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ABSTRACT:The present study specifically indicated that the crude ethanolic and aqueous extracts of the leaves of Adhatoda vasica Nees produced anthelmintic activity against african earthworm Eudrilus eugeniae. Various concentrations (10, 25, 50 mg/ml) of aqueous and ethanolic extracts were evaluated in the bioassay involving determination of time of paralysis (P) and time of death (D) of the worms. Albendazole was used as standard anthelmintic drug and distilled water was used as negative control. The results of the present study indicated that the ethanolic and aqueous extracts significantly exhibited paralysis of worms in lower doses (10, 25 and 50 mg/ml) and also caused death of worms at higher concentration of 50 mg/ml, as compared to standard drug. Further studies are in process to isolate the active principle responsible for the activity.

The objective of the present work was to engineer and characterize stable citric acid cross-linked microcomplex of the inclusion complexes of artemether with β-cyclodextrin and Kollidon VA 64 with lumefantrine to release the drugs in controlled manner for effective combinational drug treatment in malaria. The microcomplex had a hydrodynamic diameter of 1047 ± 147 nm with surface charge of -19.7 ± 0.5 mV. The microcomplex showed high encapsulation efficiencies 85.6 ± 1.78% for artemether and 91.16 ± 2.21% for lumefantrine due to the lipophilic nature of drugs. In-vitro and in-vivo drug release studies showed the controlled release of artemether and lumefantrine for a period of 24 h.