Evidence map›Paper›PMID 20856833›Full record

ReviewInternational journal of nanomedicine2010

The use of PEGylated liposomes in the development of drug delivery applications for the treatment of hemophilia.

Rivka Yatuv, Micah Robinson, Inbal Dayan-Tarshish, Moshe Baru

Open access · goldAbstract readReview
In one paragraph

Review in International journal of nanomedicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Mind the gap: a survey of how cancer drug carriers are susceptible to the gap between research and practice.Journal of controlled release : official journal of the Controlled Release Society · 2013
    Review
  9. Article
  10. Article
  11. Animal models of hemophilia.Progress in molecular biology and translational science · 2012
    Review
  12. 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

4 authors at 1 institution in 1 country.

Rivka YatuvOmri Laboratories Ltd., Nes Ziona, Israel.
Micah Robinson
Inbal Dayan-Tarshish
Moshe Baru
Weizmann Institute of Science · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hemophilia A is a rare X-linked bleeding disorder caused by lack or dysfunction of coagulation factor VIII (FVIII). Hemophilia A is treated with replacement therapy, but frequent injections of the missing FVIII often lead to the formation of inhibitory antibodies. Patients who develop high levels of inhibitors must be treated with bypassing agents such as activated FVII (FVIIa). Both FVIII and FVIIa have short half-lives and require multiple injections. Long-acting forms of these proteins would therefore reduce the frequency of injections, improve patient compliance and reduce complications. In this article we present a new platform technology that produces long-acting forms of FVIII and FVIIa and improves the efficacy of hemophilia treatment. This technology is based on the binding of proteins/peptides to the outer surface of PEGylated liposomes (PEGLip). Binding is dependent on an amino acid consensus sequence within the proteins and is highly specific. At the same time, binding is non-covalent and does not require any modification of the therapeutic agent or its production process. Association of proteins with PEGLip results in substantial enhancements in their pharmacodynamic properties following administration. These improvements seem to arise from the association of formulated proteins with platelets prior to induction of coagulation.

Indexed as

Amino Acid SequenceAnimalsChemistry, PharmaceuticalConsensus SequenceDelayed-Action PreparationsDisease Models, AnimalDrug Delivery SystemsFactor VIIaFactor VIIIHemophilia AHumansLiposomesMiceNanomedicinePolyethylene GlycolsDelayed-Action PreparationsFactor VIIaFactor VIIILiposomesPolyethylene Glycolsfactor VIIafactor VIIIPEGylated liposomespharmacodynamicstherapeutic proteins

Identifiers

PMID20856833
PMCPMC2939703
OpenAlexW1728730208

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.