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- W2372213006 abstract "OBJECTIVE:To determine the in vitro dissolution of different batches of nifedipine sustained-release tablet purchased by the General Hospital of Air Force of PLA for reference of evaluation and drug quality control.METHODS:With diluted hydrochloric acid as solvent,the in vitro dissolution of different batches of nifedipine sustained-release tablet was determined by spectrophotometry.RESULTS:The dissolution of different batches of nifedipine dissolution purchased by the General Hospital of Air Force of PLA was up to the standard of Drug Quality in China.CONCLUSION:The quality of nifedipine sustained-release tablet purchased by the General Hospital of Air Force of PLA was qualified which thus can be used clinically in this hospital." @default.
- W2372213006 created "2016-06-24" @default.
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- W2372213006 date "2013-01-01" @default.
- W2372213006 modified "2023-09-25" @default.
- W2372213006 title "Determination of Dissolution of Nifedipine Sustained Release Tablet by UV Spectrophotometry" @default.
- W2372213006 hasPublicationYear "2013" @default.
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