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A. Maya Nandkumar
Researcher at Sree Chitra Thirunal Institute for Medical Sciences and Technology
Publications - 8
Citations - 258
A. Maya Nandkumar is an academic researcher from Sree Chitra Thirunal Institute for Medical Sciences and Technology. The author has contributed to research in topics: Biocompatibility & Biomaterial. The author has an hindex of 5, co-authored 7 publications receiving 176 citations.
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Journal ArticleDOI
Synthesis and characterization of curcumin loaded PLA-Hyperbranched polyglycerol electrospun blend for wound dressing applications.
Govindaraj Perumal,Sreenath Pappuru,Debashis Chakraborty,A. Maya Nandkumar,Dillip Kumar Chand,Mukesh Doble +5 more
TL;DR: Results suggest that PLA/HPG/Cur nanofibers can be a potential wound patch dressing for acute and chronic wound applications.
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Synthesis of magnesium phosphate nanoflakes and its PCL composite electrospun nanofiber scaffolds for bone tissue regeneration.
TL;DR: Results indicated that HPG with surface decorated nMP electrospun nanocomposite scaffold can be a promising material for bone tissue engineering applications.
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Differential Adhesive and Bioactive Properties of the Polymeric Surface Coated with Graphene Oxide Thin Film.
TL;DR: A simple single-step method for coating a polymeric substrate with a thin GO film and evaluated the novel antiadhesive activity of these films, which makes thin GO films a self-sufficient surface engineering material for future biomedical applications.
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Hyaluronic acid-g-poly(HEMA) copolymer with potential implications for lung tissue engineering
TL;DR: Grafting with poly(HEMA) is a suitable method for the fabrication of stable, cytocompatible natural-synthetic polymer hybrid matrices for varied biomedical applications such as tissue engineering, wound dressings, drug delivery and so forth.
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Influence of magnesium particles and Pluronic F127 on compressive strength and cytocompatibility of nanocomposite injectable and moldable beads for bone regeneration.
TL;DR: The results indicate that the nanocomposite bone graft was cytocompatible against MG63 osteosarcoma cells and increased the osteogenic gene expression by 2-3 folds, indicating that it can be a potential defect filling biomaterial for bone tissue regeneration at the fracture site.