Design, development and optimization of s (-) Atenolol floating sustained release matrix tablets using surface response methodology
The objective of this present investigation was to develop and formulate floating sustained release matrix tablets of s (-) atenolol, by using different polymer combinations and filler, to optimize by using surface response methodology for different drug release variables and to evaluate the drug re...
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Published in: | Indian journal of pharmaceutical sciences Vol. 77; no. 5; pp. 563 - 572 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
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Medknow Publications
01-09-2015
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Abstract | The objective of this present investigation was to develop and formulate floating sustained release matrix tablets of s (-) atenolol, by using different polymer combinations and filler, to optimize by using surface response methodology for different drug release variables and to evaluate the drug release pattern of the optimized product. Floating sustained release matrix tablets of various combinations were prepared with cellulose-based polymers: Hydroxypropyl methylcellulose, sodium bicarbonate as a gas generating agent, polyvinyl pyrrolidone as a binder and lactose monohydrate as filler. The 32 full factorial design was employed to investigate the effect of formulation variables on different properties of tablets applicable to floating lag time, buoyancy time, % drug release in 1 and 6 h (D1 h,D6 h) and time required to 90% drug release (t90%). Significance of result was analyzed using analysis of non variance and P<0.05 was considered statistically significant. S (-) atenolol floating sustained release matrix tablets followed the Higuchi drug release kinetics that indicates the release of drug follows anomalous (non-Fickian) diffusion mechanism. The developed floating sustained release matrix tablet of improved efficacy can perform therapeutically better than a conventional tablet. |
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AbstractList | The objective of this present investigation was to develop and formulate floating sustained release matrix tablets of s (-) atenolol, by using different polymer combinations and filler, to optimize by using surface response methodology for different drug release variables and to evaluate the drug release pattern of the optimized product. Floating sustained release matrix tablets of various combinations were prepared with cellulose-based polymers: Hydroxypropyl methylcellulose, sodium bicarbonate as a gas generating agent, polyvinyl pyrrolidone as a binder and lactose monohydrate as filler. The 32 full factorial design was employed to investigate the effect of formulation variables on different properties of tablets applicable to floating lag time, buoyancy time, % drug release in 1 and 6 h (D1 h, D6 h ) and time required to 90% drug release (t90% ). Significance of result was analyzed using analysis of non variance and P< 0.05 was considered statistically significant. S (-) atenolol floating sustained release matrix tablets followed the Higuchi drug release kinetics that indicates the release of drug follows anomalous (non-Fickian) diffusion mechanism. The developed floating sustained release matrix tablet of improved efficacy can perform therapeutically better than a conventional tablet. The objective of this present investigation was to develop and formulate floating sustained release matrix tablets of s (-) atenolol, by using different polymer combinations and filler, to optimize by using surface response methodology for different drug release variables and to evaluate the drug release pattern of the optimized product. Floating sustained release matrix tablets of various combinations were prepared with cellulose-based polymers: Hydroxypropyl methylcellulose, sodium bicarbonate as a gas generating agent, polyvinyl pyrrolidone as a binder and lactose monohydrate as filler. The 3(2) full factorial design was employed to investigate the effect of formulation variables on different properties of tablets applicable to floating lag time, buoyancy time, % drug release in 1 and 6 h (D1 h,D6 h) and time required to 90% drug release (t90%). Significance of result was analyzed using analysis of non variance and P < 0.05 was considered statistically significant. S (-) atenolol floating sustained release matrix tablets followed the Higuchi drug release kinetics that indicates the release of drug follows anomalous (non-Fickian) diffusion mechanism. The developed floating sustained release matrix tablet of improved efficacy can perform therapeutically better than a conventional tablet. The objective of this present investigation was to develop and formulate floating sustained release matrix tablets of s (-) atenolol, by using different polymer combinations and filler, to optimize by using surface response methodology for different drug release variables and to evaluate the drug release pattern of the optimized product. Floating sustained release matrix tablets of various combinations were prepared with cellulose-based polymers: Hydroxypropyl methylcellulose, sodium bicarbonate as a gas generating agent, polyvinyl pyrrolidone as a binder and lactose monohydrate as filler. The 3 2 full factorial design was employed to investigate the effect of formulation variables on different properties of tablets applicable to floating lag time, buoyancy time, % drug release in 1 and 6 h (D 1 h, D 6 h ) and time required to 90% drug release (t 90% ). Significance of result was analyzed using analysis of non variance and P < 0.05 was considered statistically significant. S (-) atenolol floating sustained release matrix tablets followed the Higuchi drug release kinetics that indicates the release of drug follows anomalous (non-Fickian) diffusion mechanism. The developed floating sustained release matrix tablet of improved efficacy can perform therapeutically better than a conventional tablet. |
Audience | Academic |
Author | Gharge, V Shah, M Shinde, M Gunjal, P Gurjar, M Pimple, S |
AuthorAffiliation | 1 Emcure Pharmaceutical Ltd, Emcure House, Pune-411 026, India Formulation and Development Department, Zuventus Healthcare Ltd, T-184 MIDC Bhosari, Pune-411 026, India |
AuthorAffiliation_xml | – name: 1 Emcure Pharmaceutical Ltd, Emcure House, Pune-411 026, India – name: Formulation and Development Department, Zuventus Healthcare Ltd, T-184 MIDC Bhosari, Pune-411 026, India |
Author_xml | – sequence: 1 givenname: P surname: Gunjal fullname: Gunjal, P organization: Formulation and Development Department, Zuventus Healthcare Ltd, T-184 MIDC Bhosari, Pune-411 026 – sequence: 2 givenname: M surname: Shinde fullname: Shinde, M organization: Formulation and Development Department, Zuventus Healthcare Ltd, T-184 MIDC Bhosari, Pune-411 026 – sequence: 3 givenname: V surname: Gharge fullname: Gharge, V organization: Emcure Pharmaceutical Ltd, Emcure House, Pune-411 026 – sequence: 4 givenname: S surname: Pimple fullname: Pimple, S organization: Emcure Pharmaceutical Ltd, Emcure House, Pune-411 026 – sequence: 5 givenname: M surname: Gurjar fullname: Gurjar, M organization: Emcure Pharmaceutical Ltd, Emcure House, Pune-411 026 – sequence: 6 givenname: M surname: Shah fullname: Shah, M organization: Emcure Pharmaceutical Ltd, Emcure House, Pune-411 026 |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26798171$$D View this record in MEDLINE/PubMed |
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Copyright | COPYRIGHT 2015 Medknow Publications and Media Pvt. Ltd. Copyright Medknow Publications & Media Pvt Ltd Sep-Oct 2015 Copyright: © Indian Journal of Pharmaceutical Sciences 2015 |
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Keywords | hydrophilic polymers surface response methodology Buoyancy time floating lag time floating sustained release s (-) atenolol |
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SubjectTerms | Atenolol Bioavailability Cellulose Chemical properties Chemical synthesis Conflicts of interest Drug delivery systems Drug dosages Methods Optimization techniques Plasma Production processes Research Paper Tablets (Medicine) Variables |
Title | Design, development and optimization of s (-) Atenolol floating sustained release matrix tablets using surface response methodology |
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