CPT Pharmacometrics & Systems Pharmacology · 2017 · 12 citations · 26 references
MedicinePharmacokineticsPharmacologyBone MetabolismMineral MetabolismPharmacokinetic ModelingBone Density RegulationBone FormationBone MineralizationOsteogenesisOsteoporosisPhysiologically Based Pharmacokinetic ModelingBone Formation MarkersBone Mineral DensityBone Mineral Density DeclineBone Tissue MineralizationDrug Effects On Bone DensityMathematical Modeling Of Disease
Osteoporosis is caused by decreased bone mineral density (BMD) and new treatments for this disease are desperately needed. Bone morphogenetic protein 2 (BMP2) is crucial for bone formation. The mimetic peptide CK2.3 acts downstream of BMP2 and increases BMD when injected systemically into the tail vein of mice. However, the most effective dosage needed to induce BMD in humans is unknown. We developed a mathematical model for CK2.3-dependent bone mineralization. We used a physiologically based pharmacokinetic (PBPK) model to derive the CK2.3 concentration needed to increase BMD. Based on our results, the ideal dose of CK2.3 for a healthy individual to achieve the maximum increase of mineralization was about 409 µM injected in 500 µL volume, while dosage for osteoporosis patients was about 990 µM. This model showed that CK2.3 could increase the average area of bone mineralization in patients and in healthy adults.
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PaxDb, a Database of Protein Abundance Averages Across All Three Domains of Life
Meng Wang, Mona Weiss, Milan Simonovic et al. · Molecular & Cellular Proteomics · 2012 · 485 citations · Full text
Osteoblasts and bone formation
Joana Caetano‐Lopes, Helena Canhão, João Eurico Fonseca · Bone and Mineral · 1994 · 243 citations · Full text