Evidence map›Paper›PMID 31690769›Full record

ArticleScientific reports2019

Method and its Composition for encapsulation, stabilization, and delivery of siRNA in Anionic polymeric nanoplex: An In vitro- In vivo Assessment.

Nidhi Raval, Hardi Jogi, Piyush Gondaliya, Kiran Kalia, Rakesh K Tekade

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 57 citations in OpenAlex.

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  7. Targeted allele-specificMolecular therapy. Nucleic acids · 2025
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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

5 authors at 2 institutions in 1 country.

Nidhi RavalNational Institute of Pharmaceutical Education and Research (NIPER) - Ahmedabad, Palaj, (An Institute of National Importance), Opposite Air Force Station, Gandhinagar, 382355, Gujarat, India.
Hardi JogiNational Institute of Pharmaceutical Education and Research (NIPER) - Ahmedabad, Palaj, (An Institute of National Importance), Opposite Air Force Station, Gandhinagar, 382355, Gujarat, India.
Piyush GondaliyaNational Institute of Pharmaceutical Education and Research (NIPER) - Ahmedabad, Palaj, (An Institute of National Importance), Opposite Air Force Station, Gandhinagar, 382355, Gujarat, India.
Kiran KaliaNational Institute of Pharmaceutical Education and Research (NIPER) - Ahmedabad, Palaj, (An Institute of National Importance), Opposite Air Force Station, Gandhinagar, 382355, Gujarat, India.
Rakesh K TekadeNational Institute of Pharmaceutical Education and Research (NIPER) - Ahmedabad, Palaj, (An Institute of National Importance), Opposite Air Force Station, Gandhinagar, 382355, Gujarat, India. rakeshtekade@gmail.com.
National Institute of Pharmaceutical Education and Research · INDepartment of Pharmaceuticals · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small interfering RNA (siRNA) are synthetic RNA duplex designed to specifically knockdown the abnormal gene to treat a disease at cellular and molecular levels. In spite of their high potency, specificity, and therapeutic potential, the full-fledged utility of siRNA is predominantly limited to in vitro set-up. Till date, Onpattro is the only USFDA approved siRNA therapeutics available in the clinic. The lack of a reliable in vivo siRNA delivery carrier remains a foremost obstacle towards the clinical translation of siRNA therapeutics. To address the obstacles associated with siRNA delivery, we tested a dendrimer-templated polymeric approach involving a USFDA approved carrier (albumin) for in vitro as well as in vivo delivery of siRNA. The developed approach is simple in application, enhances the serum stability, avoids in vivo RNase-degradation and mediates cytosolic delivery of siRNA following the endosomal escape process. The successful in vitro and in vivo delivery of siRNA, as well as targeted gene knockdown potential, was demonstrated by HDAC4 inhibition in vitro diabetic nephropathy (DN) podocyte model as well as in vivo DN C57BL/6 mice model. The developed approach has been tested using HDAC4 siRNA as a model therapeutics, while the application can also be extended to other gene therapeutics including micro RNA (miRNA), plasmids oligonucleotides, etc.

Indexed as

Diabetic NephropathiesDrug Delivery SystemsHistone DeacetylasesPodocytesRepressor ProteinsRNA, Small InterferingAnimalsCell Line, TransformedDisease Models, AnimalHumansMiceHDAC4 protein, humanHistone DeacetylasespatisiranRepressor ProteinsRNA, Small Interfering

Identifiers

PMID31690769
PMCPMC6831632
OpenAlexW2988826640

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.