Effect of column length and elution mechanism on the separation of proteins by reversed-phase high-performance liquid chromatography

1992 ◽  
Vol 625 (2) ◽  
pp. 217-222 ◽  
Author(s):  
Junichi Koyama ◽  
Junko Nomura ◽  
Yoshihiro Shiojima ◽  
Yutaka Ohtsu ◽  
Izumi Horii
1988 ◽  
Vol 443 ◽  
pp. 381-397 ◽  
Author(s):  
K.D. Nugent ◽  
W.G. Burton ◽  
T.K. Slattery ◽  
B.F. Johnson ◽  
L.R. Snyder

1981 ◽  
Vol 101 (3) ◽  
pp. 279-282 ◽  
Author(s):  
NAOKI ASAKAWA ◽  
MASANORI TSUNO ◽  
TEIICHI HATTORI ◽  
MASAAKI UEYAMA ◽  
AISHIN SHINODA ◽  
...  

1981 ◽  
Vol 101 (8) ◽  
pp. 708-712 ◽  
Author(s):  
NAOKI ASAKAWA ◽  
MASANORI TSUNO ◽  
TEIICHI HATTORI ◽  
MASAAKI UEYAMA ◽  
AISHIN SHINODA ◽  
...  

1988 ◽  
Vol 443 ◽  
pp. 363-379 ◽  
Author(s):  
W.G. Burton ◽  
K.D. Nugent ◽  
T.K. Slattery ◽  
B.R. Summers ◽  
L.R. Snyder

Author(s):  
Raju Chandra ◽  
Manisha Pant ◽  
Harchan Singh ◽  
Deepak Kumar ◽  
Ashwani Sanghi

A reliable and reproducible reversed-phase high performance liquid chromatography (RP-HPLC) was developed for the quantitative determination of Remipril drug content from marketed bulk tablets. The active ingredient of Remipril separation achieved with C18 column using the methanol water mobile phase in the ratio of 40:60 (v/v). The active ingredient of the drug content quantify with UV detector at 215 nm. The retention time of Remipril is 5.63 min. A good linearity relation (R2=0.999) was obtained between drug concentration and average peak areas. The limit of detection and limit of quantification of the instrument were calculated 0.03 and 0.09 µg/mL, respectively. The accuracy of the method validation was determined 102.72% by recoveries method.


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