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Synthesis of Stimuli-responsive Nanogels using Aqueous One-step Crosslinking and Co-nanopolymerization
Published on: January 24, 2025
Crosslinked poly(Lactose) microgels and nanogels for biomedical applications
Mehmet Can1, Ramesh S Ayyala2, Nurettin Sahiner3
1Department of Chemistry & Nanoscience and Technology Research and Application Center, Canakkale Onsekiz Mart University Terzioglu Campus, 17100 Canakkale, Turkey.
New poly(lactose) (p(LAC)) microgels and amine-modified versions (p(LAC)-EDA) show promising blood compatibility and controlled drug release, paving the way for novel biomedical applications.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Nanotechnology
Background:
- Lactose (LAC), a milk carbohydrate, possesses unique functional and nutritional properties making it attractive for biomedical applications.
- Designing functional interfaces using lactose-derived materials is an emerging area of research.
- The development of novel biocolloids from lactose is crucial for advancing drug delivery and tissue engineering.
Purpose of the Study:
- To synthesize and characterize crosslinked poly(lactose) (p(LAC)) microgels for potential biomedical applications.
- To chemically modify p(LAC) microgels with ethylenediamine (EDA) to create amine-functionalized p(LAC)-EDA microgels with enhanced properties.
- To evaluate the blood compatibility and drug loading/release capabilities of the developed microgels.
Main Methods:
- p(LAC) microgels were synthesized via water-in-oil (w/o) microemulsion crosslinking using DiVinyl Sulfone (DVS).
- p(LAC) microgels were chemically modified with ethylenediamine (EDA) to yield p(LAC)-EDA microgels.
- Blood compatibility was assessed using hemolysis and blood clotting tests.
- Drug loading and release studies were performed using Rosmarinic Acid (RA) as a model drug.
Main Results:
- p(LAC) microgels were successfully prepared with high yield (90±5%) and a size range of 0.5-50 µm.
- Chemical modification shifted the isoelectric point (IEP) from pH 1.8 (p(LAC)) to pH 7.7 (p(LAC)-EDA).
- Both p(LAC) and p(LAC)-EDA microgels demonstrated good blood compatibility up to 2 mg/mL, with minimal impact on blood clotting.
- p(LAC)-EDA microgels exhibited a linear release profile for Rosmarinic Acid (RA) over 4 days.
Conclusions:
- Crosslinked poly(lactose) microgels, particularly the amine-modified p(LAC)-EDA variant, are biocompatible and suitable for drug delivery applications.
- The facile synthesis and tunable properties of these lactose-based microgels offer significant potential for biomedical innovations.
- These novel biocolloids represent a promising platform for developing advanced drug delivery systems with controlled release kinetics.
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