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Published on: August 2, 2016
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Functionalized Moringa oleifera Gum as pH-Responsive Nanogel for Doxorubicin Delivery: Synthesis, Kinetic Modelling
Sunita Ranote1,2,3, Marta Musioł1, Marek Kowalczuk1
1Centre of Polymer and Carbon Materials, Polish Academy of Sciences, 34. M. Curie-Skłodowska St., 41-819 Zabrze, Poland.
Polymers
|November 11, 2022
Summary
This study developed a pH-responsive nanogel from Moringa oleifera gum to deliver doxorubicin (DOX) chemotherapy drugs. The nanogel demonstrates high drug loading and targeted release in simulated tumor environments, improving cancer treatment potential.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Drug Delivery Systems
Background:
- Targeted drug delivery remains a significant challenge in chemotherapy, necessitating advanced systems for improved efficacy and reduced side effects.
- Environment-responsive nanocarriers offer a promising strategy to achieve site-specific drug release within the tumor microenvironment.
- Moringa oleifera gum presents a biocompatible and biodegradable natural polymer with potential for developing novel drug delivery platforms.
Purpose of the Study:
- To synthesize and characterize a pH-responsive nanogel (MOGN) using Moringa oleifera gum as a carrier for doxorubicin (DOX).
- To evaluate the drug loading capacity, swelling behavior, and in vitro drug release profile of the DOX-loaded MOGN.
- To assess the potential of MOGN for site-specific and controlled delivery of anticancer drugs in a simulated tumor environment.
Main Methods:
- Moringa oleifera gum-based nanogel (MOGN) synthesized via free radical polymerization using γ-irradiation, followed by hydrolysis, sonication, and ultracentrifugation.
- pH-dependent swelling behavior assessed using a gravimetric method.
- Doxorubicin (DOX) loading efficiency determined, and in vitro release studies conducted at different pH values (5.5 and 7.4).
- Drug release kinetics analyzed using Korsmeyer-Peppas and Higuchi models.
- Cytotoxicity studies performed using Rhabdomyosarcoma cells to evaluate drug release efficacy.
Main Results:
- MOGN exhibited superabsorbent properties with a swelling ratio of 365.0 g/g.
- High doxorubicin loading efficiency of 98.35% was achieved.
- In vitro studies showed significantly higher DOX release at pH 5.5 (91.92%) compared to pH 7.4 (12.18%), mimicking the tumor microenvironment.
- Drug release followed Korsmeyer-Peppas model at pH 5.5 and 6.8, and Higuchi model at pH 7.4.
- Cytotoxicity studies confirmed efficient DOX release and efficacy against Rhabdomyosarcoma cells.
Conclusions:
- The synthesized Moringa oleifera gum-based nanogel (MOGN) is a highly efficient carrier for doxorubicin.
- MOGN demonstrates excellent pH-triggered drug release, favoring the acidic tumor environment.
- This pH-responsive nanogel system shows significant promise for targeted and controlled delivery of anticancer drugs, potentially enhancing chemotherapy outcomes.
Keywords:
Moringa oleifera gum nanogelRhabdosarcoma cellsdoxorubicin deliverypH-responsiverelease kinetics
