+Facile extraction of azide in sartan drugs using magnetized anion-exchange metal-organic frameworks prior to ion chromatography
Journal of Chromatography A, ISSN: 0021-9673, Vol: 1514, Page: 29-35
2017
- 11Citations
- 16Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations11
- Citation Indexes11
- 11
- CrossRef6
- Captures16
- Readers16
- 16
Article Description
Quaternary amine functionalized metal-organic framework MIL-101(Cr) (MIL-101(Cr)-NMe 3 ) was prepared as the sorbent for the magnetic solid-phase extraction (MSPE) of azide from sartan drugs before ion chromatography determination. Magnetization of MIL-101-NMe 3 were achieved concurrently by adding MIL-101-NMe 3 and Fe 3 O 4 @SiO 2 to the sample solution under ultrasonication. The prepared Fe 3 O 4 @SiO 2 /MIL-101-NMe 3 gave the adsorption capacity of 37.5 mg g −1. The developed method had a detection limit of 0.24 μg L −1 and quantitation limit of 0.79 μg L −1 for azide. The relative standard deviations for the intra-day retention time and peak area were 0.52% and 0.36% (n = 5), respectively. The developed method was successfully applied for the determination of azide in sartan drugs with the recoveries from 96.5% to 100.5%.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0021967317310105; http://dx.doi.org/10.1016/j.chroma.2017.07.027; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85026657647&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/28780139; https://linkinghub.elsevier.com/retrieve/pii/S0021967317310105; https://dx.doi.org/10.1016/j.chroma.2017.07.027
Elsevier BV
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