Literature DB >> 26713669

Application of SPECT/CT imaging system and radiochemical analysis for investigation of blood kinetics and tissue distribution of radiolabeled plumbagin in healthy and Plasmodium berghei-infected mice.

W Sumsakul1, J Karbwang2, K Na-Bangchang3.   

Abstract

Plumbagin is a derivative of napthoquinone which is isolated from the roots of plants in several families. These compound exhibits a wide range of biological and pharmacological activities including antimalarial, antibacterial, antifungal, and anticancer activities. The aim of the study was to investigate blood kinetics and tissue distribution of plumbagin in healthy and Plasmodium berghei-infected mice using Single-Photon Emission Computed Tomography/Computed Tomography (SPECT/CT) and radiochemical analysis by gamma counter. Plumbagin was labeled with (99m)technetium and the reducing agent stannous chloride dihydrate (50 μg/ml) at pH 6.5. Blood kinetics and tissue distribution of the radiolabeled plumbagin were investigated in healthy and P. berghei-infected mice (2 males and 2 females for each experimental group). In vitro and in vivo stability of plumbagin complex suggested satisfactory stability profiles of (99m)Tc-plumbagin complex in plasma and normal saline (92.21-95.47%) within 24 h. Significant difference in blood kinetics parameters (Cmax, AUC, t1/2, MRT, Vd, and CL) were observed between P. berghei-infected and healthy mice. The labeled complex distributed to all organs of both healthy and infected mice but with high intensity in liver, followed by lung, stomach, large intestine and kidney. Accumulation in spleen was markedly noticeable in the infected mice. Plumbagin-labeled complex was rapidly cleared from blood and major routes of excretion were hepatobiliary and pulmonary routes. In P. berghei-infected mice, t1/2 was significantly decreased, while Vd and CL were increased compared with healthy mice. Result suggests that malaria disease state influenced the pharmacokinetics and disposition of plumbagin. SPECT/CT imaging with radiolabeled (99m)Tc is a viable non-invasive technique that can be applied for investigation of kinetics and biodistribution of plumbagin in animal models.
Copyright © 2016. Published by Elsevier Inc.

Entities:  

Keywords:  Biodistribution; Plumbagin; SPECT/CT imaging system; Technetium-99m

Mesh:

Substances:

Year:  2015        PMID: 26713669     DOI: 10.1016/j.exppara.2015.12.001

Source DB:  PubMed          Journal:  Exp Parasitol        ISSN: 0014-4894            Impact factor:   2.011


  2 in total

1.  Pharmacokinetics, toxicity, and cytochrome P450 modulatory activity of plumbagin.

Authors:  Wiriyaporn Sumsakul; Tullayakorn Plengsuriyakarn; Kesara Na-Bangchang
Journal:  BMC Pharmacol Toxicol       Date:  2016-11-14       Impact factor: 2.483

2.  Pharmacokinetics of gene recombined angiogenesis inhibitor Kringle 5 in vivo using 131I specific markers and SPECT/CT.

Authors:  Ge Yan; Danrong Yang; Yan Yu; Jianjun Xue; Yifan Jia; Xuanzi Sun; Boyu Wang; Zewei Zhao; Maode Wang
Journal:  J Pharm Anal       Date:  2016-09-03
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.