Controlled drug delivery from chitosan-coated heparin-loaded nanopores anodically grown on nitinol shape-memory alloy

M. Moradi, E. Salahinejad, E. Sharifi, L. Tayebi · Carbohydrate polymers, 314 (2023) 120961 · 2026

A two-stage anodized nitinol surface coated with chitosan forms a hydrophilic, nanoporous platform that controls heparin release via diffusion and shows non-cytotoxicity in vitro.

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Plain English summary

The study aims to enable local, controlled delivery of the cardiovascular drug heparin using nitinol (a shape-memory alloy) as the base material. The nitinol is treated by electrochemical anodizing to create a regular nanoporous Ni-Ti-O layer, and then coated with chitosan. Researchers analyze how the surface structure and wettability change after anodizing, including reduced water contact angle (increased hydrophilicity). They also measure heparin release behavior and fit the release kinetics using multiple models (Higuchi, first-order, zero-order, and Korsmeyer–Peppas), concluding that chitosan mainly controls release through a diffusional mechanism. In vitro cell tests using HUVEC viability indicate the samples are non-cytotoxic, with the best performance reported for the chitosan-coated specimens. The authors conclude the system is promising for cardiovascular drug delivery, particularly for stent applications.

Why this matters

A combined approach using two-stage electrochemical anodizing to form nanopores on nitinol followed by chitosan coating to control local heparin delivery, with release kinetics modeled and in vitro cytocompatibility assessed. No evidence of prototype/device integration, in vivo testing, regulatory progress, or commercial deployment is provided in the abstract.

Key findings

  • Two-stage anodizing produced a regular nanoporous Ni-Ti-O layer on nitinol.
  • Anodizing decreased sessile water contact angle, increasing hydrophilicity.
  • Chitosan coating controlled heparin release primarily via a diffusional mechanism.
  • Drug release kinetics were evaluated using Higuchi, first-order, zero-order, and Korsmeyer–Peppas models.
  • HUVEC viability assays showed non-cytotoxicity, with best performance for chitosan-coated samples.

Limitations

The abstract reports in vitro analyses only (structure/wettability, drug release kinetics, and HUVEC cytocompatibility). It does not mention in vivo performance, long-term stability, mechanical behavior under device conditions, or clinical validation.

Publication

Publisher
arXiv
Journal
Carbohydrate polymers, 314 (2023) 120961
Publication date
January 27, 2026
Research type
Paper
arXiv
2601.19962
Access
open

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Method note: Summaries and ratings on this page are generated by AI from the abstract only. Read the original paper for full context. · Model: gpt-5.4-nano-2026-03-17