Niobium oxide

Endpoint summary

Link to relevant study record(s)

Reference

Endpoint:

basic toxicokinetics in vitro / ex vivo

Type of information:

experimental study

Adequacy of study:

key study

Study period:

2016-09-29 to 2017-01-17

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

test procedure in accordance with national standard methods

Objective of study:

bioaccessibility (or bioavailability)

Qualifier:

no guideline available

Principles of method if other than guideline:

This report measured bioaccessibility of Niobium(II) oxide in body fluid simulants as a surrogate for bioavailability.

GLP compliance:

no

Radiolabelling:

no

Species:

other: not applicable

Strain:

other: not applicable

Sex:

not specified

Details on test animals or test system and environmental conditions:

not applicable

Route of administration:

other: in vitro study

Vehicle:

other: not applicable

Details on exposure:

Not applicable

Duration and frequency of treatment / exposure:

Not applicable

Dose / conc.:

0.2 other: g/L

Remarks:

Loading (Gastric bio-elution test)

Dose / conc.:

2 other: g/L

Remarks:

Loading (Sweat bio-elution test)

Dose / conc.:

2 other: g/L

Remarks:

Loading (Alveolar bio-elution test)

Dose / conc.:

2 other: g/L

Remarks:

Loading (Lyosomal bio-elution test)

No. of animals per sex per dose / concentration:

Not applicable

Control animals:

other: Not applicable

Positive control reference chemical:

Not applicable

Details on study design:

Please see box "Any other information on materials and method incl. tables"

Details on dosing and sampling:

Not applicable

Statistics:

Not applicable

Preliminary studies:

Not applicable

Details on absorption:

Not applicable

Details on distribution in tissues:

Not applicable

Details on excretion:

Not applicable

Metabolites identified:

not measured

Details on metabolites:

Not applicable

Bioaccessibility (or Bioavailability) testing results:

The results of the bio-elution tests (see tables 1-5 in box "Any other information on results incl. tables") showed a consistent very low metal release in all the arteficial media tested. The highest metal release concentration was found in lysosomal fluid with < 0.2 % after 72 hours of incubation.

Table 1: Summary of Results

Metal release in Gastric test (µg/L)				% Solubility (0.2 g/L loading)
2 h		CV, %		2 h	CV, %
5.13		2		0.0031	2
Metal release in Lyosomal fluid (µg/L)				% Solubility (2 g/L loading)
24 h	CV, %	72 h	CV, %	72 h	CV, %
1348.7	1	3298.1	15	0.198	15
Metal release in Alveolar fluid (µg/L)				% Solubility (2 g/L loading)
24 h	CV,%	72 h	CV, %	72 h	CV, %
251.7	3	1149.4	6	0.069	6
Metal release in Perspiration fluid (µg/L)				% Solubility (2 g/L loading)
24 h	CV, %	168 h	CV, %	168 h	CV, %
399.5	7	689.8	1	0.041	1

Table 2: Results of the Gastric bio-elution test

Gastric test parameters				Niobium, µg/L
	Time [h]	T [° C]	pH	Mean	SD	CV [%]
Blanks	0	37	1.51	BDL	-	-
	2	37	1.51	BDL	-	-
Nb(II)O 80K	0	37	1.51	BDL	-	-
	2	37	1.49	5.13	0.11	2

CV corresponds to the coefficient of variation between vessels. BDL: Below detection limit.

Table 3: Results of the Lyosomal bio-elution test

Lyosomal test parameters				Niobium, µg/L
	Time [h]	T [° C]	pH	Mean	SD	CV [%]
Blanks	0	37	4.45	BDL	-	-
	2	37	4.48	BDL	-	-
	24	37	4.49	BDL	-	-
	72	37	4.52	BDL	-	-
Nb(II)O 80K	0	37	4.45	BDL	-	-
	2	37	4.47	383.6	7	2
	24	37	4.47	1348.7	10.6	1
	72	37	4.47	3298.1	484.2	16

CV corresponds to the coefficient of variation between vessels. BDL: Below detection limit.

Table 4: Results of the Alveolar bio-elution test

Alveolar test parameters				Niobium, µg/L
	Time [h]	T [°C]	pH	Mean	SD	CV [%]
Blanks	0	37	7.39	BDL	-	-
	2	37	7.47	0.7	0.2	22
	24	37	7.37	0.8	0.2	28
	72	37	7.42	0.9	0.2	25
Nb(II)O 80K	0	37	7.39	BDL	-	-
	2	37	7.47	197.1	0.6	0
	24	37	7.44	251.7	7	3
	72	37	7.43	1149.4	66.9	6

CV corresponds to the coefficient of variation between vessels. BDL: Below detection limit. Nb values reported in the Blanks were equal to or below the practical quantitation level for the Alveolar media (PQL = 1.0 μg/L).

Table 5: Results of the Sweat bio-elution test

Alveolar test parameters				Niobium, µg/L
	Time [h]	T [° C]	pH	Mean	SD	CV [%]
Blanks	0	30	6.67	BDL	-	-
	24	30	6.30	BDL	-	-
	168	30	6.07	BDL	-	-
Nb(II)O 80K	0	30	6.67	BDL	-	-
	24	30	6.36	399.5	28	7
	168	30	5.82	689.8	8.75	1

CV corresponds to the coefficient of variation between vessels. BDL: Below detection limit.

Conclusions:

The release of niobium ions from Niobium oxide is very low in artifical body fluids. Based on the results, the bioavailability of Niobium oxide can be considered to be very low for all routes of administration.

Executive summary:

A study to estimate the bioaccessibility of Niobium(II) oxide 80K in different artificial media: gastric juice, lysosomal, alveolar and perspiration fluids; representing ingestion, inhalation and dermal contact routes of exposure in humans, was performed. The rate and extend of the metal released in these in vitro simulations of biological compartments can be used for human health hazard classification of this substance.

The results showed a consistent very low metal release in all the arteficial media tested. The highest niobium release concentration was found in lysosomal fluid with ca. 0.2% after 72 hours of incubation. Metal release (μg/L) and solubility results (percentage) are summarized in the Table below.

Simulated Body Fluid	pH	Extraction Time (h)	µg Nb/L sample	% Nb release
Gastric fluid	1.5	2	5.13	0.0031
Lyosomal fluid	4.5 - 5.0	24	1348.7	-
		72	3298.1	0.198
Alveolar fluid	7.4	24	251.7	-
		72	1149.4	0.069
Perspiration fluid	6.5	24	399.5	-
		168	689.8	0.041

Description of key information

A study to estimate the bioaccessibility of Niobium oxide as a surrogate for bioavailability in different artificial body fluids were conducted. Based on the results, the bioavailability of Niobium oxide can be considered to be very low for all routes of administration.

Key value for chemical safety assessment

Bioaccumulation potential:

low bioaccumulation potential

Additional information

A study to estimate the bioaccessibility of Niobium(II) oxide 80K as a surrogate for bioavailability in different artificial media: gastric juice, lysosomal, alveolar and perspiration fluids; representing ingestion, inhalation and dermal contact routes of exposure in humans, was performed. The rate and extend of the metal released in these in vitro simulations of biological compartments can be used for human health hazard classification of this substance. The results showed that the release of niobium ions is very low, with a maximum release of ca. 0.2% in lysosomal fluid. Based on the results, the bioavailability of Niobium oxide can be considered to be very low for all routes of administration.