Evidence map›Paper›PMID 34770999›Full record

ArticleMolecules (Basel, Switzerland)2021

Synthesis and Characterization of Multifunctional Nanovesicles Composed of POPC Lipid Molecules for Nuclear Imaging.

Debora Petroni, Claudia Riccardi, Domenico Cavasso, Irene Russo Krauss, Luigi Paduano, Daniela Montesarchio, Luca Menichetti

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 3 institutions in 1 country.

Debora PetroniInstitute of Clinical Physiology, National Research Council, Via Moruzzi 1, I-56124 Pisa, Italy.
Claudia RiccardiDepartment of Chemical Sciences, University of Naples Federico II, Via Cintia 21, I-80126 Naples, Italy.ORCID 0000-0002-7182-0757
Domenico CavassoDepartment of Chemical Sciences, University of Naples Federico II, Via Cintia 21, I-80126 Naples, Italy.
Irene Russo KraussDepartment of Chemical Sciences, University of Naples Federico II, Via Cintia 21, I-80126 Naples, Italy.ORCID 0000-0001-8124-6034
Luigi PaduanoDepartment of Chemical Sciences, University of Naples Federico II, Via Cintia 21, I-80126 Naples, Italy.ORCID 0000-0002-1105-4237
Daniela MontesarchioDepartment of Chemical Sciences, University of Naples Federico II, Via Cintia 21, I-80126 Naples, Italy.ORCID 0000-0001-6295-6911
Luca MenichettiInstitute of Clinical Physiology, National Research Council, Via Moruzzi 1, I-56124 Pisa, Italy.ORCID 0000-0002-3293-9616
Consorzio Interuniversitario per lo Sviluppo dei Sistemi a Grande Interfase · ITIstituto di Fisiologia Clinica · ITUniversity of Naples Federico II · IT

Funding

Fondazione Umberto Veronesi xx
6 · The paper itself

Abstract

The integration of nuclear imaging analysis with nanomedicine has tremendously grown and represents a valid and powerful tool for the development and clinical translation of drug delivery systems. Among the various types of nanostructures used as drug carriers, nanovesicles represent intriguing platforms due to their capability to entrap both lipophilic and hydrophilic agents, and their well-known biocompatibility and biodegradability. In this respect, here we present the development of a labelling procedure of POPC (1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine)-based liposomes incorporating an ad hoc designed lipophilic NOTA (1,4,7-triazacyclononane-1,4,7-triacetic acid) analogue, derivatized with an oleic acid residue, able to bind the positron emitter gallium-68(III). Based on POPC features, the optimal conditions for liposome labelling were studied with the aim of optimizing the Ga(III) incorporation and obtaining a significant radiochemical yield. The data presented in this work demonstrate the feasibility of the labelling procedure on POPC liposomes co-formulated with the ad hoc designed NOTA analogue. We thus provided a critical insight into the practical aspects of the development of vesicles for theranostic approaches, which in principle can be extended to other nanosystems exploiting a variety of bioconjugation protocols.

Indexed as

Neutron DiffractionScattering, Small AngleDrug CarriersDrug Delivery SystemsHydrophobic and Hydrophilic InteractionsLiposomesMolecular StructureNanomedicineNanoparticlesPhosphatidylcholines1-palmitoyl-2-oleoylphosphatidylcholineDrug CarriersLiposomesPhosphatidylcholinesdrug deliverygallium-68liposomeNOTAPETPOPC

Identifiers

PMID34770999
PMCPMC8587727
OpenAlexW3208012184

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.