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Characterization and Dissolution Study of Micellar Curcumin-Spray Dried Powder for Oral Delivery

INTRODUCTION: Curcumin faces a major challenge in clinical use due to its poor aqueous solubility, which affects its bioavailability over oral use. The present study was carried out to overcome this problem. METHODS: An amorphous micellar curcumin-spray dried powder (MC-SDP) with self-assembled case...

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Autores principales: Wijiani, Nina, Isadiartuti, Dewi, Rijal, M Agus Syamsur, Yusuf, Helmy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083647/
https://www.ncbi.nlm.nih.gov/pubmed/32214811
http://dx.doi.org/10.2147/IJN.S245050
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author Wijiani, Nina
Isadiartuti, Dewi
Rijal, M Agus Syamsur
Yusuf, Helmy
author_facet Wijiani, Nina
Isadiartuti, Dewi
Rijal, M Agus Syamsur
Yusuf, Helmy
author_sort Wijiani, Nina
collection PubMed
description INTRODUCTION: Curcumin faces a major challenge in clinical use due to its poor aqueous solubility, which affects its bioavailability over oral use. The present study was carried out to overcome this problem. METHODS: An amorphous micellar curcumin-spray dried powder (MC-SDP) with self-assembled casein was prepared by the addition of sucrose as a protectant. The dry powder of curcumin-loaded micelles was obtained by a spray-drying technique in the presence of sucrose as a protectant. The MC-SDP in the form of dry powder was further developed into tablets to investigate the dissolution profile. The physical properties of preformed powder were characterized by differential thermal analysis (DTA), X-ray diffraction (XRD), and scanning electron microscopy (SEM). Quantitative analysis in the form of solutions was analyzed by high-performance liquid chromatography (HPLC). RESULTS: The physical properties demonstrated that MC-SDP varies from dented to smoother surfaces as a function of sucrose. Furthermore, melting transitions of curcumin in the form of MC-SDP were broadened in all sample mixtures, as observed in the DTA thermogram. The XRD spectra showed that the sharp and very intense peaks of single curcumin crystalline structure no longer existed in all MC-SDP forms, indicating that the mixtures were amorphous. Moreover, a further dissolution study of MC-SDP showed a significant increase of drug dissolved with the presence of sucrose, where >80% of curcumin from MC-SDP was dissolved within 30 min. CONCLUSION: The study demonstrated the manufacture of micellar spray-dried powder that would contribute to the development of oral delivery of curcumin.
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spelling pubmed-70836472020-03-25 Characterization and Dissolution Study of Micellar Curcumin-Spray Dried Powder for Oral Delivery Wijiani, Nina Isadiartuti, Dewi Rijal, M Agus Syamsur Yusuf, Helmy Int J Nanomedicine Original Research INTRODUCTION: Curcumin faces a major challenge in clinical use due to its poor aqueous solubility, which affects its bioavailability over oral use. The present study was carried out to overcome this problem. METHODS: An amorphous micellar curcumin-spray dried powder (MC-SDP) with self-assembled casein was prepared by the addition of sucrose as a protectant. The dry powder of curcumin-loaded micelles was obtained by a spray-drying technique in the presence of sucrose as a protectant. The MC-SDP in the form of dry powder was further developed into tablets to investigate the dissolution profile. The physical properties of preformed powder were characterized by differential thermal analysis (DTA), X-ray diffraction (XRD), and scanning electron microscopy (SEM). Quantitative analysis in the form of solutions was analyzed by high-performance liquid chromatography (HPLC). RESULTS: The physical properties demonstrated that MC-SDP varies from dented to smoother surfaces as a function of sucrose. Furthermore, melting transitions of curcumin in the form of MC-SDP were broadened in all sample mixtures, as observed in the DTA thermogram. The XRD spectra showed that the sharp and very intense peaks of single curcumin crystalline structure no longer existed in all MC-SDP forms, indicating that the mixtures were amorphous. Moreover, a further dissolution study of MC-SDP showed a significant increase of drug dissolved with the presence of sucrose, where >80% of curcumin from MC-SDP was dissolved within 30 min. CONCLUSION: The study demonstrated the manufacture of micellar spray-dried powder that would contribute to the development of oral delivery of curcumin. Dove 2020-03-16 /pmc/articles/PMC7083647/ /pubmed/32214811 http://dx.doi.org/10.2147/IJN.S245050 Text en © 2020 Wijiani et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wijiani, Nina
Isadiartuti, Dewi
Rijal, M Agus Syamsur
Yusuf, Helmy
Characterization and Dissolution Study of Micellar Curcumin-Spray Dried Powder for Oral Delivery
title Characterization and Dissolution Study of Micellar Curcumin-Spray Dried Powder for Oral Delivery
title_full Characterization and Dissolution Study of Micellar Curcumin-Spray Dried Powder for Oral Delivery
title_fullStr Characterization and Dissolution Study of Micellar Curcumin-Spray Dried Powder for Oral Delivery
title_full_unstemmed Characterization and Dissolution Study of Micellar Curcumin-Spray Dried Powder for Oral Delivery
title_short Characterization and Dissolution Study of Micellar Curcumin-Spray Dried Powder for Oral Delivery
title_sort characterization and dissolution study of micellar curcumin-spray dried powder for oral delivery
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083647/
https://www.ncbi.nlm.nih.gov/pubmed/32214811
http://dx.doi.org/10.2147/IJN.S245050
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