Encapsulation of L-ascorbic acid via polycaprolactone-polyethylene glycol-casein bioblends

The aim of this study was to encapsulate, L-ascorbic acid, in biopolymers in order to obtain (i) enhancing its encapsulation efficiency (ii) increasing drug release ratio using different pH mediums. Microparticles based on polycaprolactone, polyethylene glycol and casein are prepared by spray drying...

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Main Authors: Ozsagiroglu Erhan, Guvenilir Yuksel Avcibasi
Format: Article
Language:English
Published: Sciendo 2015-12-01
Series:Polish Journal of Chemical Technology
Subjects:
Online Access:https://doi.org/10.1515/pjct-2015-0065
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spelling doaj-7423720a165d4664955acc612636baee2021-09-05T13:59:42ZengSciendoPolish Journal of Chemical Technology1899-47412015-12-01174323610.1515/pjct-2015-0065pjct-2015-0065Encapsulation of L-ascorbic acid via polycaprolactone-polyethylene glycol-casein bioblendsOzsagiroglu Erhan0Guvenilir Yuksel Avcibasi1Istanbul Technical University, Chemical and Metallurgical Engineering Faculty, Chemical Engineering Department, 34469, Maslak-Istanbul, TurkeyIstanbul Technical University, Chemical and Metallurgical Engineering Faculty, Chemical Engineering Department, 34469, Maslak-Istanbul, TurkeyThe aim of this study was to encapsulate, L-ascorbic acid, in biopolymers in order to obtain (i) enhancing its encapsulation efficiency (ii) increasing drug release ratio using different pH mediums. Microparticles based on polycaprolactone, polyethylene glycol and casein are prepared by spray drying technique. Microparticles are in vitro characterized in terms of yield of production, particle size, morphology, encapsulation efficiency, and drug release. In this manner, the importance of the study is producing of a stable and effective drug encapsulation system by PCL-PEG-CS polymer mixture by spray dryer. We achieved minimum 27.540±0.656 μm particle size with 0.512 m2/g surface area, 84.05% maximum drug loading, and 68.92% drug release ratio at pH 9.6. Release profiles are fitted to previously developed kinetic models to differentiate possible release mechanisms. The Korsmeyer–Peppas model is the best described each release scenario, and the drug release is governed by non-Fickian diffusion at pH 9.6. Our study proposed as an alternative or adjuvants for controlling release of L-ascorbic acid.https://doi.org/10.1515/pjct-2015-0065caseindrug encapsulationl-ascorbic acidpolycaprolactonepolyethylene glycolspray dryer
collection DOAJ
language English
format Article
sources DOAJ
author Ozsagiroglu Erhan
Guvenilir Yuksel Avcibasi
spellingShingle Ozsagiroglu Erhan
Guvenilir Yuksel Avcibasi
Encapsulation of L-ascorbic acid via polycaprolactone-polyethylene glycol-casein bioblends
Polish Journal of Chemical Technology
casein
drug encapsulation
l-ascorbic acid
polycaprolactone
polyethylene glycol
spray dryer
author_facet Ozsagiroglu Erhan
Guvenilir Yuksel Avcibasi
author_sort Ozsagiroglu Erhan
title Encapsulation of L-ascorbic acid via polycaprolactone-polyethylene glycol-casein bioblends
title_short Encapsulation of L-ascorbic acid via polycaprolactone-polyethylene glycol-casein bioblends
title_full Encapsulation of L-ascorbic acid via polycaprolactone-polyethylene glycol-casein bioblends
title_fullStr Encapsulation of L-ascorbic acid via polycaprolactone-polyethylene glycol-casein bioblends
title_full_unstemmed Encapsulation of L-ascorbic acid via polycaprolactone-polyethylene glycol-casein bioblends
title_sort encapsulation of l-ascorbic acid via polycaprolactone-polyethylene glycol-casein bioblends
publisher Sciendo
series Polish Journal of Chemical Technology
issn 1899-4741
publishDate 2015-12-01
description The aim of this study was to encapsulate, L-ascorbic acid, in biopolymers in order to obtain (i) enhancing its encapsulation efficiency (ii) increasing drug release ratio using different pH mediums. Microparticles based on polycaprolactone, polyethylene glycol and casein are prepared by spray drying technique. Microparticles are in vitro characterized in terms of yield of production, particle size, morphology, encapsulation efficiency, and drug release. In this manner, the importance of the study is producing of a stable and effective drug encapsulation system by PCL-PEG-CS polymer mixture by spray dryer. We achieved minimum 27.540±0.656 μm particle size with 0.512 m2/g surface area, 84.05% maximum drug loading, and 68.92% drug release ratio at pH 9.6. Release profiles are fitted to previously developed kinetic models to differentiate possible release mechanisms. The Korsmeyer–Peppas model is the best described each release scenario, and the drug release is governed by non-Fickian diffusion at pH 9.6. Our study proposed as an alternative or adjuvants for controlling release of L-ascorbic acid.
topic casein
drug encapsulation
l-ascorbic acid
polycaprolactone
polyethylene glycol
spray dryer
url https://doi.org/10.1515/pjct-2015-0065
work_keys_str_mv AT ozsagirogluerhan encapsulationoflascorbicacidviapolycaprolactonepolyethyleneglycolcaseinbioblends
AT guveniliryukselavcibasi encapsulationoflascorbicacidviapolycaprolactonepolyethyleneglycolcaseinbioblends
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