Evidence map›Paper›PMID 26690101›Full record

ReviewMolecules (Basel, Switzerland)2015

Polymer-Based Prodrugs: Improving Tumor Targeting and the Solubility of Small Molecule Drugs in Cancer Therapy.

Sonja Dragojevic, Jung Su Ryu, Drazen Raucher

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.8field-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

29 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
  2. Polyphosphazene-Based Nanotherapeutics.Journal of functional biomaterials · 2025
    Review
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  13. Review
  14. Nanosystems Applied to HIV Infection: Prevention and Treatments.International journal of molecular sciences · 2020
    Review
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  18. Article
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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

3 authors at 3 institutions in 1 country.

Sonja DragojevicDepartment of Biochemistry, University of Mississippi Medical Center, 2500 North State Street Jackson, MS 39216, USA. sdragojevic@umc.edu.
Jung Su RyuDepartment of Biochemistry, University of Mississippi Medical Center, 2500 North State Street Jackson, MS 39216, USA. jryu@umc.edu.
Drazen RaucherDepartment of Biochemistry, University of Mississippi Medical Center, 2500 North State Street Jackson, MS 39216, USA. draucher@umc.edu.
Jackson Memorial Hospital · USState Street (United States) · USUniversity of Mississippi Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The majority of anticancer drugs have poor aqueous solubility, produce adverse effects in healthy tissue, and thus impose major limitations on both clinical efficacy and therapeutic safety of cancer chemotherapy. To help circumvent problems associated with solubility, most cancer drugs are now formulated with co-solubilizers. However, these agents often also introduce severe side effects, thereby restricting effective treatment and patient quality of life. A promising approach to addressing problems in anticancer drug solubility and selectivity is their conjugation with polymeric carriers to form polymer-based prodrugs. These polymer-based prodrugs are macromolecular carriers, designed to increase the aqueous solubility of antitumor drugs, can enhance bioavailability. Additionally, polymer-based prodrugs approach exploits unique features of tumor physiology to passively facilitate intratumoral accumulation, and so improve chemodrug pharmacokinetics and pharmacological properties. This review introduces basic concepts of polymer-based prodrugs, provides an overview of currently emerging synthetic, natural, and genetically engineered polymers that now deliver anticancer drugs in preclinical or clinical trials, and highlights their major anticipated applications in anticancer therapies.

Indexed as

AnimalsAntineoplastic AgentsDrug CarriersHumansNeoplasmsPolymersProdrugsSolubilityAntineoplastic AgentsDrug CarriersPolymersProdrugsanticancer drugscancer therapydrug deliverygenetically engineered biopolymersmacromoleculespolymer based prodrugssynthetic and natural polymers

Identifiers

PMID26690101
PMCPMC6331894
OpenAlexW2195777023

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.