Synthesis of 14C-labeled copolymers for drug delivery studies
✍ Scribed by Sung W. Rhee; Elmer J. Reist; Marie T. Rock
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- French
- Weight
- 315 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
^14^C‐labeled polyanhydride copolymers [(20:80/1,3‐bis)(p‐carboxyphenoxy)‐propane(CPP):sebacic acid (SA)] (7 and 13) were synthesized according to schemes I and II: ^14^C‐labeled sebacic acid (2,9‐^14^C~2~) (5) and ^14^C‐labeled CPP 1,3‐bis(p‐carboxyphenoxy)‐propane (labeled at C‐1, C‐3 of the propyl group) (11) were transformed to the corresponding mixed anhydrides (6 and 12) as prepolymers respectively by reaction with acetic anhydride. The labeled mixed anhydride prepolymers (6 and 12) were condensed with unlabeled counter‐prepolymers (12′ and 6′) to give the labeled polyanhydride copolymers (7 and 13). The labeled copolymers (7 and 13) were identified and characterized by gel permeation chromatography (GPC).
📜 SIMILAR VOLUMES
## Abstract Side‐chain and ring ^14^C‐labelled styrene were synthesised from labelled benzene and acetaldehyde via bromobenzene, Grignard‐reagent and 1‐phenylethanol. Uniformly ^14^C‐labelled styrene can be also prepared using this method. By‐products were identified and the purity of products was
## Abstract p‐Toluic acid‐ring‐^14^C was synthesized by the Friedel‐Crafts p‐carbamylation of toluene‐ring‐^14^C with N,N‐disubstituted carbamyl chloride and subsequent hydrolysis. The radiochemical yield was 61%. An attempt was made to apply this method for the synthesis of benzoic acid‐ring‐^14^C
a m i n e a n d N-methylphenethyl amine as well as the 14C-labeling of c l o r g y l i n e a n d L -d e p r e n y l a r e d e s c r i b e d . L a b e l i n g was a c c o m p l i s h e d b y N -a l k y l a t l o n o f t h e f r e e b a s e o f t h e c o r r e s p o n d i n g d e s m e t h y l c o m p
## Abstract A method for labelling acamprosate (calcium __N__‐acetyl homotaurinate), an anti‐craving compound for ethanol, with ^11^C, has been developed for __in vivo__ studies with positron emission tomography (PET). The synthesis was based on the acylation of homotaurinate using [^11^C]acetyl ch
## Abstract PI‐88, uniformly labelled with [^14^C] was prepared by incorporating D‐[^14^C]glucose into the fermentation of __Pichia (Hansenula) holstii__ NRRL Y‐2448 under controlled conditions to produce [^14^C]‐labelled extracellular phosphomannan. Subsequent acid catalyzed hydrolysis gave the [^