Evidence map›Paper›PMID 31990564›Full record

ArticleMolecular pharmaceutics2020

Interactions of Oral Molecular Excipients with Breast Cancer Resistance Protein, BCRP.

Ling Zou, Joshua Pottel, Natalia Khuri, Huy X Ngo, Zhanglin Ni, Eleftheria Tsakalozou, Mark S Warren, Yong Huang, Brian K Shoichet, Kathleen M Giacomini

Open access · greenAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

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  8. Transporters in Regulatory Science: Notable Contributions from Dr. Giacomini in the Past Two Decades.Drug metabolism and disposition: the biological fate of chemicals · 2022
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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

10 authors at 3 institutions in 1 country.

Ling ZouDepartment of Bioengineering and Therapeutic Sciences, Schools of Pharmacy and Medicine, University of California, San Francisco, California 94158, United States.
Joshua PottelDepartment of Pharmaceutical Chemistry & QB3 Institute, University of California, San Francisco, California 94158, United States.
Natalia KhuriDepartment of Bioengineering, Stanford University, Stanford, California 94305, United States.ORCID 0000-0001-9031-8124
Huy X NgoDepartment of Bioengineering and Therapeutic Sciences, Schools of Pharmacy and Medicine, University of California, San Francisco, California 94158, United States.
Zhanglin NiDivision of Quantitative Methods and Modeling, Office of Research and Standards, Office of Generic Drugs, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland 20993, United States.
Eleftheria TsakalozouDivision of Quantitative Methods and Modeling, Office of Research and Standards, Office of Generic Drugs, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland 20993, United States.
Mark S WarrenOptivia Biotechnology, Inc., Santa Clara, California 95054, United States.
Yong HuangOptivia Biotechnology, Inc., Santa Clara, California 95054, United States.
Brian K ShoichetDepartment of Pharmaceutical Chemistry & QB3 Institute, University of California, San Francisco, California 94158, United States.ORCID 0000-0002-6098-7367
Kathleen M GiacominiDepartment of Bioengineering and Therapeutic Sciences, Schools of Pharmacy and Medicine, University of California, San Francisco, California 94158, United States.ORCID 0000-0001-8041-5430
University of California, San Francisco · USUnited States Food and Drug Administration · USStanford University · US

Funding

UCSF-Stanford Center of Excellence in Regulatory Science and InnovationU01FD005978 · FDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ALTMAN, RUSS BIAGIO, GIACOMINI, KATHLEEN M · 2016 to 2025
$34.5M
UCSF-Stanford Center of Excellence in Regulatory Science and InnovationU01FD004979 · FDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ALTMAN, RUSS BIAGIO, GIACOMINI, KATHLEEN M · 2014 to 2016
$5.4M
FDA HHS U01 FD004979FDA HHS U01 FD005978
6 · The paper itself

Abstract

Mechanistic-understanding-based selection of excipients may improve formulation development strategies for generic drug products and potentially accelerate their approval. Our study aimed at investigating the effects of molecular excipients present in orally administered FDA-approved drug products on the intestinal efflux transporter, BCRP (

Indexed as

Administration, OralATP Binding Cassette Transporter, Subfamily G, Member 2Coloring AgentsDrug CompoundingDrug Evaluation, PreclinicalExcipientsFemaleFlavoring AgentsHEK293 CellsHumansInhibitory Concentration 50Intestinal AbsorptionMolecular WeightNeoplasm ProteinsSignal TransductionSurface-Active AgentsABCG2 protein, humanATP Binding Cassette Transporter, Subfamily G, Member 2Coloring AgentsExcipientsFlavoring AgentsNeoplasm ProteinsSurface-Active AgentsBCRPdrug−excipient interactionexcipient

Identifiers

PMID31990564
PMCPMC8177814
OpenAlexW3003960861

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.