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Drug Delivery: Overview01:16

Drug Delivery: Overview

360
The selection of a drug's delivery route depends upon its physicochemical properties, including lipid or water solubility and ionization, as well as the therapeutic requirement, such as immediate or sustained effect. These routes can be divided into three primary categories: enteral, parenteral, and topical.
Enteral delivery involves administering drugs directly through swallowing, sublingual placement, or buccal application. Orally administered drugs predominantly navigate the...
360
Drug Delivery: Miscellaneous Routes01:22

Drug Delivery: Miscellaneous Routes

439
Drug delivery methods like oral inhalation, nasal sprays, transdermal patches, eye drops, intravitreal injection,  and rectal administration provide localized effects with reduced toxicity.
Oral inhalation and nasal sprays swiftly transfer drugs across the respiratory epithelium's mucosal layer. Inhaled glucocorticoids and bronchodilators directly target lung conditions such as asthma, while fluticasone nasal spray mitigates allergic rhinitis.
Transdermal patches transport drugs...
439
Drug Delivery: Parenteral Route01:29

Drug Delivery: Parenteral Route

745
The parenteral route is a critical method of drug administration. It delivers compounds directly into the systemic circulation and bypasses the gastrointestinal tract. This approach is particularly advantageous for drugs that exhibit poor absorption or instability when administered orally.
There are three primary parenteral routes: intravenous (IV), intramuscular (IM), and subcutaneous (SC). The IV route introduces the drug directly into the bloodstream, ensuring immediate action. The IM route...
745

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Related Experiment Video

Updated: Aug 23, 2025

Alternating Magnetic Field-Responsive Hybrid Gelatin Microgels for Controlled Drug Release
09:11

Alternating Magnetic Field-Responsive Hybrid Gelatin Microgels for Controlled Drug Release

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Magnetically Actuated Shape Memory Polymers for On-Demand Drug Delivery.

Anand Utpal Vakil1, Maryam Ramezani1, Mary Beth B Monroe1

  • 1Department of Biomedical and Chemical Engineering, BioInspired Syracuse: Institute for Material and Living Systems, Syracuse University, Syracuse, NY 13244, USA.

Materials (Basel, Switzerland)
|October 27, 2022
PubMed
Summary

New magnetically responsive shape memory polymers (SMPs) offer controlled, on-demand drug delivery. Incorporating magnetic nanoparticles allows remote activation for tunable release profiles, addressing limitations of traditional intravenous infusions.

Keywords:
actuationdrug deliverymagnetismpolyurethanesshape memory polymersthermoplasticthermoset

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Area of Science:

  • Biomaterials Science
  • Polymer Chemistry
  • Drug Delivery Systems

Background:

  • Intravenous infusions for drug delivery can lead to nerve damage, pain, and infection.
  • A need exists for advanced drug delivery methods offering on-demand and prolonged administration.
  • Existing methods lack precise control over drug release kinetics.

Purpose of the Study:

  • To develop magnetically responsive shape memory polymers (SMPs) for controlled drug release.
  • To investigate the influence of magnetic nanoparticles and polymer architecture on drug delivery.
  • To engineer a system for tunable, on-demand release of multiple drugs.

Main Methods:

  • Synthesized iron oxide magnetic nanoparticles (mnps) and incorporated them into shape memory polymers (SMPs).
  • Characterized material properties using dynamic mechanical analysis and assessed cytocompatibility with 3T3 fibroblasts.
  • Quantified drug release kinetics (doxorubicin, 6-mercaptopurine, rhodamine) using UV-Vis spectroscopy.
  • Fabricated a gradient material for dual drug loading with distinct release profiles.

Main Results:

  • All polymer composites exhibited >75% cytocompatibility over 72 hours.
  • Drug release rates were tunable by altering polymer chemistry (linear vs. cross-linked) and mnp content.
  • Faster release observed with linear polymers and higher mnp content; slower release with highly cross-linked networks and lower mnp content.
  • Polymer shape memory properties and drug hydrophobicity influenced release rates; hydrophobic drugs released slower.

Conclusions:

  • Magnetically responsive SMPs provide enhanced control over drug delivery, overcoming limitations of conventional methods.
  • Tunable drug release achieved through material design, including polymer structure, magnetic content, and drug properties.
  • A novel dual-drug delivery system with distinct release profiles was successfully synthesized from a single scaffold.
  • This technology holds promise for advanced therapeutic applications requiring precise, on-demand drug administration.