Low-cost potentiometric
and spectrophotometric procedures for cephalothin
(CPI) determination in pure and biological fluids were investigated.
The potentiometric technique is created through titration of CPI with
an aqueous medium of 0.1 M NaOH at an ionic strength of μ =
0.3 M sodium chloride and room temperature by a combined glass pH
electrode. Using the standard addition method, we found that the detection
and quantitative limits were 0.042 mg/mL, with the standard deviation
SD = 0.011, correlation coefficient R = 0.9880 (n = 5), and linear concentration ranges from 0.042 to 0.82
mg/mL. This technique was utilized to assess CPI in pure solutions,
urine, and serum with suitable results. No interference was exposed
in the presence of public components of the samples under study. Recovery
of CPI for pure and biological fluids is in the range of 98.2–101%.
Also, the spectrophotometric method has been performed through the
formation of the Prussian Blue (PB) complex. The reaction between
the acidic hydrolysis product of CPI (T = 60 °C)
and the mixture of Fe3+ with hexacyanoferrate (III) ions
(HCF(III)) was detected for the spectrophotometric determination of
the drug. The maximum absorbance of the formed complex was measured
at λ = 283 nm with 2.0 × 103 L mol–1 cm–1 molar absorptivity. Reaction states have
been advanced to acquire the PB complex of great sensitivity and longer
stability. In optimal states, the absorbent of the PB compound was
attained to grow linearly with the increase in the concentration of
CPI, which agrees with the correlation coefficient values. The detection
and quantitative limits were 0.000036 and 0.0012 mg/mL, respectively,
with the standard deviation, SD = 0.0005, correlation coefficient, R = 0.9955 (n = 5), and the linearity range
of the calibration plot 0.0005–0.02 mg/mL CPI. The planned
technique was positively utilized for the detection of CPI in both
urine and serum models. The results fit well with the data found from
the potentiometric method.