Aluminum and bone: Review of new clinical circumstances associated with Al(3+) deposition in the calcified matrix of bone

Several decades ago, aluminum encephalopathy associated with osteomalacia has been recognized as the major complication of chronic renal failure in dialyzed patients. Removal of aluminum from the dialysate has led to a disappearance of the disease. However, aluminum deposit occurs in the hydroxyapatite of the bone matrix in some clinical circumstances that are presented in this review. We have encountered aluminum in bone in patients with an increased intestinal permeability (coeliac disease), or in the case of prolonged administration of aluminum anti-acid drugs. A colocalisation of aluminum with iron was also noted in cases of hemochromatosis and sickle cell anemia. Aluminium was also identified in a series of patients with exostosis, a frequent benign bone tumor. Corrosion of prosthetic implants composed of grade V titanium (TA6V is an alloy containing 6% aluminum and 4% vanadium) was also observed in a series of hip or knee revisions. Aluminum can be identified in undecalcified bone matrix stained by solochrome azurine, a highly specific stain allowing the detection of 0.03 atomic %. Colocalization of aluminum and iron does not seem to be the fruit of chance but the cellular and molecular mechanisms are still poorly understood. Histochemistry is superior to spectroscopic analyses (EDS and WDS in scanning electron microscopy).

deposit occurs in the hydroxyapatite of the bone matrix in some clinical circumstances that are presented in this review.We have encountered aluminum in bone in patients with an increased intestinal permeability (coeliac disease), or in the case of prolonged administration of aluminum anti-acid drugs.A colocalisation of aluminum with iron was also noted in cases of hemochromatosis and sickle cell anemia.Aluminium was also identified in a series of patients with exostosis, a frequent benign bone tumor.Corrosion of prosthetic implants composed of grade V titanium (TA6V is an alloy containing 6% aluminum and 4% vanadium) was also observed in a series of hip or knee revisions.Aluminum can be identified in undecalcified bone matrix stained by solochrome azurine, a highly specific stain allowing the detection of 0.03 atomic %.Colocalization of aluminum and iron does not seem to be the fruit of chance but the cellular and molecular mechanisms are still poorly understood.Histochemistry is superior to spectroscopic analyses (EDS and WDS in scanning electron microscopy).

Introduction
Bone matrix is composed of two phases: • an organic phase is elaborated by osteoblasts and is mainly composed of type I collagen microfibrils and noncollagenous proteins; • a mineral phase which is composed of numerous hydroxyapatite crystals (HA) deposited between the collagen microfibrils (Fig. 1).
The formula for biological HA is Ca 10 (PO 4 ) 6 (OH) 2 .In mature bone, nucleation of the HA crystals seems to be due to non-collagenous proteins such as the bone sialoprotein (BSP) deposited at the mineralization front 3− , is the site for ionic substitutions.Projection sur le plan (001) de la structure cristallographique de l'hydroxyapatite montrant la localisation des petits et grands tunnels.Le grand tunnel, centré sur un groupe -OHest entouré par des PO 4 3− , il s'agit du site possible pour les substitutions anioniques.[1].Alkaline phosphatase, elaborated and secreted by osteoblasts in the osteoid tissue (seams of recently synthetized organic bone matrix) allows the development of the mature HA crystals from the crystal nuclei.The enzyme substrates are pyridoxal phosphate, ATP, ADP, AMP, glucose-1-AMPc, glucose-6-phosphate, pyrophosphate and phosphor-ethanolamin present in the extracellular fluids [2].Alkaline phosphatase also acts as a phosphate transporter to the mineralization front, allowing the accretion of phosphates on the calcium atoms of the HA crystal.
From a crystallographic point of view, the arrangement of Ca 2+ , PO 4 3− and OH − groups in the crystal can be modeled as in Fig. 2 [3].In this atomic lattice, two channels can be described: a small one (0.25 nm in diameter) and a large one (0.3-0.45 nm in diameter).In this large channel, a number of atom substitutions are possible.Hydroxide groups, for example, can be substituted by anions such as F; phosphate can be substituted by other anions (e.g.carbonate) and calcium can be replaced by metallic cations such as Fe 3+ , Sr 2+ , Pb 2+  . . .The non-exhaustive list of these substitutions appears on Table 1 [3].Some of these substitutions (F − and Sr 2+ ) have been proposed in therapeutic for the treatment of osteoporosis (these drugs are non-longer used in clinical practice).It should be noted that any substitution changes the crystal properties (e.g.F-increases acid resistance of HA to hydrolysis) with a consequence at the tissue level on the bone quality.
Histochemistry is a powerful tool to characterize mineralization of the bone matrix and to identify the presence of certain metal ions abnormally present in HA where they can alter bone quality.The Perls' staining is a worldwide admitted histochemical stain for iron.The method works on soft and hard tissues.In the presence of ferrocyanide ions, Fe 3+ (but not Fe 2+ ) is precipitated as a highly waterinsoluble blue complex also termed Prussian blue.In bone, it Lacuna Lacuna is preferable to avoid the use a counterstain dye if one wants to clearly identify the iron bands in the bone matrix [4][5][6][7].Fe 3+ is deposited in the cement or arrest lines when a BSU is formed, either in cortical and/or trabecular bone.These lines are known to contain specific proteins (osteopontin and osteocalcin) that can bind metal ions.Decalcification of bone sections abolishes the staining because Fe 3+ is bound to the HA crystals.It has been shown by a very sensitive method (micro X-ray fluorescence analysis with a synchrotron) that Zn and Pb ions which are also present in the interstitial fluid can accumulate in the cement lines by uptake in the HA crystal and attachment to these proteins [8].Histochemical identification of aluminum in bone was extensively studied in patients with renal failure who developed encephalopathy and osteomalacia (see below).The different methods only work on undecalcified bone sections [9].Aluminum can be stained by the aluminon technique using aurine tricarboxylic stain [4,10].The method was found more sensitive than atomic absorption spectrometry [11].Several authors have reported that the regressive staining with solochrome azurine B (also termed Mordant blue B or chrome azurol B -CI 43830) [12] gives better results and identifies more bands in the bone matrix [13][14][15][16].We have found that spectroscopic methods such as scanning electron microscopy (SEM) coupled with X-ray energy dispersive spectroscopy (EDS) cannot identify aluminum and iron on bone samples due to the low concentration of these metals in the HA crystals.The limit of detection of EDS is 0.05% (atomic %) [17,18].We have identified these metals by wavelength dispersive spectroscopy (WDS), coupled with SEM, and the local concentrations of these metals is in the range of 0.03-0.035%at a maximum [19].However, this method does not allow mapping images of the tissues.

In vitro models of calcification
A number of models have been described to mimic in vitro the calcification of the bone matrix.We have developed a synthetic polymer (poly (2-hydroxyethyl)

Microscopie électronique à balayage de calcosphérites développés sur un polymère fonctionnalisé avec des groupements -COOH. A) Les calcosphérites sont présents à la surface du matériau et se développent par nucléation successive dans le liquide biologique. B) Croissance des calcosphérites en présence de fer à l'intérieur du milieu de culture. La présence du fer réduit considérablement leur taille. C) Absence de développement de calcosphérites lorsque des ions aluminium sont ajoutés dans le milieu de culture. La surface du polymère, avec quelques traces calcifiées, est bien visible. D) Analyse EDS des calcosphérites présents sur la Fig. B : notez la présence d'un petit pic de fer dans l'hydroxyapatite composée de calcium et phosphate stabilisé par du magnésium. E) Analyse EDS des calcosphérites présents sur la Fig. C : la présence d'aluminium est aussi mise en évidence lorsque la concentration est supérieure à 0,05 % des atomes.
methacrylate-pHEMA) which can be chemically modified by carboxymethylation.Carboxymethylated pHEMA reproduces the structure of acid proteins of the bone matrix known to induce mineralization (e.g.BSP) [20].When placed in a synthetic body fluid having the same ionic composition than the extracellular fluids, pellets made of this polymer induce mineralization.Calcified globules made of HA develop on the polymer surface within 15 days (Fig. 3A).These mineralized globules are similar in size and composition to the calcospherites described in the cartilaginous growth plate of long bones.Calcospherites are also observed in the woven bone of rapidly forming bones (callus, metaplasia. ..).The carboxymethylated pHEMA model has been used to evaluate the effects of drugs known to interfere with calcification [21] and also metal ions which can be dissolved in the body fluid.Fe 3+ ions at the concentration of 20, 40 or 60 M/L reduce the size of the calcospherites (Fig. 3B) [22].SEM-EDS identified iron in the calcospherites at very low amount (> 0.05 atomic %) (Fig. 3D).Cobalt, nickel and chromium (these metals present in stainless-steel orthopedic prostheses) can also modify the size of calcospherites [23].Strontium has also an effect on the calcospherites in a dose dependent manner.However, Sr 2+ can be progressively eluted from the crystals [24].
We have recently investigated the influence of aluminum in this model [25].Aluminum chloride was added in the body fluid at the concentration of 20, 40, and 60 g/L Al 3+ .Aluminum strongly reduced the growth of calcospherites

A) Ostéomalacie chez un patient dialysé pour une insuffisance rénale chronique. Trichrome de Goldner : la matrice osseuse minéralisée est en vert, le tissu ostéoïde en rouge sur des coupes non décalcifiées. B) Identification histochimique de l'aluminium par la coloration au solochrome azurine. Al 3+ apparaît sous forme de bandes bleues, l'os est très légèrement coloré en orange. Notez la quantité considérable de tissu ostéoïde et l'épaisseur des bordures ostéoïdes indiquant un trouble de minéralisation.
(and the highest concentration has completely inhibited their formation) (Fig. 3D).SEM-EDS identified Al 3+ in the HA calcospherites (Fig. 3E).Furthermore, other pellets were incubated with pieces of aluminum foil and, here again, a strong inhibition of the calcospherite formation was observed.This indicates that Al 3+ can be released from aluminum foils by oxidation in the body fluid.

Bone, aluminum and kidney
During the 1970s, a series of patients with renal insufficiency, who were dialyzed, developed the dialysis encephalopathy associated with osteomalacia (a mineralization defect characterized by an accumulation of osteoid tissue) (Fig. 4A) [26,27].Encephalopathy was related to the aluminum content in the dialysate because water, at the time, was purified by alumina gels in the water treatment plants.Dialysis patients had an additional cause of aluminum intoxication: they were treated by aluminum hydroxide as a countermeasure for hyperphosphatemia.In the bone from patients with dialysis osteomalacia, the presence of aluminum was identified as linear bands by histochemical methods; this reflects the deposition of Al 3+ along the calcification front and cement lines within the calcified bone matrix (Fig. 4B) [9,11].In dialyzed patients, iron and fluoride were also identified by several authors but the consensus was that aluminum had the most deleterious effects on bone mineralization [28].Aluminum was also found to interfere

Bone, aluminum and biomaterials
Several reports have stressed the importance of aluminum released by biomaterials as a toxic for bone.A ceramic coating of prosthetic stems has been proposed to favor osseointegration.HA and alumina coatings were widely used in the 1990s.However, alumina-coated prostheses were associated with a juxta prosthetic mineralization defect (similar to the dialysis osteomalacia) due to an accumulation of Al 3+ in the anchoring bone.A direct release of Al 3+ from the coating was found after histochemical staining (Fig. 5) [32,33].A bone cement containing aluminum fluorosilicate was used in oto-surgery and caused several lethal cases of aluminum encephalopathy [34].
Biomaterials are now widely used in biomedicine and their applications are numerous: heart valves, artificial heart, dental and orthopedic implants, tracheal and vascular prostheses. . .More than half of biomaterials produced by industry are used in an intra-osseous site (cement, synthetic bone filling material or prosthesis).Biomaterials are inert objects placed in direct contact with the biological fluids.They can attack the surface of metallic biomaterials as they contain numerous anions (Cl − , PO . ..), cations (Mg 2+ , Na + , Ca 2+ , Fe 3+ . ..), dissolved oxygen and free radical oxygen species.This liquid microenvironment appears to have an oxidizing power equal to 1/3 this of the ocean water and ¼ this of the air [35].In addition, the body temperature increases the oxidizing capacity and local pH variations are frequent [36].Corrosion of metallic biomaterials can occur in different types of conditions: at the metal joint grains (as metals are polycristalline), by
We have recently reported a series of 32 patients with a revision for a total reconstruction after aseptic loosening of an alumina-on-alumina hip prosthesis [37].This type of prosthesis is known to have the best friction torque [38,39].In these patients, the periprosthetic tissues were analyzed in the search of alumina debris.In 14 patients, a small fragment of periprosthetic bone was also analyzed after undecalcified embedding.Sections were obtained on a heavy duty microtome and stained by a Goldner's trichrome (for the identification of osteoid tissue and mineralized phase), solochrome azurine staining (for identification of Al 3+ ) and Perls' staining.Alumina grains were never encountered in the soft tissues.Metal particles were present in 3 patients and SEM-EDS revealed that they were composed of the TA6V titanium alloy containing 6% aluminum and 4% vanadium.TA6V (or grade V titanium ASTM) is the metal used in orthopedics for prostheses, screws, cups. ..).Histochemical analysis revealed that the Fe 3+ was not present in the bone matrix but aluminum bands were observed for each patient.In a control series of 8 patients having received a prosthesis without alumina (e.g., metal-on-polyethylene or metal-on-metal), the same methodology of analysis was used.Al 3+ was also identified in the bone matrix from these patients as linear bands in the vicinity of the prosthesis or the metal wear debris (Fig. 6A-B).It is likely that Al 3+ comes from oxidation of the metallic parts of the prosthesis (stem, cup, screw) and an origin from the alumina cannot be excluded.However, the long term tolerance of the alumina-on-alumina prostheses, and the fact that the amount of aluminum bands in the bone matrix were similar in the other group, is a plea for an oxidation of the TA6V rather than a ionic decomposition of this very stable alumina [40].The Al 3+ ion release from alumina-on-alumina and metal-on-metal total hip prostheses was dosed in the serum from a series of patients and the Al 3+ content was not different between the two groups and with a control group without prosthesis [41].
Presence of aluminum in the bone matrix is also common in orthopedic samples obtained after ablation of titanium material.Fig. 6C-D illustrates the release of aluminum from a threaded screw in a femoral head placed more than ten years before for treating a hip fracture.The material was changed during revision for a total hip arthroplasty.In such cases, the continuous release of aluminum from the metallic biomaterial is proven by the deposition of numerous repetitive bands mimicking the growth lines on a tree trunk.In a compilation study, the release of metal ions was confirmed in the body fluids of patients with metallic biomaterials by various techniques including Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and graphite furnace atomic absorption spectrometry (GF-AAS) [42].Although titanium is protected by a film of titanium oxides, the TA6V-based devices can release aluminum after prolonged implantation [43].This will certainly be observed in the next future in dental implantology.Classically, dental implants were prepared with c.p. grade II titanium.It is more ductile than the TA6V alloy (grade V), which contains aluminum and vanadium.Some industrial companies have recently proposed TA6V implants on the market, especially short implants to be used in areas with a low bone mass.Titanium can be easily oxidized and altered in mouth by the action of numerous oxidants (fluoride containing toothpastes, reactive oxygen species from polymorphonucleated cells and bacteria, or organic acids of the saliva) [44].The release of aluminum from TA6V dental implants could represent a sanitary problem in the next decade.

Bone, aluminum and diseases associated with iron metabolism
Genetic hemochromatosis (GH) is an autosomal recessive disease responsible for an iron overload.The most frequent form is due to a mutation of the HFE gene.In these patients, osteopenia and osteoporosis are frequent (28-50% of patients), together with the liver disease which is the more severe factor [45].A positive iron staining is reported in the bone matrix of these patients and appears to form linear bands.Surprisingly, aluminum can also be detected as linear bands in the same areas in some patients (Fig. 7).
Fe 3+ is also identified by histochemistry in the bone matrix of patients with other iron-related diseases such as ␤thalassemia and sickle cell anemia [46,47].The mechanisms of the Fe 3+ localization in bone are not clearly understood but the role of metal transporter proteins (such as ferroportin) has been recently reviewed [48].In two patients with sickle cell anemia, a colocalization of Al 3+ with Fe 3+ in bone was observed in our laboratory.

Bone, aluminum and digestive diseases
Aluminum is absorbed by the gut as evidenced by a number of papers in the rat [49,50].It is also absorbed in humans as shown in patients receiving phosphate binders in dialysis patients [51].Aluminum absorption from the gut leads to a bone deposition, even in the presence of a normal kidney function.Al 3+ absorption was increased in a patient with a peptic ulcer and a long-term history of gastroprotection [52].We reported a patient with a celiac disease who was using oral medications containing aluminum.She developed osteoporosis with very low bone mineral density values (T score = −6.18 at the lumbar spine).Al 3+ was identified by solochrome azurine staining in a transiliac bone biopsy [53].We also observed similar findings in a patient with low bone mineral density (T score = −3.56 at the lumbar spine) and fractures of the os ilium.The patient had also a long history of dyspepsia and was using aluminum-containing gastroprotectors for decades; here again, Al 3+ was identified in the bone biopsy.Parenteral nutrition is also associated with an increased aluminum absorption (released from nutrition solutions containing contaminated casein, from glass vials. ..)Aluminum has also been identified as a possible environmental causal factor in Crohn's disease [55].Aluminum enhances colic inflammation in mice [56].Lessons from the past (dialysis patients) and from animal studies indicate that chronic accumulation of aluminum in the bone is likely to occur in patients with inflammatory diseases of the digestive tract.Although these inflammatory bowel diseases are known to induce osteoporosis by themselves [57], it is most probable that aluminum deposition in the bone matrix contributes to the bone loss.However, this remains to be proven by bone biopsy studies.

Calcified bone in exostosis
Exostosis is the most frequent benign tumor in children and adults.Isolated exostosis is frequent but multiple exostoses are observed in several types of Multiple Hereditary Exostosis (MHE).MHE is an autosomal genetic disease due to mutation in the Golgi-associated heparin sulfate polymerases (EXT1, EXT2 or EXT3) [58].Although the pathogenesis of isolated and MHE are not fully understood, these tumors share common characteristics: they are covered by a cape of proliferation cartilage, they possess a shell of cortical bone which surround a more or less developed network of trabecular bone containing bone marrow.We have recently reported a series of thirty patients with either isolated or multiple exostosis (three cases of MHE) [19].Histological analysis of the undecalcified tumor revealed the presence of aluminum in the bone matrix of the tumor in 2/3 of patients.Surprisingly, iron was also deposited in the same areas in 1/3 of the patients (Fig. 8).Because a dysregulation of the osteoprogenitor cell has been described in this disease, it is most probable that metabolic changes in the osteoblast function are responsible for the abnormal deposition of these two metals.

The origin of aluminum in bone
It is now well recognized that aluminum enters in the body from different sources.As mentioned above, aluminum is present in foods and beverages (the additive E173 is aluminum oxide) but other routes of penetration in the body have been identified: trans or percutaneous absorption (from vaccines and anti-sweating or antiperspirant products, e.g.alum stone) and locally released from metallic biomaterials.In the body, 95% of ingested aluminum is eliminated in the feces and the 5% remaining circulate in the blood mainly bound to transferrin and albumin (Fig. 9 summarizes the aluminum metabolism in the body).The circulating aluminum can mainly be fixed in two preferential organs: brain and bone.The metal is recognized as a neurotoxic in Alzheimer and Parkinson diseases where it can also colocalize with iron.In bone, aluminum is a cause of bone loss in laboratory animals and humans and high doses cause osteomalacia.Finally, there are a number of strange coincidences concerning the metabolism of these two metals in the body: same transporters, cytotoxic activity, impairment of osteoblastic activity at low dose, inhibition of bone mineralization at high doses.

Conclusion
Aluminum can bind to the phosphate groups of HA of the calcified bone matrix.Histochemical methods are by far superior to spectroscopic methods (EDS and WDS) because aluminum and iron are identified in the same location of the bone matrix.Although the pathophysiological mechanisms are not fully understood at the cellular and molecular levels, colocalization of aluminum and iron is certainly not the fruit of chance and much effort is still needed to improve our knowledge on the toxic activity of metals.

Figure 1
Figure 1Transmission electron microscopy of the bone matrix.A) Undecalcified ultrathin section showing the mineral phase composed of hydroxyapatite crystals in the form of tablets.B) After decalcification, the organic phase composed of collagen microfibrils is clearly unmasked.Microscopie électronique à transmission de la matrice osseuse.A) coupe ultra fine non décalcifiée montrant la phase minérale constituée de cristaux d'hydroxyapatite présents sous forme de tablettes.B) Après décalcification, la phase organique composée de microfibrilles de collagène est clairement démasquée.

Figure 2
Figure 2Projection on the plane (001) of the crystallographic structure of hydroxyapatite with the localization of the small and large channels.The large channel, centered on an OH − group and outlined by PO 4 3− , is the site for ionic substitutions.Projection sur le plan (001) de la structure cristallographique de l'hydroxyapatite montrant la localisation des petits et grands tunnels.Le grand tunnel, centré sur un groupe -OHest entouré par des PO4 3− , il s'agit du site possible pour les substitutions anioniques.

Figure 3
Figure 3 Scanning electron microscopy of calcospherites developed on a polymer.A) Control calcospherites composed of HA tablets developed in a standard body fluid.B) Calcospherites developed in the presence of iron in the body fluid; note the reduced size indicating an interaction with mineralization.C) Surface of the polymer incubated in the presence of Al 3+ ; there is an almost complete inhibition of the calcospherites growth.D) EDS analysis of the calcospherites in B indicating the presence of traces of iron in HA composed of calcium/phosphate stabilized with magnesium.E) EDS analysis of the mineral developed in C indicating the presence of trace of aluminum together with calcium, phosphate and magnesium.Microscopie électronique à balayage de calcosphérites développés sur un polymère fonctionnalisé avec des groupements -COOH.A) Les calcosphérites sont présents à la surface du matériau et se développent par nucléation successive dans le liquide biologique.B) Croissance des calcosphérites en présence de fer à l'intérieur du milieu de culture.La présence du fer réduit considérablement leur taille.C) Absence de développement de calcosphérites lorsque des ions aluminium sont ajoutés dans le milieu de culture.La surface du polymère, avec quelques traces calcifiées, est bien visible.D) Analyse EDS des calcosphérites présents sur la Fig. B : notez la présence d'un petit pic de fer dans l'hydroxyapatite composée de calcium et phosphate stabilisé par du magnésium.E) Analyse EDS des calcosphérites présents sur la Fig. C : la présence d'aluminium est aussi mise en évidence lorsque la concentration est supérieure à 0,05 % des atomes.

Figure 4 A
Figure 4 A) Osteomalacia in a patient with dialyzed renal insufficiency.Goldner's trichrome identifies mineralized bone matrix in green and osteoid tissue in red; undecalcified section.Note the considerable amount of osteoid tissue and the thickness of osteoid seams indicating a mineralization defect.B) Histochemical identification of aluminum by the solochrome azurine method.Al 3+ is in blue, bone is faintly stained in orange.A) Ostéomalacie chez un patient dialysé pour une insuffisance rénale chronique.Trichrome de Goldner : la matrice osseuse minéralisée est en vert, le tissu ostéoïde en rouge sur des coupes non décalcifiées.B) Identification histochimique de l'aluminium par la coloration au solochrome azurine.Al 3+ apparaît sous forme de bandes bleues, l'os est très légèrement coloré en orange.Notez la quantité considérable de tissu ostéoïde et l'épaisseur des bordures ostéoïdes indiquant un trouble de minéralisation.

Figure 5 A
Figure 5 A) A threaded hip prosthesis covered by a thick coating of alumina deposed by a plasma torch (arrows).Thick and polished section after undecalcified embedding; the metal is in black.B) Histochemical identification of aluminum by the solochrome azurine method in another patient who had the same type of prosthesis.The metallic part has been removed before embedding and sectioning at a 7 m thickness.Al 3+ is in blue, the calcified bone matrix in orange and non-mineralized bone is unstained (arrow) and forms a thick layer facing the prosthesis, indicating a localized mineralization defect.A) Prothèse de hanche filetée recouverte par un épais dépôt d'alumine déposé par torche à plasma (flèches) ; tranche épaisse et polie sans décalcification.Le métal apparaît en noir.B) Identification histochimique de l'aluminium par la technique au solochrome azurine.La partie métallique a été enlevée avant inclusion pour réaliser des coupes de 7 m d'épaisseur.Al 3+ est en bleu, la matrice calcifiée en orange et l'os non minéralisé est incolore (flèche) indiquant un défaut local de minéralisation.

Figure 6 A
Figure 6 A) Bone harvested in the vicinity of a TA6V hip prosthesis replaced during a hip prosthesis revision.Arrows identify black metallic debris in the marrow contained in the Haversian canals.Goldner's trichrome, undecalcified bone.B) Section from the same patient, metallic wear debris composed of TA6V are evidenced (arrow).Blue bands of aluminum are present in the calcified bone matrix of the Haversian canal surrounding the metal particles.Solochrome azurine staining.C) Bone harvested from the femoral head of a patient treated by a threaded screw for a hip fracture several years ago.Fibrosis has developed inside the threads (the metal has been removed).Goldner's trichrome, undecalcified section.D) Section from the same patient stained with solochrome azurine.Aluminum are visible as blue bands in the bone facing the screw.The soft tissues (which do not contain calcium phosphate) are unstained.A) Tissu osseux prélevé au voisinage d'une prothèse en TA6V utilisée pour le traitement d'une fracture de hanche.La vis a été laissée en place pendant de nombreuses années.Les flèches identifient des débris métalliques dans les canaux de Havers.Trichrome de Goldner, coupe non décalcifiée.B) Coupe voisine obtenue chez le même patient ; les débris métalliques sont constitués de particules d'usure du TA6V (flèche).Des bandes bleues (aluminium) sont présentes dans la matrice osseuse calcifiée, des canaux de Havers autour des particules métalliques ; coloration au solochrome azurine.C) Fragment de tête fémorale d'un patient traité par une vis filetée pour une fracture du col fémoral survenue de nombreuses années auparavant.Une fibrose s'est développée à l'intérieur du filetage (le métal a été enlevé avant l'inclusion).Coloration de Goldner, coupe non décalcifiée.D) Coupe adjacente provenant du même patient et colorée par le solochrome azurine.Des dépôts d'aluminium sont visibles sous forme de bandesbleues dans le tissu osseux en face de la vis.Les tissus mous (ne contenant pas de phosphate de calcium) sont incolores.

Figure 7 A
Figure 7 A) Genetic hemochromatosis with osteoporosis.Perl's staining identifies numerous bands of ion deposited in the bone matrix.B) Histochemical detection of aluminum by solochrome azurine in the same patient.C) Histochemical detection of aluminum in a case of sickle cell anemia.D) Histochemical detection of iron (Perl's staining) in the same patient.Note the blue lines (arrows) indicating the presence of iron in the bone matrix (unstained) and the presence of numerous siderophages containing iron in the bone marrow (blue spots).A) Hémochromatose génétique avec ostéoporose.Coloration de Perl's identifiant de nombreuses bandes de fer dans la matrice osseuse.B) Détection histochimique de l'aluminium par le solochrome azurine chez le même patient.C) Détection histochimique de l'aluminium dans un cas de drépanocytose.D) Détection histochimique du fer (coloration de Perls) chez le même patient.Notez la présence de lignes bleues (flèches) indiquant la présence de fer dans la matrice osseuse non colorée et la présence de nombreux sidérophages intramédullaires contenant du fer (tâches bleues).

Table 1
4on-exhaustive list of cationic (for Ca 2+ ) and anionic substitutions (for PO43− and OH − ).The carbonate substitution of a phosphate is called ␣ substitution, and for a hydroxide, a ␤ substitution.␤ substitution increases in the human bone matrix during ageing.