pH responsive alginate polymeric rafts for controlled drug release by using box behnken response surface design

Aim of the present work was to develop alginate raft forming tablets for controlled release pantoprazole sodium sesquihydrate (PSS). Box behnken design was used to optimize 15 formulations with three independent and three dependent variables. Physical tests of all formulations were within pharmacopo...

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Main Authors: Ghulam Abbas, Muhammad Hanif, Mahtab Ahmad Khan
Format: Article
Language:English
Published: Taylor & Francis Group 2017-01-01
Series:Designed Monomers and Polymers
Subjects:
DSC
XRD
Online Access:http://dx.doi.org/10.1080/15685551.2016.1231046
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spelling doaj-a2519e9ee495466faf3c8ca922b68c642020-11-24T21:47:05ZengTaylor & Francis GroupDesigned Monomers and Polymers1568-55512017-01-012011910.1080/15685551.2016.12310461231046pH responsive alginate polymeric rafts for controlled drug release by using box behnken response surface designGhulam Abbas0Muhammad Hanif1Mahtab Ahmad Khan2Bahauddin Zakariya UniversityBahauddin Zakariya UniversityBahauddin Zakariya UniversityAim of the present work was to develop alginate raft forming tablets for controlled release pantoprazole sodium sesquihydrate (PSS). Box behnken design was used to optimize 15 formulations with three independent and three dependent variables. Physical tests of all formulations were within pharmacopoeial limits. Raft was characterized by their strength, thickness, resilience, acid neutralizing capacity, floating lag time and total floating time. Raft strength, thickness and resilience of optimized formulation AR9 were 7.43 ± 0.019 g, 5.8 ± 0.245 cm and greater than 480 min, respectively. Buffering and neutralizing capacity were 11.2 ± 1.01 and 6.5 ± 0.56 meq, respectively. Dissolution studies were performed by using simulated gastric fluid pH 1.2 and cumulative percentage release of optimized formulation AR9 was found 98%. First order release kinetics were followed and non-fickian diffusion was observed as value of n was greater than 0.45 in korsmeyer-peppas model. PSS, polymers, tablets and rafts were further characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffractometry (XRD) and differential scanning calorimetry (DSC). FTIR spectra of PSS, polymers and raft of optimized formulation AR9 showed peaks at 3223.09, 1688.17, 1586.67, 1302.64 and 1027.74 cm−1 due to –OH stretching, ester carbonyl group (C=O) stretching, existence of water and carboxylic group in raft, C–N stretching and –OH bending vibration showed no interaction between them. XRD showed diffraction lines indicates crystalline nature of PSS. DSC thermogram showed endothermic peaks at 250 °C for PSS. The developed raft was suitable for controlled release delivery of PSS.http://dx.doi.org/10.1080/15685551.2016.1231046Sodium alginatebox-behnken designraft resiliencein vitro drug releaseFTIRDSCXRD
collection DOAJ
language English
format Article
sources DOAJ
author Ghulam Abbas
Muhammad Hanif
Mahtab Ahmad Khan
spellingShingle Ghulam Abbas
Muhammad Hanif
Mahtab Ahmad Khan
pH responsive alginate polymeric rafts for controlled drug release by using box behnken response surface design
Designed Monomers and Polymers
Sodium alginate
box-behnken design
raft resilience
in vitro drug release
FTIR
DSC
XRD
author_facet Ghulam Abbas
Muhammad Hanif
Mahtab Ahmad Khan
author_sort Ghulam Abbas
title pH responsive alginate polymeric rafts for controlled drug release by using box behnken response surface design
title_short pH responsive alginate polymeric rafts for controlled drug release by using box behnken response surface design
title_full pH responsive alginate polymeric rafts for controlled drug release by using box behnken response surface design
title_fullStr pH responsive alginate polymeric rafts for controlled drug release by using box behnken response surface design
title_full_unstemmed pH responsive alginate polymeric rafts for controlled drug release by using box behnken response surface design
title_sort ph responsive alginate polymeric rafts for controlled drug release by using box behnken response surface design
publisher Taylor & Francis Group
series Designed Monomers and Polymers
issn 1568-5551
publishDate 2017-01-01
description Aim of the present work was to develop alginate raft forming tablets for controlled release pantoprazole sodium sesquihydrate (PSS). Box behnken design was used to optimize 15 formulations with three independent and three dependent variables. Physical tests of all formulations were within pharmacopoeial limits. Raft was characterized by their strength, thickness, resilience, acid neutralizing capacity, floating lag time and total floating time. Raft strength, thickness and resilience of optimized formulation AR9 were 7.43 ± 0.019 g, 5.8 ± 0.245 cm and greater than 480 min, respectively. Buffering and neutralizing capacity were 11.2 ± 1.01 and 6.5 ± 0.56 meq, respectively. Dissolution studies were performed by using simulated gastric fluid pH 1.2 and cumulative percentage release of optimized formulation AR9 was found 98%. First order release kinetics were followed and non-fickian diffusion was observed as value of n was greater than 0.45 in korsmeyer-peppas model. PSS, polymers, tablets and rafts were further characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffractometry (XRD) and differential scanning calorimetry (DSC). FTIR spectra of PSS, polymers and raft of optimized formulation AR9 showed peaks at 3223.09, 1688.17, 1586.67, 1302.64 and 1027.74 cm−1 due to –OH stretching, ester carbonyl group (C=O) stretching, existence of water and carboxylic group in raft, C–N stretching and –OH bending vibration showed no interaction between them. XRD showed diffraction lines indicates crystalline nature of PSS. DSC thermogram showed endothermic peaks at 250 °C for PSS. The developed raft was suitable for controlled release delivery of PSS.
topic Sodium alginate
box-behnken design
raft resilience
in vitro drug release
FTIR
DSC
XRD
url http://dx.doi.org/10.1080/15685551.2016.1231046
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