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BIOASSAY OF
VITAMIN D
BIOASSAY OF VITAMIND
INTRODUCTION OF VITAMIN D
– It is a fat soluble vitamin.
– Maintains the adequate levels of Calcium in the body.
– It gives strength to bones.
– Deficiency may cause rickets (softening of bones) in children and
osteomalacia in adults.
– Vitamin D is also made from cholesterol in the presence of sunlight
and also comes from different sources like fish and cod-liver oil.
BIOASSAY OF VITAMIND
TYPES OF VITAMIN D
– Most important type is Vitamin D3 (Cholecalciferol)
– Other type is Vitamin D2 (Ergocalciferol)
– The D2 form is found in foods and in most vitamin preparations and
– supplements.
– Vitamin D3 is the form produced in the body and is also used in
some
– supplements.
– Vitamin D2 and D3 are equally effective.
BIOASSAY OF VITAMIND
BIOASSAY:
– In the biological assay of vitamin D we study the antirachitic activity
i.e. (healing of rickets induced in the lab among the test animals)
which is our activity of interest.
PRINCIPLE:
– The activity of preparation of the antirachitic vitamin (Vit.D) is
determined by comparing its antirachitic activity with that of
standard preparation of the same vitamin by using a suitable method.
BIOASSAY OF VITAMIND
METHODS OF ASSAY OF VITAMIND:
There are three methods of assay of vitamin D.
– CHROMTOGRAPHIC METHOD
– CHEMICAL METHOD
– BIOLOGICAL METHOD
BIOASSAY OF VITAMIND
BIOLOGICALMETHOD:
– The biological assay of vitamin D comprises the recording and
interpretation of observations on groups of rats maintained on
specified dietary regimens throughout specified periods of their lives
whereby the biological response to the preparation under assay is
compared with the response to USP Vitamin D Capsules RS.
USP REFERENCE STANDARDS:
– USP Cholecalciferol RS.
BIOASSAY OF VITAMIND
STANDARD PREPARATION AND UNITS:
– The standard preparation is the Second International Standard for Vitamin D3
established in 1949 and consist of activated crystalline 7-dehydrocholesterol.
– It is supplied in the bottles as a solution in vegetable oil containing 1000 units
per gram (0.025 mg of 7-dehydrocholesterol).
– Validity of the reference standard is 6 months or as specified in the official
monographs.
– A unit is contained in 0.000025 mg of the pure substance.
SAMPLE PREPARATION:
– Dilutions of sample are prepared with vegetable oils.
BIOASSAY OF VITAMIND
PRELIMINARY PERIOD:
– Throughout the preliminary period in the life of a rat, which is not
longer than 30 days,maintain litters of rats under the immediate
supervision or according to directions of, the individual responsible
for the assay.
– During the preliminary period, use a dietary regimen that provides
normal development but is limited in its content of vitamin D, so
that when placed upon the Rachitogenic Diet in the depletion
period the rats develop rickets.
– At the end of the preliminary period, reject any rat that weighs less
than 44 g or more than 60g or that shows evidence of injury, disease,
or anatomical abnormality.
BIOASSAY OF VITAMIND
DEPLETION PERIOD:
– Through the depletion period, which extends from the end of
the preliminary period to the first day of the assay period,
provide each rat ad libitum with the Rachitogenic Diet and
water, and allow access to no other food or dietary
supplement.
BIOASSAY OF VITAMIND
DEPLETION PERIOD:
– RACHITOGENIC DIET
INGREDIENT PARTS BY WEIGHT
Whole yellow corn,
ground
76
Wheat gluten, ground 20
Calcium carbonate 3
Sodium chloride 1
When a chemical analysis of the entire ration shows a Ca:P ratio of less
than 4:1 or more than 5:1, the proportion of calcium carbonate may be
varied to bring the adjusted ratio to a uniform level within this range.
BIOASSAY OF VITAMIND
ASSIGNING RATS TO GROUPS FOR ASSAY PERIOD:
– Consider a litter, suitable for the assay period when individual rats in
the litter show evidence of rickets such as enlarged joints and a
distinctive wobbly, rachitic gait, provided that the depletion period is
not less than 19 or more than 25 days. The presence of rickets may
be established also from the width of the rachitic metaphysis upon
X-ray examination or by applying the Line Test to a leg bone of
one member of each litter.
– Record the weight of each rat, and assign it to a group, in which
each rat will be fed a specified dose of the Reference Standard or of
an assay sample that is under examination for its vitamin D potency.
BIOASSAY OF VITAMIND
ASSIGNING RATS TO GROUPS FOR ASSAY PERIOD:
– For each assay sample provide one or more assay groups
and not less than two standard groups.
– The two standard groups may be used for the concurrent
assay of more than one assay sample.
– Within an interval not exceeding 30 days, complete the
assignment of rats to groups according to a design that
divides litters among the groups, to achieve a complete
balance.
BIOASSAY OF VITAMIND
ASSAY DOSES:
– Select two dosage levels of the USP Cholecalciferol RS, spaced so
that the ratio of the larger to the smaller dose is not less than 1.5 or
more than 2.5.
– Select one or two dosage levels based upon a single assumed
potency for each sample. The dosage levels of the sample are
equivalent to those of the standard or to a mid-level equal to the
square root of the product of the two dosage levels of the standard.
BIOASSAY OF VITAMIND
ASSAY DOSES:
– Select dosage levels such that, when fed to rachitic rats, they are
expected to produce degrees of calcification within the range
specified under the test of data acceptability. Before feeding, the
Reference Standard and/or sample may be diluted with cottonseed
oil, provided that not more than 0.2 mL is fed on any one day. Store
the oil solutions in well-closed bottles, protected from light, at a
temperature not exceeding 10 , and use within 5 weeks.
– Assign one group of rats to each dosage level of the standard and of
the one or more samples.
BIOASSAY OF VITAMIND
ASSAY PERIOD:
– During the assay period, which extends from the end of the
depletion period for a fixed interval of 7 to 10 days, cage each rat
individually and provide it with the Rachitogenic Diet and water.
Supply a Rachitogenic Diet prepared from the same lots of
ingredients to all rats. On the first and on the third (or fourth) day of
the assay period, feed each rat one-half of its total assigned dose.
BIOASSAY OF VITAMIND
ASSAY PERIOD:
– Throughout the assay period, maintain as uniform environmental
conditions as possible for all rats, and exclude exposure to
antirachitic radiations. At the end of a fixed period of 7 to 10 days,
weigh and kill each rat. From those rats that do not weigh less at the
end than at the start of the assay period and that have consumed each
assigned dose within 24 hours of the time it was fed, dissect out one
or more leg bones for examination by the Line Test.
BIOASSAY OF VITAMIND
LINE TEST:
– Remove the proximal end of a tibia or the distal end of a radius, and
clean adhering tissue from it, in any one assay using the same bone
from all animals.
– With a clean, sharp blade cut a median, longitudinal section through
the juncture of the epiphysis and diaphysis at the same place on each
bone.
– Rinse both sections in purified water, immerse immediately in silver
nitrate solution (1 in 50) for 1 minute, and rinse again in purified
water.
BIOASSAY OF VITAMIND
LINE TEST:
– Expose the cut surface of bone,in water, to daylight or another
source of actinic light until the calcified areas develop a clearly
defined stain without marked discoloration of the uncalcified areas.
– The staining procedure may be modified to differentiate more
clearly between calcified and uncalcified areas.
– Score the degree of calcification of the rachitic metaphysis in each
rat, according to a scale that allows the average response to be
plotted as a straight line against the logarithm of the dose.
BIOASSAY OF VITAMIND
ACCEPTABILITY:
– Observations are acceptable for use in calculation of the potency
only from those groups in which two-thirds or more but not less than
7 rats show calcification at least as great as the lowest level and not
greater than the highest level.
– If the average score of the standard group on the high dosage level is
not greater than the average score of the standard group on the low
dosage level, discard the results, and repeat the assay.
BIOASSAY OF VITAMIND
CALCULATION:
– Tabulate the scores (y), listing each litter in a separate row with
treatment groups in columns.Omit any groups that do not meet the
test forAcceptability.
– Equalize the number of observations in the acceptable groups by
disregarding the results on all litters not equally represented in the
groups .
– Total the f scores for each of the treatment groups, where f is the
number of litters, and designate each total as T with subscripts 1and
2 for the low and high dosage levels, respectively.
BIOASSAY OF VITAMIND
CALCULATION:
– Total the f scores for each of the treatment groups, where f is the
number of litters, and designate each total as T with subscripts 1and
2 for the low and high dosage levels, respectively. Compute the
slope b from the sums of ΣT1, i.e. ΣT1, and of ΣT2, i.e., ΣT2, for
the standard and sample, provided the latter is represented at both
dosage levels, from the equation:
b = (ΣT2 – ΣT1) / ifh′
–in which i is the logarithm of the ratio of the high dose to the low
dose and is the same for each preparation, and h′ is the number
of preparations represented by two dosage levels and included in
the calculation of the value of b.
BIOASSAY OF VITAMIND
CALCULATION:
– Compute the logarithm of the relative potency of each specimen
under assay from the equation:
▪ in which each mean score, bar(y)U for the assay sample and
bar(y)S for the Reference Standard, is average of the individual
scores for an intermediate dosage level or of the two means for the
high and the low dosage levels and where Tb =ΣT2 – ΣT1.
BIOASSAY OF VITAMIND
CALCULATION:
– Ta=Ti for the difference in the responses to the Standard and to the
Unknown.
– Ti=sum of products of Tt multiplied by the corresponding factorial
coefficients in each row.
– Convert each observed M′ to its antilogarithm to obtain the relative
potency of the sample. Multiply the relative potency by the assumed
potency of the assay oil in Units per g, adopted at the start of the
assay, to obtain its assayed content of vitamin D in USP Units per g.
bioassay-of-vitamin-d.pptx

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bioassay-of-vitamin-d.pptx

  • 2. BIOASSAY OF VITAMIND INTRODUCTION OF VITAMIN D – It is a fat soluble vitamin. – Maintains the adequate levels of Calcium in the body. – It gives strength to bones. – Deficiency may cause rickets (softening of bones) in children and osteomalacia in adults. – Vitamin D is also made from cholesterol in the presence of sunlight and also comes from different sources like fish and cod-liver oil.
  • 3. BIOASSAY OF VITAMIND TYPES OF VITAMIN D – Most important type is Vitamin D3 (Cholecalciferol) – Other type is Vitamin D2 (Ergocalciferol) – The D2 form is found in foods and in most vitamin preparations and – supplements. – Vitamin D3 is the form produced in the body and is also used in some – supplements. – Vitamin D2 and D3 are equally effective.
  • 4. BIOASSAY OF VITAMIND BIOASSAY: – In the biological assay of vitamin D we study the antirachitic activity i.e. (healing of rickets induced in the lab among the test animals) which is our activity of interest. PRINCIPLE: – The activity of preparation of the antirachitic vitamin (Vit.D) is determined by comparing its antirachitic activity with that of standard preparation of the same vitamin by using a suitable method.
  • 5. BIOASSAY OF VITAMIND METHODS OF ASSAY OF VITAMIND: There are three methods of assay of vitamin D. – CHROMTOGRAPHIC METHOD – CHEMICAL METHOD – BIOLOGICAL METHOD
  • 6. BIOASSAY OF VITAMIND BIOLOGICALMETHOD: – The biological assay of vitamin D comprises the recording and interpretation of observations on groups of rats maintained on specified dietary regimens throughout specified periods of their lives whereby the biological response to the preparation under assay is compared with the response to USP Vitamin D Capsules RS. USP REFERENCE STANDARDS: – USP Cholecalciferol RS.
  • 7. BIOASSAY OF VITAMIND STANDARD PREPARATION AND UNITS: – The standard preparation is the Second International Standard for Vitamin D3 established in 1949 and consist of activated crystalline 7-dehydrocholesterol. – It is supplied in the bottles as a solution in vegetable oil containing 1000 units per gram (0.025 mg of 7-dehydrocholesterol). – Validity of the reference standard is 6 months or as specified in the official monographs. – A unit is contained in 0.000025 mg of the pure substance. SAMPLE PREPARATION: – Dilutions of sample are prepared with vegetable oils.
  • 8. BIOASSAY OF VITAMIND PRELIMINARY PERIOD: – Throughout the preliminary period in the life of a rat, which is not longer than 30 days,maintain litters of rats under the immediate supervision or according to directions of, the individual responsible for the assay. – During the preliminary period, use a dietary regimen that provides normal development but is limited in its content of vitamin D, so that when placed upon the Rachitogenic Diet in the depletion period the rats develop rickets. – At the end of the preliminary period, reject any rat that weighs less than 44 g or more than 60g or that shows evidence of injury, disease, or anatomical abnormality.
  • 9. BIOASSAY OF VITAMIND DEPLETION PERIOD: – Through the depletion period, which extends from the end of the preliminary period to the first day of the assay period, provide each rat ad libitum with the Rachitogenic Diet and water, and allow access to no other food or dietary supplement.
  • 10. BIOASSAY OF VITAMIND DEPLETION PERIOD: – RACHITOGENIC DIET INGREDIENT PARTS BY WEIGHT Whole yellow corn, ground 76 Wheat gluten, ground 20 Calcium carbonate 3 Sodium chloride 1 When a chemical analysis of the entire ration shows a Ca:P ratio of less than 4:1 or more than 5:1, the proportion of calcium carbonate may be varied to bring the adjusted ratio to a uniform level within this range.
  • 11. BIOASSAY OF VITAMIND ASSIGNING RATS TO GROUPS FOR ASSAY PERIOD: – Consider a litter, suitable for the assay period when individual rats in the litter show evidence of rickets such as enlarged joints and a distinctive wobbly, rachitic gait, provided that the depletion period is not less than 19 or more than 25 days. The presence of rickets may be established also from the width of the rachitic metaphysis upon X-ray examination or by applying the Line Test to a leg bone of one member of each litter. – Record the weight of each rat, and assign it to a group, in which each rat will be fed a specified dose of the Reference Standard or of an assay sample that is under examination for its vitamin D potency.
  • 12. BIOASSAY OF VITAMIND ASSIGNING RATS TO GROUPS FOR ASSAY PERIOD: – For each assay sample provide one or more assay groups and not less than two standard groups. – The two standard groups may be used for the concurrent assay of more than one assay sample. – Within an interval not exceeding 30 days, complete the assignment of rats to groups according to a design that divides litters among the groups, to achieve a complete balance.
  • 13. BIOASSAY OF VITAMIND ASSAY DOSES: – Select two dosage levels of the USP Cholecalciferol RS, spaced so that the ratio of the larger to the smaller dose is not less than 1.5 or more than 2.5. – Select one or two dosage levels based upon a single assumed potency for each sample. The dosage levels of the sample are equivalent to those of the standard or to a mid-level equal to the square root of the product of the two dosage levels of the standard.
  • 14. BIOASSAY OF VITAMIND ASSAY DOSES: – Select dosage levels such that, when fed to rachitic rats, they are expected to produce degrees of calcification within the range specified under the test of data acceptability. Before feeding, the Reference Standard and/or sample may be diluted with cottonseed oil, provided that not more than 0.2 mL is fed on any one day. Store the oil solutions in well-closed bottles, protected from light, at a temperature not exceeding 10 , and use within 5 weeks. – Assign one group of rats to each dosage level of the standard and of the one or more samples.
  • 15. BIOASSAY OF VITAMIND ASSAY PERIOD: – During the assay period, which extends from the end of the depletion period for a fixed interval of 7 to 10 days, cage each rat individually and provide it with the Rachitogenic Diet and water. Supply a Rachitogenic Diet prepared from the same lots of ingredients to all rats. On the first and on the third (or fourth) day of the assay period, feed each rat one-half of its total assigned dose.
  • 16. BIOASSAY OF VITAMIND ASSAY PERIOD: – Throughout the assay period, maintain as uniform environmental conditions as possible for all rats, and exclude exposure to antirachitic radiations. At the end of a fixed period of 7 to 10 days, weigh and kill each rat. From those rats that do not weigh less at the end than at the start of the assay period and that have consumed each assigned dose within 24 hours of the time it was fed, dissect out one or more leg bones for examination by the Line Test.
  • 17. BIOASSAY OF VITAMIND LINE TEST: – Remove the proximal end of a tibia or the distal end of a radius, and clean adhering tissue from it, in any one assay using the same bone from all animals. – With a clean, sharp blade cut a median, longitudinal section through the juncture of the epiphysis and diaphysis at the same place on each bone. – Rinse both sections in purified water, immerse immediately in silver nitrate solution (1 in 50) for 1 minute, and rinse again in purified water.
  • 18. BIOASSAY OF VITAMIND LINE TEST: – Expose the cut surface of bone,in water, to daylight or another source of actinic light until the calcified areas develop a clearly defined stain without marked discoloration of the uncalcified areas. – The staining procedure may be modified to differentiate more clearly between calcified and uncalcified areas. – Score the degree of calcification of the rachitic metaphysis in each rat, according to a scale that allows the average response to be plotted as a straight line against the logarithm of the dose.
  • 19. BIOASSAY OF VITAMIND ACCEPTABILITY: – Observations are acceptable for use in calculation of the potency only from those groups in which two-thirds or more but not less than 7 rats show calcification at least as great as the lowest level and not greater than the highest level. – If the average score of the standard group on the high dosage level is not greater than the average score of the standard group on the low dosage level, discard the results, and repeat the assay.
  • 20. BIOASSAY OF VITAMIND CALCULATION: – Tabulate the scores (y), listing each litter in a separate row with treatment groups in columns.Omit any groups that do not meet the test forAcceptability. – Equalize the number of observations in the acceptable groups by disregarding the results on all litters not equally represented in the groups . – Total the f scores for each of the treatment groups, where f is the number of litters, and designate each total as T with subscripts 1and 2 for the low and high dosage levels, respectively.
  • 21. BIOASSAY OF VITAMIND CALCULATION: – Total the f scores for each of the treatment groups, where f is the number of litters, and designate each total as T with subscripts 1and 2 for the low and high dosage levels, respectively. Compute the slope b from the sums of ΣT1, i.e. ΣT1, and of ΣT2, i.e., ΣT2, for the standard and sample, provided the latter is represented at both dosage levels, from the equation: b = (ΣT2 – ΣT1) / ifh′ –in which i is the logarithm of the ratio of the high dose to the low dose and is the same for each preparation, and h′ is the number of preparations represented by two dosage levels and included in the calculation of the value of b.
  • 22. BIOASSAY OF VITAMIND CALCULATION: – Compute the logarithm of the relative potency of each specimen under assay from the equation: ▪ in which each mean score, bar(y)U for the assay sample and bar(y)S for the Reference Standard, is average of the individual scores for an intermediate dosage level or of the two means for the high and the low dosage levels and where Tb =ΣT2 – ΣT1.
  • 23. BIOASSAY OF VITAMIND CALCULATION: – Ta=Ti for the difference in the responses to the Standard and to the Unknown. – Ti=sum of products of Tt multiplied by the corresponding factorial coefficients in each row. – Convert each observed M′ to its antilogarithm to obtain the relative potency of the sample. Multiply the relative potency by the assumed potency of the assay oil in Units per g, adopted at the start of the assay, to obtain its assayed content of vitamin D in USP Units per g.