Identification and Characterization of a New Process Related Impurity in Terbutaline Sulfate by Accurate-Mass Q-TOF LC/MS/MS and NMR
Author:
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry,Clinical Biochemistry,Biochemistry,Analytical Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s10337-021-04021-2.pdf
Reference28 articles.
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2. Daraghmeh N, Al-Omari MM, Sara Z, Badwan AA, Jaber AMY (2002) Determination of terbutaline sulfate and its degradation products in pharmaceutical formulations using LC. J Pharm Biomed Anal 29:927–937. https://doi.org/10.1016/s0731-7085(02)00216-9
3. Ahuja S, Ashman J (1990) Terbutaline sulfate. Anal Profiles Drug Subst 19:601–605
4. USP Chapters <1086> Impurities in drug substances and drug products. USP 42. The United States Pharmacopeial Convention. August 1, 2018.
5. Liu K-T, Chen C-H (2019) In: Quality management and quality control - new trends and developments. Determination of impurities in pharmaceuticals: why and how. IntechOpen. https://doi.org/10.5772/intechopen.83849
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