Evidence map›Paper›PMID 11158617›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Polymer-based gene delivery with low cytotoxicity by a unique balance of side-chain termini.

D Putnam, C A Gentry, D W Pack, R Langer

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

102 citing papers in PubMed, 488 citations in OpenAlex.

  1. Article
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  11. Coiled coil exposure and histidine tags drive function of an intracellular protein drug carrier.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Article
  12. Review
  13. Article
  14. "Double-punch" strategy for delivery of viral immunotherapy with prolonged tumor retention and enhanced transfection efficacy.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. A proof of concept gene-activated titanium surface for oral implantology applications.Journal of tissue engineering and regenerative medicine · 2020
    Article
  20. Nano-graphene oxide with antisenseJournal of dental sciences · 2020
    Article

42 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

4 authors at 1 institution in 1 country.

D PutnamDepartment of Chemical Engineering, E25-342, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
C A Gentry
D W Pack
R Langer
Massachusetts Institute of Technology · US

Funding

CONTROLLED RELEASE OF MACROMOLECULESR01GM026698 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LANGER, ROBERT S · 1985 to 2001
$576k
NIGMS NIH HHS GM-26698NIGMS NIH HHS R01 GM026698
6 · The paper itself

Abstract

Protein expression after delivery of plasmid DNA to the cell nucleus depends on the processes of transcription and translation. Cytotoxic gene-delivery systems may compromise these processes and limit protein expression. This situation is perhaps most prevalent in current nonviral polycationic gene-delivery systems in which the polycationic nature of the delivery system can lead to cytotoxicity. To approach the problem of creating nontoxic but effective gene-delivery systems, we hypothesized that by optimizing the balance between polymer cationic density with endosomal escape moieties, effective gene transfer with low cytotoxicity could be created. As a model system, we synthesized a series of polymers whose side-chain termini varied with respect to the balance of cationic centers and endosomal escape moieties. Specifically, by polymer-analogous amidation we conjugated imidazole groups to the epsilon-amines of polylysine in varying mole ratios (73.5 mol % imidazole, 82.5 mol % imidazole, and 86.5 mol % imidazole). The primary epsilon-amine terminus of polylysine served as a model for the cationic centers, whereas the imidazole groups served as a model for the endosomal escape moieties. These polymers condensed plasmid DNA into nanostructures <150 nm and possessed little cytotoxicity in vitro. Transfection efficiency, as measured by luciferase protein expression, increased with increasing imidazole content of the polymers in a nonlinear relationship. The polymer with the highest imidazole content (86.5 mol %) mediated the highest protein expression, with levels equal to those mediated by polyethylenimine, but with little to no cytotoxicity.

Indexed as

Gene Transfer TechniquesPlasmidsPolylysineAnimalsBiocompatible MaterialsCell LineCell SurvivalCytomegalovirusDrug CarriersGenes, ReporterGenetic VectorsImidazolesIndicators and ReagentsLuciferasesMacrophagesMiceBiocompatible MaterialsDrug CarriersImidazolesIndicators and ReagentsLuciferasesPolylysine

Identifiers

PMID11158617
PMCPMC14732
OpenAlexW2013841789

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.