Glofil-125

Glofil-125 Manufacturers

• Qol Medical
  

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  Glofil-125 | Qol Medical

  

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  Dosage

  The suggested dose range employed in the average patient (70 kg) is as follows:
      Continuous intravenous infusion: 20 to 100 μCi (0.74-3.7 megabecquerels) (Sigman, et al (1) method).
      Single intravenous injection: 10 to 30 μCi (0.37-1.11 megabecquerels) (Cohen, et al (2) method).
      The patient dose should be measured by a suitable radioactivity calibration system immediately prior to administration.
  

  Technique Continuous intravenous infusion

  Sigman (1) method

  I. Preparation:

  Adequate diuresis (a urine flow exceeding 3 mL/min.) is established, preferably by an oral water load of 1,500 mL two hours prior to the beginning of the clearance study. It is not necessary to withhold breakfast or admit the patient the night before.

  II. Procedure:

  After the establishment of adequate diuresis, a number 14 or 16 French Foley catheter is aseptically inserted into the bladder. An intravenous infusion of Lactated Ringer’s (Hartmann’s) solution is started in each arm, one to maintain a site for injection of the GLOFIL®-125, the other to serve as a site for serial withdrawal of blood. A two-way stopcock connects the needle and intravenous tubing of each arm. The dose is equally divided into (1) an intravenous priming dose to be injected as is and (2) a sustaining dose to be diluted in 30 to 60 mL of isotonic sodium chloride, depending on how many collection periods are anticipated. The priming dose is slowly injected into one arm. This is immediately followed by infusion of the sustaining solution through the same site, usually at the rate of 0.5 mL/min., by means of an automatic pump. During this infusion, the Lactated Ringer’s solution in the same arm is discontinued, and 40 to 45 minutes are allowed for equilibration in order to reach a state of constant plasma concentration of radioactivity. After attaining equilibrium, consecutive 15 minute collection periods are started. From the arm opposite the injection site, 5 mL of blood (allowing duplicate plasma counting volumes) is drawn six minutes prior to the midpoint of each collection period, placed in heparinized tubes, mixed, and centrifuged. The blood samples may be obtained through the two-way stopcock after discarding the first 30 mL aspirated into the syringe. This 30 mL contains the contents of the tubing, including infusion fluid, and must be cleared in order to obtain an undiluted blood sample. If desired, this step may be eliminated and blood samples obtained by direct venipuncture. During each collection period, total urine must be accurately collected and the volume accurately measured. Three such consecutive collection periods are sufficient for most clinical studies.

  III. Clearance Calculations:

  Aliquots (1 mL each) of plasma and urine from each collection period are counted in a standard gamma-ray scintillation well detector. All counts are corrected for background activity. Glomerular filtration rate is calculated by the formula C=UV/P, in which:
        C = glomerular filtration rate in mL/min
        U= urinary concentration of radioactivity in net counts/min/mL
        V= urinary flow rate in mL/min
        P = plasma concentration of radioactivity in net counts/min/mL Average glomerular filtration rate (GFR) is calculated from the rates for the individual collection periods. GFR can be expressed in terms of body weight (mL/min/kg) or body surface area (mL/min/m2). Unilateral glomerular filtration rates can be determined by the same technique by utilizing ureteral catheterization. Single intravenous injection

  Cohen (2) method:

  The method of Cohen, et al (2) requires little preparation, few and small blood samples, no bladder catheterization, and no constant intravenous infusion. It is simple to perform, rapid, and utilizes equipment which is readily available in most modern laboratories.

  I. Preparation:

  Lugol's solution, 3 drops orally, three times a day, is administered for one or two days prior to the test.

  No diet or water restriction is necessary.

  Oral water load is begun one hour before starting the test. Start with 20 mL/kg and force any clear liquids (unless contraindicated) until the test is complete.

  II. Procedure: Record actual times for the collection of the blood and urine samples.

  Empty the bladder and label the urine Urine control. Inject 10-30 μCi GLOFIL®-125 intravenously; wait 30 to 60 minutes. Collect the entire urine and label Urine discard. Draw 4 to 5 mL of blood into a heparinized syringe. Label Plasma #1. After another 30 to 60 minutes, collect the entire urine and label Urine #1. Immediately draw another blood specimen. Label Plasma #2. After final 30 to 60 minute wait, collect the urine. Label Urine #2. Draw the last blood specimen immediately. Label Plasma #3.

  III. Clearance Calculations:

  Radioactivity of one mL aliquots of both urine and plasma are determined using a well-scintillation detector with a single channel pulse-height analyzer. Sufficiently reproducible counts are usually obtained with time settings of 2 minutes for urine samples and 20 minutes for the plasma samples. Calculations of the clearance rates are made by using the formula:(1)

         C = UV/P + 1.73/SA    where

  C = glomerular filtration rate in mL/min/1.73 m2
  U = urine radioactivity in counts/min/mL
  V = urine flow rate in mL/min
  P= mean plasma radioactivity in counts/min/mL
  SA= body surface area in m2
  

  Radiation Dosimetry

  The estimated absorbed radiation doses to an average (70 kg) patient from an intravenous dose of 100 μCi (3.7 megabecquerels) of GLOFIL®-125 are shown in Table 4. Calculations assume that there is 1% free iodide in the preparation and that the thyroid uptake of the iodine is 25%.

  Table 4. Absorbed Radiation Doses* * Data supplied by Oak Ridge Associated Universities, Radiopharmaceutical Internal Dose Information Center, Oak Ridge, TN, 1988. Absorbed radiation doses for 100 µCi (3.7 megabecquerels) 2 hour bladder voiding interval 4.8 hour bladder voiding interval Organ rads mGy rads mGy Lower Large Intestine Wall 0.00065 0.0065 0.0012 0.012 Small Intestine 0.00044 0.0044 0.00050 0.0050 Stomach 0.00047 0.0047 0.00047 0.0047 Upper Large Intestine Wall 0.00040 0.0040 0.00044 0.0044 Kidneys 0.0064 0.064 0.0064 0.064 Liver 0.0018 0.018 0.0018 0.018 Ovaries 0.00054 0.0054 0.00085 0.0085 Testes 0.0019 0.019 0.0021 0.021 Urinary Bladder Wall 0.022 0.22 0.06 0.6 Red Marrow 0.00033 0.0033 0.00034 0.0034 Thyroid 0.78 7.8 0.78 7.8 Total Body 0.00096 0.0096 0.0011 0.011 Visual Inspection

  Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

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• Iso-tex Diagnostics, Inc.
  

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  Glofil-125 | Iso-tex Diagnostics, Inc.

  

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  The suggested dose range employed in the average patient (70 kg) is as follows:

      Continuous intravenous infusion: 20 to 100 μCi (0.74-3.7 megabecquerels)

  (Sigman, et al (1) method).

      Single intravenous injection: 10 to 30 µCi (0.37-1.11 megabecquerels)

  (Cohen, et al (2) method).

        The patient dose should be measured by a suitable radioactivity calibration system

  immediately prior to administration.

  Technique
  Continuous intravenous infusion

  Sigman1 method

  I. Preparation:

  1. Adequate diuresis (a urine flow exceeding 3 mL/min.) is established, preferably

     by an oral water load of 1,500 mL two hours prior to the beginning of the

     clearance study.

  2. It is not necessary to withhold breakfast or admit the patient the night before.

  II. Procedure:

  1. After the establishment of adequate diuresis, a number 14 or 16 French Foley

      catheter is aseptically inserted into the bladder.

  2. An intravenous infusion of Lactated Ringers (Hartmanns) solution is started

      in each arm, one to maintain a site for injection of the GLOFIL-125, the other

      to serve as a site for serial withdrawal of blood. A two-way stopcock connects

      the needle and intravenous tubing of each arm.

  3. The dose is equally divided into (1) an intravenous priming dose to be injected

      as is and (2) a sustaining dose to be diluted in 30 to 60 mL of isotonic sodium

      chloride, depending on how many collection periods are anticipated.

  4. The priming dose is slowly injected into one arm. This is immediately followed

      by infusion of the sustaining solution through the same site, usually at the rate of

      0.5 mL/min., by means of an automatic pump. During this infusion, the Lactated

      Ringers solution in the same arm is discontinued, and 40 to 45 minutes are

      allowed for equilibration in order to reach a state of constant plasma

      concentration of radioactivity.

  5. After attaining equilibrium, consecutive 15 minute collection periods

     are started. From the arm opposite the injection site, 5 mL of blood (allowing

     duplicate plasma counting volumes) is drawn six minutes prior to the

     midpoint of each collection period, placed in heparinized tubes, mixed, and

     centrifuged. The blood samples may be obtained through the two-way

     stopcock after discarding the first 30 mL aspirated into the syringe. This

     30 mL contains the contents of the tubing, including infusion fluid, and must

     be cleared in order to obtain an undiluted blood sample. If desired, this step

     may be eliminated and blood samples obtained by direct venipuncture.

  6. During each collection period, total urine must be accurately collected and

      the volume accurately measured. Three such consecutive collection periods

      are sufficient for most clinical studies.

  
  III. Clearance Calculations:

  1. Aliquots (1 mL each) of plasma and urine from each collection period are

      counted in a standard gamma-ray scintillation well detector.

  2. All counts are corrected for background activity.

  3. Glomerular filtration rate is calculated by the formula C=UV/P, in which:

                     C = glomerular filtration rate in mL/min
                     U= urinary concentration of radioactivity in net counts/min/mL
                     V= urinary flow rate in mL/min
                     P = plasma concentration of radioactivity in net counts/min/mL

  
  4. Average glomerular filtration rate (GFR) is calculated from the rates for the

      individual collection periods. GFR can be expressed in terms of body

      weight (mL/min/kg) or body surface area (mL/min/m2).

  5. Unilateral glomerular filtration rates can be determined by the same technique

      by utilizing ureteral catheterization.

  
  Single intravenous injection

  Cohen2 method:

  The method of Cohen, et al2 requires little preparation, few and small blood samples,

  no bladder catheterization, and no constant intravenous infusion. It is simple to

  perform, rapid, and utilizes equipment which is readily available in most modern

  laboratories.

  I. Preparation:

  1. Lugol's solution, 3 drops orally, three times a day, is administered for one or

     two days prior to the test.

     No diet or water restriction is necessary.

  2. Oral water load is begun one hour before starting the test. Start with 20 mL/kg

      and force any clear liquids (unless contraindicated) until the test is complete.

  II. Procedure: Record actual times for the collection of the blood and urine samples.

  1. Empty the bladder and label the urine Urine control.

  2. Inject 10-30 µCi GLOFIL-125 intravenously; wait 30 to 60 minutes.

  3. Collect the entire urine and label Urine discard.

  4. Draw 4 to 5 mL of blood into a heparinized syringe. Label Plasma #1.

  5. After another 30 to 60 minutes, collect the entire urine and label Urine #1.

  6. Immediately draw another blood specimen. Label Plasma #2.

  7. After final 30 to 60 minute wait, collect the urine. Label Urine #2.

  8. Draw the last blood specimen immediately. Label Plasma #3.

  
  III. Clearance Calculations:

  1. Radioactivity of one mL aliquots of both urine and plasma are determined

      using a well-scintillation detector with a single channel pulse-height analyzer.

      Sufficiently reproducible counts are usually obtained with time settings of 2

      minutes for urine samples and 20 minutes for the plasma samples. Calculations

      of the clearance rates are made by using the formula:(1)

  C = C = UV/P + 1.73/SA where

  C = glomerular filtration rate in mL/min/1.73 m2

  U = urine radioactivity in counts/min/mL

  V = urine flow rate in mL/min

  P= mean plasma radioactivity in counts/min/mL

  SA= body surface area in m2

  
  Radiation Dosimetry
  The estimated absorbed radiation doses to an average (70 kg) patient from an

  intravenous dose of 100 µCi (3.7 megabecquerels) of GLOFIL-125 are shown in

  Table 4. Calculations assume that there is 1% free iodide in the preparation and that

  the thyroid uptake of the iodine is 25%.

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