Evidence map›Paper›PMID 26139126›Full record

ReviewNanomedicine (London, England)2015

Enabling cytoplasmic delivery and organelle targeting by surface modification of nanocarriers.

Alessandro Parodi, Claudia Corbo, Armando Cevenini, Roberto Molinaro, Roberto Palomba, Laura Pandolfi, Marco Agostini, Francesco Salvatore, Ennio Tasciotti

Abstract readReview
In one paragraph

Review in Nanomedicine (London, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

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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

9 authors.

Alessandro ParodiDepartment of Nanomedicine, Houston Methodist Research Institute, 6670 Bertner Ave., Houston, TX 77030, USA.
Claudia CorboFondazione IRCCS SDN, Via Gianturco 113, 80143 Naples, Italy.
Armando CeveniniDepartment of Molecular Medicine & Medical Biotechnology, University of Naples "Federico II", Via Sergio Pansini 5, Naples 80131, Italy.
Roberto MolinaroDepartment of Nanomedicine, Houston Methodist Research Institute, 6670 Bertner Ave., Houston, TX 77030, USA.
Roberto PalombaFondazione IRCCS SDN, Via Gianturco 113, 80143 Naples, Italy.
Laura PandolfiDepartment of Nanomedicine, Houston Methodist Research Institute, 6670 Bertner Ave., Houston, TX 77030, USA.
Marco AgostiniClinica Chirurgica I, Dipartimento di Scienze Chirurgiche Oncologiche e Gastroeterologiche, Università di Padova, Via Giustiniani 2, 35128 Padova, Italy.
Francesco SalvatoreFondazione IRCCS SDN, Via Gianturco 113, 80143 Naples, Italy.
Ennio TasciottiDepartment of Nanomedicine, Houston Methodist Research Institute, 6670 Bertner Ave., Houston, TX 77030, USA.

Funding

TRANS-NETWORK PROJECTSU54CA143837 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2009 to 2014
$10.8M
Leukocyte Membrane Cloaked Carriers to Target and Overcome Tumor VasculatureR21CA173579 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI TASCIOTTI, ENNIO · 2013 to 2014
$371k
NCI NIH HHS 1R21CA173579-01A1NCI NIH HHS 5U54CA143837NCI NIH HHS R21 CA173579NCI NIH HHS U54 CA143837
6 · The paper itself

Abstract

Nanocarriers are designed to specifically accumulate in diseased tissues. In this context, targeting of intracellular compartments was shown to enhance the efficacy of many drugs and to offer new and more effective therapeutic approaches. This is especially true for therapies based on biologicals that must be encapsulated to favor cell internalization, and to avoid intracellular endosomal sequestration and degradation of the payload. In this review, we discuss specific surface modifications designed to achieve cell cytoplasm delivery and to improve targeting of major organelles; we also discuss the therapeutic applications of these approaches. Last, we describe some integrated strategies designed to sequentially overcome the biological barriers that separate the site of administration from the cell cytoplasm, which is the drug's site of action.

Indexed as

AnimalsCoated Materials, BiocompatibleCytoplasmDrug DesignHumansMaterials TestingNanocapsulesOrganellesSurface PropertiesCoated Materials, BiocompatibleNanocapsulesbiological barrierscell surface modificationsintracellular targetingnanocarriersnanomedicine

Identifiers

PMID26139126
PMCPMC5561781

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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.