Development and Validation of Stability Indicating RP - HPLC Method and Spectroscopic Method for Gadobutrol

Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/9632

Full metadata record

DC Field	Value	Language
dc.contributor.author	Chaudhary, Karanpalsingh C.	-
dc.date.accessioned	2021-01-25T07:57:50Z	-
dc.date.available	2021-01-25T07:57:50Z	-
dc.date.issued	2019-05	-
dc.identifier.uri	http://10.1.7.192:80/jspui/handle/123456789/9632	-
dc.description.abstract	Rapid and simple analytical RP-HPLC method for the determination of Gadobutrol was developed and validated as per regulatory requirements. The separation was done with a optimized chromatographic condition and retention time for Gadobutrol was found around 4.7min.the linearity range was from 50-150μg/ml. The method was validated for accuracy, precision, linearity and specificity in compliance to international regulatory guideline.	en_US
dc.publisher	Institute of Pharmacy, Nirma University, A'bad	en_US
dc.relation.ispartofseries	PDR00597;	-
dc.subject	Dissertation Report	en_US
dc.subject	Pharmaceutical Analysis	en_US
dc.subject	17MPH	en_US
dc.subject	17MPH304	en_US
dc.subject	PDR00597	en_US
dc.title	Development and Validation of Stability Indicating RP - HPLC Method and Spectroscopic Method for Gadobutrol	en_US
dc.type	Dissertation	en_US
Appears in Collections:	M.Pharm. Research Reports, Pharmaceutical Analysis

Files in This Item:

File	Description	Size	Format
PDR00597.pdf	PDR00597	18.37 MB	Adobe PDF	View/Open

IR @ Nirma University