Abstract
Background: Poisoning with Gloriosa superba, a plant containing colchicine, is common in Sri Lanka.
Objectives: This study was to estimate release of colchicine from 5 g of different parts of Gloriosa superba in simulated gastric and intestinal media, and examine the binding efficacy of activated charcoal (AC) to colchicine within this model.
Methods: A USP dissolution apparatus-II was used to prepare samples for analysis of colchicine using HPLC.
Results: Cumulative colchicine release from tuber in gastric media at 120 minutes was significantly higher (2883 μg/g) than in intestinal media (1015 μg/g) (p < .001). Mean ± SD cumulative colchicine concentration over 2 hours from tuber, leaves and trunk in gastric medium was 2883.15 ± 1295.63, 578.25 ± 366.26 and 345.60 ± 200.08 μg/g respectively and the release in intestinal media was 1014.75 ± 268.16, 347.40 ± 262.61 and 251.55 ± 285.72 μg/g respectively. Introduction of 50 g of AC into both media made colchicine undetectable (<0.1 μg/ml).
Conclusions: The tuber released the highest quantity of colchicine. The colchicine release and elapse time to achieve saturated, equilibrium dissolution mainly depends on physicochemical properties of plant part. Significant in vitro binding of colchicine to AC suggests that AC has a role in decontamination of patients presenting to hospital after ingestion of Gloriosa superba.
Acknowledgements
We thank Dr. Lackshman Jayakody Faculty of Agriculture, University of Peradeniya for identifying the plant, the chairman and the director of QC lab of Sri Lanka Pharmaceutical Manufacturing Cooperation for providing facilities to conduct dissolution tests at their laboratory. SACTRC team, specifically managers, Clinical Research Coordinators and Clinical Research Assistants for their support in collection of plant parts from various parts of Sri Lanka. The laboratory scientists from St George’s University of London for analysing the dissolution sample using HPLC techniques at their laboratory and Dr. Nilupa department of Allied Health Sciences, University of Peradeniya, Sri Lanka for her expertise on chemistry of colchicine. The South Asian Clinical Toxicology Research Collaboration is funded by the Wellcome Trust/National Health and Medical Research Council International Collaborative Research Grant 071669MA.
Disclosure statement
No potential conflict of interest was reported by the authors.