Development and Validation of a Gas Chromatography Method for Quality Control of Residual Solvents in Azilsartan Bulk Drugs-Reference-Cited by-同舟云学术

Development and Validation of a Gas Chromatography Method for Quality Control of Residual Solvents in Azilsartan Bulk Drugs

Published:2016-12-23 Issue: Volume: Page:
ISSN:0021-9665
Container-title:Journal of Chromatographic Science
language:en
Short-container-title:J Chromatogr Sci

Author:

Guan Jin,Min Jie,Yan Feng,Xu Wen-Ya,Shi Shuang,Wang Si-Lin

Funder

Natural Science Foundation of Liaoning Province of China

Scientific Research Fund of Education Department of Liaoning Province

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Analytical Chemistry

Link

http://academic.oup.com/chromsci/article-pdf/55/4/393/10981018/bmw192.pdf

Reference14 articles.

1. International Conference on Harmonization (ICH) of Technical Requirements for the Registration of Pharmaceuticals for Human Use, Q3C (R5): Impurities: Guideline for Residual Solvents, Step 4, February, (2011).

2. Determination of residual solvent levels in bulk pharmaceuticals by capillary gas chromatography

3. Determination of volatile organic compounds (VOCs) from wrapping films and wrapped PDO Italian cheeses by using HS-SPME and GC/MS;Sara;Molecules,2014

4. Azilsartan Decreases Renal and Cardiovascular Injury in the Spontaneously Hypertensive Obese Rat

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Gas Chromatography-Head Space-Flame Ionization Sensor based assessment of four residuary solvents in rivaroxaban bulk medication;Research Journal of Pharmacy and Technology;2022-11-24

2. Shorter and Rugged Analytical GC Method for Residual Solvents Content in Active Pharmaceutical Ingredient;Journal of Chromatographic Science;2021-05-05