TY - JOUR
T1 - Single-step purification and formulation of antibody-drug conjugates using a miniaturized tangential flow filtration system
AU - Sajed, Muhammad
AU - Khan, Zahoor
AU - Ashraf, Muhammad Usman
AU - Iftikhar, Hafsa
AU - Rahat, Talha Bin
AU - Falak, Samia
AU - Fozail, Salman
AU - Gue, Quiterie
AU - Pardo, Raul
AU - Ramsey, Lance
AU - Shahzad, Muhammad Saqib
N1 - Publisher Copyright:
© 2025
PY - 2025/9/19
Y1 - 2025/9/19
N2 - Antibody-drug conjugates (ADCs) are a promising therapeutic modality that enables the delivery of cytotoxic drugs to the target cells that express the corresponding antigen. However, the purification of ADCs while ensuring product safety, homogeneity, and stability is a challenging task due to their complex and fragile structure. Size exclusion chromatography (SEC), the conventional method for ADC purification, is time-consuming as it requires multiple column washes and equilibration steps. Moreover, subsequent formulation of ADCs, typically using dead-end filtration (DEF), further complicates the production workflow. We compared SEC+DEF with the µPulse®, a miniaturized and automated tangential flow filtration system, for purification and formulation of ADCs. Quality analysis revealed that both approaches were equally gentle as comparable drug-to-antibody ratios (DARs) and monomer purities were observed in the purified samples. Most importantly, both methods exhibited equivalent cleanup efficiency with a 99.8% reduction in free linker-drug concentration. The endotoxin loads comprised 0.11 EU mg-1 for the µPulse and 0.07 EU mg-1 for SEC+DEF, ensuring validation of the safe application of purified ADCs in living systems. However, the µPulse performed purification and formulation of ADCs simultaneously as compared to SEC+DEF, which required multiple manual interventions. Our results indicate that the µPulse is a gentle, single-step, and walk-away approach for the purification of ADCs.
AB - Antibody-drug conjugates (ADCs) are a promising therapeutic modality that enables the delivery of cytotoxic drugs to the target cells that express the corresponding antigen. However, the purification of ADCs while ensuring product safety, homogeneity, and stability is a challenging task due to their complex and fragile structure. Size exclusion chromatography (SEC), the conventional method for ADC purification, is time-consuming as it requires multiple column washes and equilibration steps. Moreover, subsequent formulation of ADCs, typically using dead-end filtration (DEF), further complicates the production workflow. We compared SEC+DEF with the µPulse®, a miniaturized and automated tangential flow filtration system, for purification and formulation of ADCs. Quality analysis revealed that both approaches were equally gentle as comparable drug-to-antibody ratios (DARs) and monomer purities were observed in the purified samples. Most importantly, both methods exhibited equivalent cleanup efficiency with a 99.8% reduction in free linker-drug concentration. The endotoxin loads comprised 0.11 EU mg-1 for the µPulse and 0.07 EU mg-1 for SEC+DEF, ensuring validation of the safe application of purified ADCs in living systems. However, the µPulse performed purification and formulation of ADCs simultaneously as compared to SEC+DEF, which required multiple manual interventions. Our results indicate that the µPulse is a gentle, single-step, and walk-away approach for the purification of ADCs.
KW - Antibody-drug conjugates
KW - Bioconjugate cleanup
KW - Ultrafiltration
KW - µPulse-TFF system
KW - Size exclusion chromatography
UR - https://www.sciencedirect.com/science/article/pii/S2472630325001098
UR - https://pure.ulster.ac.uk/en/publications/e46aabc0-9e3d-4706-afd9-3ca01023875b
UR - https://www.scopus.com/pages/publications/105016316353
U2 - 10.1016/j.slast.2025.100351
DO - 10.1016/j.slast.2025.100351
M3 - Article
C2 - 40976396
SN - 2472-6303
VL - 35
SP - 1
EP - 6
JO - SLAS technology
JF - SLAS technology
M1 - 100351
ER -