Evidence map›Paper›PMID 22399387›Full record

ArticlePharmaceutical research2012

Human pancreatic polypeptide in a phospholipid-based micellar formulation.

Amrita Banerjee, Hayat Onyuksel

Erratum issuedAbstract read
In one paragraph

Article in Pharmaceutical research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. BH3-mimetics: recent developments in cancer therapy.Journal of experimental & clinical cancer research : CR · 2021
    Review
  5. Article
  6. When Is It Important to Measure Unbound Drug in Evaluating Nanomedicine Pharmacokinetics?Drug metabolism and disposition: the biological fate of chemicals · 2016
    Review
  7. Article
  8. Article
  9. The future role of gut hormones in the treatment of obesity.Therapeutic advances in chronic disease · 2014
    Review
  10. Solubilization of therapeutic agents in micellar nanomedicines.Langmuir : the ACS journal of surfaces and colloids · 2013
    Article
  11. A novel peptide nanomedicine for treatment of pancreatogenic diabetes.Nanomedicine : nanotechnology, biology, and medicine · 2013
    Article
  12. Article
  13. Biomarkers of Alzheimer's disease among Mexican Americans.Journal of Alzheimer's disease : JAD · 2013
    Article
  14. Article
  15. VIP-targeted Cytotoxic Nanomedicine for Breast Cancer.Drug delivery and translational research · 2012
    Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Amrita BanerjeeDepartment of Biopharmaceutical Sciences, University of Illinois at Chicago, Chicago, Illinois 60612, USA.
Hayat Onyuksel
University of Illinois Chicago · US

Funding

Phospholipid Nanocarriers Improve Chemotherapy by Targeted Drug DeliveryR01CA121797 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ONYUKSEL, HAYAT · 2007 to 2010
$1.2M
NCI NIH HHS CA121797NCI NIH HHS R01 CA121797
6 · The paper itself

Abstract

purposePancreatic polypeptide (PP) has important glucoregulatory functions and thereby holds significance in the treatment of diabetes and obesity. However, short plasma half-life and aggregation propensity of PP in aqueous solution, limits its therapeutic application. To address these issues, we prepared and characterized a formulation of PP in sterically stabilized micelles (SSM) that protects and stabilizes PP in its active conformation.

methodsPP-SSM was prepared by incubating PP with SSM dispersion in buffer. Peptide-micelle association and freeze-drying efficacy of the formulation was characterized in phosphate buffers with or without sodium chloride using dynamic light scattering, fluorescence spectroscopy and circular dichroism. The degradation kinetics of PP-SSM in presence of proteolytic enzyme was determined using HPLC and bioactivity of the formulation was evaluated by in vitro cAMP inhibition study.

resultsPP self-associated with SSM and this interaction was influenced by presence/absence of sodium chloride in the buffer. The formulation was effectively lyophilized, demonstrating feasibility for its long-term storage. The stability of peptide against proteolytic degradation was significantly improved and PP in SSM retained its bioactivity in vitro.

conclusionsSelf-association of PP with phospholipid micelles addressed the delivery issues of the peptide. This nanomedicine should be further developed for the treatment of diabetes.

Indexed as

Drug CarriersMicellesCell Line, TumorChemistry, PharmaceuticalChromatography, High Pressure LiquidCircular DichroismColforsinCyclic AMPDrug CompoundingDrug StabilityFreeze DryingHumansHydrogen-Ion ConcentrationHypoglycemic AgentsLightNanoparticles1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-methoxy-poly(ethylene glycol 2000)ColforsinCyclic AMPDrug CarriersHypoglycemic AgentsMicellesneuropeptide Y4 receptorPancreatic PolypeptidePhosphatidylethanolaminesPolyethylene GlycolsPPY protein, humanProtein PrecursorsReceptors, Neuropeptide YSodium Chloride

Identifiers

PMID22399387
PMCPMC3349792
OpenAlexW2094129747

What OpenQuestion holds

Textmetadata
LicenceTDM
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.