Development and Evaluation of oral multiple-unit and single-unit hydrophilic controlled-release systems
Open Access
- 1 December 2000
- journal article
- research article
- Published by Springer Nature in AAPS PharmSciTech
- Vol. 1 (4) , 62-70
- https://doi.org/10.1208/pt010434
Abstract
This study compared the release behavior of single-unit (tablets, capsules) and multiple-unit (minitablets in capsules) controlled-release systems of furosemide. The swelling and erosion behaviors of these systems, which contained the swellable hydrophilic polymers sodium alginate (high viscosity) and Carbopol 974P, were compared. Swelling and erosion experiments showed a high degree of swelling and limited erosion for the Carbopol preparations, whereas less swelling but greater erosion was observed for the sodium alginate preparations. The sodium alginate preparations were eroded in 6 hours, while Carbopol preparations exhibited limited erosion within this period of time. These results appear to be attributed to the physicochemical characteristics of the polymers used in this study. Polymer characteristics greatly influenced the release of furosemide (model drug) from the formulations prepared and tested. Sodium alginate had a less pronounced sustained release effect compared with Carbopol (ie, in 8 hours all 3 sodium alginate dosage forms displayed complete release of furosemide, while only 30% of the drug was released from Carbopol dosage forms). Finally, all 3 Carbopol dosage forms (single- and multiple-unit) displayed similar release behavior while sodium alginate dosage forms displayed a different and more distinctive behavior. Minitablets and tablets showed a greater sustained release effect compared with capsules. Evaluation of the release data indicates that the release mechanism for sodium alginate formulations may be attributed to erosion/dissolution, while for Carbopol it may be attributed mainly to polymer relaxation and diffusion of the drug from the polymer surface.Keywords
This publication has 13 references indexed in Scilit:
- Evaluation of High Molecular Weight Poly(Oxyethylene) (Polyox) Polymer: Studies of Flow Properties and Release Rates of Furosemide and Captopril from Controlled-Release Hard Gelatin CapsulesPharmaceutical Development and Technology, 2000
- Formulation and in vitro evaluation of ibuprofen-carbopol® 974P-NF controlled release matrix tablets III: influence of co-excipients on release rate of the drugJournal of Controlled Release, 1998
- Influence of pH on the Release of Propranolol Hydrochloride from Matrices Containing Hydroxypropylmethylcellulose K4M and Carbopol 974Journal of Pharmaceutical Sciences, 1996
- In Vivo Behavior of Multiparticulate Versus Single-Unit Dose FormulationsPublished by Taylor & Francis ,1994
- Compaction of Multiparticulate Oral Dosage FormsPublished by Taylor & Francis ,1994
- The Controlled Release of Prednisolone Using Alginate GelPharmaceutical Research, 1994
- Poly(Ethylene oxide) (PEO) and different molecular weight PEO blends monolithic devices for drug releaseBiomaterials, 1993
- Variation in Gastrointestinal Transit of Pharmaceutical Dosage Forms in Healthy SubjectsPharmaceutical Research, 1991
- Hydroxypropylmethylcellulose sustained release technologyDrug Development and Industrial Pharmacy, 1989
- Controlled ReleasePublished by Springer Nature ,1989