光谱学与光谱分析
光譜學與光譜分析
광보학여광보분석
SPECTROSCOPY AND SPECTRAL ANALYSIS
2014年
6期
1589-1593
,共5页
李佳渝%李华春%吴飞%谭克俊
李佳渝%李華春%吳飛%譚剋俊
리가투%리화춘%오비%담극준
盐酸巴马汀%桑色素%共振光散射
鹽痠巴馬汀%桑色素%共振光散射
염산파마정%상색소%공진광산사
Palmatine hydrochloride%Morin%Resonance light scattering
在pH 为4.6的 HAc-NaAc介质中,盐酸巴马汀与桑色素通过静电引力发生反应,得到具有疏水性的离子缔合物,致使体系在308 nm处的共振光散射信号显著增强。研究表明,体系增强的共振光散射信号强度与盐酸巴马汀的浓度在0.08~1.0μmol·L-1之间具有良好的线性关系,检测限为8.0 nmol·L-1。由此建立了用于盐酸巴马汀检测的共振光散射分析方法。研究了体系的散射光谱和吸收光谱,通过扫描电镜和动态光散射考察离子缔合物的聚集情况并研究了体系的反应机理,研究了酸度及离子强度对体系的影响,最终实验选择pH 4.6的 HAc-NaAc缓冲,不加NaCl控制体系离子强度的情况下信号最佳。探讨了体系的稳定性,结果显示本反应体系反应迅速,5 min内散射强度即可达到最大值并至少能稳定120 min。考察了可能存在的共存物质的影响,结果发现常见的金属离子,无机阴离子,部分糖类及氨基酸不影响对盐酸巴马汀的检测。该方法具有简单,快速,灵敏度高的优点。该法成功用于实际药片和胶囊中盐酸巴马汀含量的测定,RSD≤3.3%。
在pH 為4.6的 HAc-NaAc介質中,鹽痠巴馬汀與桑色素通過靜電引力髮生反應,得到具有疏水性的離子締閤物,緻使體繫在308 nm處的共振光散射信號顯著增彊。研究錶明,體繫增彊的共振光散射信號彊度與鹽痠巴馬汀的濃度在0.08~1.0μmol·L-1之間具有良好的線性關繫,檢測限為8.0 nmol·L-1。由此建立瞭用于鹽痠巴馬汀檢測的共振光散射分析方法。研究瞭體繫的散射光譜和吸收光譜,通過掃描電鏡和動態光散射攷察離子締閤物的聚集情況併研究瞭體繫的反應機理,研究瞭痠度及離子彊度對體繫的影響,最終實驗選擇pH 4.6的 HAc-NaAc緩遲,不加NaCl控製體繫離子彊度的情況下信號最佳。探討瞭體繫的穩定性,結果顯示本反應體繫反應迅速,5 min內散射彊度即可達到最大值併至少能穩定120 min。攷察瞭可能存在的共存物質的影響,結果髮現常見的金屬離子,無機陰離子,部分糖類及氨基痠不影響對鹽痠巴馬汀的檢測。該方法具有簡單,快速,靈敏度高的優點。該法成功用于實際藥片和膠囊中鹽痠巴馬汀含量的測定,RSD≤3.3%。
재pH 위4.6적 HAc-NaAc개질중,염산파마정여상색소통과정전인력발생반응,득도구유소수성적리자체합물,치사체계재308 nm처적공진광산사신호현저증강。연구표명,체계증강적공진광산사신호강도여염산파마정적농도재0.08~1.0μmol·L-1지간구유량호적선성관계,검측한위8.0 nmol·L-1。유차건립료용우염산파마정검측적공진광산사분석방법。연구료체계적산사광보화흡수광보,통과소묘전경화동태광산사고찰리자체합물적취집정황병연구료체계적반응궤리,연구료산도급리자강도대체계적영향,최종실험선택pH 4.6적 HAc-NaAc완충,불가NaCl공제체계리자강도적정황하신호최가。탐토료체계적은정성,결과현시본반응체계반응신속,5 min내산사강도즉가체도최대치병지소능은정120 min。고찰료가능존재적공존물질적영향,결과발현상견적금속리자,무궤음리자,부분당류급안기산불영향대염산파마정적검측。해방법구유간단,쾌속,령민도고적우점。해법성공용우실제약편화효낭중염산파마정함량적측정,RSD≤3.3%。
A novel resonance light scattering method for the determination of PaH was developed based on the interaction of Pal-matine hydrochloride (PaH)with Morin in pH 4. 6 HAc-NaAc buffer medium,and this interaction can result in largely enhanced resonance light scattering (RLS)signal characterized by a peak at 308. 0 nm.It was found that the enhanced RLS signals intensi-ty (IRLS)at 308. 0 nm is proportional to the concentration of PaH.The limit of detection is 8. 0 nmol·L-1 and the linear range is from 0. 08 to 1. 0 mol·L-1 .In this study,the mechanism of this reaction was investigated by scanning electron microscope (SEM),dynamic light scattering (DLS)and UV absorption spectrum.The SEM images and DLS graph show that ion-associa-tion complex aggregated after the addition of PaH .The experimental condition optimization results indicate that when the buffer medium is pH 4. 6 HAc-NaAc without adding NaCl,the system has a good response for PaH.The authors investigated the sta-bility of this system.The results indicate that this reaction system has a rapid response and the IRLS can reach the maximum within 5 min and remain stable at least for 120 min.The tolerance of coexisting foreign substances in the system was also stud-ied.The research results show that the common metal ions,inorganic anions,a part of carbohydrate and amino acids have negli-gible effects on the analysis of PaH .This proposed method has some advantages including simplicity,rapidity and sensitivity.It also has been applied to the detection of PaH in tablet and capsule samples with RSD≤3. 3%.