Evidence map›Paper›PMID 24333903›Full record

ArticleInternational journal of pharmaceutics2014

Microparticles produced by the hydrogel template method for sustained drug delivery.

Ying Lu, Michael Sturek, Kinam Park

Abstract readComparative Study
In one paragraph

Article in International journal of pharmaceutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Roadmap on nanomedicine.Nanotechnology · 2021
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. PLA micro- and nano-particles.Advanced drug delivery reviews · 2016
    Review
  13. Article
  14. Review
  15. Article
  16. In vitro-in vivo correlation of parenteral risperidone polymeric microspheres.Journal of controlled release : official journal of the Controlled Release Society · 2015
    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

3 authors.

Ying LuDepartment of Industrial and Physical Pharmacy, Purdue University, West Lafayette, IN 47906, USA.
Michael SturekDepartment of Cellular & Integrative Physiology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Kinam ParkDepartment of Industrial and Physical Pharmacy, Purdue University, West Lafayette, IN 47906, USA; Department of Biomedical Engineering, Purdue University, West Lafayette, IN 47906, USA. Electronic address: kpark@purdue.edu.

Funding

EXERCISE, DIABETES, &CORONARY SMOOTH MUSCLE Ca2+R01HL062552 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI STUREK, MICHAEL · 1999 to 2013
$4.5M
Adaptable Polymer Micelles for Tumor TargetingR01CA129287 · NCI · PURDUE UNIVERSITY · PI PARK, KINAM · 2010 to 2014
$1.5M
Hydrogel template method for protein microencapsulationR01GM095879 · NIGMS · PURDUE UNIVERSITY · PI PARK, KINAM · 2012 to 2015
$1.1M
NCI NIH HHS CA129287NCI NIH HHS R01 CA129287NHLBI NIH HHS HL062552NHLBI NIH HHS R01 HL062552NIGMS NIH HHS GM095879NIGMS NIH HHS R01 GM095879
6 · The paper itself

Abstract

Polymeric microparticles have been used widely for sustained drug delivery. Current methods of microparticle production can be improved by making homogeneous particles in size and shape, increasing the drug loading, and controlling the initial burst release. In the current study, the hydrogel template method was used to produce homogeneous poly(lactide-co-glycolide) (PLGA) microparticles and to examine formulation and process-related parameters. Poly(vinyl alcohol) (PVA) was used to make hydrogel templates. The parameters examined include PVA molecular weight, type of PLGA (as characterized by lactide content, inherent viscosity), polymer concentration, drug concentration and composition of solvent system. Three model compounds studied were risperidone, methylprednisolone acetate and paclitaxel. The ability of the hydrogel template method to produce microparticles with good conformity to template was dependent on molecular weight of PVA and viscosity of the PLGA solution. Drug loading and encapsulation efficiency were found to be influenced by PLGA lactide content, polymer concentration and composition of the solvent system. The drug loading and encapsulation efficiency were 28.7% and 82% for risperidone, 31.5% and 90% for methylprednisolone acetate, and 32.2% and 92% for paclitaxel, respectively. For all three drugs, release was sustained for weeks, and the in vitro release profile of risperidone was comparable to that of microparticles prepared using the conventional emulsion method. The hydrogel template method provides a new approach of manipulating microparticles.

Indexed as

Drug Delivery SystemsDelayed-Action PreparationsDrug CarriersDrug CompoundingHydrogelsLactic AcidMethylprednisoloneMethylprednisolone AcetateMolecular WeightPaclitaxelParticle SizePolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPolymersPolyvinyl AlcoholRisperidoneDelayed-Action PreparationsDrug CarriersHydrogelsLactic AcidMethylprednisoloneMethylprednisolone AcetatePaclitaxelPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPolymersPolyvinyl AlcoholRisperidoneSolventsControlled releaseMethylprednisolone acetatePaclitaxelPLGA microparticlePVA template methodRisperidone

Identifiers

PMID24333903
PMCPMC3920451

What OpenQuestion holds

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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.