Relevance of 3D virtual planning in predicting bony interferences between distal and proximal fragments after sagittal split osteotomy.

After sagittal split osteotomy, the mandibular distal and proximal fragments do not always align themselves passively to one another, resulting in bony interferences and subsequent anomalous settlement of the condyles. Predicting these interferences could be an important ancillary procedure for avoiding intra- and postoperative surgical complications, rendering orthognathic surgery more effective and safer. This study evaluated the relevance of virtual surgical planning in assessing the displacement of the proximal segments after virtual distal segment repositioning, for predicting bony interferences between the segments and thus avoiding related intra- and postoperative surgical complications. The presence of interferences between the distal and proximal segments was compared between virtually predicted (computer-assisted simulation surgery, Dolphin software) and real cases in 100 consecutive patients diagnosed with dentofacial deformities who underwent orthognathic surgery with mandibular repositioning (using a short lingual osteotomy (SLO)). The results indicated that clockwise rotation of the mandible was the mandibular movement most prone to segment interference. Furthermore, virtual planning was sensitive (100%) but had low specificity (51.6%) in predicting proximal and distal segment interferences. This low specificity was due to the software-based automated design of the mandibular osteotomy, where the length of the distal segment was longer than the real SLO, and the mandibular ramus sagittal split was located just behind Spix's spine. Thus, more precise simulated osteotomies are needed to further validate the accuracy of virtual planning for this purpose.

Facile production of stable silicon nanoparticles: laser chemistry coupled to in situ stabilization via room temperature hydrosilylation.

Stable, alkyl-terminated, light-emitting silicon nanoparticles have been synthesized in a continuous process by laser pyrolysis of a liquid trialkyl-silane precursor selected as a safer alternative to gas silane (SiH4). Stabilization was achieved by in situ reaction using a liquid collection system instead of the usual solid state filtration. The alkene contained in the collection liquid (1-dodecene) reacted with the newly formed silicon nanoparticles in an unusual room-temperature hydrosilylation process. It was achieved by the presence of fluoride species, also produced during laser pyrolysis from the decomposition of sulfur hexafluoride (SF6) selected as a laser sensitizer. This process directly rendered alkyl-passivated silicon nanoparticles with consistent morphology and size (<3 nm), avoiding the use of costly post-synthetic treatments.

Continuous production of iron-based nanocrystals by laser pyrolysis. Effect of operating variables on size, composition and magnetic response.

Well dispersed iron-based magnetic nanoparticles have been prepared by gas phase laser-driven decomposition of iron pentacarbonyl. Agglomeration of the newly synthesized nanoparticles could be avoided by using a liquid collection system in which the exit stream from the laser reactor was bubbled through triethylene glycol (TREG). The effect of different experimental parameters (precursor concentration, laser power, working pressure, residence time) was studied and, by selecting the appropriate conditions, the size of the resulting magnetic nanocrystals could be tuned from ultrasmall (ca. 2.5 nm) to around 12 nm. For nanoparticle sizes around 10 nm and larger a metallic iron core could be preserved. These iron/iron oxide core-shell compositions exhibit very high values of magnetization, 127 emu g(-1).

Use of a polyol liquid collection medium to obtain ultrasmall magnetic nanoparticles by laser pyrolysis.

The present work addresses the main bottleneck in the synthesis of magnetic nanoparticles by laser pyrolysis. Since the introduction of laser pyrolysis for the production of nanoparticles nearly three decades ago, this method has been repeatedly presented as a highly promising alternative, on account of two main characteristics: (i) its flexibility, since nanoparticles can be formed from a wide variety of precursors in both gas and liquid phase, and (ii) its continuous nature, avoiding the intrinsic variability of batch processing. However, the results reported to date invariably show considerable aggregation of the obtained nanoparticles, which strongly limits their application in most fields. In this work, we have been able to circumvent this problem by collecting the particles in a polyol liquid medium. This method prevents the formation of aggregates and renders a uniform distribution of well dispersed ultrasmall nanoparticles (<4 nm) in a water-compatible solvent. We consider that the effectiveness of this novel collection method for the production of well-dispersed magnetic nanoparticles will be of high interest to a wide range of scientists working in the nanoparticle synthesis field and may enable new applications wherever there is a strict requirement for non-agglomerated nanoparticles.