Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Sunitha Gurrala"'
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Vol 59 (2023)
Abstract The present study entails the systematic development and validation of a stability-indicating RP-HPLC method for the analysis of sitagliptin and ertugliflozin in a fixed-dose combination. Analytical quality by design (AQbD) concepts were use
Externí odkaz:
https://doaj.org/article/326e26a1435041f7ae217dfb51d70c4a
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 7, Iss 1, Pp 1-11 (2021)
Abstract Background Analytical quality by design driven HPLC method has been optimized for simultaneous estimation of dapagliflozin and saxagliptin in pharmaceutical dosage form. Response surface methodology was employed for optimization of experimen
Externí odkaz:
https://doaj.org/article/e0acc294277a445bbcc6709b10dca259
Autor:
Swathi Naraparaju, Durai Ananda Kumar Thirumoorthy, Sunitha Gurrala, Asra Jabeen, Pani Kumar D. Anumolu
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 6, Iss 1, Pp 1-8 (2020)
Abstract Background A simple and sensitive spectrophotometric method was developed for the quantitative measurement of dolutegravir in pure form and pharmaceutical formulation. The present method was based on redox reaction between dolutegravir and f
Externí odkaz:
https://doaj.org/article/25454ca146ce460394efc363355071ac
Autor:
Ramakrishna Kommana, Gouthami Kannabattula, Sunitha Gurrala, Venkat Raj Yeradesi, Panikumar Anumolu Durga
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Vol 50, Iss 4, Pp 895-901 (2014)
A simple, specific, precise, accurate, linear, rapid, economic and validated stability indicating an RP-HPLC method for the simultaneous quantification of cefepime and tazobactam in a dry injection dosage form has been developed. Separation was perfo
Externí odkaz:
https://doaj.org/article/2a8f3b7cc5c44bbfbcab4f4bc8099828
Autor:
Shiva Raj, Harika Nizampet, Sunitha Gurrala, Subrahmanyam Cvs, Swathi Naraparaju, Durga Panikumar Anumolu
Publikováno v:
Turk J Pharm Sci
OBJECTIVES: Design of experiments assisted spectrophotometric methods have been established for the quantification of saxagliptin in pharmaceutical formulation via charge transfer complexation and Schiff’s base formation. MATERIALS AND METHODS: Box
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42658870bafef849513bd798a388e33d
https://doi.org/10.4274/tjps.galenos.2021.93195
https://doi.org/10.4274/tjps.galenos.2021.93195
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 7, Iss 1, Pp 1-11 (2021)
Background Analytical quality by design driven HPLC method has been optimized for simultaneous estimation of dapagliflozin and saxagliptin in pharmaceutical dosage form. Response surface methodology was employed for optimization of experimental condi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a94e861be4182399bb7e8dbf29903452
https://doaj.org/article/e0acc294277a445bbcc6709b10dca259
https://doaj.org/article/e0acc294277a445bbcc6709b10dca259
Autor:
Rajesh Chakka, Vasavi Panchakatla, Panikumar D Anumolu, Veda Maddala, Sunitha Gurrala, Radhagayathri Achanta
Publikováno v:
INDIAN DRUGS. 58:59-61
A simple and sensitive spectrofluorimetric method has been developed for the estimation of mesalamine (MES). Linearity was obeyed in the range of 0.1-2.5 µg/mL in distilled water as solvent at an emission wavelength (λem) of 501 nm after excitation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1912f2a610d9e408362ba37c1a913c5
https://doi.org/10.53879/id.58.03.11074
https://doi.org/10.53879/id.58.03.11074
Autor:
Panikumar D Anumolu, Rajesh Chakka, Sahitya Menkana, Divya Gayathri Mangipudi, Archana Gellaboina, Sunitha Gurrala
Publikováno v:
Turkish Journal of Pharmaceutical Sciences, Vol 16, Iss 4, Pp 410-415 (2019)
Turkish Journal of Pharmaceutical Sciences
Turkish Journal of Pharmaceutical Sciences
Objectives Simple, specific, accurate, precise, sensitive, and cost effective spectrophotometric methods were developed and validated for quantification of the drugs lornoxicam (LOR) and mesalamine (MES) in pure form and in pharmaceutical formulation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0b89414630808d5d231f4c2c121f9e5
https://doaj.org/article/2c88e85df9934b64a3f1d4db2db2004c
https://doaj.org/article/2c88e85df9934b64a3f1d4db2db2004c
Publikováno v:
Indian Journal of Pharmaceutical Education and Research. 53:s699-s709
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ffacedf0b4118d0a2f8ea91be5eeb0d
https://doi.org/10.5530/ijper.53.4s.167
https://doi.org/10.5530/ijper.53.4s.167
Autor:
Sunitha Gurrala, Panukumar Durga Anumolu, Santoshi Vani Polisetty, Anjana Ravindran, Radhagayathri Achanta, Subrahmanyam Chavali Venkata Satya
Publikováno v:
Turkish Journal of Pharmaceutical Sciences, Vol 16, Iss 1, Pp 62-68 (2019)
Turkish Journal of Pharmaceutical Sciences
Turkish Journal of Pharmaceutical Sciences
Objectives: Nowadays, the market is flooded with combinations of drugs in various dosage forms, but there is a lack of official methods to quantify them. A single dissolution test method for the analysis of combined dosage form is preferred for simpl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63cce5347ca4aa0c4a042734ed92c15a
https://doaj.org/article/5d0239021721405db1cdcf5b219f3cfe
https://doaj.org/article/5d0239021721405db1cdcf5b219f3cfe