4.7 Article

Fabrication of phenylalanine amidated pectin using ultra-low temperature enzymatic method and its hydrogel properties in drug sustained release application

Journal

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
Volume 216, Issue -, Pages 263-271

Publisher

ELSEVIER
DOI: 10.1016/j.ijbiomac.2022.06.174

Keywords

Pectin; Hydrogel; Enzymatic method

Funding

  1. Natural Science Foundation of Fujian Province of China [2021J01997]
  2. Natural Science Foundation of Zhangzhou of China [ZZ2021J29]
  3. Foundation for Middle -Young Age Teachers in Fujian Provincial Education Office [JAT200301]

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In this study, pectin was modified with phenylalanine using an ultra-low temperature enzymatic method to enhance its gel properties. The grafting ratio of phenylalanine amidated pectin was investigated under different reaction conditions. The results showed that phenylalanine amidated pectin can form hydrogel with a certain strength under acidic conditions, and it exhibits sustained and complete drug release, making it a promising sustained-release drug carrier.
In this study, pectin was modified with phenylalanine by ultra-low temperature enzymatic method to improve its gel properties. The grafting ratio of phenylalanine amidated pectin was studied under different reaction conditions. The highest value (29.21 %) was reached a reaction temperature of -5 degrees C and time of 12 h. Further analysis indicated that phenylalanine and high methoxyl pectin combined at the solid-liquid two phase interface under the catalysis of papain to form phenylalanine amidated pectin. Moreover, the physicochemical properties of pectin hydrogel and its feasibility as a sustained-release drug carrier were discussed. The results showed that phenylalanine amidated pectin can form hydrogel with a certain strength under acidic conditions, and there is no need to add a lot of soluble solids and divalent cations. Besides, the phenylalanine amidated pectin hydrogel as a sustained release carrier of drugs showed more sustained and complete drug release.

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