Evidence map›Paper›PMID 23964749›Full record

ArticleMolecular pharmaceutics2013

Structural determinants of drug partitioning in surrogates of phosphatidylcholine bilayer strata.

Viera Lukacova, Senthil Natesan, Ming Peng, Roman Tandlich, Zhanbin Wang, Sandra Lynch, Rajesh Subramaniam, Stefan Balaz

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Protein-enhanced small molecule disruptors of ordered membrane domains.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Polarity of Hydrated Phosphatidylcholine Headgroups.Langmuir : the ACS journal of surfaces and colloids · 2019
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Viera LukacovaCollege of Pharmacy, North Dakota State University , Fargo, North Dakota 58102, United States.
Senthil Natesan
Ming Peng
Roman Tandlich
Zhanbin Wang
Sandra Lynch
Rajesh Subramaniam
Stefan Balaz
Albany College of Pharmacy and Health Sciences · USNorth Dakota State University · USRhodes University · ZA

Funding

Conceptual Prediction of Drug Bioactivities in Cell-Based Assays: cell-QSARR01GM080508 · NIGMS · ALBANY COLLEGE OF PHARMACY · PI BALAZ, STEFAN · 2009 to 2013
$1.3M
NIGMS NIH HHS R01 GM080508NIGMS NIH HHS R01 GM80508
6 · The paper itself

Abstract

The knowledge of drug concentrations in bilayer headgroups, core, and at the interface between them is a prerequisite for quantitative modeling of drug interactions with many membrane-bound transporters, metabolizing enzymes and receptors, which have the binding sites located in the bilayer. This knowledge also helps understand the rates of trans-bilayer transport because balanced interactions of drugs with the bilayer strata lead to high rates, while excessive affinities for any stratum cause a slowdown. Experimental determination of bilayer location is so tedious and costly that the data are only available for some fifty compounds. To extrapolate these valuable results to more compounds at a higher throughput, surrogate phases have been used to obtain correlates of the drug affinities for individual strata. We introduced a novel system, consisting of a diacetyl phosphatidylcholine (DAcPC) solution with the water content of the fluid bilayer as the headgroup surrogate and n-hexadecane (C16) representing the core. The C16/DAcPC partition coefficients were measured for 113 selected compounds, containing structural fragments that are frequently occurring in approved drugs. The data were deconvoluted into the ClogP-based fragment solvation characteristics and processed using a solvatochromic correlation. Increased H-bond donor ability and excess molar refractivity of compounds promote solvation in the DAcPC phase as compared to bulk water, contrary to H-bond acceptor ability, dipolarity/polarizability, and volume. The results show that aromates have more balanced distribution in bilayer strata, and thus faster trans-bilayer transport, than similar alkanes. This observation is in accordance with the frequent occurrence of aromatic rings in approved drugs and with the role of rigidity of drug molecules in promoting intestinal absorption. Bilayer locations, predicted using the C16/DAcPC system, are in excellent agreement with available experimental data, in contrast to other surrogate systems.

Indexed as

AlkanesLipid BilayersModels, TheoreticalPhosphatidylcholinesPhospholipidsAlkanesLipid Bilayersn-hexadecanePhosphatidylcholinesPhospholipids

Identifiers

PMID23964749
PMCPMC3884577
OpenAlexW2330978037

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.