4.6 Article

Antioxidant activity and controlled-release feature of Quercetin loaded amines-functionalized magnetically porous cellulose

Journal

JOURNAL OF APPLIED POLYMER SCIENCE
Volume 139, Issue 10, Pages -

Publisher

WILEY
DOI: 10.1002/app.51744

Keywords

biopolymers and renewable polymers; cellulose and other wood products; drug delivery systems; stimuli-sensitive polymers

Funding

  1. Loma Riset Sawit Mahasiswa [PENG-3/DPKS/2020]
  2. Indonesian Oil Palm Plantation Fund Management Agency

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This study successfully improved the loading efficiency and controlled release behavior of quercetin by loading it onto magnetically porous cellulose functionalized with amine-based alkoxysilane. Surface modification of PC enhanced the quercetin loading efficiency and controlled its release behavior, leading to improved antioxidant activity of quercetin. The strategy of loading quercetin within MPC-NH2 proved to be effective in enhancing loading capacity, drug-release ability, and antioxidant activity.
Loading of quercetin onto drug cargo is still progressively studied to not only improve its solubility but also control the release behavior for improving therapeutics efficacy. In this present study, we successfully prepared drug cargo based magnetically porous cellulose (PC) functionalized by amine-based alkoxysilane (MPC-NH2) for effectively carrying and sustainably delivering quercetin. The PC derived from oil palm empty fruit bunches provides high loading capacity reaching 344.48 +/- 5.69 mg/g with loading effectiveness of 67.02 +/- 1.11%. Surface modification of PC surfaces by Fe3O4 nanoparticles and aminosilane compounds not only enhances the quercetin loading effectiveness to 80.83 +/- 1.10% but also controls the quercetin release behavior either at artificial gastric or physiological condition. The kinetic release study elaborates that anomalous transport is mainly involved during release of quercetin under physiological condition, but the Fickian diffusion plays the role at artificial gastric condition. The kinetic release rate of quercetin calculated following Higuchi model indicates that the Que@MPC-NH2 has slower release rate compared to another drug carrier. Additionally, the antioxidant activity of quercetin is significantly improved after being loaded onto MPC-NH2. Finally, we recapitulate that the loading of quercetin within MPC-NH2 is a powerful strategy for improving loading capacity, drug-release ability, and antioxidant activity.

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