Fuente: Laboratorio del Dr. B. Jill Venton – Universidad de Virginia
El objetivo de muchos análisis químicos es un análisis cuantitativo, donde se determina la cantidad de una sustancia en una muestra. Para calcular con precisión la concentración de un desconocido de una muestra, preparación de muestras cuidadosa es la clave. Cada vez que una muestra es manejada o transferida, de la muestra puede ser perdido. Sin embargo, existen estrategias para minimizar la pérdida de muestra. También existen estrategias para sobrellevar la pérdida de muestra y todavía hacer mediciones precisas de la concentración.
Para minimizar la pérdida de muestra, lo ideal es minimizar el número de medidas de manejo y transferencia de muestra. Por ejemplo, reuniendo una muestra sólida directamente en un matraz que se determinara una solución reduce un paso de la transferencia. Si es necesario trasladar de un matraz a otro y se hace una dilución, luego triple enjuague la cristalería ayuda a garantizar que la muestra se transfiere. Otras estrategias son más específicos de la muestra. Por ejemplo, las muestras que se adsorben al vidrio, como las proteínas, podrían manejarse mejor en tubos desechables de polipropileno. Los tubos no son hidrofílicos, por lo que si una pequeña cantidad de muestra debe pipetearse en agua, es mejor ya haber agregado el agua al tubo, por lo que la muestra puede pipetearse directamente en el solvente. Sería mejor concentrarse en lugar de secar completamente una muestra, debido a las pérdidas de insolubilities después de la rehidratación.
Otra fuente de pérdida de muestra es a través de manipulaciones de la muestra incompleto. Por ejemplo, si se utiliza un procedimiento de derivatización y la derivatización es incompleta, entonces el monto total de la muestra no se observa. Errores como este son errores sistemáticos y pueden ser resuelto por corregir el problema, como cambiar el procedimiento de derivatización. Otra causa de error sistemático en las mediciones es efectos de matriz. Estos pueden interferir con la medición de determinadas sustancias y realizar calibraciones en la misma matriz como la muestra puede reducir este efecto.
Análisis cuantitativo se realiza típicamente usando estándares internos o externos. Para los estándares externos, se realiza una curva de calibración midiendo diferentes concentraciones conocidas del analito de interés. Luego, la muestra se ejecuta por separado de la norma. Normas internas, el estándar está en la misma muestra como el analito de interés, lo que permite la medida a adoptarse simultáneamente. Por lo general, se agrega una especie diferente llamada estándar interno y la relación de la respuesta para esa norma interna y el analito se calcula. La idea es que la relación de la respuesta, llamada el factor de respuesta, es proporcional a su concentración. Mientras que el método debe ser capaz de distinguir entre el analito de interés y del estándar interno, las pérdidas de muestra que se producen después de que se agregó el estándar interno deben ser similares para ambas sustancias y por lo tanto el cociente de la respuesta permanece igual. Un caso especial del uso de estándares internos es el método de adiciones estándar, donde cantidades crecientes de la sustancia a analisar se agrega a la solución y la cantidad original de analito es calculado por la espalda. Estándares internos pueden utilizarse en electroquímica y cromatografía y espectroscopia.
Internal standards are used in many fields, including spectroscopy and chromatography. In spectroscopy, internal standards can help correct for random errors due to changes in light source intensity. If a lamp or other light source has variable power, it will affect the absorption and consequently, emission of a sample. However, the ratio of an internal standard to analyte will stay constant, even if the light source does not. One example of this is using lithium (Li) as an internal standard for the analysis of sodium in a blood sample by flame spectroscopy. Li is chemically similar to sodium but is not natively found in blood.
For chromatography, internal standards are often used in both gas chromatography and liquid chromatography. For applications with mass spectrometry as the detector, the internal standard can be an isotopically-labeled analyte, so that the molecular weight (MW) will be different than the analyte of interest. Internal standards are commonly used in pharmaceutical or environmental analyses.
Sample loss can occur every time a sample is handled or transferred, thereby making accurate calculations of concentration difficult.
To ensure accuracy, the effects of sample loss must be minimized using careful sample preparation and by limiting the number of sample handling and transfer steps. However, sample loss can also occur due to systematic errors, such as incomplete sample manipulation, matrix effects, and variations in analytic procedure.
These sources of loss can be accounted for by adding a known concentration of a species similar, but not identical, to the compound of interest. This is called an internal standard. Any sample losses that occur to the internal standard should be similar for the analyte, allowing for the concentration to be accurately calculated.
This video will illustrate the use of an internal standard and proper lab technique to account for sample loss when determining the concentration of an unknown.
An internal standard is a substance added in a known amount to standards, samples, and blanks during an analysis.
In chromatography and spectroscopy, the ratio of the signal for the internal standard and the analyte is calculated. This ratio, called the response factor, is proportional to the ratio of the analyte and standard concentrations.
Response factor, R, can be expressed by the following equation, where A represents the analytical signals of the sample and internal standard and C represents the concentrations of the sample and internal standard.
An internal standard can compensate for both systematic and random errors. For example, random errors—such as inconsistencies when measuring a sample—will be the same for both the internal standard and the analyte. Therefore, the ratio of their signals will not change.
For systematic errors, such as matrix effects in solution, the ratio will be unaffected as long as the matrix effect is equal for both the standard and the analyte.
While internal standards provide great benefit, it can be difficult to choose one that is suitable. An internal standard must have a signal that is similar, but not identical, to the analyte. It also cannot affect the measurement of the analyte in any way.
Finally, the concentration must be well known. This is achieved by ensuring that the internal standard is not natively present in the sample; thus, the only source of it in solution is the known concentration added.
In the following experiment, the concentration of caffeine in an unknown sample will be determined by gas chromatography.
This is achieved by creating a calibration curve using known caffeine solutions, with adenine as the internal standard. The slope of the calibration curve is equal to the response factor.
Once the response factor is known, the concentration of the unknown can be calculated from its measured chromatogram area ratio.
Now that you understand the basics of internal standards, let’s take a look at the procedure.
To begin the procedure, accurately weigh 100 mg of the internal standard, adenine, into a clean beaker.
Next, dissolve it in roughly 20 mL of dimethyl sulfoxide, and mix the solution.
Once the adenine has dissolved, pour the solution into a 50-mL volumetric flask.
Rinse the beaker and stir bar with 10 mL of DMSO, and pour the rinse into the flask. Repeat this rinse twice, to ensure proper solution transfer. Fill to the calibration mark, resulting in an internal standard with a concentration of 2 mg/mL.
Next, weigh 100 mg of caffeine into a beaker to prepare a stock solution. Dissolve the caffeine with a small amount of methanol. Then, use 3 rinses to transfer this solution to a fresh 25 mL volumetric flask. This is the 4 mg/mL stock solution. Use it to create 3 caffeine standards.
Next, add 0.2 mL of the internal standard, adenine, to each flask. Fill each to the final volume with methanol. Transfer each solution to a sample vial.
Run each caffeine standard through a gas chromatograph. Calculate the ratio of peak areas for the caffeine versus the adenine standard.
First, weigh 2 g of coffee into a 100-mL beaker, and record the weight.
Next, add 20 mL of methanol to extract the caffeine from the coffee. Allow the solution to stir for 20 min.
Using a Büchner funnel, filter out the coffee grounds. Rinse the beaker with a small amount of methanol, and pour this rinse into the funnel. Repeat the rinse twice.
Measure the final volume of the filtrate; it should be approximately 35 mL.
To prepare the sample for analysis, add 1 mL of the coffee extract to a sample vial. Then, add 0.2 mL of the adenine internal standard, and place the vial into the instrument’s auto-sampler rack.
Run a gas chromatography analysis of the sample, ensuring that the conditions are such that the caffeine and adenine are separate.
After completing the analysis, compute the peak area for both the internal standard and the analyte.
Once all the samples have been analyzed, the standard calibration curve can be determined for the caffeine/adenine solutions by plotting the ratios of the peak areas versus the ratios of the concentrations. The slope of this line, which represents the response factor, was 1.8.
Next, the GC data from the extracted coffee sample is analyzed. The ratio of the peak areas was calculated to be 1.78. Using the response factor and the known concentration of the internal standard, adenine, the concentration of caffeine in the unknown sample was calculated to be 0.33 mg/mL.
Many different types of reactions, across various scientific disciples, utilize internal standards to minimize the effects of errors and sample loss.
The effects of sample loss encountered during sample preparation can be minimized using internal standards, keeping their concentration ratio nearly constant.
In this example, bioactive lipids were extracted from lysed cells using a liquid-liquid extraction process. Stable isotope internal standards were added at the beginning of extraction to account for errors during sample preparation.
Internal standards were not only critical for the preparation of the bioactive lipids, but also for the analysis. The lipids were separated using high-performance liquid chromatography, and analyzed via mass spectrometry.
In spectroscopy, internal standards can help correct for random errors due to changes in light source intensity. If a lamp or other light source has variable power, it will affect the absorption and consequently, emission of a sample. However, the ratio of an internal standard to analyte will stay constant, even if the light source does not.
In chromatography, one of the largest sources of error is the injection. Auto-samplers help minimize this, but error can still be 1–2% relative standard deviation.
In this example, vapor standards containing an internal standard were analyzed using gas chromatography to establish a calibration curve. Once this was complete, the unknown sample could then be measured and the losses due to volatility of the sample accounted for.
You’ve just watched JoVE’s introduction to internal standards. You should now understand best practices for minimizing sample loss, internal standards, and response factors.
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