Evidence map›Paper›PMID 26228987›Full record

ArticleScientific reports2015

Chemical and Physical Characteristics of Doxorubicin Hydrochloride Drug-Doped Salmon DNA Thin Films.

Bramaramba Gnapareddy, Sreekantha Reddy Dugasani, Taewoo Ha, Bjorn Paulson, Taehyun Hwang, Taesung Kim, Jae Hoon Kim, Kyunghwan Oh, Sung Ha Park

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 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.

Bramaramba Gnapareddy1] Sungkyunkwan Advanced Institute of Nanotechnology (SAINT), Sungkyunkwan University, Suwon 440-746, Korea [2] Department of Physics, Sungkyunkwan University, Suwon 440-746, Korea.
Sreekantha Reddy Dugasani1] Sungkyunkwan Advanced Institute of Nanotechnology (SAINT), Sungkyunkwan University, Suwon 440-746, Korea [2] Department of Physics, Sungkyunkwan University, Suwon 440-746, Korea.
Taewoo HaDepartment of Physics, Yonsei University, Seoul 120-749, Korea.
Bjorn PaulsonDepartment of Physics, Yonsei University, Seoul 120-749, Korea.
Taehyun Hwang1] Sungkyunkwan Advanced Institute of Nanotechnology (SAINT), Sungkyunkwan University, Suwon 440-746, Korea [2] School of Mechanical Engineering, Sungkyunkwan University, Suwon 440-746, Korea.
Taesung Kim1] Sungkyunkwan Advanced Institute of Nanotechnology (SAINT), Sungkyunkwan University, Suwon 440-746, Korea [2] School of Mechanical Engineering, Sungkyunkwan University, Suwon 440-746, Korea.
Jae Hoon KimDepartment of Physics, Yonsei University, Seoul 120-749, Korea.
Kyunghwan OhDepartment of Physics, Yonsei University, Seoul 120-749, Korea.
Sung Ha Park1] Sungkyunkwan Advanced Institute of Nanotechnology (SAINT), Sungkyunkwan University, Suwon 440-746, Korea [2] Department of Physics, Sungkyunkwan University, Suwon 440-746, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Double-stranded salmon DNA (SDNA) was doped with doxorubicin hydrochloride drug molecules (DOX) to determine the binding between DOX and SDNA, and DOX optimum doping concentration in SDNA. SDNA thin films were prepared with various concentrations of DOX by drop-casting on oxygen plasma treated glass and quartz substrates. Fourier transform infrared (FTIR) spectroscopy was employed to investigate the binding sites for DOX in SDNA, and electrical and photoluminescence (PL) analyses were used to determine the optimum doping concentration of DOX. The FTIR spectra showed that up to a concentration of 30 μM of DOX, there was a tendency for binding with a periodic orientation via intercalation between nucleosides. The current and PL intensity increased as the DOX concentration increased up to 30 μM, and then as the concentration of DOX further increased, we observed a decrease in current as well as PL quenching. Finally, the optical band gap and second band onset of the transmittance spectra were analyzed to further verify the DOX binding and optimum doping concentration into SDNA thin films as a function of the DOX concentration.

Indexed as

AnimalsDNADoxorubicinDrug CarriersLuminescent MeasurementsSalmonSpectrophotometry, UltravioletSpectroscopy, Fourier Transform InfraredDNADoxorubicinDrug Carriers

Identifiers

PMID26228987
PMCPMC4530373

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Registered trials

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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.