Improved Dissolution Properties of Ketoconazole through Application of Liquisolid Techniques
DOI:
https://doi.org/10.37285/ijpsn.2015.8.4.9Abstract
In present investigation liquisolid compact technique is investigated as a tool for enhanced dissolution of poorly water-soluble drug Ketoconazole. The liquisolid tablets were formulated with liquid medications, namely Propylene Glycol (PG) drug concentrations, 60% w/w, 70% w/w and 80% w/w. Avicel pH102 was used as a carrier material, Aerosil 200 as a coating material and Sodium starch glycollate as a super-disintegrant. Quality control tests, such as uniformity of tablet weight, uniformity of drug content, tablet hardness, friability test, disintegration and dissolution tests were performed to evaluate prepared tablets. For further confirmation of results the liquisolid compacts were evaluated by XRD and FTIR studies to prove that, solubility of Ketoconazole has been increased by liquisolid compact technique. From the results obtained, it was be speculated that such systems exhibit enhanced drug release profiles due to increased wetting properties and surface of drug available for dissolution. As liquisolid compacts demonstrated significantly higher drug release rates, in PG as compared to directly compressible tablets and conventional wet granulation, we lead to conclusion that it could be a promising strategy in improving the dissolution of poor water soluble drugs and formulating immediate release solid dosage forms.
Downloads
Metrics
Keywords:
Liquisolid compact, liquid medication, Avicel 102, KetoconazoleDownloads
Published
How to Cite
Issue
Section
References
Barzegar JM, Javadzadeh Y, Nokhodchi A and Siahi-Shadbad MR (2005). Enhancement of dissolution rate of Piroxicam using liquisolid compacts. Farmaco, 60: 361-365.
El-Houssieny BM, Wahman LF and Arafa NMS (2010). Bioavailability and biological activity of liquisolid compact formula of Repaglinide and its effect on glucose tolerance in rabbits. Bio Sci Trends, 4:17-24.
Fahmy RH and Kaseem MA (2008). Enhancement of Famotidine dissolution rate through liquisolid tablet formulation. Int J Pharm Biopharm, 69: 993-1003.
Gupta G.P and Gaud RS (2002). Practical Pharmaceutics, 1st edition, CBS publishers and distributers, New Delhi p. 241-42.
ICH (2003). Harmonised Tripartite Guideline Stability Testing Of New Drug Substances and Products Q1a (R2). Current Step 4 Version. pp. 1-23.
Indian pharmacopoeia (2007). Govt. of India, Ministry of health and family welfare, Delhi: controller of India: New Delhi, India, vol-1; appendix 4.4, p. 152, 649-650.
Jarowski CI, Rohera BD and Spireas S (1992). Powdered solution technology: principles and mechanism Pharm Res, 9:1351-1358.
Javadzadeh Y, Siahi M.R., Nookhodchi A and Asnaashari S (2007). Liquisolid technique as a tool for the enhancement of poorly water soluble drugs and evaluation of their physiochemical properties. Acta Pharm, 57: 99-109.
Khaled K.A., Asiri Y.A and El-Sayed Y.M (2001). In-vivo evaluation of hydrochlorothiazide liquisolid tablet in beagles dogs. Int J Pharm, 222: 1-6.
Khalid M.E., Samy A.M and Fetouh M.I (2010). Formulation and evaluation of Rofecoxib liquisolid tablets. Int J Pharm Sci Rev Res, 3(1): 135-42.
Lachman L, Liberman H.A and Kanig J.L (1991). The theory and practice of industrial pharmacy, 3rd Ed, Bombay: Varghese publication house; pp. 296-302.
Merisko E (2002): Liversidge nanocrystals: resolving pharmaceutical formulation issues associated with poorly soluble compounds in: J.J Matty (Ed), Particles, Marcel Dekker, Orlando, 20-22.
Naseem A, Olliff C.J, Martini L.G and Lloyd A.W (2004). Effects of plasma irradiation on the wettability and dissolution of compacts of Griseofulvin. Int. J Pharm, 269: 443-450.
Nokhodchi A, Hentzschel C.M and Leopord C.S (2011). Drug release from liquisolid system: speed it up, slow it down. Expert Opin Drug Del, 8: 191-205.
Setty C.M., Prasad D.V.K. and Gupta R.M (2008). Development of fast dispersible Aceclofenac tablet: effect of functionality of super disintegrants. Indian J Pharm Sci, 70: 180-185.
Shah T.J., Amin A.F. and Parikh J.R (2007). Process optimization and characterization of poloxamer solid dispersions of a poorly water soluble drug. AAPS Pharm Sci Tech, 8: E1-E7.
Spireas S (2002). Liquisolid System and method of preparing same. U.S Patent 6423339B1, 1-32.
Staniforth J (2002). Powder flow, In: M. Aulton (Ed.). Pharmaceutics: the science of dosage form design. Churchill Livingstone Longman group, Edinburgh, 1: 197–210.
United States of Pharmacopeia (2008). The official compendia of standards. United States Pharmacopoeia and National Formulary. Asian Ed, 1: p. 266 (699), 4670(616)-4672(618).
Wells J (2002). Pharmaceutical Preformulation: The physicochemical properties of drug substances, In: Aulton M. Pharmaceutics: The science of dosage form design, 2 nd Churchill Livingstone, Longman group, Edinburgh, pp. 114-38.
Yadav V.B. and Yadav A.V (2009). Liquisolid granulation technique for tablet manufacturing: overview. Journal of Pharmacy Research, 2(4): 670-674.