Nano gold conjugation, anti-arthritic potential and toxicity studies of snake <i style="mso-bidi-font-style:normal">Naja kaouthia</i> (Lesson, 1831) venom protein toxin NKCT1 in male albino rats and mice

Abstract

Nanoscience and Nanotechnology have found their way in the fields of pharmacology and medicine. The conjugation of drug to nanoparticles combines the properties of both. In this study, gold nanoparticle (GNP) was conjugated with NKCT1, a cytotoxic protein toxin from Indian cobra venom for evaluation of anti-arthritic activity and toxicity in experimental animal models. GNP conjugated NKCT1 (GNP-NKCT1) synthesized by NaBH₄reduction method was stable at room temperature (25±2 °C), <i>p</i>H 7.2. Hydrodynamic size of GNP-NKCT1 was <span style="color:#131413;mso-ansi-language:EN-IN;mso-fareast-language:EN-IN">68<span style="mso-fareast-font-family:AdvTT3713a231+20;color:#131413;mso-ansi-language: EN-IN;mso-fareast-language:EN-IN">–<span style="color:#131413; mso-ansi-language:EN-IN;mso-fareast-language:EN-IN">122 nm. Arthritis was developed by <span style="mso-bidi-font-style:italic">Freund's complete adjuvant induction in male albino rats and treatment was done with NKCT1/GNP-NKCT1/standard drug. The paw/ankle swelling, urinary markers, serum markers and cytokines were changed significantly in arthritic control rats which were restored after GNP-NKCT1 treatment. Acute toxicity study revealed that GNP conjugation increased the minimum lethal dose value of NKCT1 and partially reduced the NKCT1 induced increase of the serum biochemical tissue injury markers. Histopathological study showed partial restoration of toxic effect in kidney tissue after GNP conjugation. Normal lymphocyte count in culture was in the order of GNP-NKCT1>NKCT1>Indomethacine treatment. The present study confirmed that GNP conjugation increased the antiarthritic activity and decreased toxicity profile of NKCT1.

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