Formulation and evaluation of gastroretentive-floating multiparticulate system of lisinopril

Aim and Objective: The main objective of this research was to formulate and evaluate gastroretentive-floating multiparticulate system of lisinopril to prolong the gastric residence time. Materials and Methods: Gastroretentive system of lisinopril was developed by ionotropic-gelation technique using...

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Main Authors: Manasa Moganti, H N Shivakumar
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Indian Journal of Health Sciences and Biomedical Research KLEU
Subjects:
Online Access:http://www.ijournalhs.org/article.asp?issn=2542-6214;year=2017;volume=10;issue=1;spage=50;epage=56;aulast=Moganti
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spelling doaj-cbc08b07889241a695530f527c32a56a2020-11-24T21:42:06ZengWolters Kluwer Medknow PublicationsIndian Journal of Health Sciences and Biomedical Research KLEU2542-62142542-62222017-01-01101505610.4103/2349-5006.198589Formulation and evaluation of gastroretentive-floating multiparticulate system of lisinoprilManasa MogantiH N ShivakumarAim and Objective: The main objective of this research was to formulate and evaluate gastroretentive-floating multiparticulate system of lisinopril to prolong the gastric residence time. Materials and Methods: Gastroretentive system of lisinopril was developed by ionotropic-gelation technique using isabgol (Plantago ovata F.) husk mucilage (IHM) as a floating agent, sodium alginate as a mucoadhesive polymer, and sodium bicarbonate as a gas-generating agent. Results: The beads were evaluated for entrapment efficiency (EE), in vitro drug release, and ex vivo mucoadhesion. The beads of batch F-2 exhibited high-EE (96.04 ± 0.74%), complete drug release (95.27 ± 0.12%), and good mucoadhesion (50% in 8 h). The in vitro drug release from these beads exhibited first-order kinetics that followed Higuchi diffusion model. Conclusion: The beads by virtue of the high EE, complete drug release, and good mucoadhesivity that exhibit prolonged gastric residence time are likely to improve the bioavailability of the drugs having the absorption window in proximal stomach.http://www.ijournalhs.org/article.asp?issn=2542-6214;year=2017;volume=10;issue=1;spage=50;epage=56;aulast=MogantiGastroretentive drug deliverylisinoprilmucoadhesivity
collection DOAJ
language English
format Article
sources DOAJ
author Manasa Moganti
H N Shivakumar
spellingShingle Manasa Moganti
H N Shivakumar
Formulation and evaluation of gastroretentive-floating multiparticulate system of lisinopril
Indian Journal of Health Sciences and Biomedical Research KLEU
Gastroretentive drug delivery
lisinopril
mucoadhesivity
author_facet Manasa Moganti
H N Shivakumar
author_sort Manasa Moganti
title Formulation and evaluation of gastroretentive-floating multiparticulate system of lisinopril
title_short Formulation and evaluation of gastroretentive-floating multiparticulate system of lisinopril
title_full Formulation and evaluation of gastroretentive-floating multiparticulate system of lisinopril
title_fullStr Formulation and evaluation of gastroretentive-floating multiparticulate system of lisinopril
title_full_unstemmed Formulation and evaluation of gastroretentive-floating multiparticulate system of lisinopril
title_sort formulation and evaluation of gastroretentive-floating multiparticulate system of lisinopril
publisher Wolters Kluwer Medknow Publications
series Indian Journal of Health Sciences and Biomedical Research KLEU
issn 2542-6214
2542-6222
publishDate 2017-01-01
description Aim and Objective: The main objective of this research was to formulate and evaluate gastroretentive-floating multiparticulate system of lisinopril to prolong the gastric residence time. Materials and Methods: Gastroretentive system of lisinopril was developed by ionotropic-gelation technique using isabgol (Plantago ovata F.) husk mucilage (IHM) as a floating agent, sodium alginate as a mucoadhesive polymer, and sodium bicarbonate as a gas-generating agent. Results: The beads were evaluated for entrapment efficiency (EE), in vitro drug release, and ex vivo mucoadhesion. The beads of batch F-2 exhibited high-EE (96.04 ± 0.74%), complete drug release (95.27 ± 0.12%), and good mucoadhesion (50% in 8 h). The in vitro drug release from these beads exhibited first-order kinetics that followed Higuchi diffusion model. Conclusion: The beads by virtue of the high EE, complete drug release, and good mucoadhesivity that exhibit prolonged gastric residence time are likely to improve the bioavailability of the drugs having the absorption window in proximal stomach.
topic Gastroretentive drug delivery
lisinopril
mucoadhesivity
url http://www.ijournalhs.org/article.asp?issn=2542-6214;year=2017;volume=10;issue=1;spage=50;epage=56;aulast=Moganti
work_keys_str_mv AT manasamoganti formulationandevaluationofgastroretentivefloatingmultiparticulatesystemoflisinopril
AT hnshivakumar formulationandevaluationofgastroretentivefloatingmultiparticulatesystemoflisinopril
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