In Vitro and In Vivo Evaluation of Oral Controlled Release Formulation of BCS Class I Drug Using Polymer Matrix System

Diltiazem hydrochloride is a calcium channel blocker, which belongs to the family of benzothiazepines. It is commonly used to treat hypertension and atrial fibrillation. Even though the drug has high solubility, its high permeability and rapid metabolism in the liver can limit the bioavailability an...

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Main Authors: Mosab Arafat (Author), Muhammad Sarfraz (Author), Mohammad F. Bostanudin (Author), Anna Esmaeil (Author), Aisha Salam (Author), Salahdein AbuRuz (Author)
Format: Book
Published: MDPI AG, 2021-09-01T00:00:00Z.
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001 doaj_3fa1dba514734e39b69f1c6b4425a594
042 |a dc 
100 1 0 |a Mosab Arafat  |e author 
700 1 0 |a Muhammad Sarfraz  |e author 
700 1 0 |a Mohammad F. Bostanudin  |e author 
700 1 0 |a Anna Esmaeil  |e author 
700 1 0 |a Aisha Salam  |e author 
700 1 0 |a Salahdein AbuRuz  |e author 
245 0 0 |a In Vitro and In Vivo Evaluation of Oral Controlled Release Formulation of BCS Class I Drug Using Polymer Matrix System 
260 |b MDPI AG,   |c 2021-09-01T00:00:00Z. 
500 |a 10.3390/ph14090929 
500 |a 1424-8247 
520 |a Diltiazem hydrochloride is a calcium channel blocker, which belongs to the family of benzothiazepines. It is commonly used to treat hypertension and atrial fibrillation. Even though the drug has high solubility, its high permeability and rapid metabolism in the liver can limit the bioavailability and increase the dose frequencies for up to four times per day. This study focused on a polymer matrix system not only to control the drug release but also to prolong the duration of bioavailability. The polymer matrices were prepared using different ratios of poloxamer-188, hydroxypropyl methylcellulose, and stearyl alcohol. In vitro and in vivo assessments took place using 24 rabbits and the results were compared to commercially available product Tildiem<sup>®</sup> (60 mg tablet) as reference. Overall, the rate of drug release was sustained with the gradual increase of poloxamer-188 incorporated with hydroxypropyl methylcellulose and stearyl alcohol in the matrix system, achieving a maximum release period of 10 h. The oral bioavailability and pharmacokinetic parameters of diltiazem hydrochloride incorporated in polymer matrix system were similar to commercial reference Tildiem<sup>®</sup>. In conclusion, the combination of polymers can have a substantial effect on controlling and prolonging the drug release pattern. The outcomes showed that poloxamer-188 combined with hydroxypropyl methylcellulose and stearyl alcohol is a powerful matrix system for controlling release of diltiazem hydrochloride. 
546 |a EN 
690 |a diltiazem hydrochloride 
690 |a poloxamer-188 
690 |a matrix system 
690 |a polymer 
690 |a controlled release 
690 |a Medicine 
690 |a R 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceuticals, Vol 14, Iss 9, p 929 (2021) 
787 0 |n https://www.mdpi.com/1424-8247/14/9/929 
787 0 |n https://doaj.org/toc/1424-8247 
856 4 1 |u https://doaj.org/article/3fa1dba514734e39b69f1c6b4425a594  |z Connect to this object online.