丁丙诺啡、纳洛酮的路线评价和HPLC分析方法的开发及纳曲酮、纳布啡的综合效率比较

Krishnasarma Pathy
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引用次数: 3

摘要

这是一项从天然阿片类药物如底拜因(也称为可待因甲基烯醇醚)和奥利帕平合成丁丙诺啡、纳曲酮、纳洛酮和纳布啡的工艺开发工作。在这一研究过程中,已经开发了几种新的吗啡类药物n -去甲基化方法。本文追溯了各种方法的演变,并对总体效率进行了比较。建立了反相高效液相色谱法(RPHPLC),用于同时测定纯制剂和市售制剂中盐酸纳洛酮和盐酸丁丙诺啡的含量。色谱柱为Hypersil ODS C18(粒径为250 mm × 4.6mm × 5μm),流动相组成pH 6.0醋酸铵缓冲液:乙腈(68:32)v/v,等密度模式,紫外检测波长为310nm。洗脱流速为1.0mL/ min,纳洛酮和丁丙诺啡的平均保留时间分别为2.86 min和3.67 min。根据ICH指南对方法进行了验证。所有验证参数的RSD均小于2%,表明该方法具有较高的准确度和精密度。纳洛酮和丁丙诺啡浓度分别在5.30μg/ml和20 ~ 120μg/ml范围内呈线性关系。纳洛酮的LOD和LOQ分别为0.08µg/mL和0.26µg/mL,丁丙诺啡的LOD和LOQ分别为0.0078µg/mL和0.0237µg/mL。将药物分别暴露于酸性、碱性、氧化、热和光解条件下,并采用该方法对应力样品进行分析。降解研究表明,这两种药物在酸性、氧化、热和光解条件下都具有很高的稳定性。在碱性条件下,RT值比标准值更低,没有任何额外的峰。在压力条件下的高稳定性证实了该方法在纯制剂和市售制剂中同时测定盐酸纳洛酮和盐酸丁丙诺啡的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Route Evaluation and Analytical HPLC Method Development of Buprenorphine, Naloxone, and Comparison Overall Efficiency of Naltrexone Nalbuphine Traces the Evolution of Various Approaches
This is out line work on the process development for the synthesis of buprenorphine, naltrexone, naloxone, and nalbuphine from naturally occurring opiates such as Thebaine, also known as codeine methyl enol ether, and oripavine. Several new methods for N-demethylation of morphinans have been developed during the pursuit of this research. The article traces the evolution of various approaches and provides a comparison for overall efficiency. A reverse phase high performance liquid chromatographic (RPHPLC) method has been developed and validated for simultaneous estimation of Naloxone Hydrochloride and Buprenorphine Hydrochloride in pure and marketed formulations. Separation was carried out using column Hypersil ODS C18 (250 mm x 4.6mm x 5μm particle size) in isocratic mode using mobile phase composition pH 6.0 ammonium acetate Buffer: Acetonitrile (68:32)v/v and UV detection at 310nm. The compounds were eluted at a flow rate of 1.0mL/ min. The average retention times for Naloxone and Buprenorphine were 2.86 and 3.67 min, respectively. The method was validated according to the ICH guidelines. The percentage RSD of all validation parameters found to be less than 2% indicating high degree of accuracy and precision of the proposed HPLC method. The method was linear over the concentration of 5.30μg/ml and 20-120μg/ml for Naloxone and Buprenorphine respectively. The LOD and LOQ of Naloxone were found to be 0.08µg/mL and 0.26µg/mL and of Buprenorphine were found to be 0.0078µg/mL and 0.0237µg/mL. The drugs were also exposed to acidic, alkaline, oxidative, thermal and photolytic conditions and the stressed samples were analyzed by the proposed method. Degradation studies showed that the both the drugs were highly stable under acidic, oxidative, thermal and photolytic conditions. Under alkaline conditions, RT values were shifted to lower as compared to standard without any additional peaks. The high percentage of stability under stress conditions confirms the suitability of the method for simultaneous estimation of Naloxone Hydrochloride and Buprenorphine Hydrochloride in pure and marketed formulations.
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