This background material explains the theory behind the log*P *and log*D* calculation:

The mass flux of a molecule at the interface of two immiscible solvents is governed by its lipophilicity. The more lipophilic a molecule is, the more soluble it is in lipophilic organic phase. For the same reason drug penetration into a biological membrane is also influenced by the lipophilicity of the drug. When a molecule is ionizable at a given pH, it forms a hydrophilic anion or cation and subsequently fails to dissolve in organic phase. Ionization of a molecule leads to the accumulation of the hydrophilic form in the aqueous phase. In contrast, its lipophilic form decreases in both aqueous and organic phase due to the law of conservation of mass.

The partition coefficient of a molecule observed in a water–*n*-octanol system has been adopted as the standard measure of lipophilicity. The observed partition coefficient depends on the support electrolyte concentration of the bulk phase the compound is dissolved in. Extra ion-pair forming chemical agents added to the aqueous/organic phase may have a significant effect on the partitioning behaviour of a molecule.

It is often meaningful to obtain the partition coefficients of molecules by calculation. The molecular structure and extent of ionization are the primary factors in calculating the partition coefficient. The standard partition coefficient of ionized and unionized species calculated from the molecular structure is based largely on the atomic log*P* increments given in Viswanadhan et al. The extent of ionization at a given pH is obtained from the predicted p*K*_{a} of the molecule. Our calculation method takes into account the effect of the counterion concentration on log*D* and log*P*.

Throughout the document we use the following symbols:

*P*_{i}(upper case) is the macro partition coefficient, where subscript*i*refers to the ionization state of species included in*P*_{i}, e.g. i= -2, -1, 0, +1, +2*p*_{i}(lower case) is the micro partition coefficient, where subscript i refers to the microspecies, e.g. i=1,2,3,4,…*D*is the distribution coefficient- [ ] means concentration of microspecies
- log
*P*is the logarithm of the partition coefficient - log
*D*is the logarithm of the distribution coefficient

The following figure gives the definition of partition and distribution coefficients for ionized and unionized species.

Fig. 1 Partition and distribution coefficients for ionized and unionized species

The partition and distribution coefficients for multiprotic compounds are defined in much the same way as for monoprotic compounds using the following formulae.

Fig. 2 Partition and distribution coefficients for multiprotic compounds

Example

In this example we suppose that a compound A_{1}A_{2}B_{1}B_{2} contains two acidic and two basic ionization sites. This compound has 16 protonation states in aqueous solution. The microspecies which are assigned to the protonation states are summarized in the following table.

Microspecies | charge |

A_{1}A_{2}B_{1}B_{2} | 0 |

A_{1}^{-}A_{2}B_{1}B_{2} | -1 |

A_{1}A_{2}^{-}B_{1}B_{2} | -1 |

A_{1}A_{2}B_{1}^{+}B_{2} | +1 |

A_{1}A_{2}B_{1}B_{2}^{+} | +1 |

A_{1}^{-}A_{2}^{-}B_{1}B_{2} | -2 |

A_{1}^{-}A_{2}B_{1}^{+}B_{2} | 0 |

A_{1}^{-}A_{2}B_{1}B_{2}^{+} | 0 |

A_{1}A_{2}^{-}B_{1}^{+}B_{2} | 0 |

A_{1}A_{2}^{-}B_{1}B_{2}^{+} | 0 |

A_{1}A_{2}B_{1}^{+}B_{2}^{+} | +2 |

A_{1}^{-}A_{2}^{-}B_{1}^{+}B_{2} | -1 |

A_{1}^{-}A_{2}^{-}B_{1}B_{2}^{+} | -1 |

A_{1}^{-}A_{2}B_{1}^{+}B_{2}^{+} | +1 |

A_{1}A_{2}^{-}B_{1}^{+}B_{2}^{+} | +1 |

A_{1}^{-}A_{2}^{-}B_{1}^{+}B_{2}^{+} | 0 |

Fig. 3 All microspecies with their charge values generated from the initial compound

Partition and distribution coefficients then can be expressed as follows:

- Partition coefficient of the neutral species is

- Partition coefficients of the anionic and the cationic species are

and - Distribution coefficient of the original molecule is

So we can further simplify the formula for *P*_{-1} to the following. This expression reveals that *P*_{-1} does not depend on the pH of the solution:

Similarly, one could show that *P*_{0}, *P*_{+1},* P*_{-2} and *P*_{+2} are also pH-independent.

In contrast to this, the distribution coefficient *D* does depend on the solution pH (see Klopman et al.):

Log

Log*P* calculations are based on a pool of fragments predefined in the log*P* calculator. This set is based on the data set in Viswanadhan et al. Every fragment is assigned a unique name and a value. The log*P* value of a molecule is the sum of the fragment values that are present in the molecule.

log*P* plugin handled only one fragment set until version 5.1.2, but then it was extended with two additional sets. The sets are based on a published data set (see Klopman et al.) and the PhysProp^{©} database. These methods however are *not* available separately in the newer versions of the log*P *calculator.

The trainable log*P* calculation (available from version 5.1.3) offers the user to define his own log*P* database and calculate log*P* values based on experimental data. New fragment value extensions make a more precise calculation possible.

To have more information on the currently available log*P *calculation methods see this page.

Examples for log

The following examples show log*P*/log*D* results for special molecules types. The calculations were performed with the default settings of the log*P *plugin.

Example #1

The compound below is zwitterionic that has the form of a A_{1}A_{2}B_{1}B_{2} molecule mentioned in the theoretical section above. Lipophilicity of this compound reaches its maximum near to the isoelectric point. (pI is 4.43 in this case, while the global maximum of the log*D *function is 5.25. The calculated log*D *value at the pI point is 5.24.)

Fig. 3 Zwitterionic molecule and its lipophilicity plot

Example #2

Homidium is a quaternary ammonium ion with strong hydrophilic character. Its log*P* is calculated with the use of the ionic fragment of the N^{+} ion. The calculated and measured log*P* values are -0.91 and -1.10, respectively.

Fig. 4 Homidium molecule

Example #3

Ibuprofen has the typical log*D* vs. pH profile that is characteristic of acidic compounds. Lipophilic behavior of ibuprofen will be dominant when its carboxylic group is unionized (at low pH). At higher pH values the carboxylic group reaches the fully ionized state and hydrofilicity becomes more enhanced.

Fig. 6 Ibuprofen and its log*D*-pH plot

Example #4

The measured distribution coefficients also depends on the measurement method. The shake flask and the pH-metric methods are the most popular in practice. The figure below shows the calculated and measured log*D* of lignocaine as function of pH.

Fig. 7 Lignocaine and its logD-pH* *plot

References

- Viswanadhan, V. N.; Ghose, A. K.; Revankar, G. R. and Robins, R. K.,
*J.Chem.Inf.Comput.Sci.*,**1989**,*29*, 3, 163-172; doi - Klopman, G.; Li, Ju-Yun.; Wang, S.; Dimayuga, M.:
*J.Chem.Inf.Comput.Sci.*,**1994**,*34*, 752; doi - PhysProp
^{©}database, webpage - Csizmadia, F.; Tsantili-Kakoulidou, A.; Panderi, I. and Darvas, F.,
*J.Pharm.Sci.*,**1997**,*86*, 7, 865-871; doi - Bouchard, G.; Carrupt, P. A.; Testa, B.; Gobry, V. and Girault, H. H.,
*Pharm.Res.*,**2001**,*18*, 5, 702-708; doi

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