Aminohippurate Sodium information, interactions and side effects, Aminohippurate sodium is an agent to measure effective renal plasma flow (ERPF). It is the sodium salt of para-aminohippuric acid, commonly abbreviated “PAH”. It is water soluble, lipid-insoluble, and has a pKa of 3.83. The empirical formula of the anhydrous salt is C9H9N2NaO3 and its structural formula is:
It is provided as a sterile, non-preserved 20 percent aqueous solution for injection, with a pH of 6.7 to 7.6. Each 10 mL contains: Aminohippurate sodium (aminohippurate) 2 g. Inactive ingredients: Sodium hydroxide to adjust pH, water for injection, q.s.
Estimation of effective renal plasma flow.
Measurement of the functional capacity of the renal tubular secretory mechanism.
DOSAGE AND ADMINISTRATION
For intravenous use only
Clearance measurements using single injection techniques are generally inaccurate, particularly in the measurement of ERPF. For this reason, intravenous infusions at fixed rates are used to sustain the plasma PAH concentration at the desired level.
To measure ERPF, the concentration of PAH in the plasma should be maintained at 2 mg per 100 mL, which can be achieved with a priming dose of 6 to 10 mg/kg and an infusion dose of 10 to 24 mg/min.
As a research procedure for the measurement of TmPAH, the plasma level of PAH must be sufficient to saturate the capacity of the tubular secretory cells. Concentrations from 40 to 60 mg per 100 mL are usually necessary.
Technical details of these tests may be found in Smith1; Wesson2; Bauer3; Pitts4; and Schnurr5.
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to use, whenever solution and container permit.
NOTE: The normal color range for this product is a colorless to yellow/brown solution. The efficacy is not affected by color changes within this range.
Effective Renal Plasma Flow (ERPF)
The clearance of PAH, which is extracted almost completely from the plasma during its passage through the renal circulation, constitutes a measure of ERPF. Hence:
ERPF = UPAHV/ PPAH
Where UPAH = concentration of PAH (mg/mL) in the urine
V = rate of urine excretion (mL/min), and
PPAH = plasma concentration of PAH (mg/mL).
Example: UPAH = 8.0 mg/mL
V = 1.5 mL/min
PPAH = 0.02 mg/mL
ERPF = 8.0 x 1.5/0.02 = 600 mL/min
Based on PAH clearance studies, the normal values for ERPF are:
men 675 ± 150 mL/min
women 595 ± 125 mL/min
Maximum Tubular Secretory
The quantity of PAH secreted by the tubules (TmPAH) is given by the difference between the total rate of excretion (UPAHV) and the quantity filtered by the glomeruli (GFR x PPAH). Hence:
TmPAH= UPAHV – (GFR x PPAH x 0.83)
The factor, 0.83, corrects for that portion of PAH which is bound to plasma protein and hence is unfilterable. Example:
UPAH = 9.55 mg/mL
V = 16.68 mL/min
GFR = 120 mL/min
PPAH = 0.60 mg/mL
Then TmPAH = 9.55 x 16.68 – (120 x 0.60 x 0.83) = 100 mg/min. Average normal values of TmPAH are 80-90 mg/min.
The value of the expression UPAHV, used in calculations of ERPF and TmPAH, may be found by determining the amount of PAH in a measured volume of urine excreted within a specific period of time.
These calculations are based on a body surface area of 1.73 m2. Corrections for variations in surface area are made by multiplying the values obtained for ERPF and TmPAH by 1.73/A, where A is the subject surface area.
No. 95 — Aminohippurate Sodium, (aminohippurate) 20 percent sterile solution for intravenous injection, is supplied as follows:
NDC 0006-3395-11 in 10 mL vials.
Store at 25°C (77°F); excursions permitted to 15-30°C (59-86°F).
Hypersensitivity reactions including anaphylaxis, angioedema, urticaria, vasomotor disturbances, flushing, tingling, nausea, vomiting, and cramps may occur. Patients may have a sensation of warmth or the desire to defecate or urinate during or shortly following initiation of infusion.
Renal clearance measurements of PAH cannot be made with any significant accuracy in patients receiving sulfonamides, procaine, or thiazolesulfone. These compounds interfere with chemical color development essential to the analytical procedures.
Probenecid depresses tubular secretion of certain weak acids such as PAH. Therefore, patients receiving probenecid will have erroneously low ERPF and TmPAH values.
Intravenous solutions must be given with caution to patients with low cardiac reserve, since a rapid increase in plasma volume can precipitate congestive heart failure.
For measurement of ERPF, small doses of PAH are used. However, in research procedures to measure TmPAH, high plasma levels are required to saturate the capacity of the tubular cells. During these procedures, the intravenous administration of PAH solutions should be carried out slowly and with caution. The patient should be continuously observed for any adverse reactions.
Carcinogenesis, Mutagenesis, Impairment of Fertility
Long-term studies in animals have not been done to evaluate any effects upon fertility or carcinogenic potential of PAH.
Pregnancy Category C. Animal reproduction studies have not been done with PAH. It is also not known whether PAH can cause fetal harm when given to a pregnant woman or can affect reproduction capacity. PAH should be given to a pregnant woman only if clearly needed.
It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when PAH is administered to a nursing woman.
Safety and effectiveness in pediatric patients have not been established.
Clinical studies of PAH did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients.
The intravenous LD50 in female mice is 7.22 g/kg.
Hypersensitivity to this product or to its components.