PVC supported liquid membrane and carbon paste potentiometric sensors incorporating an Mn(III)-porphyrin
complex as a neutral host molecule were developed for the determination of paracetamol. The measurements were
carried out in solution at pH 5.5. Under such conditions paracetamol exists as a neutral molecule. The mechanism of
molecular recognition between the Mn(III)-porphyrin and paracetamol, leading to potentiometric signal generation,
is discussed.The sensitivity and selectivity toward paracetamol of carbon paste and polymeric liquid membrane electrodes
incorporating an Mn(III)-porphyrin host were compared. The applicability of these sensors to the direct
determination of paracetamol was checked by performing a recovery test in human plasma.
The fabrication and analytical applications of two types of potentiometric
sensors for the determination of ketoconazole (KET) are described. The
sensors are based on the use of KET-molybdophosphoric acid (MPA) ion pair
as electroactive material. The fabricated sensors include both polymer membrane
and carbon paste electrodes. Both sensors showed a linear, stable and near
Nernstian slope of 57.8mV=decade and 55.2mV=decade for PVC membrane
and carbon paste sensors respectively over a relatively wide range of KET concentration
(1×10-2-5×10-5 and 1×10-2-1×10-6). The sensors showed a fast
response time of <30 sec and <45 sec. A useful pH range of 3–6 was obtained
for both types of sensors. A detection limit of 2.96 10 5M was obtained for
PVC membrane sensor and 6.91 10 6M was obtained for carbon paste sensor.
The proposed sensors proved to have a good selectivity for KET with respect to a
large number of ions. The proposed sensors were successfully applied for the
determination of KET in pharmaceutical formulations. The results obtained
are in good agreement with the values obtained by the standard method.
Dipyrromethene-Cu(II) derivatives possessing two dodecane alkyl chains have been used for the modification of gold
electrodes. Electroactive host molecules have been incorporated into a lipophilic dodecanethiol SAM deposited onto
gold electrodes through hydrophobic and van der Waals interactions (embedment technique). The presence of
dipyrromethene-Cu(II) redox centers on the electrode surface was proved by cyclic voltammetry and Osteryoung
square-wave voltammetry. The Au electrodes incorporating redox active Cu(II)-dipyrromethene SAMs were used for
the direct voltammetric determination of paracetamol in human plasma.