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Development and validation of a stability-indicating RP–HPLC method for estimation of atazanavir sulfate in bulk
A stability-indicating reverse phase–high performance liquid chromatography (RP–HPLC) method was developed and validated for the determination of atazanavir sulfate in tablet dosage forms using C(18) column Phenomenix (250 mm×4.6 mm, 5 μm) with a mobile phase consisting of 900 mL of HPLC grade metha...
Gorde:
| Argitaratua izan da: | J Pharm Anal |
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| Egile Nagusiak: | , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Xi'an Jiaotong University
2017
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5686860/ https://ncbi.nlm.nih.gov/pubmed/29404029 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jpha.2013.12.002 |
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