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EC number: 231-840-8 | CAS number: 7758-87-4
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Endpoint summary
Administrative data
Link to relevant study record(s)
Description of key information
In the absence of specific data on the ADME of tricalcium bis(orthophosphate) (beta-TCP), its physicochemical properties and relevant toxicity data (where available) were assessed for insights into likely ADME characteristics. Although beta-TCP has a MW > 100 g/mol (310 g/mol) and is slightly soluble in water it is considered that absorption via the oral route is likely to be moderate due to its nature to ionize into phosphate and calcium. Phosphate and calcium are important biological molecules which are tightly regulated systemically as well as intra-cellular. Absorption of beta-TCP itself via inhalation route will be low due to its molecular weight and low solubility. Non-resorbed particles in the oral-nasal cavity, airways and lungs will be transferred to the gastrointestinal tract with the mucus and absorbed there. Therefore, the absorption from the gastrointestinal tract will contribute to the total systemic burden of the substance that is inhaled. Low dermal absorption is expected. Based on a precautionary approach, an absorption default value of 100% is considered appropriate for oral and inhalation route and 50% for the dermal route. Wide tissue distribution of absorbed beta-TCP itself is not expected but the ionic forms of phosphate and calcium are widely distributed due to the indispensable character of phosphate and calcium. The suggested metabolism involves hydrolysis to the more soluble and polar products, calcium and phosphate ions. Due to these factors, urinary excretion as well as via faeces and sweat is the most probable route of elimination and bioaccumulation is unlikely.
Key value for chemical safety assessment
- Bioaccumulation potential:
- no bioaccumulation potential
Additional information
There are no studies available in which the toxicokinetic behaviour of tricalcium bis(orthophosphate) (CAS 7758 -87 -4) has been investigated.
Therefore, in accordance with Annex VIII, Column 1, Section 8.8.1, of Regulation (EC) No 1907/2006 and with Guidance on information requirements and chemical safety assessment Chapter R.7c: Endpoint specific guidance (ECHA, 2014), assessment of the toxicokinetic behaviour of tricalcium bis(orthophosphate) (beta-TCP) is conducted to the extent that can be derived from the relevant available information. This comprises a qualitative assessment of the physicochemical and toxicological properties according to Guidance on information requirements and chemical safety assessment Chapter R.7c: Endpoint specific guidance (ECHA, 2014).
Tricalcium bis(orthophosphate) is a solid at 20°C with a molecular weight of 310 g/mol and a water solubility of 7.7 mg/L.
ABSORPTION
Oral
No specific data regarding oral absorption of tricalcium bis(orthophosphate) (beta-TCP) were found. ECHA guidance suggests that absorption is considered favourable for substances with a molecular weight (MW) below 500 g/mol (ECHA, 2014). The MW (310 g/mol) might be indicative of absorption. For a substance to be absorbed efficiently from the gastrointestinal tract it must be in solution. A recent study report determined the water solubility of beta-TCP to be 7.7 mg/L at neutral conditions whereas at lower pH the water solubility increased dramatically (1079 mg/L at pH4). It could be assumed that beta-TCP dissolves in the gastrointestinal fluids and the substance may (since the MW is below 500 g/mol) pass through aqueous pores or be carried through the epithelial barrier by the bulk passage of water (ECHA, 2014). However, as calcium and phosphate are key elements in various cellular processes their import and export over cell membranes is regulated via pore systems and usually tightly regulated. Hunched posture was the only clinical sign observed in rats following a single oral dose of beta-TCP. This must not be a sign of absorption since this effect can also be a result of discomfort. In the absence of specific data to the contrary, a default value for oral absorption of 100% is suggested.
Dermal
ECHA guidance suggests that absorption is considered favourable for substances with a MW below 100 g/mol (ECHA, 2014). Therefore, the MW (310 g/mol) suggests dermal absorption is not likely. For a compound to penetrate the stratum corneum, it must be sufficiently water soluble i. e. above 1 mg/L (ECHA, 2014). The aqueous solubility of beta-TCP (7.7 mg/L) indicates that dermal absorption will be low to moderate (ECHA, 2014). No logP value could be determined for beta-TCP as it is an inorganic substance, therefore the passive passage across biological membranes will be negligible. In addition, as the test substance is a solid, hindered dermal absorption has to be considered as dry particulates first have to dissolve into the surface moisture of the skin before uptake via the skin is possible (ECHA, 2014). QSAR analysis of beta-TCP suggests a very low dermal absorption rate with an absorption potential of 10%. Due to the slight soluble character of beta-TCP a conservative approach of a moderate skin absorption of 50% is recommended.
Inhalation
According to ECHA (2014) guidance, particles with aerodynamic diameters below 100 µm have the potential to be inhaled.
The granulometry study shows that tricalcium bis(orthophosphate) consists of approximately 98% of particles with a particle size of < 45µm (considered to be respirable). As such the particle size distribution indicates that beta-TCP particles can be inhaled (ECHA, 2014). Besides, the substance is not lipophilic therefore would not have the potential to be absorbed directly across the respiratory tract epithelium. However, its nature as physiological substance will probably lead to some absorption via the respiratory tract. Non-resorbed particles in the oral-nasal cavity, the airways and the lungs will be transferred to the gastrointestinal tract with the mucus and absorbed there. Therefore absorption from the gastrointestinal tract will contribute to the total systemic burden of the substance that is inhaled. On this basis, a default of 100% is proposed.
DISTRIBUTION / METABOLISM
No data were found regarding the distribution and metabolism for beta-TCP. Looking at the physicochemical parameters of beta-TCP (MW=310 g/mol, inorganic, slightly soluble) a wide tissue distribution is not assumed (ECHA, 2014). But the structure suggests beta-TCP will slowly ionise to phosphate anions and calcium species. Phosphate is dissolved as ions in blood. Calcium is partly dissolved as an ion while about 50% is bound to albumin in blood. As both ions are indispensable to life their distribution is tightly regulated systemically as well as intra-cellular. Both ions are inorganic and stable to reduction or oxidation in biological systems. Phosphate is condensed to di and triphosphates (e. g. AMP, ADT, ATP). Calcium is complexed to important biological molecules (e. g. Ca: calmodulin, calbindin, etc.).
EXCRETION
Assuming homeostasis of these indispensable nutrients the same amount is excreted as taken up. Calcium and phosphate are generally excreted mainly via kidneys but also via faeces and sweat (varying for the specific ion).
References:
ECHA (2014). Guidance on information requirements and chemical safety assessment. Chapter R.7c: Endpoint specific guidance. Version 2.0, November 2014.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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