1992
DOI: 10.1021/jf00020a035
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Mono- and polyclonal antibodies to the organophosphate fenitrothion. 1. Approaches to hapten-protein conjugation

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Cited by 93 publications
(62 citation statements)
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“…Several investigators used haptens having a bridge at the thiophosphate group to develop ELISAs for organophosphorus pesticides. [4][5][6] To synthesize such haptens, they used an aminocarboxylic acid protected at the carboxylic group to attach a bridge to phosphorus atom and then deprotected the bridge later. In our laboratory, a synthetic method for attaching an aminocarboxylic acid bridge to phosphorus without protection was developed.…”
Section: Resultsmentioning
confidence: 99%
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“…Several investigators used haptens having a bridge at the thiophosphate group to develop ELISAs for organophosphorus pesticides. [4][5][6] To synthesize such haptens, they used an aminocarboxylic acid protected at the carboxylic group to attach a bridge to phosphorus atom and then deprotected the bridge later. In our laboratory, a synthetic method for attaching an aminocarboxylic acid bridge to phosphorus without protection was developed.…”
Section: Resultsmentioning
confidence: 99%
“…This method worked well for the synthesis of three haptens used in this study. The route which Skerrit [4][5][6] used to synthesize such haptens involves seven steps including protection and deprotection at both amino and carboxyl groups of the spacer arm. The route we use instead consists of only two steps with no protection and deprotection, i.e., nucleophilic attack by phenol at the P atom of ROP(=S)Cl 2 to displace Cl, followed by nucleophilic substitution of the remaining Cl by an aminocarboxylic acid.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…One type of hapten for OP pesticides is the one with an aminocarboxylic acid bridge at the thiophosphate group, which has been used for the development of ELISA for several OP pesticides. [4][5][6][7][8][9][10][11][12] We have developed a simple method for the synthesis of such haptens, which requires far fewer steps and can provide a wider range of hapten structures. [4][5][6] We previously applied this method to the synthesis of several OP pesticides including chlorpyrifos, 4 isofenphos, 5 and cyanophos.…”
Section: Introductionmentioning
confidence: 99%
“…McAdam et al (129,130) desarrollaron un método general para sintetizar este tipo de haptenos, que ha sido aplicado con éxito al desarrollo de ELISAs para varios plaguicidas organofosforados (126,(131)(132)(133)(134). Este método se basa en la unión del brazo espaciador al grupo tiofosfato, e implica varios pasos de protección y desprotección del mismo.…”
Section: Principios Generales De Las Técnicas Inmunoquímicasunclassified