Polylactic-Co-Glycolic Acid/Alginate/Neem Oil-Reduced Graphene Oxide as a pH-Sensitive Nanocarrier for Hesperidin Drug Delivery: Antimicrobial and Acute Otitis Media Assessments
<b>Background/Objectives</b>: Hesperidin (HSP) is a potent phytochemical antioxidant and anti-inflammatory agent that protects against otitis media. However, due to its low solubility and bioavailability, a suitable delivery method is needed to overcome these problems. A hydrogel is a promising nanocarrier for controlled drug delivery in response to external stimuli, such as pH variations. <b>Methods</b>: Graphene oxide (GO)-based nanocarriers that encapsulate hesperidin (HSP) were further coated with a polylactic-co-glycolic acid/alginate (PLGA-Alg) hydrogel before being integrated into a green neem oil (N.O.) double emulsion to produce a synergistic effect and then characterized by different assays. <b>Results</b>: The nanocarriers exhibited a substantial particle size (168 ± 0.32 nm), with high encapsulation (89.86 ± 0.23%) and a zeta potential of 37 ± 0.43 mV. In vitro release studies conducted over 96 h indicated a sustained HSP release of 82% at pH 5.4 and 65% at pH 7.4. The GO-HSP-loaded neem oil double emulsion formulation exhibits substantial antibacterial activity, as evidenced by inhibition zones of 39 ± 0.02 mm against <i>Staphylococcus epidermidis</i>, and considerable antifungal activity against <i>Candida albicans</i>, with an inhibition zone of 43 ± 0.13 mm, along with biofilm inhibition activity. The formulation demonstrated antioxidant activity (5.21 µg/mL) and increased cell viability (90-95%) while maintaining low cytotoxicity in HSE-2 cells. A histopathological analysis confirmed that treatment with the nanocarriers reduced the levels of pro-inflammatory cytokines (IL-1β, TNF-α, TLR4, IL-6) and raised the levels of antioxidant markers (Nrf-2, SOD) in an in vivo rat model of otitis media. <b>Conclusions</b>: GO-based nanocarriers integrated into a neem oil double emulsion and coated with PLGA-Alg hydrogel deliver hesperidin with sustained release and enhanced antibacterial, antifungal, and antioxidant properties. This formulation may be used to treat otitis media and other oxidative stress diseases.
Authors
- Sandra Hababeh (ORCID: https://orcid.org/0000-0002-9258-3332)
- Nahla A. Elzohairy
- Tassneim M. Ewedah
- Mohamed Fathi Mohamed Elrefai (ORCID: https://orcid.org/0000-0002-4442-9867)
- Saeed A. S. Al-Zuhairy (ORCID: https://orcid.org/0000-0002-7871-3313)
- Jakline Nelson
- Sammar Fathy Elhabal (ORCID: https://orcid.org/0000-0002-7970-2288)
- Marwa Fady
- Ibrahim S. Mousa
- Ahmed M. Hamdan (ORCID: https://orcid.org/0000-0003-4930-792X)
Institutions
- Ain Shams University (EG)
- Sinai University (EG)
- Hashemite University (JO)
- Zagazig University (EG)
- Nahda University (EG)
- King Saud University (SA)
- University of Wasit (IQ)
- Modern University for Information and Technology (EG)
- Armed Forces College of Medicine (EG)
- University of Kut (IQ)
- Egyptian Russian University (EG)
- University of Tabuk (SA)
Publication Details
- Journal
- Pharmaceuticals
- Published
- 2025-03-07
- DOI
- https://doi.org/10.3390/ph18030381
- Citations
- 18
- Primary Topic
- Advanced Drug Delivery Systems
- Type
- article
- Field-Weighted Citation Impact
- 14.23