Al-Majed A A, Al-Zehouri J
Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Farmaco. 2001 Apr;56(4):291-6. doi: 10.1016/s0014-827x(01)01070-9.
Ramipril, as a secondary amine compound, reacts with 7-fluoro-4-nitrobenzo-2-oxo-1,3-diazole (NBD-F) producing the corresponding fluorescent NBD-ramipril. According to this fact, spectrophotometric and fluorimetric methods for the determination of ramipril were developed. The effect of these parameters on the reaction product were carefully studied to optimize reaction conditions. The relationship between the absorbance at 465 nm and the concentration was found to be linear over the range 1-10 microg/ml. Moreover, the fluorescence intensity was also found to be directly proportional at the concentration over the range of 20-100 ng/ml at 530 nm after excitation at 465 nm. The proposed procedure was successfully applied to the determination of ramipril in both tablet dosage form and in plasma. Spectrophotometric determination of ramipril tablets yielded a percentage recovery of 98.66+/-0.38, while the percentage recovery of spectrofluorimetric determination of ramipril in spiked human plasma was 99.08+/-1.11%. The results obtained are in good agreement with those obtained by the reference method. No interference could be observed from the co-administered drug (hydrochlorothiazines).
雷米普利作为一种仲胺化合物,与7-氟-4-硝基苯并-2-氧代-1,3-二唑(NBD-F)反应生成相应的荧光NBD-雷米普利。基于这一事实,开发了分光光度法和荧光法测定雷米普利。仔细研究了这些参数对反应产物的影响以优化反应条件。发现在1-10微克/毫升范围内,465纳米处的吸光度与浓度呈线性关系。此外,在465纳米激发后,在530纳米处,荧光强度在20-100纳克/毫升浓度范围内也与浓度成正比。所提出的方法成功应用于片剂剂型和血浆中雷米普利的测定。分光光度法测定雷米普利片剂的回收率为98.66±0.38%,而荧光分光光度法测定加标人血浆中雷米普利的回收率为99.08±1.11%。所得结果与参考方法所得结果高度一致。未观察到合用药物(氢氯噻嗪)的干扰。