Introduction
The necessity for executing the sinus lift maxilla surgery is still very significant, mainly since many patients extract the teeth from the posterior maxilla region. The responsible technician for the surgery doesn’t use any technique of bone guided regeneration, therefore the severe pneumatization maxillary sinus occurs.1 Currently, countless techniques may be used for returning masticatory function, eg, zygomatic, osteoconduction inter alia, although the most used and documented technique is the lateral window technique because it presents a surgical technique less elaborated and largely known. However, the rupture of the Schneider membrane is a common fact that usually harms the procedure running.2
Among the materials available on the market for performing the sinus lift maxilla surgery, we can cite the autogenous, xenogenic, autologous, and alloplastic grafts. In this clinic case presented, it was selected a nano biomaterial with synthetic origin (alloplastic) since this biomaterial class has been presenting countless scientific evidence that it’s possible to have greater bone and vascular formation in comparison to the other classes.3,4
Bone regeneration has been studied for a long time due to its relevance in human health and complex cell events involved in the process have emerged from this prolific research field. The medical research field is usually linked to pioneering research and testing new types of biomaterials that may promote effective bone regeneration.5
Maxillary sinus floor augmentation (MSFA), or maxillary sinus lift, is the clinical procedure in dentistry that is more beneficial in bone-guided biomaterials development that emphasizes bone regeneration.6
The use of Bone-graft biomaterials dates back to the 1960s with calcium-phosphate and other absorbable materials to replace bone loss. In the following decade, synthetic polymers, like bioglass, were cataloged as the first synthetic biomaterial enabling adhesive properties to living tissue. Bone morphogenetic proteins (BMPs) were described in the same period and consolidated bone bioengineering as a well-defined research field. In the 1980s bioglass was approved by the Federal Drug Administration (FDA) as the first bioactive material. The last 20 years witnessed the exponential development of different types of bone-graft biomaterials.7
Among the recently developed bone regeneration-inducing biomaterials, synthetic calcium-phosphate provided a friendly environment for stem cells to grow. Calcium-phosphate in hydroxyapatite (HA) form, mainly found on bone matrix, exhibited strong osteoconduction and osteoinduction properties.8,9 However, HA had some limitations in clinical applications: a very slow absorption rate in vivo, that could be as long as 20 years; a weak crack resistance, and a low stimulus to bone tissue regeneration. HA limitations induced active research in calcium-phosphate compounds that could improve upon biomaterial absorption and enhance bone cells response. Beta-tricalcium phosphate (β-TCP) best fulfilled these attributes.10
The lateral window technique (modified Caldwell-Luc approach) is usually selected for MSFA when considerable bone volume gain is needed. In addition to an adequate surgical approach, a careful biomaterial selection should be observed in these cases. Properties like the frame to withstand mechanical forces and induce a prompt bone tissue regeneration are essential to future implant installation, irrespective of dental implant technique choice (immediate or after bone healing).11
MSFA procedure success is related to the amount of vital bone formed after graft maturation and the long-term dental implant survival in this region is related to bone graft maturation as well.12
This study aimed to evaluate the clinical results with the dental implants throughout graft technique with nano-biomaterials and using these results to supply a more detailed histomorphometric evaluation of collagen fibrils using different types of staining techniques (Hematoxylin/Eosin and Sirius red) and microscopy (light and polarized) in MSFA using nano-HA/β-TCP composite as a bone graft.
Patients and Methods
Patient Data
A 52 old female non-smoker, medically fit (no systemic disease) and had no bruxism, consulted the Oral Surgery and Maxillofacial Department at São Leopoldo Mandic university (DF, Brazil) in January of 2019. The patient’s chief complaint was a missing upper premolar (#24) and molars (#26, #27) that were extracted several years ago due to periodontitis and she was looking for implant replacements. Medical data and complementary exams confirmed normal health conditions. Cone-beam computed tomography (CBCT) confirmed #24, #26, #27 absence and condemned #25 because did not have bone support. In addition, severe bone loss (mean bone height of 2.0mm) and a pneumatized maxillary sinus were evidenced in CBCT as well (Figure 1). The patient provided informed consent to publish their case details and any accompanying images and institutional approval was not required to publish the case details.
 |
Figure 1 Cone-beam computed tomography parasagittal section showing pneumatized maxillary sinus and severe crestal ridge bone loss. Dental elements areas 24 and 26. |
Treatment Planning/Execution
Treatment (maxillary sinus lift) would start with MSFA using a bone-graft biomaterial in the first surgery stage, followed by two implant installations and #25 would be extracted in the second surgery stage before a final ceramic crown installation. After the patient’s accordance and OABR department bio-ethical guideline consent form signing, treatment started.
Surgical Procedures
All surgical procedures, including follow-up evaluations, were conducted in Oral Surgery and Maxillofacial Department at Brasilia Air Force clinical facility – OABR (DF, Brazil).
Amoxicillin (Amoxil®, GlaxoSmithKlein, GB) (2g, O.I.) was administered 1h previous to surgical procedures and chlorhexidine gluconate (0.12%) (Periogard®, Colgate, USA) mouth rinse was done just before surgery.
Local anesthesia was induced by injection of lidocaine chlorhydrate (2%) epinephrine 1:100.000 (Alphacaine 100®, DFL, Brazil). According to Tatum et al (1986),9, technique, a horizontal incision, 3mm from the mucogingival border, from the tuberal region to the anterior sinus margin was made. Vertical releasing flap incisions were made, exceeding the osteotomy limits, and the mucoperiosteal flap was elevated to access the bone surface. Lateral window osteotomy was performed using #6 round bur. The sinus membrane (Schneider’s membrane) was elevated to biomaterial insertion. Nano-HA/β-TCP composite (Blue Bone®, Regener, Brazil) was used.
After surgical procedures, the patient was submitted to the radiographic (periapical and panoramic) examination and CBCT again. Potassium clavulanate/amoxicillin (Clavulin®, 785mg, Brazil) was prescribed (12/12 h) for 14 days and precautions were advised: avoid nose blow, cough or sneeze with open mouth simultaneously.
Nine months after MSFA surgery, the patient underwent new local anesthesia and the surgical procedures were conducted to install two Cone Morse implants (Avantt, Systhex®, Brazil) in #24 and #26 region (3.5 mm × 11.5 mm – implant dimensions).
Two horizontal incisions in the maxillary ridge crest were made, bone surfaces were exposed and prior to pilot drilling a bone sample for histological analysis was obtained, using a 4 mm diameter trephine (Ø=4.0 mm × length=6.8 mm) (Figure 2).
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Figure 2 Trephined bone sample assigned to histological procedures and the dental implants inside the graft. |
In constant 0.9% saline irrigation and suctioning, sequential drilling followed pilot drilling (800 rpm) (BLM 660 model, Driller, Brazil), and implants were installed with a torque of 35 N/cm. Healing caps were placed, gingival tissue repositioned, and sutured.
Oral antibiotics (Metronidazole 300mg TID and Amoxicillin 500mg TID) for 3 days were prescribed, in addition to chlorhexidine gluconate (0.12%) (Periogard®, Colgate, USA) mouthwash for 7 days. A six-month period to osseointegration was awaited (Figure 3).
 |
Figure 3 Cone-beam computed tomography parasagittal section showing implants installed after nine months of sinus floor augmentation. |
Six months after implants osseointegration, healing caps were removed, abutments were fitted, an impression was taken and a wax-bite registration was made for an accurate three crown prosthetic confection (#24, #25, #26). After impression, #25 was extracted and in the following two weeks, three crowns ceramic prosthetic was installed.
Histological Techniques Protocols
The histological bone sample was soaked in buffered formaldehyde solution (10%), pH 7.4 for 48h prior to demineralization. Phosphate-buffered (0.1M, pH 7.4) EDTA – ethylenediaminetetraacetic acid (7%) (Sigma-Aldrich, USA) for 40 days. The sample was rinsed in tap water, ethanol dehydrated (75, 90, 100%), and clarified in xylene (Sigma-Aldrich, USA).
The sample was rehydrated (100%, 90%, 75%) and embedded in Paraplast® (Sigma-Aldrich, USA) at 650C. Five micrometre sections were obtained, using a microtome (Leica, Germany). Histological sections were collected in slides and divided into two groups assigned to Hematoxylin/Eosin (H/E) and Sirius Red (SR) staining.
For H/E staining, sections received 2 baths of xylene (Sigma-Aldrich, USA), the first one at 60–55°C for 5min and the second one at room temperature for 20min. Sections were rehydrated into decreasing concentrations of ethanol (100% to 70%), washed in tap water, bathed for 30 sec in hematoxylin solution (1%) (Sigma-Aldrich, USA), and washed again. Sections were, then, bathed in eosin (0.5%) (Sigma-Aldrich, USA) for 2min washed in tap water, immersed in increasing concentrations of alcohol (100% to 70%), and a final alcohol/xylene solution (1:1) bath for 5min. After drying, slides were coverslipped with Enthelan® (Sigma-Aldrich, USA).
For SR staining, sections received 2 baths of xylene, the first one at 60–55°C for 5min and the second one at room temperature for 20min. Sections were rehydrated into decreasing concentrations of ethanol (100% to 70%), washed in tap water. Sections were bathed for 15 to 30 min in Sirius Red solution (1%) (Sigma-Aldrich, MO, USA), washed in running water, dried, and counterstained with a solution of hematoxylin blue (3%) (Sigma-Aldrich, USA). After drying, slides were coverslipped with Enthellan® (Sigma-Aldrich, USA).
Histological slides were examined and imaged at conventional or polarized light using an upright Nikon E800 microscope (Olympus, Japan) with a P6FL profluorescence camera (Optika, Italy). Five aleatory fields were selected in 100x magnification and analyzed at 200x for collagen clumpiness, density e heterogeneity in each field. Images were analyzed in Image-Pro Plus for Window software, version 7.0.1 (Media Cybernetics) (Figure 4).
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Figure 4 SR staining in bright-field (A) and polarized light microscopy (B) exemplifying five aleatory areas selection (red dotted squares) suit to architecture description and collagen morphometry. Magnification 4x. |
Statistical Analysis
The data were analyzed using one-way ANOVA followed by a Friedman test and Dunn’s post-test (p < 0.05). All analyses were conducted with specific software (GraphPad Prism Version 8.0 and BioEstat 5.0). Five areas of the histologic sample were randomly selected, then separately analyzed. The data was generated using (GraphPad Prism Version 8.0 e BioEstat 5.0).
Results
Outcome and Follow-Up
After alloy-ceramic crowns were applied, it was fine tuned in the same visit. Implant stability was tested, in addition to occlusion in all mandibular courses, cervical margin adaptation, embrasures, and aesthetics. The final results were highly satisfactory and approved by the patient. The patient was monthly followed-up in the next 6 months, and during this period the implant stability and occlusion were observed. Bone height stability and gingival health were verified as well (Figure 5).
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Figure 5 Aesthetics results achieved (A) and radiographic evaluation after three months follow-up (B). |
Histological Findings
HE histological evaluation showed a various amount of newly formed trabecular bones within or adjacent to biomaterial areas, soft tissue, and remaining grafted material particles in the biopsy after 9 months of surgery biopsies. Areas of narrow trabecular bone of varying size with bone lining cells, osteoblasts, and osteocytes, and areas between the biomaterial and soft tissue with osteoclasts were consistently observed in the biopsy. Interestingly the newly formed bone was in direct contact with – or occasionally completely engulfed within biomaterial and only a few osteoclasts were seen close to the bone. The marrow spaces were primarily filled with fibrous connective tissue with no signs of inflammation (Figure 6).
 |
Figure 6 Representative photomicrographs of longitudinal section of biopsy after 9 months of surgery. (A) Observe remaining bone and graft area of the whole biopsy in low magnification. Square dotted lines indicate areas (B–E) photographed in higher magnification. (B) Note a flocculated basophilic biomaterial with osteocytes within narrow newly formed trabecular bone and osteoclasts at periphery. (C–E) Newly formed trabecular bones within or adjacent to biomaterial areas can be observed. Bone lining cells, osteoblasts and osteocytes are observed associated to narrow trabecular bone, while osteoclasts are mostly seen associated between biomaterial and soft tissue. Hematoxylin/Eosin staining. Scale bar A = 2 mm; B and C = 200 µm; D and E = 100 µm. |
PS staining in conventional and polarized light microscopy evaluation showed both areas of low birefringence, an indicative of immature bone with disorganized collagen bundles, as well as areas of high birefringence in the newly formed bone, and indicative of mature lamellar bone with high aggregation and organization of collagen bundles (Figure 7).
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Figure 7 Representative photomicrographs of biopsy after 9 months of surgery at bright-field (left panel) and polarized light microscopy (right panel). (A) Low magnification of biopsy. Square dotted lines indicate areas (B–D) photographed in higher magnification. (B–D) Newly formed immature or mature bones within or adjacent to biomaterial areas close to soft tissue can be observed. The same areas under polarized light show typical collagen bundle (appearing as bright lines) are well arranged, suggesting mature lamellar bone, while collagen fibers undulations suggests immature (non-lamellar) bone. The dark area shows no collagen organization. Sirius Red staining. Scale bar A = 2 mm; B-D = 400 µm. |
Statistical analysis, using the Friedman test, of SR staining selected areas in polarized microscopy indicated no differences in collagen density, clumpiness, and heterogeneity (Figure 8).
 |
Figure 8 Graphics showing statistical analysis of SR staining in polarized microscopy in five aleatory selected areas (A1–A5) that evaluated mean collagen density (A) (P=0.0342), collagen fibrils clumpiness (B) (P=0.1257) and collagen heterogeneity (C) (P=0.0976). |
Discussion
Provide adequate bulk bone support to replace alveolar crest loss or sinus pneumatization is the main goal of a multitude of surgical techniques and biomaterials. Our case report illustrated the selection of a traditional surgical approach and innovative biomaterial to fulfill functional and aesthetics demanded by the patient.13
In a recent review of the trends toward biomaterials development, HA-based composites were considered the ideal framework for new bone formation.14
Synthetic-HA chemical properties are considered more stable than natural (naive) bone HA, so it is the slowest absorption rate in bone regeneration/remodeling. Aggregating a faster-absorption calcium-phosphate, like β-TCP, would provide a more uniform timeline bone regeneration/remodeling rate. These characteristics guided the Nano-HA/β-TCP composite design used in this case report and already pre-clinically and clinically tested by the authors.8,15
In addition to clinical outcomes and follow-up that were considered highly satisfactory, histological/histomorphometric evaluation was conducted using traditional staining techniques indicated to tissue architecture (H/E) and collagen fibers (PS). Despite PS-polarizing microscopy’s shortcomings, if compared to more advanced techniques (immunohistochemistry) or chemical analysis, it is reliable and very easy to use. If PS-polarizing microscopy does not provide detailed collagen chemical characteristics, it does provide thorough access to the spatial architecture of the fiber’s arrangement and enables its quantitation.16,17
Kubasiewicz et al evaluated four different types of biomaterial osteoconductors potential: micro-HA, nano-HA, nano-HA/β-TCP, and nano-HA+collagen membrane. Histomorphometric analysis indicated that every experimental group tested induced bone regeneration, ranging from 34.2% to 44.4%, against 13% of the control group (no biomaterial used).19 Moreover, in the nano-HA group, no evidence of biomaterial was found, in contrast with all other test groups in which varying amounts of biomaterial could be found. These results indicate more proper resorption of nano-HA.20 A similar finding was observed in our histologic evaluation. Nano-HA/β-TCP composite could be observed as a highly active inducer of new bone formation. Newly formed immature bone was observed in the borders of and inside particles, suggesting substitution is in due course.
Studies conducted to evaluate MSFA, using different types of biomaterials, concluded that new bone volume affects important clinical outcomes.21,22 Also, histological/histomorphometric studies highlighted different cell responses among HA, β-TCP, and HA/β-TCP composite experimental groups. They concluded that HA/β-TCP composite induced more new bone formation than HA or β-TCP alone. Histological evaluation of the herein case report supports these findings, suggesting highly active areas of bone formation/remodeling as the new bone matrix, osteoclasts, osteocytes, and bone-lining cells were evident.23,24
MSFA case report using micro-HA concluded that low-rate biomaterial resorption impaired an effective cell interaction.24 Bone defects evaluation in dogs, using micro-HA, carbonate apatite (CO3Ap) and β-TCP, concluded that CO3Ap induced a higher production of new bone, due to its superior osteoconduction and osteoinduction potential.25 The similar potential of osteoconduction and osteoinduction was demonstrated in studies using the composition of nano-HA (80%) and β-TCP (20%). Histomorphometric/histologic evaluation indicated a higher number of bone cells (Osteocytes, osteoblasts, and osteoclasts), in addition to a higher number of blood vessels and a new bone matrix.26–29
Conclusion
Based on case report outcome and follow-up in addition to histologic/histomorphometric evaluation, it was possible to conclude that nano-HA/β-TCP composite was a suit biomaterial indicated to maxillary sinus floor augmentation. Nano-HA/β-TCP composite provided a favorable nano-environment to bone cells, enhancing bone matrix production.
Funding
This research received financial support from the Brazilian agencies CNPq, FAPERJ, CAPES, LUBT, Fisclinex and UERJ.
Disclosure
The authors report no conflicts of interest in this work.
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