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Recently Investigated Natural Gums and Mucilages as Pharmaceutical Excipients: An Overview

DOI: 10.1155/2014/204849

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Abstract:

Due to advances in drug delivery technology, currently, excipients are included in novel dosage forms to fulfil specific functions and in some cases they directly or indirectly influence the extent and/or rate of drug release and drug absorption. Recent trends towards use of plant based and natural products demand the replacement of synthetic additives with natural ones. Today, the whole world is increasingly interested in natural drugs and excipients. These natural materials have many advantages over synthetic ones as they are chemically inert, nontoxic, less expensive, biodegradable, and widely available. This review discusses majority of the plant-derived polymeric compounds (gums and mucilage’s), their sources, chemical constituents, uses, and some recent investigations as excipients in novel drug delivery systems. 1. Introduction In recent years, polymers those are derived from plant origin have evoked tremendous interest because of their diverse pharmaceutical applications such as diluent, binder, disintegrant in tablets, thickeners in oral liquids, protective colloids in suspensions, gelling agents in gels, and bases in suppository [1]. They are also used in cosmetics, paints, textiles, and paper making [2]. These natural gums and mucilages are preferred over the synthetic ones because they are biocompatible, cheap, and easily available than the synthetic ones. Also the natural excipients are preferred on the synthetic and semisynthetic ones because of their lack of toxicity, low cost, soothing action, availability, and nonirritant nature of the excipients [3–6]. Demand for these substances is increasing and new sources are being developed. India, because of its geographical and environmental position, has traditionally been a good source for such products among the Asian countries. 1.1. Gums and Mucilage’s Gums are considered to be pathological products, formed by giving injury to the plant or due to unfavourable conditions, such as drought, by breakdown of cell walls (extra cellular formation: gummosis). Mucilages are generally normal products of metabolism (physiological products), formed within the cell (intracellular formation). Gums readily dissolve in water, whereas, mucilage form slimy masses. Both gums and mucilages are plant hydrocolloids yielding mixture of sugars and uronic acids on hydrolysis [7]. Classification is based on source:(a)marine origin/algal (seaweed) gums: agar, carrageenans, alginic acid, and laminarin;(b)plant origin:(i)shrubs/tree exudates: gum arabic, gum ghatti, gum karaya, gum tragacanth, and khaya and albizia

References

[1]  J. L. Zatz and G. P. Kushla, “Oral aqueous suspensions and gels,” in Pharmaceutical Dosage Forms: Disperse Systems, M. M. Reiger and G. S. Banker, Eds., vol. 2, pp. 164–405, Marcel Dekker, New York, NY, USA, 1989.
[2]  G. K. Jani, D. P. Shah, V. D. Prajapatia, and V. C. Jain, “Gums and mucilages: versatile excipients for pharmaceutical formulations,” Asian Journal of Pharmaceutical Sciences, vol. 4, no. 5, pp. 309–323, 2009.
[3]  R. L. Whistler, “Drug-release retarding polymers are the key performers,” in Industrial Gums, Academic Press, London, UK, 2nd edition, 1996.
[4]  H. K. Kakrani and N. K. Jain, “A study on investigated as drug retarding agents, each presenting a binding properties of guggal gum,” Indian Journal Hospital Different Approach to the Matrix System, vol. 18, Based on the Pharmacist, no. 3, pp. 100–102, 1981.
[5]  N. S. Bhunvara and M. L. Khorana, “Studies on usually classified into three main groups: hydrophilic, suspending properties of Hyprophila spinosa. Hydrophobic and plastic,” Hydrophilic Polymers are the Indian Drugs, vol. 22, pp. 500–502, 1985.
[6]  G. T. Kulkarni, K. Gowthamarajan, R. R. Dhobe, F. Yohanan, and B. Suresh, “Development of controlled release spheriods using natural polysaccharide as release modifier,” Drug Delivery, vol. 12, no. 4, pp. 201–206, 2005.
[7]  D. C. K. Kokate, A. P. Purohit, and S. B. Gokhale, Pharmacognosy, Nirali, 29th edition, 2008.
[8]  S. K. Baveja, K. V. R. Rao, and J. Arora, “Examination of natural gums and mucilages as sustaining materials in tablet dosage forms,” Indian Journal of Pharmaceutical Sciences, vol. 50, pp. 89–92, 1988.
[9]  S. P. Wahi, V. D. Sharma, V. K. Jain, et al., “Studies on suspending property of mucilage of Hygrophila Spinosa T. Anders and Hibiscus Esculents Linn,” Indian Drug, vol. 22, pp. 500–502, 1985.
[10]  K. R. Khandelwal, Practical Pharmacognosy, Techniques and Experiments, Nirali, 2008.
[11]  R. Mazumder, L. K. Nath, A. Haque et al., “Formulation and in vitro evaluation of natural polymers based microspheres for colonic drug delivery,” International Journal of Pharmacy and Pharmaceutical Sciences, vol. 2, no. 1, pp. 211–219, 2010.
[12]  K. Hirose, K. Endo, and K. Hasegawa, “A convenient synthesis of lepidimoide from okra mucilage and its growth-promoting activity in hypocotyls,” Carbohydrate Research, vol. 339, no. 1, pp. 9–19, 2004.
[13]  R. Kumar, M. B. Patil, S. R. Patil, and M. S. Paschapur, “Evaluation of Abelmoschus esculentus mucilage as suspending agent in paracetamol suspension,” International Journal of PharmTech Research, vol. 1, no. 3, pp. 658–665, 2009.
[14]  R. Kumar, M. B. Patil, S. R. Patil, and M. S. Paschapur, “Evaluation of disintegrating properties of Abelmoschus esculentus mucilage,” International Journal of PharmTech Research, vol. 1, no. 2, pp. 241–246, 2009.
[15]  N. P. Chodavarapu, R. B. Yendluri, H. Suryadevara, P. Reddy, and P. Chhatoi, “Formulation and evaluation of Abelmoschus esculentus mucilage based metformin hydrochloride floating matrix tablets,” International Journal of Pharmacy and Technology, vol. 3, no. 2, pp. 2725–2745, 2011.
[16]  K. B. Ilango, M. Manisha, D. Sridurga, A. Rajsekaran, M. S. Kumar, and T. Subburaju, “In vitro and in vivo evaluation of okra polysaccharide-based colon-targeted drug delivery systems,” International Journal of Pharmaceutical Sciences Review and Research, vol. 5, no. 1, pp. 138–145, 2010.
[17]  W. A. Ashton, M. Jefferies, R. G. Morley, G. Pass, G. O. Phillips, and D. M. J. Power, “Physical properties and applications of aqueous solutions of Albizia zygia gum,” Journal of the Science of Food and Agriculture, vol. 26, pp. 697–704, 1975.
[18]  US National Academy of Sciences, Tropical Legumes, National Academy of Sciences, Washington, DC, USA, 1979.
[19]  O. A. Odeku and J. T. Fell, “In-vitro evaluation of khaya and albizia gums as compression coatings for drug targeting to the colon,” Journal of Pharmacy and Pharmacology, vol. 57, no. 2, pp. 163–168, 2005.
[20]  R. Deveswaran, S. Abraham, S. Bharath, B. V. Basavaraj, S. Furtado, and V. Madhavan, “Design and characterization of Diclofenac sodium tablets containing tamarind seed polysaccharide as Release retardant,” International Journal of PharmTech Research, vol. 1, no. 2, pp. 191–195, 2009.
[21]  M. U. Mishra and J. N. Khandare, “Evaluation of tamarind seed polysaccharide as abiodegradable carrier for colon specific drug delivery,” International Journal of Pharmacy and Pharmaceutical Sciences, vol. 3, no. 1, pp. 139–142, 2011.
[22]  A. Jain, Y. Gupta, and S. K. Jain, “Perspectives of biodegradable natural polysaccharides for site-specific drug delivery to the colon,” Journal of Pharmacy and Pharmaceutical Sciences, vol. 10, no. 1, pp. 86–128, 2007.
[23]  K. Malik, G. Arora, and I. Singh, “Locust bean gum as superdisintegrant—formulation and evaluation of nimesulide orodispersible tablets,” Polimery w Medycynie, vol. 41, no. 1, pp. 17–28, 2011.
[24]  M. P. Venkatarajua, D. V. Gowdaa, K. S. Rajeshb, and H. G. Shivakumara, “Xanthan and locust bean gum (from Ceratonia siliqua) matrix tablets for oral controlled delivery of propranolol hydrochloride,” Asian Journal of Pharmaceutical Sciences, vol. 2, no. 6, pp. 239–248, 2007.
[25]  J. J. L. Jenita, K. Vijaya, R. Suma, B. Raj, and A. Siddiqca, “Formulation and evaluation of compression coated tablets of mesalazine for colon delivery,” International Journal of PharmTech Research, vol. 2, no. 1, pp. 535–541, 2010.
[26]  G. A. Petropoulos, “Fenugreek: The genus Trigonella,” in Botany, G. A. Petropoulus, Ed., pp. 9–17, Taylor & Francis, London, UK, 2002.
[27]  N. Ali, N. Hossein, K. Afagh, S. Tarifeh, V. Hadi, and J. L. Ford, “An in vitro evaluation of fenugreek mucilage as a potential excipient for oral controlled-release matrix tablet,” Drug Development and Industrial Pharmacy, vol. 34, no. 3, pp. 323–329, 2008.
[28]  J. J. L. Jenita, K. Vijaya, R. Suma, and B. Raj, “Formulation and evaluation of compression coated tablets of mesalazine for colon delivery,” International Journal of PharmTech Research, vol. 2, no. 1, pp. 535–541, 2010.
[29]  G. K. Jani and D. P. Shah, “Assessing Hibiscus rosa-sinensis Linn as an excipient in sustained-release tablets,” Pharmaceutical Technology, vol. 32, no. 1, pp. 62–75, 2008.
[30]  M. üner and T. Altinkurt, “Evaluation of honey locust (Gleditsia triacanthos Linn.) gum as sustaining material in tablet dosage forms,” Il Farmaco, vol. 59, no. 7, pp. 567–573, 2004.
[31]  Final Assessment Report: Application A546 Tara Gum As A Food Additive, Food Standards Australia New Zealand, 2006.
[32]  H. J. Shin, M. H. Ki, B. Yoon, and S. W. An, “Gastricretentive controlied release mono matrix tablet,” Tech. Rep. WO/2006/088305, Chong Kun Dang Pharmaceutical, 2006.
[33]  H. Zeng, A. Moroni, A. R. Baichwal, P. A. Goliber, S. Ketsela, and D. P. Mcnamara, “Controlled- release emulsion compositions,” Tech. Rep., Penwest Pharmaceuticals, 2007.
[34]  S. Sarojini, S. D. Kunam, R. Manavalan, and B. Jayanthi, “Effect of natural gum as a binder in the formulation of diclofenac sodium tablets,” International Journal of Pharmaceutical Sciences and Research, vol. 1, no. 3, pp. 55–60, 2010.
[35]  R. D. N. Lima, J. R. Lima, C. R. de Salis, and R. A. Moreira, “Cashew-tree (Anacardium occidentale L.) exudate gum: a novel bioligand tool,” Biotechnology and Applied Biochemistry, vol. 35, no. 1, pp. 45–53, 2002.
[36]  R. Kumar, M. B. Patil, S. R. Patil, and M. S. Paschapur, “Evaluation of Anacardium occidentale gum as gelling agent in aceclofenac gel,” International Journal of PharmTech Research, vol. 1, no. 3, pp. 695–704, 2009.
[37]  K. Ofori-Kwakye, Y. Asantewaa, and S. L. Kipo, “Physicochemical and binding properties of cashew tree gum in metronidazole tablet formulations,” International Journal of Pharmacy and Pharmaceutical Sciences, vol. 2, no. 4, pp. 105–109, 2010.
[38]  G. N. K. Ganesh, R. Sureshkumar, N. Jawahar, V. Senthil, D. N. Venkatesh, and M. S. Srinivas, “Preparation and evaluation of sustained release matrix tablet of diclofenac sodium using natural polymer,” Journal of Pharmaceutical Sciences and Research, vol. 2, no. 6, pp. 360–368, 2010.
[39]  A. B. Gangurde, S. S. Malode, and R. S. Bhambar, “Preliminary evaluation of neem gum as tablet binder,” Indian Journal of Pharmaceutical Education and Research, vol. 42, no. 4, pp. 344–347, 2008.
[40]  A. H. Abdul, K. C. Suresh, B. A. Kumar et al., “Permeation studies of diclofenac sodium from ficus carica fruit mucilage matrices for transdermal delivery,” International Journal of ChemTech Research, vol. 2, no. 2, pp. 937–941, 2010.
[41]  S. Choi and M.-H. Chung, “A review on the relationship between Aloe vera components and their biologic effects,” Seminars in Integrative Medicine, vol. 1, no. 1, pp. 53–62, 2003.
[42]  H. A. Ahad, C. S. Kumar, A. Kumar B et al., “Development and in vitro evaluation of glibenclamide Aloe barbadensis miller leaves mucilage controlled release matrix tablets,” International Journal of PharmTech Research, vol. 2, no. 2, pp. 1018–1021, 2010.
[43]  D. Panda, S. Swain, R. Gupta, S. Si, and S. K. Kanungo, “Preparation and evaluation of gels from gum of Moringa oleifera,” Indian Journal of Pharmaceutical Sciences, vol. 68, no. 6, pp. 777–780, 2006.
[44]  D. Panda, N. S. K. Choudhury, M. Yedukondalu, S. Si, and R. Gupta, “Evaluation of gum of Moringa oleifera as a binder and release retardant in tablet formulation,” Indian Journal of Pharmaceutical Sciences, vol. 70, no. 5, pp. 614–618, 2008.
[45]  B. V. Patel and D. Patel, “Study of disintegrant property of Moringa Oleifera gum and its comparison with other superdisintegrants,” International Journal of ChemTech Research, vol. 3, no. 3, pp. 1119–1124, 2011.
[46]  D. M. Morkhade, S. V. Fulzele, P. M. Satturwar, and S. B. Joshi, “Gum copal and gum damar: novel matrix forming materials for sustained drug delivery,” Indian Journal of Pharmaceutical Sciences, vol. 68, no. 1, pp. 53–58, 2006.
[47]  D. M. Morkhade and S. B. Joshi, “Evaluation of gum damar as a novel microencapsulating material for ibuprofen and diltiazem hydrochloride,” Indian Journal of Pharmaceutical Sciences, vol. 69, no. 2, pp. 263–268, 2007.
[48]  L. Osete-Cortina and M. T. Domenech-Carbo, “Analytical characterization of diterpenoid resins present in pictorial varnishes using pyrolysis-gas chromatography-mass spectrometry with on line trimethylsilylation,” Journal of Chromatography A, vol. 1065, no. 2, pp. 265–278, 2005.
[49]  M. J. Umekar and P. G. Yeole, “Characterization and evaluation of natural copal gum-resin as film forming material,” International Journal of Green Pharmacy, vol. 2, no. 1, pp. 37–42, 2008.
[50]  K. Venkaiah and J. J. Shah, “Distribution, development and structure of gum ducts in Lannea coromandelica (Houtt.) merril,” Annals of Botany, vol. 54, no. 2, pp. 175–186, 1984.
[51]  B. S. Nayak, U. K. Nayak, K. B. Patro, and P. K. Rout, “Preparation and In Vitro evaluation of lamivudine entrapped MOI microspheres for oral administration,” Research Journal of Pharmacy and Technology, vol. 1, no. 4, pp. 437–441, 2008.
[52]  B. Janaki and R. B. Sashidhar, “Subchronic (90-day) toxicity study in rats fed gum kondagogu (Cochlospermum gossypium),” Food and Chemical Toxicology, vol. 38, no. 6, pp. 523–534, 2000.
[53]  K. V. R. Murthy and G. S. V. Subramanyam, Design and Statistical Optimization of Hupu Gum Based Gastric Floating Drug Delivery Systems of Diltiazem HCl, American Association of Pharmaceutical Scientists, Atlanta, Ga, USA, 2008.
[54]  R. R. Krishna and T. E. G. K. Murthy, “Preparation and evaluation of mucoadhesive microcapsules of glipizide formulated with gum kondagogu: In vitro and in vivo,” Acta Pharmaceutica Sciencia, vol. 52, no. 3, pp. 335–344, 2010.
[55]  N. C. Ngwuluka, B. A. Idiakhoa, E. I. Nep, I. Ogaji, and I. S. Okafor, “Formulation and evaluation of paracetamol tablets manufactured using the dried fruit of Phoenix dactylifera Linn as an excipient,” Research in Pharmaceutical Biotechnology, vol. 2, no. 3, pp. 25–32, 2010.
[56]  P. L. Soni and R. Pal, “Industrial gum from. Cassia tora seeds,” Trends in Carbohydrate Chemistry, vol. 2, pp. 33–44, 1996.
[57]  S. Singh, D. S. B. Bothara, and S. Singh, “Pharmaceutical characterization of Cassia tora of seed mucilage in tablet formulations,” Scholars Research Library, vol. 2, no. 5, pp. 54–61, 2010.
[58]  A. S. Mann, N. K. Jain, and M. D. Kharya, “Evaluation of the suspending properties of Cassia tora mucilage on sulphadimidine suspension,” Asian Journal of Experimental Sciences, vol. 21, no. 1, pp. 63–67, 2007.
[59]  B. S. Nayak, U. K. Nayak, K. B. Patro, and P. K. Rout, “Design and evaluation of controlled release bhara gum microcapsules of famotidine for oral use,” Research Journal of Pharmacy and Technology, vol. 1, no. 4, pp. 433–436, 2008.
[60]  K. Singh, A. Kumar, N. Langyan, and M. Ahuja, “Evaluation of Mimosa pudica seed mucilage as sustained-release excipient,” AAPS PharmSciTech, vol. 10, no. 4, pp. 1121–1127, 2009.
[61]  C. W. Vendruscolo, I. F. Andreazza, J. L. M. S. Ganter, C. Ferrero, and T. M. B. Bresolin, “Xanthan and galactomannan (from M. scabrella) matrix tablets for oral controlled delivery of theophylline,” International Journal of Pharmaceutics, vol. 296, no. 1-2, pp. 1–11, 2005.
[62]  S. N. Kothawade, P. B. Shinde, M. R. Agrawal, P. D. Aragade, and H. V. Kamble, “Preliminary evaluation of Dendropthoe falcata mucilage as tablet binder,” International Journal of PharmTech Research, vol. 2, no. 2, pp. 1474–1476, 2010.
[63]  A. Y. Leung and S. Foster, Encyclopedia of Common Natural Ingredients Used in Food, Drugs and Cosmetics, John Wiley & Sons, New York, NY, USA, 2nd edition, 1996.
[64]  K. M. Rao, K. Gnanaprakash, and A. V. Badarinath, “Preparation and evaluation of flurbiprofen gel; mucilage of Cocculus hirsutus leaf powder as gel base,” International Journal of PharmTech Research, vol. 2, no. 2, pp. 1578–1583, 2010.
[65]  F. K. Peter, M. S. Alistair, and C. C. Shirley, “Molecular structures of gum exudates from Hakea species,” Phytochemistry, vol. 34, no. 3, pp. 709–713, 1993.
[66]  H. H. Alur, S. I. Pather, A. K. Mitra, and T. P. Johnston, “Evaluation of the gum from Hakea gibbosa as a sustained-release and mucoadhesive component in buccal tablets,” Pharmaceutical Development and Technology, vol. 4, no. 3, pp. 347–358, 1999.
[67]  I. S. Okafor, A. Chukwu, and K. Duala, “Somephysicochemical properties of grewia gum,” Nigeria Journal of Polymer Science and Technology, vol. 2, no. 1, pp. 161–167, 2001.
[68]  E. Martins, I. Christiana, and K. Olobayo, “Effect of Grewia gum on the mechanical properties of Paracetamol tablet formulations,” African Journal of Pharmacy and Pharmacology, vol. 2, pp. 1–6, 2008.
[69]  E. I. Nep and B. R. Conway, “Polysaccharide gum matrix tablets for oral controlled delivery of cimetidine,” Journal of Pharmaceutical Sciences and Research, vol. 2, no. 11, pp. 708–716, 2010.
[70]  I. Ogaji and I. S. Okafor, “Potential of Grewia gum as film coating agent: some physicochemical properties of coated praziquantel tablets,” International Journal of Pharmaceutical Research, vol. 3, no. 2, pp. 16–19, 2011.
[71]  A. K. Singh, R. P. Selvam, and T. Sivakumar, “Isolation, characterisation and formulation properties of a new plant gum obtained from Mangifera indica,” International Journal of Pharmaceutical and Biomedical Research, vol. 1, no. 2, pp. 35–41, 2010.
[72]  V. K. Shingala, A. K. Singh, S. K. Yadav, and T. Sivakumar, “Design and characterization of Diclofenac sodium tablets containing Mangifera indica resin as release retardant,” International Journal of PharmTech Research, vol. 2, no. 3, pp. 2107–2111, 2010.
[73]  K. N. Ravi, R. Sachin, and B. Mirtyunjaya, “Evaluation of disintegrating properties of mangifera indica,” RGUHS Journal of Pharmaceutical Scirnces, vol. 1, no. 1, pp. 11–20, 2011.
[74]  Y. I. Muzib and P. S. Kurri, “Formulation and evaluation of gum olibanum-based sustained release matrix tablets of ambroxol hydrochloride,” International Journal of Pharmacy and Pharmaceutical Sciences, vol. 3, no. 2, pp. 195–199, 2011.
[75]  N. L. Prasanthi, S. S. Manikiran, and N. R. Rao, “In vitro drug release studies of ziprasidone from tablets using natural gums from biosphere,” Archives of Applied Science Research, vol. 3, no. 2, pp. 513–519, 2011.
[76]  K. P. R. Chowdary, P. Mohapatra, and M. N. M. Krishna, “Evaluation of olibanum resin as microencapsulating agent for controlled drug delivery,” Rasāyan Journal of Chemistry, vol. 1, no. 1, pp. 99–104, 2008.
[77]  O. A. Bamiro, V. R. Sinha, R. Kumar, and O. A. Odeku, “Characterization and evaluation of Terminalia randii gum as a binder in carvedilol tablet formulation,” Acta Pharmaceutica Sciencia, vol. 52, no. 3, pp. 254–262, 2010.
[78]  S. C. Dinda and B. Mukharjee, “Gum cordia—a new tablet binder and emulsifier,” Acta Pharmaceutica Sciencia, vol. 51, no. 2, pp. 189–198, 2009.
[79]  R. N. Chopra, S. L. Nayar, and I. C. Chopra, Glossary of Indian Medicinal Plants, 1st edition, 1956.
[80]  N. S. Sheth, N. V. Shah, and N. C. Shah, “Extraction of mucilage from Ocimum americanum linn and its role as disintegrant in tablets formulation,” Journal of Global Pharma Technology, vol. 2, no. 12, pp. 26–31, 2010.
[81]  V. Davé and S. P. McCarthy, “Review of konjac glucomannan,” Journal of Environmental Polymer Degradation, vol. 5, no. 4, pp. 237–241, 1997.
[82]  F. Alvarez-Mance?ido, M. Landin, I. Lacik, and R. Martínez-Pacheco, “Konjac glucomannan and konjac glucomannan/xanthan gum mixtures as excipients for controlled drug delivery systems. Diffusion of small drugs,” International Journal of Pharmaceutics, vol. 349, no. 1-2, pp. 11–18, 2008.

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