TY - JOUR
T1 - Development of affinity polymeric particles for the removal of 4-dimethylaminopyridine (DMAP) from active pharmaceutical ingredient crude streams using a green technology
AU - Viveiros, Raquel
AU - Pinto, José J.
AU - Costa, Nuno
AU - Heggie, William
AU - Casimiro, Teresa
N1 - info:eu-repo/grantAgreement/FCT/Projetos de Investigação Científica e Desenvolvimento Tecnológico - 2012/PTDC%2FQEQ-PRS%2F2757%2F2012/PT#
info:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FEQU-EQU%2F32473%2F2017/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50006%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50006%2F2020/PT#
info:eu-repo/grantAgreement/FCT/OE/SFRH%2FBDE%2F51907%2F2012/PT#
info:eu-repo/grantAgreement/FCT/CEEC IND 3ed/2020.00377.CEECIND%2FCP1586%2FCT0033/PT#
Funding Information:
The Associate Laboratory for Green Chemistry for Green Chemistry - Clean Technologies and Processes - LAQV is financed by national funds from FCT/MCTES and co-financed by the ERDF under the PT2020 Partnership Agreement ( POCI-01–0145-FEDER – 007265 ).
Publisher Copyright:
© 2023
PY - 2023/3
Y1 - 2023/3
N2 - Polymeric particles with affinity for 4-dimethylaminipyridine (DMAP) were developed by molecular imprinting using supercritical carbon dioxide (scCO2) technology, for cleanup of this potentially genotoxic impurity from crude mixtures of Active Pharmaceutical Ingredients (APIs). DMAP-molecularly imprinted polymer (DMAP-MIP) and the respective control, the non-molecularly imprinted polymer (NIP) were produced by free radical polymerization using methacrylic acid as monomer, ethylene glycol dimethacrylate as crosslinker and AIBN as free-radical initiator in scCO2. The materials were obtained in high yield and were characterized chemically, physically and morphologically. Their extraction efficiency was evaluated by dynamic binding experiments using two solutions: i) a solution containing 104 ppm DMAP solution; ii) model pharmaceutical mixture containing 104 ppm of DMAP and 1018 ppm of Mometasone furoate (API). Particles were able to remove 18.3 µmol DMAP/g polymer from a 104 ppm DMAP solution (i) and 1004.6 µmol DMAP/g API (ii). In addition, high recoveries of both DMAP and API were obtained, above 99%.
AB - Polymeric particles with affinity for 4-dimethylaminipyridine (DMAP) were developed by molecular imprinting using supercritical carbon dioxide (scCO2) technology, for cleanup of this potentially genotoxic impurity from crude mixtures of Active Pharmaceutical Ingredients (APIs). DMAP-molecularly imprinted polymer (DMAP-MIP) and the respective control, the non-molecularly imprinted polymer (NIP) were produced by free radical polymerization using methacrylic acid as monomer, ethylene glycol dimethacrylate as crosslinker and AIBN as free-radical initiator in scCO2. The materials were obtained in high yield and were characterized chemically, physically and morphologically. Their extraction efficiency was evaluated by dynamic binding experiments using two solutions: i) a solution containing 104 ppm DMAP solution; ii) model pharmaceutical mixture containing 104 ppm of DMAP and 1018 ppm of Mometasone furoate (API). Particles were able to remove 18.3 µmol DMAP/g polymer from a 104 ppm DMAP solution (i) and 1004.6 µmol DMAP/g API (ii). In addition, high recoveries of both DMAP and API were obtained, above 99%.
KW - Affinity purification
KW - Genotoxin removal
KW - Molecularly imprinted polymer
KW - Solid-phase extraction
KW - Supercritical carbon dioxide
UR - http://www.scopus.com/inward/record.url?scp=85146686812&partnerID=8YFLogxK
U2 - 10.1016/j.supflu.2023.105853
DO - 10.1016/j.supflu.2023.105853
M3 - Article
AN - SCOPUS:85146686812
SN - 0896-8446
VL - 194
JO - Journal of Supercritical Fluids
JF - Journal of Supercritical Fluids
M1 - 105853
ER -