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Original Articles

System Suitability in an Optimized HPLC System

Pages 3045-3060 | Published online: 23 Oct 2006

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E. Marengo, M. C. Gennaro, V. Gianotti & S. Angelino. (2001) A TEST OF ROBUSTNESS IN IIR-RP-HPLC SEPARATION OF NINE PRIORITY POLLUTANT PHENOLS. Journal of Liquid Chromatography & Related Technologies 24:3, pages 341-353.
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DennisR. Jenke. (1996) Chromatographic Method Validation: A Review of Current Practices and Procedures. III. Ruggedness, Re-Validation and System Suitability. Journal of Liquid Chromatography & Related Technologies 19:12, pages 1873-1891.
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Articles from other publishers (17)

Rupali Mahajan, Aman Bishnani, Rekha Sapkal, Amol G. Dikundwar, Samanthula Gananadhamu & Amit Asthana. (2024) Integrative analysis of tepotinib forced degradation: Combining in‐silico and liquid chromatography‐quadrupole time‐of‐flight‐tandem mass spectrometry approaches for structural elucidation. SEPARATION SCIENCE PLUS 7:4.
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Kimber L. Barnett, Brent Harrington & Timothy W. Graul. 2023. Liquid Chromatography. Liquid Chromatography 821 843 .
Shaik Khaja Moinuddin, Rahul L Gajbhiye, Pakhuri Mehta, Bhaskar Sarmah, Upadhyayula Suryanarayana Murty, V Ravichandiran, Pavan Kumar Samudrala, Amit Alexander & Pramod Kumar. (2022) UHPLC-DAD Method Development and Validation: Degradation Kinetic, Stress Studies of Farnesol and Characterization of Degradation Products Using LC-QTOF-ESI-MS with in silico Pharmacokinetics and Toxicity Predictions . Journal of Chromatographic Science 60:9, pages 817-831.
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Vaibhav S. Adhao, Suraj R. Chaudhari, Jaya P. Ambhore, Sunil Sangolkar, Raju R. Thenge, Rameshwar S. Cheke & Amod S. Patil. (2021) Reverse phase-liquid chromatography assisted protocol for simultaneous determination of lamivudine and tenofovir disoproxil fumarate in combined medication used to control HIV infection: an investigative approach. Future Journal of Pharmaceutical Sciences 7:1.
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Vishwas Pardhi, Geetanjali Pant & S. J. S. Flora. (2020) RP-HPLC method development and validation for bedaquiline fumarate to evaluate its forced degradation behaviour and stability in official dissolution media. Future Journal of Pharmaceutical Sciences 6:1.
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Saniye Özcan, Serkan Levent, Aysun Geven, Yusuf Özkay & Nafiz Öncü Can. (2020) Stability-indicating LC-MS/MS and LC-DAD methods for robust determination of tasimelteon and high resolution mass spectrometric identification of a novel degradation product. Journal of Pharmaceutical and Biomedical Analysis 191, pages 113490.
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Telma Encarnação, António Aguiar, Cátia Palito, Alberto A.C.C. Pais, Maria G. Campos, Abílio J.F.N. Sobral & Hugh D. Burrows. (2020) Development and validation of a RP-HPLC method for the simultaneous analysis of paracetamol, ibuprofen, olanzapine, and simvastatin during microalgae bioremediation. MethodsX 7, pages 101083.
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Pulok K. Mukherjee. 2019. Quality Control and Evaluation of Herbal Drugs. Quality Control and Evaluation of Herbal Drugs 421 458 .
Kimber L. Barnett, Brent Harrington & Timothy W. Graul. 2017. Liquid Chromatography. Liquid Chromatography 533 552 .
C. Vitorino, J. J. Sousa & A. A. C. C. Pais. (2013) A rapid reversed-phase HPLC method for the simultaneous analysis of olanzapine and simvastatin in dual nanostructured lipid carriers. Analytical Methods 5:19, pages 5058.
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K.L. Barnett, B. Harrington & T.W. Graul. 2013. Liquid Chromatography. Liquid Chromatography 57 73 .
Alison E. Bretnall & Graham S. Clarke. 2011. Handbook of Modern Pharmaceutical Analysis. Handbook of Modern Pharmaceutical Analysis 429 457 .
M. Ilias Jimidar, Patrick Heylen & Maurits De Smet. 2007. HPLC Method Development for Pharmaceuticals. HPLC Method Development for Pharmaceuticals 441 458 .
Michael W. Dong. 2005. Handbook of Pharmaceutical Analysis by HPLC. Handbook of Pharmaceutical Analysis by HPLC 291 301 .
Jonathan B. Crowther. 2001. Handbook of Modern Pharmaceutical Analysis. Handbook of Modern Pharmaceutical Analysis 415 443 .
P. Bruce, P. Minkkinen & M. -L. Riekkola. (1998) Practical method validation: Validation sufficient for an analysis method. Mikrochimica Acta 128:1-2, pages 93-106.
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Graham S. Clarke. (1995) The use of temperature to empirically determine system suitability validation parameters for liquid chromatography. Journal of Pharmaceutical and Biomedical Analysis 13:4-5, pages 705-709.
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