Drug Res (Stuttg) 2013; 63(11): 558-563
DOI: 10.1055/s-0033-1347256
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Development and Validation of a High-performance Liquid Chromatography Coupled with Ultraviolet Detection Method for the Determination of Isocorydine in Rat Plasma and its Application in Pharmacokinetics

Y.-Q. Liu
1   Department of Pharmacy, Kunming General Hospital of Chengdu Military Region, Kunming, PR China
2   School of Clinical Medicine, Kunming medical university, Kunming, PR China
,
H.-L. Li
1   Department of Pharmacy, Kunming General Hospital of Chengdu Military Region, Kunming, PR China
,
J.-C. He
1   Department of Pharmacy, Kunming General Hospital of Chengdu Military Region, Kunming, PR China
,
E.-F. Feng
1   Department of Pharmacy, Kunming General Hospital of Chengdu Military Region, Kunming, PR China
,
G.-X. Rao
3   School of Pharmacy, Yunnan College of Traditional Chinese Medicine, Kunming, PR China
,
G.-L. Xu
1   Department of Pharmacy, Kunming General Hospital of Chengdu Military Region, Kunming, PR China
2   School of Clinical Medicine, Kunming medical university, Kunming, PR China
› Author Affiliations
Further Information

Publication History

received 30 November 2012

accepted 18 May 2013

Publication Date:
24 July 2013 (online)

Abstract

A new HPLC–UV method has been developed, validated and applied for the determination of isocorydine (CAS 475-67-2) in rat plasma after oral or intravenous (i. v.) administration. Caffeine was used as the internal standard (IS). The analyte and IS were extracted from rat plasma by liquid–liquid extraction (LLE) with methyl tert-butyl ether and they were separated on an XTerra C18 column (250×4.6 mm, 5 µm, pH 1–12) with UV detection at 264 nm. The mobile phase consisted of methanol and 0.02 mol/L potassium dihydrogen phosphate–phosphoric acid buffer solution (pH 3.2) (30:70, v/v) at a flow rate of 1 mL/min for 8.5 min. The retention times of isocorydine and caffeine were approximately 6.5 and 5.1 min, respectively. The good linearity of the calibration curves was observed over the concentration range of 0.05–8 µg/mL (n=8, r 2≥0.9995). The lower limit of quantification (LLOQ) was 0.05 µg/mL [signal to noise ratio (S/N)≥10], and the limit of detection (LOD) was demonstrated as 0.01 µg/mL (S/N≥3). The mean extraction recovery ranged from 83.7% to 89.5% at 3 quality control (QC) concentrations. Intra-day and inter-day precision (relative standard deviation, RSD%) were within 4.7% and accuracy (relative error, RE%) ranged from −1.2% to 4.5%. The developed method was successfully applied to determination of the pharmacokinetic properties of isocorydine in rats after oral administration at a dose of 20 mg/kg and i. v. injection at 5 mg/kg.

 
  • References

  • 1 Wang X, Dong HJ, Yang B et al. Preparative isolation of alkaloids from Dactylicapnos scandens using pH-zone-refining counter-current chromatography by changing the length of the separation column. J Chromatogr B 2011; 879: 3767-3770
  • 2 Wang FH, Hu X, Cheng HL et al. Alkaloids from Dactylicapnos scandens . Zhongguo Zhong Yao Za Zhi 2009; 34: 2057-2059
  • 3 Jiangsu new medical college Dictionary of Chinese Medicine, Shanghai Scientific and Technology Literature Publishing House, Shanghai 2006
  • 4 The people’s government of Dali Bai Autonomous Prefecture, Yunnan Province, China Dali zhong yao zi yuan zhi, Yunnan Nationalities Publishing House, Kunming 1991
  • 5 Wu M, Wang YY, Ai TM. Studies of analgesic effect and mechanism of total alkaloid extracted from Dactylicapnos scandens . Zhong Cao Yao 2003; 34: 1203-1205
  • 6 Hu RL, Dai XJ, Lu YB et al. Preparative separation of isoquinoline alkaloids from Stephania yunnanensis by pH-zone-refining counter-current chromatography. J Chromatogr B 2010; 878: 1881-1884
  • 7 He L, Zhang YH, Tang LJ et al. Alkaloids from Stephania cepharantha Hayata . Zhongguo Zhong Yao Za Zhi 2010; 35: 1272-1275
  • 8 Hung TM, Dang NH, Kim JC et al. Alkaloids from Roots of Stephania rotunda and Their Cholinesterase Inhibitory Activity. Planta Med 2010; 76: 1762-1764
  • 9 Goren AC, Zhou BN, Kingston GD. Cytotoxic and DNA damaging activity of some aporphine alkaloids from Stephania dinklagei . Planta Med 2003; 69: 867-868
  • 10 You M, Wickramaratne DB, Silva GL et al. -Roemerine, an aporphine alkaloid from Annona senegalensis that reverses the multidrug-resistance phenotype with cultured cells. J Nat Prod 1995; 58: 598-604
  • 11 Nie CX, Song YL, Cheng D et al. Studies on chemical constituents of leaves of Aquilaria sinensis. Zhongguo Zhong Yao Za Zhi 2009; 34: 858-860
  • 12 Shafiee A, Lalezari I, Rahimi O. Alkaloids of papaver genus IX. Alkaloids of Glaucium vitellinum Boiss and Buhse, population Seerjan and Glaucium pulchrum Stapf, population Elika. Lloydia 1977; 40: 352-355
  • 13 Istatkova RS, Philipov SA. Alkaloids from Isopyrum thalictroides L. Phytochemistry 2000; 54: 959-964
  • 14 Sotnikova R, Kettmann V, Kostalova D et al. Relaxant properties of some aporphine alkaloids from Mahonia aquifolium . Methods Find Exp Clin Pharmacol 1997; 19: 589-597
  • 15 Chen ZH, Zhang ZX, Wang MD. Spasmolytic effects of isocorydine on the isolated gallbladder and Oddi’s sphincter in vitro. Zhongguo Yao Li Xue Bao 1985; 6: 45-48
  • 16 Chen ZH, Zhang ZX, Wang MD et al. Spasmolytic effect of isocorydine on isolated vascular strips. Zhongguo Yao Li Xue Bao 1982; 3: 240-242
  • 17 Su HD, Huang GP. Effects of d-isocorydine on mouse vas deferens. Zhongguo Yao Li Xue Bao 1986; 7: 198-201
  • 18 Zhao DH, Yang XM, Sheng BH. Antiarrhythmic action of d-isocorydine hydrochloride. Zhongguo Yao Li Xue Bao 1986; 7: 131-134
  • 19 Yadav DK, Singh N, Dev K et al. Anti-ulcer constituents of Annona squamosa twigs. Fitoterapia 2011; 82: 666-675
  • 20 Lin CJ, Chen CH, Liu FW et al. Inhibition of intestinal glucose uptake by aporphines and secoaporphines. Life Sci 2006; 79: 144-153
  • 21 Chen KS, Ko FN, Teng CM et al. Antiplatelet and Vasorelaxing Actions of Some Aporphinoids. Planta Med 1996; 62: 133-136
  • 22 Jiang QS, Huang XN, Sun AS et al. Relation of vasodilative action of isocorydine to cyclic nucleotides. Chinese J Pharmacol Toxicol 2001; 15: 251-255
  • 23 Cheng XX, Wang DM, Jiang L et al. Topoisomerase I Inhibitory Alkaloids from Corydalis saxicola . Chem Biodivers 2008; 5: 1335-1344
  • 24 Sun HF, Hou HL, Lu P et al. Isocorydine Inhibits Cell Proliferation in Hepatocellular Carcinoma Cell Lines by Inducing G2/M Cell Cycle Arrest and Apoptosis. PLoS One 2012; 7: e36808
  • 25 Lu P, Sun HF, Zhang LX et al. Isocorydine targets the drug-resistant cellular side population through PDCD4-related apoptosis in hepatocellular carcinoma. Mol Med 2012;
  • 26 Zhou SB, Zhou QY, Guan YF et al. Analgesic effect of isocorydine on 429 Digestive system disease cases. Xin Yao Yu Lin Chuang 1987; 6: 23-25
  • 27 Cheng XX, Wang DM, Jiang L et al. Simultaneous determination of eight bioactive alkaloids in Corydalis saxicola by high-performance liquid chromatography coupled with diode array detection. Phytochem Anal 2008; 19: 420-428
  • 28 Yan TQ, Yang YF, Ai TM. Determination of isocorydine and protopine in Dactylicapnos scandens by HPLC. Zhongguo Zhong Yao Za Zhi 2004; 29: 961-963
  • 29 Huang JM, Guo JX, Duan GL. Determination of 7 bio-active alkaloids in Stephania plants by RP-HPLC. Yao Xue Xue Bao 1998; 33: 528-533
  • 30 Sun WS, Lee SS, Huang HM. Determination of lauraceous aporphine alkaloids by high-performance liquid chromatography. J Pharm Biomed Anal 1996; 14: 1383-1387
  • 31 Guo CC, Yu CH, Li L et al. Rapid determination of isocorydine in rat plasma and tissues using liquid chromatography – tandem mass spectrometry and its applications to pharmacokinetics and tissue distribution. Xenobiotica 2012; 42: 466-476
  • 32 Guidance for Industry, Bioanalytical Method Validation, US Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER), 2001 Center for Veterinary Medicine (CV), May 2001. http://www/fda.gov/cder/guidance/index.htm