Controlled delivery of levothyroxine using porous silicon as a drug nanocontainer
Abstract
Porous silicon (pSi) materials are regarded as promising drug delivery vehicles due to their biocompatibility, in vivo degradation, and resorption. We examine pSi films as a platform for the controlled delivery of levothyroxine, as a means to overcome problems with consistent dosage of this drug by oral administration. Oxidized pSi films were modified with 3-(aminopropyl)triethoxysilane (APTES), creating a surface chemistry that increased levothyroxine drug loading capacity by 50 % and sustained drug release under physiological conditions for 14 days. Release kinetics from APTES-functionalized films initially followed a zero-order release profile, which is highly desirable for drug delivery. The loading and release profiles of levothyroxine suggest that the film size required to deliver a therapeutic dose is feasible for further consideration as an implantable delivery system.
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3-(Aminopropyl) triethoxysilane was added to dramatically increase the affinity to the hydrophobic drug molecule.
“3-(Aminopropyl) triethoxysilane was added to dramatically increase the affinity to this hydrophobic drug molecule.”
From Levothyroxine: conventional and novel drug delivery formulations. (2023) · cites this paper as [269]
The porous silicon membrane height was approximately 2 μm and it bound LT4 through hydrogen bonding.
“The height of the porous silicon membrane was ∼2 µm and it bound LT4 through hydrogen bonding.”
From Levothyroxine: conventional and novel drug delivery formulations. (2023) · cites this paper as [269]
An in vitro experiment demonstrated a first-order release profile of 87% of the total contents of 21 μg in an approximately 14-day period.
“An in vitro experiment demonstrated a first-order release profile of 87% of the total contents of 21 µg in an ∼14-day period.”
From Levothyroxine: conventional and novel drug delivery formulations. (2023) · cites this paper as [269]
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References 56 · Cited by 13
- Authors
- Kashanian, S., Rostami, E., Harding, F. J., McInnes, S. J. P., Al-Bataineh, S., & Voelcker, N. H.
- Affiliations
- Razi University (IR)
- Islamic Azad University, Tehran (IR)
- University of South Australia (AU)
- CARC Centre of Excellence in Convergent Bio-Nano Science and Technology, Mawson Institute, University of South Australia, Adelaide, SA 5001, Australia.
- Corresponding author
- Kashanian, Soheila
- Voelcker, Nicolas H.
- Venue
- Australian Journal of Chemistry
- Publisher
- CSIRO Publishing
- Published
- 2015-08-31
- Volume
- 69
- Issue
- 2
- Pages
- 204-211
- ISSN
- 0004-9425 (ISSN-L)
- 1445-0038
- OpenAlex
- W2145816445
- Cited by
- 13
- References
- 56
- Citations by year
- 2025: 1 · 2024: 3 · 2023: 2 · 2022: 1 · 2019: 2 · 2018: 1 · 2016: 3
- FWCI
- 0.54
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Australian Journal of Chemistry (publishedVersion)
- Adelaide Research & Scholarship (AR&S) (University of Adelaide) (submittedVersion)
- Funders
- Australian Research Council
- National Health and Medical Research Council
- National Medical Research Council
- Topics
- Physical Sciences › Materials Science › Materials Chemistry › Silicon Nanostructures and Photoluminescence
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Keywords
- porous silicon, levothyroxine, controlled drug release, APTES surface modification, sustained drug release, zero-order release kinetics, drug loading capacity, implantable drug delivery, oral drug delivery
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