Sarkis Nazira, Sawan Abdulkader
Department of Analytical and Food Chemistry, Faculty of Pharmacy, University of Aleppo, Aleppo, Syria.
BMC Chem. 2022 Mar 18;16(1):15. doi: 10.1186/s13065-022-00809-x.
An accurate, precise, sensitive, and simple spectroscopic method was developed and validated for simultaneous quantification analysis of tretinoin (TRT) and nicotinamide (NCT) with a ratio of 1:40 (TRT: NCT) in a synthetic mixture from dermal pharmaceutical preparations (solution and cream). Wavelengths were chosen in the first and second-order derivatives which are valid for the determination of NCT with the existence of TRT and excipients of the tested pharmaceutical preparations. Wavelength 253 nm was picked for the first-order derivative. Wavelengths 245 and 269 nm were picked for the second derivative. All previous wavelengths were zero-crossing points for TRT and its pharmaceutical preparations. Zero-order spectroscopy was used to determine TRT at the wavelength 348 nm, where no interference with NCT or any substance in the previous pharmaceutical preparation. The linearity range was studied and found to be 20-120 μg/mL and 0.5-5.0 μg/mL for NCT and TRT respectively. The correlation coefficient was 0.9995-0.9999 for NCT and 0.9998-0.9999 for TRT. The limit of detection (LOD) and the limit of quantification (LOQ) of NCT were 1.510 μg/mL and 4.590 μg/mL respectively at the wavelength 269 nm of the second-order derivative.
开发并验证了一种准确、精密、灵敏且简便的光谱方法,用于同时定量分析皮肤药物制剂(溶液和乳膏)合成混合物中维甲酸(TRT)和烟酰胺(NCT),比例为1:40(TRT:NCT)。在一阶和二阶导数中选择波长,这些波长对于在存在TRT和受试药物制剂辅料的情况下测定NCT是有效的。一阶导数选择波长253 nm。二阶导数选择波长245和269 nm。所有先前的波长都是TRT及其药物制剂的零交叉点。零阶光谱法用于在波长348 nm处测定TRT,在此波长下不受NCT或先前药物制剂中任何物质的干扰。研究了线性范围,发现NCT和TRT的线性范围分别为20 - 120μg/mL和0.5 - 5.0μg/mL。NCT的相关系数为0.9995 - 0.9999,TRT的相关系数为0.9998 - 0.9999。在二阶导数波长269 nm处,NCT的检测限(LOD)和定量限(LOQ)分别为1.510μg/mL和4.