Related Experiment Video
Updated: Oct 19, 2025

Alternating Magnetic Field-Responsive Hybrid Gelatin Microgels for Controlled Drug Release
Published on: February 13, 2016
Structural changes in pH-responsive gelatin/hydroxypropyl methylcellulose phthalate blends aimed at drug-release
Satoshi Nogami1, Kazunori Kadota1, Hiromasa Uchiyama1
1Faculty of Pharmacy, Osaka Medical and Pharmaceutical University, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, Japan.
This study shows gelatin/HPMCP hydrogels inhibit drug release at low pH due to HPMCP aggregation. This pH-responsive property is useful for oral gel formulations.
Area of Science:
- Materials Science
- Pharmaceutical Sciences
- Polymer Chemistry
Background:
- Gelatin and Hydroxypropyl methylcellulose acetate succinate (HPMCP) are biocompatible polymers.
- pH-responsive drug delivery systems are crucial for targeted oral formulations.
Purpose of the Study:
- To investigate the thermal and pH-dependent gelation of gelatin/HPMCP blends.
- To understand the mechanism of pH-dependent drug release inhibition.
Main Methods:
- Ultraviolet (UV) spectrophotometry
- Viscoelasticity measurements
- Dynamic Light Scattering (DLS)
Main Results:
- Low pH (< 4.8) induced HPMCP aggregation, forming a physical barrier.
- This aggregation significantly inhibited lisinopril release from gelatin/HPMCP gels at pH 1.2.
- pH affected the transparency and viscoelastic properties of the gels.
Conclusions:
- Gelatin/HPMCP blends exhibit pH-responsive gelation and drug release behavior.
- The developed hydrogel system is suitable for oral gel formulations requiring pH-triggered drug delivery.
More Related Videos
15:33Microwave-assisted Functionalization of Polyethylene glycol and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation
Published on: October 29, 2013
08:59A Freeze-Thawing Method to Prepare Chitosan-Polyvinyl alcohol Hydrogels Without Crosslinking Agents and Diflunisal Release Studies
Published on: January 14, 2020
Related Concept Videos
Bioavailability Enhancement: Drug Stability Enhancement and GI Retention
Factors Influencing Drug Absorption: Pharmaceutical Parameters