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Perspective

Teeth Microcracks Research: Towards Multi-Modal Imaging

by
Irma Dumbryte
1,*,
Donatas Narbutis
2,
Maria Androulidaki
3,
Arturas Vailionis
4,5,
Saulius Juodkazis
6,7 and
Mangirdas Malinauskas
8
1
Institute of Odontology, Vilnius University, LT-08217 Vilnius, Lithuania
2
Institute of Theoretical Physics and Astronomy, Vilnius University, LT-10222 Vilnius, Lithuania
3
Microelectronics Research Group, Institute of Electronic Structure & Laser, Foundation for Research and Technology FORTH-Hellas, 70013 Heraklion, Crete, Greece
4
Stanford Nano Shared Facilities, Stanford University, Stanford, CA 94305, USA
5
Department of Physics, Kaunas University of Technology, LT-51368 Kaunas, Lithuania
6
Optical Sciences Centre and ARC Training Centre in Surface Engineering for Advanced Materials (SEAM), School of Science, Swinburne University of Technology, Hawthorn, VIC 3122, Australia
7
WRH Program International Research Frontiers Initiative (IRFI), Tokyo Institute of Technology, Nagatsuta-cho, Midori-ku, Yokohama 226-8503, Japan
8
Laser Research Center, Vilnius University, LT-10223 Vilnius, Lithuania
*
Author to whom correspondence should be addressed.
Bioengineering 2023, 10(12), 1354; https://doi.org/10.3390/bioengineering10121354
Submission received: 19 October 2023 / Revised: 16 November 2023 / Accepted: 21 November 2023 / Published: 25 November 2023
(This article belongs to the Special Issue Application of Bioengineering to Clinical Orthodontics)

Abstract

:
This perspective is an overview of the recent advances in teeth microcrack (MC) research, where there is a clear tendency towards a shift from two-dimensional (2D) to three-dimensional (3D) examination techniques, enhanced with artificial intelligence models for data processing and image acquisition. X-ray micro-computed tomography combined with machine learning allows 3D characterization of all spatially resolved cracks, despite the locations within the tooth in which they begin and extend, and the arrangement of MCs and their structural properties. With photoluminescence and micro-/nano-Raman spectroscopy, optical properties and chemical and elemental composition of the material can be evaluated, thus helping to assess the structural integrity of the tooth at the MC site. Approaching tooth samples having cracks from different perspectives and using complementary laboratory techniques, there is a natural progression from 3D to multi-modal imaging, where the volumetric (passive: dimensions) information of the tooth sample can be supplemented by dynamic (active: composition, interaction) image data. Revelation of tooth cracks clearly shows the need to re-assess the role of these MCs and their effect on the structural integrity and longevity of the tooth. This provides insight into the nature of cracks in natural hard materials and contributes to a better understanding of how bio-inspired structures could be designed to foresee crack propagation in biosolids.

The definition of enamel microcracks (MCs), introduced more than 20 years ago, referred to incomplete tooth fractures that usually do not cross the dentin–enamel junction (DEJ) and have no loss or visible separation of tooth structure [1]. However, between the lines, there is a hint that we may be facing a more complex issue: “a fracture plane of unknown depth and direction passing through tooth structure that, if not already involving, may progress to communicate with the pulp and/or periodontal ligament” [1]. The reasons for MC formation are known and include abnormalities in the tooth maturation process, excessive or prolonged occlusal forces, traumatic injuries (e.g., during the tooth extraction procedure), temperature variations, dental procedures where a lot of drilling or grinding is required, and removal of brackets at the end of the orthodontic treatment [2,3,4,5,6,7,8]. It has also been shown that the dehydration process can play a critical role in the formation of cracks in the extracted tooth dentin of the root [9,10,11]. Storage of samples in dry conditions creates stress that may lead to significant root damage [11]. However, little is known about whether dehydration would have the same effect on enamel MCs. Still, certain values of enamel MC parameters were found to be unaffected by the dehydration during the preparation of the samples for scanning electron microscopy [8,12].
Enamel MCs can be easily visible to the eye of both the patient and the dentist. In a world where aesthetics plays an important role in people’s daily lives, knowledge of how to look at, react to, and deal with these MCs is even more important. In addition to compromising the aesthetic appearance of the teeth, MCs can damage the integrity of the enamel, lead to the accumulation of stain and plaque on the rough microfractured surface, increase the susceptibility to carious lesions, or cause greater teeth sensitivity after the debonding procedure [3,13,14,15]. The need to document teeth with MCs and to establish monitoring, prevention, and treatment algorithms is becoming evident in everyday clinical practice. The questions of how to improve aesthetics, manage the sensitivity of teeth having MCs, or whether orthodontic treatment should be modified when seeing a patient with multiple teeth with MCs are still unanswered (Figure 1a).
Over the last two decades, the field of MC research has been expanding with advances in laboratory techniques. Methods such as staining and transillumination [16,17,41], which were previously routinely used for MC detection, have been replaced by more sophisticated two-dimensional (2D) techniques that provide information on surface interfaces. The most common methods employed to examine cracks were optical stereomicroscopy (OS), scanning electron microscopy (SEM), and confocal optical profilometry (COP) [2,3,4,5,12,18,19,20,21,22,23,24]. This has made it possible to describe MCs not only qualitatively but also quantitatively. However, in addition to 2D tooth imaging, three-dimensional (3D) scanning methods (e.g., optical coherence tomography (OCT), ultrasound) have increasingly been used to obtain volumetric information of the enamel surface, including cracks [25,27,28]. While the initial interest in tooth MC studies is still growing, there has been an upward trend in the number of publications over the last 7 years towards the use of 3D imaging techniques for tooth structure examination [33,34,35,36,37,38,39,40] (Figure 1b). At the same time, 2D methods are still being employed, but their frequency of use is likely decreasing [3,18,19,20]. The shift from 2D to 3D methods is being driven both by rapidly advancing technologies that allow us to see what could previously only be imagined and by growing scientific interest (Figure 1c,d). New clinical research opportunities are opening up that could meet doctors’ expectations.
X-ray micro-computed tomography ( μ CT) can be described as a game-changing technology in the field of MC research. In dental studies, this method was introduced in 2007 [42,43], but has only been employed to visualize the inner structure of human tooth enamel in the MC region since 2021 [37]. With previously widely used laboratory techniques for the examination of various crack characteristics (e.g., their number, direction, location, length, and width), it was possible to assess the morphology, position, and dynamics of MCs only on the outer tooth enamel surface [3,4,5,8,19] (Figure 2).
Due to the limitations of the methods employed to analyze the depth of the MCs (e.g., the insufficient penetration and scanning range of the instrument [27,32], sensitivity of the technique to surface curvature [25,32], an indirect method for measuring crack depth [33,40], the necessity to infiltrate contrast material into the cracks in order to examine the depth parameter [40], or the physical evaluation of the crack after the tooth has been sectioned [33]), it remains unclear if MCs are located only within the enamel surface, or if they spread deeper into the tooth, crossing the DEJ and reaching the dentin and even the pulp [38].
The word tomography, derived from the Greek words tómos (meaning “slice” or “section”) + gráphō (meaning “to write” or “to describe”), hints the working principle in its very name. With a microtomograph, over a thousand 2D photographs rotating a sample are produced in a few hours, from which a high-resolution 3D image of the object (a data cylinder) is reproduced using specialized software. One of the most important features of an X-ray μ CT image is the successful separation of structures of different densities in a 3D volume. In 3D, the contrast between objects of different densities is characterized by an excellent resolution of up to one-hundredth of the thickness of a human hair. Modern state-of-the-art laboratory μ CTs can achieve resolutions up to 700–1000 nm (4000–10,000 nm is usually the resolution of choice for biological samples) using geometric magnification [37,38,44]. In this way, the components of the tooth can be easily seen: cracks, enamel, dentin, and pulp chamber. This data cylinder can be viewed from different directions and in different sections. It is important to emphasize that at this stage of data processing, artificial intelligence can be successfully employed to understand and automate the spatial arrangement of the structural parts of the tooth. For this purpose, several 2D photographs of the cylinder sections are viewed by eye to determine the location of the objects. Only when the components of the tooth are well identified can the neural network be trained to segment the whole image by means of artificial intelligence and, after correcting the network’s errors and retraining, achieve good segmentation quality over the entire volume of the object [45]. This method thus helps to automate the spatial recognition of the structural parts of the tooth and to understand their position.
Once the samples are properly segmented, it is possible to experiment with custom developed [46,47,48] or commercial [49] 3D visualization software, assuming that each voxel (i.e., the equivalent of a pixel in 2D space) could emit, absorb, or reflect the light. Then, choosing how the voxels should shine or cover each other so that the result looks understandable and attractive when viewed from different directions, it is possible to highlight what is curious, e.g., just the cracks in the enamel of the tooth, the whole network of cracks, or the structures of the dentin surface [37,38].
X-ray μ CT marks the non-destructive transition from the outer towards the inner tooth structure, as it allows one to achieve a resolution of a few micrometers and to see the internal structural components of the tooth in much greater detail than in a conventional dental X-ray with the naked eye. Therefore, the application of the X-ray μ CT combined with machine learning (ML) for crack analysis has significantly expanded our knowledge of this form of tooth damage [37,38]. This has led to an understanding beyond what was known so far about MCs. Using 3D non-destructive imaging, it has become possible to identify and detect not only enamel MCs that are visible on the outer surface but also those that are buried deep inside the tooth [37,38]. X-ray μ CT scanning technique enhanced with convolutional neural network (CNN) assisted voxel classification and volume segmentation (a type of deep learning algorithm) enabled 3D non-destructive examination of all spatially resolved MCs, despite the locations within the tooth in which they originate and extend, as well as the arrangement of MCs and their structural properties [38,50,51,52]. A network of star-shaped MCs (along the main axis of the tooth) inside intact (healthy, undamaged) teeth with visible or absent MCs on the buccal surface has been disclosed, proposing the idea that the cracks might be regarded as on the structural and probably functional components of the tooth [38].
The ability to characterize cracks in 3D raises further question of whether there are changes in the tooth material within the MC compared to the enamel areas that are without cracks, and whether there is a loss of structural integrity at the site of the MC. Knowledge of the extent of damage at the crack area would help to clarify whether and where treatment strategies for teeth with MCs should be targeted. From this perception comes the idea to combine a μ CT with photoluminescence (PL) and micro-/nano-Raman spectroscopy ( μ -/n-RS) for tooth structural integrity assessment at the MC site (Figure 3).
The optical characteristics of natural teeth [53,54] and the fluorescence differences between sound teeth and teeth affected by caries lesions [55,56] or treated with bleaching agents [57] have already been studied. The photoemission spectra (illuminated with wavelengths of 337.8 nm) of healthy and decayed teeth were found to be different, and the spectral intensity of teeth with dental caries was lower [56]. It was noticed that spectral intensity varied among different carious stages, with deep cavitation displaying the weakest fluorescence [56]. An analysis of the spectral shape derived from the 405 nm laser-induced autofluorescence spectra has also shown it to be a useful tool for diagnosing and staging caries [55]. Although MCs are not classified as tooth decay, it is still unknown whether the PL spectrum at the site of the crack would be similar to that of sound or damaged enamel [58].
So what are the properties of PL and μ -/n-RS that would make these techniques particularly useful for further analysis of the chemical and elemental composition of tooth material? It is important to emphasize that interaction of light with matter shows us the optical properties, composition, and defects of the examined object. This can be achieved using basic non-destructive techniques like PL and μ -/n-RS measurements, which do not require special sample preparation. With PL, the tooth is excited with monochromatic light (laser) and the emission from the radiative process is observed in different areas of the sample. The change in intensity, peak position, and peak full width at half maximum between the good area and the cracked area can be investigated. The spectral analysis yields results on the distribution of hydroxyapatite (HAP) crystals on the outer tooth surface, inside the tooth, and at the depth of light penetration. In addition, the μ -/n-RS method can be used to determine the chemical composition inside each crack and the difference with the good area. Therefore, image measurements are extremely useful tools for analyzing how to change the concentration of chemical bonds inside and outside cracks.
More sophisticated techniques such as atomic force microscopy (AFM) can be employed to examine the surface of teeth samples even at the nano-scale. The topography, roughness, and mechanical properties of the specimen surface can be assessed by means of high-resolution and high-speed imaging [59].
The field of 3D micro-optics and its applications for imaging is rapidly expanding, especially driven by femtosecond laser direct-write 3D multi-photon lithography (MPL, also known as two-photon or multi-photon polymerization) [60]. Some showcasing examples already demonstrate its feasibility for endoscopic use in pre-clinical and clinical conditions [61]. Excellent performance and the small footprint of 3D micro-optics is foreseen to be game changing in enabling diverse sophisticated optical imaging combined with spectroscopic techniques [62] into in situ and in vivo cases for teeth investigation.
Approaching teeth with MCs from individual perspectives and using different but complementary laboratory techniques, we naturally move from 3D to multi-modal tooth imaging (Figure 4).
The volumetric (passive) information of the sample can be supplemented by dynamic (active) image data. It becomes possible to reveal the physical (mechanical) properties of the tooth by scanning under loading conditions or by modifying the environmental parameters (e.g., hydrated via dehydrated medium). Thus, a material responds to the changing surroundings. Some efforts have already been made in this direction, using synchrotron X-ray tomography for the 3D assessment of enamel demineralization in carious lesions [63] and for the analysis of internal enamel during acid exposure [64]. A time-lapse imaging sequence was generated by repeatedly scanning the changes in enamel structure because of acids [64]. Therefore, 3D study of how MCs would behave under compression would give us dynamic information—already in the four-dimensional space.
Apart from X-ray structural analysis, synchrotrons provide high brilliance (brightness) beams at far-infrared (3–30 µm) and THz (30 µm–3 mm) spectral ranges. Spectral brightness has units of time 1 · distance 2 · angle 2 · bandwidth 1 [65]. At those long wavelengths, light penetration into skin depth of ∼ λ / 4 already yields useful sub-surface characterization in reflection as well as transmission. The use of attenuated total reflection (ATR), especially in the THz spectral range, expands the versatility of THz diagnostics due to the simplicity of sample preparation and measurement, which avoids THz propagation in air where there is a strong THz absorption by water (moisture). Recently, the principle to obtain 2D slicing of optical properties at different sample orientations required for 3D rendering of volume in μ CT was demonstrated using ATR [66]. Optical near-field can be used to 3D steer the intensity of far-infrared/THz beams inside the sub-surface of the sample using different polarization azimuth of the incoming beam and analyzing the reflected beam from the sample in the ATR setting [66]. This technique provides access to orientation and anisotropy in absorption or/and birefringence of the tissue, which is present in the teeth [67]. An example of natural birefringent material that also has a linear dichroism at THz wavelengths is bamboo [68]. The four-polarization analysis of transmittance spectra [69] (also applicable to reflectance [70]) provides access to structural anisotropies in absorption and birefringence and also reveals them even when spatial resolution is low [71]. The four-polarization technique is promising for the investigation of structural changes to enamel and dentin caused by ablation with ultra-short laser pulses at a high repetition rate, which is a promising technique for dental repairs and is approaching material removal rates of ∼30 mm 3 /min and could replace currently used mechanical tools for drilling [72].
Therefore, future perspectives (their strengths, weaknesses, and opportunities) for the analysis of tooth MCs are presented in Figure 5.
It is important to note that destructive tooth examination techniques are being developed in parallel [73]. In order to determine the optimal irradiation conditions for the precise removal of dental hard tissues without structural and compositional damage, the effect of femtosecond laser on the ablation of enamel and dentin was investigated at different pulse wavelengths and pulse intervals [73]. There is a potential to examine not only naturally developed cracks due to mechanical reasons, but also damage to the tooth structure caused by laser processing.
Detailed volumetric imaging of the tooth MCs, which will be complemented by dynamic data in the near future, reveals the need to review and update the definition of crack used until now and to re-assess the role of these MCs and their effect on the structural integrity and longevity of the tooth. It also provides insight into the nature of cracks in natural hard materials and contributes to a better understanding of how bio-inspired structures could be designed to foresee crack propagation in biosolids. Future estimation of the material elemental and chemical composition in a cracked tooth area could lead to the development of new algorithms for the monitoring and treatment of teeth with MCs in daily clinical practice. Considering the quality and quantity of HAP crystals in the MC area, the idea of remineralization therapy for teeth with cracks is foreseen. Finally, artificial intelligence models for segmenting teeth from X-ray μ CT images would eliminate the necessity for manual assessment of radiographic data and promote diagnostic efficiency and treatment strategy planning in cracked areas.
Over the past few years, the field of dentistry has witnessed remarkable advancements through the application of various machine learning (ML) models. Initially, studies focused on traditional convolutional neural networks (CNNs) such as U-Net for caries detection and localization [74,75]. Subsequent progress led to the development of more sophisticated architectures, including a 3D-CNN for generating partial dental crowns, demonstrating improved validation accuracy and sensitivity [76]. The evolution continued with the introduction of self-training-based methods, leveraging unlabeled data for student model training, offering computational and performance gains over traditional supervised learning [77]. Hybrid frameworks, combining deep learning (DL) and conventional computer-aided design approaches, demonstrated high accuracy in automatic periodontitis staging [78]. In addition, new artificial intelligence systems have been developed and evaluated to help determine the severity of tooth crowding and the need for tooth extraction when planning orthodontic treatment [79]. The successful combination of DL with orthodontic photographs allowed effective categorization of the tooth crowding problem and good decision-making on the choice of orthodontic treatment strategy [79]. Furthermore, the exploration of variational autoencoders and the application of ML setups for sexual dimorphism showcased a shift towards more complex and versatile models, contributing to enhanced diagnostic capabilities in dental imaging [80,81]. These progressive developments underscore the transformative potential of ML in revolutionizing dental diagnostics and treatment planning.
The utilization of ML techniques in dentistry presents a transformative approach with notable strengths. The implementation of DL models, such as U-Net and 3D-CNN, has exhibited significant precision in tasks like caries detection and partial dental crown generation, showcasing their efficacy in complex dental imaging applications. In recent years, artificial intelligence models have been used mainly for practical applications, in particular, for tooth and alveolar bone segmentation [82] and jaw reconstruction [83,84]. A deep convolutional generative adversarial network (DCGAN) called CTGAN has been proposed to help recover mandibular morphology after disease [83]. A DL approach, based on a variational auto-encoder to extract morphological features, has proven to be a promising tool for reconstructing the shape of the mandible, even when some segments from incomplete images are missing [84]. However, challenges persist, including the dependence on limited and specific datasets, the need for robust external validation across diverse patient populations, and the interpretability of complex models. Overcoming these limitations and addressing ethical considerations will be crucial for the future success and integration of ML in dentistry, promising enhanced diagnostic capabilities and improved patient care. These new research opportunities respond to today’s clinical challenges and are moving rapidly towards the medical field.

Author Contributions

Conceptualization, I.D. and M.M.; writing—original draft preparation, I.D., D.N., M.A., A.V. and S.J.; visualization, I.D. and D.N.; writing—review and editing, I.D., D.N. and M.M. All authors have read and agreed to the published version of the manuscript.

Funding

M.M. acknowledges EU LASERLAB-EUROPE (grant agreement No. 871124, Horizon 2020 research and innovation programme) for the financial support. This work was performed under the “University Excellence Initiative programme”.

Acknowledgments

Topcat [85] and Matplotlib [46] were used to visualize data.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

The following abbreviations are used in this manuscript:
2DTwo-Dimensional
3DThree-Dimensional
AFMAtomic Force Microscopy/Microscope
ATRAttenuated Total Reflection
COPConfocal Optical Profilometry/Profilometer
CNNConvolutional Neural Network
DEJDentin–Enamel Junction
DLDeep Learning
HAPHydroxyAPatite
MCMicroCrack
MLMachine Learning
OCTOptical Coherence Tomography
OSOptical StereoMicroscopy/StereoMicroscope
PLPhotoLuminescence Spectroscopy
SEMScanning Electron Microscopy/Microscope
μ CTMicro-Computed Tomography
μ -/n-RSMicro-/Nano-Raman Spectroscopy

References

  1. Ellis, S.G. Incomplete tooth fracture–proposal for a new definition. Br. Dent. J. 2001, 190, 424–428. [Google Scholar] [CrossRef] [PubMed]
  2. Dumbryte, I.; Jonavicius, T.; Linkeviciene, L.; Linkevicius, T.; Peciuliene, V.; Malinauskas, M. Enamel cracks evaluation—A method to predict tooth surface damage during the debonding. Dent. Mater. J. 2015, 34, 828–834. [Google Scholar] [CrossRef]
  3. Dumbryte, I.; Vebriene, J.; Linkeviciene, L.; Malinauskas, M. Enamel microcracks in the form of tooth damage during orthodontic debonding: A systematic review and meta-analysis of in vitro studies. Eur. J. Orthod. 2018, 40, 636–648. [Google Scholar] [CrossRef]
  4. Shahabi, M.; Heravi, F.; Mokhber, N.; Karamad, R.; Bishara, S.E. Effects on shear bond strength and the enamel surface with an enamel bonding agent. Am. J. Orthod. Dentofac. Orthop. 2010, 137, 375–378. [Google Scholar] [CrossRef] [PubMed]
  5. Habibi, M.; Nik, T.H.; Hooshmand, T. Comparison of debonding characteristics of metal and ceramic orthodontic brackets to enamel: An in-vitro study. Am. J. Orthod. Dentofac. Orthop. 2007, 132, 675–679. [Google Scholar] [CrossRef]
  6. Kitahara-Céia, F.M.F.; Mucha, J.N.; dos Santos, P.A.M. Assessment of enamel damage after removal of ceramic brackets. Am. J. Orthod. Dentofac. Orthop. 2008, 134, 548–555. [Google Scholar] [CrossRef] [PubMed]
  7. Sorel, O.; El Alam, R.; Chagneau, F.; Cathelineau, G. Comparison of bond strength between simple foil mesh and laser-structured base retention brackets. Am. J. Orthod. Dentofac. Orthop. 2002, 122, 260–266. [Google Scholar] [CrossRef]
  8. Dumbryte, I. Evaluation of Enamel Microcracks’ Characteristics before and after Removal of Metal and Ceramic Brackets for Teeth from Younger- and Older-Age Groups: An In Vitro Study. Ph.D. Thesis, Vilnius University, Vilnius, Lithuania, 2020. [Google Scholar] [CrossRef]
  9. Versiani, M.A.; Cavalcante, D.M.; Belladonna, F.G.; Silva, E.J.N.L.; Souza, E.M.; De-Deus, G. A critical analysis of research methods and experimental models to study dentinal microcracks. Int. Endod. J. 2022, 55, 178–226. [Google Scholar] [CrossRef]
  10. De-Deus, G.; Cavalcante, D.M.; Belladonna, F.G.; Carvalhal, J.; Souza, E.M.; Lopes, R.T.; Versiani, M.A.; Silva, E.J.N.L.; Dummer, P.M.H. Root dentinal microcracks: A post-extraction experimental phenomenon? Int. Endod. J. 2019, 52, 857–865. [Google Scholar] [CrossRef]
  11. Shemesh, H.; Lindtner, T.; Portoles, C.A.; Zaslansky, P. Dehydration Induces Cracking in Root Dentin Irrespective of Instrumentation: A Two-dimensional and Three-dimensional Study. J. Endod. 2018, 44, 120–125. [Google Scholar] [CrossRef]
  12. Dumbryte, I.; Linkeviciene, L.; Malinauskas, M.; Linkevicius, T.; Peciuliene, V.; Tikuisis, K. Evaluation of enamel micro-cracks characteristics after removal of metal brackets in adult patients. Eur. J. Orthod. 2013, 35, 317–322. [Google Scholar] [CrossRef] [PubMed]
  13. Chen, C.S.; Hsu, M.L.; Chang, K.D.; Kuang, S.H.; Chen, P.T.; Gung, Y.W. Failure analysis: Enamel fracture after debonding orthodontic brackets. Angle Orthod. 2008, 78, 1071–1077. [Google Scholar] [CrossRef] [PubMed]
  14. Zachrisson, B.U.; Buyukyilmaz, T. Bonding in orthodontics. In Orthodontics: Current Principles and Techniques, 4th ed.; Graber, T.M., Vanarsdall, R.L., Vig, K.W.L., Eds.; Elsevier-Mosby: St Louis, MO, USA, 2005; pp. 612–619. [Google Scholar]
  15. Dumbryte, I.; Linkeviciene, L.; Linkevicius, T.; Malinauskas, M. Does orthodontic debonding lead to tooth sensitivity? Comparison of teeth with and without visible enamel microcracks. Am. J. Orthod. Dentofac. Orthop. 2017, 151, 284–291. [Google Scholar] [CrossRef]
  16. Clark, D.J.; Sheets, C.G.; Paquette, J.M. Definitive diagnosis of early enamel and dentin cracks based on microscopic evaluation. J. Esthet. Restor. Dent. 2003, 15, 391–401, discussion 401. [Google Scholar] [CrossRef]
  17. Rix, D.; Foley, T.F.; Mamandras, A. Comparison of bond strength of three adhesives: Composite resin, hybrid GIC, and glass-filled GIC. Am. J. Orthod. Dentofac. Orthop. 2001, 119, 36–42. [Google Scholar] [CrossRef]
  18. Baherimoghadam, T.; Akbarian, S.; Rasouli, R.; Naseri, N. Evaluation of enamel damages following orthodontic bracket debonding in fluorosed teeth bonded with adhesion promoter. Eur. J. Dent. 2016, 10, 193–198. [Google Scholar] [CrossRef] [PubMed]
  19. Dumbryte, I.; Linkeviciene, L.; Linkevicius, T.; Malinauskas, M. Enamel microcracks in terms of orthodontic treatment: A novel method for their detection and evaluation. Dent. Mater. J. 2017, 36, 438–446. [Google Scholar] [CrossRef]
  20. Dumbryte, I.; Jonavicius, T.; Linkeviciene, L.; Linkevicius, T.; Peciuliene, V.; Malinauskas, M. The prognostic value of visually assessing enamel microcracks: Do debonding and adhesive removal contribute to their increase? Angle Orthod. 2016, 86, 437–447. [Google Scholar] [CrossRef]
  21. Ahrari, F.; Heravi, F.; Fekrazad, R.; Farzanegan, F.; Nakhaei, S. Does ultra-pulse CO2 laser reduce the risk of enamel damage during debonding of ceramic brackets? Lasers Med. Sci. 2012, 27, 567–574. [Google Scholar] [CrossRef]
  22. Heravi, F.; Rashed, R.; Raziee, L. The effects of bracket removal on enamel. Aust. Orthod. J. 2008, 24, 110–115. [Google Scholar]
  23. Salehi, P.; Pakshir, H.; Naseri, N.; Baherimoghaddam, T. The effects of composite resin types and debonding pliers on the amount of adhesive remnants and enamel damages: A stereomicroscopic evaluation. J. Dent. Res. Dent. Clin. Dent. Prospects 2013, 7, 199–205. [Google Scholar] [PubMed]
  24. Heravi, F.; Shafaee, H.; Abdollahi, M.; Rashed, R. How is the enamel affected by different orthodontic bonding agents and polishing techniques? J. Dent. 2015, 12, 188–194. [Google Scholar]
  25. Culjat, M.O.; Singh, R.S.; Brown, E.R.; Neurgaonkar, R.R.; Yoon, D.C.; White, S.N. Ultrasound crack detection in a simulated human tooth. Dentomaxillofac. Radiol. 2005, 34, 80–85. [Google Scholar] [CrossRef]
  26. Al Shamsi, A.H.; Cunningham, J.L.; Lamey, P.J.; Lynch, E. Three-dimensional measurement of residual adhesive and enamel loss on teeth after debonding of orthodontic brackets: An in-vitro study. Am. J. Orthod. Dentofac. Orthop. 2007, 131, 301.e9–301.e15. [Google Scholar] [CrossRef] [PubMed]
  27. Hsieh, Y.S.; Ho, Y.C.; Lee, S.Y.; Chuang, C.C.; Tsai, J.C.; Lin, K.F.; Sun, C.W. Dental optical coherence tomography. Sensors 2013, 13, 8928–8949. [Google Scholar] [CrossRef]
  28. Leão Filho, J.C.; Braz, A.K.; de Araujo, R.E.; Tanaka, O.M.; Pithon, M.M. Enamel quality after debonding: Evaluation by optical coherence tomography. Braz. Dent. J. 2015, 26, 384–389. [Google Scholar] [CrossRef]
  29. Imai, K.; Shimada, Y.; Sadr, A.; Sumi, Y.; Tagami, J. Noninvasive cross-sectional visualization of enamel cracks by optical coherence tomography in vitro. J. Endod. 2012, 38, 1269–1274. [Google Scholar] [CrossRef]
  30. Ryf, S.; Flury, S.; Palaniappan, S.; Lussi, A.; van Meerbeek, B.; Zimmerli, B. Enamel loss and adhesive remnants following bracket removal and various clean-up procedures in vitro. Eur. J. Orthod. 2012, 34, 25–32. [Google Scholar] [CrossRef]
  31. Swain, M.V.; Xue, J. State of the art of micro-CT applications in dental research. Int. J. Oral Sci. 2009, 1, 177–188. [Google Scholar] [CrossRef]
  32. Sun, K.; Yuan, L.; Shen, Z.; Xu, Z.; Zhu, Q.; Ni, X.; Lu, J. Scanning laser-line source technique for nondestructive evaluation of cracks in human teeth. Appl. Opt. 2014, 53, 2366–2374. [Google Scholar] [CrossRef]
  33. Li, Z.; Holamoge, Y.V.; Li, Z.; Zaid, W.; Osborn, M.L.; Ramos, A.; Miller, J.T.; Li, Y.; Yao, S.; Xu, J. Detection and analysis of enamel cracks by ICG-NIR fluorescence dental imaging. Ann. N. Y. Acad. Sci. 2020, 1475, 52–63. [Google Scholar] [CrossRef] [PubMed]
  34. Jamleh, A.; Mansour, A.; Taqi, D.; Moussa, H.; Tamimi, F. Microcomputed tomography assessment of microcracks following temporary filling placement. Clin. Oral Investig. 2019, 24, 1387–1393. [Google Scholar] [CrossRef] [PubMed]
  35. Alsolaihim, A.N.; Alsolaihim, A.A.; Alowais, L.O. In vivo and in vitro diagnosis of cracked teeth: A review. J. Int. Oral Health 2019, 11, 329–333. [Google Scholar] [CrossRef]
  36. Hamba, H.; Nakamura, K.; Nikaido, T.; Muramatsu, T.; Furusawa, M.; Tagami, J. Examination of micro-cracks and demineralization in human premolars using micro-CT. Jpn. J. Conserv. Dent. 2017, 60, 89–95. [Google Scholar] [CrossRef]
  37. Dumbryte, I.; Vailionis, A.; Skliutas, E.; Juodkazis, S.; Malinauskas, M. Three-dimensional non-destructive visualization of teeth enamel microcracks using X-ray micro-computed tomography. Sci. Rep. 2021, 11, 14810. [Google Scholar] [CrossRef] [PubMed]
  38. Dumbryte, I.; Narbutis, D.; Vailionis, A.; Juodkazis, S.; Malinauskas, M. Revelation of microcracks as tooth structural element by X-ray tomography and machine learning. Sci. Rep. 2022, 12, 22489. [Google Scholar] [CrossRef]
  39. Segarra, M.; Shimada, Y.; Sadr, A.; Sumi, Y.; Tagami, J. Three-Dimensional Analysis of Enamel Crack Behavior Using Optical Coherence Tomography. J. Dent. Res. 2017, 96, 308–314. [Google Scholar] [CrossRef]
  40. Zhou, J.; Fu, J.; Xiao, M.; Qiao, F.; Fu, T.; Lv, Y.; Wu, F.; Sun, C.; Li, P.; Wu, L. New technique for detecting cracked teeth and evaluating the crack depth by contrast-enhanced cone beam computed tomography: An in vitro study. BMC Oral Health 2022, 22, 1–10. [Google Scholar] [CrossRef]
  41. Bishara, S.E.; Ostby, A.W.; Laffoon, J.; Warren, J.J. Enamel cracks and ceramic bracket failure during debonding in vitro. Angle Orthod. 2008, 78, 1078–1083. [Google Scholar] [CrossRef]
  42. Huang, T.T.; Jones, A.S.; He, L.H.; Darendeliler, M.A.; Swain, M.V. Characterisation of enamel white spot lesions using X-ray micro-tomography. J. Dent. 2007, 35, 737–743. [Google Scholar] [CrossRef]
  43. Efeoglu, N.; Wood, D.J.; Efeoglu, C. Thirty-five percent carbamide peroxide application causes in vitro demineralization of enamel. Dent. Mater. 2007, 23, 900–904. [Google Scholar] [CrossRef] [PubMed]
  44. du Plessis, A.; Broeckhoven, C.; Guelpa, A.; le Roux, S.G. Laboratory x-ray micro-computed tomography: A user guideline for biological samples. GigaScience 2017, 6, 1–11. [Google Scholar] [CrossRef]
  45. Krasikov, S.; Tranter, A.; Bogdanov, A.; Kivshar, Y. Intelligent metaphotonics empowered by machine learning. Opto-Electron Adv. 2022, 5, 210147. [Google Scholar] [CrossRef]
  46. Hunter, J.D. Matplotlib: A 2D graphics environment. Comput. Sci. Eng. 2007, 9, 90–95. [Google Scholar] [CrossRef]
  47. Joye, W.A.; Mandel, E. New Features of SAOImage DS9. In Proceedings of the Astronomical Data Analysis Software and Systems XII; Astronomical Society of the Pacific Conference Series; Payne, H.E., Jedrzejewski, R.I., Hook, R.N., Eds.; Astronomical Society of the Pacific: San Francisco, CA, USA, 2003; Volume 295, p. 489. Available online: https://ui.adsabs.harvard.edu/abs/2003ASPC..295..489J (accessed on 6 November 2023).
  48. Silversmith, W. cc3d: Connected Components on Multilabel 3D and 2D Images. Available online: https://zenodo.org/record/5535251 (accessed on 11 November 2023).
  49. Dragonfly 2022.2 [Computer Software]. Comet Technologies Canada Inc. Available online: https://www.theobjects.com/dragonfly (accessed on 11 November 2023).
  50. Developers. TensorFlow. Available online: https://zenodo.org/records/6574269 (accessed on 11 November 2023).
  51. Chen, L.C.; Zhu, Y.; Papandreou, G.; Schroff, F.; Adam, H. Encoder-Decoder with Atrous Separable Convolution for Semantic Image Segmentation. arXiv 2018, arXiv:1802.02611. [Google Scholar] [CrossRef]
  52. He, K.; Zhang, X.; Ren, S.; Sun, J. Deep residual learning for image recognition. arXiv 2015, arXiv:1512.03385. [Google Scholar] [CrossRef]
  53. Fondriest, J.F. The Optical Characteristics of Natural Teeth. Insid. Dent. 2012, 8, 1–5. Available online: https://www.aegisdentalnetwork.com/id/2012/11/the-optical-characteristics-of-natural-teeth (accessed on 6 November 2023).
  54. Lee, Y.K. Fluorescence properties of human teeth and dental calculus for clinical applications. J. Biomed. Opt. 2015, 20, 040901. [Google Scholar] [CrossRef]
  55. Ko, C.C.; Yi, D.H.; Lee, D.J.; Kwon, J.; Garcia-Godoy, F.; Kwon, Y.H. Diagnosis and staging of caries using spectral factors derived from the blue laser-induced autofluorescence spectrum. J. Dent. 2017, 67, 77–83. [Google Scholar] [CrossRef]
  56. Marouf, A.A.S.; Khairallah, Y.A. Photoluminescence spectra of sound tooth and those of different carious stages. J. Biol. Ser. 2019, 2, 071–075. [Google Scholar]
  57. Caneppele, T.M.F.; Rocha Gomes Torres, C.; Bresciani, E. Analysis of the color and fluorescence alterations of enamel and dentin treated with hydrogen peroxide. Braz. Dental J. 2015, 26, 514–518. [Google Scholar] [CrossRef]
  58. Thomas, S.; Narayanan, S. Spectroscopic Investigation of Tooth Caries and Demineralization. 2023. Available online: https://www.researchgate.net/publication/48410785_Spectroscopic_Investigation_of_Tooth_Caries_and_Demineralization (accessed on 6 November 2023).
  59. Xia, F.; Youcef-Toumi, K. Review: Advanced Atomic Force Microscopy Modes for Biomedical Research. Biosensors 2022, 12, 1116. [Google Scholar] [CrossRef]
  60. Gonzalez-Hernandez, D.; Varapnickas, S.; Bertoncini, A.; Liberale, C.; Malinauskas, M. Micro-Optics 3D Printed via Multi-Photon Laser Lithography. Adv. Optical Mater. 2023, 11, 2201701. [Google Scholar] [CrossRef]
  61. Li, J.; Thiele, S.; Quirk, B.C.; Kirk, R.W.; Verjans, J.W.; Akers, E.; Bursill, C.A.; Nicholls, S.J.; Herkommer, A.M.; Giessen, H.; et al. Ultrathin monolithic 3D printed optical coherence tomography endoscopy for preclinical and clinical use. Light Sci. Appl. 2020, 9, 124. [Google Scholar] [CrossRef]
  62. Marini, M.; Nardini, A.; Martínez Vázquez, R.; Conci, C.; Bouzin, M.; Collini, M.; Osellame, R.; Cerullo, G.; Kariman, B.S.; Farsari, M.; et al. Microlenses Fabricated by Two-Photon Laser Polymerization for Cell Imaging with Non-Linear Excitation Microscopy. Adv. Funct. Mater. 2023, 33, 2213926. [Google Scholar] [CrossRef]
  63. Besnard, C.; Harper, R.A.; Moxham, T.E.; James, J.D.; Storm, M.; Salvati, E.; Landini, G.; Shelton, R.M.; Korsunsky, A.M. 3D analysis of enamel demineralisation in human dental caries using high-resolution, large field of view synchrotron X-ray micro-computed tomography. Mater. Today Commun. 2021, 27, 102418. [Google Scholar] [CrossRef]
  64. Besnard, C.; Marie, A.; Sasidharan, S.; Harper, R.A.; Marathe, S.; Moffat, J.; Shelton, R.M.; Landini, G.; Korsunsky, A.M. Time-Lapse In Situ 3D Imaging Analysis of Human Enamel Demineralisation Using X-ray Synchrotron Tomography. Dent. J. 2023, 11, 130. [Google Scholar] [CrossRef] [PubMed]
  65. Wikipedia. Synchrotron Light Source. Available online: https://en.wikipedia.org/wiki/Synchrotron_light_source (accessed on 11 November 2023).
  66. Meguya, R.; Ng, S.H.; Han, M.; Anand, V.; Katkus, T.; Vongsvivut, J.; Appadoo, D.; Nishijima, Y.; Juodkazis, S.; Morikawa, J. Polariscopy with optical near-fields. Nanoscale Horiz. 2022, 7, 1047–1053. [Google Scholar] [CrossRef] [PubMed]
  67. Cai, J.; Guang, M.; Zhou, J.; Qu, Y.; Xu, H.; Sun, Y.; Xiong, H.; Liu, S.; Chen, X.; Jin, J.; et al. Dental caries diagnosis using terahertz spectroscopy and birefringence. Opt. Express 2022, 30, 13134–13147. [Google Scholar] [CrossRef] [PubMed]
  68. Ichikawa, H.; Takeya, K.; Tripathi, S.R. Linear dichroism and birefringence spectra of bamboo and its use as a wave plate in the terahertz frequency region. Opt. Mater. Express 2023, 13, 966–981. [Google Scholar] [CrossRef]
  69. Hikima, Y.; Morikawa, J.; Hashimoto, T. FT-IR Image Processing Algorithms for In-Plane Orientation Function and Azimuth Angle of Uniaxially Drawn Polyethylene Composite Film. Macromolecules 2011, 44, 3950–3957. [Google Scholar] [CrossRef]
  70. Kamegaki, S.; Smith, D.; Ryu, M.; Ng, S.H.; Huang, H.H.; Maasoumi, P.; Vongsvivut, J.; Moraru, D.; Katkus, T.; Juodkazis, S.; et al. Four-Polarisation Camera for Anisotropy Mapping at Three Orientations: Micro-Grain of Olivine. Coatings 2023, 13, 1640. [Google Scholar] [CrossRef]
  71. Honda, R.; Ryu, M.; Moritake, M.; Balčytis, A.; Mizeikis, V.; Vongsvivut, J.; Tobin, M.J.; Appadoo, D.; Li, J.L.; Ng, S.H.; et al. Infrared Polariscopy Imaging of Linear Polymeric Patterns with a Focal Plane Array. Nanomaterials 2019, 9, 732. [Google Scholar] [CrossRef] [PubMed]
  72. Rapp, L.; Madden, S.; Brand, J.; Walsh, L.J.; Spallek, H.; Zuaiter, O.; Habeb, A.; Hirst, T.R.; Rode, A.V. Femtosecond laser dentistry for precise and efficient cavity preparation in teeth. Biomed. Opt. Express 2022, 13, 4559–4571. [Google Scholar] [CrossRef] [PubMed]
  73. Rapp, L.; Madden, S.; Brand, J.; Maximova, K.; Walsh, L.; Spallek, H.; Zuaiter, O.; Habeb, A.; Hirst, T.; Rode, A. Investigation of laser wavelength effect on the ablation of enamel and dentin using femtosecond laser pulses. Sci. Rep. 2023, 13, 20156. [Google Scholar] [CrossRef] [PubMed]
  74. Lee, S.; Oh, S.; Jo, J.; Kang, S.; Shin, Y.; Park, J. Deep learning for early dental caries detection in bitewing radiographs. Sci. Rep. 2021, 11, 16807. [Google Scholar] [CrossRef] [PubMed]
  75. Felsch, M.; Meyer, O.; Schlickenrieder, A.; Engels, P.; Schönewolf, J.; Zöllner, F.; Heinrich-Weltzien, R.; Hesenius, M.; Hickel, R.; Gruhn, V.; et al. Detection and localization of caries and hypomineralization on dental photographs with a vision transformer model. Npj Digit. Med. 2023, 6, 198. [Google Scholar] [CrossRef]
  76. Farook, T.H.; Ahmed, S.; Jamayet, N.B.; Rashid, F.; Barman, A.; Sidhu, P.; Patil, P.; Lisan, A.M.; Eusufzai, S.Z.; Dudley, J.; et al. Computer-aided design and 3-dimensional artificial/convolutional neural network for digital partial dental crown synthesis and validation. Sci. Rep. 2023, 13, 1561. [Google Scholar] [CrossRef]
  77. Qayyum, A.; Tahir, A.; Butt, M.A.; Luke, A.; Abbas, H.T.; Qadir, J.; Arshad, K.; Assaleh, K.; Imran, M.A.; Abbasi, Q.H. Dental caries detection using a semi-supervised learning approach. Sci. Rep. 2023, 13, 749. [Google Scholar] [CrossRef]
  78. Chang, H.J.; Lee, S.J.; Yong, T.H.; Shin, N.Y.; Jang, B.G.; Kim, J.E.; Huh, K.H.; Lee, S.S.; Heo, M.S.; Choi, S.C.; et al. Deep Learning Hybrid Method to Automatically Diagnose Periodontal Bone Loss and Stage Periodontitis. Sci. Rep. 2020, 10, 749. [Google Scholar] [CrossRef]
  79. Ryu, J.; Kim, Y.H.; Kim, T.W.; Jung, S.K. Evaluation of artificial intelligence model for crowding categorization and extraction diagnosis using intraoral photographs. Sci. Rep. 2023, 13, 5177. [Google Scholar] [CrossRef] [PubMed]
  80. Joo, S.; Jung, W.; Oh, S.E. Variational autoencoder-based estimation of chronological age and changes in morphological features of teeth. Sci. Rep. 2023, 13, 704. [Google Scholar] [CrossRef] [PubMed]
  81. Franco, A.; Porto, L.; Heng, D.; Murray, J.; Lygate, A.; Franco, R.; Bueno, J.; Sobania, M.; Costa, M.M.; Paranhos, L.R.; et al. Diagnostic performance of convolutional neural networks for dental sexual dimorphism. Sci. Rep. 2022, 12, 17279. [Google Scholar] [CrossRef] [PubMed]
  82. Cui, Z.; Fang, Y.; Mei, L.; Zhang, B.; Yu, B.; Liu, J.; Jiang, C.; Sun, Y.; Ma, L.; Huang, J.; et al. A fully automatic AI system for tooth and alveolar bone segmentation from cone-beam CT images. Nat. Commun. 2022, 13, 2096. [Google Scholar] [CrossRef]
  83. Liang, Y.; Huan, J.J.; Li, J.D.; Jiang, C.H.; Fang, C.Y.; Liu, Y.G. Use of artificial intelligence to recover mandibular morphology after disease. Sci. Rep. 2020, 10, 16431. [Google Scholar] [CrossRef]
  84. Tsutsumi, M.; Saito, N.; Koyabu, D.; Furusawa, C. A deep learning approach for morphological feature extraction based on variational auto-encoder: An application to mandible shape. npj Syst. Biol. Appl. 2023, 9, 30. [Google Scholar] [CrossRef]
  85. Taylor, M.B. TOPCAT & STIL: Starlink Table/VOTable Processing Software. In Proceedings of the Astronomical Data Analysis Software and Systems XIV; Astronomical Society of the Pacific Conference Series; Shopbell, P., Britton, M., Ebert, R., Eds.; Astronomical Society of the Pacific: San Francisco, CA, USA, 2005; Volume 347, p. 29. [Google Scholar]
Figure 1. (a) Key questions for the clinician who sees a patient with MCs in the enamel; (b) overall trends in publications on two-dimensional (2D; blue) [2,3,4,5,12,16,17,18,19,20,21,22,23,24] and three-dimensional (3D; yellow) [25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40] imaging techniques for teeth MCs from 2000 to 2023; (c) X-ray 2D image of tooth; and (d) X-ray micro-computed tomography of tooth voxels identified as cracks in 3D and projected in 2D.
Figure 1. (a) Key questions for the clinician who sees a patient with MCs in the enamel; (b) overall trends in publications on two-dimensional (2D; blue) [2,3,4,5,12,16,17,18,19,20,21,22,23,24] and three-dimensional (3D; yellow) [25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40] imaging techniques for teeth MCs from 2000 to 2023; (c) X-ray 2D image of tooth; and (d) X-ray micro-computed tomography of tooth voxels identified as cracks in 3D and projected in 2D.
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Figure 2. The most common laboratory methods (2D and 3D) for the qualitative and quantitative characteristics of teeth MCs and their ability to measure various cracks parameters. DEJ—dentin–enamel junction, OS—optical stereomicroscope, SEM—scanning electron microscope, COP—confocal optical profilometer, OCT—optical coherence tomography, X-ray μ CT—X-ray micro-computed tomography.
Figure 2. The most common laboratory methods (2D and 3D) for the qualitative and quantitative characteristics of teeth MCs and their ability to measure various cracks parameters. DEJ—dentin–enamel junction, OS—optical stereomicroscope, SEM—scanning electron microscope, COP—confocal optical profilometer, OCT—optical coherence tomography, X-ray μ CT—X-ray micro-computed tomography.
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Figure 3. Progression from 3D towards multi-modal imaging of tooth microstructure. Next to the 3D volume definition (X-ray μ CT), one can obtain the material’s optical properties (PL), chemical composition ( μ -/n-RS), and the topographical, chemical, and optomechanical surface properties (AFM). X-ray μ CT—X-ray micro-computed tomography, PL—photoluminescence, μ -/n-RS—micro-/nano-Raman spectroscopy, AFM—atomic force microscopy.
Figure 3. Progression from 3D towards multi-modal imaging of tooth microstructure. Next to the 3D volume definition (X-ray μ CT), one can obtain the material’s optical properties (PL), chemical composition ( μ -/n-RS), and the topographical, chemical, and optomechanical surface properties (AFM). X-ray μ CT—X-ray micro-computed tomography, PL—photoluminescence, μ -/n-RS—micro-/nano-Raman spectroscopy, AFM—atomic force microscopy.
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Figure 4. (a,b) X-ray micro-computed tomography of tooth voxels identified as cracks in 3D shown in different view perspectives. Each color encodes a unique spatially connected network of cracks. (c) Example of photoluminescence (PL) spectra (blue lines show three Gaussian components that are summed to get a red line which represents a best-fit model to the spectra (black dots)) obtained with a laser spot in (d).
Figure 4. (a,b) X-ray micro-computed tomography of tooth voxels identified as cracks in 3D shown in different view perspectives. Each color encodes a unique spatially connected network of cracks. (c) Example of photoluminescence (PL) spectra (blue lines show three Gaussian components that are summed to get a red line which represents a best-fit model to the spectra (black dots)) obtained with a laser spot in (d).
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Figure 5. Strengths, weaknesses, and opportunities of novel techniques for tooth MC examination.
Figure 5. Strengths, weaknesses, and opportunities of novel techniques for tooth MC examination.
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Dumbryte, I.; Narbutis, D.; Androulidaki, M.; Vailionis, A.; Juodkazis, S.; Malinauskas, M. Teeth Microcracks Research: Towards Multi-Modal Imaging. Bioengineering 2023, 10, 1354. https://doi.org/10.3390/bioengineering10121354

AMA Style

Dumbryte I, Narbutis D, Androulidaki M, Vailionis A, Juodkazis S, Malinauskas M. Teeth Microcracks Research: Towards Multi-Modal Imaging. Bioengineering. 2023; 10(12):1354. https://doi.org/10.3390/bioengineering10121354

Chicago/Turabian Style

Dumbryte, Irma, Donatas Narbutis, Maria Androulidaki, Arturas Vailionis, Saulius Juodkazis, and Mangirdas Malinauskas. 2023. "Teeth Microcracks Research: Towards Multi-Modal Imaging" Bioengineering 10, no. 12: 1354. https://doi.org/10.3390/bioengineering10121354

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