Evidence map›Paper›PMID 36798609›Full record

ArticleRSC advances2023

Hyaluronic acid-coated gold nanoparticles as a controlled drug delivery system for poorly water-soluble drugs.

Hyoung-Mi Kim, Jae Hong Park, You Jin Choi, Jae-Min Oh, Junghun Park

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

12 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
  6. Article
  7. Hyaluronic Acid in Nanopharmaceuticals: An Overview.Current issues in molecular biology · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. Review
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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.

Hyoung-Mi KimBiomedical Manufacturing Technology Center (BMTC), Korea Institute of Industrial Technology (KITECH) Yeongcheon-si Gyeongsangbuk-do 38822 Republic of Korea junghunpark@kitech.re.kr.
Jae Hong ParkBiomedical Manufacturing Technology Center (BMTC), Korea Institute of Industrial Technology (KITECH) Yeongcheon-si Gyeongsangbuk-do 38822 Republic of Korea junghunpark@kitech.re.kr.
You Jin ChoiBiomedical Manufacturing Technology Center (BMTC), Korea Institute of Industrial Technology (KITECH) Yeongcheon-si Gyeongsangbuk-do 38822 Republic of Korea junghunpark@kitech.re.kr.
Jae-Min OhDepartment of Energy and Materials Engineering, Dongguk University-Seoul Seoul 04620 Republic of Korea.
Junghun ParkBiomedical Manufacturing Technology Center (BMTC), Korea Institute of Industrial Technology (KITECH) Yeongcheon-si Gyeongsangbuk-do 38822 Republic of Korea junghunpark@kitech.re.kr.ORCID https://orcid.org/0000-0002-3122-3288
Korea Institute of Industrial Technology · KRDongguk University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyaluronic acid (HA) is a natural linear polysaccharide which has been widely used in cosmetics and pharmaceuticals including drug delivery systems because of its excellent biocompatibility. In this study, we investigated the one-pot synthesis of HA-coated gold nanoparticles (AuNP-HA) as a drug delivery carrier. The HAs with different molecular weights were produced by e-beam irradiation and employed as coating materials for AuNPs. Sulfasalazine (SSZ), a poorly water-soluble drug, was used to demonstrate the efficiency of drug delivery and the controlled release behaviour of the AuNP-HA. As the molecular weight of the HA decreased, the drug encapsulation efficiency of the SSZ increased up to 94%, while drug loading capacity of the SSZ was maintained at the level of about 70%. The prepared AuNP-HA-SSZ exhibited slow release of the SSZ over a short time and excellent sensitivity to different pHs and physiological conditions. The SSZ release rate was the lowest in simulated gastric conditions and the highest in simulated intestinal conditions. In this case, the AuNP-HA protects the SSZ from release under the acidic pH conditions in the stomach; on the other hand, the drug release was facilitated in the basic environment of the small intestine and colon. The SSZ was released under simulated intestinal conditions through anomalous drug transport and followed the Korsmeyer-Peppas model. Therefore, this study suggests that AuNP-HA is a promising orally-administered and intestine-targeted drug delivery system with controlled release characteristics.

Identifiers

PMID36798609
PMCPMC9926166
OpenAlexW4320735371

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.