Evidence map›Paper›PMID 40011450›Full record

ArticleScientific reports2025

New nanomanufacturing strategy through bioinspired design, for promising treatment of Parkinson's disease.

Aliaa A Razzak, Zahraa S Al-Garawi, Adawiya J Haider, F A A N Bahaa Hassan

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Aliaa A RazzakChemistry Department, Collage of Science, Mustansiriyah University, Baghdad, Iraq.
Zahraa S Al-GarawiChemistry Department, Collage of Science, Mustansiriyah University, Baghdad, Iraq. z.mohsin@uomustansiriyah.edu.iq.ORCID http://orcid.org/0000-0003-3816-2876
Adawiya J HaiderApplied Sciences Department, Laser Science and Technology Branch, University of Technology, Baghdad, Iraq.ORCID http://orcid.org/0000-0002-2191-0500
F A A N Bahaa HassanDepartment of Neurology, Sàad Al-Wittry neuroscience hospital, Baghdad, Iraq.ORCID http://orcid.org/0000-0002-1005-4032

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study attempts to develop a new nanomanufacturing strategy for Parkinson's disease using natural biodegradable components (chitosan, albumin, and dopamine) that can penetrate the blood-brain barrier (BBB) due to biocompatibility, biodegradability, targeted delivery, and controlled drug release. It was prepared, thoroughly optimized and characterized using various biophysical and chemical techniques. Results showed that the nanomanufactured system (molar ratio of 1:0.25:0.5 and particle size range: 38-190 nm) exhibited a zeta potential of + 73 mV facilitating efficient pentration of BBB through an adsorption mechanism with the cell membrane's negative charges. The particle size of the nanomanufactured system and spherical nanoparticle clusters indicated its ability to enhance dopamine delivery to brain tissues. Encapsulation efficiency was measured at 74.31 ± 0.29 with dopamine release faster at pH 5.4 and sustained release over 96 h in both acidic media (pH 5.4) or physiological conditions (pH 7.4). Cytotoxicity studies showed a degradation rate in normal cells that never exceeded 20% and the nanomanufactured system exhibited low half-maximal inhibitory concentration (IC50) values, indicating low cytotoxicity. Albumin plays a vital and distinct role in stimulating normal cells and enhancing the transport system to the target via an adsorptive-mediated endocytosis pathway. The electron microscopy images depict distrution of heterogeneous nanoparticles, with sizes ranged from 36.86 nm to 190.3 nm and a mean average diameter of 108.1 nm. The average particle size of the nanosystem was 49.4 ± 9.9 nm, with a Polydispersity Index (PI) of 0.494. The loading efficiency was 14.78 ± 0.37% and the encapsulation efficiency was 74.31 ± 0.29%. This nanomanufactured system holds significant promise for improving Parkinson's disease treatment by enabling targeted and efficient drug delivery to the brain.

Indexed as

NanoparticlesParkinson DiseaseAnimalsBlood-Brain BarrierChitosanDopamineDrug Delivery SystemsDrug LiberationHumansParticle SizeChitosanDopamineAlbuminCytotoxicityDopamine hormoneMediated adsorptive endocytosisParkinson’s diseaseROS scavenge

Identifiers

PMID40011450
PMCPMC11865579

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Registered trials

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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.