Evidence map›Paper›PMID 27314343›Full record

ArticleInternational journal of molecular sciences2016

Bioavailability of an R-α-Lipoic Acid/γ-Cyclodextrin Complex in Healthy Volunteers.

Naoko Ikuta, Hinako Okamoto, Takahiro Furune, Yukiko Uekaji, Keiji Terao, Ryota Uchida, Kosuke Iwamoto, Atsushi Miyajima, Takashi Hirota, Norihiro Sakamoto

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

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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 2 institutions in 1 country.

Naoko IkutaGraduate School of Medicine, Kobe University, Kobe 650-0017, Japan. naoko.ikuta@people.kobe-u.ac.jp.
Hinako OkamotoGraduate School of Medicine, Kobe University, Kobe 650-0017, Japan. hinako.okamoto@cyclochem.com.
Takahiro FuruneCycloChem Bio Co., Ltd., Kobe 650-0047, Japan. takahiro.furune@cyclochem.com.
Yukiko UekajiCycloChem Bio Co., Ltd., Kobe 650-0047, Japan. yukiko.uekaji@cyclochem.com.
Keiji TeraoGraduate School of Medicine, Kobe University, Kobe 650-0017, Japan. keiji.terao@cyclochem.com.
Ryota UchidaDepartment of Biopharmaceutics, Faculty of Pharmaceutical Science, Tokyo University of Science, Chiba 278-8510, Japan. j3b13702@ed.tus.ac.jp.
Kosuke IwamotoDepartment of Biopharmaceutics, Faculty of Pharmaceutical Science, Tokyo University of Science, Chiba 278-8510, Japan. gan.ln284@gmail.com.
Atsushi MiyajimaDepartment of Biopharmaceutics, Faculty of Pharmaceutical Science, Tokyo University of Science, Chiba 278-8510, Japan. miyajima@my-pharm.ac.jp.
Takashi HirotaDepartment of Biopharmaceutics, Faculty of Pharmaceutical Science, Tokyo University of Science, Chiba 278-8510, Japan. hirotas5@rs.noda.tus.ac.jp.
Norihiro SakamotoGraduate School of Medicine, Kobe University, Kobe 650-0017, Japan. nori@med.kobe-u.ac.jp.
Kobe University · JPTokyo University of Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

R-α-lipoic acid (R-LA) is a cofactor of mitochondrial enzymes and a very strong antioxidant. R-LA is available as a functional food ingredient but is unstable against heat or acid. Stabilized R-LA was prepared through complexation with γ-cyclodextrin (CD), yielding R-LA/CD. R-LA/CD was orally administered to six healthy volunteers and showed higher plasma levels with an area under the plasma concentration-time curve that was 2.5 times higher than that after oral administration of non-complexed R-LA, although the time to reach the maximum plasma concentration and half-life did not differ. Furthermore, the plasma glucose level after a single oral administration of R-LA/CD or R-LA was not affected and no side effects were observed. These results indicate that R-LA/CD could be easily absorbed in the intestine. In conclusion, γ-CD complexation is a promising technology for delivering functional but unstable ingredients like R-LA.

Indexed as

AdultAntioxidantsBiological AvailabilityDrug Combinationsgamma-CyclodextrinsHealthy VolunteersHumansMaleThioctic AcidAntioxidantsDrug Combinationsgamma-CyclodextrinsThioctic Acidbioavailabilityclinical studycyclodextrinhealthy volunteersoral administrationpharmacokineticsR-α-lipoic acid

Identifiers

PMID27314343
PMCPMC4926482
OpenAlexW2425102531

What OpenQuestion holds

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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.