in dissolution in one tablets two molecule one is losartan & second is HCTZ losartam is complies in s1 stage & hctz is complies in s2 stage then how to report result losartan s1 stage result or losartan s2 stage result
1 2049If we have 120 minutes run time method for HPLC and you wan to decrease the Run time so what should you do??
6 11895Wath is the differenc between two column HPLC wich have the samme support , lenth , pore size, etc.. But different name .for exemple : Spherisorb / lichrosorb
NDA,
2 7029How you will select column for HPLC development depends on nature of compound and how it will work explain in brief?
3 9421The boiling point of 1,3 butadiene is -4.4 DC & the boiling point of Pentane is 36.1 DC. Then how come Pentane elute before 1,3 BD in GC analysis?
1 4654Post New Analytical Chemistry Questions
How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
could negative ions be produced by bombardment process in mass spectrometry?
effect of pore size, pore volume, partical size, column length, carbon load on retention time? what is carbon load? what is the use?
why we use a particular hplc column for a particular compound give reasons?please
How much is the standard area for glc analysis
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
calibrtion procedue of LC-MS
How you develop a method in HPLC?
For limit test of heavy metals in BP, Method C require that the substance is ignited at a temperature not exceeding 800 °C. Why confines such the temperature?
why xterra column require to use at higher ph?
why cone formation during dissolution?
what are risk assement in the analytical qbd?
What is dose dumping? why require to do?
how require to set assay concentration for standard and sample?
CAN WE DETERMINE THE PEAK PURITY IN GAS CHROMATOGRAPHY ANALYSIS?