In-vitro evaluation of khaya and albizia gums as compression coatings for drug targeting to the colon

• Published in: Journal of pharmacy and pharmacology Vol. 57; no. 2; p. 163
• Main Authors: Odeku, Oluwatoyin A, Fell, John T
• Format: Journal Article
• Language: English
• Published: England 01.02.2005
• Subjects: Acetaminophen - pharmacokinetics; Adhesives - chemistry; Adhesives - isolation & purification; Adhesives - pharmacokinetics; Albizzia - chemistry; Animals; Cecum - drug effects; Chemistry, Pharmaceutical - methods; Coated Materials, Biocompatible - chemistry; Coated Materials, Biocompatible - isolation & purification; Coated Materials, Biocompatible - pharmacokinetics; Colon - drug effects; Colon - microbiology; Drug Carriers - chemistry; Drug Carriers - pharmacokinetics; Drug Delivery Systems - methods; Drug Evaluation, Preclinical - methods; Excipients - chemistry; Excipients - pharmacokinetics; Indomethacin - pharmacokinetics; Male; Meliaceae - chemistry; Nigeria; Plant Components, Aerial - chemistry; Plant Extracts - chemistry; Plant Extracts - isolation & purification; Rats; Tablets - chemistry; Tablets - pharmacokinetics; Tablets - standards; Nigeria
• ISSN: 0022-3573; 2042-7158
• DOI: 10.1211/0022357055362

Khaya and albizia gums were evaluated as compression coatings for target drug delivery to the colon using indometacin (a water insoluble drug) and paracetamol (a water soluble drug) as model drugs. The core tablets were compression-coated with 300 and 400 mg of 100% khaya gum, 100% albizia gum and a mixture of khaya and albizia gum (1:1). Drug release studies were carried out in 0.1(M) HCl (pH 1.2) for 2 h, Sorensen's buffer (pH 7.4) for 3 h and then in phosphate-buffered saline (pH 6.8) or in simulated colonic fluid for the rest of the experiment to mimic the physiological conditions from the mouth to colon. The results indicated that khaya and albizia gums were capable of protecting the core tablet in the physiological environment of the stomach and small intestine, with albizia gum showing greater ability than khaya gum. The release from tablets coated with the mixture of khaya and albizia gums was midway between the two individual gums, indicating that there was no interaction between the gums. Studies carried out using rat caecal matter in phosphate-buffered saline at pH 6.8 (simulated colonic fluid) showed that the gums were susceptible to degradation by the colonic bacterial enzymes, leading to release of the drug. The results demonstrate that khaya gum and albizia gum have potential for drug targeting to the colon.