Evidence map›Paper›PMID 22544864›Full record

ReviewPharmacological reviews2012

Physical and chemical strategies for therapeutic delivery by using polymeric nanoparticles.

José M Morachis, Enas A Mahmoud, Adah Almutairi

Abstract readReview
In one paragraph

Review in Pharmacological reviews, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing 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

77 citing papers in PubMed.

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  20. Reactive oxygen species-responsive polymer drug delivery systems.Frontiers in bioengineering and biotechnology · 2023
    Review

17 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

3 authors.

José M MorachisUniversity of California San Diego, 9500 Gilman Dr., MC 0600, La Jolla, CA 92093-0600, USA.
Enas A Mahmoud
Adah Almutairi

Funding

Chemically amplified response strategies for medical sciences; concepts borrowedDP2OD006499 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ALMUTAIRI, ADAH · 2009 to 2009
$2.3M
NIGMS NIH HHS GM06852NIH HHS 1-DP2-OD006499-01NIH HHS DP2 OD006499
6 · The paper itself

Abstract

A significant challenge that most therapeutic agents face is their inability to be delivered effectively. Nanotechnology offers a solution to allow for safe, high-dose, specific delivery of pharmaceuticals to the target tissue. Nanoparticles composed of biodegradable polymers can be designed and engineered with various layers of complexity to achieve drug targeting that was unimaginable years ago by offering multiple mechanisms to encapsulate and strategically deliver drugs, proteins, nucleic acids, or vaccines while improving their therapeutic index. Targeting of nanoparticles to diseased tissue and cells assumes two strategies: physical and chemical targeting. Physical targeting is a strategy enabled by nanoparticle fabrication techniques. It includes using size, shape, charge, and stiffness among other parameters to influence tissue accumulation, adhesion, and cell uptake. New methods to measure size, shape, and polydispersity will enable this field to grow and more thorough comparisons to be made. Physical targeting can be more economically viable when certain fabrication techniques are used. Chemical targeting can employ molecular recognition units to decorate the surface of particles or molecular units responsive to diseased environments or remote stimuli. In this review, we describe sophisticated nanoparticles designed for tissue-specific chemical targeting that use conjugation chemistry to attach targeting moieties. Furthermore, we describe chemical targeting using stimuli responsive nanoparticles that can respond to changes in pH, heat, and light.

Indexed as

AnimalsAntibodies, MonoclonalCell-Penetrating PeptidesChemistry, PharmaceuticalDrug CarriersDrug CompoundingDrug Delivery SystemsDrug DesignEndocytosisHumansHydrogen-Ion ConcentrationLigandsLightModels, MolecularNanoparticlesParticle SizeAntibodies, MonoclonalCell-Penetrating PeptidesDrug CarriersLigandsPharmaceutical PreparationsPolymers

Identifiers

PMID22544864
PMCPMC3400833

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.