Answer Posted / harsh
L1 columns coated with octadecyl silane bonded to porous
silica, 3 to 10 µm
where L7 columns coated with octylsiliane bonded to totally
porous microsilica particles 3 to 10 µm
l1 gives better resolution then l7.
l1 have more carbon loading so good for resolution
| Is This Answer Correct ? | 9 Yes | 1 No |
Post New Answer View All Answers
how you confirm the assay method?
if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
in which situation ion pair agent require to use?
What is a difference between potency and purity?
in dissolution why pool sample needed? in which type of drug pool sample need?
I have compare C2H2-air and C2H2-N2O flame AAS on determination calcium. Both use same range of std to plot calibration curve. (2-6ppm) When i measure the sample with phosphate, KCl and LaCl, C2H2-N2O flame give false positive result, around 0.5ppm. When i measure the sample with phosphste, KCl and EDTA. C2H2-N2O flame also give 0.5ppm false positive. But both above mentioned sample would not give false positive when measured by C2H2-air flame. What is the reason?
why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?
What is the use of tlc and hplc? And when and where use?
can we use the same detector in HPLC as well GC and what could be the differences we can find in the final chromato graph in any aspects?
in which situation require to use paddle and basket?
What is diffrence between extractable volume and deliverable volume? Answer pls
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.?
how to calibrate hplc & gc
How would you decide dissolution medium for NCE compound of class I drug
If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?
