#TITLE_ALTERNATIVE#

Currently, solid dosage forms containing dry extract as active compounds are limited to capsules and conventional tablets. As an alternative product and novel innovation, herbal drugs can be developed into another more practical and efficient solid dasage form, such as effervescent. The purpose of t...

Full description

Saved in:
Bibliographic Details
Main Author: PRATIWI PUJI LESTARI (NIM 10704024); Pembimbing: Dr. Sukmadjaja Asyarie dan Dr. Heni Rachmawat, ENDAH
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/13429
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:13429
spelling id-itb.:134292012-11-12T19:11:25Z#TITLE_ALTERNATIVE# PRATIWI PUJI LESTARI (NIM 10704024); Pembimbing: Dr. Sukmadjaja Asyarie dan Dr. Heni Rachmawat, ENDAH Indonesia Final Project INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/13429 Currently, solid dosage forms containing dry extract as active compounds are limited to capsules and conventional tablets. As an alternative product and novel innovation, herbal drugs can be developed into another more practical and efficient solid dasage form, such as effervescent. The purpose of this research is to develope effervescent dosage form at ambient condition. Effervescent dosage form can be developed as effervescent pellet which contains green tea extract. Effervescent pellet were formulated using combination of tablets diluents (manitol), optimization of acid (tartaric acid), and bases composition (sodium bicarbonate and sodium carbonate), PVP concentration, in each acid and base pellet. Pellets were prepared by extrusion-spheronization method. The characterization of effervescent pellet, i.e.: taste, disintegration time, cloudiness, degree of foaming, and pH. To study whether the process influence antioxidant activity of green tea extract in the formula, we measured antioxidant activity by DPPH (2,2-diphenyl-1-picryl hydrazyl) method. Formula met effervescent dosage form criteria was composed by 32% tartaric acid, sodium bicarbonate-sodium carbonate combination (14 : 13), and 4% PVP. The antioxidant potency (EC50) of green tea extract in effervescent pellet decreased compared to unformulated extract, i.e. 122.87 ug/ml vs 44.37 ug/ml. Effervescent pellet containing extract can be developed without controlling room humidity and temperature. Formulation of extract into pellet decreased antioxidant activity of the extract. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
description Currently, solid dosage forms containing dry extract as active compounds are limited to capsules and conventional tablets. As an alternative product and novel innovation, herbal drugs can be developed into another more practical and efficient solid dasage form, such as effervescent. The purpose of this research is to develope effervescent dosage form at ambient condition. Effervescent dosage form can be developed as effervescent pellet which contains green tea extract. Effervescent pellet were formulated using combination of tablets diluents (manitol), optimization of acid (tartaric acid), and bases composition (sodium bicarbonate and sodium carbonate), PVP concentration, in each acid and base pellet. Pellets were prepared by extrusion-spheronization method. The characterization of effervescent pellet, i.e.: taste, disintegration time, cloudiness, degree of foaming, and pH. To study whether the process influence antioxidant activity of green tea extract in the formula, we measured antioxidant activity by DPPH (2,2-diphenyl-1-picryl hydrazyl) method. Formula met effervescent dosage form criteria was composed by 32% tartaric acid, sodium bicarbonate-sodium carbonate combination (14 : 13), and 4% PVP. The antioxidant potency (EC50) of green tea extract in effervescent pellet decreased compared to unformulated extract, i.e. 122.87 ug/ml vs 44.37 ug/ml. Effervescent pellet containing extract can be developed without controlling room humidity and temperature. Formulation of extract into pellet decreased antioxidant activity of the extract.
format Final Project
author PRATIWI PUJI LESTARI (NIM 10704024); Pembimbing: Dr. Sukmadjaja Asyarie dan Dr. Heni Rachmawat, ENDAH
spellingShingle PRATIWI PUJI LESTARI (NIM 10704024); Pembimbing: Dr. Sukmadjaja Asyarie dan Dr. Heni Rachmawat, ENDAH
#TITLE_ALTERNATIVE#
author_facet PRATIWI PUJI LESTARI (NIM 10704024); Pembimbing: Dr. Sukmadjaja Asyarie dan Dr. Heni Rachmawat, ENDAH
author_sort PRATIWI PUJI LESTARI (NIM 10704024); Pembimbing: Dr. Sukmadjaja Asyarie dan Dr. Heni Rachmawat, ENDAH
title #TITLE_ALTERNATIVE#
title_short #TITLE_ALTERNATIVE#
title_full #TITLE_ALTERNATIVE#
title_fullStr #TITLE_ALTERNATIVE#
title_full_unstemmed #TITLE_ALTERNATIVE#
title_sort #title_alternative#
url https://digilib.itb.ac.id/gdl/view/13429
_version_ 1820736184561696768