Evidence map›Paper›PMID 17928089›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2007

Influence of particle size and antacid on release and stability of plasmid DNA from uniform PLGA microspheres.

Neelesh K Varde, Daniel W Pack

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Polymer-Based Therapeutics.Macromolecules · 2009
    Article
  9. Precise control of PLG microsphere size provides enhanced control of drug release rate.Journal of controlled release : official journal of the Controlled Release Society · 2002
    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

2 authors at 1 institution in 1 country.

Neelesh K VardeDepartment of Chemical and Biomolecular Engineering, University of Illinois, 600 S. Mathews Ave, Urbana, IL 61801 USA.
Daniel W Pack
University of Illinois Urbana-Champaign · US

Funding

Precision Microparticles for Controlled Protein DeliveryR01EB005181 · NIBIB · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI PACK, DANIEL W · 2006 to 2009
$1.0M
Design of Microparticles for Precision Drug DeliveryR21EB002878 · NIBIB · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI PACK, DANIEL W · 2003 to 2004
$359k
NIBIB NIH HHS EB002878NIBIB NIH HHS EB005181NIBIB NIH HHS R01 EB005181NIBIB NIH HHS R21 EB002878
6 · The paper itself

Abstract

PLGA microspheres are attractive DNA delivery vehicles due to their controlled release capabilities. One major problem with PLGA microspheres is that they develop an acidic microclimate as the polymer degrades, lowering the intraparticle pH, and potentially damaging the DNA. Antacids have recently shown promise in buffering this acidic microclimate and enhancing protein stability. We manufactured uniform plasmid DNA-encapsulating PLGA microspheres of two sizes (47, 80 microm diameter) and antacid concentrations (0, 3% Mg(OH)2). Microspheres with antacid had a homogeneous surface coverage of small pores, which resulted in a significant reduction of the burst effect. The 47 microm microspheres exhibited complete release of plasmid DNA over the course of two months. Incomplete release was observed from 80 microm spheres, though microspheres with 3% Mg(OH)2 showed a higher cumulative release, suggesting that the antacid at least partially aids in increasing the stability of DNA. SEM was used to visualize the surface pore evolution and cross-sectional microsphere structure over time. Subsequent image analysis was used to quantify the increase of surface pore sizes. Cross-sectional images showed increasing internal degradation and erosion, which resulted in a hollowing-out of microspheres. Our studies show that the incorporation of antacid into the microsphere structure has potential in addressing some of the major problems associated with DNA encapsulation and release in PLGA microspheres.

Indexed as

AntacidsBiocompatible MaterialsDelayed-Action PreparationsDNADrug CompoundingLactic AcidMagnesium HydroxideMicroscopy, Electron, ScanningMicrospheresNucleic Acid ConformationParticle SizePlasmidsPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPolymersPorosityAntacidsBiocompatible MaterialsDelayed-Action PreparationsDNALactic AcidMagnesium HydroxidePolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPolymers

Identifiers

PMID17928089
PMCPMC2141539
OpenAlexW2069428482

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.