Rosa Puchades

Controlled Delivery Systems Using Antibody-Capped Mesoporous Nanocontainers

This paper describes the design of new controlled delivery systems consisting of a mesoporous support functionalized on the pore outlets with a certain hapten able to interact with an antibody that acts as a nanoscopic cap. The opening protocol and delivery of the entrapped guest is related by a displacement reaction involving the presence in the solution of the antigen to which the antibody is selective. As a proof-of-the-concept, the solid MCM-41 was selected as support and was loaded with the dye [Ru(bipy)(3)]Cl(2). Then a suitable derivative of the hapten 4-(4-aminobenzenesulfonylamino)benzoic acid was anchored on the outer surface of the mesoporous support (solid S1). Finally the pores were capped with a polyclonal antibody for sulfathiazole (solid S1-AB). Delivery of the dye in the presence of a family of sulfonamides was studied in phosphate-buffered saline (PBS; pH 7.5). A selective uncapping of the pores and dye delivery was observed for sulfathiazole. This delivery behavior was compared with that shown by other solids that were prepared as models to assess the effect of the hapten and its interaction with antibody in the dye delivery control in the presence of the antigen.

Physico-chemical and chemical properties of some coconut coir dusts for use as a peat substitute for containerised ornamental plants

Selected physico-chemical and chemical characteristics of 13 coconut coir dust (mesocarp pithy tissue plus short-length fibres) samples from Asia, America and Africa were evaluated as peat alternatives. All properties studied differed significantly between and within sources, and from the control Sphagnum peat. pH of coir dust was slightly acidic, whereas salinity varied dramatically between 39 and 597 mS m(-1) in the saturated media extract. The cation exchange capacity and carbon/nitrogen (C/N) ratio ranged from 31.7 to 95.4 cmol(c) kg(-1) and from 75 to 186, respectively. Most carbon was found as lignin and cellulose. The concentrations of available nitrogen, calcium, magnesium and micro-elements were low, while those of phosphorus and potassium were remarkably high (0.28-2.81 mol m(-3) and 2.97-52.66 mol m(-3) for P and K, respectively). Saline ion concentrations, especially chloride and sodium, were also high.

Influence of Particle Size on Physical and Chemical Properties of Coconut Coir Dust as Container Medium

The influence of particle size (diameter between <0.125 mm and >2 mm) on the physical, physico-chemical and chemical properties of a coconut coir dust from Mexico was studied. Particle size significantly affected the physical properties, especially the air–water relationships. Air content increased and water-holding capacity (total and readily available) decreased with increasing particle diameter. The easily-available water content did not reveal a clear pattern of variation, showing the largest value in the fraction 0.125–0.25 mm. Particle size equivalent to 0.5 mm brought about an important and highly significant change in the physical properties studied. Coconut coir dust particle size also affected the physico-chemical and chemical characteristics, but to a lesser degree. Both the electrical conductivity and the available macro- and micro-element concentrations were significantly higher in the smaller size ranges, the largest values being obtained in the finest particle size fraction (<0.125 mm).

Review on immunoanalytical determination of tetracycline and sulfonamide residues in edible products.

The state of the art of immunoanalysis for the determination of tetracycline and sulfonamide residues in food products is reviewed. Special attention is paid to the design and synthesis of haptens, providing an overview of the efforts spent on developing antibiotic screening methods to determine residue levels in agreement with the legislation. The results and observations published, focused on tetracycline and sulfonamide enzyme-linked immunosorbent assays, are discussed.

Development of a highly sensitive enzyme-linked immunosorbent assay for atrazine Performance evaluation by flow injection immunoassay

Specific polyclonal antibodies to the herbicide atrazine (6-chloro-N-ethyl-N′-isopropyl-1,3,5-triazine-2,4-diamine) have been raised by immunizing three New Zealand rabbits. With the antisera (As) a highly sensitive enzyme-linked immunosorbent assays (ELISA) has been developed to determine atrazine in water samples. Several usable competitive immunoassays have been obtained by screening a battery of nine enzyme tracers (ETs) and three antisera. The optimized ELISA presents an IC50 of 0.28 nM (60 ng l−1) and a detection limit of 0.043 nM (9 ng l−1). Cross-reactivity studies have proved that the immunoassay is specific for atrazine while other triazine compounds are only detected on a minor extent. The flow injection immunoanalysis (FIIA) method has an IC50 of 2 nM (0.47 μg l−1) reaching a detection limit of 0.35 nM (75 ng l−1). The performance of both methods has been evaluated by analyzing water samples containing mixtures of atrazine and other pesticides at the ppb level. For this purpose two candidate reference materials have been used (A and B) and a spiked sample stored on Empore disks (sample C). A close correspondence was found between the results obtained with both immunochemical techniques.

On-line immunoanalysis for environmental pollutants: from batch assays to automated sensors

Abstract The development of antibody-based sensors has grown steadily during recent years, and their use as routine instruments in pollution control programmes might become reality in the 21st century. The conversion from batch immunoassays to practical immunosensors has not been easy, owing to the sometimes different principles employed in these methodologies. In this review we illustrate the main difficulties found in the development and implementation of on-line immunosensors, as applied to the determination of organic pollutants such as pesticides. Some solutions to these problems are proposed, and their validities discussed critically.

Chemical surface modifications for the development of silicon-based label-free integrated optical (IO) biosensors: a review.

Increasing interest has been paid to label-free biosensors in recent years. Among them, refractive index (RI) optical biosensors enable high density and the chip-scale integration of optical components. This makes them more appealing to help develop lab-on-a-chip devices. Today, many RI integrated optical (IO) devices are made using silicon-based materials. A key issue in their development is the biofunctionalization of sensing surfaces because they provide a specific, sensitive response to the analyte of interest. This review critically discusses the biofunctionalization procedures, assay formats and characterization techniques employed in setting up IO biosensors. In addition, it provides the most relevant results obtained from using these devices for real sample biosensing. Finally, an overview of the most promising future developments in the fields of chemical surface modification and capture agent attachment for IO biosensors follows.

Multiplexed microimmunoassays on a digital versatile disk.

Multiplexed microimmunoassays for five critical compounds were developed using a digital versatile disk (DVD) as an analytical support and detecting technology. To this end, coating conjugates were adsorbed on the polycarbonate face of the disk; a pool of specific antibodies, gold labeled secondary antibodies, and silver amplification were addressed for developing the assays. The detection principle is based on the capture of attenuated analog signals with the disk drive that were proportional to optical density of the immunoreaction product. The multiplexed assay achieved detection limits (IC10) of 0.06, 0.25, 0.37, 0.16, and 0.10 microg/L, sensitivities of (IC50) 0.54, 1.54, 2.62, 2.02, and 5.9 microg/L, and dynamic ranges of 2 orders of magnitude for atrazine, chlorpyrifos, metolachlor, sulfathiazole, and tetracycline, respectively. The features of the methodology were verified by analyzing natural waters and compared with reference chromatographic methods, showing its potential for high-throughput multiplexed screening applications. Analytes of different chemical nature (pesticides and antibiotics) were directly quantified without sample treatment or preconcentration in a total time of 30 min with similar sensitivity and selectivity to the ELISA plate format using the same immunoreagents. The multianalyte capabilities of immunoassaying methods developed with digital disk and drive demonstrated the competitiveness to quantify targets that require different sample treatment and instrumentation by chromatographic methods.

Current trends in immunoassay-based kits for pesticide analysis.

Detection of pesticides and their metabolites in food and environmental samples in real time is the goal of many industries. Immunoassay technology has several attributes that make it a useful tool for screening purposes (e.g., selectivity, sensitivity, portability, and rapid turnaround time). Approximately 90% of the developed immunoassays for the pesticide residue analysis use the ELISA technique. Commercial kits are tailored to target different analytes, thus eliminating in some cases the need for clean-up steps. The manageability of the immunoassay test kit, together with its accuracy and speed of analysis, allows the rapid determination in situ of many samples simultaneously. This article gives an overview on the applications of the immunokits for pesticide analysis in drinking water and foods, as well as examples of different immunoassay formats commonly used. Special attention is given to sample extraction and clean-up procedures. Application to the determination of common pesticides and their detection limit are summarized. Immunoassay kits offer many practical advantages, and the acceptance of these methods depends on several factors, including the demonstration of quality and validity compared with reference methods. Although the advantages of the technique and their applications to food industry quality control are scarcely referred to in the literature.

Development of a group-specific immunoassay for sulfonamides: Application to bee honey analysis

A set of haptens has been synthesized in order to raise generic polyclonal antibodies against sulfonamides using different strategies. After the screening of all the immunorreagents, a highly sensitive enzyme-linked immunosorbent assay was set-up for simultaneous determination of six of these antibiotics. The developed procedure allows the screening of: sulfathiazole, sulfamethoxypyridazine, sulfapyridine, sulfamethizole, sulfasalazine and N(4)-phtalylsulfathiazole with good accuracy and precision at level 0.13ng mL(-1) in buffer. The suitability of developed ELISA for its application to honey analysis has been investigated. The antimicrobials were extracted from samples with acetate buffer, and cleaned up by solid phase extraction. The mean recovery found for honey samples, spiked from 1.5 to 4.5ng mL(-1) equivalents of sulfathiazole (24-72microg sulfathiazole kg(-1) honey), was 106%.