» Articles » PMID: 12957641

Evaluation of the Swelling, Hydration and Rupturing Properties of the Swelling Layer of a Rupturable Pulsatile Drug Delivery System

Overview
Specialty Pharmacology
Date 2003 Sep 6
PMID 12957641
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

The objective of this study was to investigate the swelling characteristics of various swellable polymers in swelling layers that induce the rupturing of an outer polymer coating in pulsatile drug delivery systems (DDS). An apparatus was designed to measure simultaneously the swelling energy/force and water uptake of discs, made of polymers. The swelling energy of several excipients decreased in the following order: croscarmellose sodium (Ac-Di-Sol) > low-substituted hydroxypropyl cellulose (L-HPC) > sodium starch glycolate (Explotab) > crospovidone (Kollidon CL) > hydroxypropyl methylcellulose (Methocel K100M). A linear correlation existed between the swelling energy and the water uptake. The swelling behavior of Ac-Di-Sol depended on the ionic strength and the pH of the medium due to a competition for free water and the acidic nature of this polymer. Analysis of the time-dependent swelling force data with a previously developed exponential equation confirmed a diffusion-controlled swelling force development, predominantly controlled by the penetration rate of the medium. The swelling behavior and the rupture of the outer polymeric coating of a pulsatile DDS were demonstrated in simulation tests.

Citing Articles

Spectroscopic and Thermodynamic Study of Biopolymer Adsorption Phenomena in Heterogeneous Solid-Liquid Systems.

Dehabadi L, Karoyo A, Wilson L ACS Omega. 2019; 3(11):15370-15379.

PMID: 31458195 PMC: 6643837. DOI: 10.1021/acsomega.8b01663.


A Review of Disintegration Mechanisms and Measurement Techniques.

Markl D, Zeitler J Pharm Res. 2017; 34(5):890-917.

PMID: 28251425 PMC: 5382187. DOI: 10.1007/s11095-017-2129-z.


Formulation and evaluation of bi-layer tablet of metoclopramide hydrochloride and ibuprofen.

Shiyani B, Gattani S, Surana S AAPS PharmSciTech. 2008; 9(3):818-27.

PMID: 18612830 PMC: 2977017. DOI: 10.1208/s12249-008-9116-y.


Effect of drug solubility on polymer hydration and drug dissolution from polyethylene oxide (PEO) matrix tablets.

Li H, Hardy R, Gu X AAPS PharmSciTech. 2008; 9(2):437-43.

PMID: 18431663 PMC: 2976924. DOI: 10.1208/s12249-008-9060-x.