1. Talluri, M.V.N.K., K.K. Keshari, P.D. Kalariya and R. Srinivas, 2015. Selective separation and characterization of the stress degradation products of ondansetron hydrochloride by liquid chromatography with quadrupole time-of-flight mass spectrometry. J. Separation Sci., 38: 1625-1632.
   CrossRef  |  Direct Link  |  
2. Talluri, M.K., L. Khatoon, P.D. Kalariya, B.B. Chavan and S. Ragampeta, 2015. LC-MS-MS characterization of forced degradation products of fidarestat, a novel aldose reductase inhibitor: Development and validation of a stability-indicating RP-HPLC method. J. Chromatographic Sci. 10.1093/chromsci/bmv061.
   CrossRef  |  
3. Paulose, J., R.P. Achuthan, M.P.L. Linsha, G. Mathai, B. Prasanth, M.V.N.K. Talluri and R. Srinivas, 2015. Protonated N-benzyl and N-(1-phenylethyl) tyrosine amides dissociate via ion/neutral Complexes. Rapid Commun. Mass Spectrom., 29: 1577-1584.
   CrossRef  |  Direct Link  |  
4. Patel, P.N., P.D. Kalariya, M. Sharma, P. Garg, M.V. Talluri, S. Gananadhamu and R. Srinivas, 2015. Characterization of forced degradation products of pazopanib hydrochloride by UHPLC‐Q‐TOF/MS and in silico toxicity prediction. J. Mass Spectrometry, 50: 918-928.
   CrossRef  |  Direct Link  |  
5. Kumar Talluri, M.V.N., S. Dharavath, P.D. Kalariya, B. Prasanth and R. Srinivas, 2015. ESI-MS/MS Structural Characterization of alkaline and oxidative stressed degradants of Lurasidone by using LC/QTOF/MS. J. Pharm. Biomed. Anal., 105: 1-9.
6. Kumar Talluri, M.V.N., 2015. Regulatory considerations for forced degradation studies to assess the stability of drugs. Pharm. Focus Asia, 22: 18-23.
7. Kumar Talluri, M.V.N., 2015. Quality by design-a rapid and systematic approach for pharmaceutical analysis. Pharm. Focus Asia, 21: 32-36.
8. Kalariya, P.D., T.J. Reddy, M. Sharma, P. Garg, T.J. Reddy, R. Srinivas and M.V.N. Kumar Talluri, 2015. LC-QTOF-MS/MS studies for characterization of degradation products of mirabegron under stressed conditions and in silico toxicity predictions of its degradation products. RSC Adv., 5: 31024-31038.
9. Kalariya, P.D., P.N. Patel, R. Srinivas and M.V.N.K. Talluri, 2015. A quality by design approach for rapid, selective UPLC separation of dolutegravir-a novel anti-HIV drug degradation products: Characterization of hydrolytic and photolytic degradation products by UPLC-QTOF-MS/MS. New J. Chem., 39: 6303-6314.
10. Kalariya, P.D., P.N. Patel, M. Sharma, P.Garg, R. Srinivas and M.V.N.K. Talluri, 2015. Characterization of stress degradation products of blonanserin by UPLC-QTOF-tandem mass spectrometry. RSC Adv., 5: 69273-69288.
    CrossRef  |  Direct Link  |  
11. Kalariya, P.D., P.N. Patel, C.V. Swamy, R. Srinivas and M.V.N. Kumar Talluri, 2015. A validated liquid chromatography mass spectrometry method for the quantification of tinoridine hydrochloride in rat plasma and its application to pharmacokinetic studies. Anal. Methods, 7: 1965-1975.
    CrossRef  |  Direct Link  |  
12. Kalariya, P.D., M.V.N. Kumar Talluri, P.N. Patel and R. Srinivas, 2015. Identification of hydrolytic and isomeric N-oxides oxidative degradants of vilazodone by on-line LC-ESI-MS/MS and APCI-MS. J. Pharm. Biomed. Anal., 102: 353-365.
    CrossRef  |  Direct Link  |  
13. Anandgaonkar, V., A. Gupta, K. Srinivas and M.V.N. Kumar Talluri, 2015. Isolation, LC-MS/MS and 2D-NMR characterization of alkaline degradants of Tenofovir disoproxil fumarate. J. Pharm. Biomed. Anal., 107: 175-185.
    CrossRef  |  
14. Saladi, S., S. Gutala, K. Yadiki, M.K. Talluri and N. Satheeshkumar, 2014. Design and study of a HPLC method for the simultaneous estimation of two anti-diabetic drugs using a statistical approach. Anal. Methods, 6: 3291-3299.
    CrossRef  |  Direct Link  |  
15. Kumar Talluri, M.V.N.,, C. Divya, D. Shrireesha and R. Srinivas, 2014. Direct analysis in real time mass spectrometry (DART-MS): Pharmaceutical and biomedical applications. Curr. Trends Pharm. Sci., 2: 18-29.
16. Kumar Talluri, M.V.N. and C. Divya, 2014. DART-MS towards rapid analysis of samples. Ingredients South Asia, 7: 52-54.
17. Kalariya, P.D., M.V. Kumar Talluri, V.D. Gaitonde, P.S. Devrukhakar and R. Srinivas, 2014. Quality by design: A systematic and rapid liquid chromatography and mass spectrometry method for eprosartan mesylate and its related impurities using a superficially porous particle column. J. Separation Sci., 37: 2160-2171.
18. Kalariya, P.D., M.K. Talluri and S. Ragampeta, 2014. Experimental design approach for selective separation of vilazodone HCl and Its degradants by LC-PDA and characterization of major degradants by LC/QTOF-MS/MS. Chromatographia, 77: 1299-1313.
    CrossRef  |  
19. Jeengar, M.K., S. Shrivastava, K. Nair, S.R. Singareddy and U.K. Putcha et al., 2014. Improvement of bioavailability and anti-inflammatory potential of curcumin in combination with emu oil. Inflammation, 37: 2139-2155.
    CrossRef  |  Direct Link  |  
20. Kumar Talluri, M.V.N., 2013. Quality by design-approach for LC method development. Ingredients South Asia, 6: 46-50.
21. Kumar Talluri, M.V.N., 2013. Enantioselective chromatography for chirals. Ingredients South Asia, 6: 82-84.
22. Kumar Talluri, M.V.N. and P.D. Kalariya, 2013. Pharma-challenges for registration of medicines. Ingredients South Asia, 6: 38-40.
23. Kumar Talluri, M.V.N. and P. Kavya, 2013. Pharma-excipients with focus on middle East. Ingredients South Asia, 6: 32-35.
24. Talluri, M.K., A. Kalyankar and S. Ragampeta, 2012. Synchronized separation of atorvastatin-an antihyperlipidemic drug with antihypertensive, antidiabetic, antithrombotic drugs by RP-LC for determination in combined formulations. J. Pharm. Anal., 2: 285-292.
    CrossRef  |  
25. Kumar Talluri, M.V.N., M.K. Bairwa, H.H. Theja Dugga and R. Srinivas, 2012. Development and validation of RP-HPLC and ultraviolet spectrophotometric methods of analysis for simultaneous determination of paracetamol and lornoxicam in pharmaceutical dosage forms. J. Liquid Chromatography Related Technol., 35: 129-140.
    CrossRef  |  Direct Link  |  
26. Kumar Talluri, M.V.N., 2012. Recent advances in analytical methodologies for the determination of drug impurities. Pharm. Focus Asia, 16: 48-53.
27. Rao, R.N., P.K. Maurya, W.D. Vitthal and M.V.N. Kumar Talluri, 2011. Development of a molecularly imprinted polymer for selective extraction followed by zwitterionic hydrophilic interaction liquid chromatography (ZIC-HILIC) determination of 3-methylflavone-8-carboxylic acid, the main active metabolite of flavoxate in human urine. J. Separation Sci., 34: 3265-3271.
28. Rao, R.N., M.K. Talluri and P.K. Maurya, 2009. Separation of stereoisomers of sertraline and its related enantiomeric impurities on a dimethylated β-cyclodextrin stationary phase by HPLC. J. Pharm. Biomed. Anal., 50: 281-286.
    CrossRef  |  Direct Link  |  
29. Rao, R.N., M.N.K. Talluri and D.D. Shinde, 2008. Simultaneous separation and determination of coenzyme Q₁₀ and its process related impurities by NARP-HPLC and atmospheric pressure chemical ionization-mass spectrometry (APCI-MS). J. Pharm. Biomed. Anal., 47: 230-237.
    CrossRef  |  Direct Link  |  
30. Rao, R.N., M.K. Talluri, T.M. Krishna and K. Ravindranath, 2008. Continuous counter current extraction, isolation and determination of solanesol in Nicotiana tobacum L. by non-aqueous reversed phase high performance liquid chromatography. J. Pharm. Biomed. Anal., 46: 310-315.
    CrossRef  |  Direct Link  |  
31. Rao, R.N., M.K. Talluri, A.N. Raju, D.D. Shinde and G.S. Ramanjaneyulu, 2008. Development of a validated RP-LC/ESI-MS-MS method for separation, identification and determination of related substances of tamsulosin in bulk drugs and formulations. J. Pharm. Biomed. Anal., 46: 94-103.
    CrossRef  |  
32. Rao, R.N., D.D. Shinde, M.K. Talluri and S.B. Agawane, 2008. LC-ESI-MS determination and pharmacokinetics of adrafinil in rats. J. Chromatography B, 873: 119-123.
    CrossRef  |  Direct Link  |  
33. Rao, R.N., D.D. Shinde and M.V.N.K. Talluri, 2008. Enantioselective HPLC resolution of synthetic intermediates of armodafinil and related substances. J. Sep. Sci., 31: 981-989.
    CrossRef  |  Direct Link  |  
34. Kumar Talluri, M.V.N., T.N. Rao and A.S.R. Krishna Murty, 2008. Estimation of trace lead impurity in haematopoietic drug samples by flame atomic absorption spectrometry. Asian Chem. Lett., 12: 57-60.
35. Rao, R.N., D.D. Shinde and M.V.N.K. Talluri, 2007. Development and validation of a reversed phase liquid chromatographic method for separation and determination of related-substances of modafinil in bulk drugs. Talanta, 73: 407-414.
    CrossRef  |  
36. Rao, R.N. and M.V.N.K. Talluri, 2007. An overview of recent applications of Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) in determination of inorganic impurities in drugs and pharmaceuticals. J. Pharmaceut. Biomed. Anal., 43: 1-13.
    CrossRef  |  Direct Link  |  
37. Murty, A.S.R.K., U.C. Kulshresta, T.N. Rao and M.V.N.K. Talluri, 2005. Determination of heavy metals in selected drug substances by inductively coupled plasma-mass spectrometry. Indian J. Chem. Technol., 12: 229-231.
    Direct Link  |  
38. Kumar Talluri, M.V.N., N.R. Kandimalla, R. Bandu, D. Chundi, R. Marupakab and R. Srinivasa, 2004. Selective separation, detection of zotepine and mass spectral characterization of degradants by LC-MS/MS/QTOF. J. Pharm. Anal., 4: 107-116.
    CrossRef  |