Evidence map›Paper›PMID 25587935›Full record

ArticleMolecular pharmaceutics2015

Oral absorption enhancement of probucol by PEGylated G5 PAMAM dendrimer modified nanoliposomes.

Qian Ma, Yingchun Han, Cong Chen, Yini Cao, Siling Wang, Wenwen Shen, Huayu Zhang, Yanzhi Li, Mallory A van Dongen, Bing He and 6 more

Open access · greenAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2015. 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
3.6field-weighted citation impact, top 7% 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, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Adapting liposomes for oral drug delivery.Acta pharmaceutica Sinica. B · 2019
    Review
  11. 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

16 authors at 4 institutions in 2 countries.

Qian MaPeking University Institute of Cardiovascular Sciences, Peking University Health Science Center, Peking University , Beijing 100191, China.
Yingchun Han
Cong Chen
Yini Cao
Siling Wang
Wenwen Shen
Huayu Zhang
Yanzhi Li
Mallory A van Dongen
Bing He
Maomao Yu
Lu Xu
Mark M Banaszak Holl
George Liu
Qiang Zhang
Rong Qi
Peking University · CNMinistry of Education of the People's Republic of China · CNUniversity of Michigan–Ann Arbor · USShenyang Pharmaceutical University · CN

Funding

The Role of Cell Membrane Disruption in Non-Viral Vector Oligonucleotide DeliveryR01EB005028 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BANASZAK HOLL, MARK M · 2006 to 2013
$2.8M
NIBIB NIH HHS R01 EB005028
6 · The paper itself

Abstract

Probucol (PB), an antioxidant drug, is commonly used as a lipid concentration lowering drug to reduce blood plasma cholesterol levels in the clinic. However, the therapeutic effects of this drug are negatively impacted by its poor water solubility and low oral absorption efficiency. In this study, a PEGylated G5 PAMAM dendrimer (G5-PEG) modified nanoliposome was employed to increase water solubility, transepithelial transport, and oral absorption of PB. The uptake mechanism was explored in vitro in Caco-2 cells with the results suggesting that the absorption improvement of G5-PEG modified PB-liposome (PB-liposome/G5-PEG) was related to P-glycoprotein (P-gp) efflux pump but was independent of caveolae endocytosis pathways. Additionally, plasma lipid concentration lowering effects of PB-liposome/G5-PEG were evaluated in vivo in a LDLR-/- hyperlipidemia mouse model. Compared with saline treated group, treatment with PB-liposome/G5-PEG significantly inhibited the increase of plasma total cholesterol (TC) and triglyceride (TG) of mice induced by a high fat diet. Moreover, its lipid concentration lowering effects and plasma drug concentration were greater than PB alone or commercial PB tablets. Our results demonstrated that PB-liposome/G5-PEG significantly increased the oral absorption of PB and therefore significantly improved its pharmacodynamic effects.

Indexed as

Drug Delivery SystemsLiposomesNanocapsulesAdministration, OralAnimalsAnticholesteremic AgentsCaco-2 CellsCholesterolDendrimersDrug StabilityHumansHyperlipidemiasIntestinal AbsorptionMaleMiceMice, KnockoutAnticholesteremic AgentsCholesterolDendrimersLiposomesNanocapsulesPAMAM StarburstPolyethylene GlycolsProbucolReceptors, LDLTriglyceridesG5-PEG PAMAM dendrimerin vivo pharmacodynamic effectsnanoliposomeprobucoltransepithelial absorption and mechanism

Identifiers

PMID25587935
PMCPMC4770526
OpenAlexW2083492650

What OpenQuestion holds

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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.