Evidence map›Paper›PMID 28782388›Full record

ArticleDrug delivery2017

Nanotechnology-based drug delivery of ropinirole for Parkinson's disease.

Emilia Barcia, Liudmila Boeva, Luis García-García, Karla Slowing, Ana Fernández-Carballido, Yaquelyn Casanova, Sofía Negro

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Review
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

7 authors at 1 institution in 1 country.

Emilia Barciaa Departamento de Farmacia y Tecnología Farmacéutica, Facultad de Farmacia , Universidad Complutense de Madrid , Madrid , Spain.
Liudmila Boevaa Departamento de Farmacia y Tecnología Farmacéutica, Facultad de Farmacia , Universidad Complutense de Madrid , Madrid , Spain.
Luis García-Garcíab Unidad de Cartografía Cerebral, Instituto Pluridisciplinar, Universidad Complutense de Madrid , Madrid , Spain.
Karla Slowingc Departamento de Farmacología, Facultad de Farmacia , Universidad Complutense de Madrid , Madrid , Spain.
Ana Fernández-Carballidoa Departamento de Farmacia y Tecnología Farmacéutica, Facultad de Farmacia , Universidad Complutense de Madrid , Madrid , Spain.
Yaquelyn Casanovaa Departamento de Farmacia y Tecnología Farmacéutica, Facultad de Farmacia , Universidad Complutense de Madrid , Madrid , Spain.
Sofía Negroa Departamento de Farmacia y Tecnología Farmacéutica, Facultad de Farmacia , Universidad Complutense de Madrid , Madrid , Spain.ORCID http://orcid.org/0000-0001-8144-0558
Universidad Complutense de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A new drug delivery system is developed for ropinirole (RP) for the treatment of Parkinson's disease (PD) consisting of biodegradable poly (D,L-lactide-co-glycolide) (PLGA) nanoparticles (NPs). The formulation selected was prepared with 8 mg RP and 50 mg PLGA 502. This formulation exhibited mean encapsulation efficiency of 74.8 ± 8.2%, mean particle size lower than 155 nm, the zeta potential of -14.25 ± 0.43 mV and zero-order in vitro release of RP (14.13 ± 0.17 μg/h/10 mg NPs) for 5 d. Daily doses of the neurotoxin rotenone (2 mg/kg) given i.p. to male Wistar rats induced neuronal and behavioral changes similar to those of PD. Once neurodegeneration was established (15 d) animals received RP in saline (1 mg/kg/d for 35 d) or encapsulated within PLGA NPs (amount of NPs equivalent to 1 mg/kg/d RP every 3 d for 35 d). Brain histology and immunochemistry (Nissl-staining, glial fibrillary acidic protein and tyrosine hydroxylase immunohistochemistry) and behavioral testing (catalepsy, akinesia, rotarod and swim test) showed that RP-loaded PLGA NPs were able to revert PD-like symptoms of neurodegeneration in the animal model assayed.

Indexed as

NanoparticlesAnimalsDrug CarriersDrug Delivery SystemsIndolesLactic AcidMaleParkinson DiseaseParticle SizePolyglycolic AcidRatsRats, WistarDrug CarriersIndolesLactic AcidPolyglycolic AcidropinirolenanoparticlesParkinson’s diseasepoly (D,L-lactide-co-glycolide)Ropinirole

Identifiers

PMID28782388
PMCPMC8241177
OpenAlexW2744332025

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.