A stability indicating method development and validation for separation of process related impurities and characterization of unknown impurities of tyrosine kinase inhibitor Nilotinib by RP-HPLC, NMR spectroscopy and ESI-MS

Rp Hplc ◽

RP-HPLC Stability Indicating Method Development and Validation for Simultaneous Determination of Grazoprevir and Elbasvir

Chemistry Africa ◽

10.1007/s42250-021-00253-9 ◽

2021 ◽

Author(s):

Aymen Labidi ◽

Sami Jebali ◽

Mehdi Safta ◽

Latifa Latrous El Atrache

Keyword(s):

Simultaneous Determination ◽

Method Development ◽

Stability Indicating ◽

Rp Hplc ◽

Stability Indicating Method Development and Validation for Valacyclovir in Bulk and Tablet Dosage Form by Rp-Hplc

Journal of Complementary Medicine Research ◽

10.5455/jcmr.2021.12.04.05 ◽

2021 ◽

Vol 12 (4) ◽

pp. 30

Author(s):

VAIJINATH DIGGE ◽

S PATIL ◽

C PANCHAL

Keyword(s):

Dosage Form ◽

Method Development ◽

Stability Indicating ◽

Rp Hplc ◽

Development And Validation ◽

Tablet Dosage

Forced Degradation and Stability Indicating Method Development and Validation of Ratinovir by RP-HPLC In Bulk and Pharmaceutical Dosage Form

American Journal of PharmTech Research ◽

10.46624/ajptr.2018.v8.i2.015 ◽

2018 ◽

Vol 8 (2) ◽

pp. 196-203

Author(s):

Merugu Manasa P. ◽

Siva Kumar N. ◽

Sahani N. ◽

Sujatha P. ◽

Sahithi .

Keyword(s):

Dosage Form ◽

Method Development ◽

Forced Degradation ◽

Stability Indicating ◽

Rp Hplc ◽

Stability Indicating Method Development and Validation for Simultaneous Estimation of the Netupitant and Palonosetron in Bulk and Pharmaceutical Dosage Form by RP-HPLC

World Journal of Pharmaceutical Sciences ◽

10.54037/wjps.2022.100112 ◽

2022 ◽

Vol 10 (01) ◽

pp. 113-120

Author(s):

Harshini Gandla ◽

M. Ajitha

Keyword(s):

Dosage Form ◽

Method Development ◽

Simultaneous Estimation ◽

Stability Indicating ◽

Rp Hplc ◽

Stability Indicating Method Development and Validation for the Estimation of Rotigotine by Rp-Hplc in Bulk and Pharmaceutical Dosage form

Oriental Journal Of Chemistry ◽

10.13005/ojc/310486 ◽

2015 ◽

Vol 31 (4) ◽

pp. 2499-2505 ◽

Cited By ~ 1

Author(s):

P Swarupa ◽

D Krishna ◽

K. R. S Prasad ◽

K Babu

Keyword(s):

Dosage Form ◽

Method Development ◽

Stability Indicating ◽

Rp Hplc ◽

Simultaneous, Stability Indicating Method Development and Validation for Related Compounds of Ibuprofen and Paracetamol Tablets by RP-HPLC Method

Journal of Chromatography & Separation Techniques ◽

10.4172/2157-7064.1000155 ◽

2012 ◽

Vol 03 (08) ◽

Cited By ~ 1

Author(s):

Gnana Raja M

Keyword(s):

Method Development ◽

Hplc Method ◽

Stability Indicating ◽

Rp Hplc ◽

Simultaneous Stability ◽

Development And Validation ◽

Related Compounds

Development and validation of RP-HPLC method for the determination of Pazopanib Hydrochloride (A tyrosine kinase inhibitor) in pharmaceutical dosage form

Research Journal of Pharmacy and Technology ◽

10.5958/0974-360x.2021.00273.0 ◽

2021 ◽

Vol 14 (3) ◽

pp. 1549-1554

Author(s):

P. Ravi Sankar ◽

K. Saisneha Latha ◽

A. Bhavani Sailu ◽

SK. Taheera ◽

B. Madhuri

Keyword(s):

Tyrosine Kinase ◽

Tyrosine Kinase Inhibitor ◽

Dosage Form ◽

Kinase Inhibitor ◽

Hplc Method ◽

Rp Hplc ◽

Stability indicating method development and validation of semaglutide by RP-HPLC in pharmaceutical substance and pharmaceutical product

Research Journal of Pharmacy and Technology ◽

10.5958/0974-360x.2021.00247.x ◽

2021 ◽

Vol 14 (3) ◽

pp. 1385-1389

Author(s):

Merugu Manasa ◽

Vijey M Aanandhi

Keyword(s):

Method Development ◽

Pharmaceutical Product ◽

Pharmaceutical Substance ◽

Stability Indicating ◽

Rp Hplc ◽

RP-HPLC separation and ESI-MS, 1H, and 13C NMR characterization of forced degradants including process related impurities of carisbamate: Method development and validation

Journal of Pharmaceutical and Biomedical Analysis ◽

10.1016/j.jpba.2013.01.001 ◽

2013 ◽

Vol 77 ◽

pp. 49-54 ◽

Cited By ~ 5

Author(s):

Ramisetti Nageswara Rao ◽

Kuntamukkala Ramakrishna ◽

Bompelli Sravan ◽

Kondapalli Santhakumar

Keyword(s):

13C Nmr ◽

Method Development ◽

Hplc Separation ◽

1H And 13C Nmr ◽

Related Impurities ◽

Rp Hplc ◽

Nmr Characterization ◽

A Rapid RP‐HPLC Stability Indicating Method Development and Validation of Moxifloxacin Hydrochloride Related Substances in Finished Dosage Forms

Biomedical Chromatography ◽

10.1002/bmc.5192 ◽

2021 ◽

Author(s):

Krishna Rao Vankalapati ◽

Pallavi Algete ◽

Sathyanarayana Boodida

Keyword(s):

Method Development ◽

Dosage Forms ◽

Stability Indicating ◽

Related Substances ◽

Rp Hplc ◽