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NORMAL CONSTITUENTS OF
URINE
Dr. Janice D’Sa
INTRODUCTION
• Urine is an excretory product of the body.
• It is formed in the kidney.
• Urine examination helps in the diagnosis of
various renal as well as systemic diseases.
URINE COLLECTION
• Urine is usually collected in a sterile wide mouthed
container.
• Different method of urine collection are –
– FIRST MORNING SAMPLE (conc urine for biochemical
analysis, casts and crystals)
– RANDOM SAMPLE(chemical screening, microscopic
examination)
– 24 HOUR URINE SAMPLE (quantitative estimation of
proteins, sugars, electrolytes, hormones)
– MID STREAM URINE
– CLEAN CATCH URINE
SAMPLE PRESERVATION
• For determination of urea, ammonia, nitrogen and
calcium – Hydrochloric acid is used.
• For determination of sodium, potassium, chloride,
bicarbonate, calcium, phosphorus, urea, ammonia,
amino acids, creatinine, proteins, reducing substances
and ketone bodies - Thymol is used
• For determination of Ascorbic acid – Acetic acid is used
• Toluene may also be used as a preservative.
COMPOSITION OF NORMAL URINE
PHYSICAL PROPERTIES
VOLUME
• Normal volume of urine excreted per day by
normal subjects is 1000-2000 ml/day.
• Night urine output < 400ml.
• Factors which influence the volume excreted :
– Intake of fluid, proteins and salt.
– Excessive perspiration and strenuous exercise
decrease the volume of urine.
COLOR
• Normal urine is pale yellow (due to presence of
pigment urochrome)
• When the output of urine is low it appears deep
yellow.
• Freshly voided urine is clear and transparent.
• Long standing urine may become turbid. (Due to
precipitation of phosphates)
ODOUR
• Normal odour of urine is aromatic in nature.
• Long standing urine may have an ammoniacal
odour (due to decomposition of urea to
ammonia).
PH
• Normal PH of urine ranges from 5.5 – 6.5.
• Factors which influence PH :
– High protein diet makes the urine more acidic
– Diet rich in vegetables and fruits make the urine
more alkaline.
• Measured using Dipsticks, Litmus Paper or Ph
paper.
SPECIFIC GRAVITY
• Specific gravity indicates the concentrating ability
of the kidneys.
• Normal range : 1.012 – 1.024
• Measured using urinometer, refractometer,
dipsticks.
• Sp. Gravity is affected by –
1. Volume of Urine excreted
2. Amount of solids present in the urine.
• Urinometer/ Hydrometer
consists of a thin stem
graduated from 1000 to
1060 corresponding to
specific gravities of 1.0 to
1.06. The bulb at the
bottom is suitably
weighed. Urinometer is
calibrated at 60 deg F (15
deg C)
METHOD OF DETERMINATION OF
SPECIFIC GRAVITY
1. Take sufficient urine in a container.
2. Allow the urinometer to float in urine
without touching the sides.
3. Observe the specific gravity reading
corresponding to the meniscus of urine.
4. Note the temperature of urine using a
thermometer.
5. Temperature correction is done for specific
gravity.
• TEMPERATURE CORRECTION
Observed sp. Gravity = 1010
Observed Room Temperature = 37 deg C
Temp of Urine = 15 deg C
Corrected Temperature = 37-15/3 = 7
Calibrated Sp. Gravity = 1010 + 7 = 1017
= 1.017
CHEMICAL CONSTITUENTS
NORMAL INORGANIC
CONSTITUENTS
CHLORIDE
• Normal chloride excreted in 24 hr urine
sample is 8 – 15 g/ day(NaCl).
INCREASED LEVELS DECREASED LEVELS
POLYDIPSIA EXCESSIVE SWEATING, FASTING,
DIARRHOEA, VOMITING
USE OF DIURETICS DIABETES INSIPIDUS
ADDISON’S DISEASE INFECTIONS
CUSHING’S SYNDROME
• TEST FOR CHLORIDE
METHOD – Take 2 ml of urine + 0.5
ml of conc. HNO3 + 1ml AgNo3.
OBSERVATION – Curdy white
precipitate
INFERENCE – Chloride is
precipitated as AgCl with Ag No3 in
presence of HNO3.
SULPHATE
• Daily excretion : 1g/ day
• Sulphur is derived from catabolism of sulphur
containing amino acids.
INCREASED LEVELS DECREASED LEVELS
HOMOCYSTEINURIA RENAL IMPAIRMENT
HIGH PROTEIN DIET
CYSTINURIA
METHOD –
2ml urine + 2ml Barium
Chloride
OBSERVATION –
White precipitate
INFERENCE – Sulphate is
precipitated as barium
sulphate with barium chloride.
CALCIUM
• Daily excretion – 200mg/day
INCREASED LEVELS DECREASED LEVELS
HYPER PARATHYROIDISM TETANY
RENAL STONES
HYPERVITAMINOSIS D
MULTIPLE MYELOMA
METHOD
5ml urine + 5 drops of 1% acetic acid + 5ml of
potassium oxalate.
OBSERVATION : Trace amount of white
precipitate
INFERENCE : Calcium is precipitated as calcium
oxalate in acid medium.
INORGANIC PHOSPHATE
• Daily excretion : 1gm/ day
INCREASED LEVELS DECREASED LEVELS
RICKETS / OSTEOMALACIA DIARRHOEA
HYPERPARATHYROIDISM NEPHRITIS
ACIDOSIS PARATHYROID HYPOFUNCTION
PREGNANCY
METHOD
5ml urine + few drops of conc HNO3
+ a pinch of ammonium molybdate.
Warm
OBSERVATION
Canary yellow precipitate.
INFERENCE : Inorganic phosphate is
precipitated as canary yellow
ammonium phosphomolybdate.
AMMONIA
• Daily excretion : 0.5-0.8gm/ day
• Urinary ammonia is derived from glutamine
and other amino acids by kidney.
INCREASED LEVELS DECREASED LEVELS
INGESTION OF ACID FORMING
FOODS
ALKALOSIS
DIABETIC KETOACIDOSIS NEPHRITIS
URINARY TRACT INFECTION
METHOD
5ml urine + 2% sodium carbonate (till
the red litmus turns blue). Boil.
During boiling, hold a piece of
moistened red litmus paper at the
mouth of the test tube.
OBSERVATION : Red litmus turns blue
INFERENCE : Ammonia liberated turns
red litmus blue.
NORMAL ORGANIC
CONSTITUENTS
UREA
• Daily excretion : 20-30 gm/day
• Urea is formed in the liver.
• End product of protein metabolism.
INCREASED LEVELS DECREASED LEVELS
FEVER LIVER DISEASE
DIABETES MELLITUS METABOLIC / RESPIRATORY ACIDOSIS
INCREASED INTAKE OF PROTEIN NEPHRITIS
SODIUM HYPOBROMITE TEST
METHOD
2ml urine + Few drops of sodium
hypobromite solution.
OBSERVATION : Brisk effervescence
INFERENCE : Hypobromite decomposes
urea to give nitrogen gas.
SPECIFIC UREASE TEST
METHOD
Label two test tubes as ‘TEST’ and ‘CONTROL’
Into TEST : 5ml urea solution + 2ml well mixed urease suspension.
Into CONTROL : 5ml urea solution + 2ml urease suspension which is
heated strongly.
Incubate both TEST and CONTROL at room temperature for 15-
20mins.
At the end, add 2 drops of phenolpthalein to both the tubes.
OBSERVATION
In TEST : Pink Color
In CONTROL : No pink color
INFERENCE
Urease converts urea into ammonia and carbonic
acid. Under the Ph of the reaction condition,
ammonia and carbonic acid are converted to
ammonium carbonate, Ph goes above 9.5. Since
the content are alkaline, phenolphthalein gives
pink color.
URIC ACID
• Daily excretion : 0.6-1gm/ day
• End product of purine metabolism.
• Increased levels of uric acid in urine is
URICOSURIA
INCREASED LEVELS DECREASED LEVELS
LEUKEMIA PURINE FREE DIET
CANCERS GOUT
PHOSPHOTUNGSTIC ACID REDUCTION TEST
METHOD
2ml urine + few drops of phosphotungstic
acid + few drops of 20% sodium
carbonate.
OBSERVATION
Blue color is formed
INFERENCE
Uric acid is a reducing agent in strong
alkaline condition. It reduces colorless
phosphotungstic acid to tungsten blue.
SCHIFF’S TEST
METHOD
Wet a piece of filter paper with a few drops of
ammoniacal silver nitrate solution. Add 1 or 2
drops of uric acid solution on the same paper.
OBSERVATION : Black color is formed
INFERENCE : Uric acid reduces ammoniacal silver
nitrate to metallic silver which is black in color.
CREATININE
• Daily excretion : 2gm/day in males, 1gm/day in females.
• Urinary creatinine is formed from muscle creatine.
INCREASED LEVELS DECREASED LEVELS
MUSCULAR DISORDERS RENAL FAILURE
MYASTHENIA GRAVIS
THYROTOXICOSIS
STARVATION
UNCONTROLLED DIABETES
MELLITUS
METHOD
Label 2 test tubes as ‘test’ and ‘control’.
Into Test : 2ml urine + 2ml saturated picric acid+
few drops of 10% NaOH
Into Control : 2ml water + 2ml saturated picric acid+
few drops of 10% NaOH
OBSERVATION
‘TEST’ – Orange Color, ‘CONTROL’ – Yellow Color
INFERENCE
Creatinine reacts with alkaline picrate solution to
form orange creatinine picrate.
ETHEREAL SULPHATE
• 100mg of organic sulphate is excreted per
day.
TEST FOR DETECTING ETHEREAL SULPHATE
METHOD
1ml urine + 2ml BaCl2 + 2ml concentrated HCl.
Mix and filter. Divide the filtrate into two
portions. Boil one and compare with the other
(control)
OBSERVATION : Trace turbidity compared to
that in control (red color may also be seen)
INFERENCE : This test is done after removing the
inorganic sulphate. Conc Hcl hydrolyses
ethereal sulphate to inorganic sulphate which
then gives precipitate with BaCl2.
UROBILINOGEN
• Increased urobilinogen concentration in urine is a
sensitive index of liver dysfunction or hemolytic
disorder.
• Urobilinogen is present in excessive amount in
prehepatic and hepatic jaundice.
• Urobilinogen is absent in urine in post hepatic
jaundice
METHOD
5ml of freshly voided urine + 1ml Ehrlich reagent,
mix. Let stand for 5 mins.
OBSERVATION
Red color is seen when viewed through the
mouth of the test tube.
INFERENCE
Urobilinogen reacts with p-dimethyl amino
benzaldehyde of the reagent to give red color.
THANK YOU 

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Normal constituents of urine

  • 2. INTRODUCTION • Urine is an excretory product of the body. • It is formed in the kidney. • Urine examination helps in the diagnosis of various renal as well as systemic diseases.
  • 3. URINE COLLECTION • Urine is usually collected in a sterile wide mouthed container. • Different method of urine collection are – – FIRST MORNING SAMPLE (conc urine for biochemical analysis, casts and crystals) – RANDOM SAMPLE(chemical screening, microscopic examination) – 24 HOUR URINE SAMPLE (quantitative estimation of proteins, sugars, electrolytes, hormones) – MID STREAM URINE – CLEAN CATCH URINE
  • 4. SAMPLE PRESERVATION • For determination of urea, ammonia, nitrogen and calcium – Hydrochloric acid is used. • For determination of sodium, potassium, chloride, bicarbonate, calcium, phosphorus, urea, ammonia, amino acids, creatinine, proteins, reducing substances and ketone bodies - Thymol is used • For determination of Ascorbic acid – Acetic acid is used • Toluene may also be used as a preservative.
  • 6.
  • 8. VOLUME • Normal volume of urine excreted per day by normal subjects is 1000-2000 ml/day. • Night urine output < 400ml. • Factors which influence the volume excreted : – Intake of fluid, proteins and salt. – Excessive perspiration and strenuous exercise decrease the volume of urine.
  • 9. COLOR • Normal urine is pale yellow (due to presence of pigment urochrome) • When the output of urine is low it appears deep yellow. • Freshly voided urine is clear and transparent. • Long standing urine may become turbid. (Due to precipitation of phosphates)
  • 10.
  • 11. ODOUR • Normal odour of urine is aromatic in nature. • Long standing urine may have an ammoniacal odour (due to decomposition of urea to ammonia).
  • 12. PH • Normal PH of urine ranges from 5.5 – 6.5. • Factors which influence PH : – High protein diet makes the urine more acidic – Diet rich in vegetables and fruits make the urine more alkaline. • Measured using Dipsticks, Litmus Paper or Ph paper.
  • 13.
  • 14. SPECIFIC GRAVITY • Specific gravity indicates the concentrating ability of the kidneys. • Normal range : 1.012 – 1.024 • Measured using urinometer, refractometer, dipsticks. • Sp. Gravity is affected by – 1. Volume of Urine excreted 2. Amount of solids present in the urine.
  • 15. • Urinometer/ Hydrometer consists of a thin stem graduated from 1000 to 1060 corresponding to specific gravities of 1.0 to 1.06. The bulb at the bottom is suitably weighed. Urinometer is calibrated at 60 deg F (15 deg C)
  • 16. METHOD OF DETERMINATION OF SPECIFIC GRAVITY 1. Take sufficient urine in a container. 2. Allow the urinometer to float in urine without touching the sides. 3. Observe the specific gravity reading corresponding to the meniscus of urine. 4. Note the temperature of urine using a thermometer. 5. Temperature correction is done for specific gravity.
  • 17. • TEMPERATURE CORRECTION Observed sp. Gravity = 1010 Observed Room Temperature = 37 deg C Temp of Urine = 15 deg C Corrected Temperature = 37-15/3 = 7 Calibrated Sp. Gravity = 1010 + 7 = 1017 = 1.017
  • 18.
  • 21. CHLORIDE • Normal chloride excreted in 24 hr urine sample is 8 – 15 g/ day(NaCl). INCREASED LEVELS DECREASED LEVELS POLYDIPSIA EXCESSIVE SWEATING, FASTING, DIARRHOEA, VOMITING USE OF DIURETICS DIABETES INSIPIDUS ADDISON’S DISEASE INFECTIONS CUSHING’S SYNDROME
  • 22. • TEST FOR CHLORIDE METHOD – Take 2 ml of urine + 0.5 ml of conc. HNO3 + 1ml AgNo3. OBSERVATION – Curdy white precipitate INFERENCE – Chloride is precipitated as AgCl with Ag No3 in presence of HNO3.
  • 23. SULPHATE • Daily excretion : 1g/ day • Sulphur is derived from catabolism of sulphur containing amino acids. INCREASED LEVELS DECREASED LEVELS HOMOCYSTEINURIA RENAL IMPAIRMENT HIGH PROTEIN DIET CYSTINURIA
  • 24. METHOD – 2ml urine + 2ml Barium Chloride OBSERVATION – White precipitate INFERENCE – Sulphate is precipitated as barium sulphate with barium chloride.
  • 25. CALCIUM • Daily excretion – 200mg/day INCREASED LEVELS DECREASED LEVELS HYPER PARATHYROIDISM TETANY RENAL STONES HYPERVITAMINOSIS D MULTIPLE MYELOMA
  • 26. METHOD 5ml urine + 5 drops of 1% acetic acid + 5ml of potassium oxalate. OBSERVATION : Trace amount of white precipitate INFERENCE : Calcium is precipitated as calcium oxalate in acid medium.
  • 27. INORGANIC PHOSPHATE • Daily excretion : 1gm/ day INCREASED LEVELS DECREASED LEVELS RICKETS / OSTEOMALACIA DIARRHOEA HYPERPARATHYROIDISM NEPHRITIS ACIDOSIS PARATHYROID HYPOFUNCTION PREGNANCY
  • 28. METHOD 5ml urine + few drops of conc HNO3 + a pinch of ammonium molybdate. Warm OBSERVATION Canary yellow precipitate. INFERENCE : Inorganic phosphate is precipitated as canary yellow ammonium phosphomolybdate.
  • 29. AMMONIA • Daily excretion : 0.5-0.8gm/ day • Urinary ammonia is derived from glutamine and other amino acids by kidney. INCREASED LEVELS DECREASED LEVELS INGESTION OF ACID FORMING FOODS ALKALOSIS DIABETIC KETOACIDOSIS NEPHRITIS URINARY TRACT INFECTION
  • 30. METHOD 5ml urine + 2% sodium carbonate (till the red litmus turns blue). Boil. During boiling, hold a piece of moistened red litmus paper at the mouth of the test tube. OBSERVATION : Red litmus turns blue INFERENCE : Ammonia liberated turns red litmus blue.
  • 32. UREA • Daily excretion : 20-30 gm/day • Urea is formed in the liver. • End product of protein metabolism. INCREASED LEVELS DECREASED LEVELS FEVER LIVER DISEASE DIABETES MELLITUS METABOLIC / RESPIRATORY ACIDOSIS INCREASED INTAKE OF PROTEIN NEPHRITIS
  • 33. SODIUM HYPOBROMITE TEST METHOD 2ml urine + Few drops of sodium hypobromite solution. OBSERVATION : Brisk effervescence INFERENCE : Hypobromite decomposes urea to give nitrogen gas.
  • 34. SPECIFIC UREASE TEST METHOD Label two test tubes as ‘TEST’ and ‘CONTROL’ Into TEST : 5ml urea solution + 2ml well mixed urease suspension. Into CONTROL : 5ml urea solution + 2ml urease suspension which is heated strongly. Incubate both TEST and CONTROL at room temperature for 15- 20mins. At the end, add 2 drops of phenolpthalein to both the tubes.
  • 35. OBSERVATION In TEST : Pink Color In CONTROL : No pink color INFERENCE Urease converts urea into ammonia and carbonic acid. Under the Ph of the reaction condition, ammonia and carbonic acid are converted to ammonium carbonate, Ph goes above 9.5. Since the content are alkaline, phenolphthalein gives pink color.
  • 36. URIC ACID • Daily excretion : 0.6-1gm/ day • End product of purine metabolism. • Increased levels of uric acid in urine is URICOSURIA INCREASED LEVELS DECREASED LEVELS LEUKEMIA PURINE FREE DIET CANCERS GOUT
  • 37. PHOSPHOTUNGSTIC ACID REDUCTION TEST METHOD 2ml urine + few drops of phosphotungstic acid + few drops of 20% sodium carbonate. OBSERVATION Blue color is formed INFERENCE Uric acid is a reducing agent in strong alkaline condition. It reduces colorless phosphotungstic acid to tungsten blue.
  • 38. SCHIFF’S TEST METHOD Wet a piece of filter paper with a few drops of ammoniacal silver nitrate solution. Add 1 or 2 drops of uric acid solution on the same paper. OBSERVATION : Black color is formed INFERENCE : Uric acid reduces ammoniacal silver nitrate to metallic silver which is black in color.
  • 39. CREATININE • Daily excretion : 2gm/day in males, 1gm/day in females. • Urinary creatinine is formed from muscle creatine. INCREASED LEVELS DECREASED LEVELS MUSCULAR DISORDERS RENAL FAILURE MYASTHENIA GRAVIS THYROTOXICOSIS STARVATION UNCONTROLLED DIABETES MELLITUS
  • 40. METHOD Label 2 test tubes as ‘test’ and ‘control’. Into Test : 2ml urine + 2ml saturated picric acid+ few drops of 10% NaOH Into Control : 2ml water + 2ml saturated picric acid+ few drops of 10% NaOH OBSERVATION ‘TEST’ – Orange Color, ‘CONTROL’ – Yellow Color INFERENCE Creatinine reacts with alkaline picrate solution to form orange creatinine picrate.
  • 41. ETHEREAL SULPHATE • 100mg of organic sulphate is excreted per day. TEST FOR DETECTING ETHEREAL SULPHATE METHOD 1ml urine + 2ml BaCl2 + 2ml concentrated HCl. Mix and filter. Divide the filtrate into two portions. Boil one and compare with the other (control)
  • 42. OBSERVATION : Trace turbidity compared to that in control (red color may also be seen) INFERENCE : This test is done after removing the inorganic sulphate. Conc Hcl hydrolyses ethereal sulphate to inorganic sulphate which then gives precipitate with BaCl2.
  • 43. UROBILINOGEN • Increased urobilinogen concentration in urine is a sensitive index of liver dysfunction or hemolytic disorder. • Urobilinogen is present in excessive amount in prehepatic and hepatic jaundice. • Urobilinogen is absent in urine in post hepatic jaundice
  • 44. METHOD 5ml of freshly voided urine + 1ml Ehrlich reagent, mix. Let stand for 5 mins. OBSERVATION Red color is seen when viewed through the mouth of the test tube. INFERENCE Urobilinogen reacts with p-dimethyl amino benzaldehyde of the reagent to give red color.