Liquid Chromatographic analysis of Methotrexate and Minocycline- Relevance to the determination in Plasma/Nanoparticulate formulations

Kumar Janakiraman, Venkateshwaran Krishnaswami, Vaidevi Sethuraman, V. Rajendran, R. Kandasamy
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Abstract

To develop an RP-HPLC method for the simultaneous estimation of methotrexate (MTX) and minocycline (MNC). Different HPLC methods were reported for the estimation of MTX/MNC individually, but there is no report for the simultaneous estimation of both MTX and MNC in a simple method. The objective of the developed method is to utilize the method for the estimation of MTX/MNC in different pharmaceutical formulations and in biological fluids. An HPLC method for the estimation of methotrexate (MTX) and minocycline (MNC) relevance to the evaluation of nanoparticulate formulations has been developed and validated. Chromatographic estimation was achieved using the mobile phase composition of sodium acetate buffer and acetonitrile (70:30% v/v) at pH 4.0 at a flow rate of 0.2 mL/min at 307 nm. The calibration curve for MTX and MNC was found to be linear at nanogram (5 to 25 ng.mL-1) and microgram (5 to 25 μg.mL-1) levels at a correlation coefficient range of 0.98 to 0.99 for both MTX/MNC. The lower limit of detection and limit of quantification were found to be 0.026 ng.mL-1 and 0.079 ng.mL-1 for MTX and MNC, respectively. The percentage relative standard deviation for validation parameters of both drugs was found to be less than 6.5%. The amount of MTX and MNC present within the nanoparticles was found to be MTX (0.84 mg/mL) and MNC (0.61 mg/mL). The in vitro release showed an immediate release pattern for MTX (64.95±2.08%) and MNC (90.90±1.78%) within 12 h. The developed analytical method for the simultaneous estimation of MTX and MNC was found to be simple, affordable, dynamic, low cost, rapid and easy to perform with good repeatability. This method is also time consuming, since the peaks were obtained within a moderate analysis time.
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甲氨蝶呤和米诺环素的液相色谱分析-与血浆/纳米颗粒制剂测定的相关性
建立反相高效液相色谱法同时测定甲氨蝶呤(MTX)和米诺环素(MNC)的含量。不同的高效液相色谱法分别测定MTX/MNC已有报道,但未见同时测定MTX和MNC的简便方法。所开发方法的目的是利用该方法估计不同药物制剂和生物液体中的MTX/MNC。建立并验证了甲氨蝶呤(MTX)和米诺环素(MNC)与纳米颗粒制剂评价相关性的高效液相色谱方法。采用醋酸钠缓冲液和乙腈(70:30% v/v)为流动相,pH为4.0,流速为0.2 mL/min,波长为307 nm,进行色谱估计。MTX和MNC在纳克(5 ~ 25 μg.mL-1)和微克(5 ~ 25 μg.mL-1)水平上均呈线性关系,相关系数范围为0.98 ~ 0.99。检测下限和定量下限均为0.026 ng。mL-1和0.079 ng。MTX和MNC分别为mL-1。两种药物验证参数的相对标准偏差百分比均小于6.5%。纳米颗粒中MTX和MNC的含量分别为MTX (0.84 mg/mL)和MNC (0.61 mg/mL)。MTX(64.95±2.08%)和MNC(90.90±1.78%)的体外释放在12 h内均呈快速释放模式。所建立的同时测定MTX和MNC的分析方法简便、经济、动态、成本低、快速、重复性好。这种方法也很耗时,因为峰是在一个适中的分析时间内获得的。
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