Evidence map›Paper›PMID 24128651›Full record

ReviewHuman vaccines & immunotherapeutics2014

Polymeric nanoparticles: potent vectors for vaccine delivery targeting cancer and infectious diseases.

Azam Bolhassani, Shabnam Javanzad, Tayebeh Saleh, Mehrdad Hashemi, Mohammad Reza Aghasadeghi, Seyed Mehdi Sadat

Abstract readReview
In one paragraph

Review in Human vaccines & immunotherapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing 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

86 citing papers in PubMed.

  1. Review
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  6. Emerging dendrimer-based RNA delivery strategies.Nanomedicine (London, England) · 2025
    Review
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26 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.

Azam BolhassaniDepartment of Hepatitis and AIDs; Pasteur Institute of Iran; Tehran, Iran.
Shabnam JavanzadDepartment of Hepatitis and AIDs; Pasteur Institute of Iran; Tehran, Iran; Department of genetics; Islamic Azad University; Tehran Medical Branch; Tehran, Iran.
Tayebeh SalehDepartment of Nanobiotechnology; Faculty of Biological Sciences; Tarbiat Modares University; Tehran, Iran.
Mehrdad HashemiDepartment of genetics; Islamic Azad University; Tehran Medical Branch; Tehran, Iran.
Mohammad Reza AghasadeghiDepartment of Hepatitis and AIDs; Pasteur Institute of Iran; Tehran, Iran.
Seyed Mehdi SadatDepartment of Hepatitis and AIDs; Pasteur Institute of Iran; Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanocarriers with various compositions and biological properties have been extensively applied for in vitro/in vivo drug and gene delivery. The family of nanocarriers includes polymeric nanoparticles, lipid-based carriers (liposomes/micelles), dendrimers, carbon nanotubes, and gold nanoparticles (nanoshells/nanocages). Among different delivery systems, polymeric carriers have several properties such as: easy to synthesize, inexpensive, biocompatible, biodegradable, non-immunogenic, non-toxic, and water soluble. In addition, cationic polymers seem to produce more stable complexes led to a more protection during cellular trafficking than cationic lipids. Nanoparticles often show significant adjuvant effects in vaccine delivery since they may be easily taken up by antigen presenting cells (APCs). Natural polymers such as polysaccharides and synthetic polymers have demonstrated great potential to form vaccine nanoparticles. The development of new adjuvants or delivery systems for DNA and protein immunization is an expanding research field. This review describes polymeric carriers especially PLGA, chitosan, and PEI as vaccine delivery systems.

Indexed as

Communicable Disease ControlAdjuvants, ImmunologicDrug CarriersHumansNanoparticlesNeoplasmsPolymersVaccinesAdjuvants, ImmunologicDrug CarriersPolymersVaccinesgene therapynatural polymernon-viral vectorssynthetic polymervaccine delivery

Identifiers

PMID24128651
PMCPMC4185908

What OpenQuestion holds

Textmetadata
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.