17
2021
In vitro Dissolution Profile at Different Biological pH Conditions of Hydroxychloroquine Sulfate Tablets Is Available for the Treatment of COVID-19

Naresh Kumar Katari , Murtaza M. Tambuwala , Kamal Dua , Thirupathi Dongala
Frontiers in Molecular Biosciences 7 613393 -613393

20
2021
A simple and rapid HPLC method for determination of parabens and their degradation products in pharmaceutical dosage forms.

Thirupathi Dongala , Lakshmi Narasimha Rao Katakam , Santhosh Kumar Ettaboina
Biomedical Chromatography

2021
QbD based development of HPLC method for simultaneous quantification of Telmisartan and Hydrochlorothiazide impurities in tablets dosage form.

Ashok K. Palakurthi , Thirupathi Dongala , Lakshmi Narasimha R. Katakam
Practical Laboratory Medicine 21

25
2020
Estimation of ramipril and telmisartan in human plasma by LC–MS/MS: Application in pharmacokinetic study

Ashok Kumar Palakurthi , Thirupathi Dongala , Siva Sankara Rao Yadlapalli
SEPARATION SCIENCE PLUS 3 ( 6) 191 -199

2020
A simple high‐performance liquid chromatography method development for Carbidopa and Levodopa impurities: Evaluation of risk assessment before method validation by Quality by Design approach

Velusamy B. Subramanian , Naresh Konduru , Naresh Kumar Katari , Thirupathi Dongala
SEPARATION SCIENCE PLUS 3 ( 11-12) 530 -539

16
2020
RP-HPLC Stability Indicating Method Development and Validation of Pseudoephedrine Sulfate and Related Organic Impurities in Tablet Dosage Forms, Robustness by QbD Approach

Thirupathi Dongala , Lakshmi Narasimha Rao Katakam , Ashok Kumar Palakurthi , Naresh Kumar Katari
Analytical Chemistry Letters 9 ( 5) 697 -710

9
2019
Stability-indicating HPLC method for simultaneous quantification of 14 impurities in excedrin tablet formulations and identification of new impurity by LC-MS in accelerated stability studies.

Thirupathi Dongala , Naresh Kumar Katari , Ashok Kumar Palakurthi , Sreekantha B. Jonnalagadda
Biomedical Chromatography 33 ( 10)

13
2019
Development and validation of a generic RP‐HPLC PDA method for the simultaneous separation and quantification of active ingredients in cold and cough medicines.

Thirupathi Dongala , Naresh Kumar Katari , Ashok Kumar Palakurthi , Sreekantha B. Jonnalagadda
Biomedical Chromatography 33 ( 11)

12
2019
Stability‐indicating RP‐HPLC method development and validation for determination of nine impurities in apixaban tablet dosage forms. Robustness study by quality by design approach

Velusamy B. Subramanian , Naresh Kumar Katari , Thirupathi Dongala , Sreekantha B. Jonnalagadda
Biomedical Chromatography 34 ( 1)

8
2020
QbD-based development of an extraction procedure for simultaneous quantification of telmisartan, amlodipine besylate and chlorthalidone in combination complex matrix formulation.

Ashok Kumar Palakurthi , Thirupathi Dongala , Ravindra Kumar Yalavarthi , Jayashree Anireddy
Biomedical Chromatography 34 ( 2) 4755

4
2020
A novel UPLC-PDA isocratic method for the quantification fulvestrant in oil-based pre-filled syringe injection matrix formulations

Thirupathi Dongala , Ashok Kumar Palakurthi , Yashodharani Vytla , Naresh Kumar Katari
Journal of Analytical Science and Technology 10 ( 1) 1 -12

16
2019
Quantitative estimation of Fulvestrant injection 505(j) composition and impurities profile by capillary gas chromatography and HPLC-PDA techniques

Thirupathi Dongala , Naresh Kumar Katari , Vishnu Murthy Marisetti , Sreekantha B. Jonnalagadda
Journal of The Iranian Chemical Society 18 ( 6) 1 -12

2021