TY - JOUR
T1 - The enzymatic degradation and transport of leucine-enkephalin and 4-imidazolidinone enkephalin prodrugs at the blood-brain barrier
AU - Lund, L.
AU - Bak, A.
AU - Friis, G.J.
AU - Hovgaard, L.
AU - Christrup, Lona Louring
PY - 1998/10/15
Y1 - 1998/10/15
N2 - In this study, the stability in and transport across a cell culture model of the blood-brain barrier (BBB) is investigated for leucine-enkephalin (Leu-enkephalin) and four 4-imidazolidinone prodrugs of Leu-enkephalin. The results show that Leu-enkephalin is degraded in the cell culture model of the BBB both by cytosolic and plasma membrane bound enzymes. It is likely that aminopeptidase is the predominant enzyme responsible for the degradation of Leu-enkephalin. All four 4-imidazolidinone prodrugs of Leu-enkephalin examined showed an increased stability of Leu-enkephalin against degradation by both plasma membrane bound and cytosolic enzymes. Consequently, the transport properties of Leu-enkephalin is also improved by up to 60% by formation of 4-imidazolidinone prodrugs. Copyright (C) 1998 Elsvier Science B.V.
AB - In this study, the stability in and transport across a cell culture model of the blood-brain barrier (BBB) is investigated for leucine-enkephalin (Leu-enkephalin) and four 4-imidazolidinone prodrugs of Leu-enkephalin. The results show that Leu-enkephalin is degraded in the cell culture model of the BBB both by cytosolic and plasma membrane bound enzymes. It is likely that aminopeptidase is the predominant enzyme responsible for the degradation of Leu-enkephalin. All four 4-imidazolidinone prodrugs of Leu-enkephalin examined showed an increased stability of Leu-enkephalin against degradation by both plasma membrane bound and cytosolic enzymes. Consequently, the transport properties of Leu-enkephalin is also improved by up to 60% by formation of 4-imidazolidinone prodrugs. Copyright (C) 1998 Elsvier Science B.V.
UR - http://www.scopus.com/inward/record.url?scp=0032531892&partnerID=8YFLogxK
U2 - 10.1016/S0378-5173(98)00192-6
DO - 10.1016/S0378-5173(98)00192-6
M3 - Journal article
AN - SCOPUS:0032531892
SN - 0378-5173
VL - 172
SP - 97
EP - 101
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
IS - 1-2
ER -