Development of tablets containing semipurified extract of guaraná (Paullinia cupana)

This study evaluated the technological feasibility of producing a semipurified extract of guaraná (Paullinia cupana Kunth, Sapindaceae) in tablet form, using a direct-compression process. Maltodextrin and gum arabic were used to produce the extract microparticles, in order to protect the microparticles against such factors as temperature, oxidation, and humidity. Using pharmacopoeial methodologies, technological and physicochemistry tests (determination of residual moisture, of bulk and tapped density, Hausner ratio, compressibility and compactibility index, appearance, mean weight, hardness, friability, disintegration time, determination of EPA amount in tablets and in vitro release profile) were conducted. The formulation containing 200 mg of microparticles, 170 mg microcrystalline cellulose, and 10 mg lactose gave the best results in terms of hardness (116 N), friabilility (0.28%), mean weight (0.3821 g), and disintegration time (25 min) for a tablet designed for oral administration. The results met pharmacopoeial specifications, and the tablets are suitable for oral administration.

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Main Authors: Klein,Traudi, Longhini,Renata, Bruschi,Marcos Luciano, Mello,João Carlos Palazzo de
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Farmacognosia 2013
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2013000100026
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spelling oai:scielo:S0102-695X20130001000262013-03-28Development of tablets containing semipurified extract of guaraná (Paullinia cupana)Klein,TraudiLonghini,RenataBruschi,Marcos LucianoMello,João Carlos Palazzo de guaraná lactose microcrystalline cellulose microparticles Paullinia cupana tablets This study evaluated the technological feasibility of producing a semipurified extract of guaraná (Paullinia cupana Kunth, Sapindaceae) in tablet form, using a direct-compression process. Maltodextrin and gum arabic were used to produce the extract microparticles, in order to protect the microparticles against such factors as temperature, oxidation, and humidity. Using pharmacopoeial methodologies, technological and physicochemistry tests (determination of residual moisture, of bulk and tapped density, Hausner ratio, compressibility and compactibility index, appearance, mean weight, hardness, friability, disintegration time, determination of EPA amount in tablets and in vitro release profile) were conducted. The formulation containing 200 mg of microparticles, 170 mg microcrystalline cellulose, and 10 mg lactose gave the best results in terms of hardness (116 N), friabilility (0.28%), mean weight (0.3821 g), and disintegration time (25 min) for a tablet designed for oral administration. The results met pharmacopoeial specifications, and the tablets are suitable for oral administration.info:eu-repo/semantics/openAccessSociedade Brasileira de FarmacognosiaRevista Brasileira de Farmacognosia v.23 n.1 20132013-02-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2013000100026en10.1590/S0102-695X2012005000147
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country Brasil
countrycode BR
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databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Klein,Traudi
Longhini,Renata
Bruschi,Marcos Luciano
Mello,João Carlos Palazzo de
spellingShingle Klein,Traudi
Longhini,Renata
Bruschi,Marcos Luciano
Mello,João Carlos Palazzo de
Development of tablets containing semipurified extract of guaraná (Paullinia cupana)
author_facet Klein,Traudi
Longhini,Renata
Bruschi,Marcos Luciano
Mello,João Carlos Palazzo de
author_sort Klein,Traudi
title Development of tablets containing semipurified extract of guaraná (Paullinia cupana)
title_short Development of tablets containing semipurified extract of guaraná (Paullinia cupana)
title_full Development of tablets containing semipurified extract of guaraná (Paullinia cupana)
title_fullStr Development of tablets containing semipurified extract of guaraná (Paullinia cupana)
title_full_unstemmed Development of tablets containing semipurified extract of guaraná (Paullinia cupana)
title_sort development of tablets containing semipurified extract of guaraná (paullinia cupana)
description This study evaluated the technological feasibility of producing a semipurified extract of guaraná (Paullinia cupana Kunth, Sapindaceae) in tablet form, using a direct-compression process. Maltodextrin and gum arabic were used to produce the extract microparticles, in order to protect the microparticles against such factors as temperature, oxidation, and humidity. Using pharmacopoeial methodologies, technological and physicochemistry tests (determination of residual moisture, of bulk and tapped density, Hausner ratio, compressibility and compactibility index, appearance, mean weight, hardness, friability, disintegration time, determination of EPA amount in tablets and in vitro release profile) were conducted. The formulation containing 200 mg of microparticles, 170 mg microcrystalline cellulose, and 10 mg lactose gave the best results in terms of hardness (116 N), friabilility (0.28%), mean weight (0.3821 g), and disintegration time (25 min) for a tablet designed for oral administration. The results met pharmacopoeial specifications, and the tablets are suitable for oral administration.
publisher Sociedade Brasileira de Farmacognosia
publishDate 2013
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2013000100026
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