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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Determination of the nutraceutical, glucosamine hydrochloride, in raw materials, dosage forms and plasma using pre-column derivatization with ultraviolet HPLC.
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Determination of the nutraceutical, glucosamine hydrochloride, in raw materials, dosage forms and plasma using pre-column derivatization with ultraviolet HPLC.

机译:使用紫外高效液相色谱柱前衍生化法测定原料药,剂型和血浆中的营养保健品氨基葡萄糖盐酸盐。

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A selective and specific high performance liquid chromatography method was developed to quantitate glucosamine hydrochloride in raw materials, dosage forms and plasma. Reverse phase chromatography using pre-column derivatization with phenylisothiocyanate, and ultraviolet detection (lambda = 254 nm) was used to quantify the eluate. The mobile phase consisted of MeOH/H2O/CH3COOH (10:89.6:0.04) and was pumped at a flow rate of 1.2 ml/min. The standard curves for glucosamine hydrochloride showed linearity (r > or = 0.99) over the selected concentration range from 6.65 to 16.63 microg/ml for raw materials and dosage forms. The precision of the dosage form assay, expressed as the % relative standard deviation (R.S.D.), was < 5% at all concentrations. The intra-day and inter-day accuracy, as indicated by the relative error (R.E.), ranged from - 2.54 to 2.70% for glucosamine hydrochloride. For the plasma assay, beagle dog plasma was used to prepare standard curves in the concentration range of 1.25-20 microg/ml. Precipitation of plasma proteins was accomplished with acetonitrile to separate interfering endogenous products from the compound of interest. The supernatant was derivatized using phenylisocyanate in phosphate buffer (pH = 8.3) and subsequently evaporated to dryness under a nitrogen stream at 42 degrees C. The residue was dissolved in 250 microl mobile phase and injected onto the chromatographic system. The assay was linear in concentration ranges of 1.25-20 microg/ml (r > or = 0.999). Intra- and inter-day precision was < or = 5.23 and 5.65%, respectively and the intra- and inter-day accuracy, indicated by R.E., ranged from - 8.6 to 10.35%. The method was found to be specific and with excellent linearity, accuracy and precision and is well suited for the quantitation of glucosamine hydrochloride in raw materials, dosage forms, and pharmacokinetic studies.
机译:开发了一种选择性和特异性的高效液相色谱法,用于定量测定原料,剂型和血浆中的氨基葡萄糖盐酸盐。反相色谱使用异硫氰酸苯酯进行柱前衍生,并使用紫外检测(λ= 254 nm)对洗脱液进行定量。流动相由MeOH / H2O / CH3COOH(10:89.6:0.04)组成,并以1.2 ml / min的流速泵送。对于原料和剂型,氨基葡萄糖盐酸盐的标准曲线在6.65至16.63 microg / ml的选定浓度范围内显示线性(r>或= 0.99)。在所有浓度下,以%相对标准偏差(R.S.D.)表示的剂型测定的精确度<5%。如相对误差(R.E.)所示,日间和日间精度对于氨基葡萄糖盐酸盐为-2.54至2.70%。对于血浆测定,使用比格犬血浆制备浓度范围为1.25-20微克/毫升的标准曲线。用乙腈完成血浆蛋白的沉淀,将干扰的内源性产物与目标化合物分离。使用在磷酸盐缓冲液(pH = 8.3)中的异氰酸苯酯将上清液衍生化,然后在42摄氏度的氮气流下蒸发至干。将残留物溶于250微升流动相中,并注入色谱系统。该测定在1.25-20微克/毫升的浓度范围内呈线性关系(r≥0.999)。日内和日间准确度分别为<或= 5.23和5.65%,R.E。表示的日内和日间准确度为-8.6至10.35%。发现该方法具有特异性,并具有出色的线性,准确性和精密度,非常适用于定量原料,剂型和药代动力学研究中的氨基葡萄糖盐酸盐。

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