ArticleNanomaterials (Basel, Switzerland)2017
3D Nanoporous Anodic Alumina Structures for Sustained Drug Release.
Article in Nanomaterials (Basel, Switzerland), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Predictive Neural Network Modeling of Nanoporous Anodic Alumina for Controlled Drug Release Implants: An Integrated Machine Learning Approach.Materials (Basel, Switzerland) · 2026Article
- Interpreting the Theranostic Applications of Alumina and Silica Substrates in Cancer.Molecules (Basel, Switzerland) · 2026Review
- Functionalised Anodised Aluminium Oxide as a Biocidal Agent.International journal of molecular sciences · 2022Article
- Article
- Conceptual Progress for Explaining and Predicting Self-Organization on Anodized Aluminum Surfaces.Nanomaterials (Basel, Switzerland) · 2021Review
- Recent Advances in Nanoporous Anodic Alumina: Principles, Engineering, and Applications.Nanomaterials (Basel, Switzerland) · 2021Review
- Comprehensive Survey on Nanobiomaterials for Bone Tissue Engineering Applications.Nanomaterials (Basel, Switzerland) · 2020Review
- Advances in Optical Biosensors and Sensors Using Nanoporous Anodic Alumina.Sensors (Basel, Switzerland) · 2020Review
- Real-Time Monitoring of Biotinylated Molecules Detection Dynamics in Nanoporous Anodic Alumina for Bio-Sensing.Nanomaterials (Basel, Switzerland) · 2019Article
- Effect of Sharp Diameter Geometrical Modulation on the Magnetization Reversal of Bi-Segmented FeNi Nanowires.Nanomaterials (Basel, Switzerland) · 2018Article
Corrections and comments
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Authors and funding
5 authors.
Funding
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Abstract
The use of nanoporous anodic alumina (NAA) for the development of drug delivery systems has gained much attention in recent years. The release of drugs loaded inside NAA pores is complex and depends on the morphology of the pores. In this study, NAA, with different three-dimensional (3D) pore structures (cylindrical pores with several pore diameters, multilayered nanofunnels, and multilayered inverted funnels) were fabricated, and their respective drug delivery rates were studied and modeled using doxorubicin as a model drug. The obtained results reveal optimal modeling of all 3D pore structures, differentiating two drug release stages. Thus, an initial short-term and a sustained long-term release were successfully modeled by the Higuchi and the Korsmeyer-Peppas equations, respectively. This study demonstrates the influence of pore geometries on drug release rates, and further presents a sustained long-term drug release that exceeds 60 days without an undesired initial burst.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.