Evidence map›Paper›PMID 31861277›Full record

ReviewMolecules (Basel, Switzerland)2019

Aptamers Chemistry: Chemical Modifications and Conjugation Strategies.

Fadwa Odeh, Hamdi Nsairat, Walhan Alshaer, Mohammad A Ismail, Ezaldeen Esawi, Baraa Qaqish, Abeer Al Bawab, Said I Ismail

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 164 papers.

0numbers the graph read from it
0cells of the map it votes in
164citing papers in PubMed
13.3field-weighted citation impact, top 1% 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

164 citing papers in PubMed, 384 citations in OpenAlex.

  1. Article
  2. Aptamer targeting proprotein convertase subtilisin/kexin type 9:Research in pharmaceutical sciences · 2026
    Article
  3. Advances in Aptamer Drug Delivery Systems for Treatment of Glioblastoma.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
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104 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

8 authors at 1 institution in 2 countries.

Fadwa OdehFaculty of Science, The University of Jordan, Amman 11942, Jordan.
Hamdi NsairatFaculty of Science, The University of Jordan, Amman 11942, Jordan.
Walhan AlshaerCell Therapy Center, The University of Jordan, Amman 11942, Jordan.
Mohammad A IsmailFaculty of Medicine, The University of Jordan, Amman 11942, Jordan.
Ezaldeen EsawiFaculty of Medicine, The University of Jordan, Amman 11942, Jordan.
Baraa QaqishFaculty of Medicine, The University of Jordan, Amman 11942, Jordan.
Abeer Al BawabFaculty of Science, The University of Jordan, Amman 11942, Jordan.
Said I IsmailFaculty of Medicine, The University of Jordan, Amman 11942, Jordan.
University of Jordan · JO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Soon after they were first described in 1990, aptamers were largely recognized as a new class of biological ligands that can rival antibodies in various analytical, diagnostic, and therapeutic applications. Aptamers are short single-stranded RNA or DNA oligonucleotides capable of folding into complex 3D structures, enabling them to bind to a large variety of targets ranging from small ions to an entire organism. Their high binding specificity and affinity make them comparable to antibodies, but they are superior regarding a longer shelf life, simple production and chemical modification, in addition to low toxicity and immunogenicity. In the past three decades, aptamers have been used in a plethora of therapeutics and drug delivery systems that involve innovative delivery mechanisms and carrying various types of drug cargos. However, the successful translation of aptamer research from bench to bedside has been challenged by several limitations that slow down the realization of promising aptamer applications as therapeutics at the clinical level. The main limitations include the susceptibility to degradation by nucleases, fast renal clearance, low thermal stability, and the limited functional group diversity. The solution to overcome such limitations lies in the chemistry of aptamers. The current review will focus on the recent arts of aptamer chemistry that have been evolved to refine the pharmacological properties of aptamers. Moreover, this review will analyze the advantages and disadvantages of such chemical modifications and how they impact the pharmacological properties of aptamers. Finally, this review will summarize the conjugation strategies of aptamers to nanocarriers for developing targeted drug delivery systems.

Indexed as

Chemical PhenomenaAptamers, NucleotideDrug CarriersDrug Delivery SystemsHumansImmunoconjugatesLigandsLipidsMolecular StructureNanoparticlesSELEX Aptamer TechniqueAptamers, NucleotideDrug CarriersImmunoconjugatesLigandsLipidsaptamerschemical modificationsconjugationdrug deliverynanocarriers

Identifiers

PMID31861277
PMCPMC6982925
OpenAlexW2995953990

What OpenQuestion holds

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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.