Tags

Type your tag names separated by a space and hit enter

Drug release from film-coated chlorpheniramine maleate nonpareil beads: water influx and development of a new drug release model.
Pharm Dev Technol. 1999; 4(4):481-90.PD

Abstract

The purpose of this work was to investigate drug release from film-coated chlorpheniramine maleate (CPM) nonpareils (sugar spheres) and the effect of water influx on the drug release mechanism. The methods used in the study involved the layering of CPM onto nonpareil cores using a fluid-bed apparatus. These CPM cores were then coated with an aqueous ethylcellulose dispersion, which was blended with a solution of hydroxylpropylmethylcellulose (HPMC) at different concentrations. The net water influx was determined by measuring water uptake during dissolution. The film surface area was calculated from bead diameters measured with an optical microscope. Drug release profiles were measured using USP dissolution method I (basket). The results showed that significant water influx occurred, which produced an internal liquid phase ranging from 0 to 1.8 x 10(3) mm3/g of sample. As a result of the water uptake, an increase in bead size was observed. The bead surface area varied over the range of 40-80 x 10(3) mm2/g sample because of a combined effect of the water uptake and the release of the bead contents. A bead geometry parameter was proposed as the ratio of the bead surface area to the volume of the internal liquid phase. This bead geometry parameter was measured as a function of time and fit to an equation using a computer curve-fitting technique. This equation was substituted into an existing drug release model to give a more appropriate mathematical model describing drug release from this system. The conclusion drawn from these results is that the influx of water during drug dissolution creates a progressive increase in the liquid phase within the nonpareil bead; this causes a corresponding increase in the bead surface area which influences the drug release rate.

Authors+Show Affiliations

Department of Pharmaceutical Sciences, University of the Sciences in Philadelphia, Pennsylvania 19104, USA.No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

10578501

Citation

Tang, L, et al. "Drug Release From Film-coated Chlorpheniramine Maleate Nonpareil Beads: Water Influx and Development of a New Drug Release Model." Pharmaceutical Development and Technology, vol. 4, no. 4, 1999, pp. 481-90.
Tang L, Wigent RJ, Schwartz JB. Drug release from film-coated chlorpheniramine maleate nonpareil beads: water influx and development of a new drug release model. Pharm Dev Technol. 1999;4(4):481-90.
Tang, L., Wigent, R. J., & Schwartz, J. B. (1999). Drug release from film-coated chlorpheniramine maleate nonpareil beads: water influx and development of a new drug release model. Pharmaceutical Development and Technology, 4(4), 481-90.
Tang L, Wigent RJ, Schwartz JB. Drug Release From Film-coated Chlorpheniramine Maleate Nonpareil Beads: Water Influx and Development of a New Drug Release Model. Pharm Dev Technol. 1999;4(4):481-90. PubMed PMID: 10578501.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Drug release from film-coated chlorpheniramine maleate nonpareil beads: water influx and development of a new drug release model. AU - Tang,L, AU - Wigent,R J, AU - Schwartz,J B, PY - 1999/12/1/pubmed PY - 1999/12/1/medline PY - 1999/12/1/entrez SP - 481 EP - 90 JF - Pharmaceutical development and technology JO - Pharm Dev Technol VL - 4 IS - 4 N2 - The purpose of this work was to investigate drug release from film-coated chlorpheniramine maleate (CPM) nonpareils (sugar spheres) and the effect of water influx on the drug release mechanism. The methods used in the study involved the layering of CPM onto nonpareil cores using a fluid-bed apparatus. These CPM cores were then coated with an aqueous ethylcellulose dispersion, which was blended with a solution of hydroxylpropylmethylcellulose (HPMC) at different concentrations. The net water influx was determined by measuring water uptake during dissolution. The film surface area was calculated from bead diameters measured with an optical microscope. Drug release profiles were measured using USP dissolution method I (basket). The results showed that significant water influx occurred, which produced an internal liquid phase ranging from 0 to 1.8 x 10(3) mm3/g of sample. As a result of the water uptake, an increase in bead size was observed. The bead surface area varied over the range of 40-80 x 10(3) mm2/g sample because of a combined effect of the water uptake and the release of the bead contents. A bead geometry parameter was proposed as the ratio of the bead surface area to the volume of the internal liquid phase. This bead geometry parameter was measured as a function of time and fit to an equation using a computer curve-fitting technique. This equation was substituted into an existing drug release model to give a more appropriate mathematical model describing drug release from this system. The conclusion drawn from these results is that the influx of water during drug dissolution creates a progressive increase in the liquid phase within the nonpareil bead; this causes a corresponding increase in the bead surface area which influences the drug release rate. SN - 1083-7450 UR - https://www.unboundmedicine.com/medline/citation/10578501/Drug_release_from_film_coated_chlorpheniramine_maleate_nonpareil_beads:_water_influx_and_development_of_a_new_drug_release_model_ L2 - https://www.tandfonline.com/doi/full/10.1081/pdt-100101385 DB - PRIME DP - Unbound Medicine ER -