Schultz Dale Reaction

Schultz Dale reaction

Schultz Dale reactionClick on the image to know more about Schultz Dale Reaction

 What is Schultz Dale Reaction

Schultz Dale reaction is an anaphylactic reaction produced in vitro during the testing of immunomodulatory drugs

 What is the rationale behind Schultz Dale Reaction

It is used to initiate the release of mediators of anaphylaxis like histamine which induce contraction in smooth muscles.

 How is Schultz Dale Reaction induced

To induce Schultz Dale reaction, guinea pigs are used generally. The animals are sensitized against egg albumin and three weeks after this, they are sacrificed. Ileum of the sacrificed animals is isolated and the contractility of the isolates is tested

Can we use any other tissues for Schultz Dale reaction?
Yes. Researchers have used lungs, tracheae of guinea pigs and trachea of mice as well.

|Humidity|- Absolute, Relative and Specific.

Humidity

Humidity is a term for water vapor in the air, and can refer to any one of several measurements of humidity.

Absolute humidity

Absolute humidity is an amount of water vapor, usually discussed per unit volume. The mass of water vapor,  m_w , per unit volume of total moist air,  V_{net} , can be expressed as follows:

 AH = {m_w \over V_{net}}.

Absolute humidity in air ranges from zero to roughly 30 grams per cubic meter when the air is saturated at 30 °C.

 

Relative humidity

Relative humidity is a term used to describe the amount of water vapor in a mixture of air and water vapor. It is defined as the ratio of the partial pressure of water vapor in the air-water mixture to the saturated vapor pressure of a flat sheet of pure water at those conditions. The relative humidity of air depends not only on temperature but also on the pressure of the system of interest.

Relative humidity is normally expressed as a percentage and is calculated by using the following equation, it is defined as the ratio of thepartial pressure of water vapor (H2O)  \left({e_w}\right)  in the mixture to the saturated vapor pressure of water  \left({{e^*}_w}\right)  at a prescribed temperature.

 \phi  =  {{e_w} \over {{e^*}_w}} \times 100%

Relative humidity is often used instead of absolute humidity in situations where the rate of water evaporation is important, as it takes into account the variation in saturated vapor pressure.

 

Specific humidity

Specific humidity is the ratio of water vapor to dry air in a particular mass, and is sometimes referred to as humidity ratio. Specific humidity ratio is expressed as a ratio of mass of water vapor,  m_v , per unit mass of dry air  m_a  .

That ratio is defined as:

 SH = {m_v \over m_a}.

Dissolution

Dissolution

Dissolution is the process by which a solid, liquid or gas forms a solution in a solvent. For the dissolution of solids, the process of dissolution can be explained as the breakdown of the crystal lattice into individual ions, atoms or molecules and their transport into the solvent

The rate of dissolution quantifies the speed of the dissolution process.

The rate of dissolution depends on:

  • nature of the solvent and solute

  • temperature (and to a small degree pressure)

  • degree of undersaturation

  • presence of mixing

  • interfacial surface area

  • presence of inhibitors (e.g., a substance adsorbed on the surface).

The rate of dissolution can be often expressed by the Noyes-Whitney Equation or the Nernst and Brunner equation[1] of the form:

\frac {dm} {dt} = A \frac {D} {d} (C_s-C_b)

where:

m – amount of dissolved material, kg

t – time, seconds

A – surface area of the interface between the dissolving substance and the solvent, m2

D – diffusion coefficient, m2/s

d – thickness of the boundary layer of the solvent at the surface of the dissolving substance, m

Cs – concentration of the substance on the surface, kg/m3

Cb – concentration of the substance in the bulk of the solvent, kg/m3

For dissolution limited by diffusion, Cs is equal to the solubility of the substance.

When the dissolution rate of a pure substance is normalized to the surface area of the solid (which usually changes with time during the dissolution process), then it is expressed in kg/m2s and referred to as “intrinsic dissolution rate”. The intrinsic dissolution rate is defined by the United States Pharmacopeia.

Dissolution rates vary by orders of magnitude between different systems. Typically, very low dissolution rates parallel low solubilities, and substances with high solubilities exhibit high dissolution rates, as suggested by the Noyes-Whitney equation. However, this is not a rule.

Diffusion

Diffusion describes the spread of particles through random motion from regions of higherconcentration to regions of lower concentration. The time dependence of the statistical distribution in space is given by the diffusion equation. The concept of diffusion is tied to that of mass transferdriven by a concentration gradient. Diffusion is invoked in the social sciences to describe the spread of ideas.

Fick’s laws of diffusion describe diffusion and can be used to solve for the diffusion coefficient, D. They were derived by Adolf Fick in the year 1855.

Fick’s first law relates the diffusive flux to the concentration under the assumption of steady state. It postulates that the flux goes from regions of high concentration to regions of low concentration, with a magnitude that is proportional to the concentration gradient (spatial derivative). In one (spatial) dimension, the law is

\bigg. J = - D \frac{\partial \phi}{\partial x} \bigg.

where

  •  J is the “diffusion flux” [(amount of substance) per unit area per unit time], example (\tfrac{\mathrm{mol}}{ \mathrm m^2\cdot \mathrm s}) J measures the amount of substance that will flow through a small area during a small time interval.

  • \, D is the diffusion coefficient or diffusivity in dimensions of [length2 time−1], example (\tfrac{\mathrm m^2}{\mathrm s})

  • \, \phi (for ideal mixtures) is the concentration in dimensions of [(amount of substance) length−3], example (\tfrac\mathrm{mol}{\mathrm m^3})

  • \, x is the position [length], example \,\mathrm m

Fick’s second law predicts how diffusion causes the concentration to change with time:

\frac{\partial \phi}{\partial t} = D\,\frac{\partial^2 \phi}{\partial x^2}\,\!

Where

  • \,\phi is the concentration in dimensions of [(amount of substance) length−3], example (\tfrac\mathrm{mol}{m^3})

  • \, t is time [s]

  • \, D is the diffusion coefficient in dimensions of [length2 time−1], example (\tfrac{m^2}{s})

  • \, x is the position [length], example \,m

Supersaturation

The term “supersaturatio” refers to a solution that contains more of the dissolved material than could be dissolved by the solvent under the solubility amount. It can also refer to a vapor of a compound that has a higher (partial) pressure than the vapor pressure of that compound.