Evidence map›Paper›PMID 27189051›Full record

ArticleScientific reports2016

Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8.

Ankur Gautam, Jagpreet Singh Nanda, Jesse S Samuel, Manisha Kumari, Priyanka Priyanka, Gursimran Bedi, Samir K Nath, Garima Mittal, Neeraj Khatri, Gajendra Pal Singh Raghava

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 79 citations in OpenAlex.

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  20. A review of lipidation in the development of advanced protein and peptide therapeutics.Journal of controlled release : official journal of the Controlled Release Society · 2019
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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

10 authors at 1 institution in 1 country.

Ankur GautamBioinformatics Centre, CSIR-Institute of Microbial Technology, Chandigarh-160036, India.
Jagpreet Singh NandaBioinformatics Centre, CSIR-Institute of Microbial Technology, Chandigarh-160036, India.
Jesse S SamuelBioinformatics Centre, CSIR-Institute of Microbial Technology, Chandigarh-160036, India.
Manisha KumariBioinformatics Centre, CSIR-Institute of Microbial Technology, Chandigarh-160036, India.
Priyanka PriyankaBioinformatics Centre, CSIR-Institute of Microbial Technology, Chandigarh-160036, India.
Gursimran BediBioinformatics Centre, CSIR-Institute of Microbial Technology, Chandigarh-160036, India.
Samir K NathDepartment of Protein Science and Engineering, CSIR-Institute of Microbial Technology, Chandigarh-160036, India.
Garima MittalExperimental Animal Facility, CSIR-Institute of Microbial Technology, Chandigarh-160036, India.
Neeraj KhatriExperimental Animal Facility, CSIR-Institute of Microbial Technology, Chandigarh-160036, India.
Gajendra Pal Singh RaghavaBioinformatics Centre, CSIR-Institute of Microbial Technology, Chandigarh-160036, India.
Institute of Microbial Technology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Skin, being the largest organ of the body, is an important site for drug administration. However, most of the drugs have poor permeability and thus drug delivery through the skin is very challenging. In this study, we examined the transdermal delivery capability of IMT-P8, a novel cell-penetrating peptide. We generated IMT-P8-GFP and IMT-P8-KLA fusion constructs and evaluated their internalization into mouse skin after topical application. Our results demonstrate that IMT-P8 is capable of transporting green fluorescent protein (GFP) and proapoptotic peptide, KLA into the skin and also in different cell lines. Interestingly, uptake of IMT-P8-GFP was considerably higher than TAT-GFP in HeLa cells. After internalization, IMT-P8-KLA got localized to the mitochondria and caused significant cell death in HeLa cells signifying an intact biological activity. Further in vivo skin penetration experiments revealed that after topical application, IMT-P8 penetrated the stratum corneum, entered into the viable epidermis and accumulated inside the hair follicles. In addition, both IMT-P8-KLA and IMT-P8-GFP internalized into the hair follicles and dermal tissue of the skin following topical application. These results suggested that IMT-P8 could be a potential candidate to be used as a topical delivery vehicle for various cosmetic and skin disease applications.

Indexed as

Administration, TopicalAnimalsBiological TransportCell DeathCell Line, TumorCell-Penetrating PeptidesDrug Delivery SystemsEpidermisGreen Fluorescent ProteinsHair FollicleHeLa CellsHumansIntercellular Signaling Peptides and ProteinsMaleMice, Inbred BALB CMitochondriaCell-Penetrating PeptidesGreen Fluorescent ProteinsIntercellular Signaling Peptides and ProteinsKLA peptidePeptidesRecombinant Fusion Proteins

Identifiers

PMID27189051
PMCPMC4870705
OpenAlexW2404014633

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.