Phenylboronic Acid-Grafted Chitosan Nanocapsules for Effective Delivery and Controllable Release of Natural Antioxidants: Olive Oil and Hydroxytyrosol

Author:

Hendawy Omnia1,Al-Sanea Mohammad2ORCID,Elbargisy Rehab3ORCID,Rahman Hidayat4ORCID,Mohamed Ahmed5ORCID,Kamal Islam6ORCID,Elshaarawy Reda78ORCID,Khedr Amgad9ORCID,El-Fattah Wesam1011ORCID

Affiliation:

1. Department of Pharmacology, College of Pharmacy, Jouf University, Sakaka 72341, Saudi Arabia

2. Department of Pharmaceutical Chemistry, College of Pharmacy, Jouf University, Sakaka 72341, Saudi Arabia

3. Department of Pharmaceutics, College of Pharmacy, Jouf University, Sakaka 72341, Saudi Arabia

4. Department of Clinical Pharmacy, College of Pharmacy, Jouf University, Sakaka 72341, Saudi Arabia

5. Department of Chemistry, College of Science, Jouf University, Sakaka 72341, Saudi Arabia

6. Department of Pharmaceutics, Faculty of Pharmacy, Port Said University, Port Said 42526, Egypt

7. Department of Chemistry, Faculty of Science, Suez University, Suez 43533, Egypt

8. Institute of Inorganic Chemistry and Structural Chemistry, Heinrich-Heine University Dusseldorf, 40225 Dusseldorf, Germany

9. Department of Pharmacognosy, Faculty of Pharmacy, Port Said University, Port Said 42526, Egypt

10. Chemistry Department, College of Science, IMSIU (Imam Mohammad Ibn Saud Islamic University), Riyadh 11432, Saudi Arabia

11. Department of Chemistry, Faculty of Science, Port Said University, Port Said 42526, Egypt

Abstract

Olives and virgin olive oil (VOO) are a staple of Mediterranean diets and are rich in several beneficial phenolic compounds, including hydroxytyrosol (HT). Therefore, VOO was extracted from Koroneiki olive fruits, and its volatile as well as phenolic components were identified. Meanwhile, in order to upgrade the pharmaceutical capabilities of VOO and HT, a new conjugate phenylboronic acid-chitosan nanoparticles (PBA-CSNPs, NF-1) was fabricated and applied as nanocapsules for implanting high loading and efficient delivery of VOO and HT nanoformulations (NF-2 and NF-3). Due to the H-bonding interactions and boronate ester formation between the hydroxyl groups of the phenolic content of VOO or HT and the PBA groups in the nanocapsules (NF-1), VOO and HT were successfully loaded into the PBA-CSNPs nanocapsules with high loading contents and encapsulation efficacies. The NF-2 and NF-3 nanoformulations demonstrated physicochemical stability, as revealed by their respective zeta potential values, and pH-triggered drug release characteristics. The in vitro studies demonstrated that the nascent nanocapsules were almost completely nontoxic to both healthy and cancer cells, whereas VOO-loaded (NF-2) and HT-loaded nanocapsules (NF-3) showed efficient anti-breast cancer efficiencies. In addition, the antimicrobial and antioxidant potentials of VOO and HT were significantly improved after nanoencapsulation.

Funder

Deanship of Scientific Research in cooperation with the Olive Research Center at Jouf University

Publisher

MDPI AG

Subject

Pharmaceutical Science

Reference47 articles.

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