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Background: Snakehead fish (Ophiocephalus striatus) is a freshwater fish that is utilized as anti-inflammatory and anticancer drug. The aim of this study was to determine the toxicity effect of snakehead fish powder (SFP), formulate it into liposome and in vitro study using sensitive and resistant breast cancer cells. Methods: Dried powder of snakehead fish was made using the atomizer then made a test solution which was divided into 7 treatment groups in different concentrations. They were exposed to zebrafish embryos then observed for 72 h post fertilization (hpf). After acquiring the half maximal inhibitory concentration (IC50) and lethal concentration (LC50) of SFP, these concentrations were used to formulate SFP into liposome by extrusion method. SFP-liposomes were characterized and stable tested. Afterwards, SFP-liposomes were evaluated in vitro using sensitive and resistant breast cancer cells. Results: The maximum allowed toxicant concentration of SFP was 0.0543 mg/mL meaning slight toxic symptoms, IC50 = 0.0945 mg/mL showing the growth inhibition of zebrafish embryos, and LC50 = 0.1549 mg/mL meaning very toxic category that has killed zebrafish embryos. The characterization results showed that size of SFP-liposome were 121 nm ± 0.29, polydispersity index 0.06 ± 0.02, zeta-potential -10.15 mV ± 0.36 and % entrapment efficiency (EE) 85.75% ± 2.24. Six weeks of stability study showed that size profile was stable at 25°C and 37°C. Moreover, SFP-liposomes inhibited breast cancer cell proliferation when evaluated with 4T1 and MDA-MB231-sensitive and resistant cells. Conclusion: SFP has bioactive compounds based on toxicity effect and can be formulated into liposome as a promising nanonutraceutical formulation.

A recent outbreak of Coronavirus SARS-CoV-2 disease also called COVID-19 in China, has rapidly spread to other countries of the world. The medical and scientific communities are working tirelessly to produce a vaccine due to the lethal nature of this virus. COVID-19 is a novel virus that requires immediate emergency therapy, thereby leading to massive fear of infection, social problems in the community, and an increase in the number of infected people. Therefore, scientists and researchers need to determine the epidemiological cases of the virus, such as its mode of transmission, effective preventive measures, and the nature of the life cycle. In addition, there needs to be current literature advances in diagnostic development such as RT-PCR, CT- Scan, Elisa as well as clinical researches on modern and herbal drugs for the treatment of infected patients. This treatment technique is classified from antiviral drugs such as entry, replication, nucleosides, nucleotides, and protease inhibitors, along with the use of heterocyclic drugs, monoclonal antibodies therapy, vaccine development and herbal formulations that have been pre-clinically tested in vitro and molecular docking. Chemical drug molecules with prospective applications in the treatment of COVID-19 have been included in this review

Background: The aim of the present study was to characterize and evaluate the nanoemulgel (NEG) of snakehead fish powder (SFP), as a transdermal delivery system for poorly water soluble drug, in order to conquer the inconveniences related to its oral conveyance. Methods: Diverse nanoemulsion components (oil, surfactant, and co-surfactant) were chosen based on solvency and emulsification capacity. SFP loaded nanoemulsion which tested by stress-stability testing was carried out for all formulations and those that passed these tests were characterized for mean droplet size, polydispersity index (PDI), zeta potential, pH, viscosity, and transmittance. After that, this was continued by permeation studies using snake skin in vitro and rabbit skin in vivo studies i.e. skin irritation study and the effectiveness test. Results: Mean droplet size and zeta potential of the optimized nanoemulsion (NE4) were found to be 98.6 ± 0.93 nm (polydispersity index, PDI = 0.1 ± 0.20) and -57.5 ± 0.3 mV respectively. Optimized nanoemulsion was converted into nanoemulgel with 1.5% w/v of gelling agent (HPMC) and evaluated for pH, viscosity, spreadability, and extrudability measurement. Ex vivo transdermal permeation value for SFP through snake skin as membrane from NEG1, NEG2, NEG3 and marketed SFP cream showed results of 55.65 ± 0.93%, 56.14 ± 0.70%, 66.75 ± 1.03% and 49.80 ± 3.42% respectively in 3 hours. Moreover, all the treatment group did not show skin irritation of each group. The effect of burn wound healing of NEG3 showed a significant (P