Evaluation of Aceclofenac Loaded Alginate Mucoadhesive Spheres Prepared by Ionic Gelation

DOI:

https://doi.org/10.37285/ijpsn.2012.5.4.4

Authors

  • M. Mohan Varma
  • H.L.N Rao

Abstract



Controlled release aceclofenac spheres were prepared in a cross-linked alginate matrix using ionotropic gelation technique. A suspension of aceclofenac in sodium alginate solution was added drop wise into 10% w/v calcium chloride solution and the resulting spheres were evaluated for their drug content, flow properties, mucoadhesive property and the dissolution rate. The aceclofenac loaded alginate spheres were prepared using various mucoadhesive polymers: sodium alginate, HPMC, sodium CMC, guar gum, methyl cellulose and carbopol. The calcium chloride was used as the crosslinking agent. Fourier transform infrared spectroscopy (FTIR) was used to evaluate the drug-polymer interaction. The alginate spheres showed good rheological properties, drug content uniformity and high entrapment efficiency. The aceclofenac release from the spheres was slow and extended up to 10 hours. The drug loaded spheres exhibited good mucoadhesive property in the in vitro wash off test. The drug release from the optimized formulation (drug-sodium alginate-HPMC K15M; 1:0.9: 0.1 ratio) followed zero order kinetics and exhibited non-Fickian diffusion. The rate of release of aceclofenac decreased with increasing concentration of sodium alginate due to slow penetration of dissolution fluid in the spheres. The results suggest that alginate spheres can potentially deliver aceclofenac at zero-order controlled release following oral administration. The FTIR studies indicated the absence of the drug-polymer interaction in the solid state.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Keywords:

Aceclofenac, Mucoadhesive, Alginate spheres, Controlled release

Downloads

Published

2013-02-28

How to Cite

1.
Varma MM, Rao H. Evaluation of Aceclofenac Loaded Alginate Mucoadhesive Spheres Prepared by Ionic Gelation. Scopus Indexed [Internet]. 2013 Feb. 28 [cited 2024 Dec. 22];5(4):1847-5. Available from: https://ijpsnonline.com/index.php/ijpsn/article/view/593

Issue

Section

Research Articles

References

Almeida FP and Almeida AJ (2004). Cross-linked alginate-gelatinbeads: a new matrix for controlled release of pindolol. J Control Release 97: 431-439.

Arica B, Calis S, Atilla P, Durlu NT, Cakar N, Kas HS and Hincal AA (2005). In vitro and in vivo studies of ibuprofen loaded biodegradable alginate beads. Journal of microencapsulation 22: 153-165.

Bajpai SK and Sharma S (2004). Investigation of swelling/ degradation behavior of alginate beads crosslinked with Ca2+ and Ba2+ ions. React Funct Polym 59: 129-140.

Belgamwar V, Shah V and Surana SJ(2009). Formulation and evaluation of oral mucoadhesive multiparticulate system containing metoprolol tartarate: An In Vitro – Ex Vivo characterization. Current Drug Delivery 6: 113-121.

Bodde HE, De Vries ME and Junginger HE (1990). Mucoadhesive polymers for the buccal delivery of peptides, structure – adhesiveness relationships. J Control Rel 13: 225-231.

Brogden RN and Wiseman LR (1996). Aceclofenac: A review of its pharmacodynamic properties and therapeutic potential in the treatment of rheumatic disorders and in pain management. Drugs 52: 113-124.

Castellanos NRJ, Zia H and Rhodes CT (1993). Mucoadhesive drug delivery systems. Drug Dev Ind Pharm 19: 143-194.

Chowdary KPR and Srinivas L (2000). Mucoadhesive drug delivery systems. Indian Drugs 37: 400-406.

Chowdary KPR and Rao YS (2003). Design and In Vitro and In Vivo evaluation of mucoadhesive microcapsules of glipizide for oral controlled release. AAPS Pharm Sci Tech 4: 39-45.

Das MK and Mourya DP (2008). Evaluation of diltiazem hydrochloride-loaded mucoadhesive microspheres prepared by emulsification-internal gelation technique. Acta Poloniae Pharmaceutica Drug Research 65: 249-259.

Gallardo A, Eguiburu JL, Berridi MJF and Roman JS (1998). Preparation and in vitro release studies of ibuprofen loaded films and microspheres made from graft copolymers of poly(L-lactic acid) on acrylic back bones. J Control Rel 55: 171-179.

Goudanavar PSM, Patil S and Manvi FV (2010). Design and characterisation of sustained release microcapsules of salbutamol sulphate. International Journal of Pharm Tech Research 2: 1144-1149.

Hari PC, Chandy T and Sharma CP (1996). Chitosan/calcium alginate microcapsules for intestinal delivery of nitrofurantoin. J Microencapsulation 13: 319 – 329.

Higuchi T (1963). Mechanism of sustained-action medication. theoretical analysis of rate of release of solid drugs dispersed in solid matrices. J Pharm Sci 51: 1145-1149.

Khazaeli P, Pardakhtya A and Hassanzadeh F (2008). Formulation of ibuprofen beads by ionotropic gelation. Iranian J Pharm Res 7: 163-170.

Kim CK and Lee EJ (1992). The controlled release of blue dextran from alginate beads. Int J Pharm 79: 11-19.

Patel H, Patel JK and Patel RR (2010). Pellets: A general overview. Int J Pharm World Res 1: 1-15.

Patel JK,Patel RP, Amin AF and Patel MM(2005). Formulation and evaluation of mucoadhesive glipizide microspheres. AAPS Pharm Sci Tech 6: E49-E55.

Patil JS, Kamalapur MV and Marapur SC (2010). Ionotropic gelation and polyelectrolyte complexation; the novel techniques to design hydrogel particulate sustained, modulated drug delivery system. Digest J Nanomat Biostru 5: 241-248.

Patil PB, Gawali VU, Patil HN, Hardikar SR and Bhosale AV (2009). Preparation and evaluation of mucoadhesive microspheres of atenolol and propranolol. Int J PharmTech Res 1: 639-643.

Patil SB and Murthy RSR (2006). Mucoadhesive polymers: means of improving drug delivery. Pharma Times 38: 25-28.

Peppas NA (1985). Analysis of fickian and non-fickian drug release from polymers. Pharma Acta Helv 60: 110-111.

Peppas NA and Bury PA (1985). Surface interfacial and molecular aspects of polymer bioadhesion on soft tissues. J Control Rel 12: 257-275.

Ponchel G and Irache J (1998). Specific and non-specific bioadhesive particulate systems for oral delivery to the gastrointestinal tract. Adv Drug Deliv Rev 34: 191-219.

Rao YM, Vani G, Chary R and Bala R (1998). Design and evaulation of mucoadhesive drug delivery systems. Indian Drugs 35: 558–565.

Sarfaraz MD, Hiremath D and Chowdary KPR (2010). Formulation and characterization of rifampicin microcapsules. Indian J Pharm Sci 72: 101–105.

Thorat YS, Modi VS and Dhavale SC (2009). Use of carbomers to design mucoadhesive microspheres for an anti- H. pylori drug, clarithromycin. Int J PharmTech Research 1: 1421-1428.

Varma MM and Vijaya S (2012). Development and evaluation of gastroretentive floating drug delivery system of atenolol. Int J Pharm Chem Sci 1: 867-876.

Vasir JK, Tambwekar K and Garg S (2003). Bioadhesive microspheres as a controlled drug delivery system. Int. J Pharm 255: 13-32.

Wamorkar VV, Varma MM, Kumar BV and Reddy VM (2010). Effect of hydrophilic and hydrophobic polymers and in vitro evaluation of hydrodynamically balanced system of metoclo-pramide HCl. Int J Pharm Sci Nanotech 3: 1129-1135.