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1.
Heliyon ; 10(8): e26840, 2024 Apr 30.
Article in English | MEDLINE | ID: mdl-38660239

ABSTRACT

This study investigates the optimal placement of locking plate screws for bone fracture stabilization in the humerus, a crucial factor for enhancing healing outcomes and patient comfort. Utilizing Finite Element Method (FEM) modeling, the research aimed to determine the most effective screw configuration for achieving optimal stress distribution in the humerus bone. A computer tomography (CT) scan of the humerus was performed, and the resulting images were used to create a detailed model in SOLIDWORKS 2012. This model was then analyzed using ANSYS Workbench V13 to develop a finite element model of the bone. Four different screw configurations were examined: 4 × 0°, 4 × 10°, 4 × 20°, 2 × 20°; 2 × 0°. These configurations were subjected to bending in the XZ and YZ planes, as well as tension and compression along the Z axis. The research identified the 2 × 20°+2 × 0° configuration as the most beneficial, with average stress values below 30 MPa and peak stress values below 50 MPa in 3-point bending at the first screw. This configuration consistently showed the lowest stress values across all loading scenarios. Specifically, stress levels ranged from 20 MPa to 50 MPa for bending in the XZ plane, 20 MPa-35 MPa for bending in the YZ plane, 20 MPa-30 MPa for extension in the Z-axis, and 18 MPa-25 MPa for compression in the Z-axis. The 4 × 10° and 4 × 20° configurations also produced satisfactory results, with stress levels not exceeding 70 MPa. However, the 4 × 0° configuration presented considerable stress during bending and compression in the Z-axis, with stress values exceeding 100 MPa, potentially leading to mechanical damage. In conclusion, the 2 × 20°; 2 × 0° screw configuration was identified as the most effective in minimizing stress on the treated bone. Future work will involve a more detailed analysis of this methodology and its potential integration into clinical practice, with a focus on enhancing patient outcomes in bone fracture treatment.

2.
Molecules ; 22(3)2017 Mar 11.
Article in English | MEDLINE | ID: mdl-28287472

ABSTRACT

The reaction between benzyl amines, triethyl orthoformate, and diethyl phosphite affords either bisphosphonic (compound 1) or N-benzylaminobenzylphosphonic (compound 2) acid depending on the reaction conditions. The final output of the reaction can be manipulated by the choice of reaction conditions, particularly the molar ratio of substrates.


Subject(s)
Benzylamines/chemistry , Diphosphonates/chemical synthesis , Formates/chemistry , Organophosphonates/chemical synthesis , Phosphites/chemistry , Catalysis , Chemistry Techniques, Synthetic , Crystallography, X-Ray , Models, Molecular
3.
Molecules ; 22(2)2017 Feb 08.
Article in English | MEDLINE | ID: mdl-28208725

ABSTRACT

The reaction of diethyl phosphite with triethyl orthoformate and a primary amine followed by hydrolysis is presented, and the reaction was suitable for the preparation of (aminomethylene)bisphosphonates. 3-Amino-1,2,4-triazole was chosen as an interesting substrate for this reaction because it possesses multiple groups that can serve as the amino component in the reaction-namely, the side-chain and triazole amines. This substrate readily forms 1,2,4-triazolyl-3-yl-aminomethylenebisphosphonic acid (compound 1) as a major product, along with N-ethylated bisphosphonates as side products. The in vitro antiproliferative effects of the synthesized aminomethylenebisphosphonic acids against J774E macrophages were determined. These compounds exhibit similar activity to zoledronic acid and higher activity than incadronic acid.


Subject(s)
Bone Density Conservation Agents/chemistry , Bone Density Conservation Agents/pharmacology , Formates/chemistry , Phosphites/chemistry , Triazoles/chemistry , Triazoles/pharmacology , Animals , Apoptosis/drug effects , Bone Density Conservation Agents/chemical synthesis , Cell Line, Tumor , Diphosphonates/pharmacology , Magnetic Resonance Imaging , Mice , Models, Molecular , Molecular Conformation , Osteoclasts/drug effects , Potentiometry , Triazoles/chemical synthesis
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