Application of a classical least-squares regression method to the assay of 1,4-dihydropyridine antihypertensives and their photoproducts.

A multicomponent UV spectrophotometric method using a classical least-squares (CLS) algorithm has been developed for the quantitative determination of 1,4-dihydropyridine (DHP) calcium antagonists and respective photoproducts. The procedure was optimized by defining a fractionation scheme for selecting the more useful wavelength ranges to be used in the calibration model. The method is potentially able to be extended to the other drugs of the same family.

Determination of hydrochlorothiazide and irbesartan in pharmaceuticals by fourth-order UV derivative spectrophotometry.

The fourth-order derivative spectrum from the alcoholic sample is used. HCT can be determined by a specific peak-trough, of low intensity, at 330-340 nm. For IST evaluation, a peak-trough around 250-310 nm is available, common to both products, whose amplitude increases linearly only for low concentration values, while it decreases at higher values.

Photodegradation monitoring of amlodipine by derivative spectrophotometry.

A derivative spectrophotometric method for the simultaneous determination of amlodipine and its pyridine photodegradation product has been developed. The analytes concentrations were linearly correlated with spectral measurements in the 3rd order UV derivative spectrum through equations obtained by simple and multiple regression analysis. The recovery values were estimated to range from 95 to 99% and the quantitation limit of the photoproduct was found to be equivalent to an impurity level of 1%, with respect to the content of amlodipine.

Propofol assay in biological fluids in pregnant women.

A rapid, accurate and sensitive UV derivative method was described for measuring the Propofol concentration in some biological fluids. Furthermore two alternative procedures, a gaschromatographic and a colorimetric, were also defined, and the results of the three methods, when applied on blood samples spiked with known amounts of analyte, were compared. The samples were preliminary purified by a solid phase extraction on octadecyl C18 cartridge.

Nasally-administered progesterone: comparison of ointment and spray formulations.

The aim of the study was to compare the bioavailability and clinical usefulness of progesterone (P) administered nasally in spray or ointment form. Twenty healthy post-menopausal women were randomly allocated to treatment by either intranasal spray (4 doses of an oil-based P solution at a concentration of 2 mg/0.1 ml, corresponding to a total dose of approximately 11 mg of P) or an ointment (quantity 0.