Author(s): Preeti, Padhi Swarupanjali

Email(s): singhpreeti2308@gmail.com

DOI: 10.5958/0974-360X.2021.00077.9   

Address: Preeti*, Padhi Swarupanjali
Pharmacy Institute, Noida Institute of Engineering and Technology,
19 Knowledge Park-II, Institutional Area, Greater Noida U.P – 201301.
*Corresponding Author

Published In:   Volume - 14,      Issue - 1,     Year - 2021


ABSTRACT:
Glipizide is an antidiabetic drug which is used to treat type 2 diabetes. Glipizide belongs to BCS class 2, which have low solubility and high permeability. Due to the solubility problem it has low bioavailability. In this experimental work attempts are made to enhance the solubility of glipizide by mixed solvency technique which consists of cosolvency and hydrotrophy methods. In cosolvency method four cosolvent namely polyethylene glycol, propylene glycol, glycine and ethanol were considered and In Hydrotropy method, three different hydrotropes, sodium benzoate, sodium citrate and sodium salicylate in concentration with % (5,10,15,20,25,30,35 & 40) were used. In cosolvency method PEG was found to be most suitable compare to other three. There was a rise in solubility of glipizide with increase in concentration of PEG but considering its toxic effect 40% of PEG was taken for further concentration. Out of the three different hydrotropes sodium salicylate showed best result with 40%. The monophasic dosages form was formulated and evaluated. The parameters like pH, viscosity, surface tension and specific gravity etc were also performed.


Cite this article:
Preeti, Padhi Swarupanjali. Formulation of Oral Dosage Form of Antidiabetic Drug Glipizide using Mixed Solvency Method. Research J. Pharm. and Tech. 2021; 14(1):427-431. doi: 10.5958/0974-360X.2021.00077.9

Cite(Electronic):
Preeti, Padhi Swarupanjali. Formulation of Oral Dosage Form of Antidiabetic Drug Glipizide using Mixed Solvency Method. Research J. Pharm. and Tech. 2021; 14(1):427-431. doi: 10.5958/0974-360X.2021.00077.9   Available on: https://rjptonline.org/AbstractView.aspx?PID=2021-14-1-77


REFERENCES:
1.    Fischer, Jnos and Ganellin and C. Robin. Analogue-based Drug Discovery. John Wiley & Sons. (2006); p. 449.
2.    Kawakami K, Oda N, Miyoshi K, Funaki T and Ida Y. Solubilization behavior of a poorly soluble drug under combined use of surfactant and cosolvent. Eur J Pharm Sci. 2006; 28:7-14.
3.    Maheshwari RK. Analysis of frusemide by application of hydrotropic solublization phenomenon. Indian Pharmacist. 2005; 4:555-558
4.    Maheshwari RK. New application of hydrotropic solublization in the spectrophotometric estimation of ketoprofen in tablet dosage form.  Pharma Review. 2005; 3:123-125
5.    Yalkowsky SH and Roseman TJ. Solubilization of drugs by cosolvents. In: Yalkowsky SH, editor. Techniques of Solubilization of Drugs. New York: Marcel Dekker Inc.; 1981. p. 91-4.
6.    Li P, Tabibi I and Yalkowsky SH. Solubilization of Flavopiridol by pH control combined with cosolvents, surfactants and complexants. J Pharm Sci. 1999; 88:945-947.
7.    Maheshwari RK. Solubilization of ibuprofen by mixed solvency approach” The Indian Pharmacist. 2009; 8:81-84 21.
8.    Maheshwari RK. Potentiation of solvent character by mixed solvency concept: A novel concept of solubilization” J Pharm Res. 2010; 3:411-413
9.    Yu H Nola, Ho NM Emmie, Tang P. W Francis and Wan S.M. Terence: To develop the simple, stability-indicating reversed-phase high-performance liquid chromatographic (RP-HPLC) method for determination of Glipizide in guinea pig plasma, Journal of Chromatography A,2008; Vol.1, Issues 1-2: 426-434.
10.    Mathis, J., Gizir, A. M., Yang and Y. Solubility of Alkylbenzenes and a Model for Predicting the Solubility of Liquid Organics on High Temperature Water. J. Chem. Eng. Data 2004, 49, 1269.
11.    Miller, D. J., Hawthorne, S. B., Gizir, A. M. and Clifford, A. A. Solubility of Polycyclic Aromatic Hydrocarbons in Subcritical Water from 298 to 498 K. J. Chem. Eng. Data 1998, 43, 1043.
12.    Saleh, A.M., Badwan, A.A., El-Khordagui and L.K.A. Study of hydrotropic salts, cyclohexanol and water system. Int. J. Pharm. 1983,17, 115–119.
13.    Saleh, A.M., Daabis, N.A. and 1974. Study of the interaction of menadione with hydrotropic salts. Pharmazie 1974,29, 525–527.
14.    Eckert, C.A., Knutson, B. I., Debenedetti and P. G. Supercritical Fluids as Solvents for Chemical and Materials Processing. Nature, 1996, 383, 313–318.
15.    Reverchon, E. Supercritical Fluid Extraction and Fractionation of Essential Oils and Related Products. J. Supercrit. Fluids, 1997, 10, 1–37.  
16.    Kuchekar B.S. and Yadav A.V: Studies on solid dispersion of Paracetamol; the Eastern Pharmacist, 1995; 38: 149.

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