A J Domb, M Rock, J Schwartz, C Perkin, G Yipchuk, B Broxup, J G Villemure
Index: Biomaterials 15(9) , 681-8, (1994)
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The metabolic disposition and elimination process of the anhydride co-polymer poly[1,3-bis(p-carboxy-phenoxypropane):sebacic acid] 20:80 [P(CPP:Sa)20:80] implanted in the rat brain was studied. Two polymers were prepared, one with [14C]SA and unlabelled CPP, and the other co-polymer with [14C]CPP and unlabelled SA. With these two polymers we were able to study the metabolic disposition of each monomer after polymer degradation. Polymer wafers loaded with N,N-bis(2-chloroethyl)-N-nitrosourea or without the drug were implanted in the rat brain. For the rats implanted with the [14C]SA-labelled polymer, approximately 40% of the radioactivity was found in the expired CO2, 10% in the urine, about 2% in the faeces and about 10% remained in the device 7 d after implantation. On the other hand, only 4% of the [14C]CPP monomer was eliminated by urine and faeces during this period. The drug-loaded polymer degraded faster than the blank polymer. This study supports the theory that the polymer is a biodegradable material that can be used for the direct and specific delivery of drugs into a targeted organ and can provide continued release of drugs over a period of time.
Structure | Name/CAS No. | Molecular Formula | Articles |
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1 3-BIS(P-CARBOXYPHENOXY)PROPANE
CAS:3753-81-9 |
C17H16O6 |
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Urich, K.E. et al.
[Macromolecules 28 , 2184, (1995)] |
Excretion of a radiolabelled anticancer biodegradable polyme...
1995-09-01 [Biomaterials 16(14) , 1069-72, (1995)] |
Molecular weight changes in polymer erosion.
1992-10-01 [Pharm. Res. 9(10) , 1279-83, (1992)] |
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