Evidence map›Paper›PMID 29526096›Full record

ArticleBiomacromolecules2018

Development of Fully Degradable Phosphonium-Functionalized Amphiphilic Diblock Copolymers for Nucleic Acids Delivery.

Yannick P Borguet, Sarosh Khan, Amandine Noel, Sean P Gunsten, Steven L Brody, Mahmoud Elsabahy, Karen L Wooley

Open access · greenAbstract read
In one paragraph

Article in Biomacromolecules, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

6 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
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

7 authors at 3 institutions in 2 countries.

Yannick P BorguetDepartments of Chemistry, Chemical Engineering, and Materials Science & Engineering, and the Laboratory for Synthetic-Biologic Interactions , Texas A&M University , College Station , Texas 77842 , United States.
Sarosh KhanDepartments of Chemistry, Chemical Engineering, and Materials Science & Engineering, and the Laboratory for Synthetic-Biologic Interactions , Texas A&M University , College Station , Texas 77842 , United States.
Amandine NoelDepartments of Chemistry, Chemical Engineering, and Materials Science & Engineering, and the Laboratory for Synthetic-Biologic Interactions , Texas A&M University , College Station , Texas 77842 , United States.
Sean P GunstenDepartment of Medicine , Washington University , St. Louis , Missouri 63110 , United States.
Steven L BrodyDepartment of Medicine , Washington University , St. Louis , Missouri 63110 , United States.
Mahmoud ElsabahyDepartments of Chemistry, Chemical Engineering, and Materials Science & Engineering, and the Laboratory for Synthetic-Biologic Interactions , Texas A&M University , College Station , Texas 77842 , United States.
Karen L WooleyDepartments of Chemistry, Chemical Engineering, and Materials Science & Engineering, and the Laboratory for Synthetic-Biologic Interactions , Texas A&M University , College Station , Texas 77842 , United States.ORCID 0000-0003-4086-384X
Texas A&M University · USWashington University in St. Louis · USAssiut University · EG

Funding

NHLBI NIH HHS HHSN268201000046C
6 · The paper itself

Abstract

To expand the range of functional polymer materials to include fully hydrolytically degradable systems that bear bioinspired phosphorus-containing linkages both along the backbone and as cationic side chain moieties for packaging and delivery of nucleic acids, phosphonium-functionalized polyphosphoester- block-poly(l-lactide) copolymers of various compositions were synthesized, fully characterized, and their self-assembly into nanoparticles were studied. First, an alkyne-functionalized polyphosphoester- block-poly(l-lactide) copolymer was synthesized via a one pot sequential ring opening polymerization of an alkyne-functionalized phospholane monomer, followed by the addition of l-lactide to grow the second block. Second, the alkynyl side groups of the polyphosphoester block were functionalized via photoinitiated thiol-yne radical addition of a phosphonium-functionalized free thiol. The polymers of varying phosphonium substitution degrees were self-assembled in aqueous buffers to afford formation of well-defined core-shell assemblies with an average size ranging between 30 and 50 nm, as determined by dynamic light scattering. Intracellular delivery of the nanoparticles and their effects on cell viability and capability at enhancing transfection efficiency of nucleic acids (e.g., siRNA) were investigated. Cell viability assays demonstrated limited toxicity of the assembly to RAW 264.7 mouse macrophages, except at high polymer concentrations, where the polymer of high degree of phosphonium functionalization induced relatively higher cytotoxicity. Transfection efficiency was strongly affected by the phosphonium-to-phosphate (P

Indexed as

Gene Transfer TechniquesAlkynesAnimalsDioxanesMacrophagesMiceNanoparticlesOrganophosphorus CompoundsPhosphorusPolymersRAW 264.7 CellsSulfhydryl CompoundsAlkynesdilactideDioxanesOrganophosphorus CompoundsPhosphorusPolymersSulfhydryl Compounds

Identifiers

PMID29526096
PMCPMC5894060
OpenAlexW2791169139

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.