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    Article

    Rapid, sensitive, and validated UPLC/Q‑TOF‑MS method for quantitative determination of vasicine in Adhatoda vasica and its in vitro culture

    Garg Madhukar1★, Ennus Tajuddin Tamboli1, Parveen Rabea2, S. H. Ansari1, M. Z. Abdin3, Ahmad Sayeed1★ Corresponding author

    1. 1Departments of Pharmacognosy and Phytochemistry, Bioactive Natural Product Laboratory, University, Hamdard Nagar, New Delhi, India.
    2. 2Pharmaceutics, Faculty of Pharmacy, India.
    3. 3Biotechnology, Faculty of Science, Hamdard University, Hamdard Nagar, New Delhi, India.

    CORRESPONDENCE

    Garg Madhukar

    Departments of Pharmacognosy and Phytochemistry, Bioactive Natural Product Laboratory, University, Hamdard Nagar, New Delhi, India.

    sahmad_jh@yahoo.co.in

    Received: 24-11-2012; Revised: 10-01-2013.

    Volume 10, Issue 37s · pp. S198–S205 · PUBLISHED 21 February 2014 · DOI: 10.4103/0973-1296.127375

    View on Pharmacogn. Mag. original site ↗

    ABSTRACT

    Background: Adhatoda vasica a perennial herb has been used in Ayurvedic and Unani system of medicines since last 2000 years and has been employed for the treatment of respiratory tract ailments. Objective: To develop and validate new, rapid, and highly sensitive high throughput ultra‑performance liquid chromatography/quadrupole‑time‑of‑flight mass‑spectrometry (UPLC/Q‑TOF‑MS) method for the quantitative estimation of vasicine in the leaves and to establish in vitro cultures of Adhatoda vasica for production of vasicine. Materials and Methods: The chromatographic separation was achieved on a Waters ACQUITY UPLCTM BEH C8 (100.0 × 2.1 mm; 1.7 µm) column packing using isocratic mobile phase consisting of acetonitrile: 20 mM ammonium acetate (90:10; v/v) in a multiple reactions monitoring mode using the transitions m/z 189.09 → 171.08 for vasicine. Results: The vasicine was eluted at 2.58 ± 0.05 min and established a dynamic range of linearity over the concentration range of 1–1000 ng/ml (r2 = 0.999 ± 0.0005). The lower limit of detection and quantification was 0.68 and 1.0 ng/ml, respectively. There was no significant difference observed in the content of vasicine (0.92-1.04%w/w) among the eleven samples collected from different locations of India. The in vitro cultures developed showed that addition of extra 28 mM KNO3 and 100 mM NaCl in MS medium supplemented with 2,4‑dichlorophenoxyacetic acid (2,4‑D) + benzyladenine (BA) + indole acetic acid (IAA) (1 ppm each) produces faster biomass and higher amount of quinazoline alkaloids. Conclusion: Rapid, efficient, and sensitive UPLC/Q‑TOF‑MS method was developed for the estimation of vasicine and an efficient protocol for development of in vitro cultures was proposed, which can be used at large scale for industrial production of vasicine using bioreactors.

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      Madhukar, G., Tamboli, E. T., Rabea, P., Ansari, S. H., Abdin, M. Z., & Sayeed, A. (2014). Rapid, sensitive, and validated UPLC/Q‑TOF‑MS method for quantitative determination of vasicine in Adhatoda vasica and its in vitro culture. Pharmacognosy Magazine, 10(37s), S198–S205. https://doi.org/10.4103/0973-1296.127375