Literature DB >> 10205604

Aqueous ethyl cellulose dispersions containing plasticizers of different water solubility and hydroxypropyl methylcellulose as coating material for diffusion pellets. I. Drug release rates from coated pellets.

M A Frohoff-Hülsmann1, A Schmitz, B C Lippold.   

Abstract

The present work investigates release mechanisms of theophylline pellets coated with an aqueous ethyl cellulose (EC) dispersion containing plasticizers and hydroxypropyl methylcellulose (HPMC) as a water soluble pore former. Three different drug release mechanisms from coated pellets can be determined as a function of the water solubility of the plasticizers and the ionic strength of the release medium. Coated pellets with the addition of more hydrophilic plasticizers such as triethyl citrate (TEC) or diethyl phthalate (DEP) show an approximate zero-order-release rate. In contrast, two-phase release profiles can be observed from pellets coated with dispersions containing hardly soluble plasticizers such as dibutyl phthalate (DBP) or dibutyl sebacate (DBS). Only in a release medium of high ionic strength the water soluble pore former will remain in the coating. Thus the drug diffuses through a hydrated swollen membrane containing EC, HPMC and insoluble plasticizer. The release mechanisms depend on the glass transition temperature of the ethyl cellulose and therefore on the migration of the plasticizers and the pore former. This was shown by investigation of the migration of the additives and the influence of the temperature of the release medium on the release. Additionally, the study investigates the effect of curing and storage conditions of coated pellets on the drug release rate.

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Year:  1999        PMID: 10205604     DOI: 10.1016/s0378-5173(98)00327-5

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  8 in total

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3.  Development and evaluation of a pH-dependent sustained release tablet for irritable bowel syndrome.

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4.  Formulation and evaluation of pH activated dosage form as minitablets in capsule for delivery of fesoterodine.

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5.  Formulation optimization and characterization of transdermal film of curcumin by response surface methodology.

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6.  Medications as a source of human exposure to phthalates.

Authors:  Russ Hauser; Susan Duty; Linda Godfrey-Bailey; Antonia M Calafat
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Review 7.  Sustained Release Drug Delivery Applications of Polyurethanes.

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8.  Transdermal delivery of Diltiazem HCl from matrix film: Effect of penetration enhancers and study of antihypertensive activity in rabbit model.

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  8 in total

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