Development and evaluation of diltiazem hydrochloride controlled-release pellets by fluid bed coating process

The aim of the present study was to develop controlled-release pellets of diltiazem HCl with ethyl cellulose and hydroxylpropyl methylcellulose phthalate as the release rate retarding polymers by fluid bed coating technique. The prepared pellets were evaluated for drug content, particle size, subjec...

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গ্রন্থ-পঞ্জীর বিবরন
প্রধান লেখক: Mikkilineni Bhanu Prasad (Author), Suryadevara Vidyadhara (Author), Reddyvalam Lankapalli C Sasidhar (Author), Talamanchi Balakrishna (Author), Pavuluri Trilochani (Author)
বিন্যাস: গ্রন্থ
প্রকাশিত: Wolters Kluwer Medknow Publications, 2013-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Mikkilineni Bhanu Prasad  |e author 
700 1 0 |a Suryadevara Vidyadhara  |e author 
700 1 0 |a Reddyvalam Lankapalli C Sasidhar  |e author 
700 1 0 |a Talamanchi Balakrishna  |e author 
700 1 0 |a Pavuluri Trilochani  |e author 
245 0 0 |a Development and evaluation of diltiazem hydrochloride controlled-release pellets by fluid bed coating process 
260 |b Wolters Kluwer Medknow Publications,   |c 2013-01-01T00:00:00Z. 
500 |a 2231-4040 
500 |a 0976-2094 
500 |a 10.4103/2231-4040.111526 
520 |a The aim of the present study was to develop controlled-release pellets of diltiazem HCl with ethyl cellulose and hydroxylpropyl methylcellulose phthalate as the release rate retarding polymers by fluid bed coating technique. The prepared pellets were evaluated for drug content, particle size, subjected to Scanning Electron Microscopy (SEM) and Differential Scanning Calori metry (DSC), and evaluated for in vitro release. Stability studies were carried out on the optimized formulations for a period of 3 months. The drug content was in the range of 97%-101%. The mean particle size of the drug-loaded pellets was in the range 700-785 μm. The drug release rate decreased as the concentration of ethyl cellulose increased in the pellet formulations. Among the prepared formulations, FDL10 and FDL11 showed 80% drug release in 16 h, matching with USP dissolution test 6 for diltiazem HCl extended-release capsules. SEM photographs confirmed that the prepared formulations were spherical in nature with a smooth surface. The compatibility between drug and polymers in the drug-loaded pellets was confirmed by DSC studies. Stability studies indicated that the pellets were stable. 
546 |a EN 
690 |a Controlled release 
690 |a diltiazem HCl 
690 |a fluid bed coating 
690 |a multiparticulate dosage forms 
690 |a sustained release 
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 4, Iss 2, Pp 101-107 (2013) 
787 0 |n http://www.japtr.org/article.asp?issn=2231-4040;year=2013;volume=4;issue=2;spage=101;epage=107;aulast=Prasad 
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/9aa1a8d82df34bb2a56503bc81d5c6c4  |z Connect to this object online.