LTD-C310 (C31H43BN7O10): Integrated Pharmacokinetic / Pharmacodynamic Framework Metformin Core · Boron Carrier · Flavonoid Payload · Vitamin E Lipid Conjugate (LDL/VLDL Channel)

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Authors: Lance Thomas Davidson
Cited by: 0

Abstract

LTD-C310 (C31H43BN7O10) is presented as an integrated physiologically based pharmacokinetic/pharmacodynamic (PBPK/PD) framework describing a multi-functional therapeutic conjugate designed for selective tumour accumulation. The model consists of 32 coupled ordinary differential equations describing dissolution, enterocyte uptake with TPGS-mediated efflux inhibition, portal and lymphatic absorption pathways, perfusion-limited organ distribution, hepatic metabolism, enterohepatic recycling, and tumour-specific retention mechanisms. Additional components include pH-dependent tumour partitioning, intracellular ion-trap retention, ROS-mediated elimination suppression, and tumour spatial heterogeneity. Pharmacodynamic behaviour follows an extended Simeoni tumour growth inhibition model with optional boron neutron capture therapy (BNCT) and adaptive resistance dynamics. The framework is derived axiomatically from physical and biochemical principles, with stability, global mass balance, and structural identifiability explicitly demonstrated.

Fields of Study & Subjects

Nanoparticle-Based Drug Delivery Boron Compounds in Chemistry Boron and Carbon Nanomaterials Research

Publication details

Journal / source
Zenodo (CERN European Organization for Nuclear Research)
Publication date
5 March 2026
Language
EN
Document type
Preprint