Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/11199
Title: Development and validation of analytical methods for quantification of new drug molecules by using high performance liquid chromatography
Researcher: Mogili Rama Kotaiah
Guide(s): Chandra Sekhar, K B
Babu Rao, Ch
Keywords: HPLC-MS/MS
Quantification of new drug molecules
Upload Date: 13-Sep-2013
University: Jawaharlal Nehru Technological University, Anantapuram
Completed Date: 19.09.2011
Abstract: Analytical method development and validation is a good research in the field of pharmaceutical analysis utilized to determine the drug content in bulk , pharmaceutical dosage forms and in biological fluids like blood serum, urine etc in view of the industrial scenario and literature, by using spectral and chromatographic techniques, revealed the utility of analytical instruments like HPLC, HPTLC and LC MS for the quantification of API s at greater accuracy and precision in quantification of drugs in formulation and in biological fluids even at low concentration. newlineDetermination of Active medicament in terms of purity is essential in the department of quality control and quality assurance for the pharmaceutical dosage form, prior to its entry into market. Now days, potency of the drugs and efficacy are playing major role in patient compliance during therapy. Hence, No matter the therapeutic agent present as individual or in the combination with other drugs, the amount of active ingredient at individual dose should be complied as per posology direction in order to achieve efficacy. However, in recent decades there are lot of analytical methods have been established for the determination of medicament in quality control and quality assurance aspects. newlineThere is a rapid advancement and developments in the field of pharmaceutical analysis where sensitive chromatographic and spectral techniques have been evoked for the determination of drugs in pharmaceutical dosage forms and in biological fluids in pharmaceutical industry, the analyst plays a vital role in newlineFDA approval of newer potent drugs with respect to method development, validation and determination of drugs. newlineThe main goal of this research work is selected based on the increasing needs of the pharmaceutical industry in developing suitable analytical methods. Among the various other available techniques the aim and objective of this work was focused on the modern chromatographic techniques such as HPLC-MS/MS which are accurate precise, sophisticated and are having wid
Pagination: 243
URI: http://hdl.handle.net/10603/11199
Appears in Departments:Department of Pharmaceutical Sciences

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abstract.pdfAttached File103.68 kBAdobe PDFView/Open
acknowledgement.pdf214.3 kBAdobe PDFView/Open
amisulpride...pdf484.7 kBAdobe PDFView/Open
certificate & declaration.pdf95.67 kBAdobe PDFView/Open
chapter - 1.pdf220.79 kBAdobe PDFView/Open
chapter -2.pdf119.83 kBAdobe PDFView/Open
chapter - 3.pdf886.79 kBAdobe PDFView/Open
chapter- 4.pdf1.02 MBAdobe PDFView/Open
chapter - 5.pdf1.01 MBAdobe PDFView/Open
chapter- 6.pdf795.76 kBAdobe PDFView/Open
chapter- 7 summary-conclusion.pdf134.24 kBAdobe PDFView/Open
contents.pdf78.16 kBAdobe PDFView/Open
east and central african journal of pharmacetical sciences.pdf103.64 kBAdobe PDFView/Open
esomoprozole.pdf278.1 kBAdobe PDFView/Open
list of publications.pdf168.08 kBAdobe PDFView/Open
list of tables & figures.pdf315.54 kBAdobe PDFView/Open
references.pdf247.03 kBAdobe PDFView/Open
rizatriptan.pdf401.51 kBAdobe PDFView/Open
title page.pdf177.14 kBAdobe PDFView/Open


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