Evaluation of the measurement of Cu(II) bioavailability in complex
aqueous media using a hollow-fiber supported liquid membrane
device (HFSLM) and two microalgae species (Pseudokirchneriella
subcapitata and Scenedesmus acutus)
Erik A. Rodríguez-Morales, Eduardo Rodríguez de San Miguel
*
, Josefina de Gyves
Departamento de Química Analítica, Facultad de Química, Universidad Nacional Aut onoma de Mexico, Ciudad Universitaria, 04510 Mexico, D.F., Mexico
article info
Article history:
Received 12 June 2015
Received in revised form
5 August 2015
Accepted 9 August 2015
Available online xxx
Keywords:
Bioavailability
Copper
Chemical surrogate
Hollow fiber
Microalgae
abstract
The environmental bioavailability of copper was determined using a hollow-fiber supported liquid
membrane (HFSLM) device as a chemical surrogate and two microalgae species (Scenedesmus acutus and
Pseudokirchneriella subcapitata). Several experimental conditions were studied: pH, the presence of
organic matter, inorganic anions, and concomitant cations. The results indicated a strong relationship
between the response given by the HFSLM and the microalgae species with free copper concentrations
measured by an ion selective electrode (ISE), in accordance with the free-ion activity model (FIAM). A
significant positive correlation was evident when comparing the bioavailability results measured by the
HFSLM and the S. acutus microalga species, showing that the synthetic device may emulate biological
uptake and, consequently, be used as a chemical test for bioavailability measurements using this alga as a
biological reference.
© 2015 Elsevier Ltd. All rights reserved.
1. Introduction
Currently, the study of metal ion bioavailability in natural sys-
tems is important for the determination of water quality because
the concept focuses specifically on the amount of metal that is
capable of crossing biological membranes and not on the total
amount of metal in the medium (McGeer et al., 2004). The different
chemical forms in which the metal ions might be present in
aqueous environments lead to different types of interactions with
biological membranes, affecting the bioassimilation and the
toxicity of such species (Slaveykova and Wilkinson, 2003;
Wilkinson and Buffle, 2004; De Schamphelaere and Janssen,
2006). Bioavailability is a concept for which no simple generic
definition can be formulated (Cui et al., 2013), although a large
number of definitions can be found in the literature. The definition
given in ISO 11074 (ISO, 2005) that “bioavailability is the degree to
which chemicals present in the soil may be absorbed or metabo-
lized by human or ecological receptors or are available for inter-
action with biological systems” implies that the metals migrate
from the environment into the organism through a boundary zone,
i.e., it relates the environmental availability measured by chemical
methods and the toxicologic bioavailability measured by biological
procedures (Harmsen, 2007). By crossing this zone, the metals
released by the soils are taken up by organisms, and for this reason,
having an estimation of the magnitude of the process is necessary
to evaluate the impact of the sorption performed by the organism.
Common ways to make such measurements are to quantify the
amount of internalized metal, evaluate the internalization fluxes, or
determine the toxicity as a function of metal amount in the bio-
logical systems (Franklin et al., 2002; Slaveykova et al., 2009).
Numerous bioavailabilities could be measured depending on the
type of target organisms and time scales using methods that are
usually time consuming because of the manipulation of biological
entities. For this reason, chemical measurements made in envi-
ronmental matrices are usually employed to determine a fraction of
a well-defined class of contaminants assumed to be available for
specific receptors, e.g., free, labile, inert (Parthasarathy and Buffle,
1994), and lipophobic (Parthasarathy et al., 2010) fractions. Some
of these methods include diffusion gradients in thin films (DGT)
(Zhang and Davison, 2000; Han et al., 2014), voltamperometry
(Buffle and Tercier-Waeber, 2000) and supported or permeation
liquid membranes (SLM, PLM, respectively) (Parthasarathy et al.,
* Corresponding author.
E-mail address: erdsmg@unam.mx (E. Rodríguez de San Miguel).
Contents lists available at ScienceDirect
Environmental Pollution
journal homepage: www.elsevier.com/locate/envpol
http://dx.doi.org/10.1016/j.envpol.2015.08.011
0269-7491/© 2015 Elsevier Ltd. All rights reserved.
Environmental Pollution 206 (2015) 712e719