Evidence map›Paper›PMID 27920529›Full record

ArticleInternational journal of nanomedicine

Synthetic high-density lipoproteins for delivery of 10-hydroxycamptothecin.

Yue Yuan, Jian Wen, Jie Tang, Qiming Kan, Rose Ackermann, Karl Olsen, Anna Schwendeman

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.7field-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

14 citing papers in PubMed, 43 citations in OpenAlex.

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  9. Dual TLR agonist nanodiscs as a strong adjuvant system for vaccines and immunotherapy.Journal of controlled release : official journal of the Controlled Release Society · 2018
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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

7 authors at 2 institutions in 2 countries.

Yue YuanDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, People's Republic of China; Department of Pharmaceutical Sciences, Biointerfaces Institute, College of Pharmacy, University of Michigan.
Jian WenDepartment of Internal Medicine, Division of Molecular Medicine and Genetics, University of Michigan Medical School, Ann Arbor, MI, USA.
Jie TangDepartment of Pharmaceutical Sciences, Biointerfaces Institute, College of Pharmacy, University of Michigan.
Qiming KanDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, People's Republic of China.
Rose AckermannDepartment of Pharmaceutical Sciences, Biointerfaces Institute, College of Pharmacy, University of Michigan.
Karl OlsenDepartment of Pharmaceutical Sciences, Biointerfaces Institute, College of Pharmacy, University of Michigan.
Anna SchwendemanDepartment of Pharmaceutical Sciences, Biointerfaces Institute, College of Pharmacy, University of Michigan.
Shenyang Pharmaceutical University · CNUniversity of Michigan–Ann Arbor · US

Funding

Synthetic HDL_a potential sepsis therapyR01GM113832 · NIGMS · UNIVERSITY OF KENTUCKY · PI LI, XIANG-AN, SCHWENDEMAN, ANNA · 2015 to 2019
$3.0M
HDL-Loaded Nanoparticles for Glioma TherapeuticsR21NS091555 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CASTRO, MARIA G · 2015 to 2016
$427k
NIGMS NIH HHS R01 GM113832NINDS NIH HHS R21 NS091555
6 · The paper itself

Abstract

The purpose of this study was to develop a novel synthetic high-density lipoprotein (sHDL) nanoparticle delivery system for 10-hydroxycamptothecin (HCPT) for treatment of colon carcinoma. HDL is recognized by scavenger receptor B-I (SR-BI) over-expressed in colon carcinomas 5- to 35-fold relative to the human fibroblasts. The sHDL nanoparticles were composed of apolipoprotein A-I mimic peptide (5A) and contained 0.5%-1.5% (w/w) of HCPT. An optimized HCPT-sHDL formulation exhibited 0.7% HCPT loading with 70% efficiency with an average size of 10-12 nm. Partitioning of HCPT in the sHDL lipid membrane enhanced drug stability in its active lactone form, increased solubilization, and enabled slow release. Cytotoxicity studies in HT29 colon carcinoma cells revealed that the IC

Indexed as

AnimalsAntineoplastic Agents, PhytogenicApolipoprotein A-ICamptothecinDrug Delivery SystemsDrug StabilityHT29 CellsHumansLactonesLipoproteins, HDLNanoparticlesRats, Sprague-Dawley10-hydroxycamptothecinAntineoplastic Agents, PhytogenicApolipoprotein A-ICamptothecinLactonesLipoproteins, HDLapolipoprotein A-I mimic peptidecamptothecincolon carcinomananodiscnanoparticlephospholipidsSR-BI receptor

Identifiers

PMID27920529
PMCPMC5125756
OpenAlexW2555119016

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.