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Because the test pad reaction is dependent on pH, false positive results can occur if the urine is highly alkaline. [ 60 ] [ 62 ] Conventional test strips are not sensitive enough to reliably detect microalbuminuria , a condition in which urine albumin levels are slightly elevated, [ 64 ] although dipsticks specialized for this measurement exist.
The pH of urine normally vary between 4.5 and 8 with the first urine produced in the morning generally being more acidic and the urine produced after meals generally more alkaline. [4] Normal reference values are not provided for urine pH as the variation is too wide and results have to be considered in the context of the other quantifiable ...
Reference ranges for urine tests are described below: Measurement Lower limit Upper limit ... pH: 5 [2] 7 [2] (unitless) Protein: 0: trace amounts [2] Glucose: n/a: 0 ...
Conversely, when pH = pK a, the concentration of HA is equal to the concentration of A −. The buffer region extends over the approximate range pK a ± 2. Buffering is weak outside the range pK a ± 1. At pH ≤ pK a − 2 the substance is said to be fully protonated and at pH ≥ pK a + 2 it is fully dissociated (deprotonated).
Urine electrolyte levels can be measured in a medical laboratory for diagnostic purposes. The urine concentrations of sodium , chlorine and potassium may be used to investigate conditions such as abnormal blood electrolyte levels, acute kidney injury , metabolic alkalosis and hypovolemia .
A urine test is any medical test performed on a urine specimen. The analysis of urine is a valuable diagnostic tool because its composition reflects the functioning of many body systems, particularly the kidneys and urinary system , and specimens are easy to obtain. [ 1 ]
The converse is true in a basic medium. For example, Naproxen is a non-steroidal anti-inflammatory drug that is a weak acid (its pKa value is 5.0). The gastric juice has a pH of 2.0. It is a three-fold difference (due to log scale) between its pH and its pKa; therefore there is a 1000× difference between the charged and uncharged concentrations.
To calibrate the electrode, it is first immersed in a standard solution, and the reading on a pH meter is adjusted to be equal to the standard buffer's value. The reading from a second standard buffer solution is then adjusted using the "slope" control to be equal to the pH for that solution. Further details, are given in the IUPAC ...