Individual and combined effect of PVP, PEG 6000 and some other diluents on the solubility and dissolution rate of Itraconazole tablets

Rajesh Pavan A (1) , Chandra Sekhar K.B (2) , Sirisha K (3) , Mounika S (4)
(1) Department of pharmaceutics, JNTUA-Oil Technological and Pharmaceutical Research Institute, Anantapuramu, Andhra Pradesh, India, India ,
(2) Department of pharmaceutics, JNTUA-Oil Technological and Pharmaceutical Research Institute, Anantapuramu, Andhra Pradesh, India, India ,
(3) Department of pharmaceutics, JNTUA-Oil Technological and Pharmaceutical Research Institute, Anantapuramu, Andhra Pradesh, India, India ,
(4) Department of pharmaceutics, JNTUA-Oil Technological and Pharmaceutical Research Institute, Anantapuramu, Andhra Pradesh, India, India

Abstract

Itraconazole, an Anti-fungal drug, which is poorly soluble in water. It requires Enhancement in dissolution rate for enhancing its oral bioavailability by several techniques. The prepared Itraconazole tablets possess good physicochemical characteristics and the in vitro dissolution and release rate kinetics were originated acceptable. Deviations were found in dissolution rate, efficiency for the Itraconazole tablets. The factors viz., used of Poly ethylene glycol 6000, Poly Vinyl Pyrrolidone and Dicalcium Phosphate, as A, B and C respectively and the combined factors also observed. Formulations F3 and F7 gave good dissolution rate and efficiency values. Addition of PVP 2% resulted in increased dissolution rate of Itraconazole tablets. A grouping of Poly ethylene glycol 6000, Poly Vinyl Pyrrolidone and Dicalcium Phosphate was suggested for making Itraconazole tablets with good dissolution characteristics.

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Authors

Rajesh Pavan A
rajeshpawan18@gmail.com (Primary Contact)
Chandra Sekhar K.B
Sirisha K
Mounika S
Rajesh Pavan A, Chandra Sekhar K.B, Sirisha K, & Mounika S. (2023). Individual and combined effect of PVP, PEG 6000 and some other diluents on the solubility and dissolution rate of Itraconazole tablets. International Journal of Research in Pharmaceutical Sciences, 8(4), 629–634. Retrieved from https://ijrps.com/home/article/view/4631

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