The influence of titanate coupling agent on the performance of barium titanate/PMMA denture base nanocomposites after SBF storage
JOURNAL OF THERMOPLASTIC COMPOSITE MATERIALS
Authors: Elshereksi, Nidal Wanis; Muchtar, Andanastuti; Azhari, Che Husna
Abstract
Poly(methyl methacrylate) (PMMA)/nanobarium titanate (NBT) composite has potential application in denture base materials. The denture base materials should be stable in the wet environment and exhibit good mechanical properties. This study aimed to evaluate the effectiveness of titanate coupling agent (TCA) on NBT behavior after soaking in the simulated body fluid (SBF) and to determine the effect of SBF exposure on fracture toughness of the PMMA nanocomposites. Silanated (Si-NBT), titanated (Ti-NBT), and pure NBT (Un-NBT) at 5% concentration (by mass) were incorporated in the PMMA matrix. NBT was sonicated in MMA prior to mixing with PMMA. SBF absorption, solubility, and leaching were measured, and fracture toughness of the PMMA nanocomposites was evaluated after soaking. The results showed that Titanated samples displayed lower SBF absorption capability and solubility values than the silanated ones. Moreover, the leachability of filler elements (Ba and Ti) was substantially reduced by titanation (54% and 61%, respectively), whereas the Si-NBT/PMMA revealed values of 12.3% and 7% respectively. Significant differences in fracture toughness were observed among the tested samples after 6 weeks of aging in SBF (p< 0.05). Although no notable changes in theK(IC)of pure PMMA and Un-NBT/PMMA samples were detected,K(IC)was improved by 20% after titanation. In addition, the fracture toughness of the titanated samples was higher than that of the silanated ones by 26%. In conclusion, TCA exhibited better stability in moisture than silane. Degradation resistance to moisture obtained with titanated NBT could lead to the promotion of clinical longevity of the composites.
Coupling Ion Specificity of the Flagellar Stator Proteins MotA1/MotB1 of Paenibacillus sp. TCA20
BIOMOLECULES
Authors: Onoe, Sakura; Yoshida, Myu; Terahara, Naoya; Sowa, Yoshiyuki
Abstract
The bacterial flagellar motor is a reversible rotary molecular nanomachine, which couples ion flux across the cytoplasmic membrane to torque generation. It comprises a rotor and multiple stator complexes, and each stator complex functions as an ion channel and determines the ion specificity of the motor. Although coupling ions for the motor rotation were presumed to be only monovalent cations, such as H(+)and Na+, the stator complex MotA1/MotB1 of Paenibacillus sp. TCA20 (MotA1(TCA)/MotB1(TCA)) was reported to use divalent cations as coupling ions, such as Ca(2+)and Mg2+. In this study, we initially aimed to measure the motor torque generated by MotA1(TCA)/MotB1(TCA)under the control of divalent cation motive force; however, we identified that the coupling ion of MotA1(TCA)MotB1(TCA) is very likely to be a monovalent ion. We engineered a series of functional chimeric stator proteins between MotB1(TCA) andEscherichia coli MotB.E. coli Delta motABcells expressing MotA1(TCA) and the chimeric MotB presented significant motility in the absence of divalent cations. Moreover, we confirmed that MotA1(TCA)/MotB1(TCA) in Bacillus subtilis Delta motAB Delta motPScells generates torque without divalent cations. Based on two independent experimental results, we conclude that the MotA1(TCA)/MotB1(TCA) complex directly converts the energy released from monovalent cation flux to motor rotation.