Abstract / Summary
This study completely overturns the obsolete paradigm of traditional empirical medicine, which relies heavily on parenchymal cell repair or organ donor transplantation. For the first time, it establishes a universal, materialistic physical foundation for the hardware compensation of internal organ functions within the living body. Terminal parenchymal organ failures—such as portal hypertension, gastric mucosal deterioration, and acute massive hemorrhagic shock—are desacralized and reduced to physical overloads of the body's circulatory bus in terms of flow rate, pressure, molecular shear rate, and nutritional balance. This protocol establishes an architectural framework utilizing a minimally invasive, permanently indwelling subcutaneous abdominal expansion slot. Its core add-on component is a multiphase composite sandwich fluid solid-state hardware cartridge with a thickness of less than 15 mm. The entire system is completely exempt from external electronic power and exogenous biochemical medication. It perfectly reverses and exploits natural human cross-organ pressure drops, swallowing pressure, respiratory movements, as well as the constant mechanical static pressure derived from the stepping motor and hanging height of clinical syringe pumps as the primary driving forces. By positioning a non-Newtonian fluid topological micro-shear barrier grid at the inlet, the whole-blood shear stress is strictly locked below the critical threshold of mechanical erythrocyte destruction. Utilizing the steric hindrance cybernetics of a synthetic solid-phase enzyme matrix on graphene walls, log-scale rigid reductions of biochemical toxin concentrations (such as blood ammonia and bilirubin) are achieved within an ultra-short 2 cm channel. Concurrently, the system establishes an esophageal-jejunal neutral retrograde endothermic track that completely bypasses the stomach. Combined with low-impedance external drainage driven by spontaneous resting physiological pressure differentials of gastric acid, it rigidly severs the positive feedback loop of gastrointestinal collapse and deterioration. During the tactical prodromal phase, the system employs a passive wearable exoskeleton vest. Completely dry perfluorocarbon (PFC) nanoporous wafers are pre-embedded within solid cartridges. Upon encountering hypothermic hemorrhagic emergencies, these wafers are instantaneously activated via mechanical kinetic energy to release liquid universal blood piston micro-droplets. The outer shell utilizes a modified chiral nematic liquid crystal elastomer (LCE). When the interstitial fluid pressure exceeds the capillary tolerance threshold, it triggers anisotropic unidirectional mechanical swelling, locking the internal pressure below an absolute safety ceiling of 12 mmHg. Following evacuation, the system utilizes the neodymium-iron-boron (NdFeB) fractal magnetic network of the vest to project a high-gradient magnetic field for zero-residue non-invasive trapping within the body. This operates in a closed-loop recycling system involving in vitro, in situ dry-state collapse and re-weaving back into the cartridge. The system achieves perfect self-consistency across the mathematical boundaries of fluid dynamics and surface catalysis physics. It aims to forcibly erase fluid biochemical deficits on the front lines of critical care and outdoor emergencies, thereby buying a precious self-healing window for native organs. All contents of the 3-series papers comply with the CC0 1.0 Universal protocol and are dedicated to all mankind without compensation.