Evidence map›Paper›PMID 23430484›Full record

ArticlePharmaceutical research2013

A mouse model to evaluate the impact of species, sex, and lipid load on lymphatic drug transport.

Natalie L Trevaskis, Suzanne M Caliph, Gary Nguyen, Patrick Tso, William N Charman, Christopher J H Porter

Open access · greenAbstract read
In one paragraph

Article in Pharmaceutical research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. An update on oral drug deliveryActa pharmaceutica Sinica. B · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Species differences in tumour responses to cancer chemotherapy.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    Review
  14. Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Natalie L TrevaskisDrug Delivery, Disposition and Dynamics Monash Institute of Pharmaceutical Sciences, Monash University (Parkville Campus), 381 Royal Parade, Parkville, Victoria, Australia, 3052, Natalie.Trevaskis@monash.edu.
Suzanne M Caliph
Gary Nguyen
Patrick Tso
William N Charman
Christopher J H Porter
Monash University · AUUniversity of Cincinnati · US

Funding

LIPID, LIPOPROTEIN, AND GLUCOSE METABOLISM COREU24DK059630 · NIDDK · UNIVERSITY OF CINCINNATI · PI TSO, PATRICK · 2001 to 2015
$12.9M
Lipid profile, lipoprotein and apolipoprotein composition, and intestinal fat absorption efficiency in germ-free and conventional miceU2CDK059630 · NIDDK · UNIVERSITY OF CINCINNATI · PI LIU, MIN · 2016 to 2021
$4.9M
Functional & molecular study of intetinal cholesterol transporters & absorptionR01DK076928 · NIDDK · UNIVERSITY OF CINCINNATI · PI TSO, PATRICK · 2007 to 2011
$1.6M
Interaction of Nutrient & Organochlorine AbsorptionR01ES014464 · NIEHS · UNIVERSITY OF CINCINNATI · PI TSO, PATRICK · 2007 to 2010
$1.3M
NIDDK NIH HHS R01 DK076928NIDDK NIH HHS U24 DK059630NIDDK NIH HHS U2C DK059630NIEHS NIH HHS R01 ES014464
6 · The paper itself

Abstract

purposeTo establish a lymph-cannulated mouse model, and use the model to investigate the impact of lipid dose on exogenous and endogenous lipid recruitment, and drug transport, into the lymph of males versus females. Finally, lymphatic transport and drug absorption in the mouse were compared to other pre-clinical models (rats/dogs).

methodsAnimals were orally or intraduodenally administered 1.6 mg/kg halofantrine in low or high (14)C-lipid doses. For bioavailability calculation, animals were intravenuosly administered halofantrine. Lymph or blood samples were taken and halofantrine, triglyceride, phospholipid and (14)C-lipid concentrations measured.

resultsLymphatic lipid transport increased linearly with lipid dose, was similar across species and in male/female animals. In contrast, lymphatic transport of halofantrine differed markedly across species (dogs>rats>mice) and plateaued at higher lipid doses. Lower bioavailability appeared responsible for some species differences in halofantrine lymphatic transport; however other systematic differences were involved.

conclusionsA contemporary lymph-cannulated mouse model was established which will enable investigation of lymphatic transport in transgenic and disease models. The current study found halofantrine absorption and lymphatic transport are reduced in small animals. Future analyses will investigate mechanisms involved, and if similar trends occur for other drugs, to establish the most relevant model(s) to predict lymphatic transport in humans.

Indexed as

AnimalsAntimalarialsBiological AvailabilityDogsFemaleLipid MetabolismLipidsLymphatic SystemMaleMiceMice, Inbred C57BLModels, AnimalPharmaceutical VehiclesPhenanthrenesPhospholipidsRatsAntimalarialshalofantrineLipidsPharmaceutical VehiclesPhenanthrenesPhospholipidsTriglycerides

Identifiers

PMID23430484
PMCPMC4136478
OpenAlexW2091872697

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.