Research reported in this publication was supported by JSPS KAKENHI JP21K09915 (MO) and the National Institute of General Medical Sciences;&#160;T34GM145509 (MM) and the National Institute of Dental and&#160;Craniofacial Research; R01DE025255 and R21DE032156&#160;(XH); R01DE029709, R21DE028715 and R15DE027851&#160;(TK); R01DE027648 and K02DE029531 (MS).

All procedures described in this protocol have been performed in accordance with guidelines and regulations for the use of vertebrate animals approved by the Institutional Animal Care Use Committee (IACUC) at Augusta University and at Nova Southeastern University which is accredited by the Association for Assessment and Accreditation of Laboratory Animal Care International (AAALAC). Note that Dr. Suzuki was employed by Augusta University where the mouse dental fluorosis experiments were completed.
1. Extraction of mandibular incisors in a mouse dental fluorosis model
<ol>
	<li>Feed fluoride-free diets to C57BL/6 mice (5-week-old, male) from 1 week prior to fluoride until termination of fluoride treatment.</li>
	<li>Prepare fluoride water by adding NaF in distilled water followed by vacuum filtration using a 0.2 &#181;m filter. Give animals fluoride water as NaF (0 ppm and 125 ppm; N=5/group) ad libitum for 6 weeks. Replace fluoride water with a freshly prepared batch every 2 days.</li>
	<li>After 6 weeks of fluoride water treatment, euthanize animals with CO2 followed by decapitation.</li>
	<li>Extract the hemi mandibular with incisor from each mouse. To collect the hemi mandibular with incisor, cut the muscles around the mandibular jaw without applying excessive force.</li>
	<li>Place the hemi mandibular in PBS and keep it at 4 &#176;C until &#956;-CT analysis (optional). Separate the incisor from the mandibular using a scalpel (#15) and scissors without damaging or breaking the specimen.</li>
	<li>Wash the isolated incisor with PBS and perform dehydration by immersing it in increasing strength of alcohol (70% and 100% ethanol) for 2-3 h. 
	NOTE: If the tissue (e.g., pulp) is not sufficiently dehydrated, resin impregnation is likely to be inhibited and subsequent evaluation will likely be inadequate.</li>
	<li>After dehydration with ethanol, embed the incisor horizontally in resin. Continue to step 3.</li>
</ol>
2. Extraction of maxillary alveolar bones in a mouse ligature-induced periodontal bone resorption (L-PBR) model
<ol>
	<li>Administer 0.8 mL of ketamine (100 mg/mL) + 0.1 mL of Xylazine (100 mg/mL) + 9.1 mL of PBS intraperitoneally (i.p.) to mouse (C57BL/6, 8-12-week-old, male) as anesthetics. The dosage is 0.01 mL/g (weight). Apply ophthalmic ointment to both eyes to prevent dryness under anesthesia.</li>
	<li>Place the anesthetized mouse on a heating pad for 5-10 min. Assess responses to tail/toe pinches and the intactness of the ocular reflex. Confirm that the mouse is unresponsive to the noxious stimuli and the reflex is absent.</li>
	<li>Place the mouse on the treatment table and keep the mouth open by means of a ligature 5-0 silk suture tied to a magnetic post on the treatment table.</li>
	<li>Under a surgical microscope, wind the ligature (Braided silk suture 6-0) around one side of the maxillary second molar (single layer)&#160;using micro needle holders. Minimize individual differences in analysis by using one side as the treatment side and the other side as the control.</li>
	<li>Tie the ligature and make a knot on the palate side. After making a knot, cut the remaining ligature as short as&#160;possible so that the excessive ligature does not interfere with chewing or eating. This is important to ensure that the ligature will not loosen by chewing during the subsequent observation period. 
	NOTE: Do not leave the animal unattended until it has regained sufficient consciousness to maintain sternal recumbency. Do not return the animal that has undergone surgery to the company of other animals until fully recovered. Maintain sterile conditions during survival.</li>
	<li>Feed diet and water to mice ad libitum for 2 weeks. After 2 weeks of ligation, euthanize mice with CO2 followed by decapitation.</li>
	<li>Extract both side maxillae (ligature side and control side) with molars from each mouse. To collect maxillae with molars, cut the muscles and bone around the maxillary jaw using scissors without applying excessive force. Place each maxilla in PBS and keep it at 4 &#176;C until &#181;CT analysis (optional).</li>
	<li>Separate the alveolar bone with molars (1st to 3rd) from the maxilla using a scalpel (#15) and scissors without damaging or breaking the specimen.</li>
	<li>Wash the isolated alveolar bone with PBS then dehydrate and degrease by immersion in increasing strength of alcohol (70% and 100% ethanol) for 2-3 h. 
	&#8203;NOTE: If&#160;the tissue (e.g., pulp and bone) is not sufficiently dehydrated, resin impregnation is likely to be inhibited and subsequent evaluation will likely be inadequate.</li>
	<li>After dehydration with ethanol, embed the alveolar bone horizontally in resin. Continue to step 3.</li>
	<li>Optional: Perform &#181;CT evaluation before microhardness testing.
	<ol>
		<li>Before microhardness testing, perform nondestructive structural analysis (e.g., &#181;CT) using the same sample for microhardness testing as a complementary evaluation (Figure 1). Structural information (3D image, mineral density, volume) by &#181;CT could support to evaluate sample mechanical properties and quality that may affect microhardness results.</li>
	</ol>
	</li>
</ol>
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/66583/66583fig01.jpg" /> 
Figure 1: Representative &#956;CT images of enamel in control and fluoride-treated mice incisors. (A) Representative &#956;CT sagittal image of mandibular incisor. (B-D) &#956;CT coronal images of control incisor (NaF 0 ppm). (E-G) &#956;CT coronal images of incisor treated with NaF (125 ppm). Representative enamel mineral density (EMD) is shown (g/cm3). <a href="https://www.jove.com/files/ftp_upload/66583/66583fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
3. Embedding samples in resin
<ol>
	<li>Continue from step 1.7 (dental fluorosis model) or step 2.10 (L-PBR model).</li>
	<li>Coat the inside surface of the mounting cup (1 inch) with a thin layer of petrolatum. Mix resin (cold setting embedding resin) according to instructions. Pour the resin and hardener into the provided plastic cup in a 15:2 volume ratio and carefully mix with a wooden spatula for at least 2 min. Avoid air bubbles.</li>
	<li>Place dehydrated and degreased incisor (Figure 2A) or alveolar bone with molars (Figure 2B) oriented horizontally and parallel to the bottom of the mounting cup (1 specimen per cup).</li>
	<li>Pour the mixed resin (just enough resin, about 1.5 mL) into the mounting cup to completely cover the specimen. Avoid adding more resin than necessary, as excess resin will impede the polishing process (Figure 2C,D). Place the mounting cup containing specimen on a hot plate at 50 &#176;C for at least 8 h to promote resin polymerization. This procedure contributes to holding the specimen in a stable position. 
	NOTE: Depending on the sample size, adjust the amount of resin to completely cover the specimen. Do not fill too much resin, otherwise more time will be needed to remove superfluous resin.</li>
	<li>After curing, remove the resin containing the specimen from the mounting cup. Remove burrs and arrange the specimen&#39;s plane and the opposite side plane as parallel and flat using an advanced grinder-polisher with rough water-resistant abrasive paper (Grit 60/P60 and 120/P120) under water flooding. Keep the height of specimen to approximately 3 mm for incisor and alveolar bone (Figure 2E,F). 
	&#8203;NOTE: When the specimen is analyzed by SEM following the microhardness measurement, the thickness of the sample should be about 3 mm so that subsequent SEM observation will not be affected. Smaller samples are more difficult to manipulate with the grinder. For the samples intended for microhardness only, the specimen height can increase to about 10-20 mm.</li>
	<li>Trim the external shape to make a rectangular solid resin block and round corners (approximately, width 30 mm, length 10 mm for incisor (Figure 2G) and width 10 mm, length 5 mm, for alveolar bone (Figure 2H)) using a precision sectioning saw.</li>
	<li>Once the rough shape correction is complete, remove debris and particles from the resin block using an ultrasonic cleaner (about 1 min). Continue to step 4.</li>
</ol>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/66583/66583fig02.jpg" /> 
Figure 2: Flow of resin-embedding and polishing procedure. (A) Dehydrated and degreased incisor. (B) Dehydrated and degreased alveolar bone in L-PBR. (C, D) Incisors and alveolar bone immersed in resin. (E, F) By cutting off the resin, it is easier to polish the target tissue surface. (G, H) Resin corners rounded for the polishing process. Abbreviations:&#160;L-PBR =&#160;ligature-induced periodontal bone resorption.&#160;<a href="https://www.jove.com/files/ftp_upload/66583/66583fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
4. Polishing of specimens
NOTE: Polishing of specimens is done manually using waterproof abrasive papers (from rough to finer) on an advanced grinder-polisher under water flooding.
<ol>
	<li>Place a rough water-resistant abrasive paper (Grit 600/P1200) on the grinder. Place the trimmed and cleaned resin block (from step 3.7) on the rough water-resistant abrasive paper.</li>
	<li>While pouring water, hold the resin block and polish the specimen&#39;s evaluation surface on the grinder-polisher (Speed 1-10 x g). At this time, be careful to hold the resin block so that the evaluation surface is parallel to the ground. To keep the evaluation surface intact, check the surface with the naked eye or under&#160;a microscope. 
	NOTE: Note that the grinder rotates clockwise, and uniform pressure can lead to an unparallel surface. To obtain a parallel surface, keep the glider rotational speed constant and press the specimen carefully for a few seconds, and then rotate the specimen 180&#176; to press for the same amount of time. Rough abrasive paper may remove not only resin but also specimen.</li>
	<li>Change the abrasive paper to the Grit 800/P2400 and place the resin block on it. Repeat step 4.2.</li>
	<li>Remove debris and particles from the resin block using an ultrasonic cleaner (about 1 min). 
	NOTE: Before proceeding, using an ultrasonic cleaner to remove any surface debris to prevent clogging is recommended.</li>
	<li>Next, perform serial polishing using finer abrasive papers; polishing order is 12 &#181;m, 9 &#181;m, 3 &#181;m, 1 &#181;m and 0.3 &#181;m.</li>
	<li>Place a lapping film (12 &#181;m) on the grinder-polisher table without rotation and place the resin block on the lapping film. 
	NOTE: In this experiment, the grinder table is suitable to get a flat surface condition under water flooding. Alternatively, a large plane mirror (or similar one) that provides parallelism can also be used.</li>
	<li>Under water cooling, carefully polish the specimen&#39;s evaluation surface on the lapping film by hand. Move the sample vertically, horizontally, and diagonally for the same number of seconds under water injection with strokes of 2 to 3 cm (1 inch). When the polishing procedure is properly achieved, the resin specimen will stick&#160;to the lapping film.</li>
	<li>Remove debris and particles as in step 4.4. Change the abrasive paper to the next size according to the serial polishing order (from 12 &#181;m to 0.3 &#181;m) and place the resin block on it.</li>
	<li>While pouring water, hold the resin block and carefully polish the specimen&#39;s surface on the lapping film by hand. Remove debris and particles as in step 4.4.</li>
	<li>Repeat steps 4.5 - 4.8 to complete the final polishing (0.3 &#181;m). After completing the final polishing (0.3 &#181;m), the specimen should have a mirror finish surface (Figure 3A).</li>
	<li>Clean the surface of the specimen with ethanol (100%) to degrease and dehydrate and store resin blocks at room temperature until microhardness testing. During storage, avoid excessive moisture and dust. Continue to step 5.</li>
</ol>
5. Vickers microhardness test
NOTE: Indentation of a mirror finish surface specimen is done using a microhardness tester. Testing is performed with a load of 25 g for 10 s with a Vickers tip.
<ol>
	<li>Vickers microhardness test for incisors (dental fluorosis model) 
	NOTE: Enamel can be divided into three layers from outside (oral cavity side) to inside (pulp side); namely, the superficial layer, the middle layer, and the deep layer (dentin-enamel junction, DEJ) (Figure 3B)16. In this protocol, three enamel layers are tested.
	<ol>
		<li>Set loading force to 25 g and loading duration to 10 s. Place the resin block on the stage.</li>
		<li>Indent 6 points in each enamel layer (superficial, middle and DEJ) and dentine in each region (cervical, middle and tip; Figure 3B).</li>
		<li>Measure the length of the two diagonals (d1 and d2; Figure 3B) to calculate the Vickers microhardness value (HV; Figure 4).</li>
	</ol>
	</li>
	<li>Vickers microhardness test for alveolar bone (L-PBR model)
	<ol>
		<li>Set loading force to 25 g and loading duration to 10 s. Place the resin block on the stage.</li>
		<li>Indent 3-6 points in each mesial and distal side of alveolar bone from the alveolar crest. Indent alveolar bones between 1st and 2nd molar (white square), and 2nd and 3rd molar. 
		NOTE: In this protocol, 6 points in each mesial and distal side (total 12 points) were evaluated for the control (intact) bone, and 3 points in each side (total 6 points) were evaluated for L-PBR. The number of indentation points depends on the conditions of the lesion (e.g., too much bone loss limits the indentation area).</li>
	</ol>
	</li>
</ol>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/66583/66583fig03v2.jpg" /> 
Figure 3: Evaluation regions of microhardness in mandibular incisor. (A) Mirror finish surface sample containing mandibular incisor. (B) Indentations in each region; cervical, middle, and tip (NaF 0 ppm). (C) Three enamel layers; from DEJ, Inner, Middle, and Outer enamel. Abbreviations: D = dentin, E = enamel, DEJ = dentin enamel junction <a href="https://www.jove.com/files/ftp_upload/66583/66583fig03largev2.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/66583/66583fig04.jpg" /> 
Figure 4: Vickers microhardness of enamel treated with or without NaF. The microhardness of dentin and three enamel layers were evaluated in each region, cervical, middle, and tip region. (A-C) Control and (D-F) NaF (125 ppm) treatment. Data are presented as mean &#177; SD. Significant differences were evaluated by one-way ANOVA with Tukey&#39;s post-hoc test. p values &#60; 0.05 were considered statistically significant. **p &#60; 0.005, ***p &#60; 0.0005, ****p &#60; 0.0001 <a href="https://www.jove.com/files/ftp_upload/66583/66583fig04large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Microhardness Protocol for Evaluating Rodent Oral Disease

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The authors declare no conflict of interest.

Microhardness is performed to evaluate mechanical properties of hard tissues like tooth and bone. To date, divergent microhardness measurement methods have been reported. Most of the measurement information, especially sample preparations and the indentation sites are likely to be insufficient. This study focused on the microhardness protocol for enamel and alveolar bone in dental fluorosis and periodontal diseases models. To obtain consistent and accurate results, the critical steps in this protocol are orientation of t...

Hardness is one of the mechanical properties (e.g., elasticity, hardness, viscoelasticity, and fracture behavior) and is commonly used to characterize the ability to resist compression deformation and fracture of a local area of a material. The static indentation hardness test is the most used method, including Vickers hardness and Knoop hardness1. The Vickers hardness test is implemented by pressing a diamond indenter into the surface under a fixed testing load. The indenter is pyramid-shaped, with a square base and an angle of 136&#176; between opposite faces. The length of both diagonals formed on the test surface is measured, and the average is used to calculate the hardness, which is determined by the ratio F/A (where F is the force and A is the surface area of the indentation). The Vickers microhardness number (HV=F/A) is usually expressed in kilograms-force (kgf) per mm2 indentation, with 1 HV &#8776; 0.1891 F/d2 (N/mm2). The Knoop hardness also consists of a diamond square pyramid indenter formed by two unequal opposite angles. The Knoop hardness number (HK) equals the ratio of applied load to the projected contact area. Hardness tests are classified into micro-indentation (microhardness) tests and macro-indentation tests, depending on the force applied to the test material. Micro-indentation tests typically use loads in the range 0.01-2 N (about 1-203 gf); meanwhile, macro-indentation tests use over 10 N (10119 gf)1.
To evaluate features of dental hard tissues in oral diseases, including tooth and alveolar bone, micro-CT (&#181;CT) and scanning electron microscopy (SEM) are used for structural analysis. &#181;CT provides 3D imaging information (volume and mineral density)2, and SEM produces microstructure images (enamel prism and bone lacuna-canalicular)3. Complementarily to structural analysis by &#181;CT and SEM, microhardness is one of the informative parameters to evaluate how structural changes alter the mechanical properties of tooth and alveolar bone in oral diseases, e.g., enamel malformation and periodontal bone resorption. The Vickers microhardness value of human enamel (HV = 283-374) is about 4 to 5 times higher than that of dentin (HV = 53-63)4,5. In rodent dental fluorosis models, enamel microhardness significantly decreases in mouse incisors treated with fluoride (HV = 136) compared to control enamel (HV = 334)6,7. This suggests that fluorosed enamel is softer and weaker with lower mineral content and higher protein content than found in non-fluorosed enamel. Microhardness is used to evaluate bone mechanical properties. Several previous studies have examined the mechanical behavior of human bone from different anatomic sites, including long bone microhardness8,9,10. The mean microhardness of human fluorosed femurs showed a significant decrease (HV = 222.4) compared to non-fluorosed femurs (HV = 294.4)11. Despite being a useful parameter, there is a scarcity of literature describing microhardness (either Vickers12 or Knoop13,14) of alveolar bone in oral diseases.
To date, divergent microhardness measurement methods have been reported. Since microhardness values vary15 depending on sample preparation (polishing and flat surface) and indentation site, diverse protocols can cause discrepancies among studies. Standardization of the microhardness testing protocol is essential for consistent and accurate evaluation in oral disease models. In the present study, we demonstrate a standardized protocol for microhardness analysis in tooth and alveolar bone in mouse dental fluorosis model and periodontal bone resorption model.

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			<td>CarbiMet PSA 60/P60</td>
			<td>Buehler</td>
			<td>36080060</td>
			<td></td>
		</tr>
		<tr>
			<td>CarbiMet PSA 600/P1200</td>
			<td>Buehler</td>
			<td>36080600</td>
			<td></td>
		</tr>
		<tr>
			<td>Castroviejo Micro Needle hilder</td>
			<td>F.S.T</td>
			<td>12060-01</td>
			<td></td>
		</tr>
		<tr>
			<td>Epofix cold setting embeding Resin</td>
			<td>Electron Microscopey Science</td>
			<td>CAT-1237</td>
			<td></td>
		</tr>
		<tr>
			<td>Fisherbrand 112xx Series Advanced Ultrasonic Cleaner</td>
			<td>Fisher Brand</td>
			<td>FB11201</td>
			<td></td>
		</tr>
		<tr>
			<td>Fluoride-free Rodent diet</td>
			<td>Bio Serv</td>
			<td>F1515</td>
			<td>&#160;AIN-76A, 1/2&#34; Pellets</td>
		</tr>
		<tr>
			<td>in-vivo microCT Skyscan 1176</td>
			<td>Bruker</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Isomet 1000 Precison saw</td>
			<td>Buehler</td>
			<td>MA112180</td>
			<td></td>
		</tr>
		<tr>
			<td>Lapping film 0.3&#181;m</td>
			<td>Maruto instrument co, LTD. Japan</td>
			<td>26-4203</td>
			<td>Alternative&#160; 
			A3-0.3 SHT, 3M USA</td>
		</tr>
		<tr>
			<td>Lapping film 1&#181;m</td>
			<td>Maruto instrument co, LTD. Japan</td>
			<td>26-4206</td>
			<td>Alternative 
			A3-1 SHT, 3M USA</td>
		</tr>
		<tr>
			<td>Lapping film 12&#181;m</td>
			<td>Maruto instrument co, LTD. Japan</td>
			<td>26-4211</td>
			<td>Alternative 
			A3-12 SHT, 3M USA</td>
		</tr>
		<tr>
			<td>Lapping film 3&#181;m</td>
			<td>Maruto instrument co, LTD. Japan</td>
			<td>26-4204</td>
			<td>Alternative 
			A3-3 SHT, 3M USA</td>
		</tr>
		<tr>
			<td>Lapping film 9&#181;m</td>
			<td>Maruto instrument co, LTD. Japan</td>
			<td>26-4201</td>
			<td>Alternative 
			A3-9 SHT, 3M USA</td>
		</tr>
		<tr>
			<td>Leica wild microscope&#160;</td>
			<td>Leica</td>
			<td>LEIC M690</td>
			<td></td>
		</tr>
		<tr>
			<td>Metaserv 2000 Variable speed Grinder polisher</td>
			<td>Buehler</td>
			<td>No: 557-MG1-1160</td>
			<td></td>
		</tr>
		<tr>
			<td>MicroCut PSA 1200/P2500</td>
			<td>Buehler</td>
			<td>36081200</td>
			<td></td>
		</tr>
		<tr>
			<td>MicroCut PSA P4000</td>
			<td>Buehler</td>
			<td>36084000</td>
			<td></td>
		</tr>
		<tr>
			<td>Microhardness tester, ALPHA-MHT-1000Z&#160;</td>
			<td>PACE Technologies</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>SamplKups &#160;1 inch</td>
			<td>Buehler</td>
			<td>No: 209178</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium Fluoride</td>
			<td>Fisher Scientific</td>
			<td>S299-100</td>
			<td></td>
		</tr>
		<tr>
			<td>West cott Stitch Scissor</td>
			<td>JEDMED</td>
			<td>Cat. #25-1180</td>
			<td></td>
		</tr>
		<tr>
			<td>ZooMed Repti Thern Undertank heater (U.T.H)</td>
			<td>Zoo Med Laboratories, Inc.</td>
			<td>RH-4</td>
			<td></td>
		</tr>
	</tbody>
</table>

microhardness measurements on tooth and alveolar bone in rodent oral disease models

The mechanical property, microhardness, is evaluated in dental enamel, dentin, and bone in oral disease models, including dental fluorosis and periodontitis. Micro-CT (&#181;CT) provides 3D imaging information (volume and mineral density) and scanning electron microscopy (SEM) produces microstructure images (enamel prism and bone lacuna-canalicular). Complementarily to structural analysis by &#181;CT and SEM, microhardness is one of the informative parameters to evaluate how structural changes alter mechanical properties. Despite being a useful parameter, studies on microhardness of alveolar bone in oral diseases are limited. To date, divergent microhardness measurement methods have been reported. Since microhardness values vary depending on the sample preparation (polishing and flat surface) and indentation sites, diverse protocols can cause discrepancies among studies. Standardization of the microhardness protocol is essential for consistent and accurate evaluation in oral disease models. In the present study, we demonstrate a standardized protocol for microhardness analysis in tooth and alveolar bone. Specimens used are as follows: for the dental fluorosis model, incisors were collected from mice treated with/without fluoride-containing water for 6 weeks; for ligature-induced periodontal bone resorption (L-PBR) model, alveolar bones with periodontal bone resorption were collected from mice ligated on the maxillary 2nd molar. At 2 weeks after the ligation, the maxilla was collected. Vickers hardness was analyzed in these specimens according to the standardized protocol. The protocol provides detailed materials and methods for resin embedding, serial polishing, and indentation sites for incisors and alveolar. To the best of our knowledge, this is the first standardized microhardness protocol to evaluate the mechanical properties of tooth and alveolar bone in rodent oral disease models.

Author Spotlight: Establishing an Accurate Microhardness Testing Protocol for Craniofacial Tissues

Microhardness Measurements on Tooth and Alveolar Bone in Rodent Oral Disease Models

In this research, we focused on establishing accurate and consistent microhardness testing. Microhardness testing is a traditional method, but fear not, the methodology is not sufficiently described in previous publications. As we demonstrated in the result, provide immediate minimal microhardness reduction depends on the intention sites of the interim, like inner, middle and outer layers.Our results suggests that the intention site is important to obtain accurate and consistent results. The scientific gap is that the previous studies did not sufficiently describe the microhardness testing methods, especially the variation sites. Due to this, microhardness result were not consistent between studies.To fill this gap, we established this protocol for accurate and effective evaluation. Our established protocol will advance mineral tissue testing in enamel, denti, and earlier bone in periodontal disease, bone origination, and oral cancer bone invasion models. We will focus on how environmental factors affect dental craniofacial pathophysiology.For example, chloride and organ rolling, PFAS. PFAS is manmade forever hazardous chemicals. Our microhardness protocol will contribute to evaluating how PFAS affect mechanical properties in mineral tissues in tooth development, periodontal bone resorption, and oral cancer bone invasion.

Dental fluorosis model: Figure 1 shows representative &#956;CT images of incisors in control and fluoride-treated mice. In the control (Figure 1B-D), the cervical region showed lower enamel mineral density (EMD) of 1.188 g/cm3 (Figure 1B) compared to the middle (1.924 g/cm3) and tip (1.819 g/cm3; Figure 1C,D). In the fluoride-treated ena...

Watch this Scientific Journal Video about Author Spotlight: Establishing an Accurate Microhardness Testing Protocol for Craniofacial Tissues at JoVE.com

Microhardness is a mechanical property and an informative parameter for evaluating hard tissue pathophysiology. Here, we demonstrate a standardized protocol (sample preparation, polishing, flat surface, and indentation sites) for microhardness analysis in tooth and alveolar bone in rodent oral disease models, namely, dental fluorosis, and ligature-induced periodontal bone resorption.

The mechanical property, microhardness, is evaluated in dental enamel, dentin, and bone in oral disease models, including dental fluorosis and ...

microhardness-measurements-on-tooth-alveolar-bone-rodent-oral-disease

Research

JoVE Journal

Biology

Vickers Microhardness Testing of Murine Dental Samples Embedded in Resin

461 Views.  Nova Southeastern University.  Microhardness is a mechanical property and an informative parameter for evaluating hard tissue pathophysiology. Here, we demonstrate a standardized protocol (sample preparation, polishing, flat surface, and indentation sites) for microhardness analysis in tooth and alveolar bone in rodent oral disease models, namely, dental fluorosis, and ligature-induced periodontal bone resorption.

Microhardness Protocol for Evaluating Rodent Oral Disease

Summary