PENGEMBANGAN FORMULA LIPOSOM KERING OVALBUMIN MENGGUNAKAN LIOPROTEKTAN MALTODEKSTRIN DAN MATRIKS HPMC 15000

Background: The present study aims to design formulation of ovalbumincontaining liposomes that are well-preserved during freeze-drying. The combination of Hydroxy Propyl Methyl Cellulose (HPMC) as matrix and lyoprotectants maltodextrin. The obtained dry products were investigated in terms of the...

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Main Author: RADITYA WEKA NUGRAHENI, 051514153014
Format: Theses and Dissertations NonPeerReviewed
Language:English
English
Published: 2018
Subjects:
Online Access:http://repository.unair.ac.id/70268/1/abstrak.pdf
http://repository.unair.ac.id/70268/2/full%20text.pdf
http://repository.unair.ac.id/70268/
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Institution: Universitas Airlangga
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spelling id-langga.702682018-02-28T22:39:31Z http://repository.unair.ac.id/70268/ PENGEMBANGAN FORMULA LIPOSOM KERING OVALBUMIN MENGGUNAKAN LIOPROTEKTAN MALTODEKSTRIN DAN MATRIKS HPMC 15000 RADITYA WEKA NUGRAHENI, 051514153014 RS Pharmacy and materia medica Background: The present study aims to design formulation of ovalbumincontaining liposomes that are well-preserved during freeze-drying. The combination of Hydroxy Propyl Methyl Cellulose (HPMC) as matrix and lyoprotectants maltodextrin. The obtained dry products were investigated in terms of their physical characteristics and ovalbumin integrity. Methods: Liposomes were prepared using thin film method and hydrated with the lyoprotectant solution. The formed liposomes were mixed with HPMC gel and freeze-dried. The obtained solid products were characterized using Differential Scanning Calorimetry (DSC), X-Ray Diffraction (XRD), and Scanning Electron Microscopy (SEM). Ovalbumin integrity was quantified using Bradford Assay. Results: The DSC thermograms of formulations with maltodextrin were relatively homogenous, yet exhibiting meta-stable properties. These results were confirmed by XRD data, in which formulations with maltodextrin showed no intensive peaks, indicating amorphous solid. The SEM images show the morphology of spherical liposomes trapped in the matrices. The SEM images also corresponded to the DSC and XRD data. The SEM data were supported by the TEM data in which showed spherical liposome after re-hydration. Ovalbumin was proved to be well preserved during freeze-drying using this systems since the highest recovery was FM1 with (99.89+5.1)%, while the lowest was FM2 (80.25+4.4)% . Maltodextrin concentration played important role in determining ovalbumin recovery (p=0,343). The higher maltodextrin concentration the lower ovalbumin recovery. Conclusion: The developed liposomes formulation using combination of HPMC matrix and maltodextrin showed potential in preserving liposomes structure and ovalbumin integrity 2018-03-01 Thesis NonPeerReviewed text en http://repository.unair.ac.id/70268/1/abstrak.pdf text en http://repository.unair.ac.id/70268/2/full%20text.pdf RADITYA WEKA NUGRAHENI, 051514153014 (2018) PENGEMBANGAN FORMULA LIPOSOM KERING OVALBUMIN MENGGUNAKAN LIOPROTEKTAN MALTODEKSTRIN DAN MATRIKS HPMC 15000. Thesis thesis, Universitas Airlangga.
institution Universitas Airlangga
building Universitas Airlangga Library
country Indonesia
collection UNAIR Repository
language English
English
topic RS Pharmacy and materia medica
spellingShingle RS Pharmacy and materia medica
RADITYA WEKA NUGRAHENI, 051514153014
PENGEMBANGAN FORMULA LIPOSOM KERING OVALBUMIN MENGGUNAKAN LIOPROTEKTAN MALTODEKSTRIN DAN MATRIKS HPMC 15000
description Background: The present study aims to design formulation of ovalbumincontaining liposomes that are well-preserved during freeze-drying. The combination of Hydroxy Propyl Methyl Cellulose (HPMC) as matrix and lyoprotectants maltodextrin. The obtained dry products were investigated in terms of their physical characteristics and ovalbumin integrity. Methods: Liposomes were prepared using thin film method and hydrated with the lyoprotectant solution. The formed liposomes were mixed with HPMC gel and freeze-dried. The obtained solid products were characterized using Differential Scanning Calorimetry (DSC), X-Ray Diffraction (XRD), and Scanning Electron Microscopy (SEM). Ovalbumin integrity was quantified using Bradford Assay. Results: The DSC thermograms of formulations with maltodextrin were relatively homogenous, yet exhibiting meta-stable properties. These results were confirmed by XRD data, in which formulations with maltodextrin showed no intensive peaks, indicating amorphous solid. The SEM images show the morphology of spherical liposomes trapped in the matrices. The SEM images also corresponded to the DSC and XRD data. The SEM data were supported by the TEM data in which showed spherical liposome after re-hydration. Ovalbumin was proved to be well preserved during freeze-drying using this systems since the highest recovery was FM1 with (99.89+5.1)%, while the lowest was FM2 (80.25+4.4)% . Maltodextrin concentration played important role in determining ovalbumin recovery (p=0,343). The higher maltodextrin concentration the lower ovalbumin recovery. Conclusion: The developed liposomes formulation using combination of HPMC matrix and maltodextrin showed potential in preserving liposomes structure and ovalbumin integrity
format Theses and Dissertations
NonPeerReviewed
author RADITYA WEKA NUGRAHENI, 051514153014
author_facet RADITYA WEKA NUGRAHENI, 051514153014
author_sort RADITYA WEKA NUGRAHENI, 051514153014
title PENGEMBANGAN FORMULA LIPOSOM KERING OVALBUMIN MENGGUNAKAN LIOPROTEKTAN MALTODEKSTRIN DAN MATRIKS HPMC 15000
title_short PENGEMBANGAN FORMULA LIPOSOM KERING OVALBUMIN MENGGUNAKAN LIOPROTEKTAN MALTODEKSTRIN DAN MATRIKS HPMC 15000
title_full PENGEMBANGAN FORMULA LIPOSOM KERING OVALBUMIN MENGGUNAKAN LIOPROTEKTAN MALTODEKSTRIN DAN MATRIKS HPMC 15000
title_fullStr PENGEMBANGAN FORMULA LIPOSOM KERING OVALBUMIN MENGGUNAKAN LIOPROTEKTAN MALTODEKSTRIN DAN MATRIKS HPMC 15000
title_full_unstemmed PENGEMBANGAN FORMULA LIPOSOM KERING OVALBUMIN MENGGUNAKAN LIOPROTEKTAN MALTODEKSTRIN DAN MATRIKS HPMC 15000
title_sort pengembangan formula liposom kering ovalbumin menggunakan lioprotektan maltodekstrin dan matriks hpmc 15000
publishDate 2018
url http://repository.unair.ac.id/70268/1/abstrak.pdf
http://repository.unair.ac.id/70268/2/full%20text.pdf
http://repository.unair.ac.id/70268/
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