Evidence map›Paper›PMID 33803208›Full record

ReviewMolecules (Basel, Switzerland)2021

Co-Opting Host Receptors for Targeted Delivery of Bioconjugates-From Drugs to Bugs.

Kristen M Tummillo, Karsten R O Hazlett

Abstract readHistorical ArticleReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Kristen M TummilloDepartment of Regenerative and Cancer Cell Biology, Albany Medical College, Albany, NY 12208, USA.
Karsten R O HazlettDepartment of Regenerative and Cancer Cell Biology, Albany Medical College, Albany, NY 12208, USA.ORCID 0000-0001-6084-7607

Funding

NIH HHS RO1AI123129U.S. Department of Defense W81XH1910661
6 · The paper itself

Abstract

Bioconjugation has allowed scientists to combine multiple functional elements into one biological or biochemical unit. This assembly can result in the production of constructs that are targeted to a specific site or cell type in order to enhance the response to, or activity of, the conjugated moiety. In the case of cancer treatments, selectively targeting chemotherapies to the cells of interest limit harmful side effects and enhance efficacy. Targeting through conjugation is also advantageous in delivering treatments to difficult-to-reach tissues, such as the brain or infections deep in the lung. Bacterial infections can be more selectively treated by conjugating antibiotics to microbe-specific entities; helping to avoid antibiotic resistance across commensal bacterial species. In the case of vaccine development, conjugation is used to enhance efficacy without compromising safety. In this work, we will review the previously mentioned areas in which bioconjugation has created new possibilities and advanced treatments.

Indexed as

Drug Delivery SystemsEstrogens, Conjugated (USP)History, 20th CenturyHistory, 21st CenturyHumansImmunoconjugatesNanoparticlesPharmaceutical PreparationsVaccines, ConjugateEstrogens, Conjugated (USP)ImmunoconjugatesPharmaceutical PreparationsVaccines, Conjugateantibioticsantibody–drug conjugatesbioconjugationconjugated vaccinesdrug deliverynanoparticlestargeted vaccinesvaccines

Identifiers

PMID33803208
PMCPMC7963163

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.