Professional Documents
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Asian Journal
of
PHARMACEUTICAL RESEARCH
Journal homepage: - www.ajprjournal.com
P a g e | 127
Asian J. Pharm. Res. Vol 5, Issue 2, 126-127, 2015.
Values
241
2-10
1.212 10-2
5.2229 104
0.152
0.046
0.999
*Amount found
mg
49.9
99.99
CONCLUSION
The developed UV spectroscopic method is
precise and accurate. This method can be applied for
routine analysis of Vilazodone from tablet dosage form.
*Percentage recovery
100.13
ACKNOWLEDGEMENT
The Authors are thankful to the management
SIMS Group of Institutions, Guntur, for providing
necessary facilities to carry out the research work.
REFERENCES
1. Parameswara Reddy B, Pramod N, Venkateswararao P, Sudhakar babu AMS. Method development and validation for the
assay of vilazodone in bulk and formulation by using RPHPLC technique, International Journal of Biological
&Pharmaceutical Research, 3(6), 2012, 789-795.
2. Kalariya PD, Talluri MV, Patel PN, Srinivas R. Identification of hydrolytic and isomeric N-oxide degradants of
vilazodone by on line LC-ESI-MS/MS and APCI-MS, Journal of Pharmaceutical and Biomedical Analysis, 102, 2015,
353-365.
3. Zeng LL, Sun LL, Zou Q, Zhou F, Wei P, Ouyang PK. Bioavailability comparison of a new form of vilazodone XVII to
IV in beagles using liquid chromatography/mass spectrometry, Biomedical Chromatography, 28(12), 2014, 1738-1743.