evaluation of calendula mucilage as a mucoadhesive and controlled release component in buccal tablets

mucoadhesive drug delivery systems were developed to sustain drug delivery via various mucus membranes for either local or systemic delivery of poorly absorbed drugs such as peptides and proteins as well as drugs that are subjected to high first-pass metabolism. the present study was undertaken to use isolated calendula mucilage as a mucoadhesive agent and to formulate controlled release buccoadhesive tablets with an intention to avoid hepatic first-pass metabolism as well as to enhance residence time of drug in the buccal cavity. the mucilage was isolated from the calendula petals by aqueous extraction method and characterized for various physiochemical parameters as well as for its adhesive properties. by using direct compression technique, tablets were prepared containing dried mucilage and chlorpheniramine maleate (cpm) as a model drug. three batches of tablets were prepared and evaluated containing three mucoadhesive components namely methocel k4m, carbopol 974p and isolated calendula mucilage in 16.66%, 33.33 % and 50 % (1:2:3 ratio) resulting in 9 different formulations. ftir studies between mucilage and cpm suggested the absence of a chemical interaction between cpm and calendula mucilage. the results of the study showed that the isolated mucilage had good physicochemical and morphological characteristics and tablets conformed to the pharmacopoeial specifications. also in vitro release studies showed controlled action of drug with increasing the concentration of the isolated calendula mucilage as a mucoadhesive agent in the formulations. permeability studies indicated that permeability behavior was not statistically different (p>0.05) by changing the mucoadhesive component. the formulated mucoadhesive tablets for buccal administration containing 75 mg calendula mucilage showed controlled drug release. thus, mucoadhesive natural calendula mucilage based buccal tablets for controlled release were successfully formulated.