MIKROENKAPSULASI PELET PROBIOTIK DENGAN METODE SUSPENSI UDARA MENGGUNAKAN FLUIDIZED BED DRYER (FBD)

Lactobacillus acidophilus were completely inactive when exposed to gastric acid condition at pH 1.2. Microencapsulation of the bacterial cells by air suspension method using Fluidized Bed Dryer (FBD) was proposed to develop technology of powder production of probiotics which can increase the surviva...

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Main Author: ADLIA , AMIRAH
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/9901
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:9901
spelling id-itb.:99012009-04-16T15:44:42ZMIKROENKAPSULASI PELET PROBIOTIK DENGAN METODE SUSPENSI UDARA MENGGUNAKAN FLUIDIZED BED DRYER (FBD) ADLIA , AMIRAH Indonesia Final Project INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/9901 Lactobacillus acidophilus were completely inactive when exposed to gastric acid condition at pH 1.2. Microencapsulation of the bacterial cells by air suspension method using Fluidized Bed Dryer (FBD) was proposed to develop technology of powder production of probiotics which can increase the survivability of probiotics in gastrointestinal system. Cells suspension was dispersed in Avicel pH 101 followed by extrusion-spheronization at ambient temperature to create pellet as a matrix that protects the probiotic in the subsequent coating using FBD at 37oC, 2-3 atm air pressure. Cell-encapsulated pellets with 280-500 3m size were film coated using sodium alginate solution-internally crosslinked with CaCl2 at various ratios. Gastric resistant permeability of the coating film was tested by using riboflavine 5'-phosphate sodium as a model. The concentration of riboflavine leached out from riboflavine microcapsules upon exposure to artificial gastric fluid was measured by spectrophotometer UV 267 nm. Encapsulated L. acidophilus were incubated in MRS Broth pH 1.2 at 37oC and sampled every 60 minutes to analyze the viability of L. acidophilus in gastric acid condition. Viable bacterial cells were enumerated by Total Plate Count technique. The optimum formula resulted in good characteristic of probiotic microcapsule was using 1.5% (w/v) sodium alginate and 1.7% (w/v) CaCl2 in HCl pH 3 where cell's population reducted only 1 log. The microencapsulation was effectively preserved probiotic cell viability at 90% of cell's population as compared to non-encapsulated cells and therefore potential for delivering the viable cells to intestine. 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 Lactobacillus acidophilus were completely inactive when exposed to gastric acid condition at pH 1.2. Microencapsulation of the bacterial cells by air suspension method using Fluidized Bed Dryer (FBD) was proposed to develop technology of powder production of probiotics which can increase the survivability of probiotics in gastrointestinal system. Cells suspension was dispersed in Avicel pH 101 followed by extrusion-spheronization at ambient temperature to create pellet as a matrix that protects the probiotic in the subsequent coating using FBD at 37oC, 2-3 atm air pressure. Cell-encapsulated pellets with 280-500 3m size were film coated using sodium alginate solution-internally crosslinked with CaCl2 at various ratios. Gastric resistant permeability of the coating film was tested by using riboflavine 5'-phosphate sodium as a model. The concentration of riboflavine leached out from riboflavine microcapsules upon exposure to artificial gastric fluid was measured by spectrophotometer UV 267 nm. Encapsulated L. acidophilus were incubated in MRS Broth pH 1.2 at 37oC and sampled every 60 minutes to analyze the viability of L. acidophilus in gastric acid condition. Viable bacterial cells were enumerated by Total Plate Count technique. The optimum formula resulted in good characteristic of probiotic microcapsule was using 1.5% (w/v) sodium alginate and 1.7% (w/v) CaCl2 in HCl pH 3 where cell's population reducted only 1 log. The microencapsulation was effectively preserved probiotic cell viability at 90% of cell's population as compared to non-encapsulated cells and therefore potential for delivering the viable cells to intestine.
format Final Project
author ADLIA , AMIRAH
spellingShingle ADLIA , AMIRAH
MIKROENKAPSULASI PELET PROBIOTIK DENGAN METODE SUSPENSI UDARA MENGGUNAKAN FLUIDIZED BED DRYER (FBD)
author_facet ADLIA , AMIRAH
author_sort ADLIA , AMIRAH
title MIKROENKAPSULASI PELET PROBIOTIK DENGAN METODE SUSPENSI UDARA MENGGUNAKAN FLUIDIZED BED DRYER (FBD)
title_short MIKROENKAPSULASI PELET PROBIOTIK DENGAN METODE SUSPENSI UDARA MENGGUNAKAN FLUIDIZED BED DRYER (FBD)
title_full MIKROENKAPSULASI PELET PROBIOTIK DENGAN METODE SUSPENSI UDARA MENGGUNAKAN FLUIDIZED BED DRYER (FBD)
title_fullStr MIKROENKAPSULASI PELET PROBIOTIK DENGAN METODE SUSPENSI UDARA MENGGUNAKAN FLUIDIZED BED DRYER (FBD)
title_full_unstemmed MIKROENKAPSULASI PELET PROBIOTIK DENGAN METODE SUSPENSI UDARA MENGGUNAKAN FLUIDIZED BED DRYER (FBD)
title_sort mikroenkapsulasi pelet probiotik dengan metode suspensi udara menggunakan fluidized bed dryer (fbd)
url https://digilib.itb.ac.id/gdl/view/9901
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