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Fundamentals of
Dermal Exposure
Thomas D. Klingner
Colormetric Laboratories, Inc.
Understanding the Skin

  The skin is the largest organ of the body
  (20,000 cm2).
  The skin has two primary functions:
      1. It serves as a physical barrier to
  infectious agents.
      2. It retains moisture in the body.
Structure of the Skin

            The skin is often conceived as
             a brick and mortar structure. The
            interstitial lipids bind the
            corneocytes together and form a
            lipophilic pathway for chemical
            absorption into the Stratum
            Corneum.
Stratum Corneum:
the initial barrier to dermal
exposure

   Comprised of layers of keratin (dead skin
   cells) held together by a lipid matrix
   (0.01-0.06 mm thick).
   Membrane coating granules (MCG)
   produce fatty oils that retain the body’s
   moisture.
The Chemistry of
Exposure
Three Basic Principles

Oil and water don’t mix
First Principle
                         Like Dissolves Like

 - chemicals will migrate from a low solubility toward a high
    solubility environment.

 This principle introduces the important concept of the octanol water partition
    coefficient or Ko/w. Chemical solubility is characterized based on how
    soluble a chemical is in each phase of a 50:50 water and octanol mixture.
    Water (hydrophillic) and octanol (lipophillic) lie at opposite ends of the
    solubility spectrum.

 The preferential solubility in either phase determines where chemicals lie in
    the solubility spectrum.
Second Principle

       Concentration gradient (Ficks Law)

Chemicals will diffuse from a high concentration toward a lower
concentration.

This occurs in air and in the skin. Spilled solvent evaporates
contaminating the air in a room to saturation. A drop of chemical on the
skin will permeate into the skin lipids until the skins solvent capacity is
saturated. This is the skin depot capacity.
Third Principle
                    Molecular Size

The lower the chemical molecular weight (MW) the more
  rapid diffusion will proceed. Large molecules will
  penetrate slowly if at all.
Small grains of sand will quickly sift through a series of
  screens where large grains will pass through slowly or
  not at all. The skins corneocytes, arranged in the brick
  and mortar structure, slow or prevent absorption of
  large molecules.
The Process of Dermal
Exposure
 Step 1 - initial dermal uptake
   The skin’s primary function is to retain water, therefore,
   the skin is an excellent barrier to water soluble
   chemicals.
   Oil soluble chemicals are readily soluble in the skin’s
   lipids and rapidly partition into the stratum corneum.

 The K o/w lipid solubility of the chemical determines how
   rapidly the chemical is absorbed into the skin. As the
   skin’s solvent capacity approaches saturation, the total
   exposed area of the skin determines the total
   exposure.
A chemical’s ability to penetrate the outer barrier of the
skin (stratum corneum) depends on two physiochemical
properties.




 Increasing molecular weight and size is a conflicting factor in skin
 penetration. Thus, where compounds may become more lipophilic
 with increasing size, the ability of these compounds to diffuse
 through the intercellular spaces is reduced.
 With solubility remaining constant, a low molecular weight chemical
 (L.M.W. 100) will penetrate 100x to 1000x faster than a high
 molecular chemical (H.M.W. 400+).
Log Kp = 2.72 + 0.71 log K o/w -0.0061 MW Potts and Guy, USEPA 1992
Chemical                     CAS No.    MW           Log K o/w    Kp (cm/hr)            This equation is used by the EPA
Nitrophenol, 4-
             4-                100027        139.1         1.91                6.1E-3
                                                                               6.1E-    to predict skin uptake or the
                                                                                        permeation constant Kp of toxic
Nitrophenol, 4-amino-2-
             4- amino-         119346        154.1         0.96                1.1E-3
                                                                               1.1E-
                                                                                        chemicals.
Nitropropane,2                  79469         110          0.55                1.0E-3
                                                                               1.0E-
Nitroso-di-n-butylamine,n-
Nitroso- di- butylamine,n-     924163        158.2         1.92                4.8E-3
                                                                               4.8E-    As the solubility increases (higher
                                                                                        K o/w) Kp also increases. As the
Nitroso-N-ethylurea,n-
Nitroso- ethylurea,n-          759739        117.1         0.23           540.0E-6
                                                                          540.0E-
                                                                                        MW increases the Kp decreases.
Nitroso-N-methylurea,n-
Nitroso- methylurea,n-         684935        103.1        -0.03           430.0E-6
                                                                          430.0E-
Nitrosodiethanolamine,n-
Nitrosodiethanolamine,n-      1116547         134         -1.58            22.0E-6
                                                                           22.0E-       Compare: Phenanthrene log K
                                                                                        o/w 4.57, MW 178.2 Kp is 0.27
Nitrosodiethylamine,n-
Nitrosodiethylamine,n-          55185          88          0.48                1.2E-3
                                                                               1.2E-
                                                                                        cm/hr. Nitrosodiethanolamine,
Nitrosodiphenylamine,p-
Nitrosodiphenylamine,p-        156105        198.2          3.5            36.0E-3
                                                                           36.0E-       n- log K o/w -1.58 MW 134.0 Kp
Nitrosomethylvinylamine,n-
Nitrosomethylvinylamine,n-    4549400         86.1           0            570.0E-6
                                                                          570.0E-       0.000022 cm/hr.
                                                                                                  cm/hr.
Nitrosomorpholine, n-
                   n-           59892        116.1        -0.44           180.0E-6
                                                                          180.0E-
                                                                                        The Phenanthrene will penetrate
Nitrosonornicotine,n-
Nitrosonornicotine,n-        16543558        177.2         0.03           170.0E-6
                                                                          170.0E-       the skin1000x faster.
Nitrosopiperidine, n-
                   n-          100754        350.3         0.36            25.0E-6
                                                                           25.0E-
Nonanol                        143088         144          3.47            73.0E-3
                                                                           73.0E-
Octanol                        111875         130          2.97            39.0E-3
                                                                           39.0E-
Parathion                       56382         291          3.83            17.0E-3
                                                                           17.0E-
PCB-chlorobiphenyl, 4-
PCB-                4-        2051629         292           6.5            1.3E+0
PCB-hexachlorobiphenyl
PCB-                         26601649         361          6.72           710.0E-3
                                                                          710.0E-
Pentachloronitrobenzene         82688        295.3         4.64            59.0E-3
                                                                           59.0E-
Pentachloropenol                87865        266.4         5.86           650.0E-3
                                                                          650.0E-
Pentanol                        71410          88          1.56                7.1E-3
                                                                               7.1E-
Pentanone, 4-methyl-2-
           4- methyl-          108101         100          1.19                3.3E-3
                                                                               3.3E-
Phenanthrene                    85018        178.2         4.57           270.0E-3
                                                                          270.0E-
Phenol                         108952          94          1.46                5.5E-3
                                                                               5.5E-
Step 2 - Systemic Uptake
Chemical Warfare Agents (CWA’s) have a low molecular weight,
  are moderately lipophillic and highly toxic. To be effective
  systemic toxins CWA’s must also demonstrate some degree of
  water solubility i.e. midrange K o/w, to partition into the blood
  stream.
More lipophilic chemicals rapidly saturate the stratum corneum
  lipids capacity, but slowly partition into the hydrophillic
  bloodstream limiting systemic toxicity. As long as the skin
  remains dry, lipophilic chemicals remain more soluble in the skin
  lipids limiting systemic absorption.
The Skin Depot – wash-in
effect
Washing with soap and water hydrates the skin and may worsen exposures to lipophilic
chemicals. The chart below shows what happened after washing with soap and water at the
24 hr. mark for four exposures.
The irony – soap and water is effective for water soluble chemicals. Water soluble chemicals
tend to be poorly absorbed via healthy and intact skin.
Washing the skin with soap and water or solvents may actually enhance absorption of
 lipophilic chemicals. R. Moody, Toxic. In Vitro,8; 1225 1994

                      0.07
                      0.06
                      0.05                                                       1
             %      0.04                                                         2
         Permeation 0.03                                                         3
                      0.02                                                       4
                      0.01
                         0
                             4 8 12 16 20 24 26 28 32 36 40 44 48
                                            Time (Hrs.)

    DDT was applied to the skin and the percentage of permeation into the bloodstream
    measured. The excess lipophillic DDT (K o/w 6.36) was washed from the skin after 24 hrs.
    and the percentage penetrating the bloodstream increased by 5 fold.
Comparison of enhancement effect of decontamination solution on rate of
                 percutaneous penetration of diethylmalonate remaining in skin samples that
   300           were decontaminated 1 hour post exposure.           Loke et. al, 1999


   250                       control                    Decontamination                Mean enhancement
                                                        in
   200                       1/4 hr. decon                 Solution                    penetration rate %
                                                        2% (w/v)anionic surfactant                141.19
                                                         2% (w/v)         cationic surfactant      138.03
   150                       1/2 hr. decon
                                                        2% (w/v)          non-ionic surfactant     135.32
                                                        de-ionized water      hypotonic solution 105.55
   100                       1 hr. decon
                                                        0.9% (w/v)saline    isotonic solution      71.27
                                                        9 % (w/v) saline hypertonic solution 23.17
   50

   0
               1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25



Time is the crucial factor in decontamination.
Diethylmalonate, a nerve agent simulant, was washed from the skin after increasing time intervals of
¼ to ½ hrs. After ½ hr. decontamination with soap and water or water increased systemic absorption
vs. the control (no decontamination). Nerve agents require a certain effective dose to be absorbed. It
is possible that controls may have lived and those decontaminated at 1 hr. would have died.
Solubility is the key.




  Note: The EPA “Recognition and Management Pesticide Poisoning” 1999 recommends washing with soap and water.


The pesticide Alachlor that is lipophillic is supplied in a solvent concentrate and applied in a diluted
water emulsion spray. As the Alachlor was, diluted from 20 parts water to 80 parts water, the
concentration was 4x lower but the systemic absorption increased 4x. Alachlor remained more soluble in
the more concentrated emulsion than in the skin.
Evaluation of compounds as barriers to dermal penetration of organophosphates using
 acetylcholinesterase inhibition.                    Olson, Carl T. et al Toxicity Letters, 55(1991) 325-334




 Ed50 Values and 95% confidence limits for acetylcholinesterase inhibition.
 OP compound                Time after exposure (min.)                                      Ed50 (95% confidence limits)
                           No barrier                                                       PEG 540 barrier
                           (mg/kg)                                                          (mg/kg)
 TGD                       30           1.90 (1.44-2.52)                                    1915 (0.05-8 X 107)
                           60           1.01 (0.81-1.26)                                    33.3 (11.0-100)
                           120          0.94 (0.710-01.23)                                  7.89 (5.44-11.4)
                           240          1.06 (0.83-1.34)                                    6.28 (4.96-7.95)
 GD                        30           0.68 (0.52-0.89)                                    14.4 (5.43-38.4)
                           60           0.56 (0.40-0.78)                                    6.17 (3.82-9.97)
                           120          0.54 (0.39-0.75)                                    4.39 (2.67-7.22)
                           240          0.49 (0.33-0.73)                                    1.76 (0.75-4.12)
 VX                        30           0.131 (0.031-0.549)                                 167 (0.9 x 103)
                           60           0.026 (0.017-0.040)                                 18.2 (0.055-6002)
                           120          0.012 (0.010-0.014)                                 3.38 (0.104-110)
                           240          0.007 (0.005-0.008)                                 10 (0.043-103)

A barrier of HMW polyethelene glycol (MW 540) was applied to the skin of rats before exposure to various CWA’s. The
 CWA was more soluble in PEG barrier than the skin and systemic absorption was slower. For example, for VX to
achieve systemic toxicity in 30 minutes, .131 mg/Kg was effective with no barrier. With PEG, .167 mg/kg was applied
to achieve the same level of toxicity. An increase of 1000x.
Like Dissolves Like
60%
50%                                                                                     4 hours
40%
30%
20%                                                                                     8 hours
10%
 0%

           water          50%                 polyglycol               corn oil
                          soap                (D-TAM)
% of MDI dose remaining in skin

   This study compared the ability of water, 50% soap and water, a polyglycol based cleanser
    and corn oil (control) to minimize absorption of isocyanate (MDI) into the skin. The data
    show that corn oil and the polyglycol based cleanser are more effective than water or soap
    and water in limiting the transfer of MDI into the skin. These results are consistent with the
    miscibility of MDI in corn oil and polyglycol.

Ronald C. Wester et al. In Vivo Evaluation of MDI Skin Decontamination Procedures. Presented
   September 1998, Polyurethane Expo.

Even after 8 hours, less than 10% of the applied dose entered the skin when decontaminated
   with non-aqueous HMW solvents. Water alone drove over 50% of the dose into the skin.
Solubility in Skin Decontamination Solvents
             A Rational Approach to Skin Decontamination,T. Buckley, Johns Hopkins Univ., M.
                Dellarco, USEPA, T. Klingner, CLI Laboratories, AIHA Conference 2001
             Comparison of Saturation
             100%
             90%
             80%                                                                                   Water
             70%                                                                                   10% soap
 Solublity




             60%
                                                                                                   D-TAM
             50%
             40%                                                                                   Glycol
             30%
                                                                                                   D-TAM Oil
             20%
             10%
             0%
                  methylenedianiline chlorpyrifos pentachlorophenol                 benzo-a-pyrene
                   log ko/w1.59**    log k o/w 4.7*** log k o/w 5.86**             log k o/w 6.5**
             *Relative to solvent with maximum solubility; maximum solubility was not always achieved
             ** solubility determined spectrophotometrically
             ***solubility determined by visual inspection of mass dissolving in solution
Premise: The more soluble the contaminant is in the decontamination agent the more effective
the decontamination process.
Skin Decontamination Selection Guide
                                                   for

   D-TAM Skin Cleanser and D-TAM Safe Solvent
 Log K o/w             0                                            3.5                               8.0
Soap and Water                          D-TAM™       Skin                           D-TAM™ Safe
                                        Cleanser (Peg Based)                        Solvent (plant oil based)

                                                                                            TDI
                     Phenol                                    Aldrin               Benzo-a-pyrene
Formaldehyde                             Aniline
                                        Di-nitro-Toluene                                     MDI
                                                               Lindane              Penatchlorphenol
Propanol
                     Acetone                                                               PCBs
                                        Trinitrobenzene
                                                               Malathion                   DDT
Hydrazine                               Dichlorethane
                                                                                    Diesel Oil

By adjusting the K o/w of the HMW D-TAM formulation effective decontamination of chemicals across the
entire solubility spectrum can be achieved.
Ineffective Decontamination:
                              A False Sense of Security
 Organophosphate poisoning from wearing a laundered
 uniform previously contaminated with parathion.
                                                   Clifford, N.J., Nies, A.S., JAMA 12, 1, 89 Vol 262 No 21


 Case 1                              Case 2                                  Case 3
 25 year old                         23 year old                             18 year old
This worker was accidentally       This worker collapsed at work           This worker also collapsed after wearing
sprayed with parathion during      after receiving the freshly laundered   the re-laundered uniform. The connection
the manufacturing process. The     uniform that was previously             was made with the earlier contamination and
contaminated uniform was removed   contaminated. There was no              it was destroyed. No further incidences
and inadvertently sent to be       obvious exposure connected to this      occurred. Patient recovered in hospital.
laundered rather than destroyed.   and the uniform was removed
Patient recovered in hospital.     and sent to be laundered. Patient
                                   recovered in hospital.
Re-use of PPC; Potential
Exposure to Pesticides
Garrod, Phillips, Pemberton, Amer. Occup. Hyg., Vol 45, No.1, 2001




       38% of agricultural workers using unapproved
       disposable gloves showed positive exposure to hands.
       95% of workers who re-used chemical protective
       gloves (protection factor 20X) had positive exposure.

    The re-use of contaminated PPC can result in significant
      unanticipated exposure. Proper decontamination of PPC can
      prevent these exposures.
“It is better to learn from someone
  else’s mistakes rather than your
  own.” Dear Ole Dad
   • 25% of medical personnel treating victims
   of the Tokyo sarin terrorist attack were
   themselves acutely poisoned.

“Good ideas are not adopted
automatically. They must be driven into
practice with courageous impatience.”
Admiral Hyman Rickover

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Klingner

  • 1. Fundamentals of Dermal Exposure Thomas D. Klingner Colormetric Laboratories, Inc.
  • 2. Understanding the Skin The skin is the largest organ of the body (20,000 cm2). The skin has two primary functions: 1. It serves as a physical barrier to infectious agents. 2. It retains moisture in the body.
  • 3. Structure of the Skin The skin is often conceived as a brick and mortar structure. The interstitial lipids bind the corneocytes together and form a lipophilic pathway for chemical absorption into the Stratum Corneum.
  • 4. Stratum Corneum: the initial barrier to dermal exposure Comprised of layers of keratin (dead skin cells) held together by a lipid matrix (0.01-0.06 mm thick). Membrane coating granules (MCG) produce fatty oils that retain the body’s moisture.
  • 5. The Chemistry of Exposure Three Basic Principles Oil and water don’t mix
  • 6. First Principle Like Dissolves Like - chemicals will migrate from a low solubility toward a high solubility environment. This principle introduces the important concept of the octanol water partition coefficient or Ko/w. Chemical solubility is characterized based on how soluble a chemical is in each phase of a 50:50 water and octanol mixture. Water (hydrophillic) and octanol (lipophillic) lie at opposite ends of the solubility spectrum. The preferential solubility in either phase determines where chemicals lie in the solubility spectrum.
  • 7. Second Principle Concentration gradient (Ficks Law) Chemicals will diffuse from a high concentration toward a lower concentration. This occurs in air and in the skin. Spilled solvent evaporates contaminating the air in a room to saturation. A drop of chemical on the skin will permeate into the skin lipids until the skins solvent capacity is saturated. This is the skin depot capacity.
  • 8. Third Principle Molecular Size The lower the chemical molecular weight (MW) the more rapid diffusion will proceed. Large molecules will penetrate slowly if at all. Small grains of sand will quickly sift through a series of screens where large grains will pass through slowly or not at all. The skins corneocytes, arranged in the brick and mortar structure, slow or prevent absorption of large molecules.
  • 9. The Process of Dermal Exposure Step 1 - initial dermal uptake The skin’s primary function is to retain water, therefore, the skin is an excellent barrier to water soluble chemicals. Oil soluble chemicals are readily soluble in the skin’s lipids and rapidly partition into the stratum corneum. The K o/w lipid solubility of the chemical determines how rapidly the chemical is absorbed into the skin. As the skin’s solvent capacity approaches saturation, the total exposed area of the skin determines the total exposure.
  • 10. A chemical’s ability to penetrate the outer barrier of the skin (stratum corneum) depends on two physiochemical properties. Increasing molecular weight and size is a conflicting factor in skin penetration. Thus, where compounds may become more lipophilic with increasing size, the ability of these compounds to diffuse through the intercellular spaces is reduced. With solubility remaining constant, a low molecular weight chemical (L.M.W. 100) will penetrate 100x to 1000x faster than a high molecular chemical (H.M.W. 400+).
  • 11. Log Kp = 2.72 + 0.71 log K o/w -0.0061 MW Potts and Guy, USEPA 1992 Chemical CAS No. MW Log K o/w Kp (cm/hr) This equation is used by the EPA Nitrophenol, 4- 4- 100027 139.1 1.91 6.1E-3 6.1E- to predict skin uptake or the permeation constant Kp of toxic Nitrophenol, 4-amino-2- 4- amino- 119346 154.1 0.96 1.1E-3 1.1E- chemicals. Nitropropane,2 79469 110 0.55 1.0E-3 1.0E- Nitroso-di-n-butylamine,n- Nitroso- di- butylamine,n- 924163 158.2 1.92 4.8E-3 4.8E- As the solubility increases (higher K o/w) Kp also increases. As the Nitroso-N-ethylurea,n- Nitroso- ethylurea,n- 759739 117.1 0.23 540.0E-6 540.0E- MW increases the Kp decreases. Nitroso-N-methylurea,n- Nitroso- methylurea,n- 684935 103.1 -0.03 430.0E-6 430.0E- Nitrosodiethanolamine,n- Nitrosodiethanolamine,n- 1116547 134 -1.58 22.0E-6 22.0E- Compare: Phenanthrene log K o/w 4.57, MW 178.2 Kp is 0.27 Nitrosodiethylamine,n- Nitrosodiethylamine,n- 55185 88 0.48 1.2E-3 1.2E- cm/hr. Nitrosodiethanolamine, Nitrosodiphenylamine,p- Nitrosodiphenylamine,p- 156105 198.2 3.5 36.0E-3 36.0E- n- log K o/w -1.58 MW 134.0 Kp Nitrosomethylvinylamine,n- Nitrosomethylvinylamine,n- 4549400 86.1 0 570.0E-6 570.0E- 0.000022 cm/hr. cm/hr. Nitrosomorpholine, n- n- 59892 116.1 -0.44 180.0E-6 180.0E- The Phenanthrene will penetrate Nitrosonornicotine,n- Nitrosonornicotine,n- 16543558 177.2 0.03 170.0E-6 170.0E- the skin1000x faster. Nitrosopiperidine, n- n- 100754 350.3 0.36 25.0E-6 25.0E- Nonanol 143088 144 3.47 73.0E-3 73.0E- Octanol 111875 130 2.97 39.0E-3 39.0E- Parathion 56382 291 3.83 17.0E-3 17.0E- PCB-chlorobiphenyl, 4- PCB- 4- 2051629 292 6.5 1.3E+0 PCB-hexachlorobiphenyl PCB- 26601649 361 6.72 710.0E-3 710.0E- Pentachloronitrobenzene 82688 295.3 4.64 59.0E-3 59.0E- Pentachloropenol 87865 266.4 5.86 650.0E-3 650.0E- Pentanol 71410 88 1.56 7.1E-3 7.1E- Pentanone, 4-methyl-2- 4- methyl- 108101 100 1.19 3.3E-3 3.3E- Phenanthrene 85018 178.2 4.57 270.0E-3 270.0E- Phenol 108952 94 1.46 5.5E-3 5.5E-
  • 12. Step 2 - Systemic Uptake Chemical Warfare Agents (CWA’s) have a low molecular weight, are moderately lipophillic and highly toxic. To be effective systemic toxins CWA’s must also demonstrate some degree of water solubility i.e. midrange K o/w, to partition into the blood stream. More lipophilic chemicals rapidly saturate the stratum corneum lipids capacity, but slowly partition into the hydrophillic bloodstream limiting systemic toxicity. As long as the skin remains dry, lipophilic chemicals remain more soluble in the skin lipids limiting systemic absorption.
  • 13. The Skin Depot – wash-in effect Washing with soap and water hydrates the skin and may worsen exposures to lipophilic chemicals. The chart below shows what happened after washing with soap and water at the 24 hr. mark for four exposures. The irony – soap and water is effective for water soluble chemicals. Water soluble chemicals tend to be poorly absorbed via healthy and intact skin. Washing the skin with soap and water or solvents may actually enhance absorption of lipophilic chemicals. R. Moody, Toxic. In Vitro,8; 1225 1994 0.07 0.06 0.05 1 % 0.04 2 Permeation 0.03 3 0.02 4 0.01 0 4 8 12 16 20 24 26 28 32 36 40 44 48 Time (Hrs.) DDT was applied to the skin and the percentage of permeation into the bloodstream measured. The excess lipophillic DDT (K o/w 6.36) was washed from the skin after 24 hrs. and the percentage penetrating the bloodstream increased by 5 fold.
  • 14. Comparison of enhancement effect of decontamination solution on rate of percutaneous penetration of diethylmalonate remaining in skin samples that 300 were decontaminated 1 hour post exposure. Loke et. al, 1999 250 control Decontamination Mean enhancement in 200 1/4 hr. decon Solution penetration rate % 2% (w/v)anionic surfactant 141.19 2% (w/v) cationic surfactant 138.03 150 1/2 hr. decon 2% (w/v) non-ionic surfactant 135.32 de-ionized water hypotonic solution 105.55 100 1 hr. decon 0.9% (w/v)saline isotonic solution 71.27 9 % (w/v) saline hypertonic solution 23.17 50 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 Time is the crucial factor in decontamination. Diethylmalonate, a nerve agent simulant, was washed from the skin after increasing time intervals of ¼ to ½ hrs. After ½ hr. decontamination with soap and water or water increased systemic absorption vs. the control (no decontamination). Nerve agents require a certain effective dose to be absorbed. It is possible that controls may have lived and those decontaminated at 1 hr. would have died.
  • 15. Solubility is the key. Note: The EPA “Recognition and Management Pesticide Poisoning” 1999 recommends washing with soap and water. The pesticide Alachlor that is lipophillic is supplied in a solvent concentrate and applied in a diluted water emulsion spray. As the Alachlor was, diluted from 20 parts water to 80 parts water, the concentration was 4x lower but the systemic absorption increased 4x. Alachlor remained more soluble in the more concentrated emulsion than in the skin.
  • 16. Evaluation of compounds as barriers to dermal penetration of organophosphates using acetylcholinesterase inhibition. Olson, Carl T. et al Toxicity Letters, 55(1991) 325-334 Ed50 Values and 95% confidence limits for acetylcholinesterase inhibition. OP compound Time after exposure (min.) Ed50 (95% confidence limits) No barrier PEG 540 barrier (mg/kg) (mg/kg) TGD 30 1.90 (1.44-2.52) 1915 (0.05-8 X 107) 60 1.01 (0.81-1.26) 33.3 (11.0-100) 120 0.94 (0.710-01.23) 7.89 (5.44-11.4) 240 1.06 (0.83-1.34) 6.28 (4.96-7.95) GD 30 0.68 (0.52-0.89) 14.4 (5.43-38.4) 60 0.56 (0.40-0.78) 6.17 (3.82-9.97) 120 0.54 (0.39-0.75) 4.39 (2.67-7.22) 240 0.49 (0.33-0.73) 1.76 (0.75-4.12) VX 30 0.131 (0.031-0.549) 167 (0.9 x 103) 60 0.026 (0.017-0.040) 18.2 (0.055-6002) 120 0.012 (0.010-0.014) 3.38 (0.104-110) 240 0.007 (0.005-0.008) 10 (0.043-103) A barrier of HMW polyethelene glycol (MW 540) was applied to the skin of rats before exposure to various CWA’s. The CWA was more soluble in PEG barrier than the skin and systemic absorption was slower. For example, for VX to achieve systemic toxicity in 30 minutes, .131 mg/Kg was effective with no barrier. With PEG, .167 mg/kg was applied to achieve the same level of toxicity. An increase of 1000x.
  • 17. Like Dissolves Like 60% 50% 4 hours 40% 30% 20% 8 hours 10% 0% water 50% polyglycol corn oil soap (D-TAM) % of MDI dose remaining in skin This study compared the ability of water, 50% soap and water, a polyglycol based cleanser and corn oil (control) to minimize absorption of isocyanate (MDI) into the skin. The data show that corn oil and the polyglycol based cleanser are more effective than water or soap and water in limiting the transfer of MDI into the skin. These results are consistent with the miscibility of MDI in corn oil and polyglycol. Ronald C. Wester et al. In Vivo Evaluation of MDI Skin Decontamination Procedures. Presented September 1998, Polyurethane Expo. Even after 8 hours, less than 10% of the applied dose entered the skin when decontaminated with non-aqueous HMW solvents. Water alone drove over 50% of the dose into the skin.
  • 18. Solubility in Skin Decontamination Solvents A Rational Approach to Skin Decontamination,T. Buckley, Johns Hopkins Univ., M. Dellarco, USEPA, T. Klingner, CLI Laboratories, AIHA Conference 2001 Comparison of Saturation 100% 90% 80% Water 70% 10% soap Solublity 60% D-TAM 50% 40% Glycol 30% D-TAM Oil 20% 10% 0% methylenedianiline chlorpyrifos pentachlorophenol benzo-a-pyrene log ko/w1.59** log k o/w 4.7*** log k o/w 5.86** log k o/w 6.5** *Relative to solvent with maximum solubility; maximum solubility was not always achieved ** solubility determined spectrophotometrically ***solubility determined by visual inspection of mass dissolving in solution Premise: The more soluble the contaminant is in the decontamination agent the more effective the decontamination process.
  • 19. Skin Decontamination Selection Guide for D-TAM Skin Cleanser and D-TAM Safe Solvent Log K o/w 0 3.5 8.0 Soap and Water D-TAM™ Skin D-TAM™ Safe Cleanser (Peg Based) Solvent (plant oil based) TDI Phenol Aldrin Benzo-a-pyrene Formaldehyde Aniline Di-nitro-Toluene MDI Lindane Penatchlorphenol Propanol Acetone PCBs Trinitrobenzene Malathion DDT Hydrazine Dichlorethane Diesel Oil By adjusting the K o/w of the HMW D-TAM formulation effective decontamination of chemicals across the entire solubility spectrum can be achieved.
  • 20. Ineffective Decontamination: A False Sense of Security Organophosphate poisoning from wearing a laundered uniform previously contaminated with parathion. Clifford, N.J., Nies, A.S., JAMA 12, 1, 89 Vol 262 No 21 Case 1 Case 2 Case 3 25 year old 23 year old 18 year old This worker was accidentally This worker collapsed at work This worker also collapsed after wearing sprayed with parathion during after receiving the freshly laundered the re-laundered uniform. The connection the manufacturing process. The uniform that was previously was made with the earlier contamination and contaminated uniform was removed contaminated. There was no it was destroyed. No further incidences and inadvertently sent to be obvious exposure connected to this occurred. Patient recovered in hospital. laundered rather than destroyed. and the uniform was removed Patient recovered in hospital. and sent to be laundered. Patient recovered in hospital.
  • 21. Re-use of PPC; Potential Exposure to Pesticides Garrod, Phillips, Pemberton, Amer. Occup. Hyg., Vol 45, No.1, 2001 38% of agricultural workers using unapproved disposable gloves showed positive exposure to hands. 95% of workers who re-used chemical protective gloves (protection factor 20X) had positive exposure. The re-use of contaminated PPC can result in significant unanticipated exposure. Proper decontamination of PPC can prevent these exposures.
  • 22. “It is better to learn from someone else’s mistakes rather than your own.” Dear Ole Dad • 25% of medical personnel treating victims of the Tokyo sarin terrorist attack were themselves acutely poisoned. “Good ideas are not adopted automatically. They must be driven into practice with courageous impatience.” Admiral Hyman Rickover