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Extaro 300

Manufactured by Zeiss
Sourced in Germany

The Extaro 300 is a surgical microscope developed by Zeiss. It provides high-quality optics and illumination for use in various medical procedures.

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6 protocols using extaro 300

1

Selection of Premolars for Endodontic Research

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After approval by the institutional ethics committee of Saint Joseph University, Beirut, Lebanon (USJ-2017-55), 85 lower premolars, extracted for reasons unrelated to the study, were cleaned using an ultrasonic insert (1S, Satelec Acteon Group, Mérignac, France) and stored in 0.1% formocresol. Teeth were inspected under an operating microscope (Zeiss Extaro 300, Oberkochen, Germany) at x25 magnification to eliminate teeth with cracks or advanced external resorption. Mesiodistal and vestibulolingual X-rays were taken (Sopix, Satelec Acteon Group, Merignac, France) to discard teeth with treated canals, pulpal calcification, or internal resorption. Cone beam computed tomography (Newtom VGI, Verona, Italy) (CBCT) was performed, and only teeth with mature apices and a single oval canal with a moderate curvature of 15 to 22 degrees according to the Schneider technique, were included in the study [18 (link),19 (link),20 (link)]. Finally, 30 mandibular premolars were selected. Access cavity was prepared using an 856 diamond bur (Komet Italia SRL, Milan, Italy) with a high-speed handpiece under running water under an operating microscope, and a size #10 k-file (Dentsply Sirona, Ballaigues, Switzerland) was introduced to verify patency. This study followed the CRIS guidelines for in vitro studies, as discussed in the 2014 concept note [21 (link)].
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2

Smear Layer Removal Effectiveness

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The crown portion of each tooth specimen was cut off under a dental operating microscope (Extaro 300, Zeiss, Jena, Germany). Roots were sectioned perpendicularly to its long axis in equal proportions with a low-speed handpiece diamond disc into the coronal third, middle third, and apical third, respectively. After dehydrating and processing the root surface with gold palladium, the sectioned specimens were viewed under a scanning electron microscope (SU3500, Hitachi Ltd., Tokyo, Japan) in 500× and 2000× magnifications to examine the remaining smear layer. An evaluation was made to evaluate the smear layer removal effectiveness by recording the dentinal tubule exposure quantity as well as the presence, quantity, and distribution of the smear layer based on the score described by Hulsmann et al. [46 (link)]. The score was graded on a four-point scale as follows: score I = dentinal tubules completely opened, score II = more than 50% of dentinal tubules opened, score III = less than 50% of dentinal tubules opened, score IV = all of the dentinal tubules covered with smear layer. Two observers were calibrated, and a blind evaluation was performed by examining the images independently. The level of agreement between the two observers was assessed with the kappa test.
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3

3D Modeling of Maxillary Premolar

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A recently extracted, non-carious, three-rooted maxillary first premolar with mature apices, normal root morphology and canal curvatures less than 20 degrees was selected. The tooth was anonymous and was extracted for periodontal reasons not related to this study. The tooth was cleaned and examined under 16X magnification by a dental operating microscope (Zeiss Extaro 300, Germany) to confirm the absence of any fractures or resorption defects. The selected premolar was scanned with a high-resolution Cone Beam Computed Tomography machine (PlanmecaProMax 3d MID; Planmeca, Helsinki, Finland), with endodontic mode, operating at 90 kV, 12 mA with a voxel dimension of 75 μm. A total of 668 images were generated and the data was obtained in the DICOM format images. Materialize interactive medical image control system (MIMICS 19.0; Materialise, Leuven, Belgium) was then used to identify enamel and dentine, as well as produce the 3-dimensional (3D) model by forming masks and automatically growing threshold regions. Data were then optimized using the 3-Matic Medical 11.0 software (Materialise NV). SolidWorks (Dassault Systems, France) was used to combine enamel and dentine as well as to establish the surrounding bone.
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4

Fluorescent Microscopy and Xpert MTB/RIF Assay for Mycobacteria Detection

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Smear for LED fluorescent microscopy were prepared according to standard procedures.11 Smears for FM were stained using auramin O. Briefly, smears were flooded with Auramin O for 10 min, destained with acid alcohol for 2 min, and then counterstained with methylene blue for one minute. With auramine O staining, Mycobacteria appear as bright yellow fluorescent rods on a dark background. The slides were examined with ZEISS EXTARO 300 at 20× magnification. The presence or absence of AFB was reported using WHO/IUATLD guideline.18
The sediment samples by cytocentrifugation were processed for Xpert MTB/RIF assay. Using a fresh transfer pipette, 2 mL of the processed sample was transferred to the Xpert MTB/RIF cartridge 10. Load the cartridge into the GeneXpert instrument as per manufacturer's instructions according to standard protocol.14 (link), 19 (link) The MTB/RIF assay interpretation is software based and not user dependent.20 (link) The sensitivity and specificity of each sample were calculated according to the following formula
Sensitivity: True positiveTrue positive+False negative×100
Specificity: True negativeTrue negative+False positive×100
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5

Enamel Samples Preparation Protocol

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Twenty teeth were collected based on the inclusion and extrusion [Figure 1]. Inclusion criteria included teeth with sound enamel, with no history of bleaching, and teeth extracted for orthodontic purposes, whereas exclusion criteria included carious teeth, cracked teeth, teeth undergone prior bleaching, hypocalcified teeth, teeth with erosion and developmental anomalies, teeth with carious lesions, and deciduous teeth.
The teeth were then cleaned using an ultrasonic scaler, autoclaved, and stored in 0.5% thymol solution.
All the teeth were thoroughly examined under the microscope (EXTARO 300, Carl Zeiss, United States) for cracks and a total of 40 enamel samples were obtained.
Each sectioned tooth was embedded in cold cure resin cylinders (DPI RR) (1.5 cm wide by 1.5 cm high) with the enamel exposed. On secondary examination, 33 intact samples were included in the study. This sample size was calculated and obtained using “Open-Epi Software”.
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6

Topographic Analysis of Interbulbar Spinal Accessory Nerve

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The research protocol was approved by the local ethics committee (protocol no:523; 25.05.2021) and was conducted in accordance with the Declaration of Helsinki. Between June 2021 and December 2021, 22 fresh human head cadavers were used to determine the topography of ibSLN. The cadavers were placed in supine position, and bilateral dissection (44 sides in total) was performed under a Zeiss Extaro 300 stereoscopic dissection microscope.
The laryngeal region was carefully dissected and thyrohyoid membrane was preserved to fully demonstrate the entrance of the ibSLN and its relationship between other consistent structures. The sternocleidomastoid muscle was laterally deviated and carotid sheet and then the vagus nerve were identi ed. By following the tracing of the vagus nerve, ibSLN and its penetrating point in the thyrohyoid membrane was identi ed. Five different distances were measured via using caliper and recorded from where the nerve pierced the membrane. The distance between penetrating point of the ibSLN to the membrane and corpus of the hyoid bone, the greater cornus of the hyoid bone, carotis bifurcation, vertical distance to superior border of thyroid cartilage, horizontal distance to thyroid notch were all measured by means of ruler and noted (Fig. 12).
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