Evidence map›Paper›PMID 36307644›Full record

ArticleArchives of pharmacal research2022

Enhancement of S(+)-zaltoprofen oral bioavailability using nanostructured lipid carrier system.

Thi Mai Anh Pham, Dong Ho Lee, Young-Guk Na, Minki Jin, Minwoo Jung, Ha-Eun Kim, Hyelim Yoo, Jong-Hee Won, Jae-Young Lee, Jong-Suep Baek and 3 more

Abstract read
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In one paragraph

Article in Archives of pharmacal research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

13 authors.

Thi Mai Anh Pham *College of Pharmacy, Chungnam National University, 99 Daehak-Ro, Yuseong-Gu, Daejeon, 34134, South Korea.
Dong Ho Lee *College of Pharmacy, Chungnam National University, 99 Daehak-Ro, Yuseong-Gu, Daejeon, 34134, South Korea.
Young-Guk Na *College of Pharmacy, Chungnam National University, 99 Daehak-Ro, Yuseong-Gu, Daejeon, 34134, South Korea.
Minki JinCollege of Pharmacy, Chungnam National University, 99 Daehak-Ro, Yuseong-Gu, Daejeon, 34134, South Korea.
Minwoo JungCollege of Pharmacy, Chungnam National University, 99 Daehak-Ro, Yuseong-Gu, Daejeon, 34134, South Korea.
Ha-Eun KimCollege of Pharmacy, Chungnam National University, 99 Daehak-Ro, Yuseong-Gu, Daejeon, 34134, South Korea.
Hyelim YooCollege of Pharmacy, Chungnam National University, 99 Daehak-Ro, Yuseong-Gu, Daejeon, 34134, South Korea.
Jong-Hee WonCollege of Pharmacy, Chungnam National University, 99 Daehak-Ro, Yuseong-Gu, Daejeon, 34134, South Korea.
Jae-Young LeeCollege of Pharmacy, Chungnam National University, 99 Daehak-Ro, Yuseong-Gu, Daejeon, 34134, South Korea.
Jong-Suep BaekDepartment of Bio-Health Convergence, Kangwon National University, Chuncheon, 24341, South Korea.
Su-Cheol HanCenter for Companion Animal New Drug Development, Jeonbuk Branch, Korea Institute of Toxicology (KIT), Jeongeup, Jeollabuk-Do, 53212, South Korea.
Hong-Ki LeeCenter for Companion Animal New Drug Development, Jeonbuk Branch, Korea Institute of Toxicology (KIT), Jeongeup, Jeollabuk-Do, 53212, South Korea. hongki.lee@kitox.re.kr.ORCID http://orcid.org/0000-0003-3670-386X
Cheong-Weon ChoCollege of Pharmacy, Chungnam National University, 99 Daehak-Ro, Yuseong-Gu, Daejeon, 34134, South Korea. chocw@cnu.ac.kr.

Funding

National Research Council of Science and Technology CRC21021-000National Research Foundation of Korea 2019R1A2C1086102
6 · The paper itself

Abstract

Zaltoprofen is a nonsteroidal anti-inflammatory drug with poor oral bioavailability. S(+)-zaltoprofen (SZPF)-loaded nanostructured lipid carriers (NLCs) were prepared to enhance oral bioavailability. SZPF-loaded NLCs (NLC-SZPF) were prepared using the hot-melting homogenization method and optimized using the Box-Behnken design. The characterization of optimized NLC-SZPF, in vitro release, cytotoxicity, cellular uptake, ex vivo permeability, and pharmacokinetic parameters were evaluated to confirm the advantages of NLC formulation. NLC-SZPF with a diameter of 105.5 ± 1.2 nm had a high encapsulation efficiency of 99.84 ± 0.01%. NLC-SZPF showed a sustained-release profile, high biocompatibility, and high permeability across the intestinal tract. The relative bioavailability of NLC-SZPF was 431.3% compared with that of SZPF after oral administration to experimental rats. NLC-SZPF was successfully optimized using experimental designs to enhance the oral bioavailability of SZPF. Hence, NLC-SZPF could be a promising approach to overcome the poor oral bioavailability of SZPF.

Indexed as

Drug CarriersNanostructuresAdministration, OralAnimalsBenzopyransBiological AvailabilityExcipientsLipidsParticle SizePropionatesRatsSolubilityBenzopyransDrug CarriersExcipientsLipidsPropionatespyranoprofenBioavailabilityBox–Behnken designNanostructured lipid carrierOptimizationS(+)-zaltoprofen

Identifiers

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Textmetadata
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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.