Abstract

The matrix tablets of diltiazem hydrochloride were prepared by direct compression using hydroxypropyl methyl cellulose (HPMC) and various amounts (2.5%, 5.0%, 10% and 20%) of citric acid, malic acid and succinic acid. The characterization of physical mixture of drug and organic acids was performed by Infra-red spectroscopy. An organic acid was incorporated to set up a system bringing about gradual release of this drug. The influence of organic acids on the release rate were described by the Peppas equation: M t /M∞ = Kt n and Higuchi’s equation: Q t = K1t1/2. The addition of organic acids and the pH value of medium could notably influence the dissolution behavior and mechanism of drug-release from matrices. Increasing amounts of organic acid produced an increase in drug release rate, which showed a good linear relationship between contents of organic acid and drug accumulate release (%) in phosphate buffer, pH 7.4. The drug release increased significantly (P < 0.05) with use of succinic acid in tablet formulation. Increasing amounts of succinic acid above 10% produced decreasing values of n and increasing values of k, in a linear relationship, which indicated there was a burst release of drug from the matrix. Optimized formulations are found to be stable upon 3-month study.

Highlights

  • Many drugs are weak bases or salts thereof and demonstrate pH-dependent solubility in the pH range of the GI tract

  • The in vitro drug release data were fitted into Korsmeyer–Peppas equation[12] Mt/M∞ = Ktn, where Mt/M∞ corresponds to the amount of drug released at time t and after an infinite time, K is a constant related to the structural and geometric properties of the drug delivery system and n is the release exponent related to the mechanism of the release

  • Its solubility at pH 3.6 is 879.03 mg/mL, at pH 6.0 is 378.68 mg/mL, and at pH 7.4 is reduced to 71.42 mg/mL

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Summary

INTRODUCTION

Many drugs are weak bases or salts thereof and demonstrate pH-dependent solubility in the pH range of the GI tract. Several attempts to overcome the problem of pH-dependent solubility of weakly basic drugs have been published They are mostly based on the presence of acidic excipients such as water soluble or insoluble polymers or organic acids.[3,4] The effect of enteric polymers on release characteristics of weakly basic drugs with different pKa and aqueous solubilities at the pH of interest (7.4) were investigated for their release from hydrophilic matrices.[5] These excipients either increase the release of drug from the delivery system by leaching out at higher pH values or keeping the pH low within the system in the intestinal pH range and the solubility of the drug high. The solubility of HPMC is pH-independent and forms a strong viscous gel on contact with aqueous media, which may be useful in controlled delivery of highly watersoluble drugs.[7,8]

MATERIALS AND METHODS
RESULTS AND DISCUSSION
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