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1.
Pharm Dev Technol ; 26(1): 60-68, 2021 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-33032496

RESUMEN

To enhance the dissolution and oral bioavailability of telmisartan (TMS), a poorly water-soluble anti-hypertensive drug, a supersaturable self-microemulsifying drug delivery system (SuSMEDDS) was developed. Amorphous alkalinized TMS (AAT) was formulated into a SMEDDS, composed of Capmul® MCM (oil), Cremophor® RH40 (surfactant), and tetraglycol (co-surfactant). Although the SMEDDS was rapidly dissolved (>80% within 5 min) in a limited condition (500 mL, pH 6.8), drug precipitation was observed over time, resulting in a decrease in dissolution levels. The precipitation was due to drug recrystallization, as determined by differential scanning calorimetry and powder X-ray diffraction analyses. Several polymers, including Soluplus® (SOL), were screened as precipitation inhibitors; ultimately, SuSMEDDS-SOL was prepared by admixing SOL and the SMEDDS at a 5:100 (w/w) ratio. SuSMEDDS-SOL was superior in terms of dissolution efficiency (>90% over 2 h) and dissolution-retaining time (no precipitation over 2 h). An in vivo pharmacokinetic study in rats revealed that the oral bioavailability of SuSMEDDS-SOL was 4.8-, 1.3-, and 1.2-fold greater than those of the TMS suspension, AAT solution, and SMEDDS, respectively. Therefore, SuSMEDDS-SOL is a promising candidate to enhance the dissolution and oral bioavailability of TMS.


Asunto(s)
Antihipertensivos/sangre , Antihipertensivos/síntesis química , Sistemas de Liberación de Medicamentos/métodos , Emulsionantes/sangre , Emulsionantes/síntesis química , Telmisartán/sangre , Telmisartán/síntesis química , Administración Oral , Animales , Antihipertensivos/administración & dosificación , Disponibilidad Biológica , Emulsionantes/administración & dosificación , Masculino , Ratas , Ratas Sprague-Dawley , Solubilidad , Telmisartán/administración & dosificación
2.
Molecules ; 25(8)2020 Apr 11.
Artículo en Inglés | MEDLINE | ID: mdl-32290380

RESUMEN

Many studies have analyzed nicotine metabolites in blood and urine to determine the toxicity caused by smoking, and assess exposure to cigarettes. Recently, hair and nails have been used as alternative samples for the evaluation of smoking, as not only do they reflect long-term exposure but they are also stable and easy to collect. Liquid-liquid or solid-phase extraction has mainly been used to detect nicotine metabolites in biological samples; however, these have disadvantages, such as the use of toxic organic solvents and complex pretreatments. In this study, a modified QuEChERS method was proposed for the first time to prepare samples for the detection of nicotine metabolite cotinine (COT) and trans-3'-hydroxycotinine (3-HCOT) in hair and nails. High-performance liquid chromatography-tandem mass spectrometry (LC-MS/MS) was used to analyze traces of nicotine metabolites. The established method was validated for selectivity, linearity, lower limit of quantitation, accuracy, precision and recovery. In comparison with conventional liquid-liquid extraction (LLE), the proposed method was more robust, and resulted in higher recoveries with favorable analytical sensitivity. Using this method, clinical samples from 26 Korean infants were successfully analyzed. This method is expected to be applicable in the routine analysis of nicotine metabolites for environmental and biological exposure monitoring.


Asunto(s)
Cotinina/análogos & derivados , Cotinina/análisis , Cabello/química , Uñas/química , Extracción en Fase Sólida/métodos , Cromatografía Liquida/métodos , Humanos , Límite de Detección , Nicotina/análisis , Nicotina/metabolismo , Espectrometría de Masas en Tándem/métodos
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