Calidad fisicoquímica de Xilonest 2% jalea producida en un laboratorio Farmacéutico nacional, 2020
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Date
2022
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Universidad Nacional de Trujillo
Abstract
El presente informe describe los ensayos realizados en xilonest 2% jalea producto terminado, con la finalidad de determinar la calidad fisicoquímica de acuerdo a las especificaciones establecidas por la Farmacopea de Estados Unidos de América (USP) 42, empleando 16 tubos de xilonest 2% jalea. Los análisis se realizaron en un laboratorio farmacéutico ubicado en la ciudad de Lima. Los ensayos realizados fueron: descripción, llenado mínimo, pH (25°C), identificación, dosaje y peso específico (25°C), dando resultado de: identificación cumple con los tiempos de retención según la valoración y con el espectro de infrarrojo, dosaje 2.01 g/100mL (100.5%), pH 6.5 y peso específico 1,0223; cumpliendo todos los resultados de acuerdo a los valores establecidos por la Farmacopeade Estados Unidos de América (USP) 42. Conforme a sus especificaciones concluyendoque el producto xilonest 2 % jalea cumple con los parámetros establecidos y es apto parasu uso.
ABSTRACT This report describes the tests carried out on xilonest 2% jelly finished product, in order to determine the physicochemical quality according to the specifications established by the Pharmacopoeia of the United States of America (USP) 42, using 16 tubes of xilonest 2% jelly. The analyzes were performed in a pharmaceutical laboratory located in the city of Lima. The tests carried out were: description, minimum filling, pH (25°C), identification, dosage and specific weight (25°C), resulting in: identification complies with the retention times according to the valuation and with the infrared spectrum, dosage 2.01 g/100mL (100.5%), pH 6.5 and specific weight 1.0223; fulfilling all the results according to the values established by the Pharmacopoeia of the United States of America (USP) 42. In accordance with its specifications, concluding that the product xilonest 2% jelly complies with the established parameters and is suitable for use.
ABSTRACT This report describes the tests carried out on xilonest 2% jelly finished product, in order to determine the physicochemical quality according to the specifications established by the Pharmacopoeia of the United States of America (USP) 42, using 16 tubes of xilonest 2% jelly. The analyzes were performed in a pharmaceutical laboratory located in the city of Lima. The tests carried out were: description, minimum filling, pH (25°C), identification, dosage and specific weight (25°C), resulting in: identification complies with the retention times according to the valuation and with the infrared spectrum, dosage 2.01 g/100mL (100.5%), pH 6.5 and specific weight 1.0223; fulfilling all the results according to the values established by the Pharmacopoeia of the United States of America (USP) 42. In accordance with its specifications, concluding that the product xilonest 2% jelly complies with the established parameters and is suitable for use.
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Keywords
xilonest, fisicoquímico, calidad.