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Development and validation of an HPLC–MS/MS method to determine clopidogrel in human plasma
A quantitative method for clopidogrel using online-SPE tandem LC–MS/MS was developed and fully validated according to the well-established FDA guidelines. The method achieves adequate sensitivity for pharmacokinetic studies, with lower limit of quantifications (LLOQs) as low as 10 pg/mL. Chromatogra...
Tallennettuna:
| Julkaisussa: | Acta Pharm Sin B |
|---|---|
| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Elsevier
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4724691/ https://ncbi.nlm.nih.gov/pubmed/26904399 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.apsb.2015.11.001 |
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