| Type of Material: | Thesis |
| Title: | Analytical method development and validation on Eslicarbazepine acetate, Asnapine maleate and key Intermediate of some drug substances |
| Researcher: | Srinivas, Mudigonda |
| Guide: | Mukkanti, K. | Sait, Shakil |
| Department: | Department of Chemistry |
| Publisher: | Jawaharlal Nehru Technological University, Hyderabad |
| Place: | Hyderabad |
| Year: | 2013 |
| Language: | English |
| Subject: | Analytical | Development | Drugs | Eslicarbazepine | Substances |
| Dissertation/Thesis Note: | PhD; Department of Chemistry, Jawaharlal Nehru Technological University, Hyderabad, Hyderabad; 2013 |
| Fulltext: | Shodhganga |
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| 001 | 454100 | |
| 003 | IN-AhILN | |
| 005 | 2024-07-22 16:48:40 | |
| 008 | __ | 240722t2013||||ii#||||g|m||||||||||eng|| |
| 035 | __ | |a(IN-AhILN)th_454100 |
| 040 | __ | |aJNTU_500028|dIN-AhILN |
| 041 | __ | |aeng |
| 100 | __ | |aSrinivas, Mudigonda|eResearcher |
| 110 | __ | |aDepartment of Chemistry|bJawaharlal Nehru Technological University, Hyderabad|dHyderabad|ein|0U-0017 |
| 245 | __ | |aAnalytical method development and validation on Eslicarbazepine acetate, Asnapine maleate and key Intermediate of some drug substances |
| 260 | __ | |aHyderabad|bJawaharlal Nehru Technological University, Hyderabad|c2013 |
| 300 | __ | |a230 p.|dNone|c- |
| 500 | __ | |a- |
| 502 | __ | |cDepartment of Chemistry, Jawaharlal Nehru Technological University, Hyderabad, Hyderabad|d2013|bPhD |
| 520 | __ | |aThe present research carried out to establish new analytical methods for active pharmaceutical ingredients (API) and the key intermediates of API in estimation of related substances and assay of new compounds and their dosage forms. The proficient research work has been divided in to six chapters. The first chapter consists of a brief introduction on the need for development of new analytical methods for related components estimation, source of impurities in pharmaceutical substances, requirement for control of impurities, pharmacopeial norms, ICH quality guidelines, FDA recommendations, multi-detection system composed of ultraviolet, evaporative light scattering detection for the analysis of pharmaceuticals by liquid chromatography, new technology of stationary phases, various hyphenated techniques, approaches for development of stability indicating methods with LC contents of method validation parameters and discussion on how develop a new method approaches on the general methodology for LC analysis. The |
| 653 | __ | |aAnalytical |
| 653 | __ | |aDevelopment |
| 653 | __ | |aDrugs |
| 653 | __ | |aEslicarbazepine |
| 653 | __ | |aSubstances |
| 700 | __ | |aMukkanti, K.|eGuide |
| 700 | __ | |aSait, Shakil|eCo-Guide |
| 856 | __ | |uhttp://shodhganga.inflibnet.ac.in/handle/10603/19965|yShodhganga |
| 905 | __ | |afromsg |
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