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使用X射线粉末衍射技术同时估算阿巴卡韦、拉米夫定和奈韦拉平复方制剂的结晶度

Simultaneous estimation of degree of crystallinity in combination drug product of abacavir, lamivudine and neverapine using X-ray powder diffraction technique.

作者信息

Kommavarapu Pavan, Maruthapillai Arthanareeswari, Allada Ravikiran, Palanisamy Kamaraj, Chappa Praveen

机构信息

Department of Chemistry, SRM University, Kattankulathur 603203, Tamil Nadu, India.

出版信息

J Young Pharm. 2013 Dec;5(4):127-32. doi: 10.1016/j.jyp.2013.10.003. Epub 2013 Nov 14.

Abstract

OBJECTIVE

In the present study, simultaneous determination of degree of crystallinity content in abacavir (ABC), lamivudine (3TC) and neverapine (NVP) from there combination drug product using X-ray powder diffraction (XRPD) technique is developed and validated.

METHODS

The X-ray procedure for the identification and determination of the degree of crystallinity in ABC, 3TC and NVP drug product is developed and validated. It is based on the X-ray diffraction from crystalline region of the drug product. The characteristic peaks of the three drugs were characterized using XRPD.

RESULTS

ABC, 3TC and NVP concentrations ranging from 70% to 130% in drug product were prepared and linearity in this concentration range is described. The % coefficient of variation (%CV) was found to be 0.9982 for ABC, 0.9978 for 3TC and 0.9984 for NVP. The mean recoveries were found to be 100.3% for ABC, 99.0% for 3TC and 100.8% for NVP. Regressions statistics and Analysis of variance (ANOVA) table results were evaluated and found to be satisfactory.

CONCLUSIONS

The method has been applied to unknown mixtures of drug formulations and stability samples. The proposed method can be useful in the quality control of combination drug products.

摘要

目的

在本研究中,开发并验证了一种使用X射线粉末衍射(XRPD)技术同时测定阿巴卡韦(ABC)、拉米夫定(3TC)和奈韦拉平(NVP)复方制剂中结晶度含量的方法。

方法

开发并验证了用于鉴定和测定ABC、3TC和NVP制剂中结晶度的X射线方法。该方法基于药物制剂结晶区域的X射线衍射。使用XRPD对三种药物的特征峰进行了表征。

结果

制备了药物制剂中ABC、3TC和NVP浓度范围为70%至130%的样品,并描述了该浓度范围内的线性关系。发现ABC的变异系数(%CV)为0.9982,3TC为0.9978,NVP为0.9984。发现ABC的平均回收率为100.3%,3TC为99.0%,NVP为100.8%。对回归统计和方差分析(ANOVA)表结果进行了评估,结果令人满意。

结论

该方法已应用于药物制剂的未知混合物和稳定性样品。所提出的方法可用于复方制剂的质量控制。

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