Polar surface area explained

The polar surface area (PSA) or topological polar surface area (TPSA) of a molecule is defined as the surface sum over all polar atoms or molecules, primarily oxygen and nitrogen, also including their attached hydrogen atoms.

PSA is a commonly used medicinal chemistry metric for the optimization of a drug's ability to permeate cells. Molecules with a polar surface area of greater than 140 angstroms squared (Å2) tend to be poor at permeating cell membranes.[1] For molecules to penetrate the blood–brain barrier (and thus act on receptors in the central nervous system), a PSA less than 90 Å2 is usually needed.[2]

TPSA is a valuable tool in drug discovery and development. By analyzing a drug candidate's TPSA, scientists can predict its potential for oral bioavailability and ability to reach target sites within the body. This prediction hinges on a drug's ability to permeate biological barriers.

Permeating these barriers, such as the Blood-Brain Barrier (BBB), the Placental Barrier (PB), and the Blood-Mammary Barrier (BM), is crucial for many drugs to reach their intended targets.

The BBB, for example, protects the brain from harmful substances. Drugs with a lower TPSA (generally below 90 Ų) tend to permeate the BBB more easily, allowing them to reach the brain and exert their therapeutic effects (Shityakov et al[3] ., 2013).

Similarly, for drugs intended to treat the fetus, a lower TPSA (below 60 Ų) is preferred to ensure they can pass through the placenta (Augustiño-Roubina[4] et al., 2019).

Breastfeeding mothers also need consideration. Here, an optimal TPSA for a drug is around 60-80 Ų to allow it to reach the breast tissue for milk production, while drugs exceeding 90 Ų are less likely to permeate the Blood-Mammary Barrier.[5]

See also

Literature

External links

Notes and References

  1. Pajouhesh H, Lenz GR . Medicinal Chemical Properties of Successful Central Nervous System Drugs. . NeuroRx . 2 . 4 . 541–553 . Oct 2005 . 10.1602/neurorx.2.4.541 . 16489364 . 1201314.
  2. Hitchcock SA, Pennington LD . Structure - Brain Exposure Relationships . J. Med. Chem. . 49 . 26 . 7559–7583 . May 2006 . 10.1021/jm060642i . 17181137 .
  3. Shityakov . Sergey . Neuhaus . Winfried . Dandekar . Thomas . Förster . Carola . 2013 . Analysing molecular polar surface descriptors to predict blood-brain barrier permeation . International Journal of Computational Biology and Drug Design . 6 . 1-2 . 146–156 . 10.1504/IJCBDD.2013.052195 . 1756-0756 . 23428480.
  4. Hester . Gabrielle . Lang . Tom . Madsen . Laura . Tambyraja . Rabindra . Zenker . Paul . January 2019 . Timely Data for Targeted Quality Improvement Interventions: Use of a Visual Analytics Dashboard for Bronchiolitis . Applied Clinical Informatics . 10 . 1 . 168–174 . 10.1055/s-0039-1679868 . 1869-0327 . 6402943 . 30841007.
  5. Web site: Δραστική: PARACETAMOL . 2024-04-10 . farmako.net . en.