Design and evaluation of cedrela gum based microparticles of theophilline.
Keywords:
Cedrela gum, Drug release, Microparticles, Spray drying, TheophyllineAbstract
Aim: The purpose of this study was to develop microparticles of theophylline employing Cedrela gum, a novel natural gums, as a polymer by spray drying method.
Materials and Methods: The process parameters were different spray drying temperatures of 110º, 130º and 150ºC. The microparticles were evaluated for characteristics like particle size, incorporation efficiency, thermal analysis, X-ray diffraction (XRD) analysis and in vitro drug release.
Results: The microparticles were spherical with distorted surface morphology. The particle size ranged from 35.6 to 58.0 μm depending on the spray drying temperature. Differential scanning calorimetry (DSC) studies revealed that theophiline was molecularly dispersed at all operating temperatures. The release of drug from the microparticles was immediate with no lag time with complete release obtained from the microparticles prepared at the highest temperature.
Conclusion: Cedrela gum could serve as a carrier for solid dispersion of drugs such as Theophilline by means of spray drying at a temperature as low as 110ºC. Microspheres obtained at this temperature were smaller, more free flowing and less susceptible to agglomeration.
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References
Morkhade DM, Joshi SB. Evaluation of gum damar as a novel
microencapsulating material for Ibuprofen and Diltiazem Hydrochloride. Indian J of Pharm Sci. 2007;263-7.
Tuncay M, Calis S, Kas HS, Ercan MT, Peksoy I, Hincal AA. In vitro and in vivo evaluation of diclofenac sodium loaded albumin microspheres. J Microencapsul. 2000;17-(2):145-55.
Jiao YY, Ubrich N, Hoffart V, Marchandarvier M, Vigneron C, Hoffman M, et al. Preparation and characterization of heparin-loaded polymeric microparticles. Drug Dev Ind Pharm. 2002;28:1033-41.
Chowdary KRP, Ratna V. Preparation and evaluation of cellulose acetate microcapsules of theophylline. Indian J Pharm Sci. 1990;52(6):279-81.
Narisawa S, Yoshino H, Hirakawa Y, Noda K. An organic acid-induced sigmoidal release system for oral controlled-release
preparations. Pharm Res. 1994;11:111-6.
Bharadwaj TR, Kanwar M, Lal R, Gupta A. Natural gums and modified natural gums as sustained-release carriers. Drug Dev Ind
Pharm. 2000;10:1025-38.
Satturwar PM, Fulzele SV, Dorle AK. Evaluation of polymerized rosin for the formulation and development of transdermal drug delivery system: a technical Note. AAPS Pharm Sci Tech. 2004;6(4):649-54.
Odeniyi MA, Jaiyeoba KT. Optimization of ascorbic acid tablet formulations containing hydrophilic polymers. Farmacia. 2009;57:(2):157-66.
Council of Europe. European Pharmacopoeia. Strasbourg: Council of Europe, 2001.
Khan IU, Rhaja NM, Mehmood HQ. Development of ethylcellulose-polyethylene glycol and ethylcellulose-polyvinyl pyrolidone blend oral microspheres of Ibuprofen. J Drug Del Sci Tech. 2010;20:(6):439-44.
Fu-De C, Ming-Shi Y, Ben-Gang Y, Yu-Ling F, Liang W, Peng Y, et al. Preparation of sustained-release nitrendipine microspheres
with eudragit RS and aerosol using quasiemulsion solvent diffusion method. Int J Pharm. 2003;259:103-13.
Mahajan HS, Gattani SG. Gellan gum based microparticles of metoclopromide for intranasal delivery: development and evaluation. Chem Pharm Bull. 2009;57:(4):388-92.
Viswanathan NB, Thomas PA, Pandit JK, Kulkarni MG, Mashelkar RA. Morphological changes in degrading PLGA and P(DL)LA
microspheres: implications for the design of controlled release systems. J Control Release. 1999;58:9-20
Giunchedi P, Gavini E, Bonacucina G, Palmieri GF. Tabletted polylactide microspheres prepared by a w/o emulsion-spray drying method. J Microencapsul. 2000;17:711-20.
Pavenetto F, Genta I, Giunchedi P, Conti B, Conte U. Spray dried albumin microspheres for the intra-articular delivery of dexamethasone. J Microencapsul. 1994;11:445-54.
Park K, Robinson JR. Bioadhesive polymers as platforms for oral controlled drug delivery: method to study bioadhesion. Int J Pharm. 1984;19:107–27.
Wee S, Gombotz WR. Protein release from alginate matrices. Adv Drug Deliv Rev. 1998; 31:(3):267-85.
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