Table of Contents
International Scholarly Research Notices
Volume 2014 (2014), Article ID 628382, 6 pages
http://dx.doi.org/10.1155/2014/628382
Research Article

Study of the Effect of Dillenia indica Fruit Mucilage on the Properties of Metformin Hydrochloride Loaded Spray Dried Microspheres

Department of Pharmaceutical Sciences, Dibrugarh University, NH-37, Dibrugarh, Assam 786004, India

Received 20 May 2014; Revised 7 September 2014; Accepted 5 November 2014; Published 20 November 2014

Academic Editor: Hamadi Fetoui

Copyright © 2014 Hemanta Kumar Sharma and Lila Kanta Nath. 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.

Abstract

Natural materials are preferred over synthetic counterparts because of their biodegradable and biocompatible nature. The present work was proposed to utilize mucilage from natural source for the development of controlled release formulation of metformin hydrochloride. Natural mucilaginous substance extracted from Dillenia indica L. (DI) fruit was used in fabricating controlled release microspheres. The microspheres were prepared by spray drying method under different formulation parameters. The prepared microspheres were studied for particle size, drug excipient compatibility, particle shape and surface morphologies, drug entrapment efficiency, mucoadhesivity, and in vitro drug release properties. The prepared microspheres exhibited mucoadhesive properties and demonstrated controlled release of metformin hydrochloride. The study reveals that the natural materials can be used for formulation of controlled release microspheres and would provide ample opportunities for further study.

1. Introduction

Microspheres can be prepared by different methods. In the present study, microspheres were prepared by spray drying method [1, 2]. Spray drying is advantageous as it is a well-established technology and the equipment is capable of high product output. Thermosensitive substances can be coated successfully by this method because the time of exposure to elevated temperature is extremely short. Nonaqueous coating systems can be used for encapsulation of moisture-sensitive materials. The biological half-life of metformin hydrochloride (MH) is 2.5 to 5 hr and gastrointestinal absorption is incomplete with an absolute bioavailability of 50–60% (under fasting condition). Reduction of gastrointestinal motility enhances the absorption of MH. The rate of absorption is slower than that of elimination.

The plant Dillenia indica L. (Family: Dilleniaceae; Synonym: Dillenia speciosa Thunb.) is known as elephant apple/indian catmon (English); Bhavya, Bharija (Sanskrit); Ou tenga (Assamese). It is distributed in India, Nepal, Bangladesh, and Sri Lanka [3]. The fruits of Dillenia indica (DI) are used by tribal and folk communities of various regions as vegetable. The fruit of DI is “globose” (Figure 1), with excrescent calyx, 12.5–15.0 cm in diameter, green when young and yellowish and sweet-scented when ripe; seeds many, compressed, embedded in hairy cells [3, 4]. The leaf, bark, and fruit of this plant are used traditionally as medicine in different forms for their therapeutic values. The mucilage of the fruit is used to wash hair and has conditioning effect. Description of D. indica is available in various ancient Indian literatures about its important common and medicinal uses [5, 6]. There are also reports that the plant parts exhibited antileukemic, anti-inflammatory, antioxidant, antiproliferative, antidiabetic, antimicrobial, antifungal, antidiarrheal, cytotoxic, and hepatoprotective activities [79].

628382.fig.001
Figure 1: Image of the fruit of D. indica.

Earlier, extraction, characterization of the mucilage, and compatibility study of the mucilage with metformin hydrochloride was reported [10]. The mucilage was extracted by heating with water at 60–70°C and the filtrate was precipitated by acetone. Quantitative estimation of pectin was carried out after detection of the presence of pectin in the mucilage by colorimetric method. DSC, FTIR, and XRD studies were carried out alone and in combination with metformin hydrochloride. No interaction was found between the mucilage and metformin hydrochloride. Metformin hydrochloride loaded microspheres were prepared using Bora rice flour in combination with sodium alginate [11]. In another study, mucilage of DI fruit, mucilage of Abelmoschus esculentus pods and Bora rice flour were used for formulation of metformin hydrochloride loaded microspheres [12].

In this study, metformin hydrochloride loaded microspheres were prepared by spray drying method using the mucilage of DI fruits alone. The effect of the mucilage concentration on the properties of the microspheres was studied. The results of this study are reported here.

2. Experimental Section

2.1. Materials

Metformin hydrochloride (MH) was received as gift sample from Ozone Pharmaceutical Ltd., Guwahati, Assam. The fruits of Dillenia indica were procured from local market. The mucilage of D. indica fruit was extracted by acetone precipitation method as described above [10, 13]. All chemicals used in this study were of analytical grade and were procured commercially (E-Merck, India). They were used as such without testing and purification. The intestinal segment of goat (Ileum), used for mucoadhesive study, was procured from local slaughter house.

3. Methods

3.1. Preparation of Microspheres

Metformin hydrochloride loaded microspheres with the mucilage of DI fruits were prepared by spray drying method. Aqueous dispersions of the mucilage of DI fruits of three different concentrations (1.0%, 2.0%, and 3.0% w/v) were prepared by heating at °C for 1 hr. The dispersions were allowed to cool to room temperature and then MH was added to dispersions at a concentration of 1.5% w/v and stirred to dissolve MH. The mixture was sonicated for 10 min. Then, the mixture was spray dried using lab spray dryer (LU-222 Advanced Labultima, India) with 0.7 mm nozzle. Parameters of spray dryer were changed and products were collected separately in each run. The composition and various processing parameters of the method used are presented in Table 1.

tab1
Table 1: It contains the composition and formulation parameters of metformin HCl loaded microspheres using mucilage of D. indica by spray drying method.
3.2. Evaluation of Microspheres

The prepared microspheres were evaluated for particle size, particle shape and surface topography, liquid uptake capacity, drug entrapment efficiency, mucoadhesive property, and in vitro drug release property.

3.3. Particle Size and Shape

The particle size of the microspheres was determined by optical microscopy method [14]. The shape and surface topography of the microspheres was investigated by using (S-3600N, HITACHI) scanning electron microscope (SEM) at 15 KV.

3.4. Liquid Uptake Capacity

The liquid uptake capacity of microspheres was determined in three aqueous media (water, 0.1 M HCl and phosphate buffer pH 7.4) at room temperature (37.5°C ± 0.5°C). Weighed quantities of the samples were taken into test tubes separately with fixed volume of media in undisturbed condition for 6 hrs. The liquid was then decanted off carefully and the final weight of microspheres was taken. The percentage liquid uptake was calculated using the following relation: where and are the initial weight and final weight of sample after 6 hrs, respectively [15, 16].

3.5. Drug Entrapment Efficiency (DEE)

Microspheres equivalent to 50.0 mg of the drug were taken and the amount of drug entrapped was estimated by dispersing the crushed microspheres in 100.0 mL of phosphate buffer (pH 7.4) by shaking on a mechanical shaker (Remi Motors, Mumbai, India) for 12 hr. The solution was filtered and the filtrate was diluted 25 times with phosphate buffer (pH 7.4) and the absorbance was measured spectrophotometrically (UV-1700, Shimadzu, Japan) at 233 nm against a blank. The amount of drug entrapped in the microspheres was calculated in percentage from the ratio of actual drug content to theoretical drug content as given in the following equation [17, 18]:

3.6. Mucoadhesive Property

The mucoadhesive property of microspheres was evaluated by in vitro wash off test method [1921]. Freshly excised pieces of goat intestinal mucosa (2 × 2 cm) were washed with phosphate buffer (pH 7.4) mounted on to glass slides with cotton thread. Microspheres were spread on to each prepared glass slide and were counted under microscope. The number of microspheres spread was not constant but ranges from 76 to 98. Then immediately thereafter, the slides were hung to USP tablet disintegration test apparatus (Lab. India, Mumbai). When the test apparatus was operated, the sample was subjected to slow up and down movement in the test fluid (phosphate buffer pH 7.4) at 37°C contained in a 1 L vessel of the apparatus. After 5 hrs, the apparatus was stopped and the number of microspheres still adhering to mucosal surface was counted with the help of microscope. This process was repeated for three times () and the average number of microspheres adhered was calculated.

3.7. In Vitro Drug Release Study

The release of drug from the microspheres was studied in phosphate buffer (pH 7.4) as dissolution medium, using USP paddle-type dissolution test apparatus (six vessels, TL 06, Electro Lab, India) at °C with a rotating speed of 100 rpm. The liquid uptake capacity and mucoadhesive property were found to be more in phosphate buffer (pH 7.4) and therefore the in vitro drug release study was carried out using phosphate buffer media (pH 7.4). A sample of microspheres equivalent to 50.0 mg of metformin hydrochloride was used in each test. 10.0 mL of the sample from each dissolution test vessel was withdrawn at predetermined time intervals (0, 0.5, 1, 1.5, 2, 4, 6, 8, and 10 hr) for 10 hrs and the same volume of media was replaced. The withdrawn samples were filtered through a membrane filter (0.45 μm) and were analyzed for drug content spectrophotometrically at 233 nm using the UV-visible spectrophotometer (UV-1700, Shimadzu, Japan) [2224].

4. Results and Discussion

4.1. Particle Size and Shape

The mean particle sizes of the formulations were found to be in the range of to μm in the formulations from SD1 to SD12. The particle size was found to be increased, when mucilage concentration was increased at constant inlet temperature, feed flow rate, and aspirator flow rate as observed in formulations SD3, SD6, SD9, and SD12 (Table 2). It was observed from the SEM photograph (Figure 2) of the samples of microspheres that the surfaces of the microspheres were rough with deepening on the surface. This was due to rapid loss of water from the surface on exposure to high temperature (Table 1). However, the microspheres were found to be almost spherical in shape.

tab2
Table 2: In vitro evaluation of the metformin hydrochloride loaded spray dried microspheres prepared using mucilage of D. indica.
628382.fig.002
Figure 2: SEM image of metformin hydrochloride loaded microspheres (SD9) prepared using mucilage of D. indica by spray drying method at 150 magnification.
4.2. Liquid Uptake Capacity

The liquid uptake capacity of microspheres was determined in water, phosphate buffer pH 7.4, and in 0.1 M HCl. The liquid uptake was found to be within the range of to % in 0.1 M HCl; to % in water, and to % in phosphate buffer (pH 7.4). Maximum water uptake was observed in formulations containing higher amounts of the mucilage (SD3, SD6, SD9, and SD12) when inlet temperature, feed flow rate, and aspirator flow rate were kept constant (Tables 1 and 2). The uptake was low in 0.1 M HCl and in water but higher in phosphate buffer (pH 7.4). The acidic mucilage (pH 5.0) developed network structures in basic pH (pH 7.4) due to which more liquid uptake was observed in comparison to water and 0.1 M HCl.

4.3. Drug Entrapment Efficiency

The entrapment efficiency of different formulations is presented in Table 2. The entrapment efficiency was found to be in the range of to (SD1 to SD12). Highest entrapment efficiency was found to be (SF-12) in the formulation containing higher amount of the mucilage of Dillenia indica. The low entrapment efficiency was due to the aqueous solubility of MH and low water uptake capacity of the mucilage which in turn the drug was made available in the bulk solution before it was entrapped by the mucilage. The increased concentration of mucilage increased water uptake due to which more amount of the drug was available in the network structure of the mucilage. During spray drying process, the water evaporated leaving the drug within the mucilage network.

4.4. Mucoadhesive Property

The results of in vitro wash-off test of the spray dried microspheres prepared using the mucilage of Dillenia indica are presented in Figure 3. It was observed that the particles of formulations SD3, SD6, SD8, SD9, SD10, and SD12 remained adhered to the mucosal surface of the intestinal membrane up to 3.5 hrs.

628382.fig.003
Figure 3: In vitro wash off test of metformin hydrochloride loaded microspheres prepared using mucilage of D. indica by spray drying method (SD1 to SD12).

The mucoadhesive property was found to be increased at increased concentration of mucilage in the formulations SD3, SD6, SD9, and SD12 (Table 1).

4.5. In Vitro Drug Release Study

In vitro drug release study of the microspheres was carried out in phosphate buffer (pH 7.4) for 10 hrs. The results exhibited maximum drug release from most of the formulations within 4 hrs during the 10 hrs study except the formulations SD2, SD5, SD8, and SD11, which exhibited maximum drug release within 6 hrs during the 10 hrs study. These four formulations contained intermediate concentration of the mucilage (2.0 g) for a particular operating condition of spray dryer (Table 1). The in vitro drug release of the formulations was best explained by Higuchi kinetics with the highest linearity in formulations SD8, SD10, and SD12. The correlation coefficient (R2) of the above formulations was 0.917, 0.863, and 0.909, respectively, which revealed that the drug diffused at a comparatively slower rate as the diffusional path length was increased. However, a direct correlation between the mucilage concentrations with the drug release kinetics could not be established due to the variation in the operating condition of the spray dryer. Moreover, the formulations also exhibited variations in the mechanism of drug release. Formulations SD1, SD2, SD3, SD7, SD8, SD9, and SD11 exhibited Fickian diffusion, whereas, SD4, SD5, SD6, SD10, and SD12 exhibited non-Fickian diffusion. This revealed that the mechanism was not directly related to the mucilage concentration but was related to the process parameters. The concentration versus time profile of the formulations ( error = ±2%) is presented in Figure 4.

628382.fig.004
Figure 4: Cumulative percent drug release versus time profile of metformin hydrochloride loaded microspheres prepared using mucilage of D. indica by spray drying method (SD1 to SD12).

5. Conclusion

The microspheres prepared using the mucilage of DI by spray drying method exhibited poor entrapment efficiency but better mucoadhesive property. The microspheres remained adhered up to 3.5 hrs. The maximum liquid uptake was only 66.05%. The liquid uptake was the maximum in alkaline media and the minimum in 0.1 M HCl. Maximum amount of drug was released within 2 hrs and a decrease of concentration was observed during the study period of 10 hrs. However, there are options for improvement of the properties of microspheres for release of drug in a more controlled manner for a prolonged period of time.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors are thankful to All India Council for Technical Education and University Grants Commission for the fund. The authors also thank Oil India Ltd., Duliajan, Assam, for the SEM study, and Ozone Pharmaceutical Ltd., Guwahati, Assam, for providing the drug as gift sample.

References

  1. J. Swarbrick, Encyclopedia of Pharmaceutical Technology, Marcel Dekker, New York, NY, USA, 2007.
  2. R. Vehring, “Pharmaceutical particle engineering via spray drying,” Pharmaceutical Research, vol. 25, no. 5, pp. 999–1022, 2008. View at Publisher · View at Google Scholar · View at Scopus
  3. C. P. Khare, Ed., Indian Medicinal Plants: An Illustrated Dictionary, Springer, New York, NY, USA, 2007.
  4. K. M. Nadkarni and A. K. Nadkarni, The Indian Materia Medica, Nadkarni and Co., Bombay, India, 1954.
  5. B. K. Pradhan and H. K. Badola, “Ethnomedicinal plant use by Lepcha tribe of Dzongu valley, bordering Khangchendzonga Biosphere Reserve, in North Sikkim, India,” Journal of Ethnobiology and Ethnomedicine, vol. 4, article 22, 2008. View at Publisher · View at Google Scholar · View at Scopus
  6. U. K. Sharma and S. Pegu, “Ethnobotany of religious and supernatural beliefs of the mising tribes of Assam with special reference to the “Dobur Uie”,” Journal of Ethnobiology and Ethnomedicine, vol. 7, article 16, 2011. View at Publisher · View at Google Scholar · View at Scopus
  7. U. Bose, K. Gunasekaran, V. Bala, and A. A. Rahman, “Evaluation of phytochemical and pharmacological properties of Dillenia indica Linn. Leaves,” Journal of Pharmacology and Toxicology, vol. 5, no. 5, pp. 222–228, 2010. View at Publisher · View at Google Scholar · View at Scopus
  8. M. H. Abdille, R. P. Singh, G. K. Jayaprakasha, and B. S. Jena, “Antioxidant activity of the extracts from Dillenia indica fruits,” Food Chemistry, vol. 90, no. 4, pp. 891–896, 2005. View at Publisher · View at Google Scholar · View at Scopus
  9. M. Lahkar, B. Thakuria, and P. Pathak, “A study of the anxiolytic-like activity of Dillenia indica linn. leaves in experimental models of anxiety in mice,” Internet Journal of Pharmacology, vol. 9, no. 2, article 78, 2011. View at Google Scholar · View at Scopus
  10. H. K. Sharma, S. Lahkar, and L. K. Nath, “Extraction, characterisation and compatibility study of polysaccharides from Dillenia indica and Abelmoschus esculentus with metformin hydrochloride for development of drug delivery system,” International Journal of PharmTech Research, vol. 5, no. 1, pp. 275–283, 2013. View at Google Scholar · View at Scopus
  11. H. K. Sharma, J. Mohapatra, and L. K. Nath, “Development and characterisation of metformin loaded spray dried Bora rice microspheres,” Pakistan Journal of Pharmaceutical Sciences, vol. 26, no. 1, pp. 17–22, 2013. View at Google Scholar · View at Scopus
  12. H. K. Sharma, S. Lahkar, and L. Kanta Nath, “Formulation and in vitro evaluation of metformin hydrochloride loaded microspheres prepared with polysaccharide extracted from natural sources,” Acta Pharmaceutica, vol. 63, no. 2, pp. 209–222, 2013. View at Publisher · View at Google Scholar · View at Scopus
  13. Y. Gao, F.-D. Cui, Y. Guan, L. Yang, Y.-S. Wang, and L.-N. Zhang, “Preparation of roxithromycin-polymeric microspheres by the emulsion solvent diffusion method for taste masking,” International Journal of Pharmaceutics, vol. 318, no. 1-2, pp. 62–69, 2006. View at Publisher · View at Google Scholar · View at Scopus
  14. L. Lachman and H. A. Liberman, The Theory and Practice of Industrial Pharmacy, Varghese Publishing House, Mumbai, India, 2nd edition, 1991.
  15. A. Martin, J. Swarbrick, and A. Cammarata, Eds., Physical Pharmacy, K.M.Varghese Company, Bombay, India, 3rd edition, 1983.
  16. H. K. Batchelor, D. Banning, P. W. Dettmar, F. C. Hampson, I. G. Jolliffe, and D. Q. M. Craig, “An in vitro mucosal model for prediction of the bioadhesion of alginate solutions to the oesophagus,” International Journal of Pharmaceutics, vol. 238, no. 1-2, pp. 123–132, 2002. View at Publisher · View at Google Scholar · View at Scopus
  17. N. A. Nafee, N. A. Boraie, F. A. Ismail, and L. M. Mortada, “Design and characterization of mucoadhesive buccal patches containing cetylpyridinium chloride,” Acta Pharmaceutica, vol. 53, no. 3, pp. 199–212, 2003. View at Google Scholar · View at Scopus
  18. T. Uchida, K. Yoshida, Y. Nakada et al., “Preparation and characterization of polylactic acid microspheres containing water-soluble anesthetics with small molecular weight,” Chemical and Pharmaceutical Bulletin, vol. 45, no. 3, pp. 513–517, 1997. View at Publisher · View at Google Scholar · View at Scopus
  19. L. Whitehead, J. H. Collett, and J. T. Fell, “Amoxycillin release from a floating dosage form based on alginates,” International Journal of Pharmaceutics, vol. 210, no. 1-2, pp. 45–49, 2000. View at Publisher · View at Google Scholar · View at Scopus
  20. K. Park and J. R. Robinson, “Bioadhesive polymers as platforms for oral-controlled drug delivery: method to study bioadhesion,” International Journal of Pharmaceutics, vol. 19, no. 2, pp. 107–127, 1984. View at Publisher · View at Google Scholar · View at Scopus
  21. R. B. Gandhi and J. R. Robinson, “Bioadhesive drug delivery system,” Indian Journal of Pharmaceutical Sciences, vol. 50, no. 3, p. 145, 1988. View at Google Scholar
  22. C.-M. Lehr, J. A. Bouwstra, J. J. Tukker, and H. E. Junginger, “Intestinal transit of bioadhesive microspheres in an in situ loop in the rat—a comparative study with copolymers and blends based on poly(acrylic acid),” Journal of Controlled Release, vol. 13, no. 1, pp. 51–62, 1990. View at Publisher · View at Google Scholar · View at Scopus
  23. I. Henriksen, K. L. Green, J. D. Smart, G. Smistad, and J. Karlsen, “Bioadhesion of hydrated chitosans: an in vitro and in vivo study,” International Journal of Pharmaceutics, vol. 145, no. 1-2, pp. 231–240, 1996. View at Publisher · View at Google Scholar · View at Scopus
  24. K. H. Yuen, K. K. Peh, and B. L. Tan, “Relating in vitro/in vivo data of two controlled-release metformin formulations,” Drug Development and Industrial Pharmacy, vol. 25, no. 5, pp. 613–618, 1999. View at Publisher · View at Google Scholar · View at Scopus