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Development and validation of an HPLC method involving solid-phase extraction for the analysis of hydrophobic drugs in the presence of polyamidoamine (PAMAM) dendrimers

机译:聚酰胺相(PAMAM)树枝状大分子存在下固相萃取用于疏水药物分析的HPLC方法的开发和验证

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摘要

Two rapid and accurate isocratic high performance liquid chromatographic (HPLC) methods of analysis for nifedipine and furosemide in the presence of poly-amidoamine (PAMAM) dendrimers is described. Solid-phase extraction (SPE) using C-18 extraction cartridges and methanol as the eluent, was used to extract the drugs from the dendrimer and dendrimer plasma solutions. For both drugs, chromatographic separation was performed with a 5 mu m, 250 x 4 mm, octadecyl silane (C18) column. In the first method, nifedipine was analyzed using methanol:water (2:1 v/v) as the mobile phase with a flow rate of 0.7 mL/min. The injection volume was 20 mu L with detection at 254 mn and a retention time of I I minutes. In the second method, furosemide was analyzed using water: acetonitrile: acetic acid (60:40:1 v/v) as the mobile phase with a flow rate of 1.0 mL/min, injection volume of 20 mu L, and detection at 272 urn. The retention time for furosemide was 8.5 minutes.
机译:描述了两种在聚丙烯酰胺胺(PAMAM)树状大分子存在下快速,准确的等度高效液相色谱(HPLC)方法分析硝苯地平和速尿。使用C-18萃取柱和甲醇作为洗脱液的固相萃取(SPE)用于从树枝状聚合物和树枝状聚合物血浆溶液中提取药物。对于这两种药物,色谱分离均使用5微米,250 x 4毫米的十八烷基硅烷(C18)色谱柱进行。在第一种方法中,使用甲醇:水(2:1 v / v)作为流动相,以0.7 mL / min的流速分析硝苯地平。进样量为20μL,检测量为254 mn,保留时间为I I分钟。在第二种方法中,使用水:乙腈:乙酸(60:40:1 v / v)作为流动相分析呋塞米,流速为1.0 mL / min,进样量为20μL,并在272处检测瓮。速尿的保留时间为8.5分钟。

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