Response surface methodology and process optimization of sustained release pellets using Taguchi orthogonal array design and central composite design

Furosemide is a powerful diuretic and antihypertensive drug which has low bioavailability due to hepatic first pass metabolism and has a short half-life of 2 hours. To overcome the above drawback, the present study was carried out to formulate and evaluate sustained release (SR) pellets of furosemid...

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Main Authors: Gurinder Singh (Author), Roopa S Pai (Author), V Kusum Devi (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2012-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Gurinder Singh  |e author 
700 1 0 |a Roopa S Pai  |e author 
700 1 0 |a V Kusum Devi  |e author 
245 0 0 |a Response surface methodology and process optimization of sustained release pellets using Taguchi orthogonal array design and central composite design 
260 |b Wolters Kluwer Medknow Publications,   |c 2012-01-01T00:00:00Z. 
500 |a 2231-4040 
500 |a 0976-2094 
500 |a 10.4103/2231-4040.93565 
520 |a Furosemide is a powerful diuretic and antihypertensive drug which has low bioavailability due to hepatic first pass metabolism and has a short half-life of 2 hours. To overcome the above drawback, the present study was carried out to formulate and evaluate sustained release (SR) pellets of furosemide for oral administration prepared by extrusion/spheronization. Drug Coat L-100 was used within the pellet core along with microcrystalline cellulose as the diluent and concentration of selected binder was optimized to be 1.2%. The formulation was prepared with drug to polymer ratio 1:3. It was optimized using Design of Experiments by employing a 3 2 central composite design that was used to systematically optimize the process parameters combined with response surface methodology. Dissolution studies were carried out with USP apparatus Type I (basket type) in both simulated gastric and intestinal pH. The statistical technique, i.e., the two-tailed paired t test and one-way ANOVA of in vitro data has proposed that there was very significant ( P≤0.05) difference in dissolution profile of furosemide SR pellets when compared with pure drug and commercial product. Validation of the process optimization study indicated an extremely high degree of prognostic ability. The study effectively undertook the development of optimized process parameters of pelletization of furosemide pellets with tremendous SR characteristics. 
546 |a EN 
690 |a Central composite design 
690 |a extrusion/spheronization 
690 |a furosemide 
690 |a statistical analysis 
690 |a Taguchi orthogonal array design 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Journal of Advanced Pharmaceutical Technology & Research, Vol 3, Iss 1, Pp 30-40 (2012) 
787 0 |n http://www.japtr.org/article.asp?issn=2231-4040;year=2012;volume=3;issue=1;spage=30;epage=40;aulast=Singh 
787 0 |n https://doaj.org/toc/2231-4040 
787 0 |n https://doaj.org/toc/0976-2094 
856 4 1 |u https://doaj.org/article/86253389b1c2437ea918ed1df2eec94b  |z Connect to this object online.