Cited by 13Silicon Nanostructures and PhotoluminescenceNanoparticle-Based Drug DeliveryAdvanced Drug Delivery Systems

Controlled delivery of levothyroxine using porous silicon as a drug nanocontainer

Kashanian, Soheila, Rostami, Elham, Harding, Frances J., McInnes, Steven J. P., Al-Bataineh, Sameer, Voelcker, Nicolas H.·2016·Australian Journal of Chemistry

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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Crossref · 10.1071/ch15315

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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.”
  • 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.”
  • 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.”

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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
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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