Speciation of Organotin Compounds in Biological Tissues by GC/ICP-MS Using the NexION 350D

APPLICATION NOTE
GC/ICP - MS
GC/ICP-MS
Authors:
Joaudimir Castro, Emmanuel Tessier,
Kenneth Neubauer* and Olivier
F.X. Donard
Laboratoire de Chimie Analytique
Bio-inorganique et Environnement
IPREM UMR 5254 CNRS
Université de Pau et des Pays de l’Adour,
Hélioparc, 64053 Pau, France
*PerkinElmer, Inc.
710 Bridgeport Avenue
Shelton, CT
Speciation of Organotin
Compounds in Biological
Tissues by GC/ICP-MS Using
the NexION 300D/350D
Introduction
The environmental concerns regarding
organotin compounds are of great
importance due to their extensive use
for agricultural, industrial and domestic applications.1 Butyl- and phenyl-tins
have been widely used as active biocides in applications such as antifouling
paints, PVC stabilizers, timber treatment, and others.2 For example, the use
of antifouling paints resulted in extensive damage to non-target organisms
at ultratrace concentration levels (ppt) and accumulation in sediments and
biota.3-4 As a result, the European Union (EU) added tributyl tin (TBT) and its
degradation products to the list of priority pollutants (Decision 2455/2001/EC
amending the Water Framework Directive 2000/60/EC).4 The U.S. Environmental
Protection Agency (EPA) established the ambient aquatic-life water quality
criteria for TBT in which the criterion to protect marine aquatic life from
chronic toxic effects is 3 ng Sn/L and from acute toxic effects 172 ng Sn/L.4 The
different toxicity levels between TBT, triphenyl tin (TPhT) and their degradation
products (di- and monosubstituted and inorganic tin,) as well as the monitoring
of their environmental impact, makes organotin speciation analysis necessary.5
Nowadays, the method of choice for trace organometals analysis is gas
chromatography coupled with inductively coupled plasma mass spectrometry
(GC/ICP-MS) due to its high sensitivity, selectivity, multielemental
and multiisotopic capabilities.3 To carry out organotin speciation via
GC/ICP-MS, a derivatization reaction with sodium tetrapropylborate or
sodium tetraethylborate is necessary to increase the volatility of the species.
In addition, for the analysis of complex matrices, such as biological tissues
and sediments, a soft extraction step is required prior to
the derivatization of the organotins in order to preserve the
original species of the analytes. Open focused microwave
extraction is the most popular extraction procedure because
it is fast and efficient.3 The work presented here encompasses
the GC/ICP-MS (Clarus® GC and NexION® ICP-MS) speciation
analysis of organotins, more specifically, mono-, di-, and tributyl-tin species in biological samples via external calibration.
Special attention is given to the optimization of the GC
transfer line parameters, which allows the coupling of the GC
and ICP-MS.
Experimental Conditions
Reagents and Chemicals
Stock solutions of monomethyltin trichloride (MMT, 97%),
dimethyltin dichloride (DMT, 97%), trimethyltin chloride
(TMT, 97%), monobutyltin trichloride (MBT, 95%), dibutyltin
dichloride (DBT, 97%), and tributyltin chloride (TBT, 96%)
were purchased from Sigma-Aldrich™ and prepared in
glacial acetic acid (HAc) (GFS Chemicals). Sodium
tetrapropylborate (NaBPr4) (Merseburger Spezialchemikalien,
Germany) was used for derivatization. The buffer solution
(0.1M, pH 4.9) used during the derivatization was prepared
by dissolving sodium acetate and glacial acetic acid (HAc) in
MQ water. HPLC-grade isooctane and Optima-grade
methanol (MeOH) were obtained from Thermo
Fisher Scientific™. High-purity ammonium
hydroxide (NH4OH), nitric acid (HNO3),
hydrochloric acid (HCl) and
tetramethylammonium hydroxide (TMAH; 25%)
were obtained from GFS Chemicals. Reference
material CRM 477 Mussel Tissue, obtained from
the Institute for Reference Materials and
Measurements (IRMM; Geel, Belgium), and an oyster tissue
sample from the Arcachon Bay in France were evaluated in
this experiment.
Instrumentation
Chromatographic analysis was performed using a
PerkinElmer® Clarus 580 Gas Chromatograph coupled to
a NexION 300D ICP Mass Spectrometer detector by means
of a PerkinElmer GC/ICP-MS transfer line (Figure 1).
The Silcosteel® tube transfer line, equipped with an
inner deactivated capillary column, was inserted into the
quartz torch and injector. Optimization of the operational
parameters (i.e. distance of the inner deactivated capillary
column, Ar makeup and oxygen (O2) flow rates) necessary
to work under this dry plasma configuration were evaluated.
An SP-D Discover focused microwave system (CEM
Corporation, Matthews, North Carolina, USA) was used
for the extraction of the organotins from the matrices.
The operating conditions are listed in Table 1.
Data collection and analysis was accomplished using
NexION ICP-MS and Chromera® CDS software.
Figure 1. Clarus 580 GC (right) connected to NexION 300D ICP-MS (left) via GC transfer line.
Table 1. GC/ICP-MS operating conditions.
GC Parameters (Clarus 580)
Conditions
Column:
Elite-5MS (5%Diphenyl-dimethylpolysiloxane)
(30 m, id 0.25 mm, d.f. 0.25 µm)
Injection port:
Splitless
Injection port temperature:
250 °C
Injection volume:
1.0 µL
He carrier gas flow (mL/min):
2.0
Transfer line temperature:
300 °C
Transfer line capillary:
Elite - Siltek deactivated fused-silica (id 0.25 mm)
Transfer line capillary position:
7 cm back from tip of Silcosteel® tube
50 °C → ramp 10 °C/min → 100 °C → ramp 45 °C/min → 290 °C (3 min)
Oven program:
2
ICP-MS Parameters (NexION 300)
Conditions
RF power:
1600 W
Nebulizer flow rate:
0.90 L/min
Auxiliary gas flow rate:
1.2 L/min
Plasma gas flow rate:
15 L/min
Oxygen gas flow rate:
0.025 L/min
Injector diameter:
1.2 mm i.d.
Isotope/dwell times:
Sn: 118, 119, 120 (30 ms)
N: 15 (30 ms)
Sample Preparation
The sample preparation, microwave extraction and
derivatization procedures were presented previously in the
literature.3-4 Stock solutions (1000 µg/mL) of the methylated
and butylated tin solutions were prepared in concentrated
HAc. Working solutions were prepared fresh daily in 1% HCl
by appropriate dilution of the stock solutions and stored in
the refrigerator. Calibration curves were generated by
triplicate injections of the standards solutions. For the
derivatization procedure, the acetate buffer solution (0.1 M,
pH 4.9) was prepared by weighing approximately 4.4 g of
sodium acetate and 1.0 mL of HAc and dissolving with MQ
water to make 500 mL. In addition, 2.5% NaBPr4 solution of
the derivatizing agent was prepared in MQ water and stored
in the dark.
It is very important to work under clean conditions for
successful analysis at low concentrations. The containers
were washed with detergent, followed by successive HNO3
and HCl baths (10% v:v in MQ water) with MQ water rinses
between steps. Once the cleaning procedure was finished,
the containers were dried under a laminar flow hood and
stored until use.
Table 2. Optimized microwave extraction conditions
CEM Microwave (SP-D Discover) Conditions
Power:
75 W
Ramp time: 1.0 min
Temperature:
70 ˚C
Hold time:
4.0 min
Microwave Extraction
For the microwave extraction of the organotin compounds
from the mussel and oyster tissue, 0.15 g of dry sample was
added to separate 10 mL extraction vials. Then, 4 mL of
25% TMAH was added to the biological tissues. A small
magnetic stir bar was added to each vial in order to fully
homogenize the resulting slurry during the extraction
process. After microwave digestion, the samples were
centrifuged (if necessary), and the supernatants transferred
to clean vials and stored in the refrigerator until analysis.
The operational conditions of the microwave program used
are listed in Table 2.
Derivatization Procedure
The derivatization step was performed in 20 mL glass vials.
First, 5 mL of the acetate buffer solution was added to 20,
50, 100 and 200 µL of a 5 ng/mL working standard solution
containing the organotin species; the pH of each solution
was then adjusted to 5.0 using HCl or NH4OH, if necessary.
Next, 1 mL isooctane and 250 µL of 2.5% NaBPr4 was added
and the vial capped and manually shaken for 5 minutes. The
organic phase was then transferred to a GC vial for analysis.
Three blank solutions were prepared in the same manner
for detection limit determination and to characterize any
contamination likely to occur during the preparation step. In
the case of the biological tissue, 5 mL of the buffer solution
was added to 30 and 300 µL of the mussel tissue and oyster
tissue extract, respectively, and the pH of each solution was
adjusted to 5.0 using HCl or NH4OH. Then, 1 mL isooctane
and 500 µL of 2.5% NaBPr4 were added, the vial capped
and manually shaken for 5 minutes. The organic phase
was transferred to a GC vial for analysis. Figure 2 shows a
summarized flow chart of the sample preparation procedure
employed throughout this work.
Extraction
Derivatization
Biological tissue
Grams of extract
0.1-0.25 g sample
5 mL acetate buffer
(0.1 M, pH=5) Re-adjust
to desired pH with
NH4OH or HCl
4 mL TMAH (25%)
Add stir bar
70 °C, 75 W, ramp for
1 min., 4 min. hold
0.5-1.0 mL isooctane
and 0.5 mL 2.5% NaBPr4
Manual agitation for
5 minutes and extract
organic phase
Centrifuge (2500 rpm,
5 minutes), if necessary
Figure 2. Flow chart of the extraction and derivatization procedures used.
3
Results and Discussion
GC Transfer Line Optimization
Optimization of the operational parameters related to the
GC transfer line and ICP-MS torch, such as the distance of
the inner capillary column, the Ar makeup gas flow rate
(i.e. the nebulizer gas) and the addition of oxygen gas (O2),
were evaluated using the continuous signal of the nitrogen
(N2) impurities (isotope 15) from the helium (He) carrier gas.
The addition of O2 is necessary to prevent the deposition of
carbon on the ICP-MS sampling cone5, resulting from the
isooctane. Although the 15N+ response was used for the
optimization here, the addition of xenon/argon gas mixture
(50 ppm) has been employed previously.6
The GC transfer line provided by PerkinElmer has been
designed to be used with the Clarus or AutoSystem™ GCs
and can be coupled to either the NexION or ELAN® ICP-MS
platforms. The GC transfer line temperature is controlled
by the Clarus GC system to maintain the analytes in the gas
phase and prevent cold spots in the transfer line.7 The Ar
makeup gas flow rate is controlled from the ICP-MS
nebulizer control and is heated as it enters the transfer
line. It is important to achieve sufficient flow to efficiently
transfer the analytes into the plasma. The O2 gas, added
through a “T”, also passes through the transfer line.
Once the setup is complete and the plasma ignited, the
15 +
N response is measured and parameters optimized. From
previous work, the optimum values for the addition of
O2 gas and the position of the inner deactivated capillary
column (relative to the end of the Silcosteel® tube in the
transfer line) were determined to be 0.025 L/min and 7 cm,
respectively.6 The Ar makeup gas flow rate (with the O2 set
at 0.025 L/min) was then optimized by varying the flow rate
between 0.8-1.0 L/min until a maximum 15N+ response was
observed. Once the optimum conditions were determined,
injection of organic solvent (e.g., isooctane, hexane,
acetone etc.) was performed to confirm that the analyte
reaches the plasma. Figure 3 shows the typical response of
Figure 4. Typical 15N+ calibration curves for Sn (120Sn+).
4
Figure 3. Typical 15N+ signal for an isooctane solvent injection.
the 15N+ isotope signal for an injection of isooctane.
The suppression of the 15N+ baseline signal at 2.5 min
corresponds to the combustion of the organic solvent in the
plasma and thus confirms efficient GC gas flow penetration
into the plasma. The optimum conditions for the GC/ICP-MS
system are listed in Table 1 (Page 2).
Analytical Performance
The analytical response characteristics were determined
for the butylated tin standard solutions. The calibration
curves were generated for the Sn isotopes (118, 119 and
120) responses for the butyl-tin compounds through
triplicate injections of 1 µL across a concentration range
from 0 (i.e. analytical blank) to 2 ng/mL in isooctane.
Good linearity and satisfactory coefficients of correlation
(R2 values) were observed for the 120Sn response functions
(Figure 4). The limits of detections (LODs = 3σblank/m) were
determined from each calibration response function, and
absolute LODs of 18, 200 and 7 fg were obtained for MBT,
DBT and TBT as 120Sn, respectively. The high absolute LOD
value observed for DBT is probably due to the high blanks
values which are related to contamination from the
containers and reagents used in the chemical preparation
procedure. This is usually observed since DBT is used in the
industrial synthesis of plastics.
DBT
5a
30000
20000
MBT
TMT
10000
TBT
15000
DMT
Intensity (cps)
MMT
25000
5000
0
40000
6
Time (min)
7
8
DBT
35000
30000
25000
9
5b
20000
TMT
0
3
4
5
6
7
Time (min)
8
9
10
11
12
Sn
Sn
DMT
MMT
5000
TMT
10000
DPhT
2
MOT
1
MPhT TBT
0
MBT
15000
5000
DMT
10000
20000
DPhT
MBT
15000
MPhT TBT
MOT
Intensity (cps)
30000
MMT
Intensity (cps)
5
40000
35000
25000
4
DBT
3
0
4
5
6
Time (min)
7
8
9
5c
DBT
3
140K
100K
80K
60K
0
6.0
6.5
7.0
7.5
8.0
8.5
Time (min)
9.0
9.5
Figures 5a-c show the chromatographic separation for
the organotin species (120Sn isotope) in a 0.25 ng/mL
standard in isooctane, oyster tissue and mussel tissue
reference material, respectively. Multiple Sn isotopes
(118, 119, 120) were monitored during method
development, but only results for 120Sn are presented
for simplicity. The chromatographic conditions (Table 1)
were chosen in a way that elution of the species was
away from the zone disturbed by the solvent elution.1
Quantification results by external calibration were
obtained for the butyl-tin compounds present in the
biological tissue samples. Triplicate extraction of the
mussel tissue reference material was used for the
validation of this methodology. The certified values for
MBT, DBT and TBT were compared to the experimental
values obtained, and the results are shown in Table 3.
Table 3 also shows the concentration values obtained
for the butyl- tin species present in the oyster tissue
sample, although these compounds were not certified.
The temperature program listed in Table 1 provided
good separation for the organotin compounds in less
than 11 minutes with peak widths of 2-3s. Figure 5a
shows the chromatogram obtained under the optimum
conditions for a 0.25 ng/mL standard in isooctane
containing methyl-tin and butyl-tin species at mass 120.
As seen in Figures 5b-c, the chromatographic separation
of the oyster and mussel tissues also shows the presence
of additional organotin species (monooctyl-, dioctyl-,
monophenyl-, diphenyl- and triphenyltin) usually
observed in environmental samples. All the peaks
observed are clearly identified in the chromatograms.
The peak around 8.5 minutes is probably due to NaBEt4
impurities in the NaBPr4 reagent employed during the
derivatization procedure which would form ethylated
forms of the organotin species. To corroborate its
identity, further work is required.
TphT
DOT
DPhT
MOT
MPhT
TMT
20K
MBT
40K
TBT
Intensity (cps)
120K
Chromatographic Separation and Method Validation
10.0
10.0
Figures 5a-5c. Chromatographic separation for the organotin species (120Sn
isotope) for a 0.25 ng/mL standard in isooctane (5a), oyster tissue (5b),
and mussel tissue reference material (5c).
Table 3. Concentration results for MBT, DBT and TBT (expressed ng/g as Sn) obtained in the analysis of the biological tissues (n=3, triplicate extraction)
Certified/Indicative Values
Experimental Values
Recovery (%)
CRM 477 - Mussel Tissue
MBT
1013 ± 189
928 ± 130
92
DBT
785 ± 61
745 ± 90
95
TBT
900 ± 78
953 ± 42
106
Oyster Tissue
MBT
-
23 ± 3
-
DBT
-
83 ± 7
-
TBT
-
26 ± 1
5
Conclusions
The successful coupling of the GC transfer line between the
Clarus GC and the NexION ICP-MS detection system for the
analysis of biological tissues was presented here. Response
functions for the butyl-tin species with satisfactory linearity
were generated, and absolute LODs were determined
after optimization of the operational parameters. The GC
chromatographic separation for the organotin compounds
was applied to the analysis of a mussel tissue reference
material and an oyster tissue. The quantification and
validation of the butyl-tin species in the biological tissues
was carried out by external calibration with recoveries of
≥ 92% and RSDs of ≤ 14%.
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