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Our findings suggest that guided-motion BCS TKA normalizes MCL strain. In this study, no significant differences were observed in the mean and peak strain measurements between native and guided-motion BCS-TKA knees at any flexion angle. The MCL provides restraint against anterior tibial translation in ACL-deficient knees [28]. Multiple previous studies have reported that MCL strain was significantly higher in post-TKA knees than in native knees [14,15,18] and postoperative MCL laxity was also higher in post-TKA knees than in native knees [16,17]. Our findings, when taken into account with previous studies, suggest that guided-motion BCS TKA successfully restored MCL strain to the level found in native knees. Additionally, free nerve endings that serve as a nociceptive system were reported to be the most commonly observed mechanoreceptors in the MCL [29]. Our findings, when taken into account with this anatomical detail, suggest that guided-motion BCS TKA may provide more normal feelings of the knee, which is strongly associated with patient satisfaction [11,12,30]. However, future studies that evaluate the MCL strain thresholds necessary to perceive the differences between normal and prosthetic knees are needed. Our findings also indicated that the standard deviations of the peak MCL strain were much higher than those of the mean MCL strain. One plausible explanation is that the difference in measuring area may affect MCL strain. In this study, the mean MCL strain was determined by measuring the strain over the whole MCL area and the peak MCL strain was found at one-fourth of the entire MCL area, and the distribution of MCL strain was evaluated at each of ROIs. Therefore, the surface strains measured at a smaller area, such as the peak MCL strain and strain at ROIs, are more susceptible to specimen-specific anatomical conditions, such as the bone contour underneath the measured MCL area and the soft tissues connected soft tissues to the MCL, than those measured at the entire MCL. 153554b96e
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Classification criteria for organic chemistry products
The classification criteria for organic chemistry products mainly include carbon skeleton structure and functional groups.
Classified by carbon skeleton:
Chain like compounds: Carbon atoms in molecules are connected to each other in a chain like structure, such as fatty hydrocarbons and their derivatives.
Cyclic compounds: Atoms in the molecule are arranged in a cyclic manner and are divided into aliphatic compounds and aromatic compounds. Acyclic compounds do not contain aromatic rings, such as cyclopropane and cyclohexene; Aromatic compounds contain aromatic rings, such as benzene, its homologues, and derivatives.
Classified by functional groups:
Hydrocarbons: composed of carbon and hydrogen, such as alkanes (hydrocarbons with single bonds, such as ethane), alkenes (hydrocarbons with carbon carbon double bonds, such as ethylene), and alkynes (hydrocarbons with carbon carbon triple bonds, such as acetylene).
Derivatives of hydrocarbons: Compounds in which the hydrogen atom in a hydrocarbon molecule is replaced by other atoms or groups, including halogenated hydrocarbons, alcohols, phenols, ethers, aldehydes, carboxylic acids, esters, nitro compounds, and amines.
Specific examples of classification
Alkanes: such as ethane (CH3 CH3), propane (CH3 CH ₂ CH3).
Alkenes: such as ethylene (C ₂ H ₄) and propylene (C ∝ H ₆).
Alkynes: such as acetylene (C ₂ H ₂) and propyne (C ∝ H ₄).
Aromatic hydrocarbons: such as benzene (C ₆ H ₆) and toluene.
Halogenated hydrocarbons: such as chloroform (CHCl3), bromoethane (C ₂ H ₅ Br).
Alcohols: such as ethanol (C ₂ H ₅ OH) and propanol (C ∝ H ₇ OH).
Phenols: such as phenol (C ₆ H ₅ OH).
Ethers: such as dimethyl ether (C ₂ H ₆ O) and ether (C ₄ H ₁ O).
Aldehydes: such as formaldehyde (HCHO), acetaldehyde (C ₂ H ₄ O).
Carboxylic acids: such as acetic acid (CH3 COOH), propionic acid (CH3 H ₆ O ₂).
Esters: such as ethyl acetate (C ₄ H ₈ O ₂), propyl propionate (C ₆ H ₁ O ₄).