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Interaction of quinolines and artemisinin based antimalarials drugs with ferriprotoporphyrin IX


par Bienvenu MAVAKALA KIAZOLUA
Tsinghua University
Traductions: Original: fr Source:

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3.4 Data analysis

It is assumed that the interaction between hemin (H) and antimalarial drug (Q) can be described according to the equilibrium shown below:

(3-2)

In diluted solutions, the association constant of complex K can be written as follows:

(3-3)

and

where is the concentration of complex and and are the initial concentrations of hemin and drug, respectively

(3-4)

(3-5)

Combining Equations (3-2), (3-3), (3-4) and (3-5), the resulting quadratic equation can be written as:

(3-6)

One of the roots of the equation (3-6) is given by:

(3-7)

The optical absorption of the system during titration can be written as:

(3-8)

where A and d are the optical density and the light path, respectively, and are the molar extinction coefficients of hemin and its complex solutions.

Combining Equations (3-4) and (3-7), with Equation (3-8), the following equation is obtained:

(3-9)

Where A0 is the molar extinction of hemin solution at =0, and ( = -) is the difference of the molar extinction coefficients between hemin complex and free hemin. The basic data are initial concentrations of hemin () and drug () and the corresponding optical absorption of hemin (A). With these data, parameters particularly the equilibrium constant K, can be fitted according to Eq. (3-9) with the help of Microsoft Origin 6.1 package.

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