Publication Type:

Journal Article

Source:

Journal of Applied Pharmaceutical Science, Volume 1, Number 4, p.76-78 (2011)

URL:

http://www.scopus.com/inward/record.url?eid=2-s2.0-84875831712&partnerID=40&md5=3bdda5bab32273bea9c61579f4b48dd5

Abstract:

{A new, simple, accurate, and precise high-performance thin-layer chromatographic (HPTLC) method has been established for quantitative analysis of valsartan in tablet formulations. Standard and sample solutions of valsartan were applied to precoated silica gel G 60 F254 HPTLC plates and the plates were developed with chloroform: acetonitrile: toluene: glacial acetic acid, in the ratio 1:8:1:0.1 (v/v) (v/v), as mobile phase. UV detection was performed at 254 nm. The retention factors of valsartan was 0.65. The calibration plot for Valsartan standard was linear with r =0.9999

Notes:

cited By (since 1996)0

Cite this Research Publication

D. G. Ta Parambi, Mathew, Mb, and Ganesan, Vc, “Quantitative analysis of valsartan in tablets formulations by high performance thin-layer chromatography”, Journal of Applied Pharmaceutical Science, vol. 1, pp. 76-78, 2011.