Evidence map›Paper›PMID 30249662›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

l-Serine-modified polyamidoamine dendrimer as a highly potent renal targeting drug carrier.

Satoru Matsuura, Hidemasa Katsumi, Hiroe Suzuki, Natsuko Hirai, Hidetaka Hayashi, Kazuhiro Koshino, Takahiro Higuchi, Yusuke Yagi, Hiroyuki Kimura, Toshiyasu Sakane and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.3field-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

32 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Article
  3. Nanoparticles in the Treatment of Renal Fibrosis.International journal of nanomedicine · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Nanotherapeutics in Kidney Disease: Innovations, Challenges, and Future Directions.Journal of the American Society of Nephrology : JASN · 2025
    Review
  12. Article
  13. Gene therapy and kidney diseases.Molecular therapy. Methods & clinical development · 2024
    Review
  14. Review
  15. Article
  16. Review
  17. Research Progress of Drug Delivery Systems Targeting the Kidneys.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  18. Review
  19. Silica-coated LiYFRSC advances · 2024
    Article
  20. 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

11 authors at 2 institutions in 2 countries.

Satoru MatsuuraDepartment of Biopharmaceutics, Kyoto Pharmaceutical University, 607-8414 Kyoto, Japan.
Hidemasa KatsumiDepartment of Biopharmaceutics, Kyoto Pharmaceutical University, 607-8414 Kyoto, Japan; hkatsumi@mb.kyoto-phu.ac.jp.
Hiroe SuzukiDepartment of Biopharmaceutics, Kyoto Pharmaceutical University, 607-8414 Kyoto, Japan.
Natsuko HiraiDepartment of Biopharmaceutics, Kyoto Pharmaceutical University, 607-8414 Kyoto, Japan.
Hidetaka HayashiDepartment of Biopharmaceutics, Kyoto Pharmaceutical University, 607-8414 Kyoto, Japan.
Kazuhiro KoshinoDepartment of Bio-Medical Imaging, National Cerebral and Cardiovascular Center Research Institute, 565-8565 Osaka, Japan.
Takahiro HiguchiDepartment of Bio-Medical Imaging, National Cerebral and Cardiovascular Center Research Institute, 565-8565 Osaka, Japan.
Yusuke YagiDepartment of Analytical and Bioinorganic Chemistry, Kyoto Pharmaceutical University, 607-8414 Kyoto, Japan.
Hiroyuki KimuraDepartment of Analytical and Bioinorganic Chemistry, Kyoto Pharmaceutical University, 607-8414 Kyoto, Japan.
Toshiyasu SakaneDepartment of Biopharmaceutics, Kyoto Pharmaceutical University, 607-8414 Kyoto, Japan.
Akira YamamotoDepartment of Biopharmaceutics, Kyoto Pharmaceutical University, 607-8414 Kyoto, Japan.
Kyoto Pharmaceutical University · JPNational Cerebral and Cardiovascular Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective delivery of drug carriers selectively to the kidney is challenging because of their uptake by the reticuloendothelial system in the liver and spleen, which limits effective treatment of kidney diseases and results in side effects. To address this issue, we synthesized l-serine (Ser)-modified polyamidoamine dendrimer (PAMAM) as a potent renal targeting drug carrier. Approximately 82% of the dose was accumulated in the kidney at 3 h after i.v. injection of

Indexed as

Drug Delivery SystemsAngiotensin-Converting Enzyme InhibitorsAnimalsCaptoprilDendrimersDrug CarriersKidney DiseasesMicePolyaminesSerineAngiotensin-Converting Enzyme InhibitorsCaptoprilDendrimersDrug CarriersPoly(amidoamine)PolyaminesSerinedendrimerdrug deliveryl-serinerenal targeting

Identifiers

PMID30249662
PMCPMC6187148
OpenAlexW2890927910

What OpenQuestion holds

Textmetadata
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.