Evidence map›Paper›PMID 27863666›Full record

ArticleInternational journal of pharmaceutics2016

Nasal powders of thalidomide for local treatment of nose bleeding in persons affected by hereditary hemorrhagic telangiectasia.

G Colombo, F Bortolotti, V Chiapponi, F Buttini, F Sonvico, R Invernizzi, F Quaglia, C Danesino, F Pagella, P Russo and 3 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of pharmaceutics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 33 citations in OpenAlex.

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  6. ADMET & DMPK · 2024
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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

13 authors at 5 institutions in 1 country.

G ColomboDepartment of Life Sciences and Biotechnology, University of Ferrara, Via Fossato di Mortara 17/19, 44121 Ferrara, Italy.
F BortolottiDepartment of Life Sciences and Biotechnology, University of Ferrara, Via Fossato di Mortara 17/19, 44121 Ferrara, Italy.
V ChiapponiDepartment of Pharmacy, University of Parma, Parco Area delle Scienze 27/A, 43124 Parma, Italy.
F ButtiniDepartment of Pharmacy, University of Parma, Parco Area delle Scienze 27/A, 43124 Parma, Italy.
F SonvicoDepartment of Pharmacy, University of Parma, Parco Area delle Scienze 27/A, 43124 Parma, Italy.
R InvernizziDepartment of Internal Medicine, University of Pavia, IRCCS Fondazione Policlinico San Matteo, Piazzale Golgi 19, 27100 Pavia, Italy.
F QuagliaDepartment of Internal Medicine, University of Pavia, IRCCS Fondazione Policlinico San Matteo, Piazzale Golgi 19, 27100 Pavia, Italy.
C DanesinoDepartment of Molecular Medicine, General Biology and Medical Genetics Unit, University of Pavia, Via Forlanini 6, 27100 Pavia, Italy.
F PagellaDepartment of Otorhinolaryngology, IRCCS Fondazione Policlinico San Matteo, Piazzale Golgi 19, 27100 Pavia, Italy.
P RussoDepartment of Pharmacy, University of Salerno, via Giovanni Paolo II 132, 84084 Fisciano, SA, Italy.
R BettiniDepartment of Pharmacy, University of Parma, Parco Area delle Scienze 27/A, 43124 Parma, Italy.
P ColomboPlumeStars srl, Strada G. Inzani 1, 43125 Parma, Italy.
A RossiDepartment of Pharmacy, University of Parma, Parco Area delle Scienze 27/A, 43124 Parma, Italy. Electronic address: alessandra.rossi@unipr.it.
University of Parma · ITUniversity of Pavia · ITUniversity of Ferrara · ITPoliclinico San Matteo Fondazione · ITUniversity of Salerno · IT

Funding

Telethon GGP13036
6 · The paper itself

Abstract

In this work nasal powder formulations of thalidomide were designed and studied to be used by persons affected by hereditary hemorrhagic telangiectasia as a complementary anti-epistaxis therapy, with the goal of sustaining the effect obtained with thalidomide oral treatment after its discontinuation for adverse effects. Three nasal powders were prepared using as carriers β-CD or its more hydrophilic derivatives such as hydropropyl-β-CD and sulphobutylether-β-CD and tested with respect to technological and biopharmaceutical features after emission with active and passive nasal powder devices. For all formulated powders, improved dissolution rate was found compared to that of the raw material, making thalidomide promptly available in the nasal environment at a concentration favouring an accumulation in the mucosa. The very limited transmucosal transport measured in vitro suggests a low likelihood of significant systemic absorption. The topical action on bleeding could benefit from the poor absorption and from the fact that about 2-3% of the thalidomide applied on the nasal mucosa was accumulated within the tissue, particularly with the β-CD nasal powder.

Indexed as

Administration, IntranasalAnimalsbeta-CyclodextrinsChemistry, PharmaceuticalDrug CarriersEpistaxisHumansNasal MucosaPowdersRabbitsSolubilityTelangiectasia, Hereditary HemorrhagicThalidomidebeta-CyclodextrinsDrug CarriersPowdersThalidomideCyclodextrinsHydroxypropyl-β-cyclodextrin (PubChem CID: 44134771)Lecithin (PubChem CID: 57369748)MucoadhesionNasal devicesNasal powdersSulphobutylether-β-cyclodextrin (PubChem CID: 91886200)TelangiectasiaThalidomideThalidomide (PubChem CID: 5426)β-cyclodextrin (PubChem CID: 444041)

Identifiers

PMID27863666
PMCPMC5120990
OpenAlexW2549160635

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.