ispaghula (Plantago ovata F.) husk mucilage- (IHM-) alginate mucoadhesive beads containing glibenclamide by ionotropic gelation technique. The effects of sodium alginate (SA) to IHM and cross-linker (CaCl2) concentration on the drug encapsulation efficiency (DEE, %), as well as cumulative drug release after 10 hours (, %), were optimized using 32 factorial design based on response surface methodology. The observed responses were coincided well with the predicted values by the experimental design. The optimized mucoadhesive beads exhibited % w/w of DEE and good mucoadhesivity with the biological membrane in wash-off test and sustained drug release profile over 10 hours. The beads were also characterized by SEM and FTIR analyses. The in vitro drug release from these beads was followed by controlled release (zero-order) pattern with super case-II transport mechanism. The optimized glibenclamide-loaded IHM-alginate mucoadhesive beads showed significant antidiabetic effect in alloxan-induced diabetic rats over prolonged period after oral administration.
The mucoadhesive polymer containing oral drug delivery systems has the capacity to prolong residence time of drugs at the absorption site and facilitate intimate contact with underlying absorptive surface to enhance bioavailability . Polymers used in the mucoadhesive formulations include natural, semisynthetic, and synthetic ones.
In recent years, a growing interest has been identified in the development of natural polymer-based drug delivery systems due to their biodegradability, biocompatibility, aqueous solubility, swelling ability, easy availability, and cost-effectiveness . Amongst various natural polymers, alginates have been widely used in the development of drug delivery applications [3–6]. It is obtained from Laminaria hyperborean, Ascophullum nodosum, and Macrocystis pyrifera . It is composed of linear copolymers of two monomeric units, that is, β-D-mannuronic acid and α-L-guluronic acid . Sodium alginate (SA) undergoes ionotropic-gelation by Ca2+ to form calcium alginate due to an ionic interaction between carboxylic acid groups of alginate chain and Ca2+ . Sodium alginate has mucoadhesive property; however, the cross-linked alginates are usually fragile [9, 10]. Therefore, blending of different mucoadhesive polymers is one of the most popular approaches to formulate ionotropically cross-linked alginate-based mucoadhesive beads [9, 11, 12]. Again, blending with suitable polymers, may improve the drug encapsulation, which is found comparatively lower in alginate-based beads prepared by ionotropic-gelation method .
Ispaghula (Plantago ovata F.) husk is an indigenous product of south Asia and is widely used herbal product both in traditional and modern medicines . The ispaghula husk mucilage (IHM) is white, hydrophilic in nature, and forms a colorless gel in presence of water [14–16]. IHM contains a high amount of highly branched neutral arabinoxylan (arabinose 22.6%, xylose 74.6%, and traces of other sugars) and about 35% of nonreducing terminal sugar residues . Few investigations had been carried out to formulate mucoadhesive beads as drug delivery matrices using both untreated ispaghula husk and alkaline treated ispaghula husk directly as polymeric blend with sodium alginate [1, 17, 18]. However, no attempt has been taken to formulate mucoadhesive alginate-based beads using isolated IHM as polymeric blend for the use in drug delivery. In the current investigation, the utility of isolated IHM, as a possible natural polymeric-blend with SA for the development of new IHM-blended alginate beads containing glibenclamide through ionotropic-gelation, was examined.
Glibenclamide is a sulfonylurea used in the treatment of non-insulin-dependent diabetes mellitus (NIDDM, type-II) [2, 19]. Its plasma half-life is 4–6 hours, which makes multiple dosing to maintain the therapeutic blood level . Therefore, it would be beneficial to develop a mucoadhesive system of glibenclamide using IHM-alginate for oral use, which might facilitate an intimate contact with the mucous membranes (i.e., mucoadhesion or bioadhesion) in the gastrointestinal tract, and thus the gastric residence could be prolonged to release glibenclamide at the target site at controlled rate over an extended period to maximize the therapeutic effect.
In the development of any pharmaceutical formulation, an important issue is to design a formulation with optimized quality in a short time period and minimum number of trials [20, 21]. Traditionally, pharmaceutical formulators develop various formulations by changing one variable at a time while keeping others fixed. This classical method is laborious and time consuming. However, many experiments do not succeed in their purpose because they are not properly thought out and designed, and even the best data analysis cannot compensate lack of planning. Therefore, it is essential to understand the influence of formulation variables on the quality of formulations with a minimal number of experimental trials and subsequent selection of formulation variables to develop an optimized formulation using established statistical tools [5, 22–24]. Factorial designs, where all the factors are studied in all possible combinations, are considered the most efficient in estimating the influence of individual variables and their interactions performing minimum numbers of experiments . A computer-aided optimization technique based on 32 (two factors and three levels) factorial design and response surface methodology was employed to investigate the effects of two independent process variables (factors), that is, SA: IHM and cross-linker (CaCl2) concentration on the properties of glibenclamide-loaded ionotropically gelled IHM-alginate beads such as drug encapsulation and drug release.
Glibenclamide (B.S. Traders Pvt. Ltd., India), SA (Central Drug House, India), ispaghula husk (Shree Baidyanath Ayurved Bhawan Pvt. Ltd., India), and calcium chloride (Merck Ltd., India) were used for this investigation. All other chemicals and reagents used were of analytical grade.
2.2. Isolation IHM from Ispaghula Husk
The mucilage from ispaghula (Plantago ovata F.) husk was extracted according to the previously reported method [26, 27]. An amount of 10 mL of 0.1 M HCl was heated to boil in a 100 mL flask and 1 gram of Plantago ovata F. husk was added. Heating was resumed and the process of husk dissolution was watched. After total change of color, the flask was finally removed from heat and the solution was filtered through a clean muslin cloth while still hot. In order to separate residual traces of mucilage, the seeds were washed twice with 5 mL of hot water and the solution obtained each time was filtered. The combined filtrate, containing the dissolved mucilage, was mixed with 60 mL of 95% ethyl alcohol, stirred, and allowed to stand for 5 hours. Finally, the supernatant liquid was decanted and the precipitate in the beaker was dried in an oven at 50°C. The dried IHM cake was grounded with a mortar and passed through a sieve (0.15 mm mesh size). The isolated IHM powders were packed in a plastic bag and kept airtight desiccators until further use.
2.3. Preparation of Glibenclamide-Loaded IHM-Alginate Beads
The glibenclamide-loaded IHM-alginate beads were prepared by ionotropic-gelation technique using calcium chloride (CaCl2) as cross-linker. Briefly, SA and IHM aqueous dispersions were prepared separately using distilled water. These dispersions were well mixed with stirring for 15 min at 1000 rpm using a magnetic stirrer (Remi Motors, India). Afterwards, glibenclamide was added to the dispersion mixture. The ratio of drug to polymer was maintained 1 : 2 in all formulations. The final mixtures were homogenized for 15 min at 1000 rpm using a homogenizer (Remi Motors, India) and ultrasonicated for 5 minutes for debubbling. The resulting dispersion was then added via a 21-gauge needle. The added droplets were retained in the CaCl2 solution for 15 min to complete the curing reaction and to produce rigid beads. The wet beads were collected by decantation and washed two times with distilled water and dried at 37°C for 24 h. The dried glibenclamide-loaded IHM-alginate beads were stored in a desiccator until used.
2.4. Experimental Design for Optimization
A 32 factorial design was employed for optimization with SA: IHM () and concentration of CaCl2 () as the prime selected independent variables, which were varied at three levels, low (–1), medium (0), and high (+1). The drug encapsulation efficiency (DEE, %) and 10 hours (, %) were used as dependent variables (responses). Design-Expert Version 220.127.116.11 software (Stat-Ease Inc., USA) was used for the generation and evaluation of the statistical experimental design. The matrix of the design including investigated responses, that is, DEE and , is shown in Table 1. The effects of independent variables upon the all measured responses were modelled using the following quadratic mathematical model generated by 32 factorial design : where is the response, is the intercept, and , , , , are regression coefficients. and are individual effects; and are quadratic effects; X1X2 is the interaction effect. One-way ANOVA was applied to estimate the significance () of generated models. Individual response parameters were evaluated using the F-test. The response surface methodology was applied to analyze the effect of independent factors (SA: IHM and CaCl2 concentration) on the measured responses (DEE and ).
2.5. Determination of
Accurately weighed, 100 mg of beads were taken and were crushed using pestle and mortar. The crushed powders of drug containing beads were placed in 500 mL of phosphate buffer, pH 7.4, and kept for 24 hours with occasionally shaking at °C. After the stipulated time, the mixture was stirred at 500 rpm for 15 min on a magnetic stirrer. The polymer debris formed after disintegration of bead was removed filtering through Whatman filter paper (No. 40). The drug content in the filtrate was determined using a UV-VIS spectrophotometer (Shimadzu, Japan) at 228.5 nm. The DEE of beads was calculated using this following formula:
2.6. Bead Size Measurement
Particle size of 100 dried beads from each batch was measured by optical microscopic method for average particle size using an optical microscope (Olympus). The ocular micrometer was previously calibrated by stage micrometer.
2.7. Surface Morphology Analysis by Scanning Electron Microscopy (SEM)
Samples were gold coated by mounted on a brass stub using double-sided adhesive tape and under vacuum in an ion sputter with a thin layer of gold (3 ~ 5 nm) for 75 seconds and at 20 kV to make them electrically conductive, and their morphology was examined by scanning electron microscope (ZEISS EVO 40, Japan).
2.8. Fourier Transform-Infrared (FTIR) Spectroscopy
Samples were reduced to powder and analyzed as KBr pellets by using a Fourier transform-infrared (FTIR) spectroscope (Perkin Elmer Spectrum RX I, USA). The pellet was placed in the sample holder. Spectral scanning was taken in the wavelength region between 4000 and 400 cm−1 at a resolution of 4 cm−1 with scan speed of 1 cm/second.
2.9. In Vitro Drug Release Studies
The release of glibenclamide from various IHM-alginate beads was tested using a dissolution apparatus USP (Campbell Electronics, India). The baskets were covered with 100-mesh nylon cloth to prevent the escape of the beads. The dissolution rates were measured at °C under 50 rpm speed. Glibenclamide-loaded IHM-alginate beads equivalent to 30 mg glibenclamide were taken in 900 mL of dissolution medium (0.1 N HCl, pH 1.2 for first 2 hours and phosphate buffer, pH 7.4 for next 8 hours). An amount of 5 mL of aliquots was collected at regular time intervals, and the same amount of fresh dissolution medium was replaced into the dissolution vessel to maintain sink condition throughout the experiment. The collected aliquots were filtered and suitably diluted to determine absorbance using a UV-VIS spectrophotometer (Shimadzu, Japan) at 228.5 nm against appropriate blank.
In order to predict and correlate the in vitro release behaviour of glibenclamide from formulated glibenclamide-loaded IHM-alginate beads, it is necessary to fit into a suitable mathematical model. The in vitro drug release data were evaluated kinetically in different mathematical models [5, 6]: (i)Zero-Order Model: , where represents the drug released amount in time , and is the start value of ; is the rate constant;(ii)First-Order Model: , where represents the drug released amount in time , and is the start value of ; is the rate constant;(iii)Higuchi Model: , where represents the drug released amount in time , and is the rate constant;(iv)Korsmeyer-Peppas Model: , where represents the drug released amount in time , is the rate constant, and is the diffusional exponent, indicative of drug release mechanism.
The Korsmeyer-Peppas model was also employed in the in vitro drug release behaviour analysis of these formulations to distinguish between competing release mechanisms [5, 6]: Fickian release (diffusion-controlled release), non-Fickian release (anomalous transport), and case-II transport (relaxation-controlled release). When is ≤0.43, it is Fickian release. The value between 0.43 and 0.85 is defined as non-Fickian release. When ≥ 0.85, it is case-II transport.
2.10. Mucoadhesion Testing
The mucoadhesivity of optimized glibenclamide-loaded IHM-alginate beads was evaluated by ex vivo wash-off method [11, 12]. Freshly excised pieces of goat intestinal mucosa (2 × 2 cm) (collected from slaughterhouse) were mounted on glass slide (7.5 × 2.5 cm) using thread. Fifty beads were spread onto the wet tissue specimen, and the prepared slide was hung onto a groove of disintegration test apparatus. The tissue specimen was given regular up and down movement in a vessel containing 900 mL of 0.1 N HCl (pH 1.2) and phosphate buffer (pH 7.4), separately, at 37°C. After regular time intervals, the machine was stopped and the number of beads still adhering to the tissue was counted.
2.11. In Vivo Evaluation
In vivo studies were performed in alloxan-induced diabetic albino rats  of either sex (weighing 266–342 grams). The acclimatized rats were kept fasting for 24 h with water ad libitum. All experiments were performed between 8 AM to 12 PM to minimize circadian influences. The experimental protocol was subjected to the scrutiny of the Institutional Animal Ethical Committee and was cleared before starting. The animals were handled as per guidelines of committee for the purpose of control and supervision on experimental animals (CPCSEA). All efforts were made to minimize both the suffering and number of animals used.
The rats were made diabetic by intraperitoneal administration of freshly prepared alloxan solution at a dose of 150 mg/kg dissolved in 2 mM citrate buffer (pH 3.0). After one week of alloxan administration, alloxanized rats with fasting blood glucose of 300 mg/dL or more were considered diabetic and were employed in the study for 12 hours. The alloxan-induced diabetic rats were divided randomly into 2 groups of 6 rats each and treated as follows. Group A was administered with pure glibenclamide in suspension form, and Group B was administered with optimized formulation of glibenclamide-loaded IHM-alginate beads, both at a dose equivalent to 5 mg glibenclamide/kg body weight using oral feeding needle. Blood samples were withdrawn (0.1 mL) from tail tip of each rat at regular time intervals under mild ether anesthesia and were analyzed for blood glucose by oxidase-peroxidase method using Accu-Chek Sensor Comfort (Roche Diagnostics, Germany) test strips.
2.12. Statistical Analysis
Statistical optimization was performed using Design-Expert Version 18.104.22.168 software (Stat-Ease Inc., USA). The in vivo data were tested for significant differences () by paired samples t-test. All other data was analyzed with simple statistics. The simple statistical analysis and paired samples t-test were conducted using MedCalc software, version 22.214.171.124.
3. Results and Discussion
IHM was isolated from ispaghula (Plantago ovata F.) husk, and the average yield of IHM was found 39.86% w/w.
For the 32 factorial design, a total of 9 trial formulations were proposed by Design-Expert Version 126.96.36.199 software. According to this trial proposal, various glibenclamide-loaded IHM-alginate beads were prepared by ionotropic-gelation technique. When various dispersion mixtures containing polymer-blend (SA and IHM) and glibenclamide were dropped into the solutions containing calcium ions, gelled glibenclamide-loaded IHM-alginate beads were formed instantaneously due to electrostatic interaction between negatively charged alginate ions and positively charged calcium ions present in the cross-linking solutions.
Overview of matrix of the design including investigated responses (DEE and ) was presented in Table 1. The values of DEE and , measured for all trial formulations, were fitted in the 32 factorial design to get model equations. The Design-Expert Version 188.8.131.52 software provided quadratic model equations involving individual main factors and interaction factors for all response parameters. The results of the ANOVA indicated that these models were significant for all response parameters (Table 2).
The model equation relating as response became ; F value = 10398.24; ).
The model equation relating as response became ( 0.9981; F value = 309.07; ).
Model simplification was carried out by eliminating nonsignificant terms from previously mentioned model equations , giving and .
Linear correlation plots between the actual, the predicted response variables are presented in Figures 1 and 2, and their corresponding residual plots showing the scatter of the residuals versus predicted values are presented in Figures 3 and 4. The influences of main effects (factors) on responses (here, DEE and ) were further elucidated by response surface methodology. Response surface methodology is a widely proficient approach in the development and optimization of drug delivery devices [5, 8, 28]. Response surface methodology encompasses the generation of model equations of the investigated responses over the experimental domain to determine optimum formulation () . The three-dimensional response surface plot is very useful in learning about the main and interaction effects of the independent variables (factors), whereas two-dimensional contour plot gives a visual representation of values of the response . The three-dimensional response surface plot relating DEE (Figure 5) indicates the increment of DEE with the lowering of SA: IHM () and increasing of CaCl2 concentration (). However, an increment in values with the increasing of SA: IHM () and lowering of CaCl2 concentration () is indicated by the three-dimensional response surface plot relating (Figure 6). All the two-dimensional contour plots relating measured responses (Figures 7 and 8) showed nonlinear relationships between independable variables, investigated for this study.
Numerical optimization technique using the desirability approach was employed to develop optimized formulations with desired response (optimum quality). The desirable ranges of the independable variables (factors) were restricted to 1.00 ≤ ≤ 1.50 and 9.50 ≤ ≤ 11.50, whereas the desirable ranges of responses were restricted to 95.00 ≤ ≤ 100.00% and 60.00 ≤ ≤ 65.00%. The optimal values of responses were obtained by numerical analysis using the Design-Expert Version 184.108.40.206 software based on the criterion of desirability. The desirability plot indicating desirable regression ranges for optimal process variable settings was presented in Figure 9, and overlay plot indicating the region of optimal process variable settings was presented in Figure 10. In order to evaluate the optimization capability of these models generated according to the results of 32 factorial design, optimized glibenclamide-loaded IHM-alginate beads were prepared using one of the optimal process variable settings proposed by the design (prediction ). The selected optimal process variable setting used for the formulation of optimized formulation was and . The optimized beads containing glibenclamide (F-O) were evaluated for and . Table 3 lists the results of experiments with predicted responses by the mathematical models and those actually observed. The optimized glibenclamide-loaded IHM-alginate beads (F-O) showed DEE of % and of % with small error values (0.94, and −3.69, resp.), indicating that mathematical models obtained from the 32 factorial design were fitted well.
The of all these glibenclamide-loaded IHM-alginate beads was within the range between and w/w (Tables 1 and 3). It was observed that was increased with the lowering of SA: IHM in polymer-blend, which may be due to increase in viscosity of the polymeric solution by the IHM addition as polymeric-blend with SA. This might have prevented drug leaching to the cross-linking solution and the elevation of cross-linking by CaCl2. Again, the of these beads was increased with increasing CaCl2 concentration in cross-linking solutions, due to the high degree of cross-linking by the concentrated calcium ions. The glibenclamide-loaded IHM-alginate beads prepared using lower CaCl2 concentration might have larger pores due to insufficient cross-linking, and drug leaching may occur through the pores that may result in lower drug encapsulation .
The average bead size of glibenclamide-loaded IHM-alginate beads was within the range of to mm (Table 4). Increase in the average size of beads was found with the increasing incorporation of IHM as a polymer-blend with SA. This could be attributed due to the increase in viscosity of polymer-blend solution with incorporation of IHM in increasing ratio that in turn increased the droplet size of polymer-blend solutions to the cross-linking solutions during preparation. Again, the decrease in average size of these formulated IHM-alginate beads was observed, when concentrated CaCl2 solution was used for cross-linking, which might be due to shrinkage of polymeric gel by higher degree of cross-linking.
The surface morphological analysis of glibenclamide-loaded IHM-alginate beads was visualized by SEM and presented in Figure 11. The SEM photograph of these beads possessed irregular shape without forming agglomeration. Their surface morphologies appeared to have rough with characteristic large wrinkles and cracks, as it was evident from the SEM photographs. These cracks and wrinkles might be caused by partly collapsing the polymeric gel network during drying.
The FTIR spectra of pure glibenclamide, glibenclamide-loaded IHM-alginate beads, and IHM-alginate beads without drug are shown in Figure 12. The FTIR spectrum of pure glibenclamide and the principal absorption peaks appeared at 3314 cm−1 due to the –NH stretching, 3116 cm−1 for aromatic hydrogen absorption, and a peak at 1717 cm−1 occurs due to –C=O absorption peak. In the FTIR spectrum of glibenclamide-loaded IHM-alginate beads, various characteristic peaks of glibenclamide appeared without any significant shifting. This indicates that glibenclamide maintained its identity after formulation of IHM-alginate beads through ionotropic-gelation technique. In both the FTIR spectra of glibenclamide-loaded IHM-alginate beads and IHM-alginate beads without drug, the strong and broad absorption band peaks had been observed between 3600–3200 cm−1 due to –OH stretching along with some complex bands in the region 1200–1030 cm−1 due to –C–O and C–O–C stretching vibrations, which are the characteristic of the natural polysaccharides. In addition, absorption bands in the regions 930–820 cm−1 and 785–730 cm−1 were also observed due to vibrational modes of pyranose rings of polysaccharides. The presence of strong asymmetric stretching absorption band between 1650 cm−1 and 1620 cm−1 and weaker symmetric stretching band near 1420 cm−1 supported the presence carboxylate anion of alginate structure. The FTIR analysis confirmed the compatibility of the glibenclamide with SA and IHM used to prepare the glibenclamide-loaded IHM-alginate beads by ionotropic-gelation technique.
The in vitro glibenclamide release studies were carried out for glibenclamide-loaded IHM-alginate beads in the 0.1 N HCl (pH, 1.2) for first 2 hours and then in phosphate buffer (pH, 7.4) for next 8 hours. All these beads showed prolonged glibenclamide release over 10 hours (Figure 13). Glibenclamide release from these IHM-alginate beads in the acidic pH was found slow due to the shrinkage of alginate at acidic pH. The trace amount of drug release at the initial stage of the dissolution study could probably be due to the surface adhered drug. After that, glibenclamide release was observed faster in phosphate buffer (pH, 7.4) comparatively, due to the higher swelling rate of these beads in phosphate buffer. The cumulative drug released from these formulated beads containing glibenclamide in 10 hours (, %) was within the range of % to %, and this was found to be higher with the decreasing SA to IHM ratio in the polymer-blend and increasing CaCl2 concentration in cross-linking solution. In case of comparatively higher IHM containing beads, the more hydrophilic property of IHM could bond better with water to form viscous gel-structure. This might blockade the pores on the surface of beads and sustain drug release profile. Again, the glibenclamide release from IHM-alginate beads prepared using higher CaCl2 concentration was comparatively sustained than the beads formulated with that of lower concentration. The higher concentration of CaCl2 (cross-linker) could produce high degree of cross-linking and thereby slower the drug release from highly cross-linked glibenclamide-loaded IHM-alginate beads.
The in vitro drug release data from various glibenclamide-loaded IHM-alginate beads were evaluated kinetically using various mathematical models like zero-order, first-order, Higuchi, and Korsmeyer-Peppas models. The accuracy and prediction ability of these models was determined using regression analysis. The result of the curve fitting () into various mathematical models is given in Table 5. When the respective of glibenclamide-loaded IHM-alginate beads was compared, it was found to follow the zero-order model ( = 0.992 to 0.997) over a period of 10 hours. This was also observed to be closest to Korsmeyer-Peppas model ( to 0.994). The best fit of zero-order model indicated that the glibenclamide release from these IHM-alginate beads followed controlled-release pattern. The values of diffusional exponent () determined from Korsmeyer-Peppas model ranged from 1.025 to 1.115, indicating the drug release from these glibenclamide-loaded IHM-alginate beads following the super case-II transport mechanism controlled by swelling and relaxation of polymeric-blend (SA-IHM) matrix. This could be attributed due to polymer dissolution and polymeric chain enlargement or relaxation.
The ex vivo wash-off behavior of optimized glibenclamide-loaded IHM-alginate beads (F-O) using goat intestinal mucosa was found faster in intestinal pH (7.4) than that in gastric pH (1.2). In gastric pH, the percentage of beads adhered onto the goat intestinal mucosal tissue varied from % over 10 hours, whereas this was % in intestinal pH (Figure 14). Thus, the results of the ex vivo wash-off test indicated that the newly developed optimized glibenclamide-loaded IHM-alginate beads had good mucoadhesivity.
In alloxan-induced diabetic rats, the comparative in vivo blood glucose level and the mean percentage reduction in blood glucose level after oral administration of pure glibenclamide and optimized glibenclamide-loaded IHM-alginate mucoadhesive beads (F-O) are presented in Figures 15 and 16, respectively. In case of the group treated with pure glibenclamide (Group A), a rapid reduction in blood glucose level was observed within 2-3 hours of administration, and after that, the blood glucose level recovered rapidly towards the normal level. In case of the group (Group B) treated with optimized glibenclamide-loaded IHM-alginate mucoadhesive beads, the reduction in blood glucose level was found slower than that of the group treated with pure glibenclamide (Group A) up to 3 hours. Significant differences () were found between the blood glucose levels after administration of pure glibenclamide and optimized glibenclamide-loaded IHM-alginate mucoadhesive beads (F-O) at each time point measured. However, the reductions in glucose level were increased gradually with the increment of time in case of Group B (treated with optimized glibenclamide-loaded IHM-alginate mucoadhesive beads) and were sustained over 10 hours. A 25% reduction in glucose level is considered a significant hypoglycemic effect . Therefore, the significant hypoglycemic effect by the optimized glibenclamide-loaded IHM-alginate mucoadhesive beads (F-O) was observed over 10 hours.
In this investigation, glibenclamide-loaded IHM-alginate mucoadhesive beads were successfully developed and optimized. These developed optimized mucoadhesive beads demonstrated high drug encapsulation, good mucoadhesivity with the biological membrane, sustained drug release profile at a controlled rate, and significant antidiabetic activity in alloxan-induced diabetic rats over prolonged period after oral administration. Therefore, these glibenclamide-loaded IHM-alginate mucoadhesive beads were found suitable for prolonged systemic absorption of glibenclamide through sustained drug release and mucoadhesive properties after oral administration maintaining tight blood glucose level and improved patient compliance in the management of non-insulin-dependent diabetes mellitus. Moreover, the technique for the preparation of these beads was found simple, economical, and consistent. This type of beads can also be exploited for drug delivery of other drugs to improve their bioavailability and therapeutic efficacy.
Conflict of Interests
The authors report no conflict of interests.
- A. K. Nayak, M. S. Hasnain, S. Beg, and M. I. Alam, “Mucoadhesive beads of gliclazide: design, development, and evaluation,” ScienceAsia, vol. 36, no. 4, pp. 319–325, 2010.
- A. K. Nayak, B. Das, and M. Maji, “Calcium alginate/gum Arabic beads containing glibenclamide: development and in vitro characterization,” International Journal of Biological Macromolecules, vol. 51, pp. 1070–1078, 2012.
- S. H. Yoo, Y. B. Song, P. S. Chang, and H. G. Lee, “Microencapsulation of α-tocopherol using sodium alginate and its controlled release properties,” International Journal of Biological Macromolecules, vol. 38, no. 1, pp. 25–30, 2006.
- P. Sriamornsak and S. Sungthongjeen, “Modification of theophylline release with alginate gel formed in hard capsules,” AAPS PharmSciTech, vol. 8, no. 3, pp. E1–E8, 2007.
- J. Malakar, A. K. Nayak, and D. Pal, “Development of cloxacillin loaded multiple-unit alginate-based floating system by emulsion-gelation method,” International Journal of Biological Macromolecules, vol. 50, pp. 138–147, 2012.
- A. K. Nayak, S. Khatua, M. S. Hasnain, and K. K. Sen, “Development of alginate-PVP K 30 microbeads for controlled diclofenac sodium delivery using central composite design,” DARU Journal of Pharmaceutical Sciences, vol. 19, pp. 356–366, 2011.
- J. Han, Z. Zhou, R. Yin, D. Yang, and J. Nie, “Alginate-chitosan/hydroxyapatite polyelectrolyte complex porous scaffolds: preparation and characterization,” International Journal of Biological Macromolecules, vol. 46, no. 2, pp. 199–205, 2010.
- Y. L. Patel, P. Sher, and A. P. Pawar, “The effect of drug concentration and curing time on processing and properties of calcium alginate beads containing metronidazole by response surface methodology,” AAPS PharmSciTech, vol. 7, no. 4, article 86, 2006.
- D. Pal and A. K. Nayak, “Development, optimization, and anti-diabetic activity of gliclazide-loaded alginate-methyl cellulose mucoadhesive microcapsules,” AAPS PharmSciTech, vol. 12, pp. 1431–1441, 2011.
- F. Llanes, D. H. Ryan, and R. H. Marchessault, “Magnetic nanostructured composites using alginates of different M/G ratios as polymeric matrix,” International Journal of Biological Macromolecules, vol. 27, no. 1, pp. 35–40, 2000.
- D. Pal and A. K. Nayak, “Novel tamarind seed polysaccharide-alginate mucoadhesive microspheres for oral gliclazide delivery: in vitro-in vivo evaluation,” Drug Delivery, vol. 19, pp. 123–131, 2012.
- S. K. Prajapati, P. Tripathi, U. Ubaidulla, and V. Anand, “Design and development of gliclazide mucoadhesive microcapsules: in vitro and in vivo evaluation,” AAPS PharmSciTech, vol. 9, no. 1, pp. 224–230, 2008.
- B. Singh, “Psyllium as therapeutic and drug delivery agent,” International Journal of Pharmaceutics, vol. 334, pp. 1–14, 2007.
- R. A. Laidlaw and E. G. V. Percival, “Studies of seed mucilages, part V: examination of a polysaccharide extracted from the seeds of Plantago ovata Forsk by hot water,” Journal of the Chemical Society, pp. 528–534, 1950.
- R. A. Laidlaw and E. G. V. Percival, “Studies on seed mucilages, part III: examination of a polysaccharide extracted from the seeds of Plantago ovata Forsk,” Journal of the Chemical Society, pp. 1600–1607, 1949.
- M. H. Fischer, N. Yu, G. R. Gray, J. Ralph, L. Anderson, and J. A. Marlett, “The gel-forming polysaccharide of psyllium husk (Plantago ovata Forsk),” Carbohydrate Research, vol. 339, no. 11, pp. 2009–2017, 2004.
- V. K. Sharma and A. Bhattacharya, “Release of metformin hydrochloride from Ispaghula-sodium alginate beads adhered on cock intestinal mucosa,” Indian Journal of Pharmaceutical Education and Research, vol. 42, no. 4, pp. 363–372, 2008.
- D. P. Maurya, Y. Sultana, M. Aqil et al., “Formulation and optimization of alkaline extracted ispaghula husk microparticles of isoniazid—in vitro and in vivo assessment,” Journal of Microencapsulation, vol. 28, pp. 472–482, 2011.
- A. A. Attama and O. J. Nwabunze, “Mucuna gum microspheres for oral delivery of glibenclamide: in vitro evaluation,” Acta Pharmaceutica, vol. 57, no. 2, pp. 161–171, 2007.
- G. A. Lewis, D. Matieu, and R. Phan-Tan-Lu, Pharmaceutical Experiment Design, Marcel Dekker, New York, NY, USA, 1999.
- B. Singh, R. Kapil, M. Nandi, and N. Ahuja, “Developing oral drug selivery systems using formulation by design: vital precepts, retrospect and prospects,” Expert Opinion in Drug Delivery, vol. 8, pp. 1341–1360, 2011.
- B. Singh, B. Garg, S. C. Chaturvedi et al., “Formulation development of gastroretentive tablets of lamivudine using floating-bioadhesive potential of optimized polymer blends,” Journal of Pharmacy and Pharmacology, vol. 64, pp. 654–669, 2012.
- B. Singh, R. Kumar, and N. Ahuja, “Optimizing drug delivery systems using systematic “design of experiments”, part I: fundamental aspects,” Critical Reviews in Therapeutic Drug Carrier Systems, vol. 22, no. 1, pp. 27–105, 2005.
- B. Singh, M. Dahiya, V. Saharan, and N. Ahuja, “Optimizing drug delivery systems using systematic “design of experiments”, part II: retrospect and prospects,” Critical Reviews in Therapeutic Drug Carrier Systems, vol. 22, no. 3, pp. 215–294, 2005.
- S. A. Joshi, S. S. Chavhan, and K. K. Sawant, “Rivastigmine-loaded PLGA and PBCA nanoparticles: preparation, optimization, characterization, in vitro and pharmacodynamic studies,” European Journal of Pharmaceutics and Biopharmaceutics, vol. 76, no. 2, pp. 189–199, 2010.
- P. K. Sharma and A. K. Koul, “Mucilage in seeds of Plantago ovata and its wild allies,” Journal of Ethnopharmacology, vol. 17, no. 3, pp. 289–295, 1986.
- M. Saeedi, K. Morteza-Semnani, F. Ansoroudi, S. Fallah, and G. Amin, “Evaluation of binding properties of Plantago psyllium seed mucilage,” Acta Pharmaceutica, vol. 60, no. 3, pp. 339–348, 2010.
- A. K. Nayak and D. Pal, “Development of pH-sensitive tamarind seed polysaccharide-alginate composite beads for controlled diclofenac sodium delivery using response surface methodology,” International Journal of Biological Macromolecules, vol. 49, pp. 784–793, 2011.
- S. Maiti, P. Dey, A. Banik, B. Sa, S. Ray, and S. Kaity, “Tailoring of locust bean gum and development of hydrogel beads for controlled oral delivery of glipizide,” Drug Delivery, vol. 17, no. 5, pp. 288–300, 2010.