Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Modified-Release Drug Delivery Systems: Stimuli-Activated01:30

Modified-Release Drug Delivery Systems: Stimuli-Activated

Stimuli-activated drug delivery systems are designed to release drugs in response to specific physical, chemical, or biological stimuli. These systems often utilize hydrogels—three-dimensional, hydrophilic polymer networks capable of swelling in aqueous environments and retaining significant fluid volumes. Upon exposure to particular stimuli, these hydrogels undergo structural transitions that allow the embedded drug to be released. Due to this adaptive behavior, such systems are also called...
Insulin Formulations: Types and Delivery01:27

Insulin Formulations: Types and Delivery

Insulin preparations are categorized by their duration of action into short-acting and long-acting types. Two strategies are used to modify insulin's absorption and pharmacokinetic profile: slowing the absorption post-subcutaneous injection, or altering human insulin's amino acid sequence or protein structure. These changes retain the insulin's ability to bind to the insulin receptor, but alter its behavior in solution or after injection.
Short-acting insulins are divided into rapid-acting...
Modified-Release Drug Delivery Systems: Rate-Programmed I01:22

Modified-Release Drug Delivery Systems: Rate-Programmed I

Rate-programmed drug delivery systems (DDS) are designed to release drugs at specific, controlled rates to maintain consistent therapeutic levels. These systems are categorized based on their release mechanisms, including dissolution-controlled DDS, diffusion-controlled DDS, and combined dissolution-diffusion-controlled DDS.In dissolution-controlled DDS, the release rate depends on the slow dissolution of the drug itself or the surrounding matrix. Drugs with inherently slow dissolution rates,...
Modified-Release Drug Delivery Systems: Rate-Programmed II01:19

Modified-Release Drug Delivery Systems: Rate-Programmed II

Rate-programmed drug delivery systems release drugs in a controlled manner to maintain therapeutic levels. Three main designs include reservoir, matrix, and hybrid systems.Reservoir systems consist of a drug core enclosed within a membrane that controls drug release. In non-swelling reservoir systems, polymers like ethyl cellulose or polymethacrylates are used. These do not hydrate in aqueous media and control release through membrane thickness, porosity, or insolubility. This type includes...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Joint color-spatial iterative interaction and metric-based motion filtering for unsupervised polyp segmentation in endoscopic videos.

Neural networks : the official journal of the International Neural Network Society·2026
Same author

AI models based on gadoxetic acid-enhanced MRI to predict treatment response and prognosis after TACE in hepatocellular carcinoma.

Frontiers in oncology·2026
Same author

Neutral BODIPY-chitosan films for photodynamic food freshness preservation.

Chemical communications (Cambridge, England)·2026
Same author

Precision Engineered Dissolving Microneedles Enable Green-Light Activated Chemo-Photodynamic Therapy for Psoriasis.

ACS applied materials & interfaces·2026
Same author

Can incorporating preoperative arterial enhancement ratio map into habitat analysis predict TACE refractoriness in unresectable hepatocellular carcinoma?

BMC medical imaging·2026
Same author

Enabling Durable Quasi-Solid-State Li-S Batteries with an Organic Nitrate Additive for Anode Protection and Polysulfide Confinement.

ACS applied materials & interfaces·2026

Related Experiment Video

Updated: May 22, 2026

Hollow Microneedle-based Sensor for Multiplexed Transdermal Electrochemical Sensing
08:19

Hollow Microneedle-based Sensor for Multiplexed Transdermal Electrochemical Sensing

Published on: June 1, 2012

Electrically Modulated Semi-Convertible Hydrogel Microneedles for Programmable Insulin Delivery.

Hongyue Jiang1, Xinze Zhang1, Xiang Li1

  • 1State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, P. R. China.

Advanced Materials (Deerfield Beach, Fla.)
|May 21, 2026
PubMed
Summary

A new wearable microneedle system uses electrical stimulation to precisely control insulin delivery for type 1 diabetes management. This innovative hydrogel technology mimics natural pancreatic function for improved blood glucose regulation.

Keywords:
gel‐sol transitioninsulin deliveryprogrammablesemi‐convertible hydrogelwearable device

More Related Videos

Fabrication of a Master Mold for Microneedles with a Micron-sized Air-vent Hole
06:25

Fabrication of a Master Mold for Microneedles with a Micron-sized Air-vent Hole

Published on: December 5, 2025

Related Experiment Videos

Last Updated: May 22, 2026

Hollow Microneedle-based Sensor for Multiplexed Transdermal Electrochemical Sensing
08:19

Hollow Microneedle-based Sensor for Multiplexed Transdermal Electrochemical Sensing

Published on: June 1, 2012

Fabrication of a Master Mold for Microneedles with a Micron-sized Air-vent Hole
06:25

Fabrication of a Master Mold for Microneedles with a Micron-sized Air-vent Hole

Published on: December 5, 2025

Area of Science:

  • Biomaterials Science
  • Drug Delivery Systems
  • Endocrinology

Background:

  • Current insulin delivery methods for type 1 diabetes often lack sustained and precise control.
  • Mimicking the pancreas's dynamic insulin secretion is a key goal for improved diabetes management.

Purpose of the Study:

  • To develop a wearable, electrically modulated microneedle system for self-regulated insulin delivery.
  • To create a system capable of sustained and precise insulin release for type 1 diabetes treatment.

Main Methods:

  • A semi-convertible hydrogel microneedle system combining silk fibroin and polyethylene glycol/chitosan was engineered.
  • Flexible electrodes induced a gel-sol phase transition in the hydrogel under 1.2 V electrical stimulation for insulin release.
  • The system's performance was evaluated in type 1 diabetic mouse models.

Main Results:

  • Electrical stimulation triggered insulin release via silk fibroin phase transition and polymer network expansion.
  • Insulin release was controlled by electrical signals, with passive diffusion occurring when stimulation ceased.
  • A single microneedle patch demonstrated segmented control, with effects lasting up to 16 hours.

Conclusions:

  • The developed microneedle system offers a versatile and precise approach to insulin delivery.
  • This technology shows significant potential for long-term, self-regulated management of type 1 diabetes.
  • The electrically modulated system provides a promising strategy for chronic disease management.