The present work proposes to find if a bio-active composite in the hemolymph or plasma of the freshwater bivalve Anodonta cygnea is able to offer immunity and specificity for meliorating the major symptoms in human SARS and COVID-19 lineage infection. The Methodology concerns in silico procedures using organic fluids from 54 bivalves (in very specific conditions) to evaluate their therapeutic effects in 6 voluntary SARS and COVID-19 infected persons with an integrative diagnosis by a computational Mora®Nova apparatus to access the basal and experimental human physiological parameters.
A deep and consistent study will be developed with an increase in the human sampling for better understanding the intervention efficacy of this intelligence medicine integrator, the Mora® Nova method. These in silico experiments when associated with the bioresonance frequencies from stimulated hemolymph compounds of the freshwater bivalve A. cygnea, may lead us to expect high plasticity and immunological potential. Obviously, additional in vitro studies in future, with adequate culture cell lineages in different conditions and with bioresonance treatment by Mora® Nova method, should also be accomplished with hemolymph/plasma interference to confirm the pertinence, and the real efficacy on SARS / COVID-19 infection as well as to clarify the respective biological mechanisms. In addition, to analyze and evaluate any specific bioactive compound from the induced hemolymph condition needs molecular experiments which can give deep structural information concerning any efficient molecule against the SARS / COVID-19 virus lineage and respective mutants. Effectively, according to current scientific opinion, the virus mutation phenomenon leads to great and problematic difficulty for maintaining the collective and human global immunization. In this case, the present Mora methodology offers a very functional, dynamic, and efficient process when combined with a biological model, as the bivalve A. cygnea, with high plasticity and eventual molecular reconstructive adaptation. This Mora procedure can extend to other immune-depressive diseases namely cancer, rheumatoid arthritis, and neurodegenerative diseases combining with respective stimulated bivalve fluids. It suggests opening a promising future perspective when applied to large human sampling as well as with in vitro cellular assays. In addition, to explore this research with in vitro cell cultures and to do the characterization and the effects from bio-compounds on similar diseases is our close objective.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
45
Marine liquid and fluids extracted from freshwater bivalve of A. cygnea (under very specific conditions)
SARS / COVID-19 fluid/liquid - impregnation
SARS / COVID-19 fluid-bivalve-incubation
Bivalve Manipulation - Stress inducing
Refrigerated fluid to check for maintained response
Instituto Politécnico de Bragança
Bragança, Portugal
ICBAS - University of Porto
Porto, Portugal
Pulmonary system
Voll Electromagnetic conductance reading (Hz) on pulmonary system biopoints
Time frame: T0 - Day 1 - Baseline
Pulmonary system change
Voll Electromagnetic conductance reading (Hz) on pulmonary system biopoints
Time frame: T1 - Day 1 - After in silico human virus infestation
Pulmonary system change
Voll Electromagnetic conductance reading (Hz) on pulmonary system biopoints
Time frame: T2 - Day 1 - After adding the interface of the original fluid
Pulmonary system change
Voll Electromagnetic conductance reading (Hz) on pulmonary system biopoints
Time frame: T3 - Day 1 - After adding the interface of virus impregnated fluid
Pulmonary system change
Voll Electromagnetic conductance reading (Hz) on pulmonary system biopoints
Time frame: T4 - Day 3 - After adding the interface of virus incubated fluid during 48 hours
Cardiac system
Voll Electromagnetic conductance reading (Hz) on cardiac system biopoints
Time frame: T0 - Day 1 - Baseline
Cardiac system change
Voll Electromagnetic conductance reading (Hz) on cardiac system biopoints
Time frame: T1 - Day 1 - After in silico human virus infestation
Cardiac system change
Voll Electromagnetic conductance reading (Hz) on cardiac system biopoints
Time frame: T2 - Day 1 - After adding the interface of the original fluid
Cardiac system change
Voll Electromagnetic conductance reading (Hz) on cardiac system biopoints
Time frame: T3 - Day 1 - After adding the interface of virus impregnated fluid
Cardiac system change
Voll Electromagnetic conductance reading (Hz) on cardiac system biopoints
Time frame: T4 - Day 3 - After adding the interface of virus incubated fluid during 48 hours
Immunologic system
Voll Electromagnetic conductance reading (Hz) on immunologic system biopoints
Time frame: T0 - Day 1 - Baseline
Immunologic system change
Voll Electromagnetic conductance reading (Hz) on immunologic system biopoints
Time frame: T1 - Day 1 - After in silico human virus infestation
Immunologic system change
Voll Electromagnetic conductance reading (Hz) on immunologic system biopoints
Time frame: T2 - Day 1 - After adding the interface of the original fluid
Immunologic system change
Voll Electromagnetic conductance reading (Hz) on immunologic system biopoints
Time frame: T3 - Day 1 - After adding the interface of virus impregnated fluid
Immunologic system change
Voll Electromagnetic conductance reading (Hz) on immunologic system biopoints
Time frame: T4 - Day 3 - After adding the interface of virus incubated fluid during 48 hours
Gastrointestinal system
Voll Electromagnetic conductance reading (Hz) on gastrointestinal system biopoints
Time frame: T0 - Day 1 - Baseline
Gastrointestinal system Change
Voll Electromagnetic conductance reading (Hz) on gastrointestinal system biopoints
Time frame: T1 - Day 1 - After in silico human virus infestation
Gastrointestinal system Change
Voll Electromagnetic conductance reading (Hz) on gastrointestinal system biopoints
Time frame: T2 - Day 1 - After adding the interface of the original fluid
Gastrointestinal system Change
Voll Electromagnetic conductance reading (Hz) on gastrointestinal system biopoints
Time frame: T3 - Day 1 - After adding the interface of virus impregnated fluid
Gastrointestinal system Change
Voll Electromagnetic conductance reading (Hz) on gastrointestinal system biopoints
Time frame: T4 - Day 3 - After adding the interface of virus incubated fluid during 48 hours
Nervous system
Voll Electromagnetic conductance reading (Hz) on nervous system biopoints
Time frame: T0 - Day 1 - Baseline
Nervous system change
Voll Electromagnetic conductance reading (Hz) on nervous system biopoints
Time frame: T1 - Day 1 - After in silico human virus infestation
Nervous system change
Voll Electromagnetic conductance reading (Hz) on nervous system biopoints
Time frame: T2 - Day 1 - After adding the interface of the original fluid
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Nervous system change
Voll Electromagnetic conductance reading (Hz) on nervous system biopoints
Time frame: T3 - Day 1 - After adding the interface of virus impregnated fluid
Nervous system change
Voll Electromagnetic conductance reading (Hz) on nervous system biopoints
Time frame: T4 - Day 3 - After adding the interface of virus incubated fluid during 48 hours
Endocrine system
Voll Electromagnetic conductance reading (Hz) on endocrine system biopoints
Time frame: T0 - Day 1 - Baseline
Endocrine system change
Voll Electromagnetic conductance reading (Hz) on endocrine system biopoints
Time frame: T1 - Day 1 - After in silico human virus infestation
Endocrine system change
Voll Electromagnetic conductance reading (Hz) on endocrine system biopoints
Time frame: T2 - Day 1 - After adding the interface of the original fluid
Endocrine system change
Voll Electromagnetic conductance reading (Hz) on endocrine system biopoints
Time frame: T3 - Day 1 - After adding the interface of virus impregnated fluid
Endocrine system change
Voll Electromagnetic conductance reading (Hz) on endocrine system biopoints
Time frame: T4 - Day 3 - After adding the interface of virus incubated fluid during 48 hours