Evidence map›Paper›PMID 26158623›Full record

ArticleNature communications2015

A drug-specific nanocarrier design for efficient anticancer therapy.

Changying Shi, Dandan Guo, Kai Xiao, Xu Wang, Lili Wang, Juntao Luo

Abstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
–field-weighted citation impact
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

67 citing papers in PubMed.

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  13. "Click" amphotericin B in prodrug nanoformulations for enhanced systemic fungemia treatment.Journal of controlled release : official journal of the Controlled Release Society · 2024
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7 more citing papers are in PubMed but not listed here.

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.

Changying ShiDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, New York 13210, USA.
Dandan GuoDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, New York 13210, USA.
Kai XiaoLaboratory of Non-human Primate Disease Model Research, National Chengdu Center for Safety Evaluation of Drugs, State Key Lab of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, China.
Xu WangDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, New York 13210, USA.
Lili WangDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, New York 13210, USA.
Juntao LuoDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, New York 13210, USA.

Funding

Size-tunable cancer nanotherapeuticsR01CA140449 · NCI · UPSTATE MEDICAL UNIVERSITY · PI LUO, JUNTAO · 2010 to 2014
$1.6M
Rational Design and High throughput synthesis of nanocarriers for efficient drug deliveryR21EB019607 · NIBIB · UPSTATE MEDICAL UNIVERSITY · PI LUO, JUNTAO · 2015 to 2016
$453k
NCI NIH HHS NIH/NCI R01CA140449NCI NIH HHS R01 CA140449NIBIB NIH HHS R21 EB019607
6 · The paper itself

Abstract

The drug-loading properties of nanocarriers depend on the chemical structures and properties of their building blocks. Here we customize telodendrimers (linear dendritic copolymer) to design a nanocarrier with improved in vivo drug delivery characteristics. We do a virtual screen of a library of small molecules to identify the optimal building blocks for precise telodendrimer synthesis using peptide chemistry. With rationally designed telodendrimer architectures, we then optimize the drug-binding affinity of a nanocarrier by introducing an optimal drug-binding molecule (DBM) without sacrificing the stability of the nanocarrier. To validate the computational predictions, we synthesize a series of nanocarriers and evaluate systematically for doxorubicin delivery. Rhein-containing nanocarriers have sustained drug release, prolonged circulation, increased tolerated dose, reduced toxicity, effective tumour targeting and superior anticancer effects owing to favourable doxorubicin-binding affinity and improved nanoparticle stability. This study demonstrates the feasibility and versatility of the de novo design of telodendrimer nanocarriers for specific drug molecules, which is a promising approach to transform nanocarrier development for drug delivery.

Indexed as

AnimalsAnthraquinonesAntineoplastic AgentsCell Line, TumorCell SurvivalCholic AcidDoxorubicinDrug CarriersHumansJurkat CellsMiceMice, Inbred BALB CMolecular Docking SimulationNanoparticlesNeoplasm TransplantationPolyethylene GlycolsAnthraquinonesAntineoplastic AgentsCholic AcidDoxorubicinDrug Carriersliposomal doxorubicinPolyethylene GlycolsPolymersrhein

Identifiers

PMID26158623
PMCPMC4499863

What OpenQuestion holds

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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.