| Type of Material: | Thesis |
| Title: | Spectroscopic and chromatographic method development and validation for the estimation of antimicrobial agents and their combinations in synthetic mixture and assay method for the pharmaceutical dosage forms |
| Researcher: | Pandya, Yogi U |
| Guide: | Patel, Samixa |
| Department: | Pharmacy |
| Publisher: | Atmiya University |
| Place: | Rajkot |
| Year: | 2022 |
| Language: | English |
| Subject: | Stability | Stress Testing | Analytical Method Development | Antimicrobial Drugs | Clinical Pre Clinical and Health | In-vitro Dissolution | Pharmacology and Pharmacy | Pharmacology and Toxicology | RP-HPLC, | Pharmacy | Medical and Health Sciences |
| Dissertation/Thesis Note: | PhD; Pharmacy, Atmiya University, Rajkot; 2022 |
| Fulltext: | Shodhganga |
| 003 | IN-AhILN | |
| 005 | 2026-10-08 17:25:46 | |
| 008 | __ | 261008t2022||||ii#||||g|m||||||||||eng|| |
| 035 | __ | |a(IN-AhILN)th_464033 |
| 040 | __ | |dIN-AhILN|aATMI_360005 |
| 041 | __ | |aeng |
| 100 | __ | |eResearcher|aPandya, Yogi U |
| 110 | __ | |aPharmacy|0U-0967|dRajkot|bAtmiya University|ein |
| 245 | __ | |aSpectroscopic and chromatographic method development and validation for the estimation of antimicrobial agents and their combinations in synthetic mixture and assay method for the pharmaceutical dosage forms |
| 260 | __ | |aRajkot|c2022|bAtmiya University |
| 300 | __ | |a361|dCD|cA4 Size |
| 502 | __ | |bPhD|d2022|cPharmacy, Atmiya University, Rajkot |
| 518 | __ | |oDate of Award|d2022 |
| 518 | __ | |d2019|oDate of Registration |
| 518 | __ | |d2022|oDate of Completion |
| 520 | __ | |aBackground: The present research work comprises of the Stability Indicating RP-HPLC analytical method development and validation for selected drugs andamp; pharmaceutical dosage forms belonging to the Antimicrobial class. The antimicrobial drugs are frequently upgraded and newly approved drugs by FDA and CDSCO are available in the markets in the form of new dosage forms as well as combined dosage forms with other drugs. For the newly approved drugs and their drug combinations, the Stability analytical methods are not available in pharmacopoeia and even dissolution methods for the solid dosage forms are also not available for the combined dosage forms. Hence there is a need of newer analytical methods, as well as stability, indicating rapid- RP-HPLC technique and it is optimised for, analysis of drug during different stress conditions as well as in pure from and solid dosage form along with the in-vitro dissolution studies carried out for solid dosage forms. Aim: The main aim of the present research work to |
| 650 | __ | |aPharmacy|2UGC |
| 650 | __ | |aMedical and Health Sciences|2AIU |
| 653 | __ | |aStability |
| 653 | __ | |aStress Testing |
| 653 | __ | |aAnalytical Method Development |
| 653 | __ | |aAntimicrobial Drugs |
| 653 | __ | |aClinical Pre Clinical and Health |
| 653 | __ | |aIn-vitro Dissolution |
| 653 | __ | |aPharmacology and Pharmacy |
| 653 | __ | |aPharmacology and Toxicology |
| 653 | __ | |aRP-HPLC, |
| 700 | __ | |eGuide|aPatel, Samixa |
| 856 | __ | |uhttp://shodhganga.inflibnet.ac.in/handle/10603/449869|yShodhganga |
| 905 | __ | |afromsg |
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