Method and apparatus for chromatographic purification
A method and an apparatus suitable for a continuous chromatography process which only needs three separation columns, and a two-step process containing two chromatographic steps, in which the first chromatographic step (capture) is performed alternating and sequentially on two separation columns, the second chromatographic step (polishing) is performed, also sequentially, on the third column.
1. A method of purifying a target molecule from one or more impurities in only one sample using an apparatus comprising
two separation units A 1 and A 2 both having the same chromatography matrix and a separation unit B having a chromatography matrix which differs from the chromatography matrix of separation units A 1 and A 2 , all separation units having a fluid inlet and a fluid outlet, whereby there is at least fluid connection between the fluid outlet of separation unit A 1 and the fluid inlet of separation unit B and fluid connection between the fluid outlet of separation unit A 2 and the fluid inlet of separation unit B
at least one valve in the fluid connection between separation units A 1 and A 2 and separation unit B that allows to switch between fluid communication between the outlet of separation unit A 1 and the fluid inlet of separation unit B and fluid communication between the outlet of separation unit A 2 and the fluid inlet of separation unit B,
at least two buffer reservoirs and at least two pumps
a reservoir containing sample solution that is in fluid connection with the inlets of separation units A 1 and A 2 ,
the method comprising:
alternately loading portions of the sample on the separation units A 1 and A 2 so that while the sample is loaded on separation unit A 1 wherein the sample is at a first pH and conductivity enabling the target molecule to be bound to separation unit A 1 , separation unit A 2 is at least part of that time in fluid communication with separation unit B so that the target molecule loaded on separation unit A 2 is eluted onto separation unit B and separation unit A 2 is re-equilibrated and while the sample is loaded on separation unit A 2 wherein the sample is at a first pH and conductivity enabling the target molecule to be bound to separation unit A 2 , separation unit A 1 is at least part of that time in fluid communication with separation unit B so that the target molecule loaded on separation unit A 1 is eluted onto separation unit B and separation unit A 1 is re-equilibrated,
recovering the target molecule from the fluid outlet of separation unit B.
2. Method according to claim 1 , wherein the target molecule is an antibody.
3. Method according to claim 1 , wherein while loading the sample onto separation unit A 1 the fluid outlet of separation unit A 1 is at least part of that time in fluid communication with the fluid inlet of separation unit A 2 to enable capturing of the target molecule that is starting to leach from the separation unit A 1 to be bound to separation unit A 2 and while loading the sample onto separation unit A 2 the fluid outlet of separation unit A 2 is at least part of that time in fluid communication with the fluid inlet of separation unit A 1 to enable capturing of the target molecule that is starting to leach from the separation unit A 2 to be bound to separation unit A 1 .
4. Method according to claim 1 , wherein a virus inactivation buffer is pumped through separation unit A 1 after loading separation unit A 1 with the target molecule and through separation unit A 2 after loading separation unit A 2 with the target molecule.
5. Method according to claim 1 , wherein while washing an unbound sample from the separation unit A 1 , separation unit A 2 is at least part of that time in fluid communication with the reservoir containing sample solution and separation unit A 1 and while washing an unbound sample from the separation unit A 2 , separation unit A 1 is at least part of that time in fluid communication with the reservoir containing sample solution and separation unit A 2 .
6. Method according to claim 1 , wherein the sample is a clarified sample.