Evidence map›Paper›PMID 30887226›Full record

ArticleDrug delivery and translational research2019

Nose-to-brain delivery of lamotrigine-loaded PLGA nanoparticles.

Kuldeep Nigam, Atinderpal Kaur, Amit Tyagi, Md Nematullah, Farah Khan, Reema Gabrani, Shweta Dang

Abstract read
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In one paragraph

Article in Drug delivery and translational research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.6field-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

39 citing papers in PubMed, 95 citations in OpenAlex.

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  7. Development,Drug delivery · 2025
    Article
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  18. Computational,Biomedicines · 2023
    Review
  19. Understanding Lamotrigine's Role in the CNS and Possible Future Evolution.International journal of molecular sciences · 2023
    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 3 institutions in 1 country.

Kuldeep NigamDepartment of Biotechnology, Jaypee Institute of Information Technology, A-10, Sector-62, Noida, 201309, India.
Atinderpal KaurDepartment of Biotechnology, Jaypee Institute of Information Technology, A-10, Sector-62, Noida, 201309, India.
Amit TyagiInstitute of Nuclear Medicine and Allied Sciences, Defence Research and Development Organisation, Timarpur, Delhi, 110054, India.
Md NematullahDepartment of Biochemistry, Faculty of Science, Jamia Hamdard, New Delhi, 110062, India.
Farah KhanDepartment of Biochemistry, Faculty of Science, Jamia Hamdard, New Delhi, 110062, India.
Reema GabraniDepartment of Biotechnology, Jaypee Institute of Information Technology, A-10, Sector-62, Noida, 201309, India.
Shweta DangDepartment of Biotechnology, Jaypee Institute of Information Technology, A-10, Sector-62, Noida, 201309, India. shweta.dang@jiit.ac.in.ORCID 0000-0002-2924-8996
Jaypee Institute of Information Technology · INJamia Hamdard · INDefence Research and Development Organisation · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Direct nose-to-brain delivery of drugs and faster onset of action have made intra-nasal route a much sought-after alternative to conventional routes of drug delivery to the brain. Lamotrigine is used for the treatment and management of neuropathic pain, and in the present work, lamotrigine (LTG)-PLGA nanoparticles were developed for intra-nasal delivery. The LTG-PLGA nanoparticles were prepared using modified nanoprecipitation method via high-speed homogenization and ultra-sonication techniques. Entrapment efficiency (EE%) of developed LTG-PLGA-NPs was found to be 84.87 ± 1.2% with drug loading of 10.21 ± 0.89%. The particle size of developed nanoparticles was found to be 184.6 nm with PDI value of 0.082 and zeta potential of - 18.8 mV. Dissolution profiles were studied in PBS (pH 7.4), simulated nasal fluid, and simulated cerebrospinal fluid where almost complete release was observed within 5 h in CSF. In vitro, cytotoxicity was analyzed using MTT assay where dose-dependent cytotoxicity was observed for developed LTG-PLGA-NPs. In vitro cytokine analysis showed positive effects of LTG-PLGA-NPs as pro-inflammatory cytokine suppressors. Further, in vivo studies were performed for radiolabeled formulation and drug (

Indexed as

Administration, IntranasalAnimalsAnticonvulsantsBrainCell Line, TumorCytokinesDrug CarriersLamotrigineMiceNanoparticlesNasal MucosaPolylactic Acid-Polyglycolic Acid CopolymerRats, Sprague-DawleyRAW 264.7 CellsAnticonvulsantsCytokinesDrug CarriersLamotriginePolylactic Acid-Polyglycolic Acid CopolymerBiodistributionGamma scintigraphyLamotrigineNanoparticlesPLGA

Identifiers

PMID30887226
OpenAlexW2922040645

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.