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Volume 37 Issue 5
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Article Navigation >  Journal of Pharmaceutical Practice and Service  > 2019  >  37(5): 450-452,480

WANG Jing, ZHANG Chuan, LI Yi, REN Jinmei, TANG Kouming. Determination of palmitul 3-(3,4-dihydroxyphenyl)-2-hydroxypropanoate liposome by HPLC method[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(5): 450-452,480. doi: 10.3969/j.issn.1006-0111.2019.05.012
Citation: WANG Jing, ZHANG Chuan, LI Yi, REN Jinmei, TANG Kouming. Determination of palmitul 3-(3,4-dihydroxyphenyl)-2-hydroxypropanoate liposome by HPLC method[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(5): 450-452,480. doi: 10.3969/j.issn.1006-0111.2019.05.012
shu

Determination of palmitul 3-(3,4-dihydroxyphenyl)-2-hydroxypropanoate liposome by HPLC method

doi: 10.3969/j.issn.1006-0111.2019.05.012
  • 1.

    Department of Pharmacy, Qingpu Branch of Zhongshan Hospital Affiliated to Fudan University, Shanghai 201700, China

  • 2.

    Department of Medicine, Shanghai University, Shanghai 200003, China

  • 3.

    Zhoupu Hospital Affiliated to Shanghai University of Medicine & Health Sciences, Shanghai 201318, China

  • Received Date: 2019-02-14
  • Rev Recd Date: 2019-05-06
  • Objective To establish a HPLC method for the assay of palmitul 3-(3,4-dihydroxyphenyl)-2-hydroxypropanoate (PDSS) in liposomes. Methods The separation was performed with an Agilent ZORBAX Eclipse Plus C18 column (4.6 mm×200 mm,5 μm) at room temperature.The mobile phase was acetonitrile-aqueous solution (500 ml water + 0.1 ml triethylamine + 0.1 ml formic acid,pH=6-7) (50:50) with the flow rate of 1 ml/min.Zidovudine palmitate was detected at 280 nm. Results PDSS had a good linear recovery between 0.05-0.45 mg/ml.The intra-day and inter-day RSD were <2%.The extracted recovery was in the range of 96% to 102%.The assay results for three batches were 97.81%,101.20% and 98.53%. Conclusion This method is simple,accurate and reliable.It can be used for the determination of PDSS in liposomes.
  • [1] 陈伟伟,高润霖,刘力生,等.中国心血管病报告2016(概要)[J].中国循环杂志,2017,32(6):521-530.
    [2] ZHOU L M,ZUO Z,CHOW M S S.Danshen:an overview of its chemistry,pharmacology,pharmacokinetics,and clinical use[J].J Clin Pharmacol,2005,45(12):1345-1359.
    [3] WU L,QIAO H,LI Y,et al.Protective roles of puerarin and Danshensu on acute ischemic myocardial injury in rats[J].Phytomedicine,2007,14(10):652-658.
    [4] YIN Y,GUAN Y,DUAN J L,et al.Cardioprotective effect of Danshensu against myocardial ischemia/reperfusion injury and inhibits apoptosis of H9c2 cardiomyocytes via Akt and ERK1/2 phosphorylation[J].Eur J Pharmacol,2013,699(1-3):219-226.
    [5] LAM F F,YEUNG J H,CHAN K M,et al.Relaxant effects of danshen aqueous extract and its constituent Danshensu on rat coronary artery are mediated by inhibition of calcium channels[J].Vascul Pharmacol,2007,46(4):271-277.
    [6] TANG Y Q,WANG M H,LE X Y,et al.Antioxidant and cardioprotective effects of Danshensu (3-(3,4-dihydroxyphenyl)-2-hydroxy-propanoic acid from Salvia miltiorrhiza) on isoproterenol-induced myocardial hypertrophy in rats[J].Phytomedicine,2011,18(12):1024-1030.
    [7] LE X Y.Effects of danshensu on the incidence of ischemia-reperfusion induced arrhythmia in hypertrophy rat heart[J].Chin J Nat Med,2009,6(6):461-465.
    [8] WANG F,LIU Y Y,LIU L Y,et al.The attenuation effect of 3,4-dihydroxy-phenyl lactic acid and salvianolic acid B on venular thrombosis induced in rat mesentery by photochemical reaction[J].Clin Hemorheol Microcirc,2009,42(1):7- 18.
    [9] TANG Y Q,WANG M H,CHEN C L,et al.Cardiovascular protection with Danshensu in spontaneously hypertensive rats[J].Biol Pharm Bull,2011,34(10):1596-1601.
    [10] LIU D,HU H Y,LIN Z X,et al.Quercetin deformable liposome:Preparation and efficacy against ultraviolet B induced skin damages in vitro and in vivo[J].J Photochem Photobiol B:Biol,2013,127:8-17.
    [11] SLINGERLAND M,GUCHELAAR H J,GELDERBLOM H.Liposomal drug formulations in cancer therapy:15 years along the road[J].Drug Discov Today,2012,17(3-4):160-166.
    [12] 纪周新,刘琳琳,李艺养,等.丹参素脂质体的制备及体外释放度研究[J].中国药师,2015,18(10):1649-1651,1660.
    [13] GUO X J,FAN X J,QIAO B,et al.A lipophilic prodrug of Danshensu:preparation,characterization,and in vitro and in vivo evaluation[J].Chin J Nat Med,2017,15(5):355-362.
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Determination of palmitul 3-(3,4-dihydroxyphenyl)-2-hydroxypropanoate liposome by HPLC method

doi: 10.3969/j.issn.1006-0111.2019.05.012
  • 1. Department of Pharmacy, Qingpu Branch of Zhongshan Hospital Affiliated to Fudan University, Shanghai 201700, China
  • 2. Department of Medicine, Shanghai University, Shanghai 200003, China
  • 3. Zhoupu Hospital Affiliated to Shanghai University of Medicine & Health Sciences, Shanghai 201318, China
  • Received Date: 2019-02-14
  • Rev Recd Date: 2019-05-06

Abstract: Objective To establish a HPLC method for the assay of palmitul 3-(3,4-dihydroxyphenyl)-2-hydroxypropanoate (PDSS) in liposomes. Methods The separation was performed with an Agilent ZORBAX Eclipse Plus C18 column (4.6 mm×200 mm,5 μm) at room temperature.The mobile phase was acetonitrile-aqueous solution (500 ml water + 0.1 ml triethylamine + 0.1 ml formic acid,pH=6-7) (50:50) with the flow rate of 1 ml/min.Zidovudine palmitate was detected at 280 nm. Results PDSS had a good linear recovery between 0.05-0.45 mg/ml.The intra-day and inter-day RSD were <2%.The extracted recovery was in the range of 96% to 102%.The assay results for three batches were 97.81%,101.20% and 98.53%. Conclusion This method is simple,accurate and reliable.It can be used for the determination of PDSS in liposomes.

WANG Jing, ZHANG Chuan, LI Yi, REN Jinmei, TANG Kouming. Determination of palmitul 3-(3,4-dihydroxyphenyl)-2-hydroxypropanoate liposome by HPLC method[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(5): 450-452,480. doi: 10.3969/j.issn.1006-0111.2019.05.012
Citation: WANG Jing, ZHANG Chuan, LI Yi, REN Jinmei, TANG Kouming. Determination of palmitul 3-(3,4-dihydroxyphenyl)-2-hydroxypropanoate liposome by HPLC method[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(5): 450-452,480. doi: 10.3969/j.issn.1006-0111.2019.05.012
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