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Ramalingam Peraman

Researcher at Gulf Medical University

Publications -  39
Citations -  476

Ramalingam Peraman is an academic researcher from Gulf Medical University. The author has contributed to research in topics: Chemistry & Medicine. The author has an hindex of 8, co-authored 33 publications receiving 326 citations.

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Analytical quality by design: a tool for regulatory flexibility and robust analytics.

TL;DR: This paper has been communicated to discuss different views of analytical scientists about implementation of AQbD in pharmaceutical quality system and also to correlate with product quality by design and pharmaceutical analytical technology (PAT).
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Polyphenolic Nutrients in Cancer Chemoprevention and Metastasis: Role of the Epithelial-to-Mesenchymal (EMT) Pathway.

TL;DR: The role of polyphenols in attenuating EMT-mediated cancer progression and metastasis is analyzed and the most important polyphenol subclasses and members of the poly phenols in reversing metastasis and targeting EMT are discussed.
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Stability-Indicating RP-HPLC Method for Simultaneous Determination of Metformin Hydrochloride and Sitagliptin Phosphate in Dosage Forms

TL;DR: In this article, a new stability-indicating high-performance liquid chromatographic method has been developed for simultaneous analysis of metformin hydrochloride (MET) and sitagliptin phosphate (SIT) in pharmaceutical dosage forms.
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Re-engineering nalidixic acid’s chemical scaffold: A step towards the development of novel anti-tubercular and anti-bacterial leads for resistant pathogens

TL;DR: The work on re-engineering nalidixic acid's chemical scaffold for newer leads is reported, it was evident that molecule with quinoxaline linked azide as side chain served as antitubercular lead whilst molecule with oxadiazole or triazole linked qu inoxaline side chainserved as anti-bacterial lead.
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Analytical Quality by Design Approach in RP-HPLC Method Development for the Assay of Etofenamate in Dosage Forms.

TL;DR: The reversed phase high performance liquid chromatographic method for routine analysis of etofenamate in dosage form has been optimized using analytical quality by design approach and validated and verified for targeted method performances, robustness and system suitability during method transfer.