Publications by authors named "Samuel Akapo"

Laminated aluminum foils are increasingly being used to protect drug products packaged in semipermeable containers (e.g., low-density polyethylene (LDPE)) from degradation and/or evaporation.

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A chiral HPLC method was validated and successfully applied for the determination of formoterol stereoisomers and their inversion products in an aqueous matrix stored at 5-70 degrees C up to 3 weeks. Analysis was performed on a Chiral-AGP column (100 x 4-mm, 5-microm) using a variable mixture of mobile phase A (50-mM sodium phosphate buffer, pH 7.0) and B (10% v/v IPA) at a flow rate of 1.

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Background: Patients with chronic obstructive pulmonary disease (COPD) are often given admixtures of nebulizable drugs to minimize the time of administration in treatment regimens.

Objective: To evaluate the physicochemical compatibility and aerodynamic characteristics of formoterol fumarate 20 microg/2 mL when mixed or sequentially nebulized with budesonide inhalation suspension 0.5 mg/2 mL, ipratropium bromide 0.

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A direct liquid immersion solid-phase microextraction-gas chromatographic (SPME-GC) method was developed and validated for the determination of 11 potential volatile organic compounds that may leach from preprinted foil laminate overwrap into aqueous pharmaceutical formulations filled in low-density polyethylene (LDPE) vials. The target compounds namely, ethanol, acetone, isopropyl alcohol, ethyl acetate, 2-butanone, n-heptane, isopropyl acetate, n-propyl acetate, toluene, diacetone alcohol and 1-propoxy-2-propanol, were suitably extracted from aqueous sample solutions by SPME using a 100-microm PDMS fiber, desorbed inside the GC inlet port, and analyzed using a J&W Scientific DB-1701 (86% polydimethylsiloxane/14% cyanopropylphenyl, 30 m x 0.53 mm i.

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A gas chromatographic method for the determination of formoterol (RS,SR)-diastereoisomer, a process impurity, in formoterol fumarate was optimized and validated. The method involves silylation of formoterol fumarate with N-(trimethylsilyl)imidazole in N,N-dimethylformamide at room temperature in an autosampler vial to produce trimethylsilyl derivatives of the enantiomers prior to GC analysis. The optimized silylation and separation conditions, respectively, produced good yield and resolution of the analytes.

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A stability-indicating reversed-phase high performance liquid chromatographic (HPLC) method has been developed and validated for the assay of formoterol fumarate and the related substances, namely, formoterol fumarate desformyl and formoterol fumarate acetamide analogs, in the active pharmaceutical ingredient. The separation was achieved by isocratic elution using an Alltech Alltima C18 (150 x 4.6 mm) column, a mobile phase consisting of ammonium acetate (50 mM; pH 5.

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Exposure of workers to diisocyanates in the polyurethane foam manufacturing industry is well documented. However, very little quantitative data have been published on exposure to diisocyanates from the use of paints and coatings. The purpose of this study was to evaluate emission of 2,4-toluene diisocyanate, 2,6-toluene diisocyanate (2,6-TDI), and isophorone diisocyanate from a commercially available two-stage concrete coating and sealant.

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