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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Online Access: | http://dx.doi.org/10.1080/15685551.2016.1231046 |
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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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